巴基斯坦西北部Koga碳酸盐岩-碱性杂岩磷灰石结构、微量元素和Sr[sbnd]Nd同位素地球化学:岩石成因和地幔源意义

IF 3.6 2区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS
Asad Khan, Zaheen Ullah, Huan Li, Shah Faisal, Yasin Rahim
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引用次数: 0

摘要

巴基斯坦西北部的古加碳酸盐岩-碱性杂岩(KCAC)位于该地区早古生代大喜马拉雅层序中,标志着一次重要的岩浆活动。杂岩主要由石英正长岩、霞石正长岩和碳酸岩岩性组成。利用阴极发光(CL)成像、微量元素和SrNd同位素组成以及LA-ICP-MS UPb年代学对这些岩性中提取的磷灰石颗粒进行了系统分析。石英正长岩(Q-Ap1)、霞石正长岩(N-Ap1)和碳酸盐正长岩(C-Ap1)中磷灰石颗粒的阴极均匀发光及其高浓度稀土(2400 ppm ~ 22130 ppm);3832 ppm - 14532 ppm;和2494 ~ 9050),特别是轻REE (LaN/YbN = 12 ~ 78;22至113;30 - 166;),表明它们的岩浆成因。从结构和化学上分带的霞石正长岩(N-Ap2)和碳酸盐(C-Ap2)磷灰石也富集轻稀土元素(LaN/YbN = 38 ~ 97和24 ~ 108);)相对于重稀土元素,这与岩浆成因一致。Q-Ap1磷灰石显示出明显的负Eu异常(0.18-0.75),表明熔融体的结晶过程经历了明显的斜长石分馏。N-Ap2磷灰石的REE + Y含量呈圆周递增趋势,其主要成因是辉石、碱长石和黑云母的分晶作用。而在C-Ap2中,REE + Y的沿边增加伴随着Na的增加和Mn的减少,表明方解石的早期结晶。粗粒霞石正长岩中N-Ap3磷灰石与N-Ap1磷灰石相比呈斑片状结构,稀土+ Y含量下降,反映了其与流体相互作用的交代性质。然而,N-Ap3与霞石正长岩(即N-Ap1)的岩浆磷灰石的初始Sr和Nd组成相似,表明参与交代蚀变的流体可能来自冷却的寄主岩浆。来自KCAC的LA-ICP-MS UPb磷灰石年代学数据与先前公布的锆石UPb年龄密切一致,表明该复合体就位后迅速冷却。磷灰石UPb定年结果表明,石英正长岩、霞石正长岩和碳酸岩的就位年龄分别为287±16 Ma、279±9 Ma和274±9 Ma;这意味着它们是在冈瓦纳北缘的二叠纪裂谷和分裂期间形成的。KCAC磷灰石的Sr和Nd同位素组成表明其为亚岩石圈地幔源,地壳污染或与交代的次大陆岩石圈地幔相互作用最小。研究表明,磷灰石结构特征结合原位微量元素和SrNd同位素组成可作为揭示碳酸盐岩-碱性杂岩复杂岩浆和热液过程以及岩浆来源性质的有效工具。
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Apatite texture, trace elements and Sr[sbnd]Nd isotope geochemistry of the Koga carbonatite-alkaline complex, NW Pakistan: Implications for petrogenesis and mantle source
The Koga Carbonatite-Alkaline Complex (KCAC) in northwestern Pakistan is emplaced within the Early Paleozoic Greater Himalayan Sequence of the region, marking a significant magmatic event. The complex primarily comprises quartz syenite, nepheline syenite, and carbonatite lithologies. Apatite grains extracted from these lithologies were systematically analyzed using cathode-luminescence (CL) imaging, trace elements and SrNd isotopic compositions, and LA-ICP-MS UPb geochronology. The homogeneous cathode luminescence of apatite grains from quartz syenite (Q-Ap1), nepheline syenite (N-Ap1) and carbonatite (C-Ap1) and their high concentrations of REE (2400 ppm – 22,130 ppm; 3832 ppm – 14,532 ppm; and 2494–9050, respectively), particularly light REE (with LaN/YbN = 12 to 78; 22 to 113; and 30–166; respectively), indicate their magmatic origin. Texturally and chemically zoned apatite from nepheline syenite (N-Ap2) and carbonatite (C-Ap2) are also enriched in light REE (LaN/YbN = 38 to 97 and 24 to 108; respectively) relative to heavy REE, which is consistent with a magmatic origin. The Q-Ap1 apatite are showing distinct negative Eu anomalies (0.18–0.75) indicative of crystallization from an evolved melt that experienced significant plagioclase fractionation. The N-Ap2 apatite exhibit a rim-ward increase in REE + Y contents, which can be attributed to fractional crystallization of pyroxene, alkali feldspar and biotite. While in C-Ap2 the rim-ward increase in REE + Y is coupled with increasing Na and decreasing Mn, suggesting early crystallization of calcite. Moreover, patchy texture and depleted REE + Y contents of N-Ap3 apatite from coarse-grained nepheline syenite compared to N-Ap1, reflect their metasomatic nature by interacting with fluids. However, N-Ap3 show similar initial Sr and Nd composition with magmatic apatite from nepheline syenite (i.e., N-Ap1) suggesting that the fluids involved in metasomatic alteration were likely originated from the cooling host magma. The LA-ICP-MS UPb apatite geochronology data from KCAC align closely with previously published zircon UPb ages, indicating rapid cooling following the emplacement of the complex. The UPb dating of apatite yields an emplacement age of 287 ± 16 Ma, 279 ± 9 Ma and 274 ± 9 Ma for the quartz syenite, nepheline syenite and carbonatite, respectively; implying their emplacement during the Permian rifting and breakup of the northern margin of Gondwana. The Sr and Nd isotopic compositions of apatite from the KCAC imply a sub-lithospheric mantle source, with minimal crustal contamination or interaction with metasomatized sub-continental lithospheric mantle. The study demonstrates that apatite textural features combined with in-situ trace elements and SrNd isotopic compositions can be an effective tool to unravel complex magmatic and hydrothermal processes and nature of the magma source of carbonatite- alkaline complexes.
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来源期刊
Chemical Geology
Chemical Geology 地学-地球化学与地球物理
CiteScore
7.20
自引率
10.30%
发文量
374
审稿时长
3.6 months
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.
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