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The 2011–2012 eruption at Cordón Caulle, Chile offers an exceptional opportunity to investigate topographic evolution of a laccolith, lava flows, and tephra during and after rhyolitic eruptions using satellite TanDEM-X and Plèiades data. We find distinct phases: rapid surface uplift from the laccolith and tephra (June–August 2011) and lava (June 2011–March 2012), followed by a reduction in the elevation of the laccolith and tephra (up to 19 m yr−1) until February 2013, and slower subsidence of all deposits until 2019 (the most recent data). The spatial distribution of subsidence-to-uplift ratios shows different volcanic and geomorphological processes occurring (degassing, cooling, crystallization, lateral movement, compaction, erosion). Pre-eruptive river channels showed elevation increases of up to 10–50 m due to tephra deposition, but this tephra was largely removed within three to four years. This research shows the potential of repeating high-resolution remote sensing elevation data to elucidate volcanic landscape evolution and yields insights into the co- and post-eruptive evolution of deposits.

 

When magmas erupt at the surface, they may have undergone many changes since their inception. While olivine drives some of these changes through crystallization and fractionation, it also records the magma evolution via mineral chemistry and by trapping mineral and melt inclusions. Olivine is an effective recorder of intensive parameters, such as temperature and melt composition, and provides an outstanding petrological tool for constraining dynamic processes, such as ascent, mixing, and cooling. Olivine sheds light on magmatic puzzles that involve both mafic and more evolved magmas, with protracted and complex magmatic histories that often obscure earlier and deeper processes. This contribution summarizes the current state of how olivine helps reconstruct source-to-surface magma assembly through its chemistry, inclusions, and textures.

 

In some ways, olivine has driven the evolution of the Solar System and likely beyond. As one of the earliest-crystallizing silicate minerals, olivine controls the initial chemical evolution of planet-wide magma oceans and individual lava flows alike. In solid aggregate form, it controls and records deformation of the mantle and smaller-scale intrusive complexes. The components of its crystal structure are mobile at high temperatures and their migration can be used to explore the timing of magmatic events. During chemical weathering, these olivine crystals capture carbon dioxide from the atmosphere as secondary minerals are formed. All of these processes take place not only on Earth, but also on other planetary bodies, making olivine ideally suited to shed light on both primordial planet-building processes and current-day volcanism and surface processes.

 

The 2011–2012 eruption at Cordón Caulle in Chile produced crystal-poor rhyolitic magma with crystal-rich mafic enclaves whose interstitial glass is of identical composition to the host rhyolite. Eruptible rhyolites are thought to be genetically associated with crystal-rich magma mushes, and the enclaves within the Cordón Caulle rhyolite support the existence of a magma mush from which the erupted magma was derived. Moreover, towards the end of the 2011–2012 eruption, subsidence gave way to inflation that has on average been continuous through at least 2020. We hypothesize that magma segregation from a crystal mush could be the source of the observed inflation. Conceptually, magma withdrawal from a crystal-poor rhyolite reservoir caused its depressurization, which could have led to upward flow of interstitial melt within an underlying crystal mush, causing a new batch of magma to segregate and partially recharge the crystal-poor rhyolite body. Because the compressibility of the crystalline matrix of the mush is expected to be lower than that of the interstitial melt, which likely contains some fraction of volatile bubbles, this redistribution of melt would result in a net increase in volume of the system and in the observed inflation. We use numerical modelling of subsurface magma flow and storage to show under which conditions such a scenario is supported by geodetic and petrologic observations.

 

Abstract Two distinct types of rare crystal-rich mafic enclaves have been identified in the rhyolite lava flow from the 2011–12 Cordón Caulle eruption (Southern Andean Volcanic Zone, SVZ). The majority of mafic enclaves are coarsely crystalline with interlocking olivine-clinopyroxene-plagioclase textures and irregular shaped vesicles filling the crystal framework. These enclaves are interpreted as pieces of crystal-rich magma mush underlying a crystal-poor rhyolitic magma body that has fed recent silicic eruptions at Cordón Caulle. A second type of porphyritic enclaves, with restricted mineral chemistry and spherical vesicles, represents small-volume injections into the rhyolite magma. Both types of enclaves are basaltic end-members (up to 9.3 wt% MgO and 50–53 wt% SiO 2 ) in comparison to enclaves erupted globally. The Cordón Caulle enclaves also have one of the largest compositional gaps on record between the basaltic enclaves and the rhyolite host at 17 wt% SiO 2 . Interstitial melt in the coarsely-crystalline enclaves is compositionally identical to their rhyolitic host, suggesting that the crystal-poor rhyolite magma was derived directly from the underlying basaltic magma mush through efficient melt extraction. We suggest the 2011–12 rhyolitic eruption was generated from a primitive basaltic crystal-rich mush that short-circuited the typical full range of magmatic differentiation in a single step. 

The conditions under which halogens partition in favor of an exsolved fluid relative to the coexisting melt are key for understanding many magmatic processes, including volcanic degassing, evolution of crustal melt bodies, and ore formation. We report new F, Cl, and Br fluid/melt partition coefficients for intermediate to silicic melts, for which F and Br data are particularly lacking; and for varying CO2-H2O contents to assess the effects of changing fluid composition (XH2O) on Br fluid/melt partitioning for the first time. The experiments were conducted at pressures 50–120 MPa, temperatures 800–1100 °C, and volatile compositions [molar XH2O = H2O/(H2O +CO2)] of 0.55 to 1, with redox conditions around the Nickel-Nickel Oxygen buffer (fO2 ≈ NNO). Experiments were not doped with Cl, Br, or F and were conducted on natural crystal-bearing volcanic products at conditions close to their respective pre-eruptive state. The experiments therefore provide realistic constraints on halogen partitioning at naturally occurring, brine-undersaturated conditions. Measurements of Br, Cl, and F were made by Secondary Ion Mass Spectrometry (SIMS) on 13 experimental glass products spanning andesite to rhyolitic compositions, together with their natural starting materials from Kelud volcano, Indonesia, and Quizapu volcano, Chile. Fluid compositions were constrained by mass balance. Average bulk halogen fluid/melt partition coefficients and standard deviations are: DClfluid/melt = 3.4 (±3.7 1 s.d.), DFfluid/melt = 1.7 (±1.7), and DBrfluid/melt = 7.1 (±6.4) for the Kelud starting material (bulk basaltic andesite), and DClfluid/melt = 11.1 (±3.5), DFfluid/melt = 0.8 (±0.8), and DBrfluid/melt = 31.3 (±20.9) for Quizapu starting material (bulk dacite). The large range in average partition coefficients is a product of changing XH2O, pressure and temperature. In agreement with studies on synthetic melts, our data show an exponential increase of halogen Dfluid/melt with increasing ionic radius, with partitioning behavior controlled by melt composition according to the nature of the complexes forming in the melt (e.g., SiF4, NaCl, KBr). The fundamental chemistry of the different halogens (differing ionic size and electronegativities) controls the way in which partitioning responds to changes in melt composition and other variables. Experimental results confirm that more Cl partitions into the fluid at higher bulk Cl contents, higher melt Na, higher fluid XH2O ratios, and lower temperatures. Bromine shows similar behavior, though it seems to be more sensitive to temperature and less sensitive to Na content and XH2O. In contrast, F partitioning into the fluid increases as the melt silica content decreases (from 72 to 56 wt% SiO2), which we attribute to the lower abundance of Si available to form F complexes in the melt. These new data provide more insights into the conditions and processes that control halogen degassing from magmas and may help to inform the collection and interpretation of melt inclusions and volcano gas data.

 

Abstract Primitive olivines from the monogenetic cones Los Hornitos, Central-South Andes, preserve dendritic, skeletal, and polyhedral growth textures. Consecutive stages of textural maturation occur along compositional gradients where high Fo–Ni cores of polyhedral olivines (Fo 92.5 , Ni ~3500 ppm) contrast with the composition of dendritic olivines (Fo < 91.5, Ni < 3000 ppm), indicating sequential nucleation. Here we present a new growth model for oscillatory Fo–Ni olivine zoning that contrasts with the standard interpretation of continuous, sequential core-to-rim growth. Olivine grows rapidly via concentric addition of open-structured crystal frames, leaving behind compositional boundary layers that subsequently fill-in with Fo–Ni-depleted olivine, causing reversals. Elemental diffusion modeling reveals growth of individual crystal frames and eruption at the surface occurred over 3.5–40 days. Those timescales constrain magma ascent rates of 40–500 m/h (0.011 to 0.14 m/s) from the deep crust. Compared to ocean island basalts, where dendritic and skeletal olivines have been often described, magmas erupted at arc settings, experiencing storage and degassing, may lack such textures due to fundamentally different ascent histories. 

Abstract Volcán Quizapu, Chile, is an under-monitored volcano that was the site of two historical eruptions: an effusive eruption in 1846–1847 and a Plinian eruption in 1932, both of which discharged ∼5 km3 (dense rock equivalent) of lava and/or tephra. The majority of material erupted in both cases is trachydacite, nearly identical for each event. We present H2O-saturated, phase equilibrium experiments on this end-member dacite magma, using a pumice sample from the 1932 eruption as the main starting material. At an oxygen fugacity (fO2) of ∼NNO + 0·2 (where NNO is the nickel–nickel oxide buffer), the phase assemblage of An25–30 plagioclase + amphibole + orthopyroxene, without biotite, is stable at 865 ± 10 °C and 110 ± 20 MPa H2O pressure (PH2O), corresponding to ∼4 km depth. At these conditions, experiments also reproduce the quenched glass composition of the starting pumice. At slightly higher PH2O and below 860 °C, biotite joins the equilibrium assemblage. Because biotite is not part of the observed Quizapu phase assemblage, its presence places an upper limit on PH2O. At the determined storage PH2O of ∼110 MPa, H2O undersaturation of the magma with XH2Ofluid = 0·87 would align Ptotal to mineral-based geobarometry estimates of ∼130 MPa. However, XH2Ofluid < 1 is not required to reproduce the Quizapu dacite phase assemblage and compositions. A second suite of experiments at lower fO2 shows that the stability fields of the hydrous silicates (amphibole and biotite) are significantly restricted at NNO – 2 relative to NNO + 0·2. Additional observations of Quizapu lava and pumice samples support the existing hypothesis that rapid pre-eruptive heating drove the effusive 1846–1847 eruption, with important refinements. We demonstrate that microlites in the end-member dacite lavas are consistent with in situ crystallization (during ascent), rather than transfer from an andesite. In one end-member dacite lava, newly identified reverse zoning in orthopyroxene and incipient destabilization of amphibole are consistent with small degrees of heating. Our work articulates a clear direction for future Quizapu studies, which are warranted given the active nature of the Cerro Azul–Descabezado Grande volcanic axis.