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  • 1
    Publication Date: 2023-07-20
    Description: Volatiles released from magma can form bubbles and leave the magma body to eventually mix with atmospheric air. The composition of those volatiles, as derived from measurements made after their emission, is used to draw conclusions on processes in the Earth's interior or their influences on Earth's atmosphere. So far, the discussion of the influence of high‐temperature mixing with atmospheric air (in particular oxygen) on the measured volcanic gas composition is almost exclusively based on thermodynamic equilibrium (TE) considerations. By modeling the combined effects of C‐H‐O‐S reaction kinetics, turbulent mixing, and associated cooling during the first seconds after magmatic gas release into the atmosphere we show that the resulting gas compositions generally do not represent TE states, with individual species (e.g., CO, H2, H2S, OCS, SO3, HO2, H2O2) deviating by orders of magnitude from equilibrium levels. Besides revealing the chemical details of high‐temperature emission processes, our results question common interpretations of volcanic gas studies, particularly affecting the present understanding of auto‐catalytic conversion of volcanic halogen species in the atmosphere and redox state determination from volcanic plume gas measurements.
    Description: Plain Language Summary: A major fraction of magmatic gas emissions are released into the atmosphere from open vents. The emission processes are characterized by fast turbulent mixing with atmospheric air (within seconds) and associated rapid cooling. Hardly anything is known about the chemical kinetics within this brief mixing and cooling period. We simulate the chemical kinetics during the first seconds of hot magmatic gases in the atmosphere and find severe deviation to common interpretations and central thermodynamic equilibrium assumptions prevailing in volcanic gas geochemistry.
    Description: Key Points: We model the chemical kinetics of high‐temperature volcanic gas emissions within the first seconds of mixing with atmospheric air. We identify key chemical processes within the magma‐atmosphere interface and quantify influences on the volcanic plume composition. Our results question common assumptions prevailing in volcanic gas geochemistry and refine interpretations of gas emissions from open vents.
    Description: German Research Foundation
    Keywords: ddc:551.9 ; volcanic gas emissions ; kinetic chemistry modeling ; atmospheric chemistry ; magmatic redox states ; reactive halogen chemistry
    Language: English
    Type: doc-type:article
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillian Magazines Ltd.
    Nature 423 (2003), S. 273-276 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The emission of volcanic gases usually precedes eruptive activity, providing both a warning signal and an indication of the nature of the lava soon to be erupted. Additionally, volcanic emissions are a significant source of gases and particles to the atmosphere, influencing tropospheric and ...
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2017-03-23
    Type: Conference or Workshop Item , NonPeerReviewed
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  • 4
    Publication Date: 2020-02-18
    Description: Long-term measurements of volcanic gas emissions conducted during the last decade suggest that under certain conditions the magnitude or chemical composition of volcanic emissions exhibits periodic variations with a period of about 2 weeks. A possible cause of such a periodicity can be attributed to the Earth tidal potential. The phenomenology of such a link has been debated for long, but no quantitative model has yet been proposed. The aim of this paper is to elucidate whether a causal link between tidal forcing and variations in volcanic degassing can be traced analytically. We model the response of a simplified magmatic system to the local tidal gravity variations and derive a periodical vertical magma displacement in the conduit with an amplitude of 0.1–1 m, depending on the geometry and physical state of the magmatic system. We find that while the tide-induced vertical magma displacement presumably has no significant direct effect on the volatile solubility, the differential magma flow across the radial conduit profile may result in a significant increase in the bubble coalescence rate at a depth of several kilometres by up to several multiples of 10 %. Because bubble coalescence facilitates separation of gas from magma and thus enhances volatile degassing, we argue that the derived tidal variation may propagate to a manifestation of varying volcanic degassing behaviour. The presented model provides a first basic framework which establishes an analytical understanding of the link between the Earth tides and volcanic degassing.
    Language: English
    Type: info:eu-repo/semantics/article
    Format: application/pdf
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  • 5
    Publication Date: 2021-06-07
    Description: Very little is known about the volatile element makeup of the gaseous emissions of Nyamulagira volcano. This paper tries to fill this gap by reporting the first gas composition measurements of Nyamulagira’s volcanic plume since the onset of its lava lake activity at the end of 2014. Two field surveys were carried out on 1 November 2014, and 13–15 October 2015. We applied a broad toolbox of volcanic gas composition measurement techniques in order to geochemically characterize Nyamulagira’s plume. Nyamulagira is a significant emitter of SO2, and our measurements confirm this, as we recorded SO2 emissions of up to ~ 14 kt/d during the studied period. In contrast to neighbouring Nyiragongo volcano, however, Nyamulagira exhibits relatively low CO2/SO2 molar ratios (〈 4) and a highH2O content (〉 92%of total gas emissions). Strong variations in the volatile composition, in particular for the CO2/SO2 ratio, were measured between 2014 and 2015, which appear to reflect the simultaneous variations in volcanic activity.We also determined the molar ratios for Cl/S, F/S and Br/S in the plume gas, finding values of 0.13 and 0.17, 0.06 and 0.11, and 2.3·10−4 and 1·10−4, in 2014 and 2015, respectively. A total gas emission flux of 48 kt/ d was estimated for 2014. The I/S ratio in 2015 was found to be 3.6·10−6. In addition, we were able to distinguish between hydrogen halides and non-hydrogen halides in the volcanic plume. Considerable amounts of bromine (18–35% of total bromine) and iodine (8–18%of total iodine) were found in compounds other than hydrogen halides. However, only a negligible fraction of chlorine was found as compounds other than hydrogen chloride.
    Description: Published
    Description: 90
    Description: 5V. Dinamica dei processi eruttivi e post-eruttivi
    Description: JCR Journal
    Keywords: Nyamulagira ; Plume composition ; Total gas flux ; 04.08. Volcanology
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 6
    Publication Date: 2021-02-17
    Description: The number concentrations and size distributions of aerosol particles 〉0.3 mm diameter were measured at the summit of Mount Etna and up to 10 km downwind from the degassing vents during July and August 2004. Aerosol number concentrations reached in excess of 9 106 L 1 at summit vents, compared to 4–8 104 L 1 in background air. Number concentrations of intermediate size particles were higher in emissions from the Northeast crater compared to other summit crater vents, and chemical composition measurements showed that Northeast crater aerosols contained a higher mineral cation content compared to those from Voragine or Bocca Nuova, attributed to Strombolian or gas puffing activity within the vent. Downwind from the summit the airborne plume was located using zenith sky ultraviolet spectroscopy. Simultaneous measurements indicated a coincidence of elevated ground level aerosol concentrations with overhead SO2, demonstrating rapid downward mixing of the plume onto the lower flanks of the volcano under certain meteorological conditions. At downwind sites the ground level particle number concentrations were elevated in all size fractions, notably in the 2.0–7.5 mm size range. These findings are relevant for assessing human health hazard and suggest that aerosol size distribution measurements may aid volcanic risk management.
    Description: Published
    Description: D10302
    Description: JCR Journal
    Description: reserved
    Keywords: aerosols ; Mount Etna ; 01. Atmosphere::01.01. Atmosphere::01.01.07. Volcanic effects
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 7
    Publication Date: 2021-06-07
    Description: The La Fossa cone of Vulcano Island (Aeolian Archipelago, Italy) is a closed conduit volcano. Today, Vulcano Island is characterized by sulfataric activity, with a large fumarolic field that is mainly located in the summit area. A scanning differential optical absorption spectroscopy instrument designed by the Optical Sensing Group of Chalmers University of Technology in Göteborg, Sweden, was installed in the framework of the European project "Network for Observation of Volcanic and Atmospheric Change", in March 2008. This study presents the first dataset of SO2 plume fluxes recorded for a closed volcanic system. Between 2008 and 2010, the SO2 fluxes recorded showed average values of 12 t.d—1 during the normal sulfataric activity of Vulcano Island, with one exceptional event of strong degassing that occurred between September and December, 2009, when the SO2 emissions reached up to 100 t.d—1.
    Description: Published
    Description: 301-308
    Description: 2V. Dinamiche di unrest e scenari pre-eruttivi
    Description: 4V. Vulcani e ambiente
    Description: 6A. Monitoraggio ambientale, sicurezza e territorio
    Description: JCR Journal
    Description: open
    Keywords: SO2 ; Differential optical absorption spectroscopy ; Vulcano Island ; Network for Observation of Volcanic and Atmospheric Change ; 01. Atmosphere::01.01. Atmosphere::01.01.07. Volcanic effects ; 04. Solid Earth::04.02. Exploration geophysics::04.02.05. Downhole, radioactivity, remote sensing, and other methods ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases ; 04. Solid Earth::04.08. Volcanology::04.08.06. Volcano monitoring ; 04. Solid Earth::04.08. Volcanology::04.08.08. Volcanic risk ; 05. General::05.02. Data dissemination::05.02.01. Geochemical data
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 8
    Publication Date: 2021-06-25
    Description: Airborne and ground-based differential optical absorption spectroscopy observations have been carried out at the volcano Nyiragongo (Democratic Republic of Congo) tomeasure SO2 and bromine monoxide (BrO) in the plume inMarch 2004 and June 2007, respectively. Additionally filter pack andmulticomponent gas analyzer system (Multi-GAS)measurements were carried out in June 2007. Ourmeasurements provide valuable information on the chemical composition of the volcanic plume emitted fromthe lava lake of Nyiragongo. The main interest of this study has been to investigate for the first time the bromine emission flux of Nyiragongo (a rift volcano) and the BrO formation in its volcanic plume. Measurement data and results from a numerical model of the evolution of BrO in Nyiragongo volcanic plume are compared with earlier studies of the volcanic plume of Etna (Italy). Even though the bromine flux from Nyiragongo (2.6 t/d) is slightly greater than that from Etna (1.9 t/d), the BrO/SO2 ratio (maximum 7 × 10 5) is smaller than in the plume of Etna (maximum 2.1 × 10 4). A one-dimensional photochemical model to investigate halogen chemistry in the volcanic plumes of Etna and Nyiragongo was initialized using data from Multi-GAS and filter pack measurements. Model runs showed that the differences in the composition of volcanic volatiles led to a smaller fraction of total bromine being present as BrO in the Nyiragongo plume and to a smaller BrO/SO2 ratio.
    Description: Published
    Description: 277-291
    Description: 4V. Vulcani e ambiente
    Description: JCR Journal
    Description: restricted
    Keywords: Intraplate volcano Nyiragongo is bromine rich although chlorine poor ; BrO/Br in volcanic plumes depends on initial plume composition ; Determination of Nyiragongo chlorine, bromine, sulfur emission strength ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 9
    Publication Date: 2017-04-04
    Description: Total CO2 output from fumaroles, soil gases, bubbling and water dissolved gases were estimated at Vulcano Island, Italy. The fumaroles output has been estimated from SO2 plume flux, while soil flux emission has been carried out through 730 CO2 fluxes measured on the island surface, performed by means of accumulation chamber method. Vulcano Island, located in the Aeolian Archipelago, is an active volcano that has been in state of solphataric activity, since the last eruption (1888-1890). At present, the main exhalative activity is in the northern part of the island, it is revealed by a wide fumaroles field, on the active edifice of “La Fossa” crater, (100°C 〈T〈450°C); by low temperature fumaroles (T〈100°C) and sea-bubbling gases in the Baia Levante area; moreover, strong soil degassing occurs in the Vulcano Porto area and around the volcanic edifice, where the active tectonic discontinuities drive CO2 to the surface. Finally, numerous carbon-rich thermal wells (up to 80°C) in the Vulcano Porto Area, testify the presence of a geothermal system with equilibrium temperature around 200°C. The preliminary results indicate an overall output of 470 T/day of CO2 from the island. The main contribution to the total output is from the summit area of the active cone (450 T/day), where 360 T/day and 90 T/day are from crater fumaroles and crater soil degassing, respectively. Peripheral areas release 8 T/day by soil degassing (Palizzi and Istmo areas mainly), a measure comparable to the contribution of water dissolved CO2 (estimated as 6 T/day) and higher than sea-bubbling CO2 (1 T/day measured in the Istmo area). The presented data (September 2007) refer to a period of moderate solphataric activity, when the highest temperature and gas/water ratio of fumaroles were 457°C and 0.17 respectively. These preliminary data allow the estimation of the background mass release and related thermal energy from the volcanic system. They represent the first complete data set, collected during moderate volcanic activity which can be compared to the new one acquired during subsequent (the next o future) evolution of the activity.
    Description: Published
    Description: Reykjavik
    Description: 1.2. TTC - Sorveglianza geochimica delle aree vulcaniche attive
    Description: open
    Keywords: solphataric activity ; co2 flux ; fumaroles ; soil gases ; 04. Solid Earth::04.02. Exploration geophysics::04.02.01. Geochemical exploration
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: Oral presentation
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  • 10
    Publication Date: 2017-04-04
    Description: Volcanoes are very strong sources of sulphur, acids and other gases, as well as particles, that are of atmospheric relevance. Some gases only behave as passive tracers, others affect the formation, growth or chemical characteristics of aerosol particles and many lead to adverse effects on vegetation and human health when deposited in the vicinity of volcanoes. In this article the main effects of volcanic emissions on atmospheric chemistry are discussed, with a focus on sulphur and halogen compounds, and to a smaller extent on climate. We primarily focus on quiescent degassing but the main effects of explosive eruptions on the troposphere and stratosphere are covered as well. The key distinction between chemistry in magmatic and hydrothermal settings and the atmosphere is that the atmosphere is oxidising whereas the chemistry is typically reducing in the former cases due to very low oxygen concentrations. Rapid catalytic cycles involving radicals are a further characteristic of atmospheric chemistry. Most reaction cycles involve the photolysis of molecules as a key part of the reaction chains. Recent measurements of halogen radicals in volcanic plumes showed that volcanic plumes are chemically very active. We explain the formation mechanism of halogen oxides in plumes as well as their relevance for the atmosphere.
    Description: Published
    Description: 131-142
    Description: 1.2. TTC - Sorveglianza geochimica delle aree vulcaniche attive
    Description: JCR Journal
    Description: reserved
    Keywords: Quiescent degassing ; Troposphere ; Halogens ; Atmospheric chemistry ; 01. Atmosphere::01.01. Atmosphere::01.01.07. Volcanic effects
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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