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Neogene Metasomatism in the Subcontinental Lithosphere beneath SE Asia—Evidence from Modal and Cryptic Phosphorus Enrichment in Peridotites and Pyroxenites from Southern Laos

Metasomatism is the prime process to create compositional heterogeneity of the upper mantle. Mineralogical and mineral chemical changes of the mantle triggered by metasomatism can be used to deduce the nature of the metasomatic agent(s) and to constrain the timing of metasomatism. This information i...

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Bibliographic Details
Published in:Journal of petrology 2019-12, Vol.60 (12), p.2413-2448
Main Authors: Konzett, Jürgen, Hauzenberger, Christoph, Krenn, Kurt, Joachim-Mrosko, Bastian, Stalder, Roland, Gröbner, Katharina, Sieberer, Anna-Katharina, Hoang, Nguyen, Khoi, Nguyen Ngoc
Format: Article
Language:English
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Summary:Metasomatism is the prime process to create compositional heterogeneity of the upper mantle. Mineralogical and mineral chemical changes of the mantle triggered by metasomatism can be used to deduce the nature of the metasomatic agent(s) and to constrain the timing of metasomatism. This information is vital for an understanding of the secular evolution of a given mantle segment and the magmatic processes occurring therein. For this study spinel-lherzolites and -websterites were collected from ∼16 Myr old alkali-basaltic lava flows that were extruded on the Bolaven Plateau in south–central Laos. These xenoliths are fragments of the shallow continental lithosphere of the SE Asian peninsula and originate from a mantle segment that acted as source for Cenozoic basaltic volcanism in the wake of the India–Asia collision. In both rock types modal metasomatism formed apatite ± whitlockite ± phlogopite ± calcic amphibole ± calcite ± orthopyroxene. The principal metasomatic phase is apatite, which appears in three varieties. Type-I apatite is ±inclusion-free and associated with phlogopite, calcic amphibole, calcite and lamellar orthopyroxene. It is high in Na and low in P and shows low analytical totals indicating a type-B carbonate–apatite component. Type-I apatite presumably precipitated from a P-alkali-rich mixed H2O–CO2 fluid with low large ion lithophile element (LILE)–light rare earth element (LREE) contents. Type-II apatite shows a spongy texture and has lower Na and higher P contents with higher analytical totals. Crosscutting discontinuous zones of type-II characteristics within type-I apatites indicate type-II formation through an exchange Na+ + CO32– = PO43– + Ca2+ by a later fluid with lower aCO2. REE-rich type-III apatite is the youngest type and formed by infiltration of basaltic melts as part of spongy rims around clinopyroxene. One lherzolite contains whitlockite in addition to apatite. Whitlockite formation is ascribed to a short-lived metasomatic event involving a fluid with extremely low aH2O. Disequilibrium between whitlockite and the bulk assemblage is indicated by hydrous silicates in the immediate vicinity of whitlockite and by substantial H2O contents of 250–370 µg g–1 in clinopyroxenes and 170–190 µg g–1 in orthopyroxenes. High-density (1·15–≥1·17 g m–3) CO2–fluid inclusions in the whitlockite-bearing sample provide evidence for the presence of low-aH2O fluids at mantle depths. The spinel-herzolites may also show cryptic metasomatism evidence
ISSN:0022-3530
1460-2415
DOI:10.1093/petrology/egaa013