Partitioning behavior of trace elements between dacitic melt and plagioclase, orthopyroxene, and clinopyroxene based on laser ablation ICPMS analysis of silicate melt inclusions

Major and trace element composition of silicate melt inclusions (SMI) and their rock-forming minerals were studied in mafic garnet granulite xenoliths from the Bakony–Balaton Highland Volcanic Field (Western-Hungary). Primary SMIs occur in clinopyroxene and plagioclase in the plagioclase-rich domains of mafic garnet granulites and in ilmenite in the vicinity of these domains in the wall rock. Based on major and trace elements, we demonstrated that the SMIs have no connection with the xenolith-hosting alkaline basalt as they have rhyodacitic composition with a distinct REE pattern, negative Sr anomaly, and HFSE depletion. The trace element characteristics suggest that the clinopyroxene hosted SMIs are the closest representation of the original melt percolated in the lower crust. In contrast, the plagioclase and ilmenite hosted SMIs are products of interaction between the silicic melt and the wall rock garnet granulite. A further product of this interaction is the clinopyroxene–ilmenite±plagioclase symplectite. Textural observations and mass balance calculations reveal that the reaction between titanite and the silicate melt led to the formation of these assemblages. We propose that a tectonic mélange of metapelites and (MOR-related) metabasalts partially melted at 0.3–0.5 GPa to form a dacitic–rhyodacitic melt leaving behind a garnet-free, plagioclase+clinopyroxene+orthopyroxene+ilmenite residuum. The composition of the SMIs (both major and trace elements) is similar to those from the middle Miocene calc-alkaline magmas, widely known from the northern Pannonian Basin (Börzsöny and Visegrád Mts., Cserhát and Mátra volcanic areas and Central Slovakian VF), but the SMIs are probably the result of a later, local process. The study of these SMIs also highlights how crustal contamination changes magma compositions during asthenospheric Miocene ascent.

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Partitioning of V and 19 other trace elements between rutile and silicate melt as a function of oxygen fugacity and melt composition: Implications for subduction zones

American Mineralogist ◽

10.2138/am-2020-7013 ◽

2020 ◽

Vol 105 (2) ◽

pp. 244-254 ◽

Cited By ~ 2

Author(s):

Megan Holycross ◽

Elizabeth Cottrell

Keyword(s):

Trace Elements ◽

Subduction Zones ◽

Silicate Melt ◽

High Field Strength ◽

Trace Element Partitioning ◽

Element Partitioning ◽

Oxygen Buffer ◽

Melt Composition ◽

Refractory Slab ◽

Partitioning Behavior

Abstract Vanadium is a multivalent element that can speciate as V2+, V3+, V4+, and V5+ over a range of geologically relevant oxygen fugacities (fO2). The abundance of V in planetary materials can be exploited as a proxy for fO2 when its partitioning behavior is known. The mineral rutile (TiO2) is an important carrier of the high field strength elements Nb and Ta in the solid Earth, but it can also incorporate substantial quantities of vanadium (up to ~2000 ppm; e.g., Zack et al. 2002). However, little work has been done to systematically investigate how the partitioning of V in rutile-bearing systems changes as a function of both fO2 and composition. We measured the partitioning of V and 19 other trace elements (Sc, Cr, Y, Zr, Nb, La, Ce, Pr, Nd, Sm, Eu, Gd, Dy, Ho, Er, Yb, Lu, Hf, and Ta) between rutile and three silicate melt compositions equilibrated at 1 atm pressure, 1300 °C and fO2 values from two log units below the quartz-fayalite-magnetite oxygen buffer (QFM-2) to air (QFM+6.5). Rutile/melt partition coefficients (DVrt/melt) change dynamically over an eight-log unit range of fO2 and are greatest at fO2 = QFM-2 in all compositions. Vanadium solubility in rutile declines continuously as fO2 increases from QFM-2 and approaches unity in air. Trace-element partitioning between rutile and melt is also correlated with melt composition, with the greatest values of Drt/melt measured in the most polymerized melt systems containing the least TiO2. We do not find any circumstances where V becomes incompatible in rutile. Our results indicate that rutile is a considerable sink for V at terrestrial fO2 values and will contribute to the retention of V in refractory slab residues in subduction zones. In agreement with previous work, we find that DTart/melt>DNbrt/melt under all conditions investigated, suggesting that rutile fractionation does not lead to low Nb/Ta ratios in Earth's continental crust.

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