Granitic pegmatite deposits, which are usually products of orogenic processes during plate convergence, can be used to demonstrate regional tectonic evolution processes. In the eastern Tibetan Plateau in China, the Jiajika, Dahongliutan, Xuebaoding, Zhawulong, and Ke’eryin rare metal pegmatite deposits are located in the southern, western, northern, midwestern, and central areas of the Songpan–Ganzê orogenic belt, respectively. In this study, we dated two muscovite Ar–Ar ages of 189.4 ± 1.1 Ma and 187.0 ± 1.1 Ma from spodumene pegmatites of the Dahongliutan deposit. We also dated one zircon U-Pb age of 211.6 ± 5.2 Ma from muscovite granite, two muscovite Ar–Ar ages of 179.6 ± 1.0 Ma and 174.3 ± 0.9 Ma, and one columbite–tantalite U-Pb age of 204.5 ± 1.8 Ma from spodumene pegmatites of the Zhawulong deposit. In addition, we dated one muscovite Ar–Ar age of 159.0 ± 1.4 Ma from spodumene pegmatite of the Ke’eryin deposit. Combining these ages and previous studies in chronology, we concluded that the granitic magma in the Jiajika, Xuebaoding, Dahongliutan, Zhawulong, and Ke’eryin deposits intruded into Triassic metaturbidites at approximately 223, 221, 220–217, 212, and 207–205 Ma, respectively, and that the crystallization of the corresponding pegmatite ceased at approximately 199–196, 195–190, 189–187, 180–174, and 159 Ma, respectively. In this study, we demonstrated that the peak in magmatic activity and the final crystallization age of the pegmatite lagged behind one another from the outer areas of the orogeny belt to the inner areas. The pegmatite–parented granitic magmas were sourced from Triassic metaturbidites that were melted by shear heating along the large-scale decollement resulting from Indosinian collisions along the North China block, Qiangtang–Changdu block, and Yangtze block. As a result, the above temporal and spatial regularities indicated that the tectonic–thermal stress resulting from the collisions of three blocks was transferred from the outer areas of the orogenic belt to the inner areas. A large amount of heat and a slow cooling rate at the convergent center of thermal stress in two directions will lead to crystallization and differentiation of magma in the Songpan–Ganzê orogenic belt, forming additional rare metal deposits.

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.

The composition and properties of ore-forming fluids are key to understanding the mechanisms of mineralization in ore deposits. These characteristics can be understood by studying fluid inclusions. Hydrates in fluid inclusions containing NaCl–H₂O and MgCl₂–H₂O were studied using cryogenic Raman spectroscopy. The intensity ratio of peaks at 3401, 3464, 3514, and 3090 cm⁻¹ shows a positive correlation with the concentration of hydrates in the inclusions, as does the ratio of the total integrated area of the MgCl₂ hydrate peak (3514 cm⁻¹) to the 3090 cm⁻¹ peak with the concentration of MgCl₂ (correlation coefficient >0.90). These correlations are important in the quantitative analysis of MgCl₂ in synthetic and natural NaCl–MgCl₂–CaCl₂–H₂O-bearing fluid inclusions. Semi-quantitative analysis of NaCl–MgCl₂–H₂O solutions indicates that peaks at 3437 and 3537 cm⁻¹ reflect the presence of NaCl in the solution. Further, a peak at 3514 cm⁻¹ is indicative of the presence of MgCl₂. The relative intensities of these peaks may be related to the relative abundances of NaCl and MgCl₂. A quantitative attempt was made on NaCl–MgCl₂–CaCl₂–H₂O system, but it was found that quantifying NaCl, MgCl₂ and CaCl₂ separately in NaCl–MgCl₂–CaCl₂–H₂O system by the secondary freezing method is difficult.