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Magma mingling and mixing are common processes at basaltic volcanoes and play a fundamental role in magma petrogenesis and eruption dynamics. Mingling occurs most commonly when hot primitive magma is introduced into cooler magma. Here, we investigate a scenario whereby cool, partially degassed lava is drained back into a conduit, where it mingles with hotter, less degassed magma. The 1959 eruption of Kīlauea Iki, Hawaiʻi involved 16 high fountaining episodes. During each episode, fountains fed a lava lake in a pit crater, which then partially drained back into the conduit during and after each episode. We infer highly crystalline tachylite inclusions and streaks in the erupted crystal-poor scoria to be the result of the recycling of this drain-back lava. The crystal phases present are dendrites of plagioclase, augite and magnetite/ilmenite, at sizes of up to 10 μm. Host sideromelane glass contains 7–8 wt% MgO and the tachylite glass (up to 0.5% by area) contains 2.5–6 wt% MgO. The vesicle population in the tachylite is depleted in the smallest size classes (< 0.5 mm) and has overall lower vesicle number densities and a higher degree of vesicle coalescence than the sideromelane component. The tachylite exhibits increasingly complex ‘stretching and folding’ mingling textures through the episodes, with discrete blocky tachylite inclusions in episodes 1 and 3 giving way to complex, folded, thin filaments of tachylite in pyroclasts erupted in episodes 15 and 16. We calculate that a lava lake crust 8–35 cm thick may have formed in the repose times between episodes, and then foundered and been entrained into the conduit during drain-back. The recycled fragments of crust would have been reheated in the conduit, inducing glass devitrification and crystallisation of pyroxene, magnetite and plagioclase dendrites and eventually undergoing ductile flow as the temperature of the fragments approached the host magma temperature. We use simple models of magma mingling to establish that stretching and folding of recycled, ductile lava could involve thinning of the clasts by up to a factor of 10 during the timescale of the eruption, consistent with observations of streaks and filaments of tachylite erupted during episodes 15 and 16, which may have undergone multiple cycles of eruption, drain-back and reheating. 

Abstract Drilling related to development of the platinum-group element deposit of the J-M Reef of the Stillwater Complex returned samples of a rare chromitite seam between anorthosite and norite in a discordant anorthositic body. Plagioclase core An concentrations are marginally higher and modestly reversely zoned on the norite side (average Ancore = 83·8; average Ancore – Anrim = –1·1) as compared with the anorthosite side (average Ancore 82·5; average Ancore – Anrim = +1·0). The anorthosites are also characterized by a slightly smaller average plagioclase grain size than plagioclase in the norite (1·41 mm and 1·54 mm, respectively). The chromite can contain single and polyphase inclusions of orthopyroxene, plagioclase, amphibole, biotite and Cl-rich apatite. These and other compositional and textural features, as well as inference from other discordant anorthositic bodies in the Banded series, are all consistent with a chromatographic model of chromite precipitation at a reaction front as a norite protolith reacts with a Cl-rich aqueous fluid saturated in plagioclase alone. Chromitite seam formation is modeled using an infiltration metasomatic model, in which a fluid becomes progressively undersaturated in pyroxene as it rises into the hotter part of the crystal pile. As this pyroxene-undersaturated fluid moves through a noritic protolith, it dissolves the Cr-bearing orthopyroxene to produce an anorthosite. Chromite precipitates at the reaction front between the anorthosite and the norite owing to liberation of Mg and Cr from pyroxene. Continuous redissolution and reprecipitation of chromite occurs as the pyroxene dissolution front moves in the direction of fluid flow, collecting the Cr lost from the anorthosite. Owing to Cr dissolved mainly as a neutral divalent cation complex, CrCl(OH)0, in the solution, but incorporated as a trivalent cation in chromite, the required redox reaction can involve concurrent precipitation of sulfide with chromite. This mechanism differs from some recent models in that the anorthosites are themselves replacement bodies and are not original precipitates from a magma nor formed by loss of mafic material by partial melting. The results show the need for experimental mineral solubility data at T and P conditions appropriate to upper crustal mafic–ultramafic intrusions.