Earthquake-induced variations in the composition of the water in the geothermal reservoir at Vulcano Island, Italy

During 1979–1989, variations were observed in the oxygen composition of the water contained in the geothermal reservoir at Vulcano Island, Italy.The reservoir water, that has a magmatic origin, showed an oxygen composition of +1.0±0.5‰ δ¹⁸O during periods without local tectonic earthquakes, and an oxygen composition of +3.4±0.5‰ δ¹⁸O after the highest-energy seismic activity that occurred recently near the island. A slight increase of the δ¹⁸O value in the reservoir water was also observed after a low-energy sequence of tectonic earthquakes that occurred at very shallow depth just beneath Vulcano Island. These ¹⁸O variations in the reservoir water are consistent with earthquake-induced increases in the contribution from high-temperature δ¹⁸O-rich magmatic condensate to the geothermal reservoir, and with subsequent decreases in the δ¹⁸O value due to ¹⁸O exchanges at the temporarily increased reservoir temperature during reactions between the highly reactive magmatic condensate and the local rocks.Only minor changes in the deuterium composition of the reservoir water occurred with time, as the δD value in the magmatic condensate released from the magma after major local earthquakes quickly approached the δD value of the water contained in the geothermal reservoir.Also the chloride concentration in the reservoir water appears to be linked to the contribution from the magmatic fluid. This chloride content seems not to have undergone major changes with time, as it may be buffered by temporary increases in the reservoir temperature up to values >300°C induced by major local earthquakes. This mechanism may possibly occur also in other magmatic–hydrothermal systems.     

Chemical and isotopic variations in fumarolic discharge and thermal waters at Vulcano Island (Aeolian Islands, Italy) during 1996: evidence of resumed volcanic activity

Gas samples from some fumaroles at ‘La Fossa' crater and Baia di Levante on Vulcano Island and from a diffuse soil gas emission were analysed during 1995–1996, along with water samples from thermal wells in the area of Vulcano Porto. During 1996, we observed a significant increase both in the gas/steam ratio and in the CO₂ concentration, as well as strong variations in δ¹³C_CO2, δD_H2O and δ¹⁸O_H2O of fumarolic gases. These variations are probably related to an increased inflow of deep fluids of magmatic origin. The temperatures of fumaroles did not show remarkable variations except for fumarole F11. In this case, temperature increased by about 80°C from February to August 1996. During the same period, remarkable variations in temperature, phreatic level and chemical and isotopic composition of water were also recorded in one of the geothermal wells in the Vulcano Porto area (Camping Sicilia; T60°C). The observed variations in this well are probably related to a pressure build-up, occurring at least in the surficial part of the system, because of increased gas flux and/or decreased permeability of the fumarolic degassing system. Chemical and isotopic composition of the water showed that during this evolutionary phase, the content of fumarolic condensate in this well was about 80 to 90%. Based on the observation of physical and chemical variables of the Camping Sicilia fluids, during this phase of activity, it is concluded that this area is affected by a phreatic eruption hazard if a volcanic episode with high energy discharge in a limited time span occurs. It follows that this well may be considered as a preferential point for volcanic activity monitoring, both in the case of normal routine surveillance and in the case of inaccessibility to the crater area.     

Structural features of the shallow plumbing system of Vulcano Island Italy

In this study, we integrate information gathered from surface geology and tectonics with the results of a shallow (0–2 km b.s.l.) seismic tomography of Vulcano Island (Italy), obtained from the analysis of local earthquakes. The observed low Vp regions correspond to caldera filling products, mainly consisting of pyroclastics, tuffs, lava flows and hyaloclastites. High-velocity anomalies represent intrusive bodies. The striking correspondence between the stratigraphy from deep wells and the calculated velocity structure allows us to reconstruct the geometry and distribution of a main intrusion and to recognize some intra-caldera depressions. The shape and location of the high and low Vp anomalies are consistent with NW–SE and N–S strikes. Eruptive centres younger than 42 kyr, as well as the structural depressions of Vulcano and of the neighbour Lipari Island, align along a N–S direction. The combined interpretation of the available structural data and of the results from the tomography suggests that magmatic reservoirs of Vulcano at shallow depth (>0.5 km) align along a NW–SE strike but their shape is controlled by N–S striking normal faults and/or cracks that accommodate the right-lateral movements of the NW–SE strike-slip fault system.Editorial responsibility: T. Druitt     

Diffuse emission of CO2 from the Fossa crater,Vulcano Island (Italy)

 Numerous measurements of CO₂ degassing from the soil, carried out with the accumulation chamber method, indicate that in the period April–July 1995 the upper part of the Fossa cone released a total output of 200 t d^–1 of CO₂, which corresponds to approximately 1000 t d^–1 of steam. These large amounts of fluids are of the same order of magnitude as those released by the high temperature fumarolic field located inside the crater. The spatial distribution of soil gas fluxes shows that the main structures releasing CO₂ are the inner slopes of the crater and a NW–SE line, located NE of the crater rim, which correspond to the main direction of Vulcano Island active faults. The comparison of the φCO₂ maps with the soil temperature distribution, derived from both direct measurements and airborne infrared images, indicates the occurrence of extensive condensation of fumarolic steam within the upper part of the Fossa cone, whose total amount is comparable to the rainfall budget. Part of the condensate which originates from this process contributes to the recharge of the phreatic aquifer of Porto Plain, modifying the chemical and isotopic composition of the groundwater. Received: 1 September 1995 / Accepted: 8 January 1996     

Genesis of chlorine and sulphur in fumarolic emissions at Vulcano Island (Italy): assessment of pH and redox conditions in the hydrothermal system

Chlorine- and sulphur-bearing compounds in fumarole discharges of the La Fossa crater at Vulcano Island (Italy) can be modelled by a mixing process between magmatic gases and vapour from a boiling hydrothermal system. This allows estimating the compounds in both endmembers. Magma degassing cannot explain the time variation of sulphur and HCl concentrations in the deep endmember, which are more probably linked to reactions of solid phases at depth, before mixing with the hydrothermal vapours. Based on the P–T conditions and speciation of the boiling hydrothermal system below La Fossa, the HCl and S_tot contents in the hydrothermal vapours were used to compute the redox conditions and pH of the aqueous solution. The results suggest that the haematite–magnetite buffer controls the hydrothermal fO₂ values, while the pH has increased since the end of the 1970s. The main processes affecting pH values may be linked to Na–Ca exchanges between evolved seawater, feeding the boiling hydrothermal system, and local rocks. While Na is removed from water, calcium enters the solution, undergoes hydrolysis and produces HCl, lowering the pH of the water. The increasing water–rock ratio within the hydrothermal system lowers the Ca availability, so the aqueous solution becomes less acidic. Seawater flowing towards the boiling hydrothermal brine dissolves a large quantity of pyrite along its path. In the boiling hydrothermal system, dissolved sulphur precipitates as pyrite and anhydrite, and becomes partitioned in vapour phase as H₂S and SO₂. These results are in agreement with the paragenesis of hydrothermal alteration minerals recovered in drilled wells at Vulcano and are also in agreement with the isotopic composition of sulphur emitted by the crater fumaroles.     

Geochemical survey of Levante Bay,Vulcano Island (Italy), a natural laboratory for the study of ocean acidification

Shallow submarine gas vents in Levante Bay, Vulcano Island (Italy), emit around 3.6t CO₂ per day providing a natural laboratory for the study of biogeochemical processes related to seabed CO₂ leaks and ocean acidification. The main physico-chemical parameters (T, pH and Eh) were measured at more than 70 stations with 40 seawater samples were collected for chemical analyses. The main gas vent area had high concentrations of dissolved hydrothermal gases, low pH and negative redox values all of which returned to normal seawater values at distances of about 400 m from the main vents. Much of the bay around the vents is corrosive to calcium carbonate; the north shore has a gradient in seawater carbonate chemistry that is well suited to studies of the effects of long-term increases in CO₂ levels. This shoreline lacks toxic compounds (such as H₂S) and has a gradient in carbonate saturation states.     

Numerical simulation of the landslide-induced tsunami of 1988 on Vulcano Island, Italy

 On 20 April 1988 a landslide of approximately 200,000 m³ occurred on the northeastern flank of the volcano La Fossa on the island of Vulcano. The landslide fell into the sea, producing a small tsunami in the bay between Punte Nere and Punta Luccia that was observed locally in the neighbouring harbour called Porto Levante. The slide occurred during a period of unrest at the volcano that was monitored very accurately. The study of this event is composed of two parts, the simulation of the landslide and the simulation of the ensuing tsunami; the former is studied by means of a Lagrangian-type numerical model in which the landslide is seen as a multibody system, an ensemble of material-deforming blocks interacting together during their motion; the latter is simulated according to the Eulerian view by solving the shallow-water approximation to Navier-Stokes equations of fluid dynamics, with the incorporation of a forcing term depending on the slide motion. Technically, the slide evolution is computed first, and this result is then used to evaluate the excitation term of the hydraulic equations and to calculate the tsunami propagation. Computed wave fronts radiate both toward the open sea, with rapid amplitude decay, and along the shore, in the form of edge waves that lose energy slowly. Comparison between model outputs and observations can be carried out only in a qualitative way owing to the absence of tide-gauge records, and results are satisfactory. Received: 14 September 1998 / Accepted: 18 December 1998     

Presence of native gold and tellurium in the active high-sulfidation hydrothermal system of the La Fossa volcano (Vulcano, Italy)

Grains of native gold and tellurium were found in siliceous hydrothermally altered rocks in the high-temperature (170–540°C) fumarolic field of the La Fossa volcano (Island of Vulcano). In addition to Au and Te, Pb–Bi sulfides (cannizzarite) and Tl-bromide chloride were found as sublimates in the hottest fumarolic vents of the crater rim. The chemical composition of altered rocks associated with sublimate deposition indicate the presence of a significant concentration of Te (up to 75 ppm), while gold concentrations are very low (<9 ppb). Pb, Bi and Tl are strongly enriched in the hottest and less oxidized fumarolic vents, reaching concentrations of 2186, 146 and 282 ppm, respectively. These elements are transported (generally as chloride complexes) to the surface by volcanic gases, and several of these (Bi, Te, Tl) are originated from magma degassing. The silicic alteration is produced by the flow of fluids with pH<2. High acidity results from introduction of magmatic gases such as SO₂, HCl and HF released by the shallow magmatic reservoir of La Fossa volcano. The silicic alteration found at Vulcano may represent an early stage of the `vuggy silica' facies which characterizes the high-sulfidation epithermal ore deposits, confirming the analogies existing between this type of ore deposit and magmatic-hydrothermal systems associated with island-arc volcanoes.     

Origin of the fumarolic fluids of Vulcano Island,Italy and implications for volcanic surveillance

Variations in D and ¹⁸O values with H₂O contents and outlet temperatures indicate that the fumaroles of La Fossa crater have discharged mixtures of magmatic water and marine hydrothermal water, since 1979. The contribution of meteoric water was low in the period 1979–1982 and very low afterwards. The ¹⁸O values of the marine-hydrothermal component of +5 to +7.2 are due to isotopic exchange with the ¹⁸O-rich silicates of the rocks under high-temperature and low-permeability conditions. The ¹⁸O value of the magmatic end-member is generally +3.5 to +4.3, although values as high as +5.5 to +6.5 were reached in the summer of 1988, when magma degassing appears to have extended into the core of the magma body. The D values of the end-member were close to -20, typical of andesitic waters. Both the isotopic values and chemical data strongly support a dry model, consisting of a central magmatic gas column and a surrounding hydrothermal envelope, in which marine hydrothermal brines move along limited fracture zones to undergo total evaporation on approaching the conduits of magmatic fluids. The vents at the eastern and western boundaries of the fumarolic field are fed by fluids whose pressure is governed by the coexistence of vapor, liquid and halite, giving rise to a high risk of phreato magmatic explosions, should magma penetrate into these wet environments. Most La Fossa eruptions were triggered by an initial hydrothermal blast and continued with a series of phreatomagmatic explosions. The fluids discharged by the Forgia Vecchia fumaroles are mixed with meteoric water, which is largely evaporated, although subordinate loss of condensed steam may be responsible for scrubbing most of the acidic gas species. The temperatures and pressures, and the risk of a sudden pressure increase, are low. A boiling hydrothermal aquifer at 230° C is present underneath the Baia di Levante beach. This area has a minor risk of hydrothermal explosions.     

Lead isotope composition of the sublimates from the fumaroles of Vulcano (Aeolian Islands,Italy): inferences on the deep fluid circulation

The fumarolic fluids of Vulcano (Aeolian Islands, Italy) consist of a mixture of both deep and shallow components. The final products, the fumarolic gases and the sublimates associated with them, provide information on the complex interactions that occur at depth. As radiogenic isotopes do not undergo fractionation after they are incorporated in a fumarolic gas, they can be used directly to characterize the components that mixed. Lead isotopes are particularly suitable, because seawater, which plays an important part in the formation of the fumarolic fluids of Vulcano, contains only negligible amounts of it (10^-12 g/g). Therefore, the lead present in the fumarolic gases (and sublimates) is derived from the magmatic component and a water-rock interaction process. The lead isotope compositions of the lead sulfosalt sublimates collected from the Fossa Crater of Vulcano in 1924, and between 1989 and 1993, are given. The lead isotope ratios of most of the samples are the same within the range of analytical error, regardless of their collection date. The only samples that display slight variations are those collected in 1993. On the whole, the compositional trend of the lead isotopes of the sublimates coincides with that of the latitic-rhyolitic activity of Fossa and differs substantially from that of the pre-Fossa trachy-basaltic activity. The lead composition of the sublimates is very different from that of the Calabrian basement rocks. The data presented here show that the magma presently degassing at Vulcano has the same lead isotopic composition as the products of the recent activity of Fossa, whereas the fumarolic fluid circulation of Vulcano has not involved basement rocks similar to the Calabrian metasediments.     

Assessment of a shallow magmatic system: the 1888–90 eruption,Vulcano Island,Italy

The magmatic system feeding the last eruption of the volcano La Fossa, Vulcano Island, Italy was studied. The petrogenetic mechanisms controlling the differentiation of erupted rocks were investigated through petrography, mineral chemistry, major, trace and rare earth element and Sr, Nd and Pb isotopic geochemistry. In addition, melt inclusion and fluid inclusion data were collected on both juvenile material and xenolithic partially melted metamorphic clasts to quantify the P-T conditions of the magma chamber feeding the eruption. A regular and continuous chemical zoning has been highlighted: rhyolites are the first erupted products, followed by trachytes and latites, whereas rhyolitic compositions were also found in the upper part of the sequence. The chemical and isotopic composition of the rhyolites indicates that they originated by fractional crystallization from latitic magmas plus the assimilation of crustal material; the trachytes represent hybrid magmas resulting from the mixing of latites and rhyolites, contaminated in the shallow magmatic system. The erupted products, primarily compositionally zoned from latites to rhyolites, are heterogeneous due to syn-eruptive mingling. The occurrence of magmacrust interaction processes, evidenced by isotopic variations (⁸⁷Sr/⁸⁶Sr=0.70474±3 to 0.70511±3; ¹⁴³Nd/¹⁴⁴Nd=0.512550±6 to 0.512614±8; ²⁰⁶Pb/²⁰⁴Pb=19.318–19.489; ²⁰⁷Pb/²⁰⁴Pb=15.642–15.782; ²⁰⁸Pb/²⁰⁴Pb=39.175–39.613), is confirmed by the presence of partially melted metamorphic xenoliths, with ⁸⁷Sr/⁸⁶Sr=0.71633±6 to 0.72505±2 and ¹⁴³Nd/¹⁴⁴Nd=0.51229±7, in rhyolites and trachytes. AFC calculations indicate a few percentage contribution of crustal material to the differentiating magmas. Thermometric measurements on melt inclusions indicate that the crystallization temperatures of the latites and trachytes were in the range of 1050–1100° C, whereas the temperature of the rhyolites appears to have been around 1000°C at the time of the eruption. Compositional data on melt inclusions reveal that the magmas involved in the eruption contained about 1–1.5 wt.% dissolved H₂O in pre-eruptive conditions. Secondary fluid inclusions found in metamorphic xenoliths give low equilibration pressure data (30–60 MPa), giving the location of the higher portions of the chamber at around 1500–2000 m of depth.     

Fluids in early stage hydrothermal alteration of high-sulfidation epithermal systems: A view from the Vulcano active hydrothermal system (Aeolian Island,Italy)

High-sulfidation (HS) epithermal systems have elements in common with passively degassing volcanoes associated with high T, acid fumarole fields or acid crater lakes. They are considered to form in two stages, the first of which involves advanced argillic alteration resulting from intense, strongly acidic fluid–rock interaction. The La Fossa hydrothermal system (Vulcano Island) represents a classic example of such an active HS system and can be considered as a modern analogue of this early stage of alteration, resulting in a core of intense silicic (90–95% pure SiO₂) alteration surrounded by alunitic alteration zones.     

Imaging and modelling the subsurface structure of volcanic calderas with high-resolution aeromagnetic data at Vulcano (Aeolian Islands,Italy)

In this paper, we present a magnetic model of the subsurface structure of Vulcano island based on high-resolution aeromagnetic data. Three profiles across the most intense magnetic anomalies over the Piano and Fossa calderas were selected for the magnetic modelling, which was constrained by structural and volcanological data, previous geophysical models, paleomagnetic data, and borehole stratigraphy obtained from two deep wells. The interpretation of the magnetic sources represents a significant contribution to the understanding of the Piano and Fossa calderas’ underlying structure, providing us with evidence of the lateral discontinuity between them at depth. We propose that the positive magnetic anomalies in the Piano caldera area are caused by: (a) the remnants of an early submarine volcano; (b) an outcropping dyke swarm related to the feeding system of the Primordial Vulcano phase (beneath Mt. Saraceno); and (c) the presence of a non-outcropping dyke system intruded along a NE–SW-oriented intra-caldera fault (beneath the eastern part of the Piano caldera). Offshore, to the west, the magnetic anomaly map suggests the presence of a submarine volcanic structure, not revealed by bathymetric data, which could represent the eruptive centre, the presence of which has been indirectly deduced from the outcrop of eastern-dipping lavas on the western seashore. Magnetic modelling of the Fossa caldera points to the presence of a highly magnetized cone-like body inside the Fossa cone, centred beneath the oldest crater rims. We interpret this body as a pile of tephritic lavas emplaced in an early phase of activity of the Fossa cone, suggesting that the volume of mafic lavas that erupted at the beginning of the construction of the Fossa edifice was more significant than has previously been deduced. Furthermore, the presence of a magnetized body inside the Fossa cone implies that high temperatures are contained in very limited spaces, do not affect its bulk inner structure, and are restricted to fumarolic conduits and vents. In addition, structures beneath the western and northern part of the Fossa caldera are revealed to have null or low magnetization, which can be ascribed to the presence of pyroclasts and hyaloclastites in this area as well as to a large volume of hydrothermally altered materials. This suggests that the hydrothermal system, with a very limited extension at present, affected a larger area in the past, especially beneath the western part of the caldera.     

A study of melt inclusions at Vulcano (Aeolian Islands, Italy): insights on the primitive magmas and on the volcanic feeding system

 This work presents the results of a microthermometric and EPMA-SIMS study of melt inclusions in phenocrysts of rocks of the shoshonitic eruptive complex of Vulcano (Aeolian Islands, Italy). Different primitive magmas related to two different evolutionary series, an older one (50–25 ka) and a younger one (15 ka to 1890 A.D.), were identified as melt inclusions in olivine Fo_88–91 crystals. Both are characterized by high Ca/Al ratio and present very similar Rb/Sr, B/Be and patterns of trace elements, with Nb and Ti anomalies typical of a subduction zone. The two basalts present the same temperature of crystallization (1180±20  °C) and similar volatile abundances. The H₂O, S and Cl contents are relatively high, whereas magmatic CO₂ concentrations are very low, probably due to CO₂ loss before low-pressure crystallization and entrapment of melt inclusions. The mineral chemistry of the basaltic assemblages and the high Ca/Al ratio of melt inclusions indicate an origin from a depleted, metasomatized clinopyroxene-rich peridotitic mantle. The younger primitive melt is characterized with respect to the older one by higher K₂O and incompatible element abundances, by lower Zr/Nb and La/Nb, and by higher Ba/Rb and LREE enrichment. A different degree of partial melting of the same source can explain the chemical differences between the two magmas. However, some anomalies in Sr, Rb and K contents suggest either a slightly different source for the two magmas or differing extents of crustal contamination. Low-pressure degassing and cooling of the basaltic magmas produce shoshonitic liquids. The melt inclusions indicate evolutionary paths via fractional crystallization, leading to trachytic compositions during the older activity and to rhyolitic compositions during the recent one. The bulk-rock compositions record a more complex history than do the melt inclusions, due to the syneruptive mixing processes commonly affecting the magmas erupted at Vulcano. The composition and temperature data on melt inclusions suggest that in the older period of activity several shallow magmatic reservoirs existed; in the younger one a relatively homogeneous feeding system is active. The shallow magmatic reservoir feeding the recent eruptive activity probably has a vertical configuration, with basaltic magma in the deeper zones and differentiated magmas in shallower, low-volume, dike-like reservoirs. Received: 11 March 1998 / Accepted: 14 July 1998     

Geochemistry of water and gas discharges from the Mt. Amiata silicic complex and surrounding areas (central Italy)

The Mt. Amiata volcano in central Italy is intimately related to the post-orogenic magmatic activity which started in Pliocene times. Major, trace elements, and isotopic composition of thermal and cold spring waters and gas manifestations indicate the occurrence of three main reservoir of the thermal and cold waters in the Mt. Amiata region. The deepest one is located in an extensive carbonate reservoir buried by thick sequences of low-permeability allochthonous and neo-autochthonous formations. Thermal spring waters discharging from this aquifer have a neutral Ca-SO₄ composition due to the presence of anhydrite layers at the base of the carbonate series and, possibly, to absorption of deep-derived H₂S with subsequent oxidation to SO₄²⁻ in a system where pH is buffered by the calcite–anhydrite pair (Marini and Chiodini, 1994). Isotopic signature of these springs and N₂-rich composition of associated gas phases suggest a clear local meteoric origin of the feeding waters, and atmospheric O₂ may be responsible for the oxidation of H₂S. The two shallower aquifers have different chemical features. One is Ca-HCO₃ in composition and located in several sedimentary formations above the Mesozoic carbonates. The other one has a Na-Cl composition and is hosted in marine sediments filling many post-orogenic NW–SE-trending basins. Strontium, Ba, F, and Br contents have been used to group waters associated with each aquifer. Although circulating to some extent in the same carbonate reservoir, the deep geothermal fluids at Latera and Mt. Amiata and thermal springs discharging from their outcropping areas have different composition: Na-Cl and Ca-SO₄ type, respectively. Considering the high permeability of the reservoir rock, the meteoric origin of thermal springs and the two different composition of the thermal waters, self-sealed barriers must be present at the boundaries of the geothermal systems. The complex hydrology of the reservoir rocks greatly affects the reliability of geothermometers in liquid phase, which understimate the real temperatures of the discovered geothermal fields. More reliable temperatures are envisaged by using gas composition-based geothermometers. Bulk composition of the 67 gas samples studied seems to be the result of a continuous mixing between a N₂-rich component of meteoric origin related to the Ca-SO₄ aquifer and a deep CO₂-rich component rising largely along the boundaries of the geothermal systems. Nitrogen-rich gas samples have nearly atmospheric N₂/Ar (=83) and

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(δ=0‰) ratios whereas CO₂-rich samples show anomalously high

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values (up to +6.13 ‰), likely related to N₂ from metamorphic schists lying below the carbonate formations. On the basis of average

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isotopic ratio (

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around 0‰), CO₂ seems to originate mainly from thermometamorphic reactions in the carbonate reservoir and/or in carbonate layers embedded in the underlying metamorphic basement. Distribution of

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isotopic ratios indicates a radiogenic origin of helium in a tectonic environment that, in spite of the presence of many post-orogenic basins and mantle-derived magmatics, can presently be considered in a compressive phase.     

Interaction of waves,currents and tides,and wave-energy impact on the beach area of Sylt Island

Erosion due to waves is an important and actual problem for most coastal areas of the North Sea. The objective of this study was to estimate the impact of wave action on the coastline of Sylt Island. From a 2-year time series (November 1999 to October 2001) of hydrological and wave parameters generated with a coupled wave–current modelling system, a period comprising storm ‘Anatol’ (3–4 December 1999) is used to investigate the effects of waves on currents and water levels and the input of wave energy into the coastline. The wave-induced stress causes an increase of the current velocity of 1 m/s over sand and an additional drift along the coast of about 20 cm/s. This produces a water level increase of more than 20 cm in parts of the tidal basin. The model system also calculates the wave energy input into the coastline. Scenario runs for December 1999 with a water level increase of 50 cm and wind velocity increased by 10% show that the input of the wave energy into the west coast of Sylt Island increases by 30% compared to present conditions. With regard to the forecasted near-future (Woth et al., Ocean Dyn 56:3–15, 2006) increase of strong storm surges, the scenario results indicate an increased risk of coastal erosion in the surf zone of Sylt Island.     

The magmatic- and hydrothermal-dominated fumarolic system at the Active Crater of Lascar volcano,northern Chile

Low-to-high temperature fumaroles discharging from the Active Crater of Lascar volcano (northern Chile) have been collected in November 2002, May 2005 and October 2006 for chemical and isotopic analysis to provide the first geochemical survey on the magmatic-hydrothermal system of this active volcano. Chemical and isotopic gas composition shows direct addition of high-temperature fluids from magmatic degassing, mainly testified by the very high contents of SO₂, HCl and HF (up to 87,800, 29,500 and 2,900 μmol/mol) and the high R/Ra values (up to 7.29). Contributions from a hydrothermal source, mainly in gas discharges of the Active Crater rim, has also been detected. Significant variations in fluid chemistry, mainly consisting of a general decrease of magmatic-related compounds, i.e. SO₂, have affected the fumarolic system during the period of observation, indicating an increase of the influence of the hydrothermal system surrounding the ascending deep fluids. The chemical composition of Active Crater fumaroles has been used to build up a geochemical model describing the main processes that regulate the fluid circulation system of Lascar volcano to be utilized in volcanic surveillance.     

Chemical composition of fumarolic gases and spring discharges from El Chichòn volcano, Mexico: causes and implications of the changes detected over the period 1998–2000

Since the March–April 1982 eruption of El Chichòn volcano, intense hydrothermal activity has characterised the 1-km-wide summit crater. This mainly consists of mud and boiling pools, fumaroles, which are mainly located in the northwestern bank of the crater lake. During the period 1998–2000, hot springs and fumaroles discharging inside the crater and from the southeastern outer flank (Agua Caliente) were collected for chemical analyses. The observed chemical fluctuations suggest that the physico-chemical boundary conditions regulating the thermodynamic equilibria of the deep rock/fluid interactions have changed with time. The chemical composition of the lake water, characterised in the period 1983–1997 by high Na⁺, Cl⁻, Ca²⁺ and SO₄²⁻ contents, experienced a dramatic change in 1998–1999, turning from a Na⁺–Cl⁻- to a Ca²⁺–SO₄²⁻-rich composition. In June 2000, a relatively sharp increase in Na⁺ and Cl⁻ contents was observed. At the same time, SO₂/H₂S ratios and H₂ and CO contents in most gas discharges increased with respect to the previous two years of observations, suggesting either a new input of deep-seated fluids or local variations of the more surficial hydrothermal system. Migration of gas manifestations, enhanced number of emission spots and variations in both gas discharge flux and outlet temperatures of the main fluid manifestations were also recorded. The magmatic-hydrothermal system of El Chichòn is probably related to interaction processes between a deep magmatic source and a surficial cold aquifer; an important role may also be played by the interaction of the deep fluids with the volcanic rocks and the sedimentary (limestone and evaporites) basement. The chemical and physical changes recorded in 1998–2000 were possibly due to variations in the permeability of the conduit system feeding the fluid discharges at surface, as testified by the migration of gas and water emanations. Two different scenarios can be put forward for the volcanic evolution of El Chichòn: (1) build-up of an infra-crater dome that may imply a future eruption in terms of tens to hundreds of years; (2) minor phreatic–phreatomagmatic events whose prediction and timing is more difficult to constrain. This suggests that, unlike the diminished volcanic activity at El Chichòn after the 1982 paroxistic event, the volcano-hydrothermal fluid discharges need to be more constantly monitored with regular and more frequent geochemical sampling and, at the same time, a permanent network of seismic stations should be installed.     

Eocene volcanism during the incipient stage of Izu–Ogasawara Arc: Geology and petrology of the Mukojima Island Group,the Ogasawara Islands

The Ogasawara Islands mainly comprise Eocene volcanic strata formed when the Izu–Ogasawara–Mariana Arc began. We present the first detailed volcanic geology, petrography and geochemistry of the Mukojima Island Group, northernmost of the Ogasawara Islands, and show that the volcanic stratigraphy consists of arc tholeiitic rocks, ultra‐depleted boninite‐series rocks, and less‐depleted boninitic andesites, which are correlatable to the Maruberiwan, Asahiyama and Mikazukiyama Formations on the Chichijima Island Group to the south. On Chichijima, a short hiatus is identified between the Maruberiwan (boninite, bronzite andesite, and dacite) and Asahiyama Formation (quartz dacite and rhyolite). In contrast, these lithologies are interbedded on Nakodojima of the Mukojima Island Group. The stratigraphically lower portion of Mukojima is mainly composed of pillow lava, which is overlain by reworked volcaniclastic rocks in the middle, whereas the upper portion is dominated by pyroclastic rocks. This suggests that volcanic activity now preserved in the Mukojima Island Group records growth of one or more volcanoes, beginning with quiet extrusion of lava under relatively deep water followed by volcaniclastic deposition. These then changed into moderately explosive eruptions that took place in shallow water or above sea level. This is consistent with the uplift of the entire Ogasawara Ridge during the Eocene. Boninites from the Mukojima Island Group are divided into three types on the basis of geochemistry. Type 1 boninites have high SiO₂ (>57.0 wt.%) and Zr/Ti (>0.022) and are the most abundant type in both Mukojima and Chichijima Island Groups. Type 2 boninites have low SiO₂ (<57.1 wt.%) and Zr/Ti (<0.014). Type 3 boninites have 57.6–60.7 wt.% SiO₂ and are characterized by high CaO/Al₂O₃ (0.9–1.1). Both type 2 and 3 boninites are common on Mukojima but are rare in the Chichijima Island Group.     

Gas geochemistry of the Valles caldera region, New Mexico and comparisons with gases at Yellowstone, Long Valley and other geothermal systems

Noncondensible gases from hot springs, fumaroles, and deep wells within the Valles caldera geothermal system (210–300°C) consist of roughly 98.5 mol% CO₂, 0.5 mol% H₂S, and 1 mol% other components. ³He/⁴He ratios indicate a deep magmatic source (R/R_a up to 6) whereas δ¹³C–CO₂ values (−3 to −5‰) do not discriminate between a mantle/magmatic source and a source from subjacent, hydrothermally altered Paleozoic carbonate rocks. Regional gases from sites within a 50-km radius beyond Valles caldera are relatively enriched in CO₂ and He, but depleted in H₂S compared to Valles gases. Regional gases have R/R_a values ≤1.2 due to more interaction with the crust and/or less contribution from the mantle. Carbon sources for regional CO₂ are varied. During 1982–1998, repeat analyses of gases from intracaldera sites at Sulphur Springs showed relatively constant CH₄, H₂, and H₂S contents. The only exception was gas from Footbath Spring (1987–1993), which experienced increases in these three components during drilling and testing of scientific wells VC-2a and VC-2b. Present-day Valles gases contain substantially less N₂ than fluid inclusion gases trapped in deep, early-stage, post-caldera vein minerals. This suggests that the long-lived Valles hydrothermal system (ca. 1 Myr) has depleted subsurface Paleozoic sedimentary rocks of nitrogen. When compared with gases from many other geothermal systems, Valles caldera gases are relatively enriched in He but depleted in CH₄, N₂ and Ar. In this respect, Valles gases resemble end-member hydrothermal and magmatic gases discharged at hot spots (Galapagos, Kilauea, and Yellowstone).