Abstract
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 evidenced by P zoning in olivine, which is characterized by P-poor (<20–130 µg g–1) cores and P-rich (170–507 µg g–1) rims, the latter in part with oscillatory zoning on a µm scale. Element correlations indicate [4]Si4+ + [6](Mg, Fe)2+ = [4]P5+ + [6]Li+, 2 [4]Si4+ + 4 [6](Mg, Fe)2+ = 2 [4]P5+ + 3 [6](Mg, Fe)2+ + [6]vac and/or 5 [4]Si4+ = 4 [4]P5+ + [4]vac as major P incorporation mechanisms. High P–T experiments conducted at 2 GPa and 950–1050 °C yield apatite-saturated P contents of olivine in the range ∼360–470 µg g–1. Most P concentrations in olivines from the xenoliths including those in the P-rich rims, however, are significantly lower than the apatite-saturated values, which indicates disequilibrium uptake of P during growth of the P-rich rims by dissolution–reprecipitation. Diffusion modeling indicates that the P zoning must have formed within decades prior to the eruption of the host basalts. This is consistent with the preservation of Li disequilibrium partitioning between olivine and pyroxenes in some of the xenoliths. All metasomatic phenomena were assigned to two metasomatic events, both of which were in close temporal relation with the eruption of the xenolith host basalts: an older event-1 formed type-I apatite, hydrous silicates, calcite and orthopyroxene and caused the modification of type-I apatite composition towards that of type-II. It is also likely to be responsible for whitlockite formation and P zoning in olivine. A younger event-2 comprises all paragenetic, textural and compositional modifications of the xenolith assemblages associated with the infiltration of basaltic melts.
