Pyrochlore-group minerals are common accessory rare-metal bearing minerals in the calcite and ankerite carbonatites of the Amba Dongar complex (India). Pyrochlore from the Amba Dongar carbonatites differs from that in other Indian complexes in Ta, Zr, Ti, rare earth element (REE) and Pb contents, but is similar with respect to Ca, Ba and Sr abundances. The evolution of pyrochlore composition was studied to understand the alteration processes and the formation of late-stage pyrochlores enriched in REE and Pb. The early magmatic pyrochlore are calcio- and niobium-dominant types and were replaced by secondary cation-deficient varieties as a consequence of the action of hydrothermal fluids and supergene weathering. These processes produce changes mainly at the A site, rarely at the B site, and the original F is replaced by OH– groups. Calcium and Na can be extracted from the structure at the alteration stage and charge balance is achieved by the introduction of REE, Th, U, Ba or Sr. At the latest supergene stages, marginal and fractured zones of pyrochlore grains are altered to Pb-rich, Si-rich and cation-deficient hydrated varieties. The magmatic pyrochlore was crystallised in a highly alkaline environment at a high activity of Ca and at temperatures near 600°C, the alteration of pyrochlore began in a hydrothermal environment at temperatures below 350°C. The major compositional changes that are associated with the alteration are summarised by the following reactions: Ca2+ + Nb5+→ REE3+ + Ti4+; Nb5+ + Fe3+ → Ti4+ + Zr4+; and 2Nb5+ + Ca2+ → Ti4+ + Si4+ + U4+.

Recent water-undersaturated phase equilibrium data on the subsystems of the granite-H2O system have provided important new constraints on the topology of the cotectic surfaces and hence on the compositional evolution of felsic magmas. The effect of water on phase relations can be deduced from a comparison of anhydrous and H2O-saturated data or from data obtained in the presence of a CO2-bearing fluid. However, although new experimental evidence indicates that the silica enrichment of evolving H2O-undersaturated, H2O-unbuffered melts during the co-precipitation of quartz and feldspar is as previously thought for orthoclase-rich compositions, it suggests that such a trend is considerably less for Ab-rich compositions. For water-poor trachytic melts, the newly recognised strong destabilisation of the sanidine melt component relative to the anorthite melt component with increasing water content indicates that the co-precipitation of two feldspars will result in saturation of the melt with ternary alkali feldspar at an earlier stage (i.e. higher melt anorthite content) than previously thought. This, in turn, implies that the melt differentiation path will have a greater component of anorthite depletion during the equilibrium co-precipitation of ternary feldspars and that the melt will remain in the peritectic region of the two feldspar plus liquid surface over a greater interval of crystallisation, thereby enhancing the possibility that the resoption of plagioclase during the early stages of equilibrium with alkali feldspar may go to completion. Comparison of CO2-free and CO2-bearing haplogranitic phase equilibrium data suggests that CO2 may be playing an independent part in the modification of phase equilibria and may induce a significant destabilisation of the orthoclase melt component.