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Patricia A. Nadeau

Publications and source records attributed to Patricia A. Nadeau.

17 recordsLinked to original sources

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↗

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↗

Growth of a passive lava lake during the 2020–2021 eruption of Kīlauea volcano, Hawaii

We investigate the growth of a passive lava lake in Halemaʻumaʻu crater during the December 2020 to May 2021 eruption of Kīlauea volcano, Hawaii. Fed by vents above their surfaces, the formation of passive lava lakes in topographic lows is an important process in the growth of basaltic volcanoes. We captured visible and thermal images during 17 helicopter overflights and applied structure-from-motion photogrammetry to create digital elevation models and orthomosaics of Halemaʻumaʻu. These data products allowed us to track eruptive activity and processes. The bulk time-averaged discharge rate (TADR) in December 2020 initially exceeded 100 m 3 s –1 but decreased to < 10 m 3 s –1 within seven days. By February 2021, TADR was < 2 m 3 s –1 and continued to decrease until the eruption ended in May 2021. A total volume of 40.6 ± 0.5 × 10 6 m 3 of lava filled Halemaʻumaʻu to a depth of 225 m. As TADR decreased, the lake progressively developed an immobile, solidified crust, beginning with surfaces farthest from the vent. This immobile surface rose endogenously, whereas exogenous surface rise occurred near the vent. Eruptive activity at a vent ended when the level of the lake surface exceeded that of the vent, which we attribute to the effects of lava sitting above the vent on ascending magma. Regular helicopter overflights, combined with field observations and the extensive monitoring network at Kīlauea, generated an unprecedented density of observations that provide insights into the emplacement of passive lava lakes and how these eruptions wane and end.

Hawaii↗

Triggering the 2022 eruption of Mauna Loa

Distinguishing periods of intermittent unrest from the run-up to eruption is a major challenge at volcanoes around the globe. Comparing multidisciplinary monitoring data with mineral chemistry that records the physical and spatio-temporal evolution of magmas fundamentally advances our ability to forecast eruptions. The recent eruption of Mauna Loa, Earth’s largest active volcano, provides a unique opportunity to differentiate unrest from run-up and improve forecasting of future eruptions. After decades of intermittent seismic and geodetic activity over 38 years of repose, Mauna Loa began erupting on 27 November 2022. Here we present a multidisciplinary synthesis that tracks the spatio-temporal evolution of precursory activity by integrating mineral and melt chemistry, fluid inclusion barometry, numerical modeling of mineral zoning, syn-eruptive gas plume measurements, the distribution and frequency of earthquake hypocenters, seismic velocity changes, and ground deformation. These diverse data indicate that the eruption occurred following a 2-month period of sustained magma intrusion from depths of 3–5 km up to 1–2 km beneath the summit caldera, providing a new model of the plumbing system at this very high threat volcano. Careful correlation of both the geochemistry and instrumental monitoring data improves our ability to distinguish unrest from the run-up to eruption by providing deeper understanding of the both the monitoring data and the magmatic system—an approach that could be applied at other volcanic systems worldwide.

Hawaii↗

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↗

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↗

Olivine diffusion constrains months-scale magma transport within Kīlauea volcano’s summit reservoir system prior to the 2020 eruption

The unprecedented 2018 summit collapse at Kīlauea and subsequent 2020–2021 eruption within the newly deepened Halema‘uma‘u Crater provide an unparalleled opportunity to understand how collapse events impact a volcano’s shallow reservoir system and magmatic processes. Glass and olivine from tephra ejected by lava fountains and several explosions on 20–21 December, within a few hours of the 2020 eruption onset, yield information about pre-eruptive magma storage and transport. The olivine population is bimodal with zoned and non-zoned phenocrysts. Normally zoned olivine crystals with core compositions around Fo 88 have 30–50 μm wide Fo 82 overgrowth rims that have skeletal textures. Two skeletal xenocrysts (cores Fo 74 and Fo 81 ) are also reversely zoned up to Fo 82 rims. The crystal cores have trace element records of at least two cycles of growth and dissolution prior to the formation of the overgrowth rims. These rims and a separate population of non-zoned Fo 82 crystals are in Fe–Mg equilibrium with their host glass (average MgO of 6.9 ± 0.4 wt% (1σ), Mg# [Mg / (Mg + Fe 2+ )] of 0.57), which suggests undercooling after intrusion of magma to shallow levels in the plumbing system. In the years prior to the 2018 collapse, non-zoned Fo 81 olivine and slightly lower MgO glasses (6.8 wt%) reflected continuous mixing and compositional buffering of magma recharge into several km 3 of stored magma in the Halema‘uma‘u reservoir (1–2 km depth). The 2020 olivine crystals lack evidence of an intrusion mixing with resident shallow magma, indicating that magma transport occurred in a disrupted system, and/or it may not have significantly mixed with stored magma remaining in the Halema‘uma‘u reservoir after the events of 2018. Diffusion modeling of Fe–Mg exchange in the zoned 2020 olivine crystals yield timescales that are mostly 60 days prior to the eruption or less, which aligns well with 22–24 October 2020 and subsequent seismic swarms at Nāmakani Paio ~ 5 km west of Kīlauea’s summit caldera. This correlation indicates that magma intruding beneath the summit (volume accommodation, recorded by the olivine crystals) was expressed by tectonic earthquakes along the Ka‘ōiki fault zone (stress accommodation). The absence of precursory SO 2 within minutes prior to eruption also indicates that the 2020 December magma may have risen from 1 to 2 km depth to the surface in as little as 10 min.

Hawaii↗

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↗

Out of the frying pan and into the fire: Effects of volcanic heat and other stressors on the conservation of a critically endangered plant in Hawaiʻi

Loss of local biodiversity resulting from abrupt environmental change is a significant environmental problem throughout the world. Extinctions of plants are particularly important yet are often overlooked. Drawing from a case in Hawai‘i, a global hotspot for plant and other extinctions, we demonstrate an effort to better understand and determine priorities for the management of an endangered plant (‘Ihi makole or Portulaca sclerocarpa ) in the face of rapid and extreme environmental change. Volcanic heat emissions and biological invasions have anecdotally been suggested as possible threats to the species. We integrated P. sclerocarpa outplanting with efforts to collect geological and ecological data to gauge the role of elevated soil temperatures and invasive grasses in driving P. sclerocarpa mortality and population decline. We measured soil temperature, soil depth, surrounding cover and P. sclerocarpa survivorship over three decades. The abundance of wild P. sclerocarpa decreased by 99.7% from the 1990s to 2021. Only 51% of outplantings persisted through 3–4 years. Binomial regression and structural equation modelling revealed that, among the variables we analysed, high soil temperatures were most strongly associated with population decline. Finding the niche where soil temperatures are low enough to allow P. sclerocarpa survival but high enough to limit other agents of P. sclerocarpa mortality may be necessary to increase population growth of this species.

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↗

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↗

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↗

Monitoring network changes during the 2018 Kīlauea Volcano eruption

In the summer of 2018, Kīlauea Volcano underwent one of its most significant eruptions in the past few hundred years. The volcano’s summit and East Rift Zone magma system partially drained, resulting in a series of occasionally explosive partial caldera collapses, and widespread lava flows in the lower East Rift Zone. The Hawaiian Volcano Observatory (HVO) operates a robust permanent monitoring network of about 250 stations, recording a variety of real‐time data streams: seismic (short‐period, broadband, strong‐motion), infrasound, Global Navigation Satellite Systems (GNSS), tilt, camera, laser rangefinder, and gas geochemistry. During the eruption, HVO staff quickly established 35 new temporary monitoring stations, to better constrain evolving volcanic hazards. The partial collapses of the caldera threatened to disrupt important telemetry links in the HVO monitoring network, and a major effort was undertaken in the midst of the eruption crisis to reroute radio telemetry and maintain continuity of data flow. In the process, a new data center was established in Hilo, to mitigate a long‐standing potential single point of failure at the HVO facility. Over the course of the eruption from May through August, lava, ashfall, wildfire, and cliff collapse destroyed or disabled 36 stations. Thousands of earthquakes damaged the main HVO facility at Uēkahuna Bluff, causing staff to evacuate the building and relocate observatory operations in the midst of the eruption response, adding more complexity to the response effort. Throughout these events, the HVO team maintained the monitoring network, provided timely information to the public and emergency managers, and collected valuable scientific data to better understand Kīlauea Volcano.

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↗

Spatial and temporal variations in SO2 and PM2.5 levels around Kīlauea volcano, Hawai'i during 2007–2018

Among the hazards posed by volcanoes are the emissions of gases and particles that can affect air quality and damage agriculture and infrastructure. A recent intense episode of volcanic degassing associated with severe impacts on air quality accompanied the 2018 lower East Rift Zone (LERZ) eruption of Kīlauea volcano, Hawai'i. This resulted in a major increase in gas emission rates with respect to usual emission values for this volcano, along with a shift in the source of the dominant plume to a populated area on the lower flank of the volcano. This led to reduced air quality in downwind communities. We analyse open-access data from the permanent air quality monitoring networks operated by the Hawai'i Department of Health (HDOH) and National Park Service (NPS), and report on measurements of atmospheric sulfur dioxide (SO 2 ) between 2007 and 2018 and PM 2.5 (aerosol particulate matter with diameter <2.5 μm) between 2010 and 2018. Additional air quality data were collected through a community-operated network of low-cost PM 2.5 sensors during the 2018 LERZ eruption. From 2007 to 2018 the two most significant escalations in Kīlauea's volcanic emissions were: the summit eruption that began in 2008 (Kīlauea emissions averaged 5–6 kt/day SO 2 from 2008 until summit activity decreased in May 2018) and the LERZ eruption in 2018 when SO 2 emission rates reached a monthly average of 200 kt/day during June. In this paper we focus on characterizing the airborne pollutants arising from the 2018 LERZ eruption and the spatial distribution and severity of volcanic air pollution events across the Island of Hawai'i. The LERZ eruption caused the most frequent and severe exceedances of the Environmental Protection Agency (EPA) PM 2.5 air quality threshold (35 μg/m 3 as a daily average) in Hawai'i in the period 2010–2018. In Kona, for example, the maximum 24-h-mean mass concentration of PM 2.5 was recorded as 59 μg/m 3 on the twenty-ninth of May 2018, which was one of eight recorded exceedances of the EPA air quality threshold during the 2018 LERZ eruption, where there had been no exceedances in the previous 8 years as measured by the HDOH and NPS networks. SO 2 air pollution during the LERZ eruption was most severe in communities in the south and west of the island, as measured by selected HDOH and NPS stations in this study, with a maximum 24-h-mean mass concentration of 728 μg/m 3 recorded in Ocean View (100 km west of the LERZ emission source) in May 2018. Data from the low-cost sensor network correlated well with data from the HDOH PM 2.5 instruments, confirming that these low-cost sensors provide a robust means to augment reference-grade instrument networks.

Hawaii↗

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↗