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Exsolution of Garnet and Clinopyroxene from High-Al Pyroxenes in Xugou Peridotite, Eastern China

机译:东部徐沟橄榄岩中高铝辉石中石榴石和斜辉石的溶解

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摘要

Serpentinized massif peridotite in the Xugou, Su-Lu ultrahigh-pressure (UHP) metamorphic belt, eastern China, preserves texturally old (porphyroclastic) ortho- and clinopyroxene with up to two generations of lamellae of garnet, clinopyroxene and Mg-chromite. Their crystallographic orientation with respect to the host pyroxene is consistent with an origin by solid-state exsolution. Comparison of integrated mineral chemistry with simplified and natural chemical datasets suggests that both aluminous precursor pyroxenes were in equilibrium at a minimum pressure of ∼4 GPa and within a temperature range of about 1300–1500°C. Steep isopleths of Ca in orthopyroxene imply that exsolution occurred during cooling. Al diffusion modelling suggests growth of widely spaced lamellae in orthopyroxene down to about 900°C. Integrated Al contents between wide lamellae record a minimum of 4 GPa pressure during cooling. Compositionally uniform exsolved minerals were formed at 4·3 ± 0·3 GPa and 730 ± 30°C and reflect a cratonic geotherm with about 33 mW m−2 surface heat flow. The peridotite matrix mineral assemblage of olivine + orthopyroxene ± garnet ± Mg-chromite ± clinopyroxene ± phlogopite records strain-induced recrystallization that partially to completely replaced precursor porphyroclasts. The recrystallized minerals lack lamellar exsolution. Recrystallized orthopyroxene, with Al2O3 at 0·13 wt %, indicates conditions of 5·5 ± 0·3 GPa and 760 ± 30°C, which are higher-grade metamorphic conditions than those preserved in the chemically equilibrated exsolution microstructures. Both estimates overlap with the range reported for the Early Mesozoic UHP metamorphism in the region (4·0–6·7 GPa and 760–970°C). Major element melt models applied to previously published Xugou peridotite data suggest high degrees of melt extraction (30–35 %) in the garnet peridotite stability field (3–4·5 GPa) until garnet and clinopyroxene exhaustion. Coincidence in pressure and in the order of temperature of equilibration of precursor pyroxenes and peridotite melting implies that peridotite formation occurred at ∼135 km depth in the subcontinental lithospheric mantle (SCLM) beneath the Archaean North China Craton. Subsequent refertilization, mineral exsolution and chemical re-equilibration during long-term cooling in the SCLM occurred prior to deformation and incorporation of the mantle fragment into the continental crust during UHP metamorphism at a minimum depth of 170 km. Because the Xugou precursor pyroxenes and peridotite formed at depths greater than the regional SCLM (c. 90 km), we infer that the orogenic peridotite massif formed part of the former hanging wall of the Archaean SCLM, which delaminated after the Late Mesozoic.
机译:中国东部苏鲁超高压(UHP)变质带蛇形化的橄榄岩橄榄石保留了质地较老的(成岩碎屑)原和斜ino石,以及多达两代的石榴石,斜cl石和镁铬铁矿片层。它们相对于主体辉石的晶体学取向与固态溶解的起源一致。综合矿物化学与简化和天然化学数据集的比较表明,两种铝质前驱体辉石均在最低压力约4 GPa且在约1300-1500°C的温度范围内处于平衡状态。邻二甲苯中Ca的陡峭等值线表明冷却期间发生了析出。 Al扩散模型表明在低至约900℃的邻二甲苯中宽间隔的薄片的生长。在冷却期间,宽薄片之间的集成Al含量最低记录为4 GPa。在4·3±0·3 GPa和730±30°C时形成了成分均匀的溶解矿物,并反射了一个地热,其地热流约为33 mW m - 2 。橄榄石+邻苯二茂铁±石榴石±镁铬铁矿±斜py石±金云母的橄榄岩基质矿物组合记录了应变诱导的重结晶,该结晶部分地完全替代了前体卟啉。重结晶的矿物缺乏层状溶解。 Al 2 O 3 为0·13 wt%的重结晶邻苯二酚表明条件为5·5±0·3 GPa和760±30°C,这是更高的条件级变质条件,而不是化学平衡的析出物微结构中保留的条件。这两个估计值都与该地区早期中生代UHP变质的报道范围重叠(4·0-6·7 GPa和760-970°C)。适用于先前发布的徐沟橄榄岩数据的主要元素熔体模型表明,在石榴石和斜dot石耗尽之前,石榴石橄榄石稳定性场(3-4-5 GPa)中的熔体抽出率很高(30-35%)。压力的重合以及前驱体辉石和橄榄岩熔融的平衡温度顺序表明,在古北华北克拉通下方的次大陆岩石圈地幔(SCLM)中,橄榄岩形成发生在约135 km的深度。在SCLM中的长期冷却过程中,随后的蒸发,矿物溶出和化学重新平衡发生在UHP变质过程中,地幔碎片在最小深度170 km变形和整合到大陆壳中之前。因为徐沟前体的辉石和橄榄岩形成的深度大于区域SCLM(约90 km),所以我们推断造山橄榄岩块体是古生界SCLM的前悬壁的一部分,该壁在中生代之后分层。

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  • 来源
    《Journal of Petrology》 |2012年第7期|p.1477-1504|共28页
  • 作者单位

    1Department of Geology and Mineralogy, Kyoto University, 606-8502 Kyoto, Japan 2Senior Research Fellow Center, Ehime University, 790-8577 Matsuyama, Japan 3Department of Earth and Environmental Sciences, Potsdam University, 14476 Potsdam, Germany 4Consiglio Nazionale Delle Ricerche, Istituto Di Geoscienze E Georisorse (Igg)-Sede Di Pavia, 27100 Pavia, Italy 5Geodynamics Research Center, Ehime University, 790-8577 Matsuyama, Japan 6Department of Earth Sciences, Kanazawa University, 920-1192 Kanazawa, Japan;

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