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  • 1
    Publication Date: 2021-02-23
    Description: We report on original geochemical data, which combine the rainfall trace metal contents from three different areas of Mt. Etna, variably fumigated by the volcanic plume, and those from soils, collected over the whole volcano. Trace element contents in rainfall appear mostly related to acidic ash leaching, while only for the most volatile elements (Cu, Zn, Cd, Pb, As, Sb, Tl, Se). We analyzed separately the labile fraction of soil samples, considered the fraction bioavailable to plants and soil organisms living in. The complexing medium used to extract the bioavailable fraction simulates the growth environment of plant roots.The contents of trace elements in the bioavailable fraction from soil samples showed peculiar patterns, apparently unrelated to the plume fumigation. The transition metal contents in the bioavailable fraction account for less than 15 % of the pseudo-total fraction and the highest contents were measured in the less acidic soil samples and farthest from the summit craters. In particular, high Fe, Mn, Co, Ni, Pb, Zn, Cd contents were paralleled by high soil organic carbon concentrations, which increased in the samples collected downwind the summit vents. Concerning immobile elements, their abundance in the bioavailable fraction was related to the degree of alteration of soils. Two elements, Se and Tl, were enriched in soil samples collected at closer distance from the summit vents. Their origin is probably related to the plume deposition.The study highlighted that the accessibility of plants to potentially harmful trace elements present in the soil is not simply related to the exposure to pollutants, but also to their fate in the pedogenetic environment.
    Description: Published
    Description: 57-78
    Description: 6A. Geochimica per l'ambiente e geologia medica
    Description: JCR Journal
    Keywords: trace elements ; Mt. Etna ; soil ; rainwater ; 03.04. Chemical and biological
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 2
    Publication Date: 2021-06-14
    Description: The eruption of Mt. Etna which occurred on December 24th 2018 was characterized by strombolian activity and fire fountains, emitted by the New South-East Crater and along a fissure that propagated towards the SE. The influence of volcanic emissions on atmospheric deposition was clearly detectable at several kilometres from the source. Wet and dry (bulk) deposition samples were collected each month, through a network of eleven collectors, in the areas of Milazzo, and Priolo between June 2018 and June 2019. They were analysed for major ions and trace elements concentrations. The pH values range from 3.9 to 8.3, while the EC values range from 7 to 396 μS cm-1. An extensive neutralization of the acidity has been recognised mainly due to the suspended alkaline dust particles, which have a buffering role in rainwater. A high load of Na+ and Cl- was observed at all sites, related to the closeness of the study areas to the coast, showing a high positive correlation (R2 = 0.989) along the line of Na+/Cl- ratio in seawater. During the eruption, the volcanic plume was carried by the winds for long distance (more than 300 km) affecting the area of Priolo but not that of Milazzo, which was upwind with respect to Mt. Etna. The impact of volcanic HF was clearly recognised in the samples collected after the eruption. Volcanic SO2 and HCl had a lower impact due to the overwhelming input of anthropogenic sulfate and marine chloride. On the contrary, the signature of the Mt. Etna eruption can be well recognised in the high concentrations of certain trace elements in the samples collected immediately after the eruption. The strongest contrast between affected and non-affected samples was recognised in Al, Cd, and especially in the volatile elements Tl and Te, which are typically enriched in volcanic emissions. The results showed that volcanic eruptions might have a relevant effect on the atmospheric chemistry and on the composition of rainwater up to distances of 80 km from the emission vents.
    Description: Published
    Description: 341-358
    Description: 6A. Geochimica per l'ambiente e geologia medica
    Description: JCR Journal
    Keywords: rainwater ; fluoride ; trace elements ; volcanic emissions ; 01. Atmosphere ; 03. Hydrosphere ; 04.08. Volcanology
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 3
    Publication Date: 2021-06-14
    Description: The complex geology of Greece includes two important parallel running ophiolitic belts. The Othrys Massif in central Greece belongs to the westernmost of them. In the current study, 33 water samples from cold hyperalkaline and hypothermal (T 〈 40°C) alkaline springs and 30 gas samples (either dissolved or free) were collected at 17 different sites in and around this wide ophiolite outcrop, aiming to determine the origin of fluids and evidence gas-water-rock interaction processes taking place in the area. Water samples were analysed for their chemical (major ions and trace elements) and isotope (δ18O-H2O, δ2H-H2O) composition. They can be subdivided into alkaline (pH 〈11) of both Mg-Ca-HCO3 and Na-HCO3 composition and hyperalkaline (pH 〉 11 and Ca-OH composition). Trace elements generally showed very low concentrations and mostly inversely correlated with pH. Gases were analysed for their chemical (He, Ne, Ar, H2, O2, N2, CH4, C2H6, CO2 and H2S) and isotope (δ13C-CH4, δ2H-CH4, δ13C-CO2) composition. Samples from alkaline waters were mainly dominated by CH4 (from 128,000 to 915,000 μmol/mol), while hyperalkaline waters showed a N2-rich composition (from 727,000 to 977,000 μmol/mol). Methane had a wide range of isotope compositions (δ13C-CH4 from -74.5 to -14.5 ‰ and δ2H-CH4 from -343 to -62 ‰). Alkaline waters present the most negative isotope values for CH4, evidencing a biogenic (both thermogenic and microbial) origin. Many of the hyperalkaline waters had CH4 isotope values compatible with an abiogenic origin through serpentinization processes but occasionaly very negative values were recorded, indicating sometimes a clear biogenic contribution. Finally, few samples both from alkaline and hyperalkaline waters showed some evidence of secondary oxidation processes.
    Description: Published
    Description: 42-56
    Description: 6A. Geochimica per l'ambiente e geologia medica
    Description: JCR Journal
    Keywords: hydrogeochemistry ; trace elements ; stable isotopes ; methane ; continental serpentinization ; 05.09. Miscellaneous
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 4
    Publication Date: 2020-05-26
    Description: 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.
    Description: Published
    Description: Athens, Greece
    Description: 6A. Geochimica per l'ambiente e geologia medica
    Keywords: groundwater quality ; Karst ; trace elements ; 03.04. Chemical and biological
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: Extended abstract
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  • 5
    Publication Date: 2023-08-29
    Description: Karst hydrosystems represent one of the largest global drinking water resources, but they are extremely vulnerable to pollution. Climate change, high population density, intensive industrial, and agricultural activities are the principal causes of deterioration, both in terms of quality and quantity, of these resources. Samples from 172 natural karst springs were collected in the whole territory of Greece. To identify any geogenic contamination and/or anthropogenic pollution, analyses of their chemical compositions, in terms of major ions and trace elements, were performed and compared to the EU limits for drinking water. Based on chloride content, the collected karst springs were divided into two groups: low-chloride (〈 100 mg L-1) and high-chloride content (〉 100 mg L-1). An additional group of springs with calcium-sulfate composition was recognised. Nitrate concentrations were always below the EU limit (50 mg L-1), although some springs presented elevated concentrations. High contents in terms of trace elements, such as B, Sr, As, and Pb, sometimes exceeding the limits, were rarely found. The Greek karst waters can still be considered a good quality resource both for human consumption and for agriculture. The main issues derive from seawater intrusion in the aquifers along the coasts. Moreover, the main anthropogenic pollutant is nitrate, found in higher concentrations mostly in the same coastal areas where human activities are concentrated. Finally, high levels of potentially harmful trace elements (e.g. As, Se) are very limited and of natural origin (geothermal activity, ore deposits, etc.).
    Description: Published
    Description: 11191
    Description: 6A. Geochimica per l'ambiente e geologia medica
    Description: JCR Journal
    Keywords: Greece ; Hydrogeochemistry ; trace elements ; water quality ; karst springs ; 03.04. Chemical and biological
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 6
    Publication Date: 2023-08-29
    Description: The concentrations of trace elements in atmospheric bulk depositions (wet plus dry) were investigated from two highly industrialised areas of Sicily (southern Italy) from June 2018 to July 2019, in order to recognise the main natural and anthropogenic sources. A side objective of this study was to improve the common sampling procedures and analytical methods used for monitoring trace elements in atmospheric deposition. The trace element VWM (Volume-Weighted Mean) concentrations ranged from less than 0.01 µg L-1 for trace elements such as Cs, Tl, and U, up to 24 µg L-1 for minor elements (Al, Zn, Sr), in the filtered aliquot, while they reached concentrations up to 144 µg L-1 for the same elements, in the unfiltered aliquot. Therefore, significant differences in concentrations between these two aliquots were found, particularly for Al, Fe, Ti, Zn, Cr, Pb, Se, Cs, and U. This implies that filtering operations may produce a consistent underestimation of concentrations of certain ‘constituents’ of the atmospheric deposition. Natural (marine spray, local and regional geogenic input, volcanic emanations) and anthropogenic sources (industrial emissions, auto vehicular traffic, and diffuse background pollution) which influence rainwater chemistry were identified. Enrichment factors (EFs), with respect to the upper crust composition, provided clear evidence of the different sources above mentioned: Ti, Fe, Al, Cs, Cr, Rb, and Co have low EFs (〈1), and are referable to the (local and/or regional) geogenic input, while Se, Sb, Zn, B, Cd, Cu, Mo, Sr, As, with high EFs (〉10), highlight the influence of marine and/or industrial sources. The study produced a novel dataset on the atmospheric deposition rate of several trace elements, which had never been studied in the investigated areas. Finally, a comparison of trace element deposition rates in the studied areas with the atmospheric deposition reported for 53 different sites, belonging to 20 different European nations, was made. The comparison showed that some elements, such as Al, V, Zn, and Mo had higher median deposition fluxes in the Sicilian sites than in European monitoring sites.
    Description: Published
    Description: 737
    Description: 6A. Geochimica per l'ambiente e geologia medica
    Description: JCR Journal
    Keywords: atmospheric deposition ; rainwater ; industrial pollution ; trace elements ; anthropogenic contribution ; 01.01. Atmosphere
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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