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Avard, Geoffroy
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Avard, Geoffroy
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- PublicationOpen AccessSynoptic analysis of a decade of daily measurements of SO2 emission in the troposphere from volcanoes of the global ground-based Network for Observation of Volcanic and Atmospheric Change(2021)
; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ;; ; ; ; ; ; ; ; ; ; ; ; ; ; ;; ; ; ; ; ; ; ; ; ; ;; ; ; ;; Volcanic plumes are common and far-reaching manifestations of volcanic activity during and be-tween eruptions. Observations of the rate of emission and composition of volcanic plumes are essential to rec-ognize and, in some cases, predict the state of volcanic activity. Measurements of the size and location of theplumes are important to assess the impact of the emission from sporadic or localized events to persistent orwidespread processes of climatic and environmental importance. These observations provide information onvolatile budgets on Earth, chemical evolution of magmas, and atmospheric circulation and dynamics. Space-based observations during the last decades have given us a global view of Earth’s volcanic emission, particularlyof sulfur dioxide (SO2). Although none of the satellite missions were intended to be used for measurementof volcanic gas emission, specially adapted algorithms have produced time-averaged global emission budgets.These have confirmed that tropospheric plumes, produced from persistent degassing of weak sources, dominatethe total emission of volcanic SO2. Although space-based observations have provided this global insight intosome aspects of Earth’s volcanism, it still has important limitations. The magnitude and short-term variabilityof lower-atmosphere emissions, historically less accessible from space, remain largely uncertain. Operationalmonitoring of volcanic plumes, at scales relevant for adequate surveillance, has been facilitated through the useof ground-based scanning differential optical absorption spectrometer (ScanDOAS) instruments since the be-ginning of this century, largely due to the coordinated effort of the Network for Observation of Volcanic andAtmospheric Change (NOVAC). In this study, we present a compilation of results of homogenized post-analysisof measurements of SO2flux and plume parameters obtained during the period March 2005 to January 2017of 32 volcanoes in NOVAC. This inventory opens a window into the short-term emission patterns of a diverseset of volcanoes in terms of magma composition, geographical location, magnitude of emission, and style oferuptive activity. We find that passive volcanic degassing is by no means a stationary process in time and thatlarge sub-daily variability is observed in the flux of volcanic gases, which has implications for emission budgetsproduced using short-term, sporadic observations. The use of a standard evaluation method allows for intercom-parison between different volcanoes and between ground- and space-based measurements of the same volcanoes.The emission of several weakly degassing volcanoes, undetected by satellites, is presented for the first time. Wealso compare our results with those reported in the literature, providing ranges of variability in emission notaccessible in the past. The open-access data repository introduced in this article will enable further exploitationof this unique dataset, with a focus on volcanological research, risk assessment, satellite-sensor validation, andimproved quantification of the prevalent tropospheric component of global volcanic emission.405 49 - PublicationRestrictedGas measurements from the Costa Rica–Nicaragua volcanic segment suggest possible along-arc variations in volcanic gas chemistryObtaining accurate estimates of the CO2 output from arc volcanism requires a precise understanding of the potential along-arc variations in volcanic gas chemistry, and ultimately of the magmatic gas signature of each individual arc segment. In an attempt to more fully constrain the magmatic gas signature of the Central America Volcanic Arc (CAVA), we present here the results of a volcanic gas survey performed during March and April 2013 at five degassing volcanoes within the Costa Rica–Nicaragua volcanic segment (CNVS). Observations of the volcanic gas plume made with a multicomponent gas analyzer system (Multi-GAS) have allowed characterization of the CO2/SO2-ratio signature of the plumes at Poás (0.30 ± 0.06, mean ± SD), Rincón de la Vieja (27.0 ±15.3), and Turrialba (2.2 ±0.8) in Costa Rica, and at Telica (3.0 ± 0.9) and San Cristóbal (4.2 ± 1.3) in Nicaragua (all ratios on molar basis). By scaling these plume compositions to simultaneously measured SO2 fluxes, we estimate that the CO2 outputs at CNVS volcanoes range from low (25.5 ± 11.0 tons/day at Poás) to moderate (918 to 1270 tons/day at Turrialba). These results add a new information to the still fragmentary volcanic CO2 output data set, and allow estimating the total CO2 output from the CNVS at 2835 ± 1364 tons/day. Our novel results, with previously available information about gas emissions in Central America, are suggestive of distinct volcanic gas CO2/ST (= SO2 + H2S)-ratio signature for magmatic volatiles in Nicaragua (∼3) relative to Costa Rica (∼0.5–1.0). We also provide additional evidence for the earlier theory relating the CO2-richer signature of Nicaragua volcanism to increased contributions from slab-derived fluids, relative to more MORB-like volcanism in Costa Rica. The sizeable along-arc variations in magmatic gas chemistry that the present study has suggested indicate that additional gas observations are urgently needed to more recisely confine the volcanic CO2 from the CAVA, and from global arc volcanism.
25 1 - PublicationOpen AccessInsights Into the Mechanisms of Phreatic Eruptions From Continuous High Frequency Volcanic Gas Monitoring: Rincón de la Vieja Volcano, Costa Rica(2019-01)
; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ;; ;Understanding the trigger mechanisms of phreatic eruptions is key to mitigating the effects of these hazardous but poorly forecastable volcanic events. It has recently been established that high-rate volcanic gas observations are potentially very suitable to identifying the source processes driving phreatic eruptions, and to eventually detecting precursory changes prior to individual phreatic blasts. In February-May 2017, we deployed a Multi-GAS instrument to continuously monitor gas concentrations in the crater lake plume of Rincón de la Vieja, a remote and poorly monitored active volcano in Costa Rica, site of frequent phreatic/phreatomagmatic eruptions. Forty-two phreatic/phreatomagmatic eruptions were seismically recorded during our investigated period, 9 of which were also recorded for gas by the Multi-GAS. To the best of our knowledge, these represent the first instrumentally measured gas compositions during individual phreatic/phreatomagmatic explosions at an active volcano. Our results show that during background quiescent degassing the Rincón de la Vieja crater lake plume was characterized by high CO2/SO2 ratios of 64 ± 59 and H2S/SO2 ratios of 0.57 ± 0.20. This composition is interpreted as reflecting hydrothermal (re)processing of magma-sourced gas in the sub-limnic environment. Phreatic blasts were recorded by the Multi-GAS as brief (1–2 min long) pulses of elevated gas mixing ratios (up to ~52 ppmv SO2 and >3,000 ppmv CO2), or more than an order of magnitude higher than during background degassing (~1 ppmv SO2 and ~450 ppmv CO2). During the phreatic eruption(s), the H2S/SO2 ratio was systematically lower (<0.18) than during background degassing, but the CO2/SO2 ratio remained high (and variable), ranging from 37 to 390. These S-poor compositions for the eruptive gas imply extensive processing of the source magmatic gas during pre-eruptive hydrothermal storage, likely by deposition of native S and/or sulfate. Our gas results are thus overall consistent with a mechanism of phreatic eruptions triggered by accumulation of magmatic-hydrothermal gases beneath a hydrothermal seal. We claim that real-time Multi-GAS monitoring is urgently needed at other crater lake-hosting volcanoes (e.g., Ruapehu, Aso), where phreatic eruptions may similarly be preceded by phases of reduced S degassing at the surface.170 120 - PublicationOpen AccessEruptive activity at Turrialba volcano (Costa Rica): Inferences from 3He/4He in fumarole gases and chemistry of the products ejected during 2014 and 2015(2016-10-17)
; ; ; ; ; ; ; ;Rizzo, Andrea Luca; Istituto Nazionale di Geofisica e Vulcanologia, Sezione Palermo, Palermo, Italia ;Di Piazza, Andrea; Istituto Nazionale di Geofisica e Vulcanologia, Sezione Roma1, Roma, Italia ;de Moor, J. Maarten; Observatorio Vulcanol ogico y Sismol ogico de Costa Rica (OVSICORI) ;Alvarado, Guillermo E.; Instituto Costarricense de Electricidad, Apdo ;Avard, Geoffroy; Observatorio Vulcanol ogico y Sismol ogico de Costa Rica (OVSICORI) ;Carapezza, Maria Luisa; Istituto Nazionale di Geofisica e Vulcanologia, Sezione Roma1, Roma, Italia ;Mora, Mauricio M.; Escuela Centroamericana de Geolog ıa, Universidad de Costa Rica; ; ; ; ; ; A new period of eruptive activity started at Turrialba volcano, Costa Rica, in 2010 after almost 150 years of quiescence. This activity has been characterized by sporadic explosions whose frequency clearly increased since October 2014. This study aimed to identify the mechanisms that triggered the resumption of this eruptive activity and characterize the evolution of the phenomena over the past 2 years. We integrate 3He/4He data available on fumarole gases collected in the summit area of Turrialba between 1999 and 2011 with new measurements made on samples collected between September 2014 and February 2016. The results of a petrological investigation of the products that erupted between October 2014 and May 2015 are also presented. We infer that the resumption of eruptive activity in 2010 was triggered by a replenishment of the plumbing system of Turrialba by a new batch of magma. This is supported by the increase in 3He/4He values observed since 2005 at the crater fumaroles and by comparable high values in September 2014, just before the onset of the new eruptive phase. The presence of a number of fresh and juvenile glassy shards in the erupted products increased between October 2014 and May 2015, suggesting the involvement of new magma with a composition similar to that erupted in 1864–1866. We conclude that the increase in 3He/4He at the summit fumaroles since October 2015 represents strong evidence of a new phase of magma replenishment, which implies that the level of activity remains high at the volcano.270 130 - PublicationRestrictedMercury fluxes from volcanic and geothermal sources: an update(Goeological society of London, 2014)
; ; ; ; ; ; ; ; ; ; ; ; ; ; ;We review the state of knowledge on global volcanogenic Hg emissions to the atmosphere and present new data from seven active volcanoes (Poa´s, Rinco ´n de la Vieja, Turrialba, Aso, Mutnovsky, Gorely and Etna) and two geothermal fields (Las Pailas and Las Hornillas). The variability of Hg contents (c. 4–125 ng m23) measured in gaseous emissions reflects the dynamic nature of volcanic plumes, where the abundances of volatiles are determined by the physical nature of degassing and variable air dilution. Based on our dataset and previous work, we propose that an average Hg/SO2 plume massratio of c. 7.8 × 1026 (+1.5 × 1026; 1SE,n ¼ 13)isbestrepre sentative of open-conduit quiescent degassing. Taking into account the uncertainty in global SO2 emissions, we infer a global volcanic Hg flux from persistent degassing of c. 76+30 t a21. Our data are derived from active volcanoes during non-eruptive periods and we do not have any direct constraint on the Hg flux during periods of elevated SO2 flux associated with large-scale effusive or explosive eruptions. This suggests that the time-averaged Hg flux from these volcanoes is even larger if the eruptive contribution is considered. Conversely, closed-conduit degassing and geothermal emissions contribute modest amounts of Hg.20 1 - PublicationRestrictedMeasurements of volcanic SO2 and CO2 fluxes by combined DOAS, Multi-GAS and FTIR observations: a case study from Turrialba and Telica volcanoes(2014)
; ; ; ; ; ; ; ; ; ; ; ; ; Over the past few decades, substantial progress has been made to overcome the technical difficulties of continuously measuring volcanic SO2 emissions. However, measurements of CO2 emissions still present many difficulties, partly due to the lack of instruments that can directly measure CO2 emissions and partly due to its strong atmospheric background. In order to overcome these difficulties, a commonly taken approach is to combine differential optical absorption spectroscopy (DOAS) by using NOVAC scan-DOAS instruments for continuous measurements of crateric SO2 emissions, and electrochemical/NDIR multi-component gas analyser system (multi-GAS) instruments for measuring CO2/SO2 ratios of excerpts of the volcanic plume. This study aims to quantify the representativeness of excerpts of CO2/SO2 ratios measured by Multi-GAS as a fraction of the whole plume composition, by comparison with simultaneously measured CO2/SO2 ratios using cross-crater Fourier transform infrared spectroscopy (FTIR). Two study cases are presented: Telica volcano (Nicaragua), with a homogenous plume, quiescent degassing from a deep source and ambient temperature, and Turrialba volcano (Costa Rica), which has a non-homogeneous plume from three main sources with different compositions and temperatures. Our comparison shows that in our “easier case” (Telica), FTIR and Multi-GAS CO2/SO2 ratios agree within a factor about 3 %. In our “complicated case” (Turrialba), Multi-GAS and FTIR yield CO2/SO2 ratios differing by approximately 13–25 % at most. These results suggest that a fair estimation of volcanic CO2 emissions can be provided by the combination of DOAS and Multi-GAS instruments for volcanoes with similar degassing conditions as Telica or Turrialba. Based on the results of this comparison, we report that by the time our measurements were made, Telica and Turrialba were emitting approximately 100 and 1,000 t day−1 of CO2, respectively.52 2