Effect of water on the glass transition of a potassium-magnesium carbonate melt.

Calorimetric measurements of the glass transition temperatures (Tg) of hydrous carbonate melts are reported on a near-eutectic composition of 55 mol% K2CO3 - 45 mol% MgCO3 with up to 42 mol% bulk H2O dissolved in the carbonate melt. Hydrous melts were quenched from 750°C to transparent and crystal-free glasses and were subsequently analysed for water content before and after measuring Tg by high-sensitivity differential scanning calorimetry. The glass transition and limited fictive temperatures as a function of the water content were determined at 10 K/min cooling/heating rates resulting in Tg ranging from 245°C at nominally anhydrous conditions to 83°C in the presence of 42 mol% H2O in the glass. Through a generalized Gordon-Taylor analysis, the factors k (7.27), k0 (3.2) and the interaction parameter Ax (0.49) were derived. The limited fictive temperature of a hypothetically, zero water containing 55 mol% K2CO3 - 45 mol% MgCO3 glass is 232 ± 5°C (505 K). The high value of the interaction parameter A indicates strong specific molecular interactions between water and the carbonates in the glassy state and a large decrease in the excess enthalpy of mixing during the conversion of the glassy into the liquid state at the glass transition. This article is part of the theme issue 'Exploring the length scales, timescales and chemistry of challenging materials (Part 1)'.

Glass transition temperatures and crystallization kinetics of a synthetic, anhydrous, amorphous calcium-magnesium carbonate.

We report the first calorimetric observations of glass transition temperatures and crystallization rates of anhydrous, amorphous calcium-magnesium carbonate using fast scanning differential scanning calorimetry. Hydrous amorphous Ca0.95Mg0.05CO3 · 0.5H2O (ACMC) solid was precipitated from a MgCl2-NaHCO3 buffered solution, separated from the supernatant, and freeze-dried. An aliquot of the freeze-dried samples was additionally dried at 250°C for up to 6 h in a furnace and in a high-purity N2 atmosphere to produce anhydrous ACMC. The glass transition temperature of the anhydrous Ca0.95Mg0.05CO3 was determined by applying different heating rates (1000-6000 K s-1) and correcting for thermal lag to be 376°C and the relaxational heat capacity was determined to be Cp = 0.16 J/(g K). Additionally, the heating rate dependence of the temperature that is associated with the corrected crystallization peaks is used to determine the activation energy of crystallization to be 275 kJ mol-1. A high-resolution transmission electron microscopy study on the hydrous and anhydrous samples provided further constraints on their compositional and structural states. This article is part of the theme issue 'Exploring the length scales, timescales and chemistry of challenging materials (Part 1)'.

Bubble rise in molten glasses and silicate melts during heating and cooling cycles.

The Hadamard-Rybczynski equation describes the steady-state buoyant rise velocity of an unconfined spherical bubble in a viscous liquid. This solution has been experimentally validated for the case where the liquid viscosity is held constant. Here, we extend this result for non-isothermal conditions, by developing a solution for bubble position in which we account for the time-dependent liquid viscosity, liquid and gas densities, and bubble radius. We validate this solution using experiments in which spherical bubbles are created in a molten silicate liquid by cutting gas cavities into glass sheets, which are stacked, then heated through the glass transition interval. The bubble-bearing liquid, which has a strongly temperature-dependent viscosity, is subjected to various heating and cooling programs such that the bubble rise velocity varies through the experiment. We find that our predictions match the final observed position of the bubble measured in blocks of cooled glass to within the experimental uncertainty, even after the application of a complex temperature-time pathway. We explore applications of this solution for industrial, artistic, and natural volcanological applied problems.

Thermal vesiculation during volcanic eruptions.

Terrestrial volcanic eruptions are the consequence of magmas ascending to the surface of the Earth. This ascent is driven by buoyancy forces, which are enhanced by bubble nucleation and growth (vesiculation) that reduce the density of magma. The development of vesicularity also greatly reduces the 'strength' of magma, a material parameter controlling fragmentation and thus the explosive potential of the liquid rock. The development of vesicularity in magmas has until now been viewed (both thermodynamically and kinetically) in terms of the pressure dependence of the solubility of water in the magma, and its role in driving gas saturation, exsolution and expansion during decompression. In contrast, the possible effects of the well documented negative temperature dependence of solubility of water in magma has largely been ignored. Recently, petrological constraints have demonstrated that considerable heating of magma may indeed be a common result of the latent heat of crystallization as well as viscous and frictional heating in areas of strain localization. Here we present field and experimental observations of magma vesiculation and fragmentation resulting from heating (rather than decompression). Textural analysis of volcanic ash from Santiaguito volcano in Guatemala reveals the presence of chemically heterogeneous filaments hosting micrometre-scale vesicles. The textures mirror those developed by disequilibrium melting induced via rapid heating during fault friction experiments, demonstrating that friction can generate sufficient heat to induce melting and vesiculation of hydrated silicic magma. Consideration of the experimentally determined temperature and pressure dependence of water solubility in magma reveals that, for many ascent paths, exsolution may be more efficiently achieved by heating than by decompression. We conclude that the thermal path experienced by magma during ascent strongly controls degassing, vesiculation, magma strength and the effusive-explosive transition in volcanic eruptions.

Assessment of the potential for in-plume sulphur dioxide gas-ash interactions to influence the respiratory toxicity of volcanic ash.

BACKGROUND: Volcanic plumes are complex environments composed of gases and ash particles, where chemical and physical processes occur at different temperature and compositional regimes. Commonly, soluble sulphate- and chloride-bearing salts are formed on ash as gases interact with ash surfaces. Exposure to respirable volcanic ash following an eruption is potentially a significant health concern. The impact of such gas-ash interactions on ash toxicity is wholly un-investigated. Here, we study, for the first time, whether the interaction of volcanic particles with sulphur dioxide (SO2) gas, and the resulting presence of sulphate salt deposits on particle surfaces, influences toxicity to the respiratory system, using an advanced in vitro approach. METHODS: To emplace surface sulphate salts on particles, via replication of the physicochemical reactions that occur between pristine ash surfaces and volcanic gas, analogue substrates (powdered synthetic volcanic glass and natural pumice) were exposed to SO2 at 500 °C, in a novel Advanced Gas-Ash Reactor, resulting in salt-laden particles. The solubility of surface salt deposits was then assessed by leaching in water and geochemical modelling. A human multicellular lung model was exposed to aerosolised salt-laden and pristine (salt-free) particles, and incubated for 24 h. Cell cultures were subsequently assessed for biological endpoints, including cytotoxicity (lactate dehydrogenase release), oxidative stress (oxidative stress-related gene expression; heme oxygenase 1 and NAD(P)H dehydrogenase [quinone] 1) and its (pro-)inflammatory response (tumour necrosis factor α, interleukin 8 and interleukin 1ß at gene and protein levels). RESULTS: In the lung cell model no significant effects were observed between the pristine and SO2-exposed particles, indicating that the surface salt deposits, and the underlying alterations to the substrate, do not cause acute adverse effects in vitro. Based on the leachate data, the majority of the sulphate salts from the ash surfaces are likely to dissolve in the lungs prior to cellular uptake. CONCLUSIONS: The findings of this study indicate that interaction of volcanic ash with SO2 during ash generation and transport does not significantly affect the respiratory toxicity of volcanic ash in vitro. Therefore, sulphate salts are unlikely a dominant factor controlling variability in in vitro toxicity assessments observed during previous eruption response efforts.

Kimberlite ascent by assimilation-fuelled buoyancy.

Kimberlite magmas have the deepest origin of all terrestrial magmas and are exclusively associated with cratons. During ascent, they travel through about 150 kilometres of cratonic mantle lithosphere and entrain seemingly prohibitive loads (more than 25 per cent by volume) of mantle-derived xenoliths and xenocrysts (including diamond). Kimberlite magmas also reputedly have higher ascent rates than other xenolith-bearing magmas. Exsolution of dissolved volatiles (carbon dioxide and water) is thought to be essential to provide sufficient buoyancy for the rapid ascent of these dense, crystal-rich magmas. The cause and nature of such exsolution, however, remains elusive and is rarely specified. Here we use a series of high-temperature experiments to demonstrate a mechanism for the spontaneous, efficient and continuous production of this volatile phase. This mechanism requires parental melts of kimberlite to originate as carbonatite-like melts. In transit through the mantle lithosphere, these silica-undersaturated melts assimilate mantle minerals, especially orthopyroxene, driving the melt to more silicic compositions, and causing a marked drop in carbon dioxide solubility. The solubility drop manifests itself immediately in a continuous and vigorous exsolution of a fluid phase, thereby reducing magma density, increasing buoyancy, and driving the rapid and accelerating ascent of the increasingly kimberlitic magma. Our model provides an explanation for continuous ascent of magmas laden with high volumes of dense mantle cargo, an explanation for the chemical diversity of kimberlite, and a connection between kimberlites and cratons.

Fault rheology beyond frictional melting.

During earthquakes, comminution and frictional heating both contribute to the dissipation of stored energy. With sufficient dissipative heating, melting processes can ensue, yielding the production of frictional melts or "pseudotachylytes." It is commonly assumed that the Newtonian viscosities of such melts control subsequent fault slip resistance. Rock melts, however, are viscoelastic bodies, and, at high strain rates, they exhibit evidence of a glass transition. Here, we present the results of high-velocity friction experiments on a well-characterized melt that demonstrate how slip in melt-bearing faults can be governed by brittle fragmentation phenomena encountered at the glass transition. Slip analysis using models that incorporate viscoelastic responses indicates that even in the presence of melt, slip persists in the solid state until sufficient heat is generated to reduce the viscosity and allow remobilization in the liquid state. Where a rock is present next to the melt, we note that wear of the crystalline wall rock by liquid fragmentation and agglutination also contributes to the brittle component of these experimentally generated pseudotachylytes. We conclude that in the case of pseudotachylyte generation during an earthquake, slip even beyond the onset of frictional melting is not controlled merely by viscosity but rather by an interplay of viscoelastic forces around the glass transition, which involves a response in the brittle/solid regime of these rock melts. We warn of the inadequacy of simple Newtonian viscous analyses and call for the application of more realistic rheological interpretation of pseudotachylyte-bearing fault systems in the evaluation and prediction of their slip dynamics.

Magma mixing induced by particle settling.

A time series of experiments at high temperature have been performed to investigate the influence of particle settling on magma mixing. A natural rhyolite glass was held above a natural basalt glass in a platinum crucible. After melting of the glasses at superliquidus temperatures, a platinum sphere was placed on the upper surface of the rhyolitic melt and sank into the experimental column (rhyolitic melt above basaltic melt). Upon falling through the rhyolitic-basaltic melt interface, the Pt sphere entrained a filament of rhyolitic melt in its further fall. The quenched products of the experiments were imaged using X-ray microCT methods. The images of our time series of experiments document the formation of a rhyolite filament as it is entrained into the underlying basalt by the falling platinum sphere. When the Pt particle reached the bottom of the crucible, the entrained rhyolitic filament started to ascend buoyantly up to the initial rhyolitic-basaltic interface. This generated a significant thickness increase of a comingled "melange" layer at the interface due to "liquid rope coiling" and piling up of the filament. As a consequence, the basalt/rhyolite interface was greatly enlarged and diffusive hybridisation greatly accelerated. Further, bubbles, originating at the interface, are observed to have risen into the overlying rhyolite dragging basalt filaments with them. Upon crossing the basalt/rhyolite interface, the bubbles have non-spherical shapes as they adapt to the differing surface tensions of basaltic and rhyolitic melts. Major element profiles, measured across the rhyolite filaments, exhibit asymmetrical shapes from the rhyolite into the basalt. Na and Ti reveal uphill diffusion from the rhyolite towards the interface in the filament cross sections. These results reveal the potential qualitative complexity of the mingling process between rhyolitic and basaltic magmas in the presence of sinking crystals. They imply that crystal-rich magma mingling may be expected to be accelerated with respect to crystal-poor systems. We urge the further fluid dynamic analysis of these phenomena, obtainable for the first time using detailed tomographic imaging.

Rapid ascent of rhyolitic magma at Chaitén volcano, Chile.

Rhyolite magma has fuelled some of the Earth's largest explosive volcanic eruptions. Our understanding of these events is incomplete, however, owing to the previous lack of directly observed eruptions. Chaitén volcano, in Chile's northern Patagonia, erupted rhyolite magma unexpectedly and explosively on 1 May 2008 (ref. 2). Chaitén residents felt earthquakes about 24 hours before ash fell in their town and the eruption escalated into a Plinian column. Although such brief seismic forewarning of a major explosive basaltic eruption has been documented, it is unprecedented for silicic magmas. As precursory volcanic unrest relates to magma migration from the storage region to the surface, the very short pre-eruptive warning at Chaitén probably reflects very rapid magma ascent through the sub-volcanic system. Here we present petrological and experimental data that indicate that the hydrous rhyolite magma at Chaitén ascended very rapidly, with velocities of the order of one metre per second. Such rapid ascent implies a transit time from storage depths greater than five kilometres to the near surface in about four hours. This result has implications for hazard mitigation because the rapidity of ascending rhyolite means that future eruptions may provide little warning.

Oxide nanolitisation-induced melt iron extraction causes viscosity jumps and enhanced explosivity in silicic magma.

Explosivity in erupting volcanoes is controlled by the degassing dynamics and the viscosity of the ascending magma in the conduit. Magma crystallisation enhances both heterogeneous bubble nucleation and increases in magma bulk viscosity. Nanolite crystallisation has been suggested to enhance such processes too, but in a noticeably higher extent. Yet the precise causes of the resultant strong viscosity increase remain unclear. Here we report experimental results for rapid nanolite crystallisation in natural silicic magma and the extent of the subsequent viscosity increase. Nanolite-free and nanolite-bearing rhyolite magmas were subjected to heat treatments, where magmas crystallised or re-crystallised oxide nanolites depending on their initial state, showing an increase of one order of magnitude as oxide nanolites formed. We thus demonstrate that oxide nanolites crystallisation increases magma bulk viscosity mainly by increasing the viscosity of its melt phase due to the chemical extraction of iron, whereas the physical effect of particle suspension is minor, almost negligible. Importantly, we further observe that this increase is sufficient for driving magma fragmentation depending on magma degassing and ascent dynamics.

Nanoscale silicate melt textures determine volcanic ash surface chemistry.

Explosive volcanic eruptions produce vast quantities of silicate ash, whose surfaces are subsequently altered during atmospheric transit. These altered surfaces mediate environmental interactions, including atmospheric ice nucleation, and toxic effects in biota. A lack of knowledge of the initial, pre-altered ash surface has required previous studies to assume that the ash surface composition created during magmatic fragmentation is equivalent to the bulk particle assemblage. Here we examine ash particles generated by controlled fragmentation of andesite and find that fragmentation generates ash particles with substantial differences in surface chemistry. We attribute this disparity to observations of nanoscale melt heterogeneities, in which Fe-rich nanophases in the magmatic melt deflect and blunt fractures, thereby focusing fracture propagation within aureoles of single-phase melt formed during diffusion-limited growth of crystals. In this manner, we argue that commonly observed pre-eruptive microtextures caused by disequilibrium crystallisation and/or melt unmixing can modify fracture propagation and generate primary discrepancies in ash surface chemistry, an essential consideration for understanding the cascading consequences of reactive ash surfaces in various environments.

Volcanic sintering: Timescales of viscous densification and strength recovery.

[1] Sintering and densification are ubiquitous processes influencing the emplacement of both effusive and explosive products of volcanic eruptions. Here we sinter ash-size fragments of a synthetic National Institute of Standards and Technology viscosity standard glass at temperatures at which the resultant melt has a viscosity of ∼108-109 Pa.s at 1bar to assess sintering dynamics under near-surface volcanic conditions. We track the strength recovery via uniaxial compressive tests. We observe that volcanic ash sintering is dominantly time dependent, temperature dependent, and grain size dependent and may thus be interpreted to be controlled by melt viscosity and surface tension. Sintering evolves from particle agglutination to viscous pore collapse and is accompanied by a reduction in connected porosity and an increase in isolated pores. Sintering and densification result in a nonlinear increase in strength. Micromechanical modeling shows that the pore-emanated crack model explains the strength of porous lava as a function of pore fraction and size.

Experimental generation of fulgurite under realistic lightning discharge conditions.

Fulgurites have been documented in geological deposits from throughout Earth's history. They have also been assigned a potential role in prebiotic chemistry as a source of reactants. Fulgurites are generated in nature by cloud-to-ground lightning strikes. The unpredictability in space and time of the occurrence of lightning events has limited the investigation of both the mechanisms by, and the conditions under, which fulgurites form. A laboratory-based approach can mitigate these limitations. Here, we describe experimentally generated fulgurites generated from Laacher See volcanic ash. We employ a DC source with a trigger-pulse setup in a high voltage laboratory, whose capabilities enable experimental conditions that correspond closely to the electrical characteristics of natural lightning strikes. The experimentally generated fulgurites closely resemble naturally-occurring fulgurites in both state and texture. These experimental investigations yield a high reproducibility of the characteristic of fulgurites generated under well-constrained conditions, enabling some inferences to be made regarding the processes involved in the generation of fulgurites in nature. This work provides a basis for a systematic characterization of experimental fulgurites and the characteristic of lightning discharges.

The porosity of felsic pyroclasts: laboratory validation of field-based approaches.

Volcanic eruptions are driven by magma rising through Earth's crust. The style of an eruption depends on intrinsic and extrinsic parameters and is commonly a dynamic process. Thorough and holistic investigation of the related products is key to understanding eruptive phenomena and assessment of volcano-specific hazards. Models of such phenomena are constrained by quantification of the dispersal, the grain size distribution, and pyroclast textures. Pyroclast texture may be described in part by measurements of density and porosity, which depend on pyroclast volume determination. Yet volume determination of irregularly shaped pyroclasts cannot be achieved with geometrical laws, instead necessitating the use of alternative methodologies. Here, we test three methodologies to quantify pyroclast volume on a set of clasts collected from the Minoan eruption deposits from Santorini, Greece. We compare (1) a manual method for obtaining the lengths of three orthogonal axes of the pyroclast with a caliper, (2) an optical method to measure the longest and shortest axes of the pyroclast via multiple photographs, and (3) an Archimedean buoyancy-based method. While the optical and manual methods provide almost identical values of pyroclast volume when tested under laboratory conditions, there is a discrepancy between these two methods and the Archimedean method, which produces an overestimation of ca. 13% in volume. This discrepancy has little impact on the subsequent assessment of porosity and density for which the natural variability of values is observed to be broader. We therefore propose using the manual approach in the field as a simple and fast, yet reliable, method to obtain large volumes of quantitative data on the texture of erupted products, and we also provide a correction factor for in-field volume assessment of rhyodacitic pumices. Supplementary Information: The online version contains supplementary material available at 10.1007/s00445-023-01679-4.

Molten-Volcanic-Ash-Phobic Thermal Barrier Coating based on Biomimetic Structure.

Volcanic ash is a major threat to aviation safety. The softening/melting temperatures of volcanic ash lie far below typical aero-engine operating temperatures. Thus, molten ash can accelerate the failure of thermal barrier coatings (TBCs). Here, inspired by natural superhydrophobic surfaces (e.g., the lotus leaf), a molten-volcanic-ash-phobic TBC, which provides a large possibility to eliminate molten ash issues of TBCs, is developed. A hierarchically structured surface is first prepared on a (Gd0.9 Yb0.1 )2 Zr2 O7 (GYbZ) pellet by ultrafast laser direct writing technology, aiming to confirm the feasibility of the biomimetic microstructure to repel molten volcanic ash wetting. Then biomimetic-structured GYbZ TBCs are successfully fabricated using plasma spray physical vapor deposition, which reveals "silicate" phobicity at high temperatures. The exciting molten-volcanic-ash-phobic attribute of the designed surfaces is attributed to the lotus-leaf-like dual-scale microstructure, emulating in particular the existence of nanoparticles. These findings may be an important step toward the development of next-generation aviation engines with greatly reduced vulnerability to environmental siliceous debris.

The physics of dancing peanuts in beer.

In Argentina, some people add peanuts to their beer. Once immersed, the peanuts initially sink part way down into the beer before bubbles nucleate and grow on the peanut surfaces and remain attached. The peanuts move up and down within the beer glass in many repeating cycles. In this work, we propose a physical description of this dancing peanuts spectacle. We break down the problem into component physical phenomena, providing empirical constraint of each: (i) heterogeneous bubble nucleation occurs on peanut surfaces and this is energetically preferential to nucleation on the beer glass surfaces; (ii) peanuts enshrouded in attached bubbles are positively buoyant in beer above a critical attached gas volume; (iii) at the beer top surface, bubbles detach and pop, facilitated by peanut rotations and rearrangements; (iv) peanuts containing fewer bubbles are then negatively buoyant in beer and sink; and (v) the process repeats so long as the beer remains sufficiently supersaturated in the gas phase for continued nucleation. We used laboratory experiments and calculations to support this description, including constraint of the densities and wetting properties of the beer-gas-peanut system. We draw analogies between this peanut dance cyclicity and industrial and natural processes of wide interest, ultimately concluding that this bar-side phenomenon can be a vehicle for understanding more complex, applied systems of general interest and utility.

Complex geometry of volcanic vents and asymmetric particle ejection: experimental insights.

Explosive volcanic eruptions eject a gas-particle mixture into the atmosphere. The characteristics of this mixture in the near-vent region are a direct consequence of the underlying initial conditions at fragmentation and the geometry of the shallow plumbing system. Yet, it is not possible to observe directly the sub-surface parameters that drive such eruptions. Here, we use scaled shock-tube experiments mimicking volcanic explosions in order to elucidate the effects of a number of initial conditions. As volcanic vents can be expected to possess an irregular geometry, we utilise three vent designs, two "complex" vents and a vent with a "real" volcanic geometry. The defining geometry elements of the "complex" vents are a bilateral symmetry with a slanted top plane. The "real" geometry is based on a photogrammetric 3D model of an active volcanic vent with a steep and a diverging vent side. Particle size and density as well as experimental pressure are varied. Our results reveal a strong influence of the vent geometry, on both the direction and the magnitude of particle spreading and the velocity of particles. The overpressure at the vent herby controls the direction of the asymmetry of the gas-particle jet. These findings have implications for the distribution of volcanic ejecta and resulting areas at risk.

Universal scaling for the permeability of random packs of overlapping and nonoverlapping particles.

Constraining fluid permeability in porous media is central to a wide range of theoretical, industrial, and natural processes. In this Letter, we validate a scaling for fluid permeability in random and lattice packs of spheres and show that the permeability of packs of both hard and overlapping spheres of any sphere size or size distribution collapse to a universal curve across all porosity ϕ in the range of ϕ_{c}<ϕ<1, where ϕ_{c} is the percolation threshold. We use this universality to demonstrate that permeability can be predicted using percolation theory at ϕ_{c}<ϕ≲0.30, Kozeny-Carman models at 0.30≲ϕ≲0.40, and dilute expansions of Stokes theory for lattice models at ϕ≳0.40. This result leads us to conclude that the inverse specific surface area, rather than an effective sphere size or pore size is a universal controlling length scale for hydraulic properties of packs of spheres. Finally, we extend this result to predict the permeability for some packs of concave nonspherical particles.

Interparticle and Brownian forces controlling particle aggregation and rheology of silicate melts containing platinum-group element particles.

We study the rheology of silicate melts containing platinum-group element (PGE) particles. They exhibit a shear-thinning behaviour, an intense aggregation tendency, and an anomalously high apparent viscosity in the low shear rate limit, even at very low particle volume fraction. Using a compilation of published experimental data, we analyse these effects in three steps. Firstly, we observe that the viscosities of these suspensions are much higher than those of natural silicate crystal-bearing melts for low shear rate regimes. Secondly, we demonstrate that the viscosities at low shear rate limit cannot be estimated by classical rheological models but rather may be understood as the result of particle aggregation, trapping dead fluid, and thereby increasing the effective particle volume fraction. Finally, we scale the critical shear rates for shear-thinning using a Peclet number analysis-invoking a competition between random thermal particle motion and hydrodynamic shearing motion-and, using an empirical extension, we additionally account for the particle-particle interaction energetics. We propose a framework in which the rheology of this family of particle-bearing melts can be predicted, and demonstrate that at low Peclet numbers, PGE-bearing particle aggregation is driven by interparticle forces and Brownian motion.

Inflated pyroclasts in proximal fallout deposits reveal abrupt transitions in eruption behaviour.

During explosive eruption of low viscosity magmas, pyroclasts are cooled predominantly by forced convection. Depending on the cooling efficiency relative to other timescales, a spectrum of deposits can be formed. Deposition of hot clasts, above their glass transition temperature, can form spatter mounds, ramparts and clastogenic lava flows. Clasts may also be deposited cold, producing tephra cones and blankets. Thus, the deposit and pyroclast type can provide information about eruption dynamics and magma properties. Here we examine pyroclasts from Tseax volcano, British Columbia, Canada. These newly identified inflated pyroclasts, are fluidal in form, have undergone post-depositional expansion, and are found juxtaposed with scoria. Detailed field, chemical and textural observations, coupled with high temperature rheometry and thermal modelling, reveal that abrupt transitions in eruptive behaviour - from lava fountaining to low-energy bubble bursts - created these pyroclastic deposits. These findings should help identify transitions in eruptive behaviour at other mafic volcanoes worldwide.