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We present data for lithospheric mantle xenoliths sampled from two alkali basalts in south‐central Vietnam, Pleiku and Xuan Loc, including fertile spinel peridotites. To better determine the origins of the Indochinese subcontinental lithospheric mantle (SCLM), including impacts of posited tectonic extrusion, we present major and trace elements, and 87Sr/86Sr, 143Nd/144Nd, 176Hf/177Hf, 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb in xenolith mineral separates. Most peridotites from Pleiku and Xuan Loc have fertile major element compositions, “depleted” and “spoon‐shaped” rare earth element (REE) patterns, interpreted to record prior melt depletion followed by melt metasomatism, and variable but generally depleted isotopic signatures (e.g., 87Sr/86Sr = 0.70238–0.70337 and 143Nd/144Nd = 0.512921–0.514190). A small group of refractory peridotites have “enriched” REE patterns suggesting more extensive metasomatism and enriched isotope ratios (87Sr/86Sr = 0.70405 and 143Nd/144Nd = 0.512755–0.512800). The presence of both fertile and refractory xenoliths records a heterogeneous SCLM beneath Vietnam. Based on geothermobarometry calculations, fertile xenoliths have equilibrium temperatures of 923–1,034°C and pressures of 11.7–15.8 kbar, while refractory xenoliths have comparable temperatures of 923–1,006°C, but lower pressures of 7.1–10.0 kbar, suggesting refractory rocks are dominantly present at shallower depths. We suggest that the lithospheric mantle has experienced variable melt extraction around 1.0–1.3 Ga, producing heterogeneous major element compositions. While we cannot rule out partial removal and replacement of the lithosphere, large‐scale delamination is not necessary to explain observed characteristics. The entire SCLM was more recently metasomatized by melts resembling Cenozoic basalts, suggesting recent asthenospheric melting has modified the SCLM by melt infiltration. 

Spring waters from across the Costa Rica margin were analyzed for their Li and He isotope compositions to determine the utility of Li isotopes as a tracer of volatile sources in subduction zones. Li isotope ratios systematically decrease with increasing depth to the subducting slab: averaging +15.0‰ ± 9.2‰ in the outer forearc (<40 km to the slab), +9.3‰ ± 4.3‰ in the forearc (40–80 km to the slab), and +5.8‰ ± 2.8‰ in the arc (>80 km to the slab). In contrast, air-corrected 3He/4He values (reported relative to the ratio in air, RA) range from 0.4 to 7.5 RA and increase from predominantly crustal values near the trench to mantle values in the arc. Together, these data support progressive devolatilization of the subducting plate with slab-derived Li components sourced from shallowly expelled pore fluids in the outer forearc, sedimentary and/or altered oceanic crust contributing to the forearc, and limited slab input beneath the arc. 

Abstract Mantle plumes contain heterogenous chemical components and sample variable depths of the mantle, enabling glimpses into the compositional structure of Earth's interior. In this study, we evaluated ocean island basalts (OIB) from nine plume locations to provide a global and systematic assessment of the relationship betweenfO₂and He‐Sr‐Nd‐Pb‐W‐Os isotopic compositions. Ocean island basalts from the Pacific (Austral Islands, Hawaii, Mangaia, Samoa, Pitcairn), Atlantic (Azores, Canary Islands, St. Helena), and Indian Oceans (La Réunion) reveal thatfO₂in OIB is heterogeneous both within and among hotspots. Taken together with previous studies, global OIB have elevated and heterogenousfO₂(average = +0.5 ∆FMQ; 2SD = 1.5) relative to prior estimates of global mid‐ocean ridge basalts (MORB; average = −0.1 ∆FMQ; 2SD = 0.6), though many individual OIB overlap MORB. Specific mantle components, such as HIMU and enriched mantle 2 (EM2), defined by radiogenic Pb and Sr isotopic compositions compared to other OIB, respectively, have distinctly highfO₂based on statistical analysis. ElevatedfO₂in OIB samples of these components is associated with higher whole‐rock CaO/Al₂O₃and olivine CaO content, which may be linked to recycled carbonated oceanic crust. EM1‐type and geochemically depleted OIB are generally not as oxidized, possibly due to limited oxidizing potential of the recycled material in the enriched mantle 1 (EM1) component (e.g., sediment) or lack of recycled materials in geochemically depleted OIB. Despite systematic offset of thefO₂among EM1‐, EM2‐, and HIMU‐type OIB, geochemical indices of lithospheric recycling, such as Sr‐Nd‐Pb‐Os isotopic systems, generally do not correlate withfO₂.