{"title":"Apatite composition and phase equilibrium modelling unravel F and Cl behavior during crustal anatexis in the Himalayan orogen","authors":"Min Ji , Xiao-Ying Gao , Cong Tu , Xuan-Jin Chen","doi":"10.1016/j.chemgeo.2025.122978","DOIUrl":null,"url":null,"abstract":"<div><div>Fluorine (F) and chlorine (Cl) are crucial in the evolution of magmatic–hydrothermal systems, but their behavior during crustal anatexis is not well understood. To address this, we combined electron probe micro-analysis of apatite in anatectic rocks and phase equilibrium modelling for partial melting of potential source rock in this study. Apatites in two types of rocks formed under different anatectic pressure–temperature–fluid conditions from the Cona area in the eastern Himalaya have contrasting major-minor element compositions. Apatites in Type I rocks, associated with fluid-present (hydration) melting under low pressures and temperatures, have systematically lower FeO, MnO, Na<sub>2</sub>O, and F contents, lower F/Cl ratios, and higher Cl contents than those in Type II rocks, related to fluid-absent (dehydration) melting under high pressures and temperatures. Using measured apatite volatile contents and theoretically constrained exchange coefficients, we estimated F and Cl contents in coexisting melts. The results show that Type I melts consistently exhibit lower F/Cl ratios than Type II melts, which can be ascribed to the differences in anatectic conditions rather than melt evolution. Forward phase equilibrium modelling and element partitioning further show that F and Cl partition preferentially into melts, depleting the solid restites. Lower pressures and fluid addition decrease F/Cl ratios in melts, as observed in the Type I rocks. Given that rare metals (e.g., Li, Be, Ta, W, Sn) are also primarily hosted by muscovite and biotite, similar to F and Cl, in the metapelite, we also modelled their behavior during partial melting. The results indicate that high-pressure dehydration melting enriches F, Cl, and rare metals in melts, offering favorable conditions for rare metal mineralization. These findings not only improve our understanding of F and Cl behavior during crustal anatexis but also shed new light on the role of anatexis in rare metal enrichment.</div></div>","PeriodicalId":9847,"journal":{"name":"Chemical Geology","volume":"692 ","pages":"Article 122978"},"PeriodicalIF":3.6000,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Geology","FirstCategoryId":"89","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0009254125003687","RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GEOCHEMISTRY & GEOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
Fluorine (F) and chlorine (Cl) are crucial in the evolution of magmatic–hydrothermal systems, but their behavior during crustal anatexis is not well understood. To address this, we combined electron probe micro-analysis of apatite in anatectic rocks and phase equilibrium modelling for partial melting of potential source rock in this study. Apatites in two types of rocks formed under different anatectic pressure–temperature–fluid conditions from the Cona area in the eastern Himalaya have contrasting major-minor element compositions. Apatites in Type I rocks, associated with fluid-present (hydration) melting under low pressures and temperatures, have systematically lower FeO, MnO, Na2O, and F contents, lower F/Cl ratios, and higher Cl contents than those in Type II rocks, related to fluid-absent (dehydration) melting under high pressures and temperatures. Using measured apatite volatile contents and theoretically constrained exchange coefficients, we estimated F and Cl contents in coexisting melts. The results show that Type I melts consistently exhibit lower F/Cl ratios than Type II melts, which can be ascribed to the differences in anatectic conditions rather than melt evolution. Forward phase equilibrium modelling and element partitioning further show that F and Cl partition preferentially into melts, depleting the solid restites. Lower pressures and fluid addition decrease F/Cl ratios in melts, as observed in the Type I rocks. Given that rare metals (e.g., Li, Be, Ta, W, Sn) are also primarily hosted by muscovite and biotite, similar to F and Cl, in the metapelite, we also modelled their behavior during partial melting. The results indicate that high-pressure dehydration melting enriches F, Cl, and rare metals in melts, offering favorable conditions for rare metal mineralization. These findings not only improve our understanding of F and Cl behavior during crustal anatexis but also shed new light on the role of anatexis in rare metal enrichment.
氟(F)和氯(Cl)在岩浆-热液系统的演化中起着至关重要的作用,但它们在地壳深熔过程中的行为尚不清楚。为了解决这一问题,本研究结合了对隐晶岩中磷灰石的电子探针微观分析和潜在烃源岩部分熔融的相平衡模型。东喜马拉雅地区Cona地区两种不同成岩压力-温度-流体条件下形成的磷灰石具有明显的主-次元素组成差异。ⅰ型岩石中的磷灰石与低压和高温下有流体熔融(水化)有关,其FeO、MnO、Na2O和F含量较ⅱ型岩石低,F/Cl比较低,Cl含量较高,与高压和高温下无流体熔融(脱水)有关。利用测量的磷灰石挥发性含量和理论约束交换系数,我们估计了共存熔体中F和Cl的含量。结果表明,ⅰ型熔体的F/Cl比值始终低于ⅱ型熔体,这与熔体演化的差异无关,而与熔融条件的差异有关。正相平衡模型和元素分配进一步表明,F和Cl优先分配到熔体中,消耗固体残余物。在I型岩石中观察到,较低的压力和流体加入降低了熔体中的F/Cl比。考虑到稀有金属(如Li, Be, Ta, W, Sn)也主要由白云母和黑云母(类似于F和Cl)在变长岩中赋存,我们也模拟了它们在部分熔融过程中的行为。结果表明,高压脱水熔融富集了熔体中的F、Cl和稀有金属,为稀有金属成矿提供了有利条件。这些发现不仅提高了我们对F和Cl在地壳深熔过程中的行为的认识,而且对深熔在稀有金属富集中的作用也有了新的认识。
期刊介绍:
Chemical Geology is an international journal that publishes original research papers on isotopic and elemental geochemistry, geochronology and cosmochemistry.
The Journal focuses on chemical processes in igneous, metamorphic, and sedimentary petrology, low- and high-temperature aqueous solutions, biogeochemistry, the environment and cosmochemistry.
Papers that are field, experimentally, or computationally based are appropriate if they are of broad international interest. The Journal generally does not publish papers that are primarily of regional or local interest, or which are primarily focused on remediation and applied geochemistry.
The Journal also welcomes innovative papers dealing with significant analytical advances that are of wide interest in the community and extend significantly beyond the scope of what would be included in the methods section of a standard research paper.