Monazite-(Ce) and xenotime-(Y) microinclusions in fluorapatite of the pegmatites from the Volta Grande Mine, Minas Gerais State, southeast Brazil, as witnesses of the dissolution-reprecipitation process
Monazite-(Ce) and xenotime-(Y) microinclusions in fluorapatite of the pegmatites from the Volta Grande Mine, Minas Gerais State, southeast Brazil, as witnesses of the dissolution-reprecipitation process
Mineralogical Magazine (August 2019) 83 (4): 595-606
- alkali metals
- Brazil
- cathodoluminescence
- cerium
- electron microscopy data
- fluid inclusions
- fluorapatite
- formula
- gold ores
- granites
- igneous rocks
- inclusions
- lithium
- metal ores
- metals
- Minas Gerais Brazil
- mineral assemblages
- mineral inclusions
- monazite
- pegmatite
- phosphates
- plutonic rocks
- precipitation
- rare earths
- SEM data
- solution
- South America
- trace elements
- xenotime
- yttrium
- Volte Grande Mine
Fluorapatite with monazite-(Ce) and xenotime-(Y) microinclusions occurs in the lithium-caesium-tantalum pegmatite body A of the Volta Grande mine, Minas Gerais state, Southeast Brazil. The fluorapatite displays faint zoning, detected mainly by cathodoluminescence. Electron probe and laser ablation analyses indicate that zoning in the fluorapatite corresponds to variation in Mn and rare-earth element (REE) content. Such compositional variation is attributed to partial removal of the REE from the fluorapatite structure during a dissolution-reprecipitation process, forming monazite-(Ce) and xenotime-(Y) microinclusions in the REE-depleted zones of the fluorapatite. These inclusions exhibit an inherited geochemical signature, manifested by low Th and U concentrations when compared to monazite and xenotime crystallised from melts. Rhodochrosite and calcite inclusions are also associated with monazite-(Ce) and xenotime-(Y) and are probably products of the same process, recycling Ca, Mn, and CO (sub 3) (super 2-) from the fluorapatite through the following reaction: [Ca (sub (5-2a-b-1/2x)) , Na (sub a) , (Y+ REE) (sub a) , Mn (sub b) ][(PO (sub 4) ) (sub 3-x) (CO (sub 3) ) (sub x) (F)] + Fluid[a(2Ca (super 2+) +P (super 5+) ) + (x-b)(Ca (super 2+) )+H (sub 2) O)] --> [Ca (sub 5) (PO (sub 4) ) (sub 3) (F,OH)] + a[(Y+REE)PO (sub 4) ] + b[Mn(CO (sub 3) )] + (x-b)[Ca(CO (sub 3) )] + Fluid a[Na (super +) ]. On the basis of new fluid-inclusion analyses, we propose that a hot (T>204.5 degrees C), salty (16 wt.% eq. NaCl, attributed to LiCl), hydrous fluid mediated the dissolution-reprecipitation of the fluorapatite. This fluid corresponds to similarly described Li-rich fluids which were suggested to have re-equilibrated the mineralogical assemblage at the Volta Grande mine.