Search Results (93)

The Sar-e-Sang lapis lazuli deposit has a mining history exceeding 5000 years, producing the world’s finest lapis lazuli. Recently, gem-quality forsterite has been discovered in the marble containing spinel, dolomite, and phlogopite at the periphery of the lapis lazuli ore body at the Pitawak mine, located east of the Sar-e-Sang deposit. The mineral assemblage indicates that the protolith of this marble is dolomite with aluminous and siliceous components. These forsterite crystals occur as colorless, transparent anhedral grains, exhibiting distinct red fluorescence under 365 nm ultraviolet light. To investigate the gemological and spectroscopic characteristics of the Pitawak mine forsterite, this study conducted and analyzed data from basic gemological analysis, electron probe microanalysis (EPMA), Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), ultraviolet–visible absorption spectroscopy (UV-VIS), Fourier-transform infrared spectroscopy (FTIR), laser Raman spectroscopy (RAMAN), and photoluminescence spectroscopy (PL) on four forsterite samples from the Pitawak mine. The analysis results reveal that the samples indicate a composition close to ideal forsterite with a crystal chemical formula of (Mg_2.00Fe_0.02)_Σ2.02Si_0.99O₄. The trace elements present include Fe, Mn, Ca, and minor amounts of Cr and Ni. The UV-VIS spectroscopy results show that the samples possess high transmittance across the visible light range with very weak absorption bands, contributing to the colorless and transparent appearance of Pitawak mine forsterite. This phenomenon is attributed to the extremely low content of chromophoric elements, which have a negligible effect on the forsterite’s color. PL spectroscopy indicates that the red fluorescence of the samples is caused by an emission peak near 642 nm. This emission peak arises from the spin-forbidden ⁴T₁ → ⁶A₁ transition of Mn²⁺ ions situated in octahedral sites within the forsterite structure. Full article

Sulfides are essential tracers for understanding the redox conditions, diffusion processes, and thermal mechanisms involved in the formation of ordinary chondrites. Their mineralogical and textural evolution provides valuable constraints on the metamorphic history of parent bodies. In this context, the Ksar El Goraane meteorite, which fell in Morocco in 2018 and is classified as an H5 ordinary chondrite, represents a particularly instructive case for investigating sulfur behavior during thermal metamorphism. Petrographic observations combined with geochemical data obtained by electron probe microanalysis (EPMA) and energy-dispersive X-ray spectroscopy (EDS) were used to characterize the main silicate and sulfide phases and to evaluate their degree of chemical equilibration. The compositions of olivine (Fa_18–20), Mg-Rich orthopyroxene, and sodic plagioclase (An_10–15) display limited analytical dispersion and well-recrystallized textures, confirming that Ksar El Goraane experienced an equilibrated metamorphic grade consistent with an H5 ordinary chondrite. The sulfide assemblage is dominated by troilite (FeS), iron-rich pyrrhotite (Fe_1−xS), and pentlandite ((Fe,Ni)₉S₈), with minor occurrences of pyrite (FeS₂). Textural relationships and chemical homogeneity observed in backscattered electron images and elemental maps indicate progressive re-equilibration during thermal metamorphism. Formation and transformation temperatures of the sulfide phases are inferred through comparison with experimental and empirical constraints reported in the literature. These results suggest early high-temperature crystallization of troilite, followed by sulfur depletion leading to pyrrhotite formation, subsequent low-temperature exsolution of pentlandite, and localized late-stage pyrite crystallization. Full article

A large, low-grade Fe–Ti–V oxide deposit occurs within the Xiaohaizi Ultramafic–Mafic intrusion. Based on petrographic observations and electron probe microanalysis (EPMA) of amphibole, this study examines the magmatic evolution and ore-forming processes of the intrusion through analyses of amphibole occurrence, mineral chemistry, and crystallization conditions. Five textural types of amphibole were identified: (i) inclusions, (ii) co-crystallization with early silicates, (iii) reaction rims, (iv) co-crystallization with late Fe–Ti oxides, and (v) phenocrysts. The amphiboles are calcic varieties, mainly composed of magnesio-hastingsite, kaersutite, and tschermakite. Crystallization occurred at temperatures of 901–1013 °C and pressures of 254–424 MPa, with ΔNNO values ranging from −1.3 to +2.8 and estimated melt H₂O contents of 3.3–7.1 wt.%, corresponding to crystallization depths of 9.6–16.0 km. Importantly, the crystallization interval of the Fe–Ti oxides is defined by these amphibole-assemblage conditions, as evidenced by their direct intergrowth. Integration of mineralogical and geochemical data indicates that the Xiaohaizi intrusion underwent four distinct stages of magmatic evolution. During these stages, the crystallization of Fe–Ti oxides was accompanied by notable fluctuations in oxygen fugacity and melt water content. These results suggest that fractional crystallization played a dominant role in ore formation, with possible late-stage liquid immiscibility observed at the mineral scale. Overall, this study proposes that the Xiaohaizi Fe–Ti–V oxide deposit represents a magmatic conduit-type ore-forming system developed within a crystal mush. The enrichment of Fe–Ti oxides is strongly associated with hydrous melts and elevated oxygen fugacity conditions. Full article

The mineralogical, geochemical, and statistical characteristics of recent fluvial deposits from the Brahmaputra–Jamuna River, Bangladesh, were examined to determine their provenance, transport dynamics, and depositional environment. Sediments were analyzed using X-ray diffraction (XRD), wavelength dispersive X-ray fluorescence (WD-XRF), field emission scanning electron microscopy (FE-SEM), and electron probe microanalysis (EPMA). Grain size analysis revealed a predominance of medium-to-fine sand (mean grain size 1.77–3.43 ϕ), with moderately well-sorted textures (sorting: 0.33–0.77 ϕ), mesokurtic to leptokurtic distributions, and skewness values ranging from −0.21 to +0.30. Mineralogical results show a high quartz content with minor feldspar, mica, zircon, rutile, and iron-bearing minerals. Geochemical data indicates high SiO₂ (63.39%–70.94%) and Al₂O₃ (12.25%–14.20%) concentrations and calculated chemical index of alteration (CIA) values ranging from 60.90 to 66.82. The microstructural study revealed angular to sub-angular grains with conchoidal fractures and stepped microcracks, indicating brittle deformation under high-energy conditions, which is consistent with short transport distances, limited sedimentary recycling, and a derivation from mechanically weathered source rocks. Multivariate analyses (PCA and K-means clustering) of grain size parameters reveal two distinct sedimentary regimes, namely Cluster 1 as finer-grained (2.36 ϕ), poorly sorted sediments, and Cluster 2 as coarser (2.98 ϕ), well-sorted deposits. Discriminant function values (Y₂: 78.82–119.12; Y₃: −6.01 to −2.56; V₁: 1.457–2.442; V₂: 1.409–2.323) highlight shallow water, fluvial/deltaic aspects, and turbidite depositional environments. These findings advance the understanding of sedimentary dynamics within large, braided river basins and support future investigations into the sustainable management of fluvial depositional environments. Full article

Thorium-rare earth-iron oxide deposits of the Lemhi Pass district, Idaho and Montana, are enriched in the middle rare earth elements (REE), and particularly neodymium (Nd). Overall, thorium (Th) and total rare earth oxide (TREO) grades of the deposits are sub equal at 0.4 wt. % but locally exceed 1 wt. % TREO. Nd-monazite, the major REE phase (35 wt. % Nd₂O₃) occurs in hydrothermal Th-REE mineralized quartz veins and biotite-rich shear zones of enigmatic origin. Hosted in Mesoproterozoic metasedimentary rocks, the deposits are modest in size but present over a large area with no obvious source pluton exposed. This paper documents the geochemistry of the monazite and provides the first geochronological data to constrain its origin. Elemental mapping and U-Th-total Pb EPMA dating of the monazite and thorite document a Paleozoic age for mineralization centered in the Late Devonian at approximately 355 Ma ± 20 Ma. A second period of volumetrically minor Th and REE remobilization is dated as Mesozoic (ca. 100 Ma). For context, a reactivated passive continental margin was present during the Devonian in eastern Idaho, while the Mesozoic was a time of major accretionary tectonics and arc magmatism further west. Nd and Pb isotopic data require a significant interaction of the fluids with an ancient crustal component represented by regional Mesoproterozoic metasedimentary rocks and granitoids. A source–transport–deposition model is hypothesized with metasomatic fractionation and enrichment of Nd during regional hydrothermal circulation. The aqueous fluids were hot, oxidizing, and likely saline, but the exact source of the Th and REEs and the mechanism of enrichment remains problematic. Additional analytical work and increased knowledge of the regional and district geology will improve this unconventional hypothesis for formation of Lemhi Pass’ unusual Nd-rich Th-REE-Fe mineralization. Full article

The Upryamoye ore field is located in the Chukotka metallogenic belt in Northeast Russia. The orebodies are hosted within Late Jurassic–Early Cretaceous greenschist-facies metamorphosed rocks and structurally controlled by NW-trending fold-and-thrust dislocations. Based on geological exploration, petrographic, mineralogical, and geochronological studies, new data on the geological structure and composition of gold–quartz mineralization of the Upryamoye ore field are presented. Optical and scanning microscopy were used to study the lithological features of the host rocks and determine the ore textures and the morphology and internal structure of native gold, auriferous pyrite, and arsenopyrite. Qualitative and quantitative characterization of the ore minerals was carried out using SEM-EDS and EPMA. To determine the age of the gold mineralization, Re-Os dating of arsenopyrite and U-Th/He dating of pyrite were performed. The results show that the orebodies comprise carbonate–quartz and sulphide–carbonate–quartz saddle reef veins in both the fold hinge and limbs, as well as mineralized shatter zones and mylonite zones that trace thrust faults. The main ore minerals are arsenopyrite and pyrite, associated with minor amounts of galena, sphalerite, chalcopyrite, tetrahedrite, and bournonite. Native gold is distributed extremely unevenly, forming thin and finely dispersed inclusions in pyrite and arsenopyrite. U-Th/He isotopic analyses of auriferous pyrites suggest that gold mineralization in the Upryamoye ore field occurred at 123 ± 4 Ma. The data obtained by Re–Os dating of auriferous arsenopyrite are inconsistent with direct geological observations but indicate that Os in the arsenopyrite was derived from the crustal source. According to a number of characteristic features of mineralization, the Upryamoye ore field is attributed to a metamorphic genetic type of orogenic low-sulphide gold–quartz deposits. The ore-forming process was long and multi-stage, occurring during the final collisional phase and the beginning of the extensional phase of the Chukotka orogen. Full article

Accurate phase identification is essential for characterising complex mineral systems but remains a challenge in SEM-based automated mineralogy (AM) for compositionally variable rock-forming or accessory minerals. While platforms such as the Tescan Integrated Mineral Analyzer (TIMA) offer high-resolution phase mapping through BSE-EDS data, classification accuracy depends on the quality of the user-defined phase library. Generic libraries often fail to capture site-specific mineral compositions, resulting in misclassification and unclassified pixels, particularly in systems with solid solution behaviour, compositional zoning, and textural complexity. We present a refined approach to developing and validating custom TIMA phase libraries. We outline strategies for iterative rule refinement using mineral chemistry, textures, and BSE-EDS responses. Phase assignments were validated using complementary microanalytical techniques, primarily electron probe microanalysis (EPMA) and laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS). Three Queensland case studies demonstrate this approach: amphiboles in an IOCG deposit; cobalt-bearing phases in a sediment-hosted Cu-Au-Co deposit; and Li-micas in an LCT pegmatite system. Targeted refinement of phases improves identification, reduces unclassified phases, and enables rare phase recognition. Expert-guided phase library development strengthens mineral systems research and downstream applications in geoscience, ore deposits, and critical minerals while integrating datasets across scales from cores to mineral mapping. Full article

Eight diffusion couples were fabricated to systematically investigate the composition-dependent interdiffusion behavior in hcp Dy-Y, Dy-Nd, Sm-Nd, and Sm-Tb binary alloys. The interdiffusion coefficients were determined at two representative temperatures using the Sauer–Freise method based on concentration–distance profiles measured by electron probe microanalysis (EPMA). These experimentally obtained diffusivities, together with available thermodynamic data, were subsequently employed to assess the atomic mobilities of each system by means of the CALTPP (CALculation of Thermo Physical Properties) program within the CALPHAD (CALculation of PHAse Diagrams) framework. The optimized mobility parameters provide a reliable description of the diffusion behavior in all investigated alloys. This reliability is confirmed by the close agreement between the calculated and experimentally measured interdiffusion coefficients, as well as by the strong consistency between the model-predicted and experimental concentration profiles. The present work thus establishes the first set of critically evaluated atomic mobility parameters for these hcp rare-earth binary systems. These results fill an important gap in the kinetic database of rare-earth alloys and lay a robust foundation for future multi-component CALPHAD-based simulations, thereby supporting the design and optimization of advanced rare-earth permanent magnets with improved coercivity and thermal stability. Full article

The Southern Great Xing’an Range (SGXR), an important W–Sn polymetallic metallogenic belt in northern China, hosts multiphase magmatism and has witnessed recent discoveries of multiple tungsten–tin polymetallic deposits. The W–Sn mineralization in this area is intimately associated with Early Cretaceous highly fractionated granites. The Chamuhan deposit, a small-sized W–Mo polymetallic deposit in SGXR, is genetically linked to a concealed fine-grained porphyritic alkali feldspar granite intrusion. In this study, we present the LA-ICP-MS zircon U-Pb ages, whole-rock geochemical, and electron probe microanalysis (EPMA) mineral chemistry to constrain the petrogenesis and metallogenic implications of this granite. Zircon U–Pb dating yields a crystallization age of 141.3 ± 1.2 Ma, consistent with molybdenite Re–Os ages. The granite is characterized by elevated SiO₂ (76.9–79.1 wt%) and total alkalis (7.3–8.5 wt%), and exhibits peraluminous high-K calc-alkaline affinity (A/CNK = 1.37–1.57). Geochemical signatures reveal enrichment in large ion lithophile elements (LILEs, e.g., Rb, Th, U) coupled with depletion in high-field strength elements (HFSEs, e.g., Ba, Sr, P, Eu, Ti, Nb, Ta), and are accompanied by right-sloping REE patterns with LREE enrichment and HREE depletion. EPMA data indicate that the mica in the intrusion is primarily zinnwaldite and Li-rich phengite, whereas the plagioclase occurs as albite. The feldspar thermobarometry yields crystallization temperatures of 689–778 °C and 313 MPa–454 MPa, while the melt H₂O content and oxygen fugacity are 8.61–11.1 wt% and −22.58–−14.48, respectively. These geochemical signatures indicate that the granites are highly fractionated I-type granites with extensive fractional crystallization of various minerals like plagioclase, K-feldspar, and apatite, etc. From the Late Jurassic to the Early Cretaceous, the subduction and rollback of the Paleo-Pacific Ocean plate resulted in extensional tectonic environments in eastern China. Asthenospheric upwelling and lower crustal melting generated parental magmas, wherein progressive fractional crystallization during ascent concentrated ore-forming elements and volatiles within residual melts. This process played a key role in the formation of the Chamuhan deposit, exemplifying the metallogenic potential of highly evolved granitic systems in the SGXR. Full article

Zircon is one of the most common accessory minerals in all types of granitoids. Due to its resistance to secondary processes, it preserves information about the composition of magma and conditions at the time of crystallization. Madeira albite granite, Brazil, offers optimum conditions for the study of chemistry and shape of zircon and the relation between the contents of particular trace elements in magma vs. in crystallizing zircon. Textural and chemical zircon data obtained using scanning electron microscopy (BSE) and cathodoluminescence (CL) imaging, automated mineralogy by TESCAN Integrated Mineral Analyzer (TIMA), and electron probe microanalyses (EPMA) enabled us to define four albite granite facies containing zircons of specific structures and chemistry. Zircon in the Madeira albite granite was formed during several, largely temporally and spatially independent episodes. During the crystallization of the common facies, occupying most of the intrusion volume, Zr/Hf value in zircon decreased from 40 to 20. This zircon, in some episodes, incorporated a higher amount of Th, which was later unmixed in the form of thorite inclusions. The pegmatoidal facies, representing crystallization of residual magma, contains zircon without thorite inclusions with a Zr/Hf value from 35 to 5. The Th/U and Y/Yb values during this evolution scattered but generally evolved to Th, Yb-enriched compositions (Th/U up to >10, Y/Yb down to 0.1). The Li-poor facies, located in the center of the stock near the cryolite deposit, contains zircon with comparatively high Zr/Hf = 45–70 and higher U and Y contents. Later, part of the common facies was hydrothermally altered to border facies, but zircon did not change noticeably during this process. The contents of minor elements in all zircon varieties are generally low (U + Th + Y + REE ˂ 0.05 apfu); Y and REE are incorporated exclusively in the xenotime component. Many crystals have low analytical totals, down to 95 wt%, and are enriched in Al, Fe, Mn, Ca, and F but this process does not influence the primary Zr/Hf, Th/U, and Y/Yb ratios. Zircons from other Madeira granite facies, including the neighboring Europa pluton, differ mainly in much higher Y/Yb values and in having (Y + REE) >> P, indicating a different than xenotime substitution mechanism. Zircon from the Madeira albite granite differs from zircons from many metaluminous rare-metal granites in low contents of minor elements and a common assemblage with thorite, instead of forming Zrn–Thr–Xnt solid solutions. Full article

Megacrystalline uraninite within Neoproterozoic migmatites in the Haita area of the Kangdian region of China provides a unique condition for the investigation of uraninite typomorphism under high-temperature conditions. The present study represents the first systematic characterization of the typomorphic signatures and genetic significance of megacrystalline uraninite via optical microscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XRS), and electron probe microanalysis (EPMA). The results show that uranium mineralization occurs as euhedral megacrystalline uraninite (black grains ≤ 10 mm) hosted in quartz veins, exhibiting frequent rhombic dodecahedral and subordinate cubic–octahedral morphologies. The paragenetic assemblage is quartz–uraninite–titanite–apatite–molybdenite. The investigated uraninite is characterized by elevated unit-cell parameters and a reduced oxygen index, with complex chemical compositions enriched in ThO₂ and Y₂O₃. These typomorphic characteristics indicate crystallization under high-temperature reducing conditions with gradual cooling. Post-crystallization tectonic fragmentation and uplift-facilitated oxidation occur, generating secondary uranium minerals with concentric color zonation (orange–red to yellow–green halos). Mineralization was jointly controlled by migmatization and late-stage tectonism, with the breakup of the Rodinia supercontinent serving as the key driver of fluid mobilization and ore deposition. The data materialized in the present study improve our knowledge about uranium mineralization during continental breakup events. Full article

The phase equilibria of the Si-C-Cu ternary system at 700 °C and 810 °C were experimentally investigated for the first time. Fifteen key alloys were prepared via powder metallurgy and analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and electron probe microanalysis (EPMA). Isothermal sections were constructed based on the identified equilibrium phases. At 700 °C, eight single-phase regions and six three-phase regions—(C)+(Cu)+hcp, (C)+hcp+γ-Cu₃₃Si₇, (C)+γ-Cu₃₃Si₇+SiC, γ-Cu₃₃Si₇+SiC+ε-Cu₁₅Si₄, SiC+ε-Cu₁₅Si₄+η-Cu₃Si(ht), and SiC+(Si)+η-Cu₃Si(ht)—were determined. At 810 °C, nine single-phase regions and seven three-phase regions were identified. The solubility of C and Si/Cu in the various phases was quantified and found to be significantly higher at 810 °C compared to 700 °C. Key differences include the presence of the bcc (β) and liquid phases at 810 °C. The results demonstrate that higher temperatures promote increased mutual solubility and reaction tendencies among Cu, C, and Si. Motivated by these findings, the influence of vacuum hot pressing parameters on SiC-fiber-reinforced Cu composites (SiC_f/Cu) was investigated. The optimal processing condition (1050 °C, 60 MPa, 90 min) yielded a high bending strength of 998.61 MPa, attributed to enhanced diffusion and interfacial bonding facilitated by the high-temperature phase equilibria. This work provides essential fundamental data for understanding interactions and guiding processing in SiC-reinforced Cu composites. Full article

The “yellow-skinned” Nanhong agate represents a unique variety of Nanhong agate found in northeastern Yunnan, China, and it is highly valued for its distinctive yellow exterior and clear red–yellow interface. Owing to the limited research on this variety, the present study provides the first comprehensive analysis. Field surveys and various laboratory techniques—including polarizing microscopy, scanning electron microscopy (SEM), Fourier-transform infrared (FTIR) spectrometry, ultraviolet–visible (UV-VIS) absorption spectrometry, Raman spectroscopy, micro X-ray diffraction (µ-XRD) with Rietveld refinement, electron microprobe analysis (EPMA), and laser ablation–inductively coupled plasma mass spectrometry (LA-ICP-MS)—were utilized to investigate its gemological, microtextural, spectroscopic, and geochemical characteristics. Field surveys identified the occurrence states of the “yellow-skinned” Nanhong agate. The laboratory results indicate that the agate primarily consists of α-quartz, with minor amounts of moganite, goethite, and hematite. The coloring mechanism observed in this study is consistent with the findings of previous studies: the external yellow coloration is due to goethite, while the internal red hue is attributed to hematite. Its unique pseudo-granular silica (Type III) structure provides a foundational basis for the later formation of the “yellow-skinned” agate variety, and geochemical data reveal the distribution patterns of elements. Based on geological surveys and experimental data, the formation of the “yellow-skinned” Nanhong agate in northeastern Yunnan can be divided into two stages: first, hydrothermal fluids filled the vesicles in the Permian Emeishan Basalt Formation (P₂β), leading to the formation of primary Nanhong agate. Subsequently, the Type III primary agate underwent weathering, erosion, transport, and deposition in the red–brown sandy mudstone of the Lower Triassic Feixianguan Formation (T₁f). The sedimentary environment in the second stage facilitated the conversion of outer hematite into goethite, resulting in the distinct “yellow-skinned” appearance with a clear red–yellow boundary. Based on the occurrence and stratigraphic relations, this study constrains the formation age of the “yellow-skinned” Nanhong agate to approximately 261.6 Ma. Full article

In recent years, domestic research on the ion substitution behavior and chromaticity of the mineral composition of “Ya’an Green” remains insufficient, while there is almost no relevant research on “Ya’an Green” abroad. In this study, X-ray powder diffraction (XRD), electron probe microanalysis (EPMA), infrared spectroscopy (IR), ultraviolet–visible spectroscopy (UV-Vis), and colorimetry were employed. The results indicate that the green and yellow matrices of “Ya’an Green” are primarily composed of muscovite, with rutile also present in the yellow matrix. In contrast, the white–green samples are mainly composed of quartz, with muscovite as a secondary mineral. Additionally, it was observed that the (004) crystal plane of muscovite exhibits a peak shift to lower 2θ angles, attributed to the substitution of Al³⁺ by ions with larger radii, such as Ba²⁺, Cr³⁺, and Fe²⁺, leading to an increase in unit cell parameters and a consequent shift in the peak to lower wavenumbers. The main elements of “Ya’an Green” are Al, Si, and K, with minor elements including Na, Fe, and Cr. Furthermore, Mg²⁺, Ca²⁺, Ti⁴⁺, Cr³⁺, and Fe²⁺ in the samples can substitute for Al³⁺ through isomorphic substitution. The infrared spectrum of muscovite in the ‘Ya’an Green’ sample shows three typical absorption peaks, 422 cm⁻¹ and 513 cm⁻¹ caused by Si-O bending vibration, 697 cm⁻¹ and 837 cm⁻¹ caused by Si-O-Al vibration, 948 cm⁻¹ caused by O-H bending vibration, and 3647 cm⁻¹ caused by O-H stretching vibration. The peak at 837 cm⁻¹ exhibits varying degrees of shift due to the substitution of Al³⁺ by ions with larger radii. The ultraviolet–visible spectra display two broad absorption bands at 422 nm and 615 nm, which are caused by Cr³⁺ transition, indicating that Cr is the chromogenic element responsible for the green color. A correlation was observed between the Cr³⁺ content and the hue angle h in “Ya’an Green” samples: the higher the Cr³⁺ content, the closer the hue angle is to 136^°, resulting in a darker green color, while lower Cr³⁺ content leads to a deviation from the dark green hue. This study establishes for the first time the correlation between the mineral composition of ‘Ya’an Green’ and its chromatic parameters and explores the linear relationship between its color and the number of color-causing elements and elemental substitution, which provide data support and theoretical models for the study of the color of seal stones. Full article

Grossular, a widely recognized colored gemstone in the market, attains premium quality when exhibiting pale-toned orange-yellow to golden-yellow hues with high transparency. Recently, our research team identified abundant gem-grade grossular associated with skarn-type polymetallic deposits in the Mt.Bozhushan area. However, these grossular specimens are currently discarded as mining waste. To promote their sustainable utilization, we conducted a systematic sampling of Mt.Bozhushan grossular and performed comprehensive analyses including fundamental gemological testing, spectroscopic characterization, and compositional profiling through EPMA and LA-ICP-MS. This multidisciplinary approach aims to establish an objective valuation framework for Mt.Bozhushan-derived grossular. The compositional and spectral data obtained in this study provide critical theoretical foundations and technical references for developing the gemstone resources of southeastern Yunnan’s Mt.Bozhushan grossular while establishing an evaluative baseline for grossular specimens from other regional deposits. Full article