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  • 01. Atmosphere::01.01. Atmosphere::01.01.03. Pollution  (3)
  • 04. Solid Earth::04.08. Volcanology::04.08.06. Volcano monitoring  (2)
  • 05. General::05.02. Data dissemination::05.02.01. Geochemical data
  • E31
  • J24
  • Life Sciences (General)
  • Elsevier Science Limited  (6)
Collection
Years
  • 1
    Publication Date: 2017-04-03
    Description: A geologically reasonable working hypothesis is proposed for the lithology of the basement underlying the Campi Flegrei caldera in the ca. 4–8 km depth range. In most current geophysical modeling, this portion of crust is interpreted as composed of Meso-Cenozoic carbonate rocks, underlain by a ca. 1 km thick sill of partially molten rock, thought to be a main magma reservoir. Shallower magma reservoirs likely occur in the 3–4 km depth range. However, the lack of carbonate lithics in any Campi Flegrei caldera volcanic rocks does not support the hypothesis of a limestone basement. Considering the major caldera-forming eruptions, which generated widespread and voluminous ignimbrites during late Quaternary times, including the Campanian Ignimbrite and Neapolitan Yellow Tuff eruptions, the total volume of trachytic to phonolitic ejected magma is conservatively estimated at not less than 350 km3. Results of least-squared mass-balance calculations suggest that this evolved magma formed through fractional crystallization from at least 2500 km3 of parent shoshonitic magma, in turn derived from even more voluminous, more mafic, K-basaltic magma. Calculations suggest that shoshonitic magma, likely emplaced at ca. 8 km depth, must have crystallized about 2100 km3 of solid material, dominated by alkali-feldspar and plagioclase, with a slightly lower amount of mafic minerals, during its route toward shallower magma reservoirs, before feeding the Campi Flegrei large-volume eruptions. The calculated volume of cumulate material, likely syenitic in composition at least in its upper portions, is more than enough to completely fill the basement volume in the 4–8 km depth range beneath the Campi Flegrei caldera, estimated at ca. 1250 km3. Thus, it is proposed that the basement underlying the Campi Flegrei caldera below 4 km is composed mostly of crystalline igneous rocks, as for many large calderas worldwide. Syenite sensu lato would meet physical properties requirements for geophysical data interpretations, explain some geochemical and isotopic features of the past 15 ka volcanics, and justify the carbon isotopic composition of fumaroles at the Campi Flegrei caldera. This implies that Meso-Cenozoic limestones, if still present today beneath the Campi Flegrei caldera, no longer constitute significant portions of its basement.
    Description: Published
    Description: 91–98
    Description: JCR Journal
    Description: restricted
    Keywords: Campi Flegrei caldera ; 04. Solid Earth::04.08. Volcanology::04.08.06. Volcano monitoring
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 2
    Publication Date: 2017-04-03
    Description: Fluorine adsorption experiments were performed on 28 samples of the first 5 cm of topsoil collected on the flanks of Mt. Etna. The soil samples were equilibrated with F-rich rainwater (3.25 mg/L) at a soil/water weight ratio of 1/25. Aliquots of the supernatant were collected after 1, 7, 72, 720 and 5640 h and analysed for F content. The soil samples could be subdivided into three groups based on their F-adsorption behaviours after 1 h and at the end of the experiment: (1) negative adsorption (F released from the soil to the solution) after 1 h and negative or moderately positive adsorption at the end, (2) from negative after 1 h to strongly positive adsorption at the end, and (3) always strong positive adsorption. The adsorption capacity of the soils was positively correlated with the soil pH, the contents of finer granulometric fractions (clay and silt) and the weathering stage (as quantified by the chemical alteration index). The most F adsorbing soils are found at the periphery of the volcano where aquifers are more vulnerable to contamination due to the shallower depth of the water table. This study further evidences the importance of the Etnean soils in protecting groundwater from an excessive magmatic F input.
    Description: Published
    Description: 1179–1188
    Description: 4.4. Scenari e mitigazione del rischio ambientale
    Description: JCR Journal
    Description: restricted
    Keywords: volcanic soils ; fluoride adsorption ; Mt. Etna ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases ; 04. Solid Earth::04.08. Volcanology::04.08.08. Volcanic risk ; 05. General::05.02. Data dissemination::05.02.01. Geochemical data ; 05. General::05.08. Risk::05.08.01. Environmental risk
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 3
    Publication Date: 2017-04-04
    Description: About 120 rainwater samples were collected through a network of five bulk collectors in the area of the Louros basin (Epirus, Greece) during the wet season from October 2008 to August 2009. They were analysed for their isotopic (δD and δ18O) and chemical (H+, Na+, K+, Mg2+, Ca2+, NH4 +, F−, Cl−, Br−, NO3 −, SO4 2 −) composition. A local meteoric water line (δD‰ = 5.80 ± 0.02 δ18O‰ + 0.02 ± 0.12) and a local isotopic lapse rate (−0.18 δ18O‰/100 m) were obtained considering the volume-weighted means of the five sampling sites. These results agree well with those obtained in nearby areas. The chemical composition of the samples allows to identify an almost entirely marine origin for chloride and sodium with decreasing deposition values at increasing distance from the coast. Nitrate and ammonium are almost completely of anthropogenic origin, calcium and potassium are overwhelmingly geogenic, sulphate has a prevailingly anthropogenic origin with a significant marine contribution and magnesium has a mixedmarine and soil dust origin. Finally, as for most of the Mediterranean area, rainwater acidity is buffered by the dissolution of the abundant geogenic carbonate aerosol.
    Description: Published
    Description: 399-410
    Description: 4.4. Scenari e mitigazione del rischio ambientale
    Description: JCR Journal
    Description: restricted
    Keywords: Precipitation ; Neutralization ; Stable isotopes ; Chemical composition ; Bulk deposition ; 01. Atmosphere::01.01. Atmosphere::01.01.02. Climate ; 01. Atmosphere::01.01. Atmosphere::01.01.03. Pollution ; 01. Atmosphere::01.01. Atmosphere::01.01.07. Volcanic effects ; 02. Cryosphere::02.03. Ice cores::02.03.06. Precipitation ; 04. Solid Earth::04.04. Geology::04.04.12. Fluid Geochemistry
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 4
    Publication Date: 2017-04-04
    Description: We installed a permanent SO2 camera system on Stromboli, Italy, in May 2013, in order to improve our capacity to monitor the SO2 emissions from this volcano. The camera collects images of SO2 concentrations with a period of ~ 10 s, allowing quantification of short-term processes, such as the gas released during the frequent explosions which are synonymous with Stromboli. It also allows quantification of the quiescent gas flux, and therefore comparison with the FLAME network of scanning ultraviolet spectrometers previously installed on the island. Analysis of results from the SO2 camera demonstrated a good agreement with the FLAME network when the plume was blown fully into the field of view of the camera. Permanent volcano monitoring with SO2 cameras is still very much in its infancy, and therefore this finding is a significant step in the use of such cameras for monitoring, whilst also highlighting the requirement of a favourable wind direction and strength. We found that the explosion gas emissions are correlated with seismic events which have a very long period component. There is a variable time lag between event onset time and the increase in gas flux observed by the camera as the explosion gas advects into the field of view of the camera. This variable lag is related to the plume direction, as shown by comparison with the plume location detected with the FLAME network. The correlation between explosion gas emissions and seismic signal amplitude show is consistent with a gas slug-driven mechanism for seismic event production. Comparison of the SO2 camera measurements of the quiescent gas flux shows a fair quantitative agreement with the SO2 flux measured with the FLAME network. Overall, the SO2 camera complements the FLAME network well, as it allows frequent quantification of the explosion gas flux produced by Stromboli, whose signal is in general too brief to be measured with the FLAME network. Further work is required, however, to fully automate the calculation of SO2 flux from the SO2 images captured with the camera, and to adequately account for scattering effects.
    Description: Published
    Description: 95-102
    Description: 3V. Dinamiche e scenari eruttivi
    Description: 5V. Sorveglianza vulcanica ed emergenze
    Description: JCR Journal
    Description: restricted
    Keywords: Stromboli ; SO2 flux ; VLP ; Explosion ; SO2 camera ; volcano monitoring ; 04. Solid Earth::04.06. Seismology::04.06.08. Volcano seismology ; 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::04.08.07. Instruments and techniques
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 5
    Publication Date: 2024-05-09
    Description: Real-time measurements of GEM and H2S discharged fromnatural and anthropogenic sources are a valuable tool to investigate the dispersion dynamics of these contaminants in air. In this study, a new approach to measure GEM and H2S concentrations in air, carried out by coupling a portable Zeeman atomic absorption spectrometer with high frequency modulation of light polarization (Lumex RA-915M) and a pulsed fluorescence gas analyzer (Thermo Scientific Model 450i), was applied to two distinct areas: (i) in the surroundings of Piancastagnaio (Siena, Central Italy), located in the eastern flanks ofMt. Amiata (a 200,000 years old volcano), where three geothermal plants are operating and whose exhaust gases are dispersed in the atmosphere after passing through the turbines and an abatement system to mitigate the environmental impact on air, and (ii) at Solfatara Crater (Campi Flegrei, Southern Italy), a volcanic apparatus characterized by intense hydrothermal activity. In 2014, seven GEMand H2S surveys were carried out in the two areas along pre-defined pathways performed by car at both the study sites. The lowest and highest recorded GEM and H2S concentrations at Piancastagnaio were up to 194 and 77 ng/m3, respectively, whilst at Solfatara Crater were up to 690 and 3392 μg/m3, respectively. Although the GEM concentrations at Piancastagnaio were lower than the limit value recommended by local regulations for outdoor environment (300 ng/m3), they were almost one order of magnitude higher than the GEM background both in Tuscany (~3.5 ng/m3) and Mt. Amiata (3–5 ng/m3), suggesting that the main source of GEM was likely related to the geothermal plants. At Solfatara Crater, the highest GEM values were recognized in proximity of the main fumarolic gas discharges. As far as the H2S concentrations are concerned, the guideline value of 150 μg/m3, recommended by WHO (2000), was frequently overcome in the study areas. Dot (in the surroundings of Piancastagnaio) and contour (at Solfatara Crater) maps for GEM and H2S concentrations built for each survey highlighted the important effects played by the meteorological parameters, the latter being measured by a Davis® Vantage Vue weather station. In particular, the GEM and H2S plumes were strongly affected by the wind speed and direction thatwere able to modify the dispersion of the two parameters in air in a matter of hours, indicating that the proposed analytical approach is able to produce a more realistic picture of the distribution of these air pollutants than that provided by using passive traps. Finally, the H2S/GEMratio, calculated by normalizing the measured GEM and H2S concentrations to their highest values (nH2S/GEM),was used as a good proxy for the chemical-physical processes that these two gas species can suffer once emitted in the air. In particular, H2S resulted to be more affected by secondary processes than GEM, possibly related to photochemical oxidation reactions.
    Description: Published
    Description: 48-58
    Description: 4V. Vulcani e ambiente
    Description: JCR Journal
    Description: restricted
    Keywords: Real-time measurements ; gaseous elemental mercury ; Hydrogen sulphide ; Gaseous contaminants ; Solfatara crater ; Mt. Amiata ; 01. Atmosphere::01.01. Atmosphere::01.01.03. Pollution ; 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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  • 6
    Publication Date: 2024-05-09
    Description: In this study, hydrogen sulfide (H2S) measurements in air carried out using (a) passive/diffusive samplers (Radiello® traps) and (b) a high-frequency (60 s) real-time analyzer (Thermo® 450i) were compared in order to evaluate advantages and limitations of the two techniques. Four different sites in urban environments (Florence, Italy) and two volcanic areas characterized by intense degassing of H2S-rich fluids (Campi Flegrei and Vulcano Island, Italy) were selected for such measurements. The concentrations of H2S generally varied over 5 orders of magnitude (from 10 1e103 mg/m3), the H2S values measured with the Radiello® traps (H2SR) being significantly higher than the average values measured by the Thermo® 450i during the trap exposure (H2STa), especially when H2S was 〈30 mg/m3. To test the reproducibility of the Radiello® traps, 8 passive/diffusive samplers were contemporaneously deployed within an 0.2 m2 area in an H2S-contaminated site at Mt. Amiata (Tuscany, Italy), revealing that the precision of the H2SR values was ±49%. This large uncertainty, whose cause was not recognizable, is to be added to that related to the environmental conditions (wind speed and direction, humidity, temperature), which are known to strongly affect passive measurements. The Thermo® 450i analyzer measurements highlighted the occurrence of short-term temporal variations of the H2S concentrations, with peak values (up to 5732 mg/m3) potentially harmful to the human health. The Radiello® traps were not able to detect such temporal variability due to their large exposure time. The disagreement between the H2SR and H2STa values poses severe concerns for the selection of an appropriate methodological approach aimed to provide an accurate measurement of this highly toxic air pollutant in compliance with the WHO air quality guidelines. Although passive samplers may offer the opportunity to carry out low-cost preliminary surveys, the use of the high-frequency H2S analyzer is preferred when an accurate assessment of air quality is required. In fact, the latter provides precise real-time measurements for a reliable estimation of the effective exposure to hazardous H2S concentrations, giving insights into the mechanisms regulating the dispersion of this air pollutant in relation to the meteorological parameters.
    Description: Published
    Description: 51-58
    Description: 4V. Vulcani e ambiente
    Description: JCR Journal
    Description: restricted
    Keywords: active analysers ; Passive/diffusive samplers ; Gaseous contaminants ; Air quality monitoring ; Hydrogen sulphide ; 01. Atmosphere::01.01. Atmosphere::01.01.03. Pollution ; 01. Atmosphere::01.01. Atmosphere::01.01.07. Volcanic effects ; 01. Atmosphere::01.01. Atmosphere::01.01.08. Instruments and techniques
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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