Anastasia O. Mikhno, Anton F. Shatskiy, Andrey V. Korsakov, Yulia G. Vinogradova, Jasper Berndt, Stephan Klemme, Sergey V. Rashchenko
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The most Mg-rich calcite from Type A inclusions coexisting with aragonite inclusions in one garnet growth zone shows X<sub>Ca</sub> = 0.935 implying their crystallization during a retrograde metamorphic stage at <i>P</i> ~ 2.3 GPa and <i>T</i> ~ 870°C along the <i>P–T</i> path. Type A calcite and aragonite inclusions were also found coexisting in one growth zone with K-bearing clinopyroxene inclusion (ω[K<sub>2</sub>O] = 0.5 wt.%). Such a high K<sub>2</sub>O-content in clinopyroxene testify that the pressure of inclusion capture exceeded 3.5 GPa, which contradicts the <i>P–T</i> conditions estimated by X<sub>Ca</sub> in magnesian calcite. Thus, Type A calcite inclusions were initially captured as an aggregate of aragonite+ magnesian calcite at ultrahigh pressure metamorphic stage (<i>P</i> ≥ 3.5 GPa, <i>T</i> = 900–1,000°C) and then re-equilibrated at lower conditions (<i>P</i> ≤ 2.3 GPa and <i>T</i> ≤ 870°C). The trace element composition of aragonite and Type A and Type B calcite from inclusions was also studied to clarify calcite genesis in these inclusions. Aragonite shows high LREE (5–57 ppm) and Sr-content (600–800 ppm). Calcite from Type A inclusions shows low LREE (2.9–19.8 ppm) and Sr-content (490–670 ppm). Calcite from Type B inclusions forms two groups according to the LREE and Sr content distribution (Type B1 and Type B2). Trace element distribution in Type B1 calcite is identical to that of Type A calcite, while Type B2 calcite shows high LREE (6.8–64.9 ppm) concentrations along with low Sr-content (180–340 ppm). Type A and Type B1 calcite is interpreted to have been re-equilibrated. Type B2 calcite inclusions crystallized from the hydrous carbonatitic melt.</p>","PeriodicalId":16472,"journal":{"name":"Journal of Metamorphic Geology","volume":"42 2","pages":"143-170"},"PeriodicalIF":3.5000,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The origin of calcite in calc-silicate rocks from the Kokchetav ultrahigh-pressure metamorphic complex\",\"authors\":\"Anastasia O. Mikhno, Anton F. Shatskiy, Andrey V. Korsakov, Yulia G. Vinogradova, Jasper Berndt, Stephan Klemme, Sergey V. Rashchenko\",\"doi\":\"10.1111/jmg.12749\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Understanding calcite genesis in ultrahigh-pressure crustal rocks is a key to the reconstruction of the evolution of ultrahigh-pressure metacarbonate rocks. Here, we present new data and a new model on the genesis and the <i>P–T</i> conditions of the formation of calcite found in the ultrahigh-pressure calc-silicate rocks from the Kokchetav massif. In the studied sample aragonite inclusions coexist with Type A calcite inclusions (previously interpreted as mineral inclusions) and the inclusions of Type B calcite (previously interpreted as derived from the crystallization of carbonatitic melt) in cores of garnet porphyroblasts. The most Mg-rich calcite from Type A inclusions coexisting with aragonite inclusions in one garnet growth zone shows X<sub>Ca</sub> = 0.935 implying their crystallization during a retrograde metamorphic stage at <i>P</i> ~ 2.3 GPa and <i>T</i> ~ 870°C along the <i>P–T</i> path. Type A calcite and aragonite inclusions were also found coexisting in one growth zone with K-bearing clinopyroxene inclusion (ω[K<sub>2</sub>O] = 0.5 wt.%). Such a high K<sub>2</sub>O-content in clinopyroxene testify that the pressure of inclusion capture exceeded 3.5 GPa, which contradicts the <i>P–T</i> conditions estimated by X<sub>Ca</sub> in magnesian calcite. Thus, Type A calcite inclusions were initially captured as an aggregate of aragonite+ magnesian calcite at ultrahigh pressure metamorphic stage (<i>P</i> ≥ 3.5 GPa, <i>T</i> = 900–1,000°C) and then re-equilibrated at lower conditions (<i>P</i> ≤ 2.3 GPa and <i>T</i> ≤ 870°C). The trace element composition of aragonite and Type A and Type B calcite from inclusions was also studied to clarify calcite genesis in these inclusions. Aragonite shows high LREE (5–57 ppm) and Sr-content (600–800 ppm). Calcite from Type A inclusions shows low LREE (2.9–19.8 ppm) and Sr-content (490–670 ppm). Calcite from Type B inclusions forms two groups according to the LREE and Sr content distribution (Type B1 and Type B2). Trace element distribution in Type B1 calcite is identical to that of Type A calcite, while Type B2 calcite shows high LREE (6.8–64.9 ppm) concentrations along with low Sr-content (180–340 ppm). Type A and Type B1 calcite is interpreted to have been re-equilibrated. 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引用次数: 0
摘要
了解超高压地壳岩石中方解石的成因是重建超高压偏碳酸盐岩演化的关键。在这里,我们展示了关于来自科克切塔夫丘陵的超高压钙硅酸盐岩中方解石形成的成因和P-T条件的新数据和新模型。在所研究的样本中,文石包裹体与石榴石斑岩岩芯中的 A 型方解石包裹体(以前被解释为矿物包裹体)和 B 型方解石包裹体(以前被解释为碳酸盐岩熔体结晶)共存。在一个石榴石生长带中与文石包裹体共存的 A 型包裹体中镁含量最高的方解石显示 XCa = 0.935,这意味着它们是在 P ~ 2.3 GPa 和 T ~ 870°C 的逆变质阶段沿 P-T 路径结晶的。在一个生长带中还发现了A型方解石和文石包裹体与含K的挛辉石包裹体(ω[K2O] = 0.5 wt.%)共存。霞石中如此高的 K2O 含量证明包裹体的捕获压力超过了 3.5 GPa,这与镁方解石中 XCa 估算的 P-T 条件相矛盾。因此,A 型方解石包裹体最初是在超高压变质阶段(P ≥ 3.5 GPa,T = 900-1,000°C)作为文石+菱镁方解石的集合体被捕获的,然后在较低的条件下(P ≤ 2.3 GPa,T ≤ 870°C)重新平衡。为了弄清包裹体中方解石的成因,还研究了包裹体中文石以及 A 型和 B 型方解石的微量元素组成。文石显示出较高的 LREE(5-57 ppm)和 Sr-含量(600-800 ppm)。A 型包裹体中的方解石显示出较低的 LREE(2.9-19.8 ppm)和 Sr-含量(490-670 ppm)。根据 LREE 和 Sr 含量的分布,B 型包裹体中的方解石分为两组(B1 型和 B2 型)。B1 型方解石的微量元素分布与 A 型方解石相同,而 B2 型方解石的 LREE 含量高(6.8-64.9 ppm),Sr 含量低(180-340 ppm)。据解释,A 型和 B1 型方解石已经过再钙化。B2型方解石包裹体由含水碳酸盐岩熔体结晶而成。
The origin of calcite in calc-silicate rocks from the Kokchetav ultrahigh-pressure metamorphic complex
Understanding calcite genesis in ultrahigh-pressure crustal rocks is a key to the reconstruction of the evolution of ultrahigh-pressure metacarbonate rocks. Here, we present new data and a new model on the genesis and the P–T conditions of the formation of calcite found in the ultrahigh-pressure calc-silicate rocks from the Kokchetav massif. In the studied sample aragonite inclusions coexist with Type A calcite inclusions (previously interpreted as mineral inclusions) and the inclusions of Type B calcite (previously interpreted as derived from the crystallization of carbonatitic melt) in cores of garnet porphyroblasts. The most Mg-rich calcite from Type A inclusions coexisting with aragonite inclusions in one garnet growth zone shows XCa = 0.935 implying their crystallization during a retrograde metamorphic stage at P ~ 2.3 GPa and T ~ 870°C along the P–T path. Type A calcite and aragonite inclusions were also found coexisting in one growth zone with K-bearing clinopyroxene inclusion (ω[K2O] = 0.5 wt.%). Such a high K2O-content in clinopyroxene testify that the pressure of inclusion capture exceeded 3.5 GPa, which contradicts the P–T conditions estimated by XCa in magnesian calcite. Thus, Type A calcite inclusions were initially captured as an aggregate of aragonite+ magnesian calcite at ultrahigh pressure metamorphic stage (P ≥ 3.5 GPa, T = 900–1,000°C) and then re-equilibrated at lower conditions (P ≤ 2.3 GPa and T ≤ 870°C). The trace element composition of aragonite and Type A and Type B calcite from inclusions was also studied to clarify calcite genesis in these inclusions. Aragonite shows high LREE (5–57 ppm) and Sr-content (600–800 ppm). Calcite from Type A inclusions shows low LREE (2.9–19.8 ppm) and Sr-content (490–670 ppm). Calcite from Type B inclusions forms two groups according to the LREE and Sr content distribution (Type B1 and Type B2). Trace element distribution in Type B1 calcite is identical to that of Type A calcite, while Type B2 calcite shows high LREE (6.8–64.9 ppm) concentrations along with low Sr-content (180–340 ppm). Type A and Type B1 calcite is interpreted to have been re-equilibrated. Type B2 calcite inclusions crystallized from the hydrous carbonatitic melt.
期刊介绍:
The journal, which is published nine times a year, encompasses the entire range of metamorphic studies, from the scale of the individual crystal to that of lithospheric plates, including regional studies of metamorphic terranes, modelling of metamorphic processes, microstructural and deformation studies in relation to metamorphism, geochronology and geochemistry in metamorphic systems, the experimental study of metamorphic reactions, properties of metamorphic minerals and rocks and the economic aspects of metamorphic terranes.