Tourmaline bearing leucogranite occurs as a pluton with pegmatitic veins intruding the Archaean granodiorite in the Bastipadu area, Kurnool district of Andhra Pradesh. We present field and petrographic relations, mineral chemistry and geochemical data for the leucogranite. It is essentially a two-mica granite, composed of quartz, perthite, microcline, albite, tourmaline and muscovite alongwith minor biotite and titanite. The euhedral tourmalines are regularly distributed in the rock. The geochemical studies show that the leucogranite is calc-alkaline, peraluminous to metaluminous which formed in a syn-collisional to volcanic arc-related setting. It displays strong ‘S’ type signatures with high K/Na ratios, moderately fractionated light rare earth elements, relatively flat heavy rare earth elements with $\rm{[Ce/Yb]_{N}} \leq 27.8$ and a strong negative Eu anomaly. The geochemical characteristics indicate that the leucogranite melt might have been generated from partial melting of metasediments. Electron probe microanalyser data show the presence of alkali group tourmaline in leucogranite represented by schorl and dravite. Tourmaline compositions plot in the Li-poor granitoids and associated pegmatites and aplites and metapelites/metasammites fields. Partial melting of boron-enriched source rocks is linked with the development of tourmalines in the leucogranite.

Carbonate hosted intermetallic compound in the Umarvaniyan area is localized within the intensively sheared (mylonitised) dolomite in a NW–SE shear zone ($\sim$15 km), belongs to Salumber Ghatol metallogenic belt, in Debari Group of Aravalli Craton, Rajasthan, India. It is characterized by extensive silicification and ferruginisation with hematite, goethite, magnetite and native gold specks. The intermetallic compound within the dolomite is composed of varying proportion of Cu–Zn–Ni–Os–Fe which has been detected by electron probe microanalysis (EPMA) study. The EMPA (WDS) results of the intermetallic compounds also reveal occurrences of intermetallic compounds of Cu–Zn–Ni–Os–Fe and native Au. The occurrence of these non-separable compounds is probably because these metals were formed at very high temperatures and in reducing condition during the evolving shear with low oxygen and low sulfur fugacity. The fast cooling effect thereafter probably made the geochemical environment least conducive for reaction between Cu/Zn/Ni and sulphur or oxygen.