Regional Zoning of a Li-Cs-Ta Pegmatite Field: Insights from Monazite-Cheralite Chemistry, U-Th-Pb and Sm-Nd Isotopes

伟晶岩 独居石 地质学 钠长石 地球化学 微斜长石 白云母 淡色花岗岩 铀矿 黑云母 矿物学 变质岩 铀 石英 片麻岩 锆石 材料科学 古生物学 冶金
作者
Cheng Wang,Yongjun Shao,Peter A. Cawood,Jianfeng Chen,Yi-Qu Xiong,Yuejun Wang
出处
期刊:Journal of Petrology [Oxford University Press]
卷期号:64 (7) 被引量:14
标识
DOI:10.1093/petrology/egad044
摘要

Abstract Li-Cs-Ta (LCT ) rare-element pegmatites occur as late-stage and highly fractionated bodies at the margins of regionally zoned granite pegmatite fields. The evolution of the granitic pegmatite system, including its rare-metal metallogeny, is often difficult to determine due to complex textures involving variable crystal size and a heterogeneous chemical composition. The Renli-Chuanziyuan pegmatite field (South China) displays a well-developed regional zonation sequence, involving a core of biotite-, two-mica- and muscovite monzogranites (MMs) that grades outward into microcline (K-zone), microcline-albite (K-Na-zone), albite (Na-zone) and albite-spodumene (Na-Li-zone) pegmatites. Monazite and the Th, Ca–end-member (i.e. cheralite) provide valuable age, rare earth element (REE) geochemical and Sm-Nd isotopic data for understanding the regional zoning process within the Renli-Chuanziyuan pegmatite. Monazite (from the MM and the K-, K-Na- and Na-zone pegmatites) and cheralite (from the Na-Li-zone pegmatite) have variable compositions and complex internal microtextures. The monazite and cheralite grains contain irregular areas with subtle heterogeneous BSE response along cracks and grain margins, suggesting that they have experienced alkali-bearing fluid-aided modification. However, these features are rarely seen in monazite from the K-zone pegmatite. Common Pb contamination and/or Pb loss during fluid-aided modification may have disturbed the monazite and cheralite U-Th-Pb isotopic system, due to the differential mobility of U, Th and Pb. The unaltered Na-zone monazite and Na-Li-zone cheralite yielded Th-Pb ages of 140.42 ± 2.30 Ma (2 σ, mean standard weighted deviation (MSWD) = 2.4, n = 14) and 139.58 ± 2.15 Ma (2 σ, MSWD = 2.9, n = 21), respectively. The unaltered MM, K-zone and K-Na-zone monazite yielded 206Pb-238U ages of 138.03 ± 2.18 (2 σ, MSWD = 2.5, n = 18), 140.39 ± 2.18 (2 σ, MSWD = 3.0, n = 20) and 140.58 ± 2.14 Ma (2 σ, MSWD = 2.0, n = 52), respectively. These ages for the four pegmatite zones are temporally consistent with a syngenetic origin for the magmatic sequence of biotite-, two-mica- and MM and the pegmatite system and rare-metal (Li-Nb-Ta-Rb-(Cs)-(Be)) mineralization. The Sm-Nd isotopic analyses of the unaltered monazite and cheralite from the MM and four pegmatite zones yield similar initial Nd isotopic composition with εNd(t) = −9.9 to −7.9, indicating an identical single-source region (i.e. the Neoproterozoic South China lower crust). The Sm/Nd ratios display a gradual decrease across the four pegmatite zones from the unaltered K-zone monazite to Na-Li-zone cheralite, i.e. 0.39–0.63 (avg. = 0.43) for K-zone, 0.29–0.35 (avg. = 0.31) for K-Na-zone, 0.26–0.30 (avg. = 0.28) for Na-zone and 0.21–0.27 (avg. = 0.24) for Na-Li-zone. Such progressive variations suggest their derivation from the same parental magma, which experienced varying degrees of fractionation before the extraction of pegmatitic melts. Comprehensive monazite and cheralite geochemistry, as well as in situ U-Th-Pb and Sm-Nd isotopic results indicate that Rayleigh-type fractional crystallization controls the mineralogical and geochemical evolution from a chemically zoned granite source.
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