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Scandium (Sc) is a dispersed metal in Earth's lithosphere, with an average abundance of 16 to 22 ppm. In the meantime, it is widely considered as a critical metal because of its paramount significance in scientific research and technical innovation. With surging demands that are not backed-up by current supplies globally, the market price of Sc oxide is astonishingly five times more than the most expensive rare earth oxide of terbium (Tb). Production of Sc is significantly held back due to scarcity of economically viable grades at explorable depths within the crust, compared with other critical metals such as REE, Nb and Ta. Nevertheless, typical high- to intermediate-grade Sc deposits, as compiled in this review, consistently show close relationships to specific magmatic (e.g. ultramafic-mafic and carbonatitic), supergene and hydrothermal processes during Sc enrichment, especially the former two. Known potential Sc deposits are tentatively classified based on their host rocks and metallogeny, including those hosted in the ultramafic-mafic rocks and related laterites, in carbonatite and related laterites, in bauxite residue and processed coals, hydrothermal Sc deposits and Sc deposits related to syenite intrusions, pegmatites or marine sediments. We also discuss the Sc enrichment mechanism and associated tectonics and partition coefficients of Sc among diverse minerals and melts, which reveal the preference of Sc for clinopyroxene, garnet and iron oxides by isomorphic replacement or ion absorption during diverse magmatic and supergene Sc enrichment processes. Lastly, Sc resources in the world-class Bayan Obo deposit are discussed in detail as an illustrative benchmark example, where hydrothermal aegirine may host majority of carbonatite-derived Sc. [ABSTRACT FROM AUTHOR]

[Display omitted] • Fluorocarbonates and monazites have recorded geochemical evolution of REE-rich magma and fluids. • Fluorocarbonates and monazites has potential as indicators to REE mineralization processes. • Mesoproterozoic REE minerals inherit geochemical features from carbonatite melt. • Mesoproterozoic and Paleozoic hydrothermal REE minerals reveal contamination of crustal materials. Fluorocarbonates and monazite are common economic REE minerals in carbonatite-related REE deposits, such as the largest known REE deposit at Bayan Obo, China. The geochemical evolution of REE minerals is a sensitive and effective indicator of delicate REE mineralization processes. In this study, the fluorocarbonates and monazites were classified into three generations, corresponding to three REE mineralizing stages. The first generation (Gen-1) of bastnäsite and monazite are generally characterized by elevated La/Ce, La/Nd and La/Lu ratios, with right-declining chondrite normalized REE distribution patterns. They have low Th and radiogenic Sr content, with forming age of about 1.3 Ga and εNd(t) around 0, indicating a primary origin and orthomagmatic crystallization from carbonatite melts. The second generation (Gen-2) of REE minerals, formed at 1.25–1.2 Ga, normally constitute banded aggregates with associated hydrothermal gangue minerals (fluorite, aegirine, sodium amphibole etc.). The Gen-2 REE minerals are featured by moderate-low La/Ce, La/Nd, La/Lu ratios but slightly elevated 87Sr/86Sr 0 ratios, indicating a Mesoproterozoic hydrothermal origin related to carbonatitic fluids. Gen-2 bastnäsite and monazite precipitated earlier in low-fluid/rock-ratio environment with right-declining LREE distribution patterns, while the subsequent Gen-2 parisite and huanghoite display convex LREE patterns and higher OH/F ratios, indicative of relative La-depletion and increased ambient fluid/rock ratios during progressive hydrothermal REE mineralization. The third generation (Gen-3) of REE minerals are generally megacrysts in the vein-type ores formed in the early Paleozoic REE mineralization stage (470–420 Ma). The Gen-3 REE minerals are typified by significantly variable REE, Sr and Nd isotopic components, indicating extensive hydrothermal metasomatism and intense contamination of crustal material. Induced by activities of early Paleozoic subduction-related fluids, Gen-3 REE minerals were formed through local REE re-enrichment within the ore-hosting dolomite, rather than by introduction of REE from external sources. In this case study, a comprehensive model of the delicate REE mineralization processes of the giant Bayan Obo REE-Nb-Fe deposit has been established. This study highlights the great potential of fluorocarbonates and monazites widely distributed in carbonatite-related REE deposits as universal geochemical indicators of late-stage evolution of carbonatite and delicate magmatic-hydrothermal REE mineralization processes. [ABSTRACT FROM AUTHOR]

[Display omitted] • The Bayan Obo deposit has notable differences with skarn/BIF in mineralogy and magnetite geochemistry. • Trace element contents in Bayan Obo magnetite controlled by coexisting mineral, f O 2 and T. • Bayan Obo iron deposit was a hydrothermal deposit related to igneous carbonatite. The giant Bayan Obo REE deposit bears a large amount of iron resources as well. However, the genesis of iron mineralization is still highly controversial with limited research. In this study, new data of trace elements of magnetite from Bayan Obo ores, Eastern contact zone skarn and Heinaobao BIF are obtained by Laser ablation (LA) ICP-MS analyses, revealing the genesis of Bayan Obo iron resources through comparing study. The Bayan Obo deposit contains disseminated, banded and massive ores, and in which magnetite is associated with REE minerals, fluorite, aegirine, riebeckite, and biotite. Euhedral magnetite in the skarn of Eastern contact zone is usually associated with pyrite, biotite, fluorite, and bastnaesite. There are two types of magnetite in the Heinaobao BIF: (1) euhedral to subhedral magnetite associated with quartz and a small amount of amphibole; (2) anhedral magnetite associated with quartz, garnet, plagioclase, amphibole and biotite. Magnetite in the Bayan Obo is enriched in Ni, but depleted in Mg, Al, Ti, Ge, Mn, Ga and Zn, showing low and variable concentrations, which is similar to the hydrothermal magnetite. The contents of some trace elements (e.g. Ti, Mn, Sc, Zn, Nb and REE) of magnetite from the skarn ores are generally higher, indicating a relatively high formation temperature. Magnetite in the Heinaobao BIF is generally characterized by low and uniform trace element contents, except for the abnormal values of Ti, Al, Cr and Mn, suggesting the involvement of terrigenous clastic materials. Compared with Bayan Obo magnetite, the skarn magnetite has the highest Sn/Ga, Co/Ni, Nb/Ta, La/Yb, Ti/V and Ti/Al ratios, while magnetite in the BIF has the highest Al/Co and lowest Nb/Ta ratios. The significant difference in mineralogical and trace element characteristics among the three types of magnetite indicates that the iron resources in Bayan Obo deposit are unlikely to be a skarn Fe deposit nor a BIF deposit. However, the Bayan Obo magnetite shows similar geochemical characteristics to hydrothermal magnetite related to carbonatite, both of which are depleted in high field strength elements, such as Zr, Hf and Ta, and show strong positive anomalies of Mn and Zn and negative anomalies of Co and Ga. In addition, in the diagrams of Ti vs. Nb + Ta and Ti vs. Zr + Hf, the Bayan Obo magnetite falls into the field of hydrothermal magnetite associated with carbonatite. In conclusion, it is recommended that the Bayan Obo iron deposit is a typical hydrothermal deposit related to carbonatite. In this contribution, the skarn magnetite formed at high temperature and the BIF magnetite was contaminated by terrigenous materials deviating from the expected region in discriminant diagrams. It is therefore proposed that the validity of these diagrams depends on a full understanding of mineralogical characteristics of samples and magnetite precipitation environment, and that multiple discrimination diagrams should be used in combination. [ABSTRACT FROM AUTHOR]