22 research outputs found

    Dynamics of Outgassing and Plume Transport Revealed by Proximal Unmanned Aerial System (UAS) Measurements at Volcán Villarrica, Chile

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    Volcanic gas emissions are intimately linked to the dynamics of magma ascent and outgassing, and, on geological timescales, constitute an important source of volatiles to the Earth’s atmosphere. Measurements of gas composition and flux are therefore critical to both volcano monitoring and to determining the contribution of volcanoes to global geochemical cycles. However, significant gaps remain in our global inventories of volcanic emissions, (particularly for CO2, which requires proximal sampling of a concentrated plume) for those volcanoes where the near-vent region is hazardous or inaccessible. Unmanned Aerial Systems (UAS) provide a robust and effective solution to proximal sampling of dense volcanic plumes in extreme volcanic environments. Here, we present gas compositional data acquired using a gas sensor payload aboard a UAS flown at Volcán Villarrica, Chile. We compare UAS-derived gas timeseries to simultaneous crater rim multi-GAS data and UV camera imagery to investigate early plume evolution. SO2 concentrations measured in the young proximal plume exhibit periodic variations that are well-correlated with the concentrations of other species. By combining molar gas ratios (CO2/SO2 = 1.48–1.68, H2O/SO2 = 67–75 and H2O/CO2 = 45–51) with the SO2 flux (142 ± 17 t/day) from UV camera images, we derive CO2 and H2O fluxes of ~150 t/day and ~2850 t/day, respectively. We observe good agreement between time-averaged molar gas ratios obtained from simultaneous UAS- and ground-based Multi-GAS acquisitions. However, the UAS measurements made in the young, less diluted plume reveal additional short-term periodic structure that reflects active degassing through discrete, audible gas exhalations.Alfred P. Sloan Foundation; Leverhulme Trus

    Ground-Based Measurements of the 2014–2015 Holuhraun Volcanic Cloud (Iceland)

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    The 2014–2015 Bárðarbunga fissure eruption at Holuhraun in central Iceland was distinguished by the high emission of gases, in total 9.6 Mt SO2, with almost no tephra. This work collates all ground-based measurements of this extraordinary eruption cloud made under particularly challenging conditions: remote location, optically dense cloud with high SO2 column amounts, low UV intensity, frequent clouds and precipitation, an extensive and hot lava field, developing ramparts, and high-latitude winter conditions. Semi-continuous measurements of SO2 flux with three scanning DOAS instruments were augmented by car traverses along the ring-road and along the lava. The ratios of other gases/SO2 were measured by OP-FTIR, MultiGAS, and filter packs. Ratios SO2/HCl = 30–110 and SO2/HF = 30–130 show a halogen-poor eruption cloud. Scientists on-site reported extremely minor tephra production during the eruption. OPC and filter packs showed low particle concentrations similar to non-eruption cloud conditions. Three weather radars detected a droplet-rich eruption cloud. Top of eruption cloud heights of 0.3–5.5 km agl were measured with ground- and aircraft-based visual observations, web camera and NicAIR II infrared images, triangulation of scanning DOAS instruments, and the location of SO2 peaks measured by DOAS traverses. Cloud height and emission rate measurements were critical for initializing gas dispersal simulations for hazard forecasting

    Ground-Based measurements of the 2014-2015 holuhraun volcanic cloud (Iceland)

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    The 2014-2015 Bárðarbunga fissure eruption at Holuhraun in central Iceland was distinguished by the high emission of gases, in total 9.6 Mt SO2, with almost no tephra. This work collates all ground-based measurements of this extraordinary eruption cloud made under particularly challenging conditions: remote location, optically dense cloud with high SO2 column amounts, low UV intensity, frequent clouds and precipitation, an extensive and hot lava field, developing ramparts, and high-latitude winter conditions. Semi-continuous measurements of SO2 flux with three scanning DOAS instruments were augmented by car traverses along the ring-road and along the lava. The ratios of other gases/SO2 were measured by OP-FTIR, MultiGAS, and filter packs. Ratios of SO2/HCl = 30-110 and SO2/HF = 30-130 show a halogen-poor eruption cloud. Scientists on-site reported extremely minor tephra production during the eruption. OPC and filter packs showed low particle concentrations similar to non-eruption cloud conditions. Three weather radars detected a droplet-rich eruption cloud. Top of eruption cloud heights of 0.3-5.5 km agl were measured with ground-and aircraft-based visual observations, web camera and NicAIR II infrared images, triangulation of scanning DOAS instruments, and the location of SO2 peaks measured by DOAS traverses. Cloud height and emission rate measurements were critical for initializing gas dispersal simulations for hazard forecasting

    Gradual caldera collapse at Bárdarbunga volcano, Iceland, regulated by lateral magma outflow

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    Large volcanic eruptions on Earth commonly occur with a collapse of the roof of a crustal magma reservoir, forming a caldera. Only a few such collapses occur per century, and the lack of detailed observations has obscured insight into the mechanical interplay between collapse and eruption.We usemultiparameter geophysical and geochemical data to show that the 110-squarekilometer and 65-meter-deep collapse of Bárdarbunga caldera in 2014-2015 was initiated through withdrawal of magma, and lateral migration through a 48-kilometers-long dike, from a 12-kilometers deep reservoir. Interaction between the pressure exerted by the subsiding reservoir roof and the physical properties of the subsurface flow path explain the gradual, nearexponential decline of both collapse rate and the intensity of the 180-day-long eruption.</p

    Magma degassing at piton de la fournaise volcano

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    Since about 1860 AD, magmatic gas release at Piton de la Fournaise volcano is very weak during intra-eruptive phases and essentially occurs during the relatively short-lived eruptions. Recent gas measurements performed during an eruption in October 2010, combined with detailed review of melt and fluid inclusion composition in magmas erupted over the past 50\ua0kyrs, indicate that most PdF eruptions extrude magmas having variably degassed at shallow depth (P\ua0&lt;\ua01\ua0kbar). The average low gas flux results from the low volume of both the magma recharges (from P\ua0&gt;\ua01\ua0kbar) and the shallow magmas, whose fluids are efficiently scrubbed by the hydrothermal system and the water table. Quantification of SO2 fluxes permits to track syn-eruptive magma ascent at shallow level (above sea level). Deeper exsolution of CO2 (below sea level) provides a potential long-term geochemical precursor for the detection of new magma recharges and volcano unrest

    Financial Innovation in the Management of Catastrophe Risk

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    Like the preceding article, this article argues that the high costs of reinsurance present the opportunity for hedging instruments to be offered to primary insurers that are both competitive with current reinsurance and that offer investors high rates of return. But the combination of high reinsurance premiums and the vast capacity of the capital market for diversification is not sufficient to ensure the success of these new instruments. If new instruments such as catastrophe options and catastrophelinked bonds are to compete successfully with reinsurance, they must provide a cost-effective means of resolving incentive conflicts between the primary insurer and the ultimate risk bearer that are known as "moral hazard." Without an effective solution of this moral hazard problem, the use of past insurance loss data to estimate the potential returns for purchasers of catastrophe bonds and other such instruments will be misleading and unreliable. 1997 Morgan Stanley.

    Bioindication of volcanic mercury (Hg) deposition around Mt. Etna (Sicily)

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    Mt. Etna is a major natural source of Hg to the Mediterranean region. Total mercury concentrations, [Hg]tot, in Castanea sativa (sweet chestnut) leaves sampled 7–13 km from Etna's vents (during six campaigns in 2005–2011) were determined using atomic absorption spectroscopy. [Hg]tot in C. sativa was greatest on Etna's SE flank reflecting Hg deposition from the typically overhead volcanic plume. [Hg]tot also showed Hg accumulation over the growing season, increasing with leaf age and recent eruptive activity. [Hg]tot in C. sativa was not controlled by [Hg]tot in soils, which instead was greatest on Etna's NW flank, and was correlated with the proportion of organic matter in the soil (% Org). An elevated [Hg]tot/% Org ratio in soils on Etna's SE flank is indicative of increased Hg deposition. This ratio was also found to decrease with local soil pH, suggesting that Hg deposited to the low pH and organic-poor soils on Etna's SE flank may not be retained but will instead be released to groundwater or re-emitted to the atmosphere. These results show that the deposition of volcanic Hg has clear impacts and confirm that Etna is an important source of Hg to the local environmen

    Gases as Precursory Signals: Experimental Simulations, New Concepts and Models of Magma Degassing

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    International audienceVolatile release during magma ascent in volcanic conduits (magma degassing) forms the basis for using volcanic gases as precursory signals. Recent high temperature high pressure experimental simulations have yielded results that challenge key assumptions related to magma degassing and are important for the interpretation of glass inclusion and gas data and for using volcanic gas as precursory signals. The experimental data show that, for ascent rates expected in natural systems, pure H2O basaltic melts will evolve mostly close to equilibrium when decompressed from 200 to 25 MPa. In the same way, degassing of H2O–S species evolves at near equilibrium, although this conclusion is limited by the number of S solubility data available for basaltic melts. However, degassing of CO2 is anomalous in all studies, whether performed on basaltic or rhyolitic melts. CO2 stays concentrated in the melt at levels far exceeding solubilities. The anomalous behaviour of CO2, when associated with near equilibrium H2O losses, yields post-decompression glasses with CO2 concentrations systematically higher than equilibrium degassing curves. Therefore, there is strong experimental support for disequilibrium degassing during ascent of CO2-bearing magmas. The existence of volatile concentration gradients around nucleated gas bubbles suggests that degassing is controlled by the respective mobilities (diffusivities) of volatiles within the melt. The recently formulated diffusive fractionation model reproduces the main characteristics, especially the volatile concentrations, of experimental glasses. The model also shows that the gas phase is more H2O-rich than expected at equilibrium because CO2 transfer toward the gas phase is hampered by its retention within the melt. However, only integrated gas compositions are calculated. Similarly, only bulk experimental fluid compositions are determined in recent experiments. Thus, constraints on the local gas phase are becoming necessary for the application to volcanoes. This stresses the need for the direct analysis of gas bubbles nucleated in decompression experiments. Pre-eruptive changes in volcanic CO2/SO2 and H2O/CO2 gas ratios are interpreted to reflect different pressures of gas-melt segregation in the conduit, an approach that assume gas-melt equilibrium. However, if disequilibrium magma degassing is accepted, the use of volatile saturation codes is no longer possible and caution must be exercised with the application of local equilibrium to volcanic gases. Future developments in the interpretation of gas data require progress from both sides, experimental and volcanological. One priority is to reduce the gap in scales between experiments and gas measurements
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