Minerals of the apatite group commonly occur in granite pegmatites, and their ability to incorporate a wide range of trace elements makes them a good indicator of magma composition and magmatic–hydrothermal processes. Gem-quality purple apatite crystals from the Dara-e-Pech pegmatite field in Afghanistan have rarely been reported. Here, we investigated apatite crystals originated from this locality, using gemological testing, chemical analysis, and in situ U–Pb dating, with the purpose of identifying their origin, the constraints on the magma source in which the apatite crystals were formed, and the timing of the magmatic–hydrothermal activity. Our findings demonstrate that the purple apatite crystals were impure fluorapatite, characterized by heavy rare-earth element (HREE) enrichment, intermediate Eu anomalies, and non-CHARAC Y/Ho ratios. The results showed that these apatite crystals yielded a lower intercept age of 135.8 ± 6.9 Ma. We proposed that the pegmatitic apatite samples formed in a transitional magmatic–hydrothermal pegmatitic system with moderate fO₂ in the Early Cretaceous (~135 Ma). Our study helps to constrain the magmatic–hydrothermal activities of the little-known Dara-e-Pech pegmatite field.

Spinel is a precious gem with a long history, but people are far less familiar with it. Previous studies on Mogok spinel from Myanmar focused on inclusion analysis, chromogenic mechanism with a single-color gemstone and heat treatment, whereas systematic studies on varicolored gem-grade spinel are lacking. In this study, the gemological and geochemical analysis of four colors of spinel samples from Mogok were carried out for basic gemology, inclusion morphology and identification, spectroscopy and geochemistry. The aim was to explore the occupation of elements of spinels in the crystal structure, as well as the chromogenic mechanism of varicolored spinels and the geological and geodynamic conditions of the formation. Mogok spinel samples are characterized by octahedral negative crystals filled with calcite and chondrodite inclusions, indicating that they are derived from a marble metamorphic-type deposit. The spinel samples of four colors are magnesia–alumina spinel (MgAl₂O₄). The contents of V and Cr in Mogok spinel are generally high, with a significant high content of Zn being the most characteristic, and trace elements vary greatly. The infrared spectra of spinel samples in different colors are basically similar. According to the UV–Vis spectrum, pink and red samples are mainly colored by Cr and/or V, whereas orange samples are mainly colored by V. Two wide absorption bands in the range 300~600 nm are mainly attributed to the spin-allowed transition and spin-forbidden transition of Cr³⁺ and/or V³⁺. The purple samples are mainly colored by Fe and the UV–Vis spectrum is mainly attributed to the spin-forbidden transition of ^TFe²⁺. This study is a favorable supplement to the research on Mogok spinels of various colors from multiple perspectives.

The Mogok metamorphic belt (MMB) of Myanmar is a famous geographical origin acknowledged by the whole world for its large mineral resources. In this study, basic gemological tests (density, UV fluorescence, refractive index, etc.), spectroscopic tests (infrared spectrum, Raman spectrum, and ultra-violet visible spectrum) and chemical composition analysis (electron microprobe and laser ablation inductively coupled plasma mass spectrometer) were carried out on scapolites from Myanmar. This paper explores the mineralogical characteristics of Burmese scapolites and provides additional information on its origin. Burmese scapolites are colorless and transparent with a yellow tone and belong to Cl-rich dipyre. The infrared spectra of the samples show the vibrations of Si-O and Al-O (400–1300 cm⁻¹), (CO₃)²⁻ (1400–300 cm⁻¹), and OH (3048 cm⁻¹ and 3568 cm⁻¹). The Raman spectra are mainly the vibrational spectra of Si (Al)-O-Si (Al) and the absorption peaks at 992 cm⁻¹ and 1110 cm⁻¹ caused by the vibrations of sulfate and carbonate ions, respectively. Black inclusions were found inside the scapolites, and the dark inclusions were identified as graphite by Raman spectroscopy. Moreover, the composition of the scapolite could be influenced by the αCl⁻/α(CO₃)²⁻ of the fluid. The Cl activity degree could control the scapolite content as the ion exchange between scapolite and plagioclase was gradually balanced. The enrichment of rare earth elements and the apparent positive Eu anomaly indicate that Burmese scapolites have a high degree of light and heavy rare earth element differentiation and an oxidizing environment of mineralization.

Gem-quality garnets, with their high closure temperature (750–800 °C), high transparency, uniform composition, and purity, offer promising prospects for U-Pb dating. Despite decades of recognition that garnets can be dated using the U-Pb method, direct dating remains extremely limited. Tsavorite is a rare gem-quality green vanadium-rich grossular hosted in the Neoproterozoic Metamorphic Mozambique Belt (NMMB). Until now, the accurate crystallization age of the tsavorite in Kenya and Lemshuku (Tanzania) has remained unknown. Here, we conducted in situ laser U-Pb geochronological analysis on gem-quality tsavorite samples from Tanzania and Kenya. U-Pb dating of tsavorite sourced from the Lemshuku mine (Tanzania) and the Tsavorite mine (Kenya) yielded ages of 643.9 ± 3.2 Ma and 617.4 ± 4.8 Ma, respectively. The high closure temperature of the U-Pb system within garnets renders it more inclined to preserve crystallization ages rather than documenting cooling events or metamorphic overprinting. Consequently, these ages are indicative of the tsavorite mineralization epochs. These findings align with the most significant metamorphic period documented in the Mozambique Belt, known as the East African Orogen, which occurred between 640 and 600 Ma. U-Pb data have revealed distinct formation times for each district. Dating specific deposits can provide more precise information about the origin of tsavorite, rather than solely relying on isotope or trace element data that have long been used for provenance studies of tsavorite.

With mineral in situ testing technology and ore deposit geochemistry development, calcite has become a hot topic in studying carbonate minerals. Four large-grain calcite crystals from Fujian, China, were used for a detailed study. This study provides a comprehensive data set through mineralogical standard properties and spectral characteristics, including Fourier transform infrared, X-ray fluorescence spectrum, and Raman spectroscopy. Major elements were analyzed using X-ray fluorescence (XRF) and Micro-XRF. A high-resolution gas-source stable isotope ratio mass spectrometer was used to test C-O isotope characteristics. The four samples’ spectral characteristics and phase composition show excellent uniformity, all with the same characteristic peaks, indicating that they are pure calcite without other impurity minerals. C-O isotope characteristics indicate that Fujian calcite has mantle genetic characteristics, which may be affected by marine carbonate dissolution or sedimentary rock contamination. The variation of Fe and Mn contents may indicate that the four samples formed at different metallogenic stages.

Titanite is a widespread accessory mineral in igneous, metamorphic, and hydrothermal rocks, but few comply with gem-grade requirements. Previous studies on Moroccan titanite focused on elementary composition and U-Pb dating. In this study, two gem-grade titanites (MA-1 and MA-2) from the Moroccan Central High Atlas were investigated through gemological and chemical studies, including infrared spectrum, Raman spectrum, SEM-EDS, and LA-ICP-MS. Two titanite samples are yellow, transparent–translucent with a greasy luster, 3.5 and 2.5 mm long. MA-1 and MA-2 have similar gemological properties, the refractive index (RI) is beyond the range of the refractometer (>1.78), the specific gravity (SG) values fall in the range of 3.52~3.54 and both are inert to short-wave and long-wave UV radiation. The spectral characteristics have high consistency with the RRUFF database. The major elements’ composition shows a negative correlation between Al, Fe, V, and Ti, suggesting the titanites underwent substitutions such as (Al, Fe³⁺) + (F, OH) ↔ Ti + O. The titanite samples, characterized by a low abundance of REE (802~4088 ppm) and enriched in LREE, exhibit positive Eu (δEu: 1.53~7.79) and Ce (δCe: 1.08~1.33) anomalies, indicating their formation in a hydrothermal environment with low oxygen fugacity. The ²³⁸U/²⁰⁶Pb and ²⁰⁷Pb/²⁰⁶Pb ratios of the titanites yield lower intercept ages of 152.6 ± 2.2 and 151.4 ± 5.3 Ma (1s), consistent with their weighted average ²⁰⁶Pb/²³⁸U ages of 152.3 ± 2.0 and 150.7 ± 3.2 Ma (1s) respectively. The results of U-Pb dating are matched with the second main magmatic activities in the High Atlas intracontinental belt of Morocco during the Mesozoic to Cenozoic period. Moreover, the two titanite samples have almost no radiational damage. All the results show that the titanite from High Atlas, Morocco, has the potential to be a reference material for LA-ICP-MS U–Pb dating, but further experiments are needed to be sure.