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  • 04. Solid Earth::04.08. Volcanology::04.08.01. Gases  (11)
  • Fluid geochemistry  (6)
  • 04. Solid Earth::04.08. Volcanology::04.08.08. Volcanic risk  (2)
  • Arezzo  (2)
Collection
  • 1
    Publication Date: 2021-06-16
    Description: This study performed the first assessment of the volcanic gas output from the Central Volcanic Zone (CVZ) of northern Chile. We present the fluxes and compositions of volcanic gases (H2O, CO2, H2, HCl, HF, and HBr) from five of the most actively degassing volcanoes in this region—Láscar, Lastarria, Putana, Ollagüe, and San Pedro—obtained during field campaigns in 2012 and 2013. The inferred gas plume compositions for Láscar and Lastarria (CO2/Stot = 0.9–2.2; Stot/HCl = 1.4–3.4) are similar to those obtained in the Southern Volcanic Zone of Chile, suggesting uniform magmatic gas fingerprint throughout the Chilean arc. Combining these compositions with our own UV spectroscopy measurements of the SO2 output (summing to ~1800 t d 1 for the CVZ), we calculate a cumulative CO2 output of 1743–1988 t d 1 and a total volatiles output of 〉20,200 t d 1. 1.
    Description: Published
    Description: 4961-4969
    Description: 5V. Sorveglianza vulcanica ed emergenze
    Description: JCR Journal
    Description: restricted
    Keywords: Gas output from the Central Volcanic Zone ; 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: 2017-04-04
    Description: Methane (CH4) emanating from a continental volcanichydrothermal system in Nisyros, Greece, is processed through the abiogenic reduction of mantle- and marine limestonederived CO2 [1]. Evidence for the occurrence of abiogenic hydrothermal reduction of CO2 is from the chemical and carbon isotopic equilibrium patterns. We have further characterized this abiogenic methane (C1) source for the concentrations of ethane (C2) and propane (C3), as well as for the hydrogen isotopic composition of CH4, H2O, H2 and H2S. C1/C2+ ratios are significantly higher than those typically observed for purely thermogenic sources. Hydrocarbon distribution ratios for other continental-hydrothermal sources rich in CO2 are comparable to those of the Nisyros fumaroles implying that abiogenic methane might be significantly more widespread than previously assumed [2]. Relative concentrations of hydrocarbons in continental-hydrothermal discharges are even indistinguishable from those measured in ultramafic hydrothermal emissions. The fact that redox conditions do not seem to exert any control on the relative concentrations of hydrocarbons in hydrothermal emissions in general, implies that the same two sources account for hydrocarbon production in continental and ultramafic environments. One source generates methane exclusively through the selective abiogenic reduction of CO2 (Sabatierreaction). The other source produces minor amounts of methane, ethane and propane by a random process and represents either the thermal cracking of organic matter or the polymerization starting from methane. Hydrogen isotope partitioning between H2O, H2S, H2 and CH4 in Nisyros fumaroles reveals that isotopic exchange rates are highest for H2O-H2S followed by H2O-H2. In contrast to H2 and H2S, the hydrogen isotopic composition of methane exhibits almost no local variations. This is in agreement with its predominantly abiogenic hydrothermal origin and with the low temperature sensitivity of the hydrogen isotope fractionation factor between water vapor and methane.
    Description: Published
    Description: Davos, Switzerland
    Description: 1.2. TTC - Sorveglianza geochimica delle aree vulcaniche attive
    Description: open
    Keywords: hydrothermal gases ; methane ; ethane ; propane ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: Oral presentation
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  • 3
    Publication Date: 2017-04-04
    Description: In the past, variations in the chemical contents (SO4 2−, Cl−, cations) of crater lake water have not systematically demonstrated any relationships with eruptive activity. Intensive parameters (i.e., concentrations, temperature, pH, salinity) should be converted into extensive parameters (i.e., fluxes, changes with time of mass and solutes), taking into account all the internal and external chemical–physical factors that affect the crater lake system. This study presents a generalized box model approach that can be useful for geochemical monitoring of active crater lakes, as highly dynamic natural systems. The mass budget of a lake is based on observations of physical variations over a certain period of time: lake volume (level, surface area), lake water temperature, meteorological precipitation, air humidity, wind velocity, input of spring water, and overflow of the lake. This first approach leads to quantification of the input and output fluxes that contribute to the actual crater lake volume. Estimating the input flux of the "volcanic" fluid (Qf - kg/s) –– an unmeasurable subsurface parameter –– and tracing its variations with time is the major focus during crater lake monitoring. Through expanding the mass budget into an isotope and chemical budget of the lake, the box model helps to qualitatively characterize the fluids involved. The (calculated) Cl− content and dD ratio of the rising "volcanic" fluid defines its origin. With reference to continuous monitoring of crater lakes, the present study provides tips that allow better calculation of Qf in the future. At present, this study offers the most comprehensive and up-to-date literature review on active crater lakes.
    Description: Published
    Description: 161-173
    Description: 1.2. TTC - Sorveglianza geochimica delle aree vulcaniche attive
    Description: JCR Journal
    Description: open
    Keywords: Geochemical monitoring ; Active crater lakes, ; Box model ; Mass budget ; Isotope and chemical budget ; 03. Hydrosphere::03.02. Hydrology::03.02.02. Hydrological processes: interaction, transport, dynamics ; 04. Solid Earth::04.04. Geology::04.04.12. Fluid Geochemistry ; 04. Solid Earth::04.08. Volcanology::04.08.06. Volcano monitoring ; 04. Solid Earth::04.08. Volcanology::04.08.07. Instruments and techniques ; 04. Solid Earth::04.08. Volcanology::04.08.08. Volcanic risk
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 4
    Publication Date: 2017-04-04
    Description: The chemistry of Yellowstone fumarole gases shows the existence of two component waters, type MC, influenced by the addition of deep mantle fluid, and type CC, influenced by crustal interactions (CC). MC is high in 3He/4He (22 Ra) and low in 4He/40Ar ( 1), reflecting input of deep mantle components. The other water is characterized by 4He concentrations 3–4 orders of magnitude higher than air-saturated meteoric water (ASW). These high He concentrations originate through circulation in Pleistocene volcanic rocks, as well as outgassing of Tertiary and older (including Archean) basement, some of which could be particularly rich in uranium, a major 4He source. Consideration of CO2–CH4–CO–H2O–H2 gas equilibrium reactions indicates equilibration temperatures from 170 C to 310 C. The estimated temperatures highly correlate with noble-gas variations, suggesting that the two waters differ in temperature. Type CC is 170 C whereas the MC is hotter, at 340 C. This result is similar to models proposed by previous studies of thermal water chemistry. However, instead of mixing the deep hot component simply with cold, meteoric waters we argue that addition of a 4He-rich component, equilibrated at temperatures around 170 C, is necessary to explain the range in fumarole gas chemistry.
    Description: Published
    Description: 265–278
    Description: 2.4. TTC - Laboratori di geochimica dei fluidi
    Description: 4.5. Studi sul degassamento naturale e sui gas petroliferi
    Description: JCR Journal
    Description: restricted
    Keywords: hydrothermal fluids ; Yellowstone Plateau ; 04. Solid Earth::04.03. Geodesy::04.03.06. Measurements and monitoring ; 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: article
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  • 5
    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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  • 6
    Publication Date: 2024-05-09
    Description: Since 2000 a joint project between the Department of Earth Science of Florence and the Unit of Environment and Health of the Municipality of Arezzo has allowed to geochemically characterise the superficial and ground waters of the municipal territory of Arezzo in order to establish the water quality and to investigate the main natural and anthropic processes responsible of their composition. The available geochemical data-base consists of more than 500 samples sites (90% of which are private wells and 7 and 3% are springs and running waters, respectively) on which physical parameters (temperature and electrical conductivity) and major, minor and trace dissolved species (pH, Ca, Mg, Na, K, NH4, HCO3, SO4, NO3, NO2, Cl, Br, F, heavy metals) have been performed by using the same sampling procedure and analytical methodology in order to have a consistent set of data. Fifteen selected sites have been analysed twice per year to evidence possible seasonal effects. No significant differences have been recorded. The Arezzo Basin, formed since Upper Pliocene, is a structural depression limited to the North and to the East by the Pratomagno and Chianti belts, respectively, and to the South and to the East by two tectonic lineaments (Val d’Arbia-Val Marecchia transversal and Chitignano normal faults). Along these tectonic discontinuities CO2-rich manifestations either seep out or exploited by private companies. Hydrogeologically, three main aquifers are recognised: i) a relatively deep aquifer hosted in Tertiary sandstone formations; ii) an intermediate aquifer hosted in Quaternary fluvio-lacustrine sediments and iii) a shallow aquifer in recent alluvional sediments. The content in Total Dissolved Solids (TDS) allows to classify the Arezzo waters in: oligomineral (69%), medium-mineral (30%) and mineral (1%) and they can be regarded as Ca(Mg)-HCO3 (87 %), Na(K)-HCO3 (7%), Ca(Mg)-SO4 (5%) and Na(K)-Cl (1%). It is noteworthy to point of that the Na(K)-HCO3 waters are aligned along the above mentioned tectonic systems. The quality of Arezzo waters has been referred to the Italian legislation that is addressed to the definition of the Maximum Admissible Concentration (MAC, DPR 236/88, Dlgs 31/01) and the Reference Value (RV, DPR 236/88) in terms of waters for the human consumption. Waters from the northern area of Arezzo overcome MAC for chlorides, sulphates and sodium; if we consider nitrogen species (NH4, NO2, NO3) the values overcome CMA for those waters collected into the city, its peripheral areas and in the south-western suburbs. Thematic maps has been produced, on the basis of the principles of linear Geostatistics, in order to analyse the spatial behaviour of the analysed variables. The aim was to find correlations with lithology, use of the soils, drainage density, pressure of antrophic activities and so on, and to identify sensible areas to monitor in their time evolution. The investigation has been developed starting from a detailed variographic analysis by means of the geochemical behaviour of each variable has been analysed in the different directions of the space while the estimation procedure to obtain the maps has been based on the application of sequential Gaussian simulation procedures.
    Description: Published
    Description: Spoleto, Italy
    Description: 2.4. TTC - Laboratori di geochimica dei fluidi
    Description: open
    Keywords: geochemical atlas ; Arezzo ; water quality ; ground-running waters ; 03. Hydrosphere::03.02. Hydrology::03.02.03. Groundwater processes
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: Oral presentation
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  • 7
    Publication Date: 2024-05-09
    Description: In January 2002, Nyiragongo volcano erupted 14–34 × 106 m3 of lava from fractures on its southern flanks. The nearby city of Goma was inundated by two lava flows, which caused substantial socioeconomic disruption and forced the mass exodus of the population, leaving nearly 120,000 people homeless. Field observations showed marked differences between the lava erupted from the northern portion of the fracture system and that later erupted from the southern part. These observations are confirmed by new 238U and 232Th series radioactive disequilibria data, which show the presence of three different phases during the eruption. The lavas first erupted (T1) were probably supplied by a residual magma batch from the lava lake activity during 1994–1995. These lavas were followed by a fresh batch erupted from fissure vents as well as later (May–June 2002) from the central crater (T2). Both lava batches reached the surface via the volcano's central plumbing system, even though a separate flank reservoir may also have been involved in addition to the main reservoir. The final phase (T3) is related to an independent magmatic reservoir located much closer (or even beneath) the city of Goma. Data from the January 2002 eruption, and for similar activity in January 1977, suggest that the eruptive style of the volcano is likely to change in the future, trending toward more common occurrence of flank eruptions. If so, this would pose a significant escalation of volcanic hazards facing Goma and environs, thus requiring the implementation of different volcano-monitoring strategies to better anticipate where and when future eruptions might take place.
    Description: Published
    Description: B09202
    Description: 3.6. Fisica del vulcanismo
    Description: JCR Journal
    Description: reserved
    Keywords: Nyiragongo ; forecasting ; volcanic hazard ; 04. Solid Earth::04.08. Volcanology::04.08.08. Volcanic risk
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 8
    Publication Date: 2024-05-09
    Description: On 3rd November 2002, at about 3 km off-shore of Panarea Island (Aeolian Islands, Southern Italy), a series of gas vents suddenly and violently opened from the seafloor at the depth of 10-15 m, with an unusually high gas flux and superimposing on the already existing submarine fumarolic field. Starting from the 12th November 2002 a discontinuous geochemical monitoring program was carried out. The emissions consisted in an emulsion whose liquid phase derived from condensation of an uprising vapor phase occurring close to the fluid outlets without significant contamination by seawater. The whole composition of the fluids was basically H2O- and CO2-dominated, with minor amounts of typical «hydrothermal» components (such as H2S, H2, CO and light hydrocarbons), atmospheric-related compounds, and characterized by the occurrence of a significant magmatic gas fraction (mostly represented by SO2, HCl and HF). According to the observed temporal variability of the fluid compositions, between November and December 2002 the hydrothermal feeding system was controlled by oxidizing conditions due to the input of magmatic gases. The magmatic degassing phenomena showed a transient nature, as testified by the almost complete disappearance of the magmatic markers in a couple of months and by the restoration, since January 2003, of the chemical features of the existing hydrothermal system. The most striking feature of the evolution of the «Panarea degassing event» was the relatively rapid restoration of the typical reducing conditions of a stationary hydrothermal system, in which the FeO/Fe1.5O redox pair of the rock mineral phases has turned to be the dominating redox controlling system.
    Description: Published
    Description: JCR Journal
    Description: open
    Keywords: Aeolian Islands ; Panarea ; submarine fumaroles ; gas chemistry ; geochemical monitoring ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases ; 04. Solid Earth::04.08. Volcanology::04.08.06. Volcano monitoring
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
    Format: 1571798 bytes
    Format: application/pdf
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  • 9
    Publication Date: 2024-05-09
    Description: Gli elementi chimici disciolti nelle acque continentali provengono dall’alterazione della crosta terrestre. L’acqua erode e dissolve i minerali delle rocce attraverso l’alterazione chimica avvalendosi del contributo dei gas presenti in atmosfera o nel sottosuolo. Il nitrato, una delle sostanze responsabili delle più gravi forme di inquinamento delle acque nei paesi in via di sviluppo, è un nutriente essenziale per la crescita delle piante e rappresenta un anello fondamentale del ciclo biogeochimico dell'azoto, in quanto viene prodotto dai batteri a partire dall'azoto atmosferico. In quantità eccessive il nitrato può essere dannoso per gli uomini e per gli animali. Elevati livelli di nitrato nell'acqua sono causati in larga misura dall'uso di fertilizzanti ricchi di nitrato e dal letame. In questo contesto, le condizioni redox delle acque naturali, che controllano la speciazione dei composti dell’azoto, sono altamente variabili perché controllate prevalentemente dall’attività biologica. In particolare, il bilancio fra i due processi dell’attività biologica, la fotosintesi e la respirazione (o decomposizione della sostanza organica), determina la presenza nel sistema di condizioni ossidanti o riducenti. I composti dell’azoto possono quindi essere considerati utili indicatori dello stato di salute di un acquifero superficiale. In questo lavoro sono analizzati i dati relativi ai tenori delle specie dell’azoto NH4 +, NO2 - e NO3 - relativi ad acque di falda campionate nell’area aretina nel corso della realizzazione dell’Atlante Geochimico delle Acque di Falda e di Scorrimento Superficiale del Comune di Arezzo. I dati sono analizzati proponendo nuove metodologie grafiche e numeriche per visualizzare lo stato del territorio nei confronti della pressione antropica come rilevata dal comportamento spaziale e temporale delle specie suddette.
    Description: Published
    Description: Accademia Nazionale dei Lincei, Roma
    Description: 2.4. TTC - Laboratori di geochimica dei fluidi
    Description: open
    Keywords: Arezzo ; groundwaters ; 03. Hydrosphere::03.02. Hydrology::03.02.03. Groundwater processes
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: Extended abstract
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  • 10
    Publication Date: 2024-05-09
    Description: Geological storage is presently one of the most promising options for reducing anthropogenic emissions of CO2. Among the several projects investigating the fate of CO2 stored at depth, the EnCana's CO2 injection EOR (Enhancing Oil Recovery) project at Weyburn (Saskatchewan, Canada) is the most important oil production development that hosts an international monitoring project. In the Weyburn EOR Project CO2 is used to increase recovery of heavy oil from the Midale Beds, a Mississippian reservoir consisting of shallow marine carbonate, where about 3 billions standard m3 of supercritical CO2 have been injected since 2000 with an injection rate of 5000 ton/day. In this work the available dataset (bulk mineralogy of the reservoir, gas-cap composition and selected preand post-CO2 injection water samples) provided by the International Energy Agency Weyburn CO2 Monitoring & Storage Project has been used in order to: i) reconstruct the pre-injection reservoir chemical composition (including pH and the boundary conditions at 62 °C and 15 MPa); ii) assess the evolution of the reservoir subjected to CO2 injection and predict dissolution/precipitation processes of the Weyburn brines over 100 years after injection; iii) validate the short-term (September 2000–2003) evolution of the in situ reservoir fluids due to the CO2 injection, by comparing the surface analytical data with the composition of the computed depressurized brines. To achieve these goals the PRHEEQC (V2.14) Software Package was used with both modified thermodynamic database and correction for supercritical CO2 fugacity. The oil–gas–water interaction and the non-ideality of the gas phase (with exception of CO2) were not considered in the numerical simulations. Despite intrinsic limitations and uncertainties of geochemical modeling, the main results can be summarized, as follows: 1) the calculated pre-injection chemical composition of the Midale Beds brine is consistent with the analytical data of the waters collected in 2000 (baseline survey), 2) the main reservoir reactions (CO2 and carbonate dissolution) take place within the first year of simulation, 3) the temporal evolution of the chemical features of the fluids in the Weyburn reservoir suggests that CO2 can safely be stored by solubility (as CO2(aq)) and mineral trapping (via dawsonite precipitation). The short-term validation performed by calculating chemical composition of the reservoir fluids (corrected for surface conditions) after the simulation of 3 years of CO2 injection is consistent (error ≤5%) with the analytical data of the wellhead water samples collected in 2003, with the exception of Ca and Mg (error N90%), likely due to complexation effect of carboxilic acid.
    Description: Published
    Description: 181-197
    Description: 2.4. TTC - Laboratori di geochimica dei fluidi
    Description: JCR Journal
    Description: partially_open
    Keywords: CO2 ; Geochemical modeling ; geological storage ; Fluid geochemistry ; EOR Weyburn Oil Field Brines ; 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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