Rare earth elements (REEs) are considered critical elements in modern society due to their irreplaceable role in new innovative and energy technologies. The giant carbonatite-related Bayan Obo deposit contributes most REE resources in the world’s market, while its origin is still unclear because of the complicated and diverse REE ore mineralogy and texture. Thescanning electron mircroscopy SEM)-based automated mineralogy allows for the numeric assessment of rocks and ores’ compositional and textural properties. Here, we use TIMA (TESCAN Integrated Mineral Analyzer) to quantitatively characterize REE ore mineralogy from the deep drill core within the H8 unit (“dolomite marble”) to better understand the deposit. The mineral composition, occurrence, and Ce elemental deportment of the borehole ores at different depths (i.e., 1107 m, 1246 m, 1406 m, 1546 m, and 1682 m) were obtained. The results show that the main types of ores in the investigated samples can be divided into banded REE-Fe ores, banded REE ores, disseminated REE-Fe ores, and veined REE ores. REE and gangue minerals vary significantly in abundance and occurrence. Monazite-(Ce) and bastnäsite-(Ce) are the primary REE host minerals, and both contribute the most to the REE budget. Other REE minerals, such as parisite-(Ce)/synchysite-(Ce), cerite-(Ce), huanghoite-(Ce)/cebaite-(Ce), and aeschynite-(Ce), are significant contributors. The gangue minerals generally include fluorite, barite, magnetite, pyrite, quartz, magnesio-arfvedsonite, and minerals of the biotite and apatite groups, among others. Combined with the newly published mineral-scale chronological and isotopic geochemical analyses, it is reasonable to conclude that the later hydrothermal fluids remobilized and redistributed the original Mesoproterozoic carbonatitic REE minerals and formed a high variable ore mineral assemblage. Furthermore, it is demonstrated that the mineralogical study using TIMA can provide accurate and reliable mineralogy data for the comprehensive interpretation of the complex REE ores, and extend our understanding of the deposit.

Selenium (Se) is an essential trace element for humans and animals, and an excess of or deficiency in Se is harmful to health. Research on the selenium enrichment zone began in the late 1970s in Shuang’an, Ziyang, southern Shaanxi Province. Naore village is only one selenosis area in Shuang’an, Ziyang, China. Different scholars have conducted systematic studies on the occurrence of selenium, its organic geochemistry and biomarkers, and its content and enrichment patterns in this area. This study applied the TIMA (TESCAN integrated mineral analyzer) for the first time to conduct detailed mineralogical work. The minerals included quartz, carbonate minerals (calcite and dolomite), feldspar (plagioclase, albite, and orthoclase), biotite and muscovite, clay minerals (chlorite and kaolinite), hematite, pyrite, and accessory minerals (almandine, olivine, zircon, and apatite) in Naore village, Ziyang, Shaanxi Province. The ATi index (100 × apatite/(apatite + tourmaline)) is used to determine the source of heavy minerals and the degree of heavy minerals’ weathering. The content POS (100 × (pyroxene + olivine + spinel)/transparent heavy mineral) of olivine, pyroxene, and spinel in heavy minerals can reflect the contribution of basic and ultrabasic rocks in the source area. The ATi and POS indexes for the heavy minerals in the research area were 91.83~99.96 and 0.01~18.75, respectively, reflecting the abundance of volcanic rock material in their source. In addition, the migration, transformation, bioavailability, and toxicity of selenium in the environment are closely related to its species. The species of selenium in various selenium-rich areas (Naore, Wamiao, and Guanquan) mainly include unusable residues and organic forms, followed by humic-acid-bound selenium. The proportions of water-soluble, exchangeable, and carbonate-bound selenium are relatively small, and the proportion of Fe-Mn oxide-bound selenium is the lowest.

The Xiaobaihegou fluorite deposit is located in the southwest of the Altyn-Tagh Orogen, NW China. However, the provenance, thermodynamic properties, and enrichment mechanisms of the ore-forming fluids in this deposit remain unclear. Fluorite mineralization primarily occurs in the vicinity of the contact zone between the granite and the wall rocks. The zircon U-Pb age of the alkali-feldspar granite in the Xiaobaihegou fluorite deposit is 482.3 ± 4.1 Ma. The ore-hosting lithologies are mainly calcareous rock series of the Altyn Group. The ore bodies are controlled by NE-trending faults and consist primarily of veined, brecciated, massive, and banded ores. The ore mineral assemblage is primarily composed of calcite and fluorite. The rare earth element (REE) patterns of fluorite and calcite in the Xiaobaihegou deposit exhibit right-dipping LREE enrichment with distinct negative Eu anomalies, which closely resemble those of the alkali-feldspar granite. This similarity suggests that the REE distribution patterns of fluorite and calcite were likely inherited from the pluton. The ore-forming process can be divided into an early stage and a late stage. The massive ores formed in the early stage contain mainly gas-rich two-phase fluid inclusions and CO₂-bearing three-phase inclusions, with homogenization temperatures ranging from 235 °C to 426 °C and salinities from 28.59% to 42.40% NaCl equivalent. In the late stage, brecciated and stockwork ores were formed. They host liquid-rich two-phase and gas-rich two-phase fluid inclusions, with homogenization temperatures ranging from 129 °C to 350 °C and salinities from 0.88% to 21.61% NaCl equivalent. The results of hydrogen and oxygen isotope studies indicate that the ore-forming fluids were derived from a mixture of magmatic–hydrothermal and meteoric water. Fluorite precipitation in the early stage was mainly due to the mixing of magmatic–hydrothermal solution and meteoric water, as well as a water–rock reaction. In the late stage, fluid mixing further occurred, resulting in a decrease in temperature and the formation of brecciated and stockwork ores. The ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd ratios of fluorite from the deposit range from 0.71033 to 0.71272 and 0.511946 to 0.512073, respectively, indicating that the ore-forming material originates from the crust. Based on the ore-forming characteristics, it is proposed that Ca may be primarily leached from the strata formation, while F may predominantly originate from magmatic–hydrothermal solutions. The formation of fluorite deposits is closely related to the transition of the Central Altyn-Tagh Block and Qaidam Block from a compressional orogenic environment to an extensional tectonic environment.

Barite is an abundant sulfate mineral in nature. Especially, the variety of morphologies of barite is often driven by the mixing of Ba-bearing hydrothermal fluid and sulfate-bearing seawater around hydrothermal chimneys. In order to better understand the factors affecting the morphology and precipitation mechanism(s) of barite in seafloor hydrothermal systems, we synthesized barite by a new method of in-situ mixing of BaCl₂ and Na₂SO₄ solutions at 200 °C while varying Ba concentrations and ratios of Ba²⁺/SO₄²⁻, and at room temperature for comparison. The results show that barite synthesized by in-situ mixing of BaCl₂ and Na₂SO₄ solutions at 200 °C forms a variety of morphologies, including rod-shaped, granular, plate-shaped, dendritic, X-shaped, and T-shaped morphologies, while room temperature barites display relatively simple, granular, or leaf-like morphologies. Thus, temperature affects barite morphology. Moreover, dendritic barite crystals only occurred at conditions where Ba²⁺ is in excess of SO₄²⁻ at the experimental concentrations. The dendritic morphology of barite may be an important typomorphic feature of barite formed in high-temperature fluids directly mixing with excess Ba²⁺ relative to SO₄²⁻.