Search

Karst systems represent the main drinking water source for 20-25% of world’s population, although covering only 7-10% of the global land surface (Ford & Williams, 2007). Karst aquifers are highly vulnerable to external pollution, so their protection and management is of critical importance to sustain water resources. In Greece, starting from the 1970’s, water demands for agricultural, domestic and industrial use increased significantly, mainly in coastal areas (Daskalaki & Voudouris, 2008). The main Hellenic aquifers are hosted in alluvial deposits, in Neogene deposits and in carbonate rocks. The latter cover about 35% of the country and are located in Western, Central and Southern Greece (Daskalaki & Voudouris, 2008). Karst aquifers are developed in limestones and dolomites (Triassic – Cretaceous), and in marbles (Paleozoic – Mesozoic). Their hydrogeological behaviour is controlled by tectonic deformation. About 45% of them is located inland, while the rest is in coastal areas (Voudouris & Kazakis, 2018). During several field sampling campaigns from 2016 to 2020, 126 karst water samples were collected in Greece. Physicochemical parameters (temperature, pH, electric conductivity and redox potential) were measured in situ. Analyses of major ions and trace elements were performed at the laboratories of INGVPalermo. Results were compared with the limits set by the Directive 98/83/EC that fixes quality standards for drinking water. Temperatures of sampled waters ranged from 8.7 to 31 °C, pH from 6.5 to 8.4, whilst Total Dissolved Solids from 206 to 25,617 mg L-1. Most of the samples showed a typical alkaline-earth bicarbonate composition, whilst those sited along the coastline presented elevated concentrations of Na+ (up to 7,680 mg L-1), Cl- (up to 14,200 mg L-1) and SO4 2- (up to 1,940 mg L-1), sometimes exceeding the EC limits, suggesting a seawater contamination. Furthermore, karst springs contaminated by seawater, displayed high concentrations of B (up to 3,870 μg L-1) and Sr (up to 7,080 μg L-1). Nitrate concentrations were always below the EC limit (50 mg L-1), indicating a low contamination from fertilizers. Few low chloride waters showed a metal enrichment, such as Tempi springs (Thessaly) that presented enrichments in Sr (up to 242 μg L-1), Mo (up to 2.27 μg L-1), Cs (up to 1.57 μg L-1) and As (up to 17 μg L-1). Such enrichments could be attributed to the local petrological environment. Generally, karst water samples can be considered suitable for human consumption. Water quality degradation of Hellenic karst springs is mainly due to seawater intrusion or to local geogenic contamination.

Fluid anomalies were often considered as possible precursors before earthquakes. However, fluid properties at the surface can change for a variety of reasons, including environmental changes near the surface, the response of the superficial fluid system to loads associated with the mechanical nucleation of earthquake fractures, or as a result of transients in fluid flow from the depths. A key problem is to understand the origin of the anomaly and to distinguish between different causes. We present a new approach to monitor geochemical and geophysical fluid properties along a vertical profile in a set of drillings from a depth of a few hundred meters to the surface. This setup can provide hints on the origin of temporal variations, as the migration direction and speed of properties can be measured. In addition, potential admixtures of fluids from a deep crustal or mantle origin with meteoric fluids can be better quantified. A prototype of a multi-level gas monitoring system comprising flow and pressure probes, as well as monitoring of fluid-geochemical properties and stable isotopes is being implemented in a mofette field with massive CO2 (up to 97 tons per day) degassing. The mofette is believed a gas emission site where CO2 ascends through crustal-scale conduits from as deep as the upper mantle, and may therefore provide a natural window to ongoing magmatic processes at mantle depth. Fluids from three adjacent boreholes—30, 70, and 230 m deep—will be continuously monitored at high sampling rates.

Karst aquifers are considered to be one of the most important aquifer types, as they constitute the main drinking water resource for the majority of the global population (Ford et al., 2007). They are generated from the dissolution of carbonate rocks (e.g. limestone, dolomite, marble etc.), a phenomenon commonly known as “karstification”. This process is mainly caused by the acidity of water enriched in dissolved CO2, with the concentration of the latter being dependent on both the temperature and the CO2 partial pressure of the atmosphere in contact with the water (Bakalowicz, 2005). Carbonate rocks cover about 35% of the land surface of Greece and are mainly located in the western, central and southern parts of the country (Daskalaki et al., 2008). The Hellenic karst aquifer resources are more abundant in the western part of Greece, which receives the highest amount of precipitation (1800 mm/a) (Mimikou, 2005). The karst system constitutes a strategic resource of water in the region and preserving its quantity and quality is of the utmost importance for the sustainability of the area. Seventy samples of natural water were collected from karst springs in the northern (Macedonia-Thrace) and in the central parts of Greece, during 3 campaigns from 2016 to 2018. Sampling sites were selected on the basis of the springs flow rates (> 50 L/s). Water temperature, pH, Eh and electric conductivity were measured in situ with portable instruments; major ions were determined by Ionic Chromatography (IC) on filtered (anions) or filtered and acidified (cations) samples, whereas trace elements were determined by Inductively Coupled Plasma Mass Spectrometry (ICP-MS) on filtered and acidified samples. All analyses were performed at the laboratories of INGV of Palermo. Chemical compositions were compared with the limits fixed by the Directive 98/83/EC, which is the most recent EU legislation that sets quality standards for drinking water. Regulations concerning the quality of drinking water as established by the Directive allow Member States to adapt the monitoring of water quality to local conditions (Karavoltsos et al., 2008). Temperatures of the sampled waters ranged from 8 to 25 °C, pH from 6.5 to 8.4, whilst Total Dissolved Solids (TDS) from 206 to 15,418 mg/L. The highest concentrations of sodium, potassium, chloride and sulfate were found in the karst springs of Central Greece (26.6-5610 mg/L; 1.56-204 mg/L; 81.06-9467 mg/L; 15-2420 mg/L, respectively), where values had sometimes exceeded the limits set by the Directive 98/83/EC, indicating a contamination due to sea water intrusion. Based on the chloride concentrations, samples were subdivided into low (Cl- < 100 mg/L) and high (Cl- > 100 mg/L) chloride karst waters. All water samples were plotted in a Langelier Ludwig diagram (Fig. 1) with the low chloride waters presenting a typical alkaline-earth bicarbonate composition. Exception is the samples of Kaliakuda, Sidirokastro and Koromilia that display enrichment in alkalis possibly due to hydrothermal activity. On the other hand, the most chloride-rich waters plot close to the sea water composition point while two samples (Rema, Mylos Kokkosi) are aligned along the seawater-groundwater mixing line (Fig. 1). Concentration ranges of major and trace elements for all waters are presented in Fig. 2, with low and high chloride samples being plotted with different symbols. High chloride group displays much higher values for Mg, SO4, Cl, Na, K, Sr, B, Li, Rb and Cs with respect to low chloride, with differences in the median values between two and three orders of magnitude. Species deriving from carbonate dissolution (Ca and HCO3) show the lowest range of concentrations both for low and high chloride waters (Fig. 2). Low chloride waters show a wide range of concentrations (three to four orders of magnitude) for trace elements such as Li, Fe, Rb, As, Mn, Cu and Cs. Trace elements were above the legislation limits (Directive 98/83/EC) mostly in the case of high chloride karst springs, showing elevated concentrations of Boron (up to 1861 μg/L), Strontium (up to 5026 μg/L) and Arsenic (up to 12.1 μg/L). In terms of Boron and Strontium, the exceeding values seem to be generally related to the intrusion of sea water. On the other hand, Arsenic, whose maximum admissible level is 10 μg/L, was above limit also in the low chloride water (17 μg/L) of Tempi, Thessalia. Few low chloride waters show a metal enrichment, such as Tempi (Sr = 242 μg/L, Mo = 2.27 μg/L, and Cs = 1.57 μg/L) and Kaliakuda (V = 3.89 μg/L, Mn = 3.65 μg/L, Fe = 71.26 μg/L, Cu = 11.55 μg/L, Zn = 22.61 μg/L, Rb = 54.7 μg/L), whilst nitrate concentrations that could indicate contamination from fertilizers or from septic tanks, are always below the maximum admissible value (50 mg/L). Most of the analyzed waters can be considered suitable for human consumption. Water quality deterioration of Hellenic karst springs is mainly due to sea water intrusion, whilst only few low chloride waters show significant enrichments in trace metals that rarely exceeds the drinking water standards. These higher contents are probably of natural origin due to local geological setting.

Earthquakes and volcanic eruptions represent a hazard. However, the impact of gases released in geodynamically active areas should not be underestimated. It is commonly known that geogenic sources release great amounts of gases, which, apart from having an important influence on the global climate, can also have a strong impact on human health causing both acute and chronic effects. In particular, CO2 and sulphur gases (mainly H2S and SO2) are the main compounds responsible for acute mortality due to their asphyxiating and/or toxic properties. One of the most known and also worst episodes occurred, took place on the 21th of August 1986 at Lake Nyos, Cameroon, when about 1700 people were killed and 850 injured by a massive CO2 release (D’Alessandro, 2006). Like other geodynamically active areas, Greece is also affected by a large number of geogenic gas manifestations (Daskalopoulou et al., 2018a). These occur either in the form of point sources (fumaroles, mofettes, bubbling gases) or of diffuse soil gas emanations (Daskalopoulou et al., 2018b). D’Alessandro and Kyriakopoulos (2013) made a preliminary estimation of the risk related to geogenic gases in Greece for the time period of 1992-2011; the whole population of the country was considered. In that period, at least two fatal episodes with a total of three victims took place, likely caused to the exposure to geogenic gases (specifically CO2). This would give a risk of 1.310-8 fatality from geogenic gas manifestations per annum. This value, although probably underestimated, is much lower than many other natural or anthropogenic risks. Since deaths due to natural gases are often wrongly attributed, it cannot be excluded that some fatal episode has not been recognized and thus that the risk is somewhat higher than assessed. Although very low, this risk should not be neglected, not only because it is possibly underestimated, but also because simple countermeasures could be adopted for risk reduction. Dangerous areas could be easily identified and delimited by geochemical prospecting and their hazards properly highlighted. Apart from the sites where fatal episodes occurred, many other hazardous sites have been recognized in Greece. Here we present data collected at Loutra Ypatis (central Greece). Study area Sperchios Basin – Evoikos Gulf Graben is a 130 km long actively spreading graben in Central Greece (1 cm/a). The high geothermal gradient of the area is evident by the presence of many thermal springs with temperatures that vary from 24 to 82 °C. In the waters of these springs, discharging along the normal faults bordering the graben, an abundant gas phase is bubbling. Loutra Ypatis is one of the emerging springs and its waters (31 °C) are exploited by a spa. The water is currently drained by a gallery and therefore the water level is about 5 m below ground at the bottom of a funnel-like hole (Fig. 1 left). For safety reasons the hole was covered by a closed building (Fig. 1 left and center). The gas, which is vigorously bubbling in the spring, is mostly (> 96%) composed of CO2 (D’Alessandro et al., 2014). The walls of the hole are covered of sulfur that derives from the partial oxidation of the H2S (2500 ppm) contained in the released gas (D’Alessandro et al., 2014). Methods In October 2015 atmospheric concentrations of CO2 were measured with a Licor LI820 NDIR spectrometer (range 0 to 20,000 ppm, accuracy of 2%), whilst in April 2016, the atmospheric concentrations of CO2 and H2S were measured with a Multi-GAS analyser manufactured by INGV-Palermo equipped with Licor LI-840 NDIR spectrometer (CO2 0-20,000 ppm) and an EZ3H electrochemical sensor by City Technology Ltd. (H2S 0–100 ppm). Simultaneous CO2, CH4 (both 0- 100%), CO, H2S (both 0-500 ppm) and O2 (0 – 25%) concentrations within the building were measured with a portable gas analyser GA2000 (Geotechnical Instruments). Results and discussion Due to the fact that a building covers the thermal spring, the intense bubbling activity of its waters creates a strong gas accumulation inside. The main component of the released gases is CO2, which has a higher density with respect to atmospheric air, thus creating the conditions for gas accumulation. About 2 m above the water level, CO2 concentrations of >95% and non-detectable O2 concentrations were measured. At higher levels above the water, CO2 concentrations were decreased but never below 50%. Such concentrations within the building are lethal for both animals and human beings. Of course, access is forbidden, but as the building is not perfectly sealed, the gases permeate to the outside through fissures and cracks. Figure 2 shows the CO2 concentrations measured in the air on October 2015 at 1.5 m height while walking around the walls of the edifice at about 2 m distance. Leaking of CO2 from the edifice is made evident by concentrations reaching values of more than 6000 ppm. The highest values were measured close to the entrance of the edifice were fissures and cracks are concentrated. Due to the tendency of CO2 to accumulate at lower levels, in this place, close to the ground, CO2 levels lethal to small animal can be reached. This was made evident by a dead bird found in that occasion (Fig. 1). In April 2016, due to the much windier conditions, CO2 concentrations at the same places reached values never exceeding 1000 ppm while H2S was always below 1 ppm. These values sharply increased getting closer to the fissures around the main entrance of the building and reached saturation of the sensors (CO2 > 20,000 ppm and H2S > 100 ppm) at a distance of few centimeters. The intense CO2 degassing observed at Loutra Ypatis may be responsible for elevated levels that can have an impact on human beings. It is worth noting that values measured in the atmosphere close to the building exceed the Occupational Recommended Exposure Limit of 5000 ppm (NIOSH, 2005). In closed spaces lethal levels can be easily reached. An older inhabitant of the close by village told us that in his childhood a playmate died by going inside the gallery that drains the thermal water out of the spa due to the high CO2 levels. Such episode underscores the need not to disregard the gas hazard created by intense natural gas manifestations like the thermal spring of Loutra Ypatis.

Volatiles are transported from the deep crust or mantle to the surface in geodynamically active areas where seismic, volcanic and geothermal activity is present; the circulation of hydrothermal fluids in the crust is enhanced. In such areas, faults may act as preferential pathways for advective gas-carrying fluid transport. Towards the surface, pressure decrease allows the gases to escape from the fluids into soil gas and eventually into the atmosphere (King, 1986). The migration of carbon-bearing crustal and mantle fluids contributes to Earth’s carbon cycle (Berner & Kothavala 2001). However, till now, the mechanisms, magnitudes and time variations of carbon transfer from depth to the surface remain the least understood parts of the global carbon budget. Carbon dioxide and methane are the main contributors of the total amount of C-degassing from geological (volcanic and non-volcanic) sources. From the beginning of the last century, high attention has been paid to the reservoirs of CO2 and CH4 in the atmosphere because they represent the most dangerous species in terms of global warning. The increased amount of carbon dioxide and methane in the atmosphere has important implications for the energy balance and the chemical composition of the atmosphere. Mörner and Etiope (2002) calculated that 102-103 Mt of CO2 are presumably involved in the carbon cycle every year. This estimation though, is affected by high uncertainty as a number of sources and C-degassing environments that account for this high leakage were not taken into consideration. Greece belongs to the most geodynamically active regions of the world and as such, it has to be considered an area of intense geogenic degassing. Regarding carbon, the territory is characterized by the high hydrothermal and volcanic activity of the South Aegean Active Volcanic Arc (SAAVA), and by widespread geological seeps of buried carbon dioxide and methane. In the present work, we present more than 700 literature data of free gases spread along the whole Hellenic territory to get insight on geographic distribution and composition of the released fluids. Moreover, we review all the published studies on CO2 and/or CH4 output of high degassing areas of Greece that are mainly concentrated along the SAAVA in a first attempt to estimate the total geologic output of the nation. Helium isotope data propose that the highest mantle contribution (50 to 90%) is found along the SAAVA, whereas the lowest in continental Greece (0-20%), with the atmospheric contribution being mostly negligible. Based on the geographical distribution of the gases, it is evident that the R/RA ratios and CO2 concentrations increase in areas characterized by: i) thin crust; ii) elevated heat flow values; iii) recent (Pleistocene-Quaternary) volcanic activity; and iv) deep routed extensional or transtensional regional faults. The highest values are therefore found along the SAAVA and the lowest in the western part of Greece where CH4 emission is prevailing. Furthermore, it was noticed that the majority of the samples present a prevailing limestone C component, whilst only few samples have a prevailing mantle C component (Sano and Marty, 1995). It seems barely possible though to distinguish CO2 deriving from crustal and slabrelated limestones. Additionally, due to the complex geodynamic history, the mantle C isotope composition could be affected by subduction-related metasomatism and, similarly to the nearby Italian area (Martelli et al., 2008), the C isotope composition could be more positive. In this case, the mantle contribution is probably underestimated. In terms of geogenic carbon degassing, the best studied and most exhaling area is the SAAVA, which releases 104,090 t/a of CO2 and 20.26 t/a of CH4. Continental Greece on the contrary, is much less studied but may release CO2 in the same order of magnitude in its eastern-central and northern part. The western and south-western parts of Greece are conversely the main area of methane and higher hydrocarbon degassing. Methane output of Greece is much less constrained but the presence on its territory of one of the biggest thermogenic gas seepages of Europe releasing about 200 t/a of CH4 to the atmosphere underscores its potentially high contribution. Approximately 114,310 t/a of CO2 and 221 t/a of CH4 are released from the whole Hellenic territory (Daskalopoulou et al., submitted). This estimation though, should be considered minimum as there are processes and sources that have not been taken into consideration yet. More specifically, in the submarine manifestations found at greater depths, gases cannot reach the sea surface due to the dissolution process that takes place along the water column; this is especially true for CO2 that is more soluble in water respect to other gases (eg. Milos - Dando et al., 1995; Kolumbo - Rizzo et al., 2016 etc). Moreover, the geological and geodynamic regime can contribute in the formation of CO2 reservoirs. This is the case of Florina Basin (Pearce et al., 2004) where more than one CO2 reservoirs were created, with one of them being exploited by the company Air Liquide Greece. It is worth noting that this reservoir, found at a depth of approximately 300 m, produces 30,000 t/a of CO2 (Pearce et al., 2004). Moreover, in the same area, water is also used for water supply and irrigation purposes. This water though contains a great amount of dissolved CO2 great part of which is released to the atmosphere when the water is pumped to the surface. Another source that should be underscored is the quantification of geogenic CO2 dissolved in big karstic aquifers. Chiodini et al. (1999, 2000) demonstrated that the relatively high solubility of CO2 in water plays an important role in the quantification of carbon. This approach was proved for central Italy and it might be the case for continental Greece due to the similar geodynamic history. Finally, in ophiolitic sequences where serpentinization takes place, if and when the conditions are adequate (i.e. presence of effective catalysts – Etiope and Ionescu, 2015) an abiogenic origin for CH4 seems to be favored even at low temperatures. Ophiolitic sequences crop out widely in Greece along two N-S trending belts, whilst more hyperalkaline springs or dry seeps may be present. However, their flux in generally is very low and therefore their contribution to the total natural CH4 output has probably to be considered negligible.

Greece belongs to the most geodynamically active regions of the world and as such, it has to be considered an area of intense geogenic degassing. In terms of carbon, the territory is characterized by the high hydrothermal and volcanic activity of the South Aegean Active Volcanic Arc (SAAVA), and by widespread geological seeps of buried carbon dioxide and methane. In the present work, we investigate the island of Gyali located in the volcanic system Kos-Gyali-Nisyros. Nine gas samples have been collected on the island of Gyali in areas found both on land, in a small lake (∼2000 m2) along its beach, and in the sea close to the shore at shallow depths (

A multidisciplinary field campaign was carried out at Nisyros Island (Greece). Hydrothermal gases were sampled and analysed, and CH4 and CO2 fluxes from the soils were measured with the accumulation chamber method. The sampling area (Lakki plain) covers an area of about 0.08 km2, and includes the main fumarolic areas of Kaminakia, Stefanos, Ramos, Lofos and Phlegeton. Flux values measured at 130 sites range from −3.4 to 1420 mg m−2 d−1 for CH4 and from 0.1 to 383 g m−2 d−1 for CO2. The fumarolic areas show very different CH4 degassing patterns, Kaminakia showing the highest CH4 output values (about 0.8 t a−1 from an area of about 30,000 m2) and Phlegeton the lowest (about 0.01 t a−1 from an area of about 2500 m2). The total output from the entire geothermal system of Nisyros should not exceed 2 t a−1. Previous indirect estimates of the CH4 output at Nisyros, based on soil CO2 output and CH4/CO2 ratios in fumarolic gases, were more than one order of magnitude higher. The present work further underscores the utmost importance of direct CH4 flux data because indirect methods totally disregard methanotrophic activity within the soil. Ten soil samples were collected for CH4 consumption experiments and for metagenomic analysis. Seven of the soil samples showed small but significant CH4 consumption (up to 39.7 ng g−1 h−1) and were positive for the methanotrophs-specific gene (pmoA) confirming microbial CH4 oxidation in the soil, notwithstanding the harsh environmental conditions (high temperature and H2S concentrations and low pH). © 2020 Elsevier B.V.

Samples of efflorescences and encrustations of hydrothermal origin have been collected at three fumarolic areas in Greece. The three sites are Sousaki, Thiafi (Methana) and Kokkino Nero (Kos) and all belong to the South Aegean Active Volcanic Arc. Samples were analysed for their mineralogical (XRD and SEM-EDS) and chemical composition. Solutions obtained from both mineralization with HNO3 and leaching with distilled water, were analysed for major (ICP-OES), minor and trace metals (ICP-MS) and for sulfate contents (IC). Results show that their composition is mainly controlled by the petrological composition of the substrate (ultramafic rocks at Sousaki, felsic volcanic rocks at Methana and low-grade metamorphic rocks at Kos). The microenvironmental conditions (humidity, oxidizing or anoxic, exposed or sheltered from meteoric agents) as well as the rainfall regime of the area play also an important role. The presence of highly soluble sulfate minerals with elevated contents of many metals further underscores the significant influence of hydrothermal activity on elements’ mobility. The sometimes very high concentrations in toxic elements like Al, As, Co, Cr, Ni evidence also a potential environmental impact.

In the period from 2004 to 2017, more than 350 samples of free and dissolved gases were collected along the whole Hellenic area. Some literature data have also been taken into consideration (Rizzo et al., 2016). Samples have been analysed for their chemical and isotope composition. The concentrations range from 0.10 to 3370 μmol/mol for He, 600 to 995,000 μmol/mol for N2, 0.60 to 915,000 μmol/mol for CH4 and 17 to 1,002,000 μmol/mol for CO2, whereas the isotope values range from 0.01 to 7.10 for R/RA and -29.91 to +6.00 for δ13C-CO2. Considering the R/RA and 4He/20Ne ratios the atmospheric, mantle and crustal contributions for He have been calculated (Sano and Wakita, 1985). The highest mantle contribution (50 to 90%) is found in the South Aegean Active Volcanic Arc (SAAVA), whereas the lowest in continental Greece (0-20%). Atmospheric contribution is mostly negligible. Taking into consideration the geographical distribution of the gases, it is evident that the R/RA increases in areas characterized by: i) thin crust; ii) elevated heat flow values; iii) recent (Pleistocene-Quaternary) volcanic activity; and iv) deep routed extensional or transtensional regional faults. The highest values are therefore found along the SAAVA and the lowest in the western part of Greece. Furthermore, based on the CO2/3He and δ13C-CO2 values (Sano and Marty, 1995), the contribution of Sediment, Mantle and Limestone end-members for CO2 was determined. The majority of the collected samples present a prevailing limestone C component and only few samples have a prevailing mantle C component. However, with the present data, it is not possible to distinguish CO2 deriving from crustal and slab-related limestones. Additionally, due to the complex geodynamic history, the mantle C isotopic composition could be affected by subduction-related metasomatism and, similarly to the nearby Italian area (Martelli et al., 2008), the C isotope composition could be more positive. In this case, the mantle contribution is probably underestimated.

Mount Etna, located in eastern Sicily, is the largest stratovolcano in Europe and one of the most intensely degassing volcanoes of the world (Allard et al., 1991; Gerlach, 1991). In particular, previous estimates highlighted that Mt Etna emits about 1.6 % of global H2O fluxes from arc volcanism (Aiuppa et al., 2008) and 10 % of global average volcanic emission of CO2 and SO2 (D’Alessandro et al., 1997; Caltabiano et al., 2004). Furthermore, Gauthier and Le Cloarec (1998) underscored that Mt. Etna is an important source of volcanic particles, having a mass flux of particle passively released from the volcano during non-eruptive period estimated between 7 to 23 tons/day (Martin et al., 2008; Calabrese et al., 2011). In general, Etna is considered to be still under evolution and rather ‘friendly’, which, along with the above, makes it a favorable natural laboratory to study volcanic geochemistry. During the previous years, 6 field campaigns and the first 2 editions of the “Etna International Training School of Geochemistry. Science meets practice” were carried out at Mt. Etna and hosted in the Volcanological Observatory of Pizzi Deneri, a picturesque building located at the base of the N-E Crater at an altitude of 2850 m a.s.l, on the rim of the Ellittico caldera. The basic idea was to share scientific knowledge and experiences in a multidisciplinary community, using local resouces with a low-cost organisation. The “Etna International Training School of Geochemistry, 2018. Science meets practice” is addressed to senior graduate students, postdoctoral researchers, fellows, and newly appointed assistant professors, aiming to bring together the next generation of researchers active in studies concerning the geochemistry and the budget of volcanic gases. Direct sampling of high-to-low temperature fumaroles, plume measurement techniques (using CO2/SO2 sensors such as Multi-GAS instruments, MAX-DOAS instruments and UV SO2 cameras, alkaline traps and particle filters) and measurement of diffuse soil gas fluxes of endogenous gases (CO2, Hg0, CH4 and light hydrocarbons) are introduced during brief theoretical sessions before being directly applied in the field. An active participation of the students to the fieldwork is always requested. Hence, the teaching approach includes frontal lesson, practical demonstrations and field applications. “Etna International Training School of Geochemistry, 2017. Science meets practice” was partially funded by EGU. Highlights of the 2016 and 2017 summer school will be presented and a new summer school for 2018 is announced. . .

The Sperchios Basin is an actively spreading rift area with deeply rooted extensional faults and also a site of quaternary volcanic activity. Such geologic conditions favoured the formation of many hydrothermal systems, whose surface expressions are among the biggest thermal springs of the whole Greece. Degassing of deeply derived geogenic CO2 is highlighted by strong bubbling within the main pools of the springs. Flux measurements were made in the Thermopyles spring with the floating chamber method and results showed that bubbling gases in the spring release about 1 ton/day of CO2. The outgoing stream has a flow of more than 250 l/s of water rich in CO2 (about 16 mmol/l). Although no bubbling is visible along the stream, after 300 m, the CO2 content decreases to 2 mmol/l, indicating an intense CO2 degassing. This was quantified in more than 10 tons/day, suggesting that most of the degassing is not visible. Output estimations at the close by thermal springs of Psoroneria and Ypatis have not been made yet, but considering that the bubbling in their pools and the water outflow rates are similar, the CO2 emitted will be of the same order of magnitude. Further contributions from the Sperchios area may come from the Kamena Vourla springs and from diffuse soil degassing. To sum up, the best estimate of the total CO2 output of the studied area is in the order of many tens of tons/day. Such output is comparable to that of the single active volcanic systems along the South Aegean Volcanic Arc (Sousaki, Methana, Milos, Santorini, Kos and Nisyros) and it highlights the importance of hidden degassing along CO2-oversaturated streams.

Several gas samples have been collected from natural gas manifestations in the island of Milos. Most of them are located underwater along its coasts, whereas three anomalous degassing fumarolic areas (Kalamos, Paleochori and Adamas) were identified on land. Almost all the gases have CO2 as the prevailing gas species, with concentrations ranging from 88 to 99% for the samples taken underwater, while the on-land manifestations present a wider range (15-98%), being sometimes heavily contaminated by air. Methane reaches up to 1.0%, H2 up to 3.2% and H2S up to 3.5% indicating a hydrothermal origin of the gases. The isotope composition of He shows values ranging from 2.55 to 3.39 R/RA, highlighting a significant mantle contribution with the highest values measured at Adamas. C-isotope composition of CO2 is in the range from -1.9 to +1.3‰ vs. V-PDB, with most of the values found around -0.5‰ indicating a prevailing limestones origin. Isotope composition of CH4, ranging from -18.4 to-5.0‰ vs. V-PDB for C and from -295 to +7‰ vs. V-SMOW for H, points to a geothermal origin with sometimes evident secondary oxidation processes. CO2-flux measurements showed values up to 1100, 1500 and 8000 g/m2/day in the areas of Kalamos, Paleochori and Adamas respectively and up to about 23,000 g/m2/day in the marine area of Kanava. The south-western part of the island was covered with a lower density prospection, revealing only few anomalous CO2 flux values (up to 650 g/m2/day). Preliminary CO2 output estimations gave values of 1.1, 0.6 and 5.5 tons/day for the three fumarolic areas and of 1.1 tons/day for Kanava. The total output of the island (about 10 tons/day) is comparable to the other volcanic/geothermal systems of the south Aegean active volcanic arc (Nisyros, Kos, Nea Kameni, Methana and Sousaki).

Greece belongs to the most geodynamically active regions of the world and as such it has to be considered an area of intense geogenic degassing. Here we review all the papers already published in the scientific literature on both the geochemistry of gas manifestations and the CO2 and CH4 release, in an attempt to obtain the first nationwide inventory of the natural output of these carbon gases in Greece. The best studied and most exhaling area is the South Aegean Active Volcanic Arc (SAAVA), which releases more than 1.3 × 105 tons of CO2 per year. Continental Greece, on the contrary, is much less studied but may release CO2 in the same order of magnitude in its eastern-central and northern parts. The western and south-western parts of Greece are conversely the main areas in which methane and higher hydrocarbons degas. Methane output of Greece is much less constrained, but the presence of one of the biggest thermogenic gas seepages of Europe, which releases about 200 tons of CH4 per year to the atmosphere, underscores its potentially high contribution. © 2019 Elsevier Ltd

Nisyros Island (Greece) is an active volcano hosting a high-enthalpy geothermal system. During June 2013, an extensive survey on Hg concentrations in different matrices (fumarolic fluids, atmosphere, soils, and plants) was carried out at the Lakki Plain, an intracaldera area affected by widespread soil and fumarolic degassing. Concentrations of gaseous elemental mercury (GEM), together with H2S and CO2, were simultaneously measured in both the fumarolic emissions and the atmosphere around them. At the same time, 130 samples of top soils and 31 samples of plants (Cistus creticus and salvifolius and Erica arborea and manipuliflora) were collected for Hg analysis. Mercury concentrations in fumarolic gases ranged from 10,500 to 46,300 ng/m3, while Hg concentrations in the air ranged from high background values in the Lakki Plain caldera (10-36 ng/m3) up to 7100 ng/m3 in the fumarolic areas. Outside the caldera, the concentrations were relatively low (2-5 ng/m3). The positive correlation with both CO2 and H2S in air highlighted the importance of hydrothermal gases as carrier for GEM. On the other hand, soil Hg concentrations (0.023-13.7 μg/g) showed no significant correlations with CO2 and H2S in the soil gases, whereas it showed a positive correlation with total S content and an inverse one with the soil pH, evidencing the complexity of the processes involving Hg carried by hydrothermal gases while passing through the soil. Total Hg concentrations in plant leaves (0.010-0.112 μg/g) had no direct correlation with soil Hg, with Cistus leaves containing higher values of Hg with respect to Erica. Even though GEM concentrations in the air within the caldera are sometimes orders of magnitude above the global background, they should not be considered dangerous to human health. Values exceeding the WHO guideline value of 1000 ng/m3 are very rare (

Forty-five gas samples have been collected from natural gas manifestations at the island of Kos - the majority of which are found underwater along the southern coast of the island. On land, two anomalous degassing areas have been recognized. These areas are mainly characterized by the lack of vegetation and after long dry periods by the presence of sulfate salt efflorescence. Carbon dioxide is the prevailing gas species (ranging from 88 to 99%), while minor amounts of N2 (up to 7.5%) and CH4 (up to 2.1%) are also present. Significant contents of H2 (up to 0.2%) and H2S (up to 0.3%) are found in the on-land manifestations. Only one of the underwater manifestations is generally rich in N2 (up to 98.9%) with CH4 concentrations of up to 11.7% and occasionally extremely low CO2 amounts (down to 0.09%). Isotope composition of He ranges from 0.85 to 6.71 R/RA, indicating a sometimes-strong mantle contribution; the highest values measured are found in the two highly degassing areas of Paradise beach and Volcania. C-isotope composition of CO2 ranges from -20.1 to 0.64‰ vs. V-PDB, with the majority of the values being concentrated at around -1‰ and therefore proposing a mixed mantle - limestone origin. Isotope composition of CH4 ranges from -21.5 to +2.8‰ vs. V-PDB for C and from -143 to +36‰ vs. V-SMOW for H, pointing to a geothermal origin with sometimes-evident secondary oxidation processes. The dataset presented in this work consists of sites that were repeatedly sampled in the last few years, with some of which being also sampled just before and immediately after the magnitude 6.6 earthquake that occurred on the 20th of July 2017 about 15 km ENE of the island of Kos. Changes in the degassing areas along with significant variations in the geochemical parameters of the released gases were observed both before and after the seismic event; however, no coherent model explaining those changes was obtained. CO2 flux measurements showed values of up to about 104 g×m-2×d-1 in both the areas of Volcania and Kokkino Nero, 5×104 g×m-2×d-1 at Paradise beach, and 8×105 g×m-2×d-1 at Therma spring. CO2 output estimations gave values of 24.6, 16.8, 12.7, and 20.6 t×d-1, respectively, for the above four areas. The total output of the island is 74.7 t×d-1 and is comparable to those of the other active volcanic/geothermal systems of Greece (Nisyros, Nea Kameni, Milos, Methana, and Sousaki). © 2019 Kyriaki Daskalopoulou et al.

Nisyros is the easternmost island of the South Aegean Active Volcanic arc in Greece. It is an active stratovolcano known for its intense hydrothermal activity. In this study we present the results of the mineralogical analyses of 20 soil samples collected in the caldera area. Samples were analysed through X-ray diffraction and the results allow us to divide them in two groups: Lakki Plain and Stefanos Crater. In their majority the soils of Lakki Plain have a main mineralogical assemblage that consists of quartz, feldspar and gismondine (Ca2Al4Si4O16·9H2O). Gismondine as well as stellerite (CaAl2Si7O18·7H2O), which is appearing in some samples, derive from hydrothermal alteration, whilst wollastonite (CaSiO3) is also found as a product of thermally metamorphosed siliceous carbonates. In the Stefanos Crater soils, due to the acid environment and the relatively high temperatures of the fumaroles (about 100°C), the main assemblages mostly comprises hydrothermal alteration minerals like quartz, sulfur, wollastonite, gypsum and gismondine. The lower amount of feldspars with respect to the Lakki Plain soils can be justified by the high percentage of gismondine, their alteration products. Voltaite (K2Fe(II)5Fe(III)3Al(SO4)12·18H2O) was also found in some of the samples as a product of hydrothermal alteration of Si deposits. Close to the fumaroles, the occurrence of alunogen (Al2(SO4)3·17H2O), a sulphide alteration mineral found in fumarolic environments, is also noticeable.

The geologic emissions of greenhouse gases (CO2 and CH4) give an important natural contribution to the global carbon budget. However, the contribution of these emissions to the global carbon cycle and their possible role on the climate change remain still poorly quantified (Guliyev and Feizullayev, 1997; Milkov, 2000; Etiope et al., 2015 and references therein). Methane, the most abundant organic compound in Earth's atmosphere, may be created either from existing organic matter or synthesized from inorganic molecules. Accordingly, it can be differentiated in two main classes: a) biotic (either microbial or thermogenic) and b) abiotic. For this study, 115 gas samples of fumarolic, thermal and cold discharges from all over the Hellenic territory were collected and both chemical (CO2, H2S, CH4, N2, O2, Ar, H2 and light hydrocarbons) and isotopic (13C-CO2, 13C-CH4, D-CH4) analyses were performed, in order to investigate the genetic processes that produced CH4 in fluids related with the complex geodynamic setting of Greece. On the basis of the spatial distribution of the gas discharges and their type of emission, the whole dataset was subdivided into 3 main “domains”, as follows: 1) Volcanic Arc (VA) - 34 samples; 2) External Hellenides (EH) - 23 samples of cold emissions and of hyperalkaline aqueous solutions; 3) Internal Hellenides (IH) - 62 samples of cold and geothermal emissions. Almost each group is characterized, as long as subdivided in 3 groups based on the type of emission (on-land free or dissolved gases and subaqueous gases) and a 4th group includes literature data.

Several gas samples have been collected from natural gas manifestations at the island of Kos. Most of them are found underwater along the southern coast of the island. On land two anomalous degassing areas have been recognized. These are characterised by lack of vegetation and after long dry periods by the presence of sulfate salts efflorescences. Almost all the gases are CO2-dominated (CO2 ranging from 88 to 99%) with minor amounts of N2 (up to 7%) and CH4 (up to 2.6%). Only the on-land manifestations have also significant contents of H2 (up to 0.2%) and H2S (up to 0.3%). Only one underwater manifestation is N2-dominated (61-99%) with CH4 (0.6-11%) and low CO2 (0.1-26%). The isotopic composition of He shows values ranging from 0.84 to 6.72 R/RA indicating a sometimes strong mantle contribution with the highest values measured in two of the most strongly degassing areas (Paradise Beach and Volcania). C-isotopic composition of CO2 is in the range from -3.6 to 0.6 ‰ vs V.PDB with most of the values around -1‰ indicating a mixed mantle – limestones origin. Isotopic composition of CH4, ranging from -21.5 to 2.8‰ for C and from -143 to 36‰ for H, points to a geothermal origin with sometimes evident secondary oxidation processes. CO2-flux measurements showed values up to about 10,000 g/m2/day in the areas of Volcania and Kokkino Nero and up to about 50,000 g/m2/day at Paradise beach. Preliminary CO2 output estimations gave values of 8.8 and 4 tons/day for the first two areas and of 2.7 tons/day for the latter. The total output of the island (15.5 tons/day) should be considered a minimum estimation because of the incomplete coverage of the area and is comparable to the other active volcanic/geothermal systems of Greece (Nisyros, Nea Kameni and Methana).

The Greek territory belongs to the geodynamically active Alpine-Himalayan orogenic belt. As such, it shows intense seismic activity, active volcanic systems and areas of enhanced geothermal fluxes. One of these areas is the Sperchios basin and the northern part of Evia island in central Greece, which present widespread thermal manifestations (D’Alessandro et al., 2014). Five of them with temperatures from 33 to 80°C present bubbling gases whose dominating species are either CO2 or N2. All gases contain from 27 to 4000 ppm of CH4. The isotopic composition of CH4 in these gases covers a wide range with δ13C values ranging from -21.7 to +16.9 ‰ and δ2H values ranging from -124 to +301 ‰. The hottest manifestation displays the lowest isotopic values within the typical range of volcanic and geothermal systems. All the remaining samples fit a methane oxidation trend reaching very positive values. If we consider the lowest values as the deep hydrothermal marker the obtained ΔH/ΔC values range between 5 and 13 which are close to those typical of microbially driven oxidation (Kinnaman et al., 2007). Although the outlet temperature of the hottest manifestations is at the upper limit for methanotrophic microrganisms (Sharp et al., 2014), we can hypothesize that environmental conditions are not favorable for their survival at this site while they can thrive in the other, strongly consuming methane and producing very positive isotopic values. D’Alessandro, W., Brusca, L., Kyriakopoulos, K., Bellomo, S., Calabrese S. (2014): A geochemical traverse along the "Sperchios Basin-Evoikos Gulf" Graben (Central Greece): origin and evolution of the emitted fluids. Mar. Petrol. Geol., 55, 295-308. Kinnaman, F.S., Valentine, D.L., Tyler, P.A. (2007): Carbon and hydrogen isotope fractionation associated with the aerobic microbial oxidation of methane, ethane, propane and butane. Geochim. Cosmochim. Acta, 71, 271-283. Sharp, C.E., Smirnova, A.V., Graham, J.M., Stott, M.B., Khadka, R., Moore, T.R., Grasby, S.E., Strack, M., Dunfield, P.F. (2014): Distribution and diversity of Verrucomicrobia methanotrophs in geothermal and acidic environments. Environ. Microbiol., 16, 1867-1878.

The Greek territory belongs to the geodynamically active Alpine-Himalayan orogenic belt. As such, it shows intense seismic activity, active volcanic systems and areas of enhanced geothermal fluxes. One of these areas is the Sperchios basin and the northern part of Evia island in central Greece, which present widespread thermal manifestations [1]. Five of them with temperatures from 33 to 80°C present bubbling gases whose dominating species are either CO2 or N2. All gases contain from 27 to 4000 ppm of CH4. The isotopic composition of CH4 in these gases covers a wide range with δ13C values ranging from -21.7 to +16.9‰ and δ2H values ranging from -124 to +301‰. The hottest manifestation displays the lowest isotopic values within the typical range of volcanic and geothermal systems. All the remaining samples fit a methane oxidation trend reaching very positive values. If we consider the lowest values as the deep hydrothermal marker the obtained ΔH/ΔC values range between 5 and 13 which are close to those typical of microbially driven oxidation [2]. Although the outlet temperature of the hottest manifestations is at the upper limit for methanotrophic microrganisms [3], we can hypothesize that environmental conditions are not favorable for their survival at this site while they can thrive in the other strongly consuming methane and producing very positive isotopic values. [1] D’Alessandro et al. (2014), Mar. Petrol. Geol. 55, 295-308; [2] Kinnaman et al. (2007), Geochim. Cosmochim. Acta 71, 271-283; [3] Sharp et al. (2014), Environ. Microbiol. 16, 1867-1878

The geologic emissions of greenhouse gases (CO2 and CH4) have an important natural contribution in the global carbon budget. Tectonics, through faults in geothermal and oil producing areas, play a significant role in the release of C-gases in many non-volcanic regions of the Earth. Methane, the most abundant organic compound in Earth’s atmosphere, has a potential global warming that is 28 times higher than that of CO2 on a 100-year time horizon. In this study, δ13C-CH4, δ2H-CH4 and light hydrocarbon (alkane: CH4, C2H6, C3H8, C3H6, i-C4H10, n-C4H10; alkene C3H6, iC4H8; and aromatic C6H6) gas concentration data of 119 gas samples (103 unpublished data and 16 literature data) from volcanic-hydrothermal, geothermal and cold discharges are used to shed light on the genetic processes that have formed CH4 in the complex geodynamic setting of Greece. On the basis of the spatial distribution of the gas discharges and their type of emission, the whole dataset was subdivided into 4 main “domains”, as follows: 1) Volcanic Arc (VA); 2) External Hellenides (EH); 3) Internal Hellenides (IH); 4) Hellenic Hinterland (HH). Almost each group is characterized, as long as subdivided, in 3 groups based on the type of emission (on-land free or dissolved gases and submarine gases) and a 4th group includes literature data. Concentrations of CH4 range from < 2 to 925,200 µmol/mol and its isotopic ratios cover a wide range (δ13C from -79.8 ‰ to +45 ‰; δ2H from -311 ‰ to +301 ‰) indicating the different primary sources and the secondary post-genetic processes (oxidation) that can significantly affect the origin of this gas compound. Hydrocarbons in the CH4-dominated gases discharged from the EH are showing a clear biotic origin. In particular, those collected in the Gavrovo-Tripolis zone are showing a dominating biotic origin, whereas it is also noticeable that some gas samples of the Ionian zone are produced by both microbial activity and thermal maturation of sedimentary organic matter. The CO2-dominated gas discharges from the main geothermal systems of the IH and from the VA most likely predominantly contain abiogenic CH4 deriving from CO2 reduction. However, some of the gas discharges of the geothermal and volcanic-hydrothermal systems located in the neritic sedimentary Pelagonian, Gavrovo-Tripolis and Attico-cycladic zones (IH) and in Rhodope massif (HH), seem to exhibit significant contributions from thermogenic sources. The presence of abiotic methane was also recognized in the hyperalkaline aqueous solutions that are issuing from the ophiolites of Othrys and Argolida (Pindos zone (EH)). Most of the geothermal gases of Subpelagonian and Vardar/Axios zones (IH), the cold manifestations of the Rhodope massif (HH) and some of the volcanic-hydrothermal ones of the Attico-cycladic zone (VA) are presenting a microbial oxidation of CH4.

The Aegean area, which is geodynamically very active, is characterised by intense seismic activity, presence of active volcanic systems and anomalous geothermal gradients. Like other regions of intense geodynamic activity it is also characterized by extensive geogenic degassing. Gas manifestations are not only widespread on land but are also very frequent underwater. Many of these, as for example those of Milos and Santorini, are known since long time and have been previously studied although the targets were generally the hot waters or the sediments affected by the emissions (Smith and Cronan 1978, Dando et al. 1995, Price et al. 2013, Megalovassilis 2014).The present study aims at producing the first catalogue of the shallow submarine gas manifestations of the Aegean Sea andto characterizegeochemically the emitted gases.

Greece, a country characterised by intense seismic and volcanic activity, has a complex geodynamic and geological setting that favours the occurrence of many gas manifestations. In this study, we address the origin of CH4 and light hydrocarbons in cold and thermal emissions discharging along the Hellenic territory. Also, we investigate their possible relationship with the main geochemical composition of the gases and the different geological settings of the sampling sites. For this purpose we collected 101 new samples that were analysed for their chemical (O2, N2, CH4, CO2, He, Ne, Ar, H2, H2S and C2-C6 hydrocarbons) and isotopic (R/RA, δ13C-CO2, δ13C-CH4 and δ2H-CH4) composition. Results show that CH4 presents a wide range of concentrations (from

Hyperalkaline mineral springs related to active continental serpentinization are a theme of growing interest since they may contain significant amounts of abiotic gas and have important implications for energy resource exploration, subsurface microbiology and astrobiology. We report the discovery of a new hyperalkaline (pH∼12) spring issuing in the Agioi Anargyroi monastery at Ermioni (Greece), connected to serpentinization of peridotites of the Argolis ophiolite. Two water samples have been collected from separated springs and analysed for the chemical composition of major, minor and trace elements, and isotopic composition (2H and 18O) of water by IC, ICP-OES, ICP-MS and IRMS, and for the chemical (H2, O2, N2, CH4, CO2 and C2H6) and isotopic (He, δ2H-CH4 and δ13C-CH4) composition of dissolved gases. The Iliokastron Mélange Unit, comprising abundant serpentinized harzburgite, represent the aquifer feeding the hyperalkaline springs. The isotopic composition of water indicates a recent meteoric recharge probably through the close by and stratigraphically higher limestones of the Faniskos Unit. The Ca-OH water composition resulted to be similar to other hyperalkaline waters of Greece and worldwide. Although the concentrations of dissolved H2 are very low (tens of nmol/L) compared to other gases collected in similar manifestations, the concentrations of CH4 are considerable (38–314 μmol/L) and display isotopic compositions indicating a substantial if not exclusive abiogenic origin. Methane oxidation is also hypothesized in one of the two springs. © 2017 Elsevier Ltd

Twenty gas samples have been collected from the natural gas manifestations of Milos Island, the majority of which is found underwater along its coast. Furthermore, three anomalous degassing fumarolic areas (Kalamos, Paleochori and Adamas) have been recognized on-land. Almost all the gases are CO2-dominated with CO2 ranging from 88 to 99% vol for the samples taken underwater, while the on-land manifestations show a wider range (15–98%) due to air contamination. Methane reaches up to 1.0% vol, H2 up to 3.2% vol and H2S up to 3.5% vol indicating a hydrothermal origin of the gases. The isotope composition of He points out to mantle contributions up to 45%, while the C-isotope composition of CO2 (from −1.9 to +1.3‰ vs. V-PDB with most of the values around −0.5‰) suggests a prevailing limestone origin. Isotope composition of CH4, ranging from −18.4 to −5.0‰ vs. V-PDB for C and from −295 to +7‰ vs. V-SMOW for H, points to a geothermal origin with sometimes evident secondary oxidation processes. Additionally, CO2-flux measurements showed high values in the three fumarolic areas (up to 1100, 1500 and 8000 g/m2/d at Kalamos, Paleochori and Adamas respectively) with the highest CO2-flux values (up to about 23,000 g/m2/d) being measured in the sea at Kanavas with a floating chamber. The south-western part of the island was covered with a lower density prospection revealing only few anomalous CO2 flux values (up to 650 g/m2/d). The total output of the island (30.5 t/d) is typical of quiescent closed-conduit volcanoes and comparable to the other volcanic/geothermal systems of the south Aegean active volcanic arc (Nisyros, Kos, Nea Kameni, Methana and Sousaki). © 2018 Elsevier B.V.

A comprehensive hydrogeochemical study of the cold and thermal groundwaters of the presently quiescent volcanic system at Methana was undertaken that involved collecting 71 natural water samples. Methana is a peninsula in Peloponnesus, Greece whose arid climate and hydrological situation is similar to that of the nearby small islands of the Aegean Sea. Similarly, the chemical and isotopic compositions of its water are dominated by the mixing of seawater with meteoric water both through direct intrusion and meteoric recharge. However, the simple mixing trends at Methana are modified by water–rock interaction processes, enhanced by the dissolution of endogenous CO2, which lead to strong enrichments in alkalinity, Ca, Ba, Fe and Mn. The thermal waters show very high salinity that is sometimes close to that of seawater [total dissolved solids (TDS) = 8.5–40 g/l]. Although the cold groundwaters sometimes also show elevated TDS values (up to 6.3 g/l), their overall quality is acceptable due to the trace metal and nitrate contents mostly being below acceptable limits. While the saltiest groundwaters are not acceptable for human consumption, they are used for irrigation without exerting toxic effects on plants, which is probably due to the high permeability of the soils not supporting salt accumulation and salinity-resistant crops being cultivated. © 2017 Elsevier B.V.

Biomonitoring techniques have been widely used in environmental studies to monitor anthropogenic pollutant. Recently such techniques have been applied also to ascertain the impact of contaminants naturally released by volcanic activity. In the present study a biomonitoring surveys has been performed in many different active volcanic systems: Mt. Etna and Vulcano (Italy), Nisyros (Greece), Nyiragongo (DRC), Masaya (Nicaragua), Gorely (Kamchatka, Russia). We sampled leaves of different species Betulla aethnensis, Pinus nigra, Populus tremula, Senecio aethnensis and Rumex aethnensis on Etna, Cistus creticus and salvifolius on Vulcano and Nisyros, Senecio ssp. on Nyiragongo, a Fern on Masaya and Salix arctica at Gorely. All samples were analyzed by ICP-MS and ICP-OES for 49 elements after acid digestion with a microwave oven (HNO3 + H2O2). Major constituents in leaves are K, Ca, Mg, Na, Si, Al and Fe ranging from about 10 3 to 105 ppm. Manganesium, Sr, Rb, Ba, Zn, B, Cu show also relatively high concentrations (100-103 ppm) while the remaining elements (As, Bi, Cd, Ce, Co, Cr, Cs, Ga, Li, Mo, Ni, Pb, Sb, Sc, Se, Th, Tl, U, V, Y and lanthanide series) display much lower values (10-4-101 ppm). Nearly all investigated elements show their highest concentrations in the samples collected closest to the main degassing vents (open craters, fumarolic fields). Increased concentrations are also found in the samples collected in the downwind direction where volcanic emissions are prevailingly dispersed. Leaves collected along radial transects from the active vents, highlight that the levels of metals decrease from one to two orders of magnitude with increasing distance from the source. The decrease is stronger for volatile elements, which are highly enriched in volcanic emissions, (As, Bi, Cd, Cs, Pb, Sb, Tl) than for more refractory elements (Al, Ba, Sc, Si, Sr, Th, U). The different species of plants show significant differences in the bioaccumulation processes for most of the analyzed elements, in particular lanthanides, which are systematically enriched in Rumex leaves. Needles of pine (non-deciduous tree) represent a good tool for biomonitoring investigation because they are important tracers of accumulation with time. The high concentrations of many toxic elements in the leaves allow us to consider some of these plants as highly tolerant species to the volcanic emissions, and suitable for biomonitoring researches further confirming their strong potential in tracing the impact and geographic distribution of these natural contaminants.

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. © 2014, Editrice Compositori s.r.l., All rights reserved.