Selected Crater and Small Caldera Lakes in Alaska: Characteristics and Hazards

This study addresses the characteristics, potential hazards, and both eruptive and non-eruptive role of water at selected volcanic crater lakes in Alaska. Crater lakes are an important feature of some stratovolcanoes in Alaska. Of the volcanoes in the state with known Holocene eruptive activity, about one third have summit crater lakes. Also included are two volcanoes with small caldera lakes (Katmai, Kaguyak). The lakes play an important but not well studied role in influencing eruptive behavior and pose some significant hydrologic hazards. Floods from crater lakes in Alaska are evaluated by estimating maximum potential crater lake water volumes and peak outflow discharge with a dam-break model. Some recent eruptions and hydrologic events that involved crater lakes also are reviewed. The large volumes of water potentially hosted by crater lakes in Alaska indicate that significant flowage hazards resulting from catastrophic breaching of crater rims are possible. Estimates of maximum peak flood discharge associated with breaching of lake-filled craters derived from dam-break modeling indicate that flood magnitudes could be as large as 103–106 m3/s if summit crater lakes drain rapidly when at maximum volume. Many of the Alaska crater lakes discussed are situated in hydrothermally altered craters characterized by complex assemblages of stratified unconsolidated volcaniclastic deposits, in a region known for large magnitude (>M7) earthquakes. Although there are only a few historical examples of eruptions involving crater lakes in Alaska, these provide noteworthy examples of the role of external water in cooling pyroclastic deposits, acidic crater-lake drainage, and water-related hazards such as lahars and base surge.

Rare Earth Elements Variations in a Hyperacid Crater Lake and Their Relations With Changes in Phreatic Activity, Physico-Chemical Parameters, and Chemical Composition: The Case of Poás Volcano (Costa Rica)

Decades of geochemical monitoring at active crater lakes worldwide have confirmed that variations in major elements and physico-chemical parameters are useful to detect changes in volcanic activity. However, it is still arduous to identify precursors of single phreatic eruptions. During the unrest phase of 2009–2016, at least 679 phreatic eruptions occurred at the hyperacid and hypersaline crater lake Laguna Caliente of Poás volcano (Costa Rica). In this study, we investigate the temporal variations of Rare Earth Elements (REE) dissolved in Laguna Caliente in order to 1) scrutinize if they can be used as a new geochemical tool to monitor changes of phreatic activity at hyperacid crater lakes and 2) identify the geochemical processes responsible for the variations of REE concentrations in the lake. The total concentration of REE varies from 950 to 2,773 μg kg−1. (La/Pr)N-local rock ratios range from 0.93 to 1.35, and Light REE over Heavy REE (LREE/HREE)N-local rock ratios vary from 0.71 to 0.95. These same parameters vary in relation to significant changes in phreatic activity; in particular, the (La/Pr)N-local rock ratio increases as phreatic activity increases, while that of (LREE/HREE)N-local rock decreases when phreatic activity increases. REE concentrations and their ratios were compared with the variations of major elements and physico-chemical parameters of the lake. Calcium versus (La/Pr)N-local rock and versus (LREE/HREE)N-local rock ratios show different trends compared to the other major elements (Na, K, Mg, Al, Fe, SO4, and Cl). Moreover, a higher loss of Ca (up to 2,835 ppm) in lake water was found with respect to the loss of Al, K, and Na. This loss of Ca is argued to be due to gypsum precipitation, a process corroborated by the mass balance calculation simulating the precipitation of gypsum and the contemporaneous removal of REE from the lake water. The observed relations between REE, changes in phreatic activity, and the parameters commonly used for the monitoring of hyperacid volcanic lakes encourage investigating more on the temporal and cause-effect relationship between REE dynamics and changes in phreatic activity at crater lake-bearing volcanoes.

Hydrochemical and Hydroacoustic Investigation of the Yugama Acid Crater Lake, Kusatsu-Shirane, Japan

The gases dissolved in the waters of volcanic lakes can present a serious hazard if the physical-chemical conditions change due to variations in the supply of magmatic gases. The monitoring of gases such as CO2 and He help us understand the degassing process and their connection with magmatic/hydrothermal system. One of the most acidic volcanic lakes on the planet is the Yugama, on Kusatsu Shirane volcano (Japan). We report the results of an interdisciplinary study carried out in August 2013 at Yugama consisting of the first estimation of rate of diffuse CO2 emission, the chemical and isotopic analysis of water and dissolved gases in samples from vertical lake profiles, and an echo-sounding survey. The lake water has an average temperature of 24-25°C, pH 1.01, concentrations of SO42- between 1,227 and 1,654 mgL−1 and Cl− between 1,506 and 2,562 mgL−1, with gas bubbling at several locations and floating sulfur globules with sulfide inclusions. A total of 66 CO2 efflux measurements were taken at the lake surface by means of the floating accumulation chamber method to estimate the diffuse CO2 output from the studied area. CO2 efflux values ranged from 82 up to 25,800 g m−2 d−1. Estimation of the diffuse CO2 emission at Yaguma Crater Lake was 30 ± 12 t d−1. Normalized CO2 emission rate (assuming an area of 0.066 km2) was 454 t km−2 d−1, a value within the range of acid volcanic lakes. Vertical profiles of major ions and dissolved gases showed variations with increases in ion content and dissolved CO2 and He with depth. Acoustic imaging shows the presence of intense bubbling and provides important information on the bathymetry of the lake. The 50–200 kHz echograms exhibit frequent vertical plumes of rising gas bubbles. Within the crater-lake, three circular submarine vents have been identified showing flares due to a significant activity of sublacustrine emissions. This work shows the first data of diffuse CO2 degassing, dissolved gases in water and echosounding (ES) from Yugama Crater Lake. Periodic hydrogeochemical and hydroacoustic surveys at Yugama Crater Lakemay thus help to document changes in the state of activity of this high-risk volcanic area.

Groundwater Interacting at Depth With Hot Plastic Magma Triggers Phreatic Eruptions at Yugama Crater Lake of Kusatsu-Shirane Volcano (Japan)

Interpreting the triggering mechanisms for phreatic eruptions is a key to improving the hazard assessment of crater lakes. Yugama Crater Lake at Kusatsu-Shirane volcano, Japan, is the site of frequent phreatic eruptions with the recent eruptions in 1982–83, 1989, and 1996, as well as volcanic unrest, including earthquake swarms in 2014 and 2018. To understand the magma–hydrothermal interaction beneath Yugama Crater Lake, we analyzed lake waters from November 2005 to May 2021. From 2005 to 2012, Cl and SO4 concentrations decreased slowly, suggesting the development of a self-sealing zone surrounding the crystallizing magma. We focused on Ca, Al, and Si concentrations as representatives of the breach and dissolution of minerals comprising the self-sealing zone and the Mg/Cl ratio as an indicator for enhanced interaction between groundwater and hot plastic rock within the self-sealing zone. In 2006–2007, the Ca, Al, Si concentrations and the Mg/Cl ratio increased. No Cl and SO4 increase during this period suggests the self-sealing zone was leached by deep circulating groundwater rather than by magmatic fluids injection. After the 2014 earthquakes, Ca, Al, and Si increased again but were associated with a significant Cl increase and a pH decrease. We believe that the HCl-rich magmatic fluids breached the self-sealing zone, leading to fluids injection from the crystallizing magma to the Yugama crater. During this period, the Mg/Cl ratio did not increase, meaning that magmatic fluids ascending from the breached area of the self-sealing zone inhibited deep intrusion of groundwater into the hot plastic rock region. In 2018, magmatic fluids ascended through the self-sealing zone again with less intensity than in 2014. All eruptions since 1982 have been accompanied by a Mg/Cl ratio increase and a Cl decrease, whereas, when a significant HCl input occurs, as in 2014, no eruptions and no Mg/Cl ratio increase occurred. This demonstrates that the groundwater–hot plastic rock interaction, rather than the magmatic fluids input, played an essential role in triggering phreatic eruptions; i.e., phreatic eruptions can potentially occur without clear signs of fresh magma intrusions.

Volatile transport of metals in the andesitic magmatic-hydrothermal system of White Island

<p>Volcanic gases observed at active volcanoes originate from the magma at depth. These volatiles exsolve as a result of decompression, crystallization and cooling of the silicate melt. The transport of metals in a magmatic volatile phase arises from complexation with the main volatile species, sulfur and halides. Composition of the magma, temperature, pressure and redox state have thus strong implications on metal mobility in these environments. Moreover, a variety of interactions and phase separations can affect these fluids after exsolution from the parental magma. This thesis aims at constraining the volatile transport of trace metals at White Island, a subduction-related magmatic-hydrothermal system, through a characterization and metal budget of the magmatic reservoir and the different atmospheric discharges. The metal content of the reservoir, as well as the effects of degassing and magma mixing on the magma are explored through the study of ejecta from the 1976-2000 eruptive cycle. CO₂, SO₂ and H₂O are degassing from a mafic melt at ~ 5 km depth, regularly feeding a shallower and evolved reservoir at ~ 800 m. Average contents of 164 ppm of Cu, 73 ppm of Zn, 12 ppm of Pb and 0.4 ppm of Au and Ag were detected in melt inclusions. A fraction of these metals partition into the exsolving aqueous fluid. Onset of magnetite crystallization may trigger exsolution of sulphide melt, found to contain around 30 wt% of Cu, and as much as 36 wt% Ni, 21 wt% Ag, 0.10 wt% Au in small inclusions, representing a considerable source of metals available for an aqueous fluid phase upon resorption. The volatile transport of metals is indicated by their enrichment in a variety of discharges at the surface. The hyperacidic waters of the crater lake absorb metals from the magmatic gases injected at subaqueous vents. Concentrations of ~ 12 ppm of As and Zn, 6 ppm of Cu and Pb were observed. Hydrolysis of the host rock by the reactive waters is responsible for the high cation contents of the fluids. Precipitation of secondary minerals such as silica, anhydrite, gypsum, sulfur and alunite occurs within and underneath the crater lake. The predicted speciation of metals greatly varies, dominated by CuI and FeII chloride complexes in the more reduced environment at the lake bottom, whereas CuII and FeIII are stable in the oxidized surficial waters. Arsenic is mainly present as As(OH)₃ at depth, with H₃AsO₄ dominating at the surface. Ag, Pb and Zn are complexed with chloride, and are not redox dependent. The presence of a body of molten sulfur at the bottom of the lake is indicated by sulfur spherules, both floating at the lake surface and in sediments. Pyrite crystals coat the surface of some globules, and chemical analyses reveal an enrichment in a variety of chalcophile metals (Tl, Sb, Bi, Au, As, Ag. Re, Cu). The volcanic gases emitted at fumaroles are enriched in metals compared to the magma. The effective transport of Se, Te, Sb, B, Au, As, and Bi is indicated by enrichment factors larger than 1000. In contrast, Cu is relatively depleted, suggesting deposition in the subsurface environment. Variations in composition are observed with time, mainly depending on temperature and major composition of the emissions. Values > 100 ppb of Sb, Bi, Ni, Zn, As and Se, > 10 ppb of Te, Pb, and Cu, and up to 8 ppb of Tl were recorded. Chloride is predicted to be the main ligand responsible for metal transport, even at higher temperature. The lack of thermodynamic data for complex solvated metal clusters may nevertheless bias our results. The low temperature of the studied fumaroles (maximum 192.5 °C) is in accordance with the small abundance of sulfides in the sublimates, whereas the high proportion of sulfates indicates oxidized conditions. The volcanic plume is enriched in metals such as Bi, Cd, Tl, Se, Te and Sb. The most common particles emitted are sulfates, halides, silicates, sulphuric acid and Zn ± Cu oxides. Metal emission rates are in the range of 1-10 kg/day for As, Se, Cu and Zn, 0.1-1 kg/day for Pb, Tl and Bi. Emissions of high-temperature magmatic gases are indicated by elevated SO₂/HCl ratio and the presence of Au in the particulate phase. Mass balance calculations in White Island magmatic-hydrothermal system indicate a segregation of around 4900 tons of copper per year, either accumulated from a dense brine at ~ 500 m depth, or deposited by low-density vapors on their way to the surface. Metal-rich sulfide blebs trapped in phenocrysts may also retain Cu at depth. These results thus reinforce the belief that White Island is an actively forming porphyry copper deposit.</p>

Volatile transport of metals in the andesitic magmatic-hydrothermal system of White Island

<p>Volcanic gases observed at active volcanoes originate from the magma at depth. These volatiles exsolve as a result of decompression, crystallization and cooling of the silicate melt. The transport of metals in a magmatic volatile phase arises from complexation with the main volatile species, sulfur and halides. Composition of the magma, temperature, pressure and redox state have thus strong implications on metal mobility in these environments. Moreover, a variety of interactions and phase separations can affect these fluids after exsolution from the parental magma. This thesis aims at constraining the volatile transport of trace metals at White Island, a subduction-related magmatic-hydrothermal system, through a characterization and metal budget of the magmatic reservoir and the different atmospheric discharges. The metal content of the reservoir, as well as the effects of degassing and magma mixing on the magma are explored through the study of ejecta from the 1976-2000 eruptive cycle. CO₂, SO₂ and H₂O are degassing from a mafic melt at ~ 5 km depth, regularly feeding a shallower and evolved reservoir at ~ 800 m. Average contents of 164 ppm of Cu, 73 ppm of Zn, 12 ppm of Pb and 0.4 ppm of Au and Ag were detected in melt inclusions. A fraction of these metals partition into the exsolving aqueous fluid. Onset of magnetite crystallization may trigger exsolution of sulphide melt, found to contain around 30 wt% of Cu, and as much as 36 wt% Ni, 21 wt% Ag, 0.10 wt% Au in small inclusions, representing a considerable source of metals available for an aqueous fluid phase upon resorption. The volatile transport of metals is indicated by their enrichment in a variety of discharges at the surface. The hyperacidic waters of the crater lake absorb metals from the magmatic gases injected at subaqueous vents. Concentrations of ~ 12 ppm of As and Zn, 6 ppm of Cu and Pb were observed. Hydrolysis of the host rock by the reactive waters is responsible for the high cation contents of the fluids. Precipitation of secondary minerals such as silica, anhydrite, gypsum, sulfur and alunite occurs within and underneath the crater lake. The predicted speciation of metals greatly varies, dominated by CuI and FeII chloride complexes in the more reduced environment at the lake bottom, whereas CuII and FeIII are stable in the oxidized surficial waters. Arsenic is mainly present as As(OH)₃ at depth, with H₃AsO₄ dominating at the surface. Ag, Pb and Zn are complexed with chloride, and are not redox dependent. The presence of a body of molten sulfur at the bottom of the lake is indicated by sulfur spherules, both floating at the lake surface and in sediments. Pyrite crystals coat the surface of some globules, and chemical analyses reveal an enrichment in a variety of chalcophile metals (Tl, Sb, Bi, Au, As, Ag. Re, Cu). The volcanic gases emitted at fumaroles are enriched in metals compared to the magma. The effective transport of Se, Te, Sb, B, Au, As, and Bi is indicated by enrichment factors larger than 1000. In contrast, Cu is relatively depleted, suggesting deposition in the subsurface environment. Variations in composition are observed with time, mainly depending on temperature and major composition of the emissions. Values > 100 ppb of Sb, Bi, Ni, Zn, As and Se, > 10 ppb of Te, Pb, and Cu, and up to 8 ppb of Tl were recorded. Chloride is predicted to be the main ligand responsible for metal transport, even at higher temperature. The lack of thermodynamic data for complex solvated metal clusters may nevertheless bias our results. The low temperature of the studied fumaroles (maximum 192.5 °C) is in accordance with the small abundance of sulfides in the sublimates, whereas the high proportion of sulfates indicates oxidized conditions. The volcanic plume is enriched in metals such as Bi, Cd, Tl, Se, Te and Sb. The most common particles emitted are sulfates, halides, silicates, sulphuric acid and Zn ± Cu oxides. Metal emission rates are in the range of 1-10 kg/day for As, Se, Cu and Zn, 0.1-1 kg/day for Pb, Tl and Bi. Emissions of high-temperature magmatic gases are indicated by elevated SO₂/HCl ratio and the presence of Au in the particulate phase. Mass balance calculations in White Island magmatic-hydrothermal system indicate a segregation of around 4900 tons of copper per year, either accumulated from a dense brine at ~ 500 m depth, or deposited by low-density vapors on their way to the surface. Metal-rich sulfide blebs trapped in phenocrysts may also retain Cu at depth. These results thus reinforce the belief that White Island is an actively forming porphyry copper deposit.</p>

Contributions to the Geology of Mt. Ruapehu, New Zealand

<p>During the passage of the lahar, shortly after 10 o'clock on Christmas Eve 1953, a portion of the Whangaehu River rail bridge at Tangiwai was demolished by a raging torrent of mud and boulders which originated from the Crater Lake of Mt. Ruapehu, nearly twenty miles distant. This mudflow, or lahar, damaged the railway bridge piers and the Wellington-Auckland express plunged into the torrent. As a result, one hundred and fifty-one people lost their lives. During tramping and ski-ing trips over the past five years the writer has become well acquainted with the National Park area. Close inspection of the Crater Lake was made on 1 January 1954, and again on 22 January. On the latter date the writer was accompanied by two chemists from the Chemistry Department, Victoria University College, and one from the Dominion Laboratory of the Department of Scientific and Industrial Research, who collected samples of the lake water. On 24 January, the Whangaehu River was followed from the Desert Road to where it emerges from a deep gorge on the lower slopes of Mt. Ruapehu. A number of braided channels were examined on the alluvial fan that extends east from the outlet gorge almost to the Desert Road. On the same day the scene of the disaster at Tangiwai was also inspected</p>