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  • 1
    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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  • 2
    Publication Date: 2019-01-09
    Description: Greece has a very complex geodynamic setting deriving from a long and complicat-ed geological history being characterized by intense seismic activity and enhanced geothermal gradient. This activity, with the contribution of an active volcanic arc, favours the existence of many gas manifestations. Depending on the prevailing gas species, the latter can be subdivided in three main groups: CO2-, N2- and CH4-dominated. In the present work, we focus on methane and light hydrocarbons (C2-C6) to define their origin. CH4 concentrations (〈2 to 915,200 μmol/mol) and isotop-ic ratios (δ13C -79.8 to +16.9 ‰, δD -298 to +264‰) cover a wide range of values indicating different origins and/or secondary post-genetic processes. Samples from gas discharged along the Ionian coast and in northern Aegean Sea have a prevail-ing microbial origin. Cold and thermal gas manifestations of central and northern Greece display a prevalent thermogenic origin. Methane in gases released along the active volcanic arc is prevailingly abiogenic, although thermogenic contributions cannot be excluded. Gases collected in the geothermal areas of Sperchios basin and northern Euboea are likely affected by strong secondary oxidation processes, as suggested by their highly positive C and H isotopic values (up to +16.9‰ and +264‰ respectively) and low C1/(C2+C3) ratios.
    Description: Submitted
    Description: Thessaloniki, Greece
    Description: 4V. Vulcani e ambiente
    Description: open
    Keywords: Hellenic territory ; hydrothermal gases ; cold gas emissions ; origin of hydrocarbon gases ; 03. Hydrosphere::03.04. Chemical and biological::03.04.05. Gases ; 03. Hydrosphere::03.04. Chemical and biological::03.04.06. Hydrothermal systems ; 04. Solid Earth::04.04. Geology::04.04.12. Fluid Geochemistry ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: Conference paper
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  • 3
    Publication Date: 2022-05-04
    Description: Abstract San Miguel volcano, El Salvador, erupted on 29 December 2013, after a 46 year period characterized by weak activity. Prior to the eruption a trend of increasing SO2 emission rate was observed, with all values measured after mid-November greater than the average value of the previous year (~310 t d 1). During the eruption, SO2 emissions increased from the level of ~330 t d 1 to 2200 t d 1, dropping after the eruption to an average level of 680 t d 1. Wind measurements and SO2 emission rates during the preeruptive, syneruptive, and posteruptive stages were used to model SO2 dispersion around the volcano. Atmospheric SO2 concentration exceeded the dangerous threshold of 5 ppm in the crater region and in some sectors with medium elevation of the highly visited volcanic cone. Combining the SO2 emission rate with measured CO2/SO2, HCl/SO2, and HF/SO2 plume gas ratios, we estimate the CO2, HCl, and HF outputs for the first time on this volcano.
    Description: Published
    Description: 5847–5854
    Description: 3V. Dinamiche e scenari eruttivi
    Description: JCR Journal
    Description: restricted
    Keywords: SO2 flux, Clorine and CO2 at San miguel, cloud dispersion and hazard ; 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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