Monitoring of volcanic eruptions at Yugama crater lake by aqueous sulfur oxyanions

Variations of polythionates (sulfane disulfonates) and sulfate in the Yugama crater lake, Japan, have been monitored for more than 25 years. Just before the 1982 eruption at the crater lake, polythionate ions decreased to zero from the normal level of about 2000 ppm and sulfate ions increased from 2500 to 5000 ppm. During the 1982 eruption polythionate and sulfate ions varied inversely in concentration and the variations exactly coincided with the frequency of volcanic earthquakes and subsequent explosions. These observations are interpreted in terms of aqueous reactions of fumarolic SO₂-H₂S gases, resulting in precipitation of alunite. The behavior of polythionate and sulfate ions strongly suggests that they are useful indicator for prediction of impending volcanic hazards from active crater lakes.     

Investigating crater lake warming using ASTER thermal imagery: Case studies at Ruapehu,Poás,Kawah Ijen,and Copahué Volcanoes

A two-channel or split-window algorithm designed to correct for atmospheric conditions was applied to thermal images taken by the Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) of Lake Yugama on Kusatsu–Shirane volcano in Japan in order to measure the temperature of its crater lake. These temperature calculations were validated using lake water temperatures that were collected on the ground. Overall, the agreement between the temperatures calculated using the split-window method and ground truth is quite good, typically ± 1.5 °C for cloud-free images. Data from fieldwork undertaken in the summer of 2004 at Kusatsu–Shirane allow a comparison of ground-truth data with the radiant temperatures measured using ASTER imagery. Further images were analyzed of Ruapehu, Poás, Kawah Ijen, and Copahué volcanoes to acquire time-series of lake temperatures. A total of 64 images of these 4 volcanoes covering a wide range of geographical locations and climates were analyzed. Results of the split-window algorithm applied to ASTER images are reliable for monitoring thermal changes in active volcanic lakes. These temperature data, when considered in conjunction with traditional volcano monitoring techniques, lead to a better understanding of whether and how thermal changes in crater lakes aid in eruption forecasting.     

Bathymetric and geochemical investigation of Kawah Ijen Crater Lake, East Java, Indonesia

A bathymetric survey of Kawah Ijen crater lake was conducted by acoustic sounding in 1996 to compare the lake morphology with those measured in 1922, 1925 and 1938, and to calculate the present lake volume. Even though the lake experienced several hydrothermal eruptions, the maximum depth became shallower (182 m) than before (200 m), resulting in a reduced lake volume (3.0×10⁷ m³).Fifty-two major and minor constituents including rare earth elements and polythionates (PT) of the lake waters at various depths were determined by ICP-AES, ICP-MS and HPLC, respectively. These ions except for several volatile elements are taken up by lake fringe through congruent dissolution of pyroclastics of Kawah Ijen volcano. Most ions are homogeneously distributed throughout the lake, although PT showed a considerable vertical variation. Rare earth elements (REE) in the Kawah Ijen water as well as those from other hyper-acidic crater lakes show distribution patterns likely due to the three rock dissolution (preferential, congruent and residual) types, and their logarithmic concentrations linearly depend upon the pH values of the lake waters.Using the PT degradation kinetics data, production rates of PT, injection rates of SO₂ and H₂S into the lake were estimated to be 114, 86 and 30 tons/day, respectively. Also travel time of the spring water at the Banyupahit Riverhead from Kawah Ijen was estimated to be 600–1000 days through the consideration of decreasing rates of PT. Molten sulfur stocks containing Sn, Cu, Bi sulfides and Pb-barite exposed on the inner crater slope were presumed to be extinct molten sulfur pools at the former lake bottom. This was strongly supported by the barite precipitation temperature estimated through the consideration of the temperature dependence of Pb-chlorocomplex formation.     

Groundwater transport of crater-lake brine at Poa´s Volcano, Costa Rica

Poa´s Volcano is an active stratovolcano in Costa Rica that has a lake in its active crater. The crater lake has high temperatures (50–90 °C), high acidity (pH ≈ 0.0), and a high dissolved-solids content (100 g/kg). The volcano has numerous freshwater springs on its flanks, but a few on the northwestern flank are highly acidic (pH = 1.6–2.5) and have high dissolved-solids concentrations (2–22 g/kg). This study analyzes the regional groundwater system at Poa´s and demonstrates the likelihood that the water discharging from the acidic springs in the Rio Agrio watershed originates at the acidic crater lake. Both heat and solute transport are analyzed on a regional scale through numerical simulations using the HST3D finite-difference model, which solves the coupled equations for fluid flow, heat transport, and solute transport. The code allows fluid viscosity and density to be functions of both temperature and solute concentration. The simulations use estimates for recharge to the mountain and a range of values and various distributions of permeability and porosity. Several sensitivity analyses are performed to test how the uncertainty in many of the model parameters affects the simulation results. These uncertainties yield an estimated range of travel times from the crater lake to the Rio Agrio springs of 1–30 years, which is in close agreement with the results of tritium analyses of the springs. Calculated groundwater fluxes into and out of the crater lake are both about several hundred kg/s. These fluxes must be accounted for in water budgets of the crater lake.     

Aqueous sulfur speciation possibly linked to sublimnic volcanic gas-water interaction during a quiescent period at Yugama crater lake,Kusatsu–Shirane volcano,Central Japan

After the phreatic eruption in 1982–83, volcanic activities at Kusatsu–Shirane volcano had been decreasing and reached a minimum in 1990, had turned to a temporal rise in activity up to 1994 and then decreased again at least up to 1997. During this low-activity period we observed a relatively short (≤ 1 y) cyclic variation in polythionates (PT) in the Yugama lake water. Spectral power density analysis of the PT time-series by an autoregressive (maximum entropy spectral estimation, MESE) method indicates that the major frequency in the PT variations is 1.0 y^− 1 and the minor is 2–3 y^− 1 (1.0 and 0.3–0.5 y in periodicity, respectively). Annual variations in the lake temperature are ruled out for explaining these periodicities. We attribute these cyclic variations to a cyclic magnification-reduction in meteoric-water injection into a hydrothermal regime where volcanic gases from cooling magma bodies at depth and cooler oxidized groundwater come into contact with each other. This interaction may result in a periodical change in the composition and flux of SO₂ and H₂S gases being discharged into the lake and forming PT. From a phase deviation (2–3 months) in the cycles between the annual precipitation, including snowmelt, and the PT time-series, we estimated the maximal depth of a hydrothermal reservoir beneath the lake assuming a vertical hydraulic conductivity (5 × 10^− 3 cm/s) of the volcanic detritus around the summit hydrothermal system. Chloride in the lake water reached a maximum 1.5 years faster than PT. This is most likely due to a gradual elevation of the potentiometric front of a concentrated sublimnic solution in the hydrothermal reservoir. Variations of dissolved SO₂ and H₂S in the lake water were not consistent with those of the fumarolic gases on the north flank of the volcano. This fact together with additional observations strongly suggests that these fumaroles may have the same origin but are chemically modified by a subsurface aquifer. The PT monitoring at active crater lakes during a quiescent period can provide insight into the annual expansions and reductions of a volcano-hosted hydrothermal reservoir.     

Geochemistry of the Albano and Nemi crater lakes in the volcanic district of Alban Hills (Rome,Italy)

Lake Albano, located 20 km to the SE of Rome, is hosted within the most recent crater of the quiescent Alban Hills volcanic complex that produced hydromagmatic eruptions in Holocene times. Stratigraphic, archaeological and historical evidence indicates that the lake level underwent important variations in the Bronze Age. Before the IV century B.C. several lahars were generated by water overflows from the lake and in the IV century B.C. Romans excavated a drainage tunnel. The lake is located above a buried carbonate horst that contains a pressurized medium-enthalpy geothermal reservoir from which fluids escape to the surface to produce many important gas manifestations of mostly CO₂. Previous studies recognized the presence of gas emissions also from the crater bottom. In 1997 the possibility of a Nyos-type event triggered by a lake rollover was considered very low, because the CO₂ water concentration at depth was found to be far from saturation. However, considering the high population density nearby, the Italian Civil Protection Department recommended that periodical monitoring be carried out. To this scope we initiated in 2001 a systematic geochemical study of the lake. Thirteen vertical profiles have been repeatedly carried out in 2001–2006, especially in the deepest part of the lake (167 m in 2006), measuring T, pH, dissolved O₂ and electrical conductivity. Water samples were collected from various depths and chemically and isotopically analysed. Two similar profiles have been measured also in the nearby Nemi crater lake. Results indicate that in the 4.5 years of monitoring the pressure of gas dissolved in the Lake Albano deep waters remained much lower than the hydrostatic pressure. A CO₂ soil survey carried out on the borders of the two lakes, indicates the presence of some zones of anomalous degassing of likely magmatic origin. A water overturn or a heavy mixing of deep and shallow waters likely occurred in winter 2003–2004, when cold rainfall cooled the surface water below 8.5 °C. Such overturns cause only a limited gas exsolution from the lake when the deep water is brought to a few meters depth but can explain the observed decrease with time of dissolved CO₂ at depth and related water pH increase. A gas hazard could occur in the case of a sudden injection through the lake bottom of a huge quantity of CO₂-rich fluids, which might be caused by earthquake induced fracturing of the rock pile beneath the lake. A limnic gas eruption might also occur should CO₂ concentration build up within the lake for a long time.     

Hydrochemical dynamics of the “lake–spring” system in the crater of El Chichón volcano (Chiapas,Mexico)

El Chichón volcano (Chiapas, Mexico) erupted violently in March–April 1982, breaching through the former volcano–hydrothermal system. Since then, the 1982 crater has hosted a shallow (1–3.3 m, acidic (pH ∼ 2.2) and warm (∼ 30 °C) crater lake with a strongly varying chemistry (Cl/SO₄ = 0–79 molar ratio). The changes in crater lake chemistry and volume are not systematically related to the seasonal variation of rainfall, but rather to the activity of near-neutral geyser-like springs in the crater (Soap Pool). These Soap Pool springs are the only sources of Cl for the lake. Their geyser-like behaviour with a long-term (months to years) periodicity is due to a specific geometry of the shallow boiling aquifer beneath the lake, which is the remnant of the 1983 Cl-rich (24,000 mg/l) crater lake water. The Soap Pool springs decreased in Cl content over time. The zero-time extrapolation (1982, year of the eruption) approaches the Cl content in the initial crater lake, meanwhile the extrapolation towards the future indicates a zero-Cl content by 2009 ± 1. This particular situation offers the opportunity to calculate mass balance and Cl budget to quantify the lake–spring system in the El Chichón crater. These calculations show that the water balance without the input of SP springs is negative, implying that the lake should disappear during the dry season. The isotopic composition of lake waters (δD and δ¹⁸O) coincide with this crater lake-SP dynamics, reflecting evaporation processes and mixing with SP geyser and meteoric water. Future dome growth, not observed yet in the post-1982 El Chichón crater, may be anticipated by changes in lake chemistry and dynamics.     

A water flow model of the active crater lake at Aso volcano,Japan: fluctuations of magmatic gas and groundwater fluxes from the underlying hydrothermal system

The first crater of Nakadake, peak of Aso volcano, Japan, contains a hot water lake that shows interesting variations in water level and temperature. These variations were discovered by precise, continuous observations of the lake independent of precipitation. We developed a numerical model of a hot crater lake and compared with observational data for the period from July 2006 to January 2009. The numerical model revealed seasonal changes in mass flux (75–132 kg/s) and enthalpy (1,840–3,030 kJ/kg) for the fluid supplied to the lake. The relation between the enthalpy and mass flux indicates that the bottom input fluid is a mixture of high- and low-temperature fluids. Assuming a mixture of high-temperature steam at 800°C and liquid water at 100°C, we evaluated the liquid and steam fluxes. The liquid water flux shows a seasonal increase lagging behind the rainy season by 2 months, suggesting that the liquid water is predominantly groundwater. The fluctuation pattern in the flux of the high-temperature steam shows a relation with the amplitude of volcanic tremor, suggesting that heating of the hydrothermal system drives the tremor. Consequently, precise observations of a hot crater lake represent a potential method of monitoring volcanic hydrothermal systems in the shallow parts of the volcanoes.     

The time-dependent variation of hydrogeochemical characteristics, thermal regime, and biocenoses in the fresh and thermal waters of the Lake Karymskii basin following the catastrophic underwater eruption of 1996 in the Akademii Nauk Caldera, Kamchatka

The results of biohydrogeochemical monitoring are used to study time-dependent variations in the hydrogeochemical characteristics of the Lake Karymskii water mass, the state and characteristics of underwater discharge zones in the Tokarev crater (formed in 1996), hydrogeochemical characteristics of thermal springs around the lake, and the biota succession in the lake for the period 1996–2006 (2007). We detected a stratification in the chemical composition of water over depth and the presence of persistent zones of increased concentrations of dissolved oxygen. We found an alkalization of lake water and a decrease in its total salinity. The new thermal springs and underwater discharges of thermal water and gases were found to be continuing. The first data were obtained on the concentration of microelements in the thermal springs of the Karymskii basin. The biodiversity of algae in Lake Karymskii was largely increased by the species diversity of benthic Bacillariophyta. The plankton phytocomponent of the precatastrophic period was found to have been regenerated in the lake as of April 2007.     

Chemical evolution and volcanic activity of the active crater lake of Poás volcano, Costa Rica, 1993–1997

Concentrations of chloride and sulfate and pH in the hot crater lake (Laguna Caliente) at Poás volcano and in acid rain varied over the period 1993–1997. These parameters are related to changes in lake volume and temperature, and changes in summit seismicity and fumarole activity beneath the active crater. During this period, lake level increased from near zero to its highest level since 1953, lake temperature declined from a maximum value of 70°C to a minimum value of 25°C, and pH of the lake water increased from near zero to 1.8. In May 1993 when the lake was nearly dry, chloride and sulfate concentrations in the lake water reached 85,400 and 91,000 mg l⁻¹, respectively. Minimum concentrations of chloride and sulfate after the lake refilled to its maximum volume were 2630 and 4060 mg l⁻¹, respectively. Between January 1993 and May 1995, most fumarolic activity was focused through the bottom of the lake. After May 1995, fumarolic discharge through the bottom of the lake declined and reappeared outside the lake within the main crater area. The appearance of new fumaroles on the composite pyroclastic cone coincided with a dramatic decrease in type B seismicity after January 1996. Between May 1995 and December 1997, enhanced periods of type A seismicity and episodes of harmonic tremor were associated with an increase in the number of fumaroles and the intensity of degassing on the composite pyroclastic cone adjacent to the crater lake. Increases in summit seismic activity (type A, B and harmonic tremor) and in the height of eruption plumes through the lake bottom are associated with a period of enhanced volcanic activity during April–September 1994. At this time, visual observations and remote fumarole temperature measurements suggest an increase in the flux of heat and gases discharged through the bottom of the crater lake, possibly related to renewed magma ascent beneath the active crater. A similar period of enhanced seismic activity that occurred between August 1995 and January 1996, apparently caused fracturing of sealed fumarole conduits beneath the composite pyroclastic cone allowing the focus of fumarolic degassing to migrate from beneath the lake back to the 1953–1955 cone. Changes in the chemistry of summit acid rain are correlated changes in volcanic activity regardless of whether fumaroles are discharging into the lake or are discharging directly into the atmosphere.     

云南腾冲青海——酸性湖泊的环境特征

火山口湖成因和持续酸性地下水补给是腾冲青海呈现酸性湖泊环境的地质基础,通过对青海环境的实际调查和水、土、生物样品的分析、鉴定,结果表明：湖水具较低pH值、极低的阳离子组成和矿化度;沉积物中Ca、Mg、Al、Fe等元素有明显流失;湖泊生物种群少且生物量低,缺失蓝藻和腹足类、瓣鳃类、甲壳类动物等为区别于一般中、碱性湖泊最显著的特点,酸性水介质湖泊系统元素地球化学行为的变化及其对生物的影响－－生物贫化和耐酸种扩张,既是腾冲青海的基本特点,也是酸性湖泊环境形成的动力机制。     

Geochemistry of the magmatic–hydrothermal system of Kawah Ijen volcano, East Java, Indonesia

Samples from Kawah Ijen crater lake, spring and fumarole discharges were collected between 1990 and 1996 for chemical and isotopic analysis. An extremely low pH (<0.3) lake contains SO₄–Cl waters produced during absorption of magmatic volatiles into shallow ground water. The acidic waters dissolve the rock isochemically to produce “immature” solutions. The strong D and ¹⁸O enrichment of the lake is mainly due to enhanced evaporation at elevated temperature, but involvement of a magmatic component with heavy isotopic ratios also modifies the lake D and ¹⁸O content. The large Δ_SO4–S⁰ (23.8–26.4‰) measured in the lake suggest that dissolved SO₄ forms during disproportionation of magmatic SO₂ in the hydrothermal conduit at temperatures of 250280°C. The lake δ¹⁸O_SO4 and δ¹⁸O_H2O values may reflect equilibration during subsurface circulation of the water at temperatures near 150°C. Significant variations in the lake's bulk composition from 1990 to 1996 were not detected. However, we interpret a change in the distribution and concentration of polythionate species in 1996 as a result of increased SO₂-rich gas input to the lake system.Thermal springs at Kawah Ijen consist of acidic SO₄–Cl waters on the lakeshore and neutral pH HCO₃–SO₄–Cl–Na waters in Blawan village, 17 km from the crater. The cation contents of these discharges are diluted compared to the crater lake but still do not represent equilibrium with the rock. The SO₄/Cl ratios and water and sulfur isotopic compositions support the idea that these springs are mixtures of summit acidic SO₄–Cl water and ground water.The lakeshore fumarole discharges (T=170245°C) have both a magmatic and a hydrothermal component and are supersaturated with respect to elemental sulfur. The apparent equilibrium temperature of the gas is 260°C. The proportions of the oxidized, SO₂-dominated magmatic vapor and of the reduced, H₂S-dominated hydrothermal vapor in the fumaroles varied between 1979 and 1996. This may be the result of interaction of SO₂-bearing magmatic vapors with the summit acidic hydrothermal reservoir. This idea is supported by the lower H₂S/SO₂ ratio deduced for the gas producing the SO₄–Cl reservoir feeding the lake compared with that observed in the subaerial gas discharges. The condensing gas may have equilibrated in a liquid–vapor zone at about 350°C.Elemental sulfur occurs in the crater lake environment as banded sediments exposed on the lakeshore and as a subaqueous molten body on the crater floor. The sediments were precipitated in the past during inorganic oxidation of H₂S in the lake water. This process was not continuous, but was interrupted by periods of massive silica (poorly crystallized) precipitation, similar to the present-day lake conditions. We suggest that the factor controlling the type of deposition is related to whether H₂S- or silica-rich volcanic discharges enter the lake. This could depend on the efficiency with which the lake water circulates in the hydrothermal cell beneath the crater. Quenched liquid sulfur products show δ³⁴S values similar to those found in the banded deposits, suggesting that the subaqueous molten body simply consists of melted sediments previously accumulated at the lake bottom.     

Subaqueous geothermal activity revealed by lacustrine sediments of the acidic Nakadake crater lake, Aso Volcano, Japan

Lacustrine sediments were sampled from the inaccessible acidic (pH = 0.43) Nakadake crater lake of Aso Volcano, Japan by a simple method. The sediments contain an extremely high content (74 wt.%) of sulfur, which exits as elemental sulfur, gypsum and anhydrite. The abundant elemental sulfur is likely formed by the reaction of SO₂ and H₂S gases and by the SO₂ disproportionation reaction in magmatic hydrothermal system below the crater lake. Based on the sulfur content of sediments and measurements of elevation change of the crater bottom, the sulfur accumulation rate at the Nakadake crater lake was calculated as 250 tonne/day, which is comparable with the SO₂ emission rate (200–600 tonne/day) from the Nakadake crater. The sediments include a small amount (9%) of clear glass shards that are apparently not altered in spite of the high reactivity of hyperacid lake water. This finding suggests that the clear glass shards are fragments of recently emitted magmas from fumaroles on the bottom of the crater lake and the magma emissions continuously occur even in quiescent periods.     

Hydroacoustic noise precursors of the 1990 eruption of Kelut Volcano, Indonesia

The results of a hydroacoustic monitoring experiment in the Kelut Crater lake, Indonesia, prior to its 1990 eruption, are presented, with the benefit of hindsight. Indeed, the underwater noise levels in three widely separated frequency bands, together with the lake water temperature, was radio-transmitted and almost continuously recorded from a period of quiescence of the volcano till the onset of its 10 February 1990, eruption, which destroyed the monitoring buoy. The comparative analysis of the noise variations in the three bands, together with seismic and temperature data, have shed light on the mechanisms underlying the pre-eruptive activity. The three acoustic levels had shown conspicuous, yet distinctive, changes prior to the eruption. Acoustic level in the low-frequency (1–50 Hz) band, which increased one year before the resumption of seismic activity and the lake warming up, is interpreted as the result of boiling at depth. The source of high-acoustic level in the audiometric (500–5000 Hz) range is clearly the bubbling of volcanic gases, occurring as a strong convective column in the middle of the lake. From the variations of this audiometric level, we have estimated that the degassing rate in the lake increased by a hundred-fold during the pre-eruptive period. Variations of ultrasonic (20–100 kHz) frequency acoustic level seem to be related with pressure and thermal changes within the hydrothermal system and its rock matrix beneath the lake. In conclusion, this experiment demonstrates the potential of hydroacoustic monitoring as an early warning system at crater lake volcanoes.     

Estimating thermal inflow to El Chichón crater lake using the energy-budget,chemical and isotope balance approaches

El Chichón crater lake appeared immediately after the 1982 catastrophic eruption in a newly formed, 1-km wide, explosive crater. During the first 2 years after the eruption the lake transformed from hot and ultra-acidic caused by dissolution of magmatic gases, to a warm and less acidic lake due to a rapid “magmatic-to-hydrothermal transition” — input of hydrothermal fluids and oxidation of H₂S to sulfate. Chemical composition of the lake water and other thermal fluids discharging in the crater, stable isotope composition (δD and δ¹⁸O) of lake water, gas condensates and thermal waters collected in 1995–2006 were used for the mass-balance calculations (Cl, SO₄ and isotopic composition) of the thermal flux from the crater floor. The calculated fluxes of thermal fluid by different mass-balance approaches become of the same order of magnitude as those derived from the energy-budget model if values of 1.9 and 2 mmol/mol are taken for the catchment coefficient and the average H₂S concentration in the hydrothermal vapors, respectively. The total heat power from the crater is estimated to be between 35 and 60 MW and the CO₂ flux is not higher than 150 t/day or ~ 200 gm^− 2 day^− 1.     

The crater lake and hydrothermal system of Mount Pinatubo,Philippines: evolution in the decade after eruption

The June 1991 eruption of Mount Pinatubo, Philippines breached a significant, pre-eruptive magmatic-hydrothermal system consisting of a hot (>300 °C) core at two-phase conditions and surrounding, cooler (<260 °C) liquid outflows to the N and S. The eruption created a large, closed crater that accumulated hydrothermal upwellings, near-surface aquifer and meteoric inflows. A shallow lake formed by early September 1991, and showed a long-term increase in level of ~1 m/month until an artificial drainage was created in September 2001. Comparison of the temporal trends in lake chemistry to pre- and post-eruptive springs distinguishes processes important in lake evolution. The lake was initially near-neutral pH and dominated by meteoric influx and Cl–SO₄ and Cl–HCO₃ hydrothermal waters, with peaks in SO₄ and Ca concentrations resulting from leaching of anhydrite and aerosol-laden tephra. Magmatic discharge, acidity (pH~2) and rock dissolution peaked in late 1992, during and immediately after eruption of a lava dome on the crater floor. Since cessation of dome growth, trends in lake pH (increase from 3 to 5.5), temperature (decline from 40 to 26 °C), and chemical and isotopic composition indicate that magmatic degassing and rock dissolution have declined significantly relative to the input of meteoric water and immature hydrothermal brine. Higher concentrations of Cl, Na, K, Li and B, and lower concentrations of Mg, Ca, Fe, SO₄ and F up to 1999 highlight the importance of a dilute hydrothermal contribution, as do stable-isotope and tritium compositions of the various fluids. However, samples taken since that time indicate further dilution and steeper trends of increasing pH and declining temperature. Present gas and brine compositions from crater fumaroles and hot springs indicate boiling of an immature Cl–SO₄ geothermal fluid of near-neutral pH at approximately 200 °C, rather than direct discharge from magma. It appears that remnants of the pre-eruptive hydrothermal system invaded the magma conduit shortly after the end of dome emplacement, blocking the direct degassing path. This, along with the large catchment area (~5 km²) and the high precipitation rate of the area, led to a rapid transition from a small and hot acid lake to a large lake with near-ambient temperature and pH. This behavior contrasts with that of peak-activity lakes that have more sustained volcanic gas influx (e.g., Kawah Ijen, Indonesia; Poas and Rincón de la Vieja, Costa Rica).Editorial responsibility: H. Shinohara     

Temporal changes in the chemistry of lake water within Yugama Crater,Kusatsu-Shirane Volcano,Japan: Implications for the evolution of the magmatic hydrothermal system

The chemical composition and temperature of lake water within Yugama Crater, Kusatsu-Shirane Volcano, Japan, have fluctuated markedly over the period 1966 to 2005. From 1966 to 1981, water temperature was relatively low, and Cl⁻ and SO₄²⁻ concentrations gradually decreased. These trends are explained by the growth of a sealing zone that formed between the region of hot rock surrounding the degassing magma and cool crust saturated with groundwater. The sealing zone acted to restrict the emission of magmatic volatiles.     

Brownish discoloration of the summit crater lake of Mt. Shinmoe-dake,Kirishima Volcano,Japan: volcanic–microbial coupled origin

A drastic change in lake water color from blue-green to brown was observed in the summit crater lake of Mt. Shinmoe-dake, Kirishima Volcano about 8 months after its 2008 eruption. The color change lasted for about 2 months (April–June 2009). The discoloration was attributed to a brownish color suspension that had formed in the lake water. X-ray fluorescence and Fourier transform infrared analyses of a sample of the suspension identified schwertmannite (Fe₈O₈(OH)₆(SO₄)). A cultivation test of iron-oxidizing bacteria for the sampled lake water with lakebed sediment revealed that the crater lake hosts iron-oxidizing bacteria, which likely participated in schwertmannite formation. We suggest that pyrite (FeS₂) provided an energy source for the iron-oxidizing bacteria since the mineral was identified in hydrothermally altered tephra ejected by the August 2008 eruption. From consideration of these and other factors, the brownish discoloration of the summit crater lake of Mt. Shinmoe-dake was inferred to have resulted from a combined volcanic–microbial process.     

Modeling Groundwater Inflow to the New Crater Lake at Kīlauea Volcano,Hawai'i

During the 2018 eruption of Kīlauea Volcano, Hawai'i, scientists relied heavily on a conceptual model of explosive eruptions triggered when lava-lake levels drop below the water table. Numerical modeling of multiphase groundwater flow and heat transport revealed that, contrary to expectations, liquid water inflow to the drained magma conduit would likely be delayed by months to years, owing to the inability of liquid water to transit a zone of very hot rock. The summit of Kīlauea subsequently experienced an ∼2-month period of consistent repeated collapses, and the crater now extends below the equilibrium position of the water table. Liquid water first emerged into the deepened crater in late July 2019. The timing of first appearance of liquid water (about 14 months postcollapse) and the rate of crater lake filling (currently ∼27 kg/s) were well-predicted by the numerical modeling done in late spring 2018, which forecast liquid inflow after 3 to 24 months at rates of 10 to 100 kg/s. A second-generation groundwater model, reflecting the current crater geometry, forecasts lake filling over the next several years. The successful 2018 to present forecasts with both models are based on unadjusted in situ permeability estimates (1 to 6 × 10⁻¹⁴ m²) and water-table elevations (600 to 800 m) from a nearby research drillhole and geophysical surveys. Important unknowns that affect the reliability of longer-term forecasts include the equilibrium water-table geometry, the rate of evaporation from the hot and growing crater lake (currently ∼29,000 m² at 70-80 °C), and heterogenous permeability changes caused by the 2018 collapse.     

Using Crater Lake chemistry to predict volcanic activity at Poás Volcano,Costa Rica

Monitoring of crater lake chemistry during the recent decline and disappearance of the crater lake of Poás Volcano revealed that large variations in SO₄/Cl, F/Cl, and Mg/Cl ratios were caused by the enhanced release of HCl vapor from the lake surface due to increasing lake temperature and solution acidity. Variation in the concentration of polythionic acids (H₂S_xO₆, x=4–6) was the most reliable predictor of renewed phreatic eruptive activity at the volcano, exhibiting sharp decreases three months prior to the initiation of phreatic eruptions in June 1987. Polythionic acids may offer a direct indicator of changing subsurface magmatic activity whereas chloride-based element ratios may be influenced by surface volatilization of HCl and subsequent recycling of acidic fluids in crater lake volcanoes.