4.7 Article

Lithium, Phosphorus, and rare earth elements in magmatic garnets from granitic Pegmatites: Coupled substitution and petrogenetic implications

Journal

ORE GEOLOGY REVIEWS
Volume 153, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.oregeorev.2022.105284

Keywords

Garnet; Granitic pegmatite; Trace element; Zoning; Substitution; Petrogenesis

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This study investigates the substitution mechanisms for lithium, phosphorus, and rare earth elements (including yttrium) in garnets from different pegmatite fields in China. The results show that lithium and sodium can enter the garnet lattice through coupled substitution with other elements. The dominant substitution mechanism depends on the bulk chemistry of the pegmatite-forming melts. Rating: 9 out of 10.
The general chemical formula of garnet can be expressed as X3Y2(ZO4)3 where X, Y, and Z represent dodeca-hedral, octahedral, and tetrahedral sites, respectively. Lithium, phosphorus, and rare earth elements (including yttrium) in garnets from the Luanzhuang-Guanpo and Ziyugou (ZYG) pegmatite fields in the East Qinling orogen and the Kalu'an (KLA) Li pegmatites in the Chinese Altay orogen have been investigated both at a mineral scale and in the context of pegmatite types to identify the substitution mechanisms for these elements. Our results show that Y + REE or P can enter the garnet lattice through coupled substitution with Li (+Na) that can compensate the charge differences due to Y + REE in the X-site or P in the Z-site of the garnet. Two substitutions, namely [X(Li,Na)+ X(Y,REE)3+ XR2+ 1 1 (R2+)-2] and [X(Li,Na)1 ZP1 Z Si-1], are likely the most important and can account for-1 incorporation of the majority of Y + REE, P, and Li + Na in pegmatite garnets. Whichever substitution becomes predominant in garnets is strongly dependent on the bulk chemistry of pegmatite-forming melts. Consequently, the first substitution dominates in garnets from NYF (niobium-yttrium-fluorine) pegmatites and mixed-type pegmatites with NYF affinity whereas the other one dominates in garnets from relatively P-rich LCT (lithium -cesium-tantalum) and barren pegmatites. Incorporation of Sc and Ti in garnet may also need Li + Na, although Sc and Ti are not as much as Y and REE in pegmatite garnet. The zonings of Y, REE, and Sc in garnet are mainly controlled by the composition of pegmatite-forming melt and consumption of these elements due to the growth of garnet itself and other minerals enriched in Y + REE (e.g., xenotime, fergusonite, monazite, etc.) or Sc (e.g., biotite). Additionally, our results, combined with the data in the literature, show that garnets from NYF peg-matites and mixed-type pegmatites with NYF affinity commonly contain elevated Y (up to -20000 ppm), REE (up to -20000 ppm), and Sc (up to -2400 ppm) but low P (<100 ppm) compared to those from LCT and barren pegmatites. Nevertheless, individual garnets with low concentrations of Y, REE, Sc, and P can occur in any types of pegmatites. Therefore, the coupled substitution between Li + Na and Y + REE or P along with zonings and concentrations of Y, REE, and Sc in garnet should be investigated on a regular basis to interpret pegmatite petrogenesis.

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