Oxy-thermobarometry of grospydite and high-Ca eclogite xenoliths from Zagadochnaya kimberlite pipe (Yakutia, Siberian craton)

IF 1.1 4区 地球科学 Q3 GEOCHEMISTRY & GEOPHYSICS
Giulia Marras, Denis Mikhailenko, Catherine A. McCammon, Alla Logvinova, Darko Hanžel, Luigi Dallai, Vincenzo Stagno
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引用次数: 0

Abstract

Grospydites are a rare variety of eclogites composed of grossular–pyroxene – disthene (kyanite) occurring only in a few kimberlite pipes worldwide. The pressures, temperatures and redox conditions of formation for grospydites have been poorly investigated, even though such parameters are needed to better understand their origin and the scarcity of elemental carbon (graphite/diamond), a common feature of these rocks. In this study, we determined the chemical composition and Fe3+/∑Fe of coexisting garnet and clinopyroxene from nine C-free kyanite-bearing eclogite xenoliths from Zagadochnaya pipe (Yakutia). Five samples show garnet with Ca# >45 mol% [Ca# = Ca/(Ca + Mg + Fe + Mn)] and are classified as grospydites, while the remaining samples are high-Ca eclogites with Ca# of 23–38 mol%. Fe3+/ΣFe of garnet ranges between 0.03 and 0.09 (± 0.02), overlapping with values measured for eclogitic garnets equilibrated at mantle conditions. Fe3+/ΣFe in clinopyroxene spans from 0.21 to 0.46 (± 0.03), slightly higher than values measured in eclogites from other localities worldwide. The calculated equilibration pressures (3.7–6.7 GPa for grospydites and 4.3–5.6 GPa for high-Ca eclogites) and temperatures (920–1220 °C for grospydites and 1010–1060 °C for high-Ca eclogites) result in fo2 values ranging from − 2.0 to − 0.2 log units for grospydites and − 1.9 to −1.7 for high-Ca eclogites relative to the fayalite-magnetite-quartz buffer. The δ18O values measured in two garnet-clinopyroxene pairs confirm that samples equilibrated at mantle conditions. Our study extends the knowledge of grospydites in terms of Fe3+/ΣFe and P-T-fo2 within the global eclogite database. Despite the finding that equilibration P-T-fo2 values are compatible with the stability of graphite/diamond, the lack of elemental C in the investigated samples can be explained as either (1) these rocks formed from a slab that lost C during subduction, or (2) these rocks underwent metasomatism with C-poor fluids/melts or (3) a carbon-free layer was sampled by the ascending kimberlitic melts.

雅库特-西伯利亚克拉通Zagadochnaya金伯利岩管中粗闪岩和高钙榴辉岩捕虏体的氧-热气压测定
辉长岩是一种由辉长岩-辉长岩-二辉石(蓝晶石)组成的罕见榴辉岩,仅产于世界上少数金伯利岩管中。尽管需要这些参数来更好地了解它们的起源和元素碳(石墨/金刚石)的稀缺性(这是这些岩石的共同特征),但对粗晶岩形成的压力、温度和氧化还原条件的研究却很少。本文对来自雅库特扎加多奇纳亚(Zagadochnaya)管道的9块含无c蓝晶石榴辉岩捕虏体中石榴石和斜辉石的化学组成和Fe3+/∑Fe进行了测定。其中5个样品为ca# >;45 mol%的石榴石[ca# = Ca/(Ca + Mg + Fe + Mn)],属于粗长辉长岩,其余样品为高Ca榴辉岩,ca#为23 ~ 38 mol%。石榴石的Fe3+/ΣFe在0.03 ~ 0.09(±0.02)之间,与在地幔条件下平衡的榴辉岩的测量值重叠。斜辉石的Fe3+/ΣFe介于0.21 ~ 0.46(±0.03)之间,略高于世界其他地区榴辉岩的Fe3+/ΣFe。计算出的平衡压力(粗长岩3.7 ~ 6.7 GPa,高钙榴辉岩4.3 ~ 5.6 GPa)和温度(粗长岩920 ~ 1220℃,高钙榴辉岩1010 ~ 1060℃)导致相对于铁矾石-磁铁矿-石英缓冲带,粗长岩的fo2值在- 2.0 ~ - 0.2 log单位之间,高钙榴辉岩的fo2值在- 1.9 ~ - 1.7 log单位之间。两对石榴石斜辉石的δ18O值证实了样品在地幔条件下的平衡。我们的研究扩展了全球榴辉岩数据库中Fe3+/ΣFe和P-T-fo2对榴辉岩的认识。尽管发现平衡P-T-fo2值与石墨/金刚石的稳定性是相容的,但样品中缺乏元素C可以解释为:(1)这些岩石是由俯冲过程中失去C的板块形成的,或者(2)这些岩石经历了与缺乏C的流体/熔体的交代作用,或者(3)上升的金伯利岩熔体采集了无碳层。
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来源期刊
Mineralogy and Petrology
Mineralogy and Petrology 地学-地球化学与地球物理
CiteScore
2.60
自引率
0.00%
发文量
0
审稿时长
1 months
期刊介绍: Mineralogy and Petrology welcomes manuscripts from the classical fields of mineralogy, igneous and metamorphic petrology, geochemistry, crystallography, as well as their applications in academic experimentation and research, materials science and engineering, for technology, industry, environment, or society. The journal strongly promotes cross-fertilization among Earth-scientific and applied materials-oriented disciplines. Purely descriptive manuscripts on regional topics will not be considered. Mineralogy and Petrology was founded in 1872 by Gustav Tschermak as "Mineralogische und Petrographische Mittheilungen". It is one of Europe''s oldest geoscience journals. Former editors include outstanding names such as Gustav Tschermak, Friedrich Becke, Felix Machatschki, Josef Zemann, and Eugen F. Stumpfl.
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