First-principles calculations of equilibrium isotope fractionation of Cl, Ca, and O in apatites and amphiboles

IF 4.5 1区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS
Shanqi Liu, Yongbing Li, Zhiming Yang, Huiquan Tian, Jianming Liu
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引用次数: 0

Abstract

Apatites and amphiboles are common hydrous minerals in igneous and metamorphic rocks, which can be found from the crust to the lithospheric mantle. These minerals can incorporate chlorine (Cl) and fluorine (F) by substituting for hydroxyl groups (OH). The isotopic compositions of Cl, Ca, and O of apatites and amphiboles are valuable geochemical tools for understanding the terrestrial and extraterrestrial processes over a wide range of temperatures. In the present study, first-principles methods were used to investigate the equilibrium isotope fractionation of Cl, Ca, and O in apatites and amphiboles. Our results reveal that amphiboles are generally more enriched in 37Cl compared to apatites. In apatites, increasing the Cl/(Cl + F) and Cl/(Cl + OH) ratios reduces the βCl-factors of Cl-F-apatites and Cl-OH-apatites, respectively, while substitution between F and OH has a small impact. In amphiboles, Cl contents have little effect on the βCl-factors. For Ca isotopes, the βCa-factors are largely unaffected by substitutions among Cl, F, and OH in either mineral. For O isotopes, the βO-factors vary depending on the type of oxygen atoms. In Cl-F-apatites and Cl-OH-apatites, the βO-factors for total oxygen atoms decrease with increasing Cl/(Cl + F) ratios but increase with Cl/(Cl + OH) ratios, respectively. Hydroxyl oxygen sites in amphiboles exhibit higher βO-factors than those in apatites, whereas silicate oxygen sites are more enriched in 18O than phosphate oxygen sites. Correlations between bond lengths and isotope fractionation properties are also observed: in both apatites and amphiboles, the βCl-factor is negatively correlated with the Cl–Cation bond length, except in the cases of actinolite and richterite, while the βO-factors of phosphate oxygen and silicate oxygen correlate with the O–P and O–Si bond lengths, respectively. These results can enhance our understanding of Cl, Ca, and O isotope behavior in halogen-bearing phosphates and silicates, providing valuable insights into the role of apatites and amphiboles as indicators of evolutionary processes on Earth and in extraterrestrial bodies.
磷灰石和角闪石中Cl、Ca和O平衡同位素分馏的第一性原理计算
磷灰石和角闪石是火成岩和变质岩中常见的含水矿物,从地壳到岩石圈地幔均有分布。这些矿物质可以通过取代羟基(OH)来吸收氯(Cl)和氟(F)。磷灰石和角闪石的Cl、Ca和O同位素组成是了解大范围温度下地球和地外过程的宝贵地球化学工具。本研究采用第一性原理方法研究了磷灰石和角闪石中Cl、Ca和O的平衡同位素分馏。结果表明,与磷灰石相比,角闪石中37Cl的富集程度更高。在磷灰石中,增加Cl/(Cl + F)和Cl/(Cl + OH)比值分别降低了Cl-F-磷灰石和Cl-OH-磷灰石的βCl-因子,而F和OH之间的取代影响较小。在角闪石中,Cl含量对βCl因子的影响不大。对于Ca同位素,βCa因子在很大程度上不受Cl、F和OH取代的影响。对于O同位素,βO因子的变化取决于氧原子的类型。在Cl-F-磷灰石和Cl-OH-磷灰石中,总氧原子β o因子分别随Cl/(Cl + F)比的增大而减小,随Cl/(Cl + OH)比的增大而增大。角闪石中羟基氧位点的β o因子高于磷灰石,而硅酸盐氧位点在18O中的富集程度高于磷酸盐氧位点。键长与同位素分异性质之间的相关性也被观察到:在磷灰石和角闪石中,β cl -因子与cl -阳离子键长呈负相关,但在放线石和黄辉石中除外,而磷酸盐氧和硅酸盐氧的β o -因子分别与O-P和O-Si键长相关。这些结果可以增强我们对含卤磷酸盐和硅酸盐中Cl、Ca和O同位素行为的理解,为磷灰石和角闪石作为地球和地外天体进化过程指标的作用提供有价值的见解。
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来源期刊
Geochimica et Cosmochimica Acta
Geochimica et Cosmochimica Acta 地学-地球化学与地球物理
CiteScore
9.60
自引率
14.00%
发文量
437
审稿时长
6 months
期刊介绍: Geochimica et Cosmochimica Acta publishes research papers in a wide range of subjects in terrestrial geochemistry, meteoritics, and planetary geochemistry. The scope of the journal includes: 1). Physical chemistry of gases, aqueous solutions, glasses, and crystalline solids 2). Igneous and metamorphic petrology 3). Chemical processes in the atmosphere, hydrosphere, biosphere, and lithosphere of the Earth 4). Organic geochemistry 5). Isotope geochemistry 6). Meteoritics and meteorite impacts 7). Lunar science; and 8). Planetary geochemistry.
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