Utilising Y2O3, Sm2O3, LuPO4, and EuPO4 and a 2N NaOH solution, Y, Sm, Lu, and Eu are metasomatically incorporated into a natural, inclusion-free, almandine–pyrope garnet (Gore Mountain) at 900°C and 1000 MPa (sealed Pt capsule, CaF2 setup with graphite oven, piston cylinder press) via a coupled dissolution–reprecipitation process. Incorporation of Y+REE takes place via a series of coupled substitutions involving the dodecahedral site in garnet, i.e. VIII(Y,REE)3+ + IVAl3+ = VIII(Fe,Mg,Mn,Ca)2+ + IVSi4+; 2VIII(Y+REE)3+ + VIII□ = 3 VIII(Fe,Mg,Mn,Ca)2+; VIII(Y,REE)3+ + VIIINa+ = 2 VIII(Fe+Mg+Mn+Ca)2+; and VIII(Y,REE)3+ + VI(Fe,Mg)2+ = VIII(Fe,Mg)2+ + VI(Al,Fe)3+. In comparison to the slower, solid-state diffusion of Y+REE in garnet under high-grade (700–900°C; 500–1000 MPa) conditions, the results from these experiments indicate that efficient, rapid incorporation (or depletion) of Y+REE in garnet could occur by fluid-aided coupled dissolution–reprecipitation during metamorphism. The results from these experiments have important implications with regard to the effect of metasomatic/metamorphic events on Lu-Hf and Sm-Nd age determination in garnet, the use of Y exchange between xenotime and garnet as a geothermometer in metamorphic rocks, and the effect of metamorphic fluids on the coupling between the Y and δ18O signal in garnets.