Geochemical analysis reveals distinct mantle origins for carbonatite systems, demonstrating that zircon trace-element signatures reliably fingerprint magmatic rare earth element sources.
The mantle sources of carbonatite and alkaline magmatic systems that host rare earth element (REE) deposits are difficult to constrain because whole-rock compositions are commonly altered. Alteration-resistant zircon trace-element compositions are used to fingerprint mantle sources at Mountain Pass, California, the largest REE deposit in the United States, and extend this approach to a global carbonatite−alkaline rock dataset. Autocrystic zircon samples from the Mountain Pass intrusive suite record subduction-like U-Sc-Nb-Yb compositions, oxidized fO2 (0.8−2.4 relative to fayalite-magnetite-quartz buffer [ΔFMQ]), and Ti-in-zircon temperatures up to ∼970 °C, indicating a lithospheric mantle source enriched and oxidized by Paleoproterozoic subduction and subsequently tapped during Mesoproterozoic postcollisional lithospheric thinning. This contrasts with the ocean island basalt−like enriched mantle recorded by Mesoproterozoic zircon from the Bayan Obo carbonatite complex, China, demonstrating that world-class REE deposits of comparable age can reflect fundamentally different mantle sources. New classifiers separate subduction-metasomatized from non-subduction-enriched mantle domains with ∼90% accuracy, providing a zircon-based tool for fingerprinting the mantle source regions of magmatic REE deposits.
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Hillenbrand et al. (2026) studied this question.
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