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  • 04. Solid Earth::04.04. Geology::04.04.12. Fluid Geochemistry  (14)
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Years
  • 1
    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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  • 2
    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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  • 3
    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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  • 4
    Publication Date: 2019-01-09
    Description: Nisyros Island, Greece, is a stratovolcano known for its intense hydrothermal activity. On June 2013, during a multidisciplinary field campaign, soil samples were collected in the caldera area to determinate the main mineralogical assemblages and to investigate the distribution of trace element concentrations and the possible relationship to the contribution of fluids of deep origin. Soil samples were analysed with XRD and for the chemical composition of their leachable (deionized water) and pseudo total (microwave digestion) fraction both for major and trace elements. The results allow to divide the samples in 2 groups: Lakki Plain and Stefanos Crater. The latter, where a fumarolic area is located, shows a mineralogical assemblage dominated by phases typical of hydrothermal alteration. Their very low pH values (1.9 – 3.4) show the strong impact of fumarolic gases which are probably also the cause of strong enrichments in these soils of highly volatile elements like S, As, Se, Bi, Sb, Tl and Te.
    Description: Published
    Description: 2SR. VULCANI - Servizi e ricerca per la Società
    Description: JCR Journal
    Description: open
    Keywords: Trace elements ; Hydrothermal alteration ; 01. Atmosphere::01.01. Atmosphere::01.01.07. Volcanic effects ; 03. Hydrosphere::03.04. Chemical and biological::03.04.06. Hydrothermal systems ; 04. Solid Earth::04.02. Exploration geophysics::04.02.01. Geochemical exploration ; 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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  • 5
    Publication Date: 2017-04-04
    Description: The most tragic event of gas driven lake eruption occurred at Lake Nyos (Cameroon) on 21 August 1986, when a dense cloud of CO2 suffocated more than 1700 people and an uncounted number of animals in just one night. The event stimulated a series of researches aimed to understand gas origins, gas release mechanisms and strategies for gas hazard mitigation. Very few studies have been carried out for describing the transport of dense CO2 clouds in the atmosphere. Although from a theoretical point of view, gas dispersion can be fully studied by solving the complete equations system for mass, momentum and energy transport, in actual practice, different simplified models able to describe only specific phases or aspects have to be used. In order to simulate dispersion of a heavy gas and to assess the consequent hazard we used a model based on a shallow layer approach (TWODEE2). This technique which uses depthaveraged variables to describe the flow behavior of dense gas over complex topography represents a good compromise between the complexity of computational fluid dynamic models and the simpler integral models. Recently the model has been applied for simulating CO2 dispersion from natural gas emissions in Central Italy. The results have shown how the dispersion pattern is strongly affected by the intensity of gas release, the topography and the ambient wind speed. Here for the first time we applied TWODEE2 code to simulate the dispersion of the large CO2 clouds released by limnic eruptions. An application concerns the case of the 1986 event at lake Nyos. Some difficulties for the simulations were related to the lack of quantitative information: gas flux estimations are not well constrained, meteorological conditions are only qualitatively known, the digital model of the terrain is of poor quality. Different scenarios were taken into account in order to reproduce the qualitative observations available for such episode. The observations regard mainly the effects of gas on the people living in the surrounding areas. Simulation results are in good agreement with these observations. Another application is focused on a hypothetical gas release from lake Albano (Italy), a volcanic lake that probably degassed on the past as reported in historical chronicles by the Roman historian Titus Livius. At the present time the lake is far from saturation conditions and the occurrence of such an event is impossible. However a recent re-interpretation of literature data clearly show the presence of anomalous CO2 enrichment of the lake waters during the last seismic crisis which affected the area. For these reasons a future limnic eruption can not be ruled out completely. The simulations we present show the potential effect of a gas driven eruption from lake Albano in this densely populated area located 20 km south-east from the centre of Rome.
    Description: Published
    Description: S.Francisco California USA
    Description: 1.2. TTC - Sorveglianza geochimica delle aree vulcaniche attive
    Description: open
    Keywords: Modeling CO2 ; gas ; eruptions ; 04. Solid Earth::04.04. Geology::04.04.12. Fluid Geochemistry ; 04. Solid Earth::04.08. Volcanology::04.08.06. Volcano monitoring ; 05. General::05.08. Risk::05.08.01. Environmental risk
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: Conference paper
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  • 6
    Publication Date: 2024-05-09
    Description: A geochemical survey of thermal waters collected from submarine vents at Panarea Island (Aeolian Islands, southern Italy) was carried out from December 2002 to March 2007, in order to investigate i) the geochemical processes controlling the chemical composition of the hydrothermal fluids and ii) the possible relations between the chemical features of the hydrothermal reservoir and the activity of the magmatic system. Compositional data of the thermal water samples were integrated in a hydrological conceptual model, which describes the formation of the vent fluid by mixing of seawater, seawater concentrated by boiling, and a deep, highly-saline end-member, whose composition is regulated by water-rock interactions at relatively high temperature and shows clear clues of magmatic-related inputs. The chemical composition of concentrated seawater was assumed to be represented by that of the water sample having the highest Mg content. The composition of the deep end-member was instead calculated by extrapolation assuming a zero-Mg end-member. The Na–K–Ca geothermometer, when applied to the thermal end-member composition, indicated an equilibrium temperature of approximately 300 °C, a temperature in agreement with the results obtained by gas-geothermometry.
    Description: Published
    Description: 246-254
    Description: 3V. Proprietà chimico-fisiche dei magmi e dei prodotti vulcanici
    Description: JCR Journal
    Description: reserved
    Keywords: low-pH waters; shallow submarine hydrothermal springs; Panarea Island ; 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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  • 7
    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)
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  • 8
    Publication Date: 2024-05-09
    Description: Abstract A geochemical survey of fumarolic and submerged gases from fluid discharges located in the Nea Kameni and Palea Kameni islets (Santorini Island, Greece) was carried out before, during, and after the unrest related to the anomalously high seismic and ground deformation activity that affected this volcanic system since January 2011. Our data show that from May 2011 to February 2012, the Nea Kameni fumaroles showed a significant increase of H2 concentrations. After this period, an abrupt decrease in the H2 contents, accompanied by decreasing seismic events, was recorded. A similar temporal pattern was shown by the F−, Cl−, SO4 2−, and NH4 + concentrations in the fumarolic condensates. During the sharp increase of H2 concentrations, when values up to 158 mmol/ mol were measured, the δ13C–CO2 values, which prior to January 2011 were consistent with a dominant CO2 thermometamorphic source, have shown a significant decrease, suggesting an increase of mantle CO2 contribution. Light hydrocarbons, including CH4, which are controlled by chemical reactions kinetically slower than H2 production from H2O dissociation, displayed a sharp increase in March 2012, under enhanced reducing conditions caused by the high H2 concentrations of May 2011–February 2012. The general increase in light hydrocarbons continued up to July 2012, notwithstanding the contemporaneous H2 decrease. The temporal patterns of CO2 concentrations and N2/Ar ratios increased similarly to that of H2, possibly due to sealing processes in the fumarolic conduits that diminished the contamination related to the entrance of atmospheric gases in the fumarolic conduits. The compositional evolution of the Nea Kameni fumaroles can be explained by a convective heat pulse from depth associated with the seismic activation of the NE–SW-oriented Kameni tectonic lineament, possibly triggered by either injection of new magma below Nea Kameni island, as apparently suggested by the evolution of the seismic and ground deformation activity, or increased permeability of the volcanic plumbing system resulting from the tectonic movements affecting the area. The results of the present study demonstrate that the geophysical and geochemical signals at Santorini are interrelated and may be precursory signals of renewed volcanic activity and encourage the development of interdisciplinary monitoring program to mitigate the volcanic risk in the most tourist-visited island of the Mediterranean Sea.
    Description: Published
    Description: 711
    Description: 1.2. TTC - Sorveglianza geochimica delle aree vulcaniche attive
    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: Santorini Island . ; Fluid geochemistry ; Geochemical monitoring ; Seismic crisis ; 03. Hydrosphere::03.02. Hydrology::03.02.04. Measurements and monitoring ; 04. Solid Earth::04.04. Geology::04.04.12. Fluid Geochemistry ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases ; 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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  • 9
    Publication Date: 2024-05-09
    Description: Copahue volcano is part of the Caviahue–Copahue Volcanic Complex (CCVC),which is located in the southwestern sector of the Caviahue volcano-tectonic depression (Argentina–Chile). This depression is a pull-apart basin accommodating stresses between the southern Liquiñe–Ofqui strike slip and the northern Copahue–Antiñir compressive fault systems, in a back-arc setting with respect to the Southern Andean Volcanic Zone. In this study, we present chemical (inorganic and organic) and isotope compositions (δ13C-CO2, δ15N, 3He/4He, 40Ar/36Ar, δ13C-CH4, δD-CH4, and δD-H2O and δ18O-H2O) of fumaroles and bubbling gases of thermal springs located at the foot of Copahue volcano sampled in 2006, 2007 and 2012. Helium isotope ratios, the highest observed for a Southern American volcano (R/Ra up to 7.94), indicate a non-classic arc-like setting, but rather an extensional regime subdued to asthenospheric thinning. δ13C-CO2 values (from −8.8‰ to −6.8‰ vs. V-PDB), δ15N values (+5.3‰ to +5.5‰ vs. Air) and CO2/3He ratios (from 1.4 to 8.8 × 109) suggest that the magmatic source is significantly affected by contamination of subducted sediments. Gases discharged from the northern sector of the CCVC show contribution of 3He-poor fluids likely permeating through local fault systems. Despite the clear mantle isotope signature in the CCVC gases, the acidic gas species have suffered scrubbing processes by a hydrothermal system mainly recharged by meteoric water. Gas geothermometry in the H2O-CO2-CH4-CO-H2 system suggests that CO and H2 re-equilibrate in a separated vapor phase at 200°–220 °C. On the contrary, rock–fluid interactions controlling CO2, CH4 production from Sabatier reaction and C3H8 dehydrogenation seem to occur within the hydrothermal reservoir at temperatures ranging from 250° to 300 °C. Fumarole gases sampled in 2006–2007 show relatively low N2/He and N2/Ar ratios and high R/Ra values with respect to those measured in 2012. Such compositional and isotope variations were likely related to injection of mafic magma that likely triggered the 2000 eruption. Therefore, changes affecting the magmatic systemhad a delayed effect on the chemistry of the CCVC gases due to the presence of the hydrothermal reservoir. However, geochemical monitoring activities mainly focused on the behavior of inert gas compounds (N2 and He), should be increased to investigate the mechanism at the origin of the unrest started in 2011.
    Description: Published
    Description: 44–56
    Description: 1.2. TTC - Sorveglianza geochimica delle aree vulcaniche attive
    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: Fluid geochemistry ; Copahue volcano ; Fumarolic fluid ; Hydrothermal reservoir ; Volcanic unrest ; 03. Hydrosphere::03.02. Hydrology::03.02.04. Measurements and monitoring ; 04. Solid Earth::04.04. Geology::04.04.12. Fluid Geochemistry ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases ; 04. Solid Earth::04.08. Volcanology::04.08.07. Instruments and techniques
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
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  • 10
    Publication Date: 2024-05-09
    Description: Measurements of soil fluxes of hydrothermal gases, with special emphasis on C6H6, as well as chemical composition of mono-aromatic compounds in fumaroles and air, were carried out in April 2012 at the Solfatara crater (Campi Flegrei, Southern Italy) to investigate the distribution and behavior of these species as they migrate through the soil from their deep source to the atmosphere. Soil fluxes of CO2, CH4 and C6H6 exhibit good spatial correlation, suggesting that diffuse degassing is mainly controlled by local fractures. The calculated total output of diffuse C6H6 from Solfatara is 0.10 kg day 1, whereas fluxes of CO2 and CH4 are 79 103 and 1.04 kg day 1, respectively. A comparison between soil gas fluxes and fumarole composition reveals that within the crater soil CH4 is significantly affected by oxidation processes, which are more efficient for low gas fluxes, being dependent on the residence time of the uprising hydrothermal gases at shallow depth. Benzene degradation, mainly proceeding through oxidation via benzoate, seems to be strongly controlled by the presence of a shallow SO2 4 -rich aquifer located in the central and southwestern sectors of the crater, suggesting that the process is particularly efficient when SO2 4 acts as terminal electron acceptor (SO4 reduction). Relatively high C6H6/C7H8 ratios, typical of hydrothermal fluids, were measured in air close to the main fumarolic field of Solfatara crater. Here, C6H6 concentrations, whose detection limit is 0.1 lgm 3, are more than one order of magnitude higher than the limit value for ambient air (5 lgm 3). This suggests that hydrothermal fluids have a strong impact on air quality in the immediate surroundings of the fumarolic vents. Significant concentrations of endogenous mono-aromatics were also detected in air samples collected from the northern and western sides of the crater, where these gas compounds are mostly fed by diffuse degassing through the crater bottom soil.
    Description: Published
    Description: 142–153
    Description: 1.2. TTC - Sorveglianza geochimica delle aree vulcaniche attive
    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 gases ; Solfatara crater ; 03. Hydrosphere::03.02. Hydrology::03.02.04. Measurements and monitoring ; 04. Solid Earth::04.04. Geology::04.04.12. Fluid Geochemistry ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases ; 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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