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High U/Th partitioning by clinopyroxene from alkali silicate and carbonatite metasomatism: an origin for Th/U disequilibrium in mantle melts?
Author(s) -
Foley S. F.,
Petibon C. M.,
Jenner G. A.,
Kjarsgaard B. A.
Publication year - 2001
Publication title -
terra nova
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.353
H-Index - 89
eISSN - 1365-3121
pISSN - 0954-4879
DOI - 10.1046/j.1365-3121.2001.00323.x
Subject(s) - carbonatite , metasomatism , geochemistry , geology , mantle (geology) , peridotite , silicate , eclogite , kimberlite , petrology , subduction , tectonics , paleontology , chemistry , organic chemistry
Clinopyroxene/melt pairs in strongly potassic silicate and carbonatite melts exhibit unusually high U/Th partitioning ratios of ˜ 3 and ˜ 2, respectively. These values are much higher than those found for aluminous clinopyroxenes in peridotite, and have the potential to cause significant ( 230 Th)/( 238 U) isotope enrichment in volcanics. The potassic silicate (lamproite) and carbonatite melts correspond closely to the main agents of mantle metasomatism, indicating that clinopyroxene in metasomatized regions of the mantle may greatly affect U/Th disequilibria. Recycling of alkali pyroxenite veins in the oceanic lithosphere formed by solidification of melt in the extremities of the MORB melting region presents an alternative to eclogite recycling in MORB and OIB genesis.