Geology topics

Christoph Kern

Publications and source records attributed to Christoph Kern.

At least 19 recordsLinked to original sources

USGS2026

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↗

USGS2026

Insights from more than a year of ongoing episodic lava fountaining at Kilauea

Episodic lava fountaining is rare globally, with only three occurrences from Kīlauea (Hawaii) since 1823. Beginning in December 2024, an eruption within the summit crater, Halemaʻumaʻu, has produced 52 fountaining episodes to date, each lasting typically for hours and separated by days to weeks. Although multiple mechanisms have been proposed, fundamental questions remain about how magma reservoir pressure, conduit permeability, and volatile exsolution control fountaining onset. We present a multi-parameter record of episodic fountaining at Kīlauea using modern geochemical, geophysical, and geologic monitoring. These observations revealed systematic correlations between fountaining and summit inflation, enabling unprecedented quantitative forecasts. This eruption will provide new constraints on the timing, evolution, and processes driving episodic fountaining globally, and highlights Kīlauea’s role as a natural laboratory for studying volcanic processes.

Hawaii↗

USGS2025

Origins and fluxes of gas emissions from the Central Volcanic Zone of the Andes

We present geochemical data from gas samples from ∼1200 km of arc in the Central Volcanic Zone of the Andes (CVZA), the volcanic arc with the thickest (∼70 km) continental crust globally. The primary goals of this study are to characterize and understand how magmatic gases interact with hydrothermal systems, assess the origins of the major gas species, and constrain gas emission rates. To this end, we use gas chemistry, isotope compositions of H, O, He, C, and S, and SO 2 fluxes from the CVZA. Gas and isotope ratios (CO 2 /S T , CO 2 /CH 4 , H 2 O/S T , δ 13 C, δ 34 S, 3 He/ 4 He) vary dramatically as magmatic gases are progressively affected by hydrothermal processes, reflecting removal and crustal sequestration of reactive species (e.g., S) and addition of less reactive meteoric and crustal components (e.g., He). The observed variations are similar in magnitude to those expected during the magmatic reactivation of volcanoes with hydrothermal systems. Carbon and sulfur isotope compositions of the highest temperature emissions (97–408 °C) are typical of arc magmatic gases. Helium isotope compositions reach values similar to upper mantle in some volcanic gases indicating that transcustal magma systems are effective conduits for volatiles, even through very thick continental crust. However, He isotopes are highly sensitive to even low degrees of hydrothermal interaction and radiogenic overprinting. Previous work has significantly underestimated volatile fluxes from the CVZA; however, emission rates from this study also appear to be lower than typical arcs, which may be related to crustal thickness.

Central Volcanic Zone of the Andes↗

USGS2025

The ghost plume phenomenon and its impact on zenith-facing remote sensing measurements of volcanic SO2 emission rates

A large source of error in SO 2 emission rates derived from mobile Differential Optical Absorption Spectroscopy (DOAS) of volcanic gas plumes is the uncertainty in atmospheric light paths between the sun and the instrument, particularly under non-ideal atmospheric conditions, such as the presence of low clouds. DOAS instruments measure the SO 2 column density along the effective light path, so changes to that pathway directly affect the measured SO 2 signal. Due to complex radiative transfer mechanisms when a cloud is between the DOAS viewing position and a volcanic plume, measured plumes can appear spatially offset from their true location, a phenomenon informally referred to as “ghost plumes.” In addition to the appearance of ghost plumes, DOAS measurements recorded in non-ideal conditions have poorly characterized errors and are often discarded, limiting the data available to characterize volcanic degassing. In this study we simulate the radiative transfer associated with zenith-facing mobile DOAS traverses using the McArtim radiative transfer model for scenarios when there is a cloud layer between the instrument and the volcanic plume. In total, 217 permutations of atmospheric optical conditions are considered with varying cloud opacities (AOD = 0, 1, 2, 4, 8, 20), plume opacities (AOD = 0, 1, 2, 4, 8), solar zenith angles (SZA = 1°, 30°, 60°), and cloud thicknesses (200, 400, 800 m). We first develop objective criteria for selecting SO 2 baseline absorption levels and plume spatial extents. The simulated plume traverses are then integrated to obtain the SO 2 cross-sectional burdens which, after multiplication with the wind speed, yield SO 2 emission rates. We find large modification in the shape of the modeled cross-sectional burdens even under translucent (low AOD) cloud conditions in our modeled scenarios. Despite modification of the plume shape, the presence of a low cloud layer is typically not a large source of error in the SO 2 cross-sectional burden or emission rate obtained from zenith-facing DOAS traverses. We find that all measured cross-sectional burdens simulated using an aerosol-free plume in the above conditions and SZA ≤ 30° are within ±25% of the true value.

Journal of Volcanology and Goethermal Research↗

USGS2025

Ultraviolet and visible remote sensing of volcanic gases

As magma rises in volcanic systems, volatile species exsolve from the silicate melt and are emitted as gases into the atmosphere. Measuring the magnitude and composition of gas emissions from volcanoes provides insights into processes occurring deep within the Earth and helps constrain the impact of volcanic degassing on atmospheric chemistry. Optical remote sensing techniques allow volcanic gas emissions to be characterized without the need to access hazardous areas near active volcanic vents. This paper reviews the state of the art in ultraviolet and visible volcanic gas remote sensing from the ground, air, and space. Special attention is given to discussing the physics of atmospheric radiative transfer on which these techniques are based. The functionality and limitations of different remote sensing instruments are examined, making clear that the ideal choice of instrumentation will depend on the volcanic system to which it is applied and the sought measurement parameters. Common algorithms for determining trace gas column densities, gas burdens, and volcanic emission rates from measurements of spectral radiance are outlined and compared, showing how some algorithms attempt to model the physics of the measurement while others maximize sensitivity. Several examples demonstrate how remote sensing measurements continue to advance our understanding of volcanic systems and their impact on the atmosphere. Finally, a few promising directions of inquiry are suggested that could lead to improvements in remote sensing instrumentation and analysis techniques. By combining spectroscopic and imaging techniques, improving our understanding of atmospheric radiative transfer, expanding the suite of target gases, and increasing the coverage and frequency of observations, we stand to significantly improve our ability to detect and quantify volcanic gas emissions and gain new insights into important Earth-system processes.

Journal of Volcanology and Geothermal Research↗

USGS2024

Volcanic gas monitoring

Introduction As magma rises through the crust, decreasing pressure conditions allow volatiles to exsolve from the magma. These volatiles then migrate upward through the crust, where they can be stored at shallower levels or escape to the atmosphere. Rising magma also heats rock masses beneath volcanic centers, causing water in shallow aquifers and hydrothermal systems to boil and release additional gases and steam (see chapter F , this volume; Ingebritsen and Hurwitz, 2024). The chemistry and quantity of gases that reach the surface during periods of quiescence or volcanic unrest can reveal that gas-rich magma is ascending, crystallizing, or alternatively stalling, with important implications for volcanic hazard (for example, Sutton and others, 1992; Aiuppa and others, 2007, 2021; Werner and others, 2009, 2011, 2012; Moretti and others, 2013; de Moor and others, 2016; Lewicki and others, 2019; Edmonds and others, 2022; Kern and others, 2022; Kunrat and others, 2022). Most volcanoes in Alaska and the western United States are characterized by weak degassing, with one or more low-temperature fumaroles (typically near the local boiling temperature of water) and connect to a deeper and sometimes extensive hydrothermal system (for example, McGee and others, 2001; Symonds and others, 2003a, b). Hydrothermal systems will affect the chemistry of rising gases exsolved from deeper magma (Symonds and others, 2001), including sulfur dioxide (SO 2 ), hydrogen chloride (HCl), and water vapor (for example, Doukas and Gerlach, 1995; Gerlach and others, 1998, 2008; Symonds and others, 2001; Werner and others, 2013). As an example, depending on factors such as temperature, pressure, and oxidation state, rising SO 2 will react with groundwater to form hydrogen sulfide (H 2 S) gas, dissolved sulfate (SO 4 2− ), or elemental sulfur (Christenson, 2000; Symonds and others, 2001; Werner and others, 2008). The reaction and dissolution of SO 2 into shallow groundwater is commonly referred to as scrubbing, and can reduce the likelihood that ascending, degassing magma can be detected. Carbon dioxide, however, in addition to exsolving from magma early in the ascent process, is not easily removed by hydrothermal fluids (Lowenstern, 2001). As scrubbing and other processes take place, the SO 2 /H 2 S, CO 2 /SO 2 , and CO 2 /H 2 S ratios may change. High rates of SO 2 emission indicate that magma has moved to relatively shallow levels in the volcano and that the system has heated up enough to establish dry pathways from depth to the surface. Monitoring multiple gas species and the total output of those species is thereby useful for volcano monitoring during both periods of quiescence, to establish background degassing conditions, and during unrest, when gas geochemistry and emission rates can provide information on changing conditions, such as magma ascent. To provide context for multidisciplinary volcano forecasts, we focus on the following two key required capabilities: (1) characterizing baseline geochemistry and gas discharge from volcanoes and volcanic regions and (2) monitoring changes in gas geochemistry and discharge to inform forecasts of volcanic eruptions and their effects. Sufficient baseline data must be collected to identify and interpret anomalous degassing associated with volcanic unrest (for example, Sorey and others, 1998; Rouwet and others, 2014). Differences in volcano type, baseline degassing rates, local hydrology, and geography (for example, high versus low latitude) will result in a different baseline for each volcano. Volcanoes of any threat level that exhibit one or more degassing phenomena would ideally be monitored by techniques needed to establish baseline degassing data, with the sampling frequency of baseline data dictated by the threat level (table E1). Additional monitoring techniques become necessary during periods of unrest. In general, three of the most important techniques for gas monitoring are (1) direct sampling of fumarole, spring, and soil gases for laboratory geochemical measurements, (2) measurements of the chemical composition of the volcanic plume and emission rates of major gas species (for example, H 2 O, CO 2 , SO 2 , and H 2 S) by satellite, airborne, or ground-based techniques, and (3) measurements of diffuse emissions of CO 2 and other gases through soils. Various methods and instruments may be useful both for baseline studies and during unrest.

Scientific Investigations Report↗

USGS2023

Editorial: Remote sensing of volcanic gas emissions from the ground, air, and space

When magma rises in volcanic systems, volatile species exsolve from the melt and are outgassed to the atmosphere. The melt composition and temperature, depth at which degassing occurs, extent of gas-water-rock interactions, and volume of ascending magma are all factors that determine the composition and rate of gas emissions at the surface. Interpreted in a petrological framework, gas measurements thus provide information on these fundamental parameters of volcanic systems. Volcanic gases have traditionally been sampled in the field and later analyzed with standard laboratory methods, but remote sensing measurements are playing an increasingly central role in characterizing emissions and the volcanoes from which they originate. The 17 contributions in this Research Topic summarize the state-of-the-art in volcanic gas remote sensing and identify key areas in which the field could further improve our understanding of global volcanism and its impact on Earth’s environment in the next decade.

Frontiers in Earth Science↗

USGS2023

An algorithm for correction of atmospheric scattering dilution effects in volcanic gas emission measurements using skylight differential optical absorption spectroscopy

Differential Optical Absorption Spectroscopy (DOAS) is commonly used to measure gas emissions from volcanoes. DOAS instruments measure the absorption of solar ultraviolet (UV) radiation scattered in the atmosphere by sulfur dioxide (SO 2 ) and other trace gases contained in volcanic plumes. The standard spectral retrieval methods assume that all measured light comes from behind the plume and has passed through the plume along a straight line. However, a fraction of the light that reaches the instrument may have been scattered beneath the plume and thus has passed around it. Since this component does not contain the absorption signatures of gases in the plume, it effectively “dilutes” the measurements and causes underestimation of the gas abundance in the plume. This dilution effect is small for clean-air conditions and short distances between instrument and plume. However, plume measurements made at long distance and/or in conditions with significant atmospheric aerosol, haze, or clouds may be severely affected. Thus, light dilution is regarded as a major error source in DOAS measurements of volcanic degassing. Several attempts have been made to model the phenomena and the physical mechanisms are today relatively well understood. However, these models require knowledge of the local atmospheric aerosol composition and distribution, parameters that are almost always unknown. Thus, a practical algorithm to quantitatively correct for the dilution effect is still lacking. Here, we propose such an algorithm focused specifically on SO 2 measurements. The method relies on the fact that light absorption becomes non-linear for high SO 2 loads, and that strong and weak SO 2 absorption bands are unequally affected by the diluting signal. These differences can be used to identify when dilution is occurring. Moreover, if we assume that the spectral radiance of the diluting light is identical to the spectrum of light measured away from the plume, a measured clean air spectrum can be used to represent the dilution component. A correction can then be implemented by iteratively subtracting fractions of this clean air spectrum from the measured spectrum until the respective absorption signals on strong and weak SO 2 absorption bands are consistent with a single overhead SO 2 abundance. In this manner, we can quantify the magnitude of light dilution in each individual measurement spectrum as well as obtaining a dilution-corrected value for the SO 2 column density along the line of sight of the instrument. This paper first presents the theory behind the method, then discusses validation experiments using a radiative transfer model, as well as applications to field data obtained under different measurement conditions at three different locations; Fagradalsfjall located on the Reykjanaes peninsula in south Island, Manam located off the northeast coast of mainland Papua New Guinea and Holuhraun located in the inland of north east Island.

Frontiers in Earth Science↗

USGS2023

Weak degassing from remote Alaska volcanoes characterized with a new airborne Imaging DOAS instrument and a suite of in situ sensors

Gas emissions from volcanoes occur when volatile species exsolve from magmatic and hydrothermal systems and make their way to the surface. Measurements of emitted gases therefore provide insights into volcanic processes. On 16 July 2021, we made airborne measurements of weak gas plumes emitted from four remote Alaska volcanoes: Iliamna Volcano, Mount Douglas, Mount Martin, and Mount Mageik. Integrated into a small fixed-wing aircraft, a new Imaging Differential Optical Absorption Spectroscopy (DOAS) instrument was used to map the spatial extent of SO 2 plumes as they drifted downwind. Contrary to conventional Mobile DOAS instruments, which provide only a single viewing direction, the Imaging DOAS simultaneously measures SO 2 column density along 48 individual viewing directions oriented in a swath above or below the aircraft. Each of the individual measurements have a comparable precision and sensitivity to those obtained by conventional instruments. Together, they provide high resolution 2D imagery of the volcanic plumes and allow calculation of limited emission rate time series information. Although zenith-facing DOAS measurements achieve greater accuracy and are performed here, the application of the Imaging DOAS in a nadir-facing setup is also discussed and compared to satellite observations made in similar geometries. Also onboard the aircraft, a suite of electrochemical and optical sensors measured the relative abundances of the six major volcanic volatile species H 2 O, CO 2 , SO 2 , H 2 S, HCl, and HF as the aircraft passed through the plumes. Mean SO 2 emission rates of 90 ± 10, 20 ± 3, and 13 ± 3 t/d were measured at Iliamna Volcano, Mount Douglas, and Mount Martin, respectively. SO 2 emissions were below the DOAS detection limit at Mount Mageik but CO 2 and H 2 S could be measured with the in situ sensors. The information gleaned from these measurements was used to assess and compare activity at these volcanoes, all of which were found to be in a state of background degassing but whose emissions pointed to different source conditions ranging from mixed magmatic-hydrothermal to purely hydrothermal in character. Additional measurements at Mount Spurr, Redoubt Volcano, and Augustine Volcano failed to detect the very weak gas concentrations downwind of these persistently degassing vents.

Alaska↗

USGS2023

A new permanent, low-cost, low-power SO2 camera for continuous measurement of volcanic emissions

Since its introduction to volcanology in the mid-2000 s, the SO 2 camera has become an important instrument for the acquisition of accurate and high time-resolution SO 2 emission rates, aiding in hazard assessment and volcanological research. However, with the exception of a few locations (Stromboli, Etna, Kīlauea), hitherto the majority of measurements have been made on discrete field campaigns, which provide only brief snapshots into a volcano’s activity. Here, we present the development of a new, low-cost, low-power SO 2 camera for permanent deployment on volcanoes, facilitating long-term, quasi-continuous (daylight hours only) measurements. We then discuss preliminary datasets from Lascar and Kīlauea volcanoes, where instruments are now in continuous operation. Further proliferation of such instrumentation has the potential to greatly improve our understanding of the transient nature of volcanic activity, as well as aiding volcano monitoring/eruption forecasting.

Frontiers in Earth Science↗

USGS2023

Estimates of volcanic mercury emissions from Redoubt Volcano, Augustine Volcano, and Mount Spurr eruption ash

Ash is a potential sink of volcanically sourced atmospheric mercury (Hg), and the concentration of particle-bound Hg may provide constraints on Hg emissions during eruptions. We analyze Hg concentrations in 227 bulk ash samples from the Mount Spurr (1992), Redoubt Volcano (2009), and Augustine Volcano (2006) volcanic eruptions to investigate large-scale spatial, temporal, and volcanic-source trends. We find no significant difference in Hg concentrations in bulk ash by distance or discrete eruptive events at each volcano, suggesting that in-plume reactions converting gaseous Hg 0 to adsorbed Hg 2+ are happening on shorter timescales than considered in this study (minutes) and any additional in-plume controls are not discernable within intra-volcanic sample variability. However, we do find a significant difference in Hg concentration of ash among volcanic sources, which indicates that volcanoes may emit comparatively high or low quantities of Hg. We combine our Hg findings with total mass estimates of ashfall deposits to calculate minimum, first-order Hg emissions of 8.23 t Hg for Mount Spurr (1992), 1.25 t Hg for Redoubt Volcano (2009), and 0.16 t Hg for Augustine Volcano (2006). In particular, we find that Mount Spurr is a high Hg emitting volcano, and that its 1992 particulate Hg emissions likely contributed substantially to the global eruptive volcanic Hg budget for that year. Based on our findings, previous approaches that use long-term Hg/SO 2 mass ratios to estimate eruptive total Hg under-account for Hg emitted in explosive events, and global volcanogenic Total Hg estimates need revisiting.

Alaska↗

USGS2023

Tracking carbon from subduction to outgassing along the Aleutian-Alaska Volcanic Arc

Subduction transports volatiles between Earth’s mantle, crust, and atmosphere, ultimately creating a habitable Earth. We use isotopes to track carbon from subduction to outgassing along the Aleutian-Alaska Arc. We find substantial along-strike variations in the isotopic composition of volcanic gases, explained by different recycling efficiencies of subducting carbon to the atmosphere via arc volcanism and modulated by subduction character. Fast and cool subduction facilitates recycling of ~43 to 61% sediment-derived organic carbon to the atmosphere through degassing of central Aleutian volcanoes, while slow and warm subduction favors forearc sediment removal, leading to recycling of ~6 to 9% altered oceanic crust carbon to the atmosphere through degassing of western Aleutian volcanoes. These results indicate that less carbon is returned to the deep mantle than previously thought and that subducting organic carbon is not a reliable atmospheric carbon sink over subduction time scales.

Alaska↗

USGS2022

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↗

USGS2022

A golden era for volcanic gas geochemistry?

The exsolution, rise, expansion, and separation of volatiles from magma provides the driving force behind both effusive and explosive volcanic eruptions. The field of volcanic gas geochemistry therefore plays a key role in understanding volcanism. In this article, we summarize the most important findings of the past few decades and how these shape today’s understanding of volcanic degassing. We argue that the recent advent of automated, continuous geochemical monitoring at volcanoes now allows us to track activity from unrest to eruption, thus providing valuable insights into the behavior of volatiles throughout the entire sequence. In the next 10 years, the research community stands to benefit from the expansion of geochemical monitoring networks to many more active volcanoes. This, along with technical advances in instrumentation, and in particular the increasing role that unoccupied aircraft systems (UAS) and satellite-based observations are likely to play in collecting volcanic gas measurements, will provide a rich dataset for testing hypotheses and developing diagnostic tools for eruption forecasts. The use of consistent, well-documented analytical methods and ensuring free, public access to the collected data with few restrictions will be most beneficial to the advancement of volcanic gas science.

Bulletin of Volcanology↗

USGS2022

Characterizing unrest: A retrospective look at 20 years of gas emissions and seismicity at Iliamna Volcano, Alaska

Episodes of unrest are not as well documented as eruptions at most volcanoes globally. Iliamna is an andesitic stratovolcano in the Cook Inlet of Alaska that has experienced several episodes of unrest. Unrest in 1996 was previously studied. Here we present data from a minor period of unrest between 2002 and 2006, and a more significant period in 2012. None of the episodes led to an eruption. A dike intrusion was suggested for the 1996 unrest based on increases in gas emissions and seismic analysis. The 2002–2006 period was characterized by a slight increase in the rate of seismicity to 13 events per day and was particularly notable due to an increase in deep long period (DLP) seismic events between 15 and 37 km that were not observed at other times. This period also included one airborne gas measurement with and elevated CO 2 /SO 2 molar ratio (17). In 2012, Iliamna unrest was characterized by significantly elevated gas emissions (up to 582 t/d SO 2 and 1385 t/d CO 2 ) and up to 49 located earthquakes per day (M > 0), and was remarkably similar to the 1996 unrest. Differences in the observed evolution of the CO 2 /SO 2 gas ratio in 2012 (2.2–4) compared to that in 1996 (up to 18) suggests that no new deep magma was involved in 2012, however this does not preclude the movement of a previously intruded magma. A months-long increase in the SO 2 /H 2 S molar ratio from 8 to 17 during the peak of the activity could reflect a temperature increase on the order of 10–30 °C of the emitted gas. Compared to pre-eruptive unrest at other Cook Inlet volcanoes, Iliamna unrest in 2012 differed in that gas emissions were < 1500 t/d and seismicity lacked a rapidly escalating sequence of earthquakes and volcanic tremor, which is normally observed in the hours to days before eruption. The observation of DLPs, the fact that Iliamna produces moderately elevated degassing over decadal timeframes, and the persistent dominance of SO 2 over H 2 S, suggests that periodic input of fresh magma from the lower crust sustains the shallower magmatic system over time, which sets it apart from neighboring volcanoes in the Cook Inlet that show minimal activity between eruptions. Various scenarios could explain why Iliamna did not proceed to eruption in 2012. Finally, we present criteria by which monitoring data may suggest an increased likelihood of eruption at Iliamna in the future.

Alaska↗

USGS2021

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↗

USGS2021

Volatile metal emissions from volcanic degassing and lava–seawater interactions at Kīlauea Volcano, Hawai’i

Volcanoes represent one of the largest natural sources of metals to the Earth’s surface. Emissions of these metals can have important impacts on the biosphere as pollutants or nutrients. Here we use ground- and drone-based direct measurements to compare the gas and particulate chemistry of the magmatic and lava–seawater interaction (laze) plumes from the 2018 eruption of Kīlauea, Hawai’i. We find that the magmatic plume contains abundant volatile metals and metalloids whereas the laze plume is further enriched in copper and seawater components, like chlorine, with volatile metals also elevated above seawater concentrations. Speciation modelling of magmatic gas mixtures highlights the importance of the S 2− ligand in highly volatile metal/metalloid degassing at the magmatic vent. In contrast, volatile metal enrichments in the laze plume can be explained by affinity for chloride complexation during late-stage degassing of distal lavas, which is potentially facilitated by the HCl gas formed as seawater boils.

Hawaii↗

USGS2021

Rapid metal pollutant deposition from the volcanic plume of Kīlauea, Hawai’i

Long-lived basaltic volcanic eruptions are a globally important source of environmentally reactive, volatile metal pollutant elements such as selenium, cadmium and lead. The 2018 eruption of Kīlauea, Hawai’i produced exceptionally high discharge of metal pollutants, and was an unprecedented opportunity to track them from vent to deposition. Here we show, through geochemical sampling of the plume that volatile metal pollutants were depleted in the plume up to 100 times faster than refractory species, such as magnesium and iron. We propose that this rapid wet deposition of complexes containing reactive and potentially toxic volatile metal pollutants may disproportionately impact localised areas close to the vent. We infer that the relationship between volatility and solubility is an important control on the atmospheric behaviour of elements. We suggest that assessment of hazards from volcanic emissions should account for heterogeneous plume depletion of metal pollutants.

Hawaii↗