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首页> 外文期刊>Contributions to Mineralogy and Petrology >Petrological significance of manganese carbonate inclusions in spessartine garnet and relation to the stability of spessartine in metamorphosed manganese-rich rocks
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Petrological significance of manganese carbonate inclusions in spessartine garnet and relation to the stability of spessartine in metamorphosed manganese-rich rocks

机译:硒化石榴石中碳酸锰夹杂物的岩石学意义及其与富硒变质岩中硒乙草胺的稳定性的关系

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摘要

Idioblastic spessartine garnet pervasively developed in Mn-rich rocks and impure manganese carbonate ore at the Lower Proterozoic Nsuta manganese deposit, Western Ghana, contains abundant inclusions of micritic and microconcretionary carbonates and, to a lesser extent, quartz. Detailed mineralogical and microprobe studies indicate all the carbonate phases (i.e. carbonate inclusions in garnet, carbonates coexisting with garnet and carbonates not directly in contact with garnet, the latter hereafter referred to as matrix carbonates) lie within the rhodochrosite–kutnahorite solid solution series, i.e. ~Mn55–80(Ca + Mg)20–45CO3 to Ca42(Mn + Mg)58(CO3)2. Minor compositional differences occur in the various carbonate phases, but partition of major elements among coexisting phases indicate most carbonate minerals strongly fractionate Ca and Mg over coexisting spessartine. The nature, composition and textural relationship of coexisting minerals and inclusions in porphyroblastic spessartine indicate that the latter formed from metamorphic reactions in which rhodochrosite and/or kutnahorite and quartz were consumed, in part corroborating earlier observations on a rhodochrosite precursor for spessartine. Spessartine formation is thus envisaged to have taken place when the predominantly Mn carbonate–quartz assemblage became unstable in the presence of minor amounts of an unknown aluminous phase. Because all the carbonates appear to be low-temperature phases with no indications of significant recrystallisation or homogenisation, it could be argued that the spessartine + rhodochrosite ± kutnahorite ± quartz ± pyrite assemblage stabilised during very low-grade greenschist facies metamorphism under relatively low but uniform f O2 conditions. These observations also suggest the stability field of spessartine could extend to relatively lower temperatures than currently envisaged.
机译:在加纳西部元古界下段Nsuta锰矿床中,富锰锰岩和不纯的碳酸锰矿中普遍形成了成岩性的塞贝斯汀石榴石,其中含有大量的微碳酸盐岩和微凝碳酸盐岩,以及程度较小的石英岩。详细的矿物学和微探针研究表明,所有碳酸盐相(即石榴石中的碳酸盐夹杂物,与石榴石共存的碳酸盐和不直接与石榴石接触的碳酸盐,以下称其为基质碳酸盐)都位于菱锰铁矿-钾钠辉石固溶体系列中,即〜Mn55–80 (Ca + Mg)20–45 CO3 到Ca42 (Mn + Mg)58 (CO3 )2 < / sub>。在不同的碳酸盐相中会发生微小的成分差异,但是在共存相之间的主要元素分配表明,大多数碳酸盐矿物会比共存的司贝沙汀更强烈地分离Ca和Mg。杂卟啉sspesartine中共存的矿物和内含物的性质,组成和结构关系表明,后者是由变质反应形成的,其中消耗了菱锰矿和/或库特钠钙石和石英,这部分证实了早期关于spessartine菱锰矿前体的观察。因此,当少量的未知铝相存在时,以碳酸锰-石英为主的组合物变得不稳定时,就会发生斯贝沙汀的形成。由于所有碳酸盐似乎都是低温相,没有迹象表明存在明显的重结晶或均质化,因此可以认为,在相对较低但均一的极低级格林西斯相变质作用下,spessartine +菱锰矿±kutnahorite±石英±黄铁矿组合稳定。 f O2 条件。这些观察结果还表明,塞斯帕汀的稳定性可以扩展到比目前设想的更低的温度。

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  • 来源
    《Contributions to Mineralogy and Petrology》 |2001年第6期|733-746|共14页
  • 作者

    F. Nyame;

  • 作者单位

    Department of Geology Rand Afrikaans University P.O. Box 524 Auckland Park 2006 Johannesburg South Africa;

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