Two main REE-bearing minerals are identified: xenotime [(Y,REE)PO4], which is HREE selective; and subordinate florencite [(REEAl3(PO4)2(OH)6] which is LREE selective. Two morphological generations of xenotime are recognised; compositions are however consistent. Xenotime contains Dy (up to 6.5 wt. % ), Er (up to 4.35 wt. % ), Gd (up to 7.56 wt. % ), Yb (up to 4.65 wt. % ) and Y (up to 43.3 wt. % ). Laser Ablation ICP-MS element mapping revealed a subtle compositional zoning in some xenotime grains. LREE appear concentrated in the grain cores or closest to the initial point of growth whereas HREE, particularly Tm, Yb and Lu, are highest at the outer margins of the grains. The HREE enrichment at the outer margins is mimicked by As, Sc, V, Sr, U, Th and radiogenic Pb. Florencite is commonly zoned and contains Ce (up to 11.54 wt. % ), Nd (up to 10.05 wt. % ) and La (up to 5.40 wt. % ) and is also notably enriched in Sr (up to 11.63 wt. % ) and Ca. Zircon (which is not a significant contributor of REEs overall due to its low abundance in the rocks) is also enriched in REE (up to 13 wt. % ¦²REE) and is the principal host of Sc (up to 0.8 wt. % ).
Early, coarse euhedral xenotime has undergone fracturing, partial breakdown and replacement by florencite. Second generation xenotime occurs as abundant small blades commonly associated with acicular hematite. Mineralization is attributed to percolation of a volatile-rich, acidic fluid, possibly granite-derived, through porous arkose units. Late hematite may suggest mixing with meteoric water and subsequent oxidation. Field observations suggest that faults acted as fluid conduits and that brecciation, possibly associated with release of volatiles from the fluid, occurred along these faults.
The data provide valuable constraints on chemical compositional trends in xenotime and coexisting minerals. Given the current surge in exploration for REE, this information will assist in the development of exploration models for comparable terranes.