Fresh samples of basalts were collected by dredging from the Nanyue intraplate seamount in the Southwest sub-basin of the South China Sea (SCS). These are alkali basalts displaying right-sloping, chondrite-normalized rare earth element (REE) profiles. The investigated basalts are characterized by low Os content (60.37–85.13 ppt) and radiogenic 187Os/188Os ratios (~0.19 to 0.21). Furthermore, 40Ar/39Ar dating of the Nanyue basalts showed they formed during the Tortonian (~8.3 Ma) and, thus, are products of (Late Cenozoic) post-spreading volcanism. The Sr–Nd–Pb–Hf isotopic compositions of the Nanyue basalts indicate that their parental melts were derived from an upper mantle reservoir possessing the so-called Dupal isotopic anomaly. Semiquantitative isotopic modeling demonstrates that the isotopic compositions of the Nanyue basalts can be reproduced by mixing three components: the average Pacific midocean ridge basalt (MORB), the lower continental crust (LCC), and the average Hainan ocean island basalt (OIB). Our preferred hypothesis for the genesis of the Nanyue basalts is that their parental magmas were produced from an originally depleted mantle (DM) source that was much affected by the activity of the Hainan plume. Initially, the Hainan diapir caused a thermal perturbation in the upper mantle under the present-day Southwest sub-basin of the SCS that led to erosion of the overlying LCC. Eventually, the resultant suboceanic lithospheric mantle (SOLM) interacted with OIB-type components derived from the nearby Hainan plume. Collectively, these processes contributed crustal- and plume-type components to the upper mantle underlying the Southwest sub-basin of the SCS. This implies that the Dupal isotopic signature in the upper mantle beneath the SCS was an artifact of in situ geological processes rather than a feature inherited from a Southern Hemispheric, upper mantle source.
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Trace Element and Isotopic Evidence for Recycled Lithosphere from Basalts from 48 to 53°E, Southwest Indian Ridge
Abstract Mantle source heterogeneity and magmatic processes have been widely studied beneath most parts of the Southwest Indian Ridge (SWIR). But less is known from the newly recovered mid-ocean ridge basalts from the Dragon Bone Amagmatic Segment (53°E, SWIR) and the adjacent magmatically robust Dragon Flag Segment. Fresh basalt glasses from the Dragon Bone Segment are clearly more enriched in isotopic composition than the adjacent Dragon Flag basalts, but the trace element ratios of the Dragon Flag basalts are more extreme compared with average mid-ocean ridge basalts (MORB) than the Dragon Bone basalts. Their geochemical differences can be explained only by source differences rather than by variations in degree of melting of a roughly similar source. The Dragon Flag basalts are influenced by an arc-like mantle component as evidenced by enrichment in fluid-mobile over fluid-immobile elements. However, the sub-ridge mantle at the Dragon Flag Segment is depleted in melt component compared with a normal MORB source owing to previous melting in the subarc. This fluid-metasomatized, subarc depleted mantle is entrained beneath the Dragon Flag Segment. In comparison, for the Dragon Bone axial basalts, their Pb isotopic compositions and their slight enrichment in Ba, Nb, Ta, K, La, Sr and Zr and depletion in Pb and Ti concentrations show resemblance to the Ejeda–Bekily dikes of Madagascar. Also, Dragon Bone Sr and Nd isotopic compositions together with the Ce/Pb, La/Nb and La/Th ratios can be modeled by mixing the most isotopically depleted Dragon Flag basalts with a composition within the range of the Ejeda–Bekily dikes. It is therefore proposed that the Dragon Bone axial basalts, similar to the Ejeda–Bekily dikes, are sourced from subcontinental lithospheric Archean mantle beneath Gondwana, pulled from beneath the Madagascar Plateau. The recycling of the residual subarc mantle and the subcontinental lithospheric mantle could be related to either the breakup of Gondwana or the formation and accretion of Neoproterozoic island arc terranes during the collapse of the Mozambique Ocean, and is now present beneath the ridge.
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- Award ID(s):
- 1657826
- PAR ID:
- 10208790
- Date Published:
- Journal Name:
- Journal of Petrology
- ISSN:
- 0022-3530
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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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.more » « less
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