Comparison of Fused Glass Beads and Pressed Powder Pellets for the Quantitative Measurement of Al,Fe, Si and Ti in Bauxite by Laser‐Induced Breakdown Spectroscopy

Due to matrix interference and sample particle size effects, some of the most important and difficult issues in laser‐induced breakdown spectroscopy (LIBS) analysis are the calibration and quantitative measurement of a complex matrix. This study proposes the use of borate fusion as an alternative sample preparation procedure for the quantitative measurement of Al, Fe, Si and Ti in bauxite by LIBS. Analytical calibration curves were made using bauxite certified reference materials (CRM), and the precision and accuracy of the methods were evaluated by analysing an additional bauxite CRM, using two different approaches: pressed powder pellets and fused glass beads. The borate fusion method was the most suitable sample preparation technique, since particle size effects and matrix interference could be minimised, obtaining better linearity on the analytical calibration curves (r²), and more accurate and more precise results for bauxite analysis.     

Monazite behaviour during isothermal decompression in pelitic granulites: a case study from Dinggye,Tibetan Himalaya

Monazite is a key accessory mineral for metamorphic geochronology, but interpretation of its complex chemical and age zoning acquired during high-temperature metamorphism and anatexis remains a challenge. We investigate the petrology, pressure–temperature and timing of metamorphism in pelitic and psammitic granulites that contain monazite from the Greater Himalayan Crystalline Complex (GHC) in Dinggye, southern Tibet. These rocks underwent isothermal decompression from pressure of >10 kbar to ~5 kbar at temperatures of 750–830 °C, and recorded three metamorphic stages at kyanite (M₁), sillimanite (M₂) and cordierite-spinel grade (M₃). Monazite and zircon crystals were dated by microbeam techniques either as grain separates or in thin sections. U–Th–Pb ages are linked to specific conditions of mineral growth on the basis of zoning patterns, trace element signatures, index mineral inclusions (melt inclusions, sillimanite and K-feldspar) in dated domains and textural relationships with co-existing minerals. The results show that inherited domains (500–400 Ma) are preserved in monazite even at granulite-facies conditions. Few monazites or zircon yield ages related to the M₁-stage (~30–29 Ma), possibly corresponding to prograde melting by muscovite dehydration. During the early stage of isothermal decompression, inherited or prograde monazites in most samples were dissolved in the melt produced by biotite dehydration-melting. Most monazite grains crystallized from melt toward the end of decompression (M₃-stage, 21–19 Ma) and are chemically related to garnet breakdown reactions. Another peak of monazite growth occurred at final melt crystallization (~15 Ma), and these monazite grains are unzoned and are homogeneous in composition. In a regional context, our pressure–temperature–time data constrains peak high-pressure metamorphism within the GHC to ~30–29 Ma in Dinggye Himalaya. Our results are in line with a melt-assisted exhumation of the GHC rocks.