scholarly journals Evolution and Li Mineralization of the No. 134 Pegmatite in the Jiajika Rare-Metal Deposit, Western Sichuan, China: Constrains from Critical Minerals

Minerals ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 45
Author(s):  
Zhen Wang ◽  
Jiankang Li ◽  
Zhenyu Chen ◽  
Qinggao Yan ◽  
Xin Xiong ◽  
...  

The Jiajika rare-metal deposit located in western Sichuan Province (China) is renowned as the largest lithium deposit in Asia, and the No. 134 pegmatite dike is the largest lithium pegmatite under mining conditions in the area. On the basis of a detailed characterization of textures and minerals in the Jiajika No. 134 pegmatite, two zones (the barren Zone Ⅰ and the spodumene Zone Ⅱ) and three subzones (Zone Ⅱ was subdivided into microcrystalline, medium-fine grained and coarse-grained spodumene zones) have been identified. The detailed mineralogical characteristics of lithium minerals and other indicator minerals from each zone were evaluated by EPMA for illustrating the magmatic–hydrothermal evolution and the cooling path of the Jiajika No. 134 pegmatite. From the outer zone inwards, grain size gradually increased, the typical graphic pegmatite zone was absent, and spodumene randomly crystallized throughout nearly the whole pegmatite body. This evidence indicated a Li-saturated melt prior to pegmatite crystallization, which could be the main cause of the super-large-scale Li mineralization of the Jiajika No. 134 pegmatite. A comparison of the Cs content between primary beryl in the Jiajika No. 134 pegmatite and other important Li-Cs-Ta pegmatites in the world indicates that No. 134 pegmatite shows a high degree of fractional crystallization. The evolution of mica species from muscovite to Li-micas from Zone Ⅰ to Zone Ⅱ marks the transition from the magmatic to the hydrothermal stage in pegmatite evolution. The absence of individual lepidolite and the relatively limited scale of alteration of spodumene (<10 vol%) suggest that the activity of the hydrothermal fluids in the system is limited, which contributes to the preservation of the easily altered Li ores and is also an important controlling factor of the super-large-scale Li mineralization of the pegmatite. Spodumene–quartz intergrowth (SQI) usually occurs partly along the rims of the spodumene grains in the Jiajika No. 134 pegmatite. Combined with the pegmatite mineral equilibria, the results of fluid inclusion studies of the pegmatite and the metamorphic conditions in the area, a constrained P-T path of the magmatic–hydrothermal crystallization of the Jiajika No. 134 pegmatite is proposed. The unusual steeply sloped cooling path of the No. 134 pegmatite could be attributed to the fast pressure drop triggered by the intrusion of a pegmatitic melt along the fractures surrounding the Majingzi granite, which could also be the dominant evolution process for other spodumene pegmatites with similar SQI features in the world. The feature of limited internal geochemical fractionation suggested by mineral-scale geochemical analyses of spodumene and micas, combined with the clear textural zoning of the No. 134 pegmatite, can best be ascribed to the effect of undercooling during pegmatite formation. This effect might be one of the non-negligible rules of pegmatite petrogenesis, and would significantly upgrade the potential of Li mineralization by minimizing diffusional Li transfer to the country rocks.

2021 ◽  
Vol 62 (10) ◽  
pp. 1175-1187
Author(s):  
A.D. Nozhkin ◽  
O.M. Turkina ◽  
K.A. Savko

Abstract —The paper presents results of a petrogeochemical and isotope–geochronological study of the granite–leucogranite association of the Pavlov massif and felsic volcanics from the Elash graben (Biryusa block, southwest of the Siberian craton). A characteristic feature of the granite–leucogranites is their spatial and temporal association with vein aplites and pegmatites of the East Sayan rare-metal province. The U–Pb age of zircon from granites of the Pavlov massif (1852 ± 5 Ma) is close to the age of the pegmatites of the Vishnyakovskoe rare-metal deposit (1838 ± 3 Ma). The predominant biotite porphyritic granites and leucogranites of the Pavlov massif show variable alkali ratios (K2O/Na2O = 1.1–2.3) and ferroan (Fe*) index and a peraluminous composition; they are comparable with S-granites. The studied rhyolites of the Tagul River (SiO2 = 71–76%) show a low ferroan index, a high K2O/Na2O ratio (1.6–4.0), low (La/Yb)n values (4.3–10.5), and a clear Eu minimum (Eu/Eu* = 0.3–0.5); they are similar to highly fractionated I-granites. All coeval late Paleoproterozoic (1.88–1.85 Ga) granites and felsic volcanics of the Elash graben have distinct differences in composition, especially in the ferroan index and HREE contents, owing to variations in the source composition and melting conditions during their formation at postcollisions extension. The wide range of the isotope parameters of granites and felsic volcanic rocks (εNd from +2.0 to –3.7) and zircons (εHf from +3.0 to +0.8, granites of the Toporok massif) indicates the heterogeneity of the crustal basement of the Elash graben, which formed both in the Archean and in the Paleoproterozoic.


2017 ◽  
Vol 472 (1) ◽  
pp. 67-71 ◽  
Author(s):  
A. E. Starikova ◽  
V. V. Sharygin ◽  
E. V. Sklyarov

2019 ◽  
Vol 487 (1) ◽  
pp. 88-92 ◽  
Author(s):  
A. E. Starikova ◽  
E. V. Sklyarov ◽  
V. V. Sharygin

We provide the results of study of the extremely enriched in Y-REE carbonate-fluorine isolations from biotite-arfvedsonite granite of the Katugin rare metal deposit. New chemical data of isolations mineral phases - gagarinite-(Y), tveitite-(Y), fluocerite-(Ce), basnaesite, fluornatropyroclore, are delivered. Carbonate-fluoride globule in quartz of hosting granite gives possibility to estimate crystallization order. This finding might be the evidence of silicate-fluorine immiscibility suggested before for Y-REE segregations in the Katugin granites. Fluorine melt segregation took likely place at the magmatic stage of biotite-arfvedsonite granite formation. It causes host granite depletion with fluorine and redistribution of REE and Y in fluorine salt melt.


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