“…Four relevant scenarios are interpreted in K 2 O-H 2 O space (arrows in Figure 9a; Blundy & Cashman, 2005): (i) melt H 2 O and an incompatible element increase in tandem, dictating that the melt is experiencing H 2 O-undersaturated, isobaric crystallization; (ii) melt H 2 O remains constant whilst an incompatible element increases, interpreted as isobaric, H 2 O-saturated crystallization; (iii) melt H 2 O decreases as an incompatible element increases, reflecting a suite of H 2 O-saturated samples derived from different amounts of crystallization at different crustal pressures that is analogous to decompression-driven crystallization; (iv) syneruptive degassing, during which a melt undergoes near isothermal decompression. In the Lesser Antilles, the sub-alkalic magmas (Macdonald et al, 2000;Metcalfe et al, 2023) and low-K 2 O cumulates (Brown et al, 2021;Camejo-Harry et al, 2018;Cooper et al, 2016;Melekhova et al, 2017Melekhova et al, , 2019Melekhova et al, , 2022Stamper et al, 2014;Tollan et al, 2012) mean that K is demonstrably an incompatible element such that increasing WR K 2 O is a crystallization proxy. The plagioclase-rich Lesser Antilles cumulates along with additional anhydrous and low-K 2 O cocrystallizing phases such as pyroxene and olivine result in bulk partition coefficients for K and H 2 O that are much less than one.…”