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Allan Lerner

Publications and source records attributed to Allan Lerner.

15 recordsLinked to original sources

Erupted volume during the 2014–2023 Semisopochnoi unrest and eruption constrained by multi-platform InSAR and volcanic gas observations

Volcano deformation data provide important constraints on magma dynamics during volcanic unrest and eruptions. From these observations, we can estimate subsurface pressure changes and relate them to volume change in the reservoir. However, because magma and rock are compressible, this volume change cannot be directly equated with eruptive volume. When we combine geodetic analyses with gas observations, petrologic constraints, volatile solubility modeling, and magma compressibility equations, however, we can estimate realistic lower and upper bounds of eruptive volume. Leveraging multi‐platform InSAR time series and satellite SO 2 data, we apply these methods to the 2014–2023 unrest and eruption of Semisopochnoi, Alaska. We find that this phreatomagmatic eruption sequence was fed by a spherical magma source at 6.5–7.5 km depth bsl, centered beneath the caldera, ∼5 km offset to the east from the vent. Volatile solubility modeling indicates that ∼50% of the initial dissolved CO 2 has exsolved at depths consistent with the geodetic source depth, increasing the magma compressibility. Combining geodetic model constraints with SO 2 observations, petrologic constraints, solubility models, and magma compressibility findings yields 12–32 Mm 3 as the most‐likely juvenile, dense‐rock equivalent eruptive volume, with a best estimate of 20 Mm 3 . Stress change modeling suggests that the local stress field encouraged conduit formation west of the pre‐eruptive inflation center, and that the 2014 M7.9 Rat Island earthquake, ∼65 km to the west of Semisopochnoi, reduced the compressive stress underneath the volcano, supporting prolonged eruptive activity.

Alaska↗

Thermal infrared and ultraviolet remote sensing of sulfur dioxide gas emitted during the 2018 lower East Rift Zone eruption of Kilauea, Hawaiʻi

Ultraviolet (UV) remote sensing is widely used to detect volcanic sulfur dioxide (SO₂) due to its high sensitivity and favorable spatial and temporal resolution. However, significant discrepancies have been reported between ground-based and satellite-based UV observations of dense volcanic plumes. A notable example is the 2018 lower East Rift Zone eruption of Kīlauea, where SO₂ emission rates derived from ground-based Differential Optical Absorption Spectroscopy (DOAS) measurements differed substantially from those obtained by the spaceborne Tropospheric Monitoring Instrument (TROPOMI). In this study, we investigate these differences by applying thermal infrared (TIR) satellite retrievals using a modified version of the SO₂-ALTA algorithm to Moderate Resolution Imaging Spectroradiometer (MODIS) observations. The resulting TIR-derived SO₂ fluxes are compared with ground-based DOAS data, satellite UV observations, and petrological estimates of gas emissions. Our results show strong agreement between TIR-derived fluxes, ground-based DOAS measurements, and petrological estimates, particularly during the peak and plateau phases of the eruption. In contrast, satellite UV-derived SO₂ emissions are systematically lower. We find that TIR observations are more effective in quantifying high-concentration SO₂ plumes in the near-vent region, while UV measurements are more sensitive under lower-concentration conditions but more affected by scattering in optically dense plumes. These findings highlight the complementary strengths of UV and TIR remote sensing techniques and emphasize the importance of accounting for plume density and observation geometry when interpreting satellite SO₂ retrievals.

Hawaii↗

Magmatic source of the opening phase of Kīlauea’s 2018 Lower East Rift Zone eruption

The 2018 eruption of Kīlauea volcano in its Lower East Rift Zone began with the discharge of evolved high-Ti basalt as weak lava fountains and short, slow-moving lava flows. The lavas were quickly geochemically recognized as being derived from magmas stored within the rift zone and remobilized by a new intrusion, a sequence that is common at Kīlauea. This initial phase of the 2018 eruption, referred to as phase 1a, lasted for 6 days and was followed by extrusion of mixed magma after a 3-day pause. Even though remobilization of older rift zone magmas is common within Kīlauea’s rift zones, it is difficult to determine which past intrusion(s) may have initially emplaced those stored magmas. This difficulty stems from the tendency for Kīlauea magmas to follow very similar differentiation paths without significant variations in major, minor, or even trace element chemistry. We investigate possible magma sources for the lavas erupted during phase 1a of the 2018 eruption using whole-rock, mineral, and glass major and trace element compositions from historical East Rift Zone eruptions with adjacent fissures. We consider two primary hypotheses for the phase 1a source: magmas associated with the 1955 Lower East Rift Zone eruption or the nine eruptions in the Middle and Upper East Rift Zone during the 1960s. Our results suggest that magma associated with the earliest phases of Kīlauea’s 1955 eruption was the most likely source of the 2018 phase 1a remobilized magma. We determine volatile saturation pressures from melt inclusion chemistry and find similar storage depths for the 2018 phase 1a and early 1955 magmas. The phase 1a and early 1955 lavas are nearly indistinguishable in all of the compositional criteria considered, implying that the leftover 1955 magma body barely cooled and differentiated in the 63 years between eruptions (cooling rates of ~0.1 °C/year). This study sheds light on the potential for protracted storage of eruptible magmas in rift zones at Kīlauea, and highlights some of the challenges and solutions to identifying genetic relationships between magmas at Kīlauea.

Hawaii↗

Petrologic and geochemical characterization of the first year of the 2024–ongoing episodic Halemaumau eruption of Kilauea (Episodes 1–39)

Kīlauea has been erupting episodically since December 23, 2024 (and is ongoing at the time of this writing in 2026) with two consistently active vents in Halema‘uma‘u producing lava fountains ranging in height from 40 to 540 m. In the first year of the eruption (through December 24, 2025, episode 39), the U.S. Geological Survey's Hawaiian Volcano Observatory collected 178 samples for eruption monitoring purposes and used a subset of 80 for near-real-time geochemical analyses. Tephra, lava, and recycled lava lake ooze-out samples have been studied on inter-episode timescales using diverse microanalytical techniques, where research-scale investigations have proven to be advantageous pseudo-near-real-time techniques. Here we present a geochemical and petrologic overview of episodes 1–39 to better understand eruption dynamics and identify changes at Kīlauea following the 2018 summit caldera collapse. There are no significant intra-episode geochemical changes that might be related to variable fountain heights or episode durations, suggesting that eruption dynamics are instead primarily controlled by viscosity and conduit geometry changes throughout a single episode and between episodes. There is variable but clear influence of the still-molten lava lake interior on compositions of this eruption, including in tephra samples from lava fountains, indicating that the vent conduits are connected in some way at depth with the still molten passive lava lake core. Tephra glasses (7.0–7.8 wt.% MgO) show cyclic changes in MgO that were decoupled from lava fountain heights and behavior in episodes 1–28 but positively correlated after episode 29. Additionally, whole-rock and glass compositions are enriched in minor elements such as K 2 O and TiO 2 compared to 2008–2023 summit eruptions, tracking the arrival of a new magma composition that may be related to the prolonged episodic eruptive behavior. Olivine-hosted melt inclusions from five episodes have ~0.35–0.43 wt.% H2O, < 300 ppm CO 2 and < 1500 ppm S, with no significant variations between episodes. Melt and fluid inclusion barometry show that magmas driving these episodes are stored and sourced from the shallow 1–2 km Halemaʻumaʻu reservoir, as were olivine from the 2023 summit eruption. The ongoing episodic eruption also has higher bulk-rock MgO compared to the five previous summit eruptions (2020−2023) and the forsterite (Fo) content of olivine has varied systematically from 2015 to 2025 with the equilibrium olivine composition of the Halema‘uma‘u reservoir increasing from Fo 80.7 in 2015 to Fo 82.7 by 2025. We argue that the Halemaʻumaʻu reservoir is heating up because the rate of magma supply is outpacing effusion and cooling following caldera collapse in 2018.

Hawaii↗

Utilizing crystal records to determine the underlying architecture and timescales of magmatic processes during the 2022 Mauna Loa eruption

Details of Mauna Loa’s plumbing system and magma storage dynamics are relatively poorly constrained, relative to nearby Kīlauea volcano. Recent studies have begun to address this gap in knowledge using geophysical imaging or olivine-focused petrology. Here, we use the crystal cargo from the 2022 summit and Northeast Rift Zone eruption to advance our understanding of Mauna Loa’s storage regions and pre˗eruptive processes. We identify textural and geochemical populations of olivine, orthopyroxene, clinopyroxene, and plagioclase macrocrysts as well as evolved glomerocrysts consisting of orthopyroxene, clinopyroxene, and plagioclase. Summit versus rift zone trends can be distinguished between specific crystal populations and are used to infer magma transfer pathways. Melt inclusion barometry from three orthopyroxene populations indicate crystallization depths of ~2–3 km which coincide with previous olivine˗hosted fluid inclusion barometry across Mauna Loa’s recent 200˗yr eruptive history. We combine orthopyroxene˗hosted melt inclusion barometry with diffusion chronometry on the same crystals using Fe˗Mg interdiffusion to estimate timescales of mixing and recharge prior to the eruption. Summit orthopyroxene yield timescales of weeks to months, aligning with geophysically recognized pre˗eruptive intrusion events and previously determined olivine timescales. Northeast Rift Zone orthopyroxene crystals have resorbed cores and yield short pre˗eruptive mixing timescales on the order of hours to days. Chemistry and timescales from the orthopyroxene populations suggest some of the 2022 magmas may have bypassed the shallowest portions of the summit reservoir system and were transferred directly into the rift zone syn˗eruptively.

Hawaii↗

Chemistry, growth, and fate of the unique, short-lived (2019–2020) water lake at the summit of Kīlauea Volcano, Hawaii

Less than a year after the 2018 Kīlauea caldera collapse and eruption, water appeared in newly deepened Halemaʻumaʻu crater. The lake—unprecedented in the written record—grew to a depth of ∼50 m before lava from the December 2020 eruption boiled it away. Surface water heightened concerns of potential phreatic or phreatomagmatic explosions but also offered a new means of possibly identifying eruption precursors. The U.S. Geological Survey Hawaiian Volcano Observatory (HVO) monitored the lake via direct visual observation, webcams, thermal imaging, colorimetry, and laser rangefinders. HVO also employed uncrewed aircraft systems to sample the water and measure near-lake gas composition. The lake's δD and δ 18 O indicate a groundwater source with substantial evaporation. The initial sample had a salinity (total dissolved solids concentration) of 71,000 mg/L and was rich in sulfate (∼53,000 mg/L), iron (∼500 mg/L), and magnesium (∼10,000 mg/L). Subsequent samples were slightly more dilute. The water's pH (∼4), δ 34 S (+4.3‰), and surface temperatures (up to 85°C) suggest, rather than significant scrubbing of magmatic volatiles, leaching of basalt and reactions with sulfate minerals resulted in high concentrations of sulfate and other solutes. Thermodynamic modeling and precipitate mineralogy indicate that water composition was controlled by iron oxidation and sulfate dissolution. Although the lake exhibited no detectable precursors before the next eruption, and phreatic or phreatomagmatic explosions did not materialize, our multi-parameter approach to monitoring yielded an enhanced understanding of the hydrologic, geologic, and magmatic conditions that led to the formation of the unique and short-lived lake.

Hawaii↗

Insights into magma storage depths and eruption controls at Kīlauea Volcano during explosive and effusive periods of the past 500 years based on melt and fluid inclusions

Kīlauea Volcano experiences centuries-long cycles of explosive and effusive eruptive behavior, but the relation, if any, between these eruptive styles and changing conditions in the magma plumbing system remains poorly known. We analyze olivine-hosted melt and fluid inclusions to determine magma storage depths during the explosive-era Keanakākoʻi Tephra eruptions (∼1500–1840 CE) and compare these results to modern effusive-era Kīlauea eruptions (1959 Kīlauea Iki, 1960 Kapoho, 2018 lower East Rift Zone). We find that shallow (1–3 km) magma storage has persisted for centuries at Kīlauea, spanning both explosive and effusive periods. In contrast, mid-crustal zones of magma storage shallowed over time, from 5 to 8 km during the Keanakākoʻi sequence to 3–5 km during the modern effusive period. Melt and fluid inclusions in high-forsterite olivine (Fo 86–89 ) trapped at shallow depths indicate that high-temperature magmas (1200 to ∼1300 °C) commonly reach depths of ≤3 km. CO 2 -rich fluid inclusions are present in olivine from all investigated Kīlauea eruptions but are larger and much more abundant in Keanakākoʻi units, which we interpret as indicating that a greater volume fraction of exsolved CO 2 -rich fluid was present in pre-eruptive Keanakākoʻi melts. Increased amounts of CO 2 -rich fluids in the Keanakākoʻi-era magmas would have increased magma buoyancy and driven rapid magma ascent, thereby increasing eruption energy and enhancing near-surface magma-water interactions compared to the current effusive period.

Hawaii↗

Origins and nature of large explosive eruptions in the lower East Rift Zone of Kīlauea volcano, Hawaii: Insights from ash characterization and geochemistry

Several powerful explosive eruptions have taken place in the populated lower East Rift Zone of Kīlauea within the past ∼750 years. These have created distinctive landforms, including a tephra rim enclosing Puʻulena Crater immediately south of the Puna Geothermal Venture power station, a tuff cone at Kapoho Crater near the eastern cape of the Island of Hawaiʻi, and a set of littoral cones, the Sand Hill in Nānāwale, where the 1840 lava flow poured into the ocean. Kapoho Crater tuff cone is the largest of these recent pyroclastic features. Mineral, glass, and melt inclusion analyses of tuff cone ash and later fissure-related scoriaceous materials also found within the crater indicate slightly evolved basaltic magmas (1120–1130 °C) that are compositionally similar to parts of the effusive lower East Rift Zone eruptions in 1955 and 2018. Tuff cone magmas were stored at depths of ∼2.5–3.5 km and had pre-eruptive volatile contents (0.5–0.8 wt% H 2 O, 280–340 ppm CO 2 , 1400–1800 ppm S) similar to other Kīlauea eruptions (e.g., 1959, 1960), suggesting that internal magma properties were unlikely to account for the unusual explosiveness of this eruption. Tephra componentry, grain-size analyses, and field observations confirm that the cone grew during a phreatomagmatic eruption mostly of vitric ash, probably where a fissure opened across the coastline or shallow ocean floor nearby. Supporting this hypothesis is the identification of at least two genera of marine diatoms within tuff cone strata. Sand Hill littoral cone ash is also vitric like that of Kapoho Crater, but distinctly coarser with abundant fluidal ejecta represented. In contrast, the Puʻulena Crater eruption deposited lithic ash and related blocks with minor juvenile magmatic contribution; a phreatomagmatic eruption that was dominantly phreatic. Differences in eruption styles are related to unique mechanics that tephra analyses help us interpret. While powerful explosive eruptions in the lower East Rift Zone are rare, they present a definite future hazard for inhabitants in this part of Hawaii.

Hawaii↗

Forecasting explosions at Sinabung Volcano, Indonesia, based on SO2 emission rates

Dome-building volcanic eruptions are often associated with frequent Vulcanian explosions, which constitute a substantial threat to proximal communities. One proposed mechanism driving such explosions is the sealing of the shallow volcanic system followed by pressurization due to gas accumulation beneath the seal. We investigate this hypothesis at Sinabung Volcano (Sumatra, Indonesia), which has been in a state of eruption since August 2010. In 2013, the volcano began erupting a lava dome and lava flow, and frequent explosions produced eruptive columns that rose many kilometers into the atmosphere and at times sent pyroclastic density currents down the southeast flanks. A network of scanning Differential Optical Absorption Spectrometers (DOAS) was installed on the volcano’s eastern flank in 2016 to continuously monitor SO 2 emission rates during daytime hours. Analysis of the DOAS data from October 2016 to September 2017 revealed that passive SO 2 emissions were generally lower in the 5 days leading up to explosive events (∼100 t/d) than was common in 5-day periods leading up to days on which no explosions occurred (∼200 t/d). The variability of passive SO 2 emissions, expressed as the standard deviation, also took on a slightly wider range of values before days with explosions (0–103 t/d at 1-sigma) than before days without explosions (43–117 t/d). These observations are consistent with the aforementioned seal-failure model, where the sealing of the volcanic conduit blocks gas emissions and leads to pressurization and potential Vulcanian explosions. We develop a forecasting methodology that allows calculation of a relative daily explosion probability based solely on measurements of the SO 2 emission rate in the preceding days. We then calculate forecast explosion probabilities for the remaining SO 2 emissions dataset (October 2017—September 2021). While the absolute accuracy of forecast explosion probabilities is variable, the method can inform the probability of an explosion occurring relative to that on other days in each test period. This information can be used operationally by volcano observatories to assess relative risk. The SO 2 emissions-based forecasting method is likely applicable to other open vent volcanoes experiencing dome-forming eruptions.

Frontiers in Earth Science↗

Trace elements in olivine fingerprint the source of 2018 magmas and shed light on explosive-effusive eruption cycles at Kīlauea Volcano

Understanding magma genesis and the evolution of intensive parameters (temperature, pressure, composition, degree of melting) in the mantle source of highly active volcanic systems is crucial for interpreting magma supply changes over time and recognizing cyclic behavior to anticipate future volcanic behavior. Major and trace elements in olivine are commonly used to study variations in mantle lithologies and melting conditions (e.g., temperature, pressure, oxygen fugacity) affecting the mantle over time. Here, we track the temporal evolution of primary melts through the most recent cycle of explosive and effusive eruptions at Kīlauea (Hawai‘i), which spans the last ∼500 years. We report major and trace elements in olivine from the last explosive period (∼1500 – early 1820’s Keanakāko‘i Tephra) and the most recent decade of the current effusive period (2018 LERZ, 2015–2018 Pu‘u‘ō‘ō, 2008–2018 lava lake and 2020 eruption in Halema‘uma‘u). Scandium concentrations in olivine allow characterizing changes in mantle source between 1500 and 2018, and suggest that the recent (2015–2018) magma feeding the Pu‘u‘ō‘ō cone did not significantly interact with the magma that erupted in the LERZ in 2018. The evolution of olivine and melt compositions over the past 500 years is not easily reconcilable with variations in mantle potential temperature, pressure of mantle melt pooling and storage, or oxygen fugacity. Instead, Sc, Mn, and Co concentrations and Ni/Mg ratio in high forsterite (Fo >87) olivine advocate for an increase in the proportion of clinopyroxene in the mantle source associated with a slightly higher degree of partial melting from 1500 to 2018. Changes in primitive melt compositions and degrees of mantle melting may well modulate magma supply to the crust and formation-replenishment of steady or ephemeral summit reservoirs, and thereby control transitions between explosive and effusive periods at Kīlauea. Analyzing trace elements in olivine at Kīlauea and elsewhere could therefore provide important clues on subtle changes occurring at the mantle level that might herald changes in volcanic behavior.

Hawaii↗

The petrologic and degassing behavior of sulfur and other magmatic volatiles from the 2018 eruption of Kīlauea, Hawaiʻi: Melt concentrations, magma storage depths, and magma recycling

Kīlauea Volcano’s 2018 lower East Rift Zone (LERZ) eruption produced exceptionally high lava effusion rates and record-setting SO 2 emissions. The eruption involved a diverse range of magmas, including primitive basalts sourced from Kīlauea’s summit reservoirs. We analyzed LERZ matrix glasses, melt inclusions, and host minerals to identify melt volatile contents and magma storage depths. The LERZ glasses and melt inclusions span nearly the entire compositional range previously recognized at Kīlauea. Melt inclusions in Fo 86-89 olivine from the main eruptive vent (fissure 8) underwent 70–170 °C cooling during transport in LERZ carrier melts, causing extensive post-entrapment crystallization and sulfide precipitation. Many of these melt inclusions have low sulfur (400–900 ppm) even after correction for sulfide formation. CO 2 and H 2 O vapor saturation pressures indicate shallow melt inclusion trapping depths (1–5 km), consistent with formation within Kīlauea’s Halemaʻumaʻu and South Caldera reservoirs. Many of these inclusions also have degassed δ 34 S values (− 1.5 to − 0.5‰). Collectively, these results indicate that some primitive melts experienced near-surface degassing before being trapped into melt inclusions. We propose that decades-to-centuries of repeated lava lake activity and lava drain-back during eruptions (e.g., 1959 Kīlauea Iki) recycled substantial volumes of degassed magma into Kīlauea’s shallow reservoir system. Degassing and magma recycling from the 2008–2018 Halemaʻumaʻu lava lake likely reduced the volatile contents of LERZ fissure 8 magmas, resulting in lower fountain heights compared to many prior Kīlauea eruptions. The eruption’s extreme SO 2 emissions were due to high lava effusion rates rather than particularly volatile-rich melts.

Hawaii↗

Quantifying gas emissions associated with the 2018 rift eruption of Kīlauea Volcano using ground-based DOAS measurements

Starting on 3 May 2018, a series of eruptive fissures opened in Kīlauea Volcano’s lower East Rift Zone (LERZ). Over the course of the next 3 months, intense degassing accompanied lava effusion from these fissures. Here, we report on ground-based observations of the gas emissions associated with Kīlauea’s 2018 eruption. Visual observations combined with radiative transfer modeling show that ultraviolet light could not efficiently penetrate the gas and aerosol plume in the LERZ, complicating SO 2 measurements by differential optical absorption spectroscopy (DOAS). By applying a statistical method that integrates a radiative transfer model with the DOAS retrievals, we were able to calculate sulfur dioxide (SO 2 ) emission rates along with estimates of their uncertainty. We find that sustained SO 2 emissions were highest in June and early July, when approximately 200 kt SO 2 were emitted daily. At the 68% confidence interval, we estimate that 7.1–13.6 Mt SO 2 were released from the LERZ during the entire May to September eruptive episode. Scaling our results with in situ measurements of plume composition, we calculate that 11–21 Mt H 2 O and 1.5–2.8 Mt CO 2 were also emitted. The gas and aerosol emissions caused hazardous conditions in areas proximal to the active vents, but plume dispersion modeling shows that the eruption also significantly impacted air quality hundreds of kilometers downwind. Combined with petrologic studies of the erupted lavas, our measurements indicate that 1.1–2.3 km 3 dense-rock equivalent of lava were erupted from the LERZ, which is approximately twice the concomitant collapse volume of the volcano’s summit.

Hawaii↗

Direct measurements of copper speciation in basaltic glasses: Understanding the relative roles of sulfur and oxygen in copper complexation in melts

Micro-analytical determination of copper (Cu) speciation in natural magmatic glasses, equilibrated below the nickel – nickel oxide (NNO) buffer, reveals that two copper species are commonly stabilized in such basaltic melts. X-ray absorption fine structure (XAFS) spectroscopic analysis of basaltic matrix glasses and melt inclusions (MI) from samples of mid-ocean ridge basalt (MORB), and from Nyamuragira, Etna and Kīlauea volcanoes show that both Cu(I)-sulfide and Cu(I)-oxide species are stabilized. The proportion of each species correlates with the measured sulfur (S) abundance of the glass. In glasses with S abundances greater than ~1000 ppm, Cu(I)-sulfide species are dominant, whereas in glasses with S abundances between 500 and 1000 ppm, both species are found to coexist. The Cu(I)-oxide species dominate at S concentrations below 500 ppm. In 1 atm S-free experimental glasses of basaltic composition that we analyzed, only Cu(I)-oxide species are detectable, regardless of the oxygen fugacity (fO2), even at relatively high fO2 values well above the NNO buffer. Our results demonstrate that XAFS techniques are highly sensitive in measuring Cu speciation in reduced (below NNO) basaltic glasses and that both oxide and sulfide complexes can be stabilized. The relative proportion of these two species is highly dependent on the concentration of S in the melt, and thus the Cu speciation in natural melts changes as S is lost from the melt by low pressure degassing.

Hawaii↗

Gas and ash emissions associated with the 2010–present activity of Sinabung Volcano, Indonesia

Sinabung Volcano (Sumatra, Indonesia) awoke from over 1200 years of dormancy with multiple phreatic explosions in 2010. After a period of quiescence, Sinabung activity resumed in 2013, producing frequent explosions, lava dome extrusion, and pyroclastic flows from dome collapses, becoming one of the world's most active volcanoes and displacing over 20,000 citizens. This study presents a compilation of the geochemical datasets collected by the Indonesian Center for Volcanology and Geological Hazard Mitigation (CVGHM) from 2010 - current (2016), which provides insights into the evolution of the eruption. Based on observations of SO2 emissions, ash componentry, leachate chemistry, and bulk ash geochemistry, the eruption can be split into five distinct phases. The initial stage of phreatic summit explosions occurred from August - October 2010, during which background SO2 emissions averaged ~550 ± 180 t/d (1 s.d.). An eruptive pause (phase two) starting in October 2010 abruptly ended in September 2013 with a resumption of conduit-clearing eruptions. This third phase had a relatively modest background SO2 emission rate (avg. ~410 ± 275 t/d) and produced ash consisting entirely of accidental ejecta with high S/Cl leachate ratios (up to 30), suggestive of deep-sourced magma and the incorporation of hydrothermal sulfur-bearing phases. The most intense phase of the eruption (phase four) occurred from December 2013 to February 2014, when juvenile magma first reached the surface. This period included dozens of large eruptions per day, high SO2 emission rates (average: 1,120 ± 1,030 t/d, peak: ~3,800 t/d), the onset of lava dome extrusion, and a dramatic drop in S/Cl ash leachates to ratios < 5, all reflecting increased degassing from shallow magma and the clearing out of sulfurous phases from the old hydrothermal system. From late February 2014 through the time of writing (September 2016), Sinabung settled into a relatively steady state of lower activity (phase five). Ash emissions now consist of dominantly juvenile material, and background SO2 emission rates have been progressively decreasing to an average of ~250 - 300 t/d. Starting August 2016, SO2 emissions started being measured in a continuous manner using a network of permanent scanning DOAS instruments. We find that long-term SO2 emission rates have been gradually declining at Sinabung since early 2014, consistent with an apparent decrease in magma supply. Our degassing model suggests that large explosions and pyroclastic flows could continue in the near-term owing to conduit plugging and dome collapses, remaining a major threat until the magma supply rate decreases further and the eruption ends.

Sumatra↗

The 2018 rift eruption and summit collapse of Kilauea Volcano

In 2018, Kīlauea Volcano experienced its largest lower East Rift Zone (LERZ) eruption and caldera collapse in at least 200 years. After collapse of the Pu'u 'Ō'ō vent on 30 April, magma propagated downrift. Eruptive fissures opened in the LERZ on 3 May, eventually extending ~6.8 km. A 4 May earthquake (M6.9) produced ~5 m of fault slip. Lava erupted at rates exceeding 100 m3/s, eventually covering 35.5 km2. The summit magma system partially drained, producing minor explosions and near-daily collapses releasing energy equivalent to M4.7-M5.4 earthquakes. Activity declined rapidly on 4 August. Summit collapse and lava flow volume estimates are roughly equivalent--about 0.8 km3. Careful historical observation and monitoring of Kīlauea enabled successful forecasting of hazardous events.

Hawaii↗