Search

In the Tethyan realm, leucocratic rocks were recognized as dikes and layers outcropping in the ophiolitic rocks of the Western Alps, in Corsica, and in the Northern Apennines. Several authors have suggested that the origin of leucocratic rocks is associated with partial melting of cumulate gabbro. Major and trace elements composition and paragenesis provided information about the leucocratic rocks genetic processes. This research aims at disclosing, for the first time, the petrographical and geochemical features of Timpa delle Murge leucocratic rocks, Pollino Massif (southern Italy), in order to discuss their origin and geodynamic significance through a comparison with other Tethyan leucocratic rocks. These rocks are characterized by high amounts of silica with moderate alumina and iron-magnesium contents showing higher potassium contents than plagiogranites, due to plagioclase alteration to sericite. Plagioclase fractionation reflects negative Eu anomalies indicating its derivation from gabbroic crystal mushes. The chondrite normalized REEs patterns suggest the participation of partial melts derived from a metasomatized mantle in a subduction environment. The results reveal some similarities in composition with other Tethyan leucocratic rocks, especially those concerning Corsica and the Northern Alps. These new data provide further clues on the origin of these leucocratic rocks and the Tethyan area geodynamic evolution.

The Pietra del Pertusillo freshwater reservoir is a major artificial lake of environmental, biological, and ecological importance located in the Basilicata region, southern Italy. The reservoir arch-gravity dam was completed in 1963 for producing hydroelectric energy and providing water for human use, and nearby there are potential sources of anthropogenic pollution such as urban and industrial activities. For the first time, the minero-chemistry of the lake and fluvio-lacustrine sediments of the reservoir have been evaluated to assess the environmental quality. Moreover, the composition of fluvial sediments derived from the peri-lacual zone of the reservoir and of local outcropping bedrock were also studied to understand the factors affecting the behavior of elements in the freshwater reservoir, with particular attention paid to heavy metals. In Italy, specific regulatory values concerning the element threshold concentration for lake and river sediments do not exist, and for this reason, soil threshold values are considered the standard for sediments of internal waters. The evaluation of the environmental quality of reservoir sediments has been performed using enrichment factors obtained with respect to the average composition of a reconstructed local upper continental crust. We suggest this method as an innovative standard in similar conditions worldwide. In the studied reservoir sediments, the trace elements that may be of some environmental concern are Cr, Cu, Zn, As, and Pb although, at this stage, the distribution of these elements appears to be mostly driven by geogenic processes. However, within the frame of the assessment and the preservation of the quality of aquatic environments, particular attention has to be paid to As (which shows median value of 10 ppm, reaching a maximum value of 26 ppm in Quaternary sediments), constantly enriched in the lacustrine samples and especially in the fine-grained fraction (median = 8.5 ppm).

In the Tethyan realm the carbonate-dominated Meso-Cenozoic South Tethyan Phosphogenic Province is of considerable economic importance since it represents the greatest accumulation of sedimentary phosphorites. In southern Italy, in the Salentine peninsula (the southern part of the Apulian Carbonate Platform, ACP), is well documented the occurrence of Cenozoic P-rich levels consisting of nodules and pebbles and showing a large P2O5 fluctuation (4.07–22.07 wt%), due to variable calcite abundance. The mainly observed P-bearing minerals are hydroxyapatite and carbonate fluorapatite and U, together with Sr and Pb, preferentially acts as Ca substitutes in both lattices. Minor authigenic monazite (LREE-bearing phosphate) and xenotime (HREE+Y-bearing phosphate), likely formed during sediment burial compaction and diagenesis. The total REEs' abundances and the shape of the shale-normalized REE-patterns in the P-rich nodules are in the range of those typically observed in Paleocene-Eocene through Pleistocene-Recent P-rich sediments, supporting the idea of a broadly consistent ocean chemistry in this span of geological time. The (La/Yb)N proxy is within the modern seawater range, signifying early diagenetic adsorption played only a minor role in affecting the REEs' distribution. The Ce and Pr anomalies suggest some P-rich nodules experienced very localized hypoxic to anoxic conditions promoting Ce/Ce* spurious results in a generally oxic to hypoxic environment causing real negative Ce anomaly. This scenario is reinforced by the lack of the coupled uranium-vanadium enrichment typically observed in an anoxic environment. Since the Pliocene the eastern Mediterranean was variously affected by oxygenation and productivity and it is likely the ACP phosphate-rich sediments formed under low sedimentation rates and authigenesis in a bottom current-dominated regime, as also indicated by the glauconite occurrence. Transgressions and sea levels rising following major glaciations may have favored the deposition of phosphate sediments by creating new restricted basin configurations and increased nutrient input promoted by upwelling processes.

The Sardinia microplate in the western Mediterranean represents an ideal example for examining the relationship between fluid geochemistry, tectonic and heat sources in hydrothermal circuits. It consists of a portion of Variscan basement partly covered by sedimentary (mainly carbonate) and volcanic successions that record significant Permian to Pliocene geodynamic events within the southern European margin. The regional structure of the northern Sardinia is dominated by Tertiary ENE–WSW trending strike-slip and NNW–SSE trending normal faults, both capable of controlling deep and shallow fluid circulation. In this paper, results of a detailed geochemical investigation of waters and gases coming from a W-E trending section of central-north Sardinia are presented in order to explain the contrasting thermal and geochemical features of two - already known groups - of fluids. The Volcanic Logudoro Waters (VLW) is a group of cold to hypothermal Na–HCO3 waters characterised by high CO2 contents and mantle-derived He, that are localized in the volcanic-dominated Tertiary grabens. The He mantle signature within the VLW waters is associated with Plio-Pleistocene Quaternary volcanism where the outgassing of mantle-derived fluids is reasonably due recently active magma sources at depth. The currently active emission of mantle-derived gas linked to cold and hypothermal waters, provides evidence that the heat diffusion associated with the Plio-Pleistocene volcanism has already ended. In contrast, the Granite Variscan Basement Waters (GBW) group is characterised by hot-NaCl-rich waters, containing high concentrations of both dissolved N2 and radiogenic 4He. The high contribution of 4He produced by radiogenic decay of U and Th in the crust indicates a supply of radiogenic heat to the hydrothermal system localized within the granitic basement or in the tectonic contact between granite and Tertiary covers.

This work focuses on two fault-controlled deposits, the Atella and Rapolla travertines, which are associated with high-angle extensional faults of the Bradano Trough, southern Apennines (Italy). The Atella travertine is along a NW-SE striking, deep-seated extensional fault, already described in literature, which crosscuts both Apulian carbonates and the overlying foredeep basin infill. The Rapolla travertine is on top of a NE-SW striking, shallow-seated fault, here described for the first time, which is interpreted as a tear fault associated with a shallow thrust displacing only the foredeep basin infill. The results of structural, sedimentological, mineralogical, and C and O isotope analyses are here reported and discussed to assess the provenance of mineralizing fluids, and to evaluate the control exerted by the aforementioned extensional faults on deep, mantle-derived and shallow, meteoric fluids. Sedimentological analysis is consistent with five lithofacies in the studied travertines, which likely formed in a typical lacustrine depositional environment. Mineralogical analysis show that travertines mainly consist of calcite, and minor quartz, feldspar and clay minerals, indicative of a terrigenous supply during travertine precipitation. The isotope signature of the two studied travertines shows different provenance for the mineralizing fluids. At the Atella site, the δ13CPDB values range between + 5.2 and + 5.7‰ and the δ18OPDB values between − 9.0 and − 7.3‰, which are consistent with a mantle-derived CO2 component in the fluid. In contrast, at the Rapolla site the δ13CPDB values vary from − 2.7 to + 1.5‰ and the δ18OPDB values from − 6.8 to − 5.4‰, suggesting a mixed CO2 source with both biogenic-derived and mantle-derived fluids. The results of structural analyses conducted along the footwall damage zone of the fault exposed at the Rapolla site, show that the whole damage zone, in which fractures and joints likely channeled the mixed fluids, acted as a distributed conduit for both fault-parallel and cross-fault fluid migration.

In this paper we provide a systematic geochemical study of the Monticchio maar lakes, on the Mt. Vulture volcano, southern Italy, to understand the processes affecting the distribution of chemical elements. A high-resolution conductivity–temperature–depth profile was obtained, and water samples were collected at various depths for analyses of major and trace elements. Although the two lakes are separated by less than 200 m, they exhibit different behaviour. The Ca–Na–HCO 3 composition of “Lago Grande” water suggests that low-temperature fluids are leached from the host volcanic rocks. Na–Ca–HCO 3 in near-surface “Lago Piccolo” water is derived from the dissolution of local volcanic rocks, while the deepest water samples are bicarbonate alkaline-earth in composition and generally show an enrichment in solutes with respect to the epilimnion layer (except for SO 4 2 − content). The hypolimnion water is principally governed by both the input of saline groundwater from the lake bottom and authigenic processes within bottom sediments. In addition, the occurrence of anoxic conditions and microbial activity is responsible for the transformation of sulphates to hydrogen sulphide, and for the precipitation of Fe sulphide phases. Both processes cause a change in the chemical composition of saline groundwater as it moves upwards. Overall, the water chemistry of the Monticchio lakes is principally affected by: i) the input of CO 2 -rich volcanic gas; ii) evaporative processes that deplete near-surface water in some elements; and iii) the occurrence of chemical, physical and biological conditions causing the transformation of molecular complexes and consequently promoting mineral precipitation.

The Mount Vulture basin, which mainly consists of pyroclastic and subordinate lava flow layers, is one of the most important aquifers for drinking water and irrigation supply in southern Italy. In this study, we investigated the geochemical behaviour of the rare earth elements (REEs) in the groundwater of this aquatic system, assessing fractionation patterns and performing speciation calculations to elucidate the geochemical processes affecting the REEs' distribution. The groundwater collected was separated into two subsets corresponding to recharge and discharge water. Overall, the groundwater exhibited REE concentrations well below 1000 ng/l, and the average content measured in the discharge water is approximately three times higher than that of the recharge water. In the recharge water, the shale normalised patterns are characterised by a more negative average Ce anomaly, a more positive average Eu anomaly, and a larger average (La/Yb)PAAS. The observed relationship between Ce anomalies and dissolved oxygen (DO) supports the idea that Ce oxidative scavenging has a role in determining the size and shape of the Ce anomaly. Further, the less negative average size of the Ce anomaly in the discharge zone also suggests Ce desorption due to changes in redox conditions. As for the Eu anomalies, the largest Eu* are associated with the recharge zone, characterised by higher average Eh and DO values. The volcanics in the Mt. Vulture lithologies have post-Archean average shale (PAAS) normalised patterns showing positive Eu anomalies due to feldspars occurrence. This indicates that the Eu* of groundwater in the recharge zone is mostly produced by the dissolution of feldspars. In the discharge zone, most samples are in equilibrium with smectite and Eu2+ adsorption onto the clay phase surface or its inclusion in the mineral structure as exchangeable cations likely lead to the smaller average size of Eu*. The possible occurrence of secondary minerals preferentially scavenging light REEs may also explain the difference in the (La/Yb)PAAS index observed between the recharge and discharge zones. Speciation calculations indicate that dissolved REEs consist mainly of carbonato complexes (LnCO3+) whereas the percentage of dicarbonato complexes (Ln(CO3)2−) increases in samples with circa-neutral pH. At acidic pH, the Ln3+ species are numerous and, in samples with large amounts of dissolved sulphate, derived by feldspathoids dissolution, from the discharge zone, the percentage of LnSO4+ species is not negligible.

Mantle volatiles are mainly lost from the Earth to the atmosphere through subaerial and submarine volcanism. Recent studies have shown that degassing of mantle volatiles also occurs from inactive volcanic areas and in tectonically active areas. A new challenge in Earth science is to quantify the mantle-derived flux of volatiles (e.g., CO2) which is important for understanding such diverse issues as the evolution of the atmosphere, the relationships between magma degassing and volcanic activity, gas pressure and seismogenic processes, and the hazards posed by volcanic lakes. Here we present a detailed study of mantle-derived CO2 budget from Mt. Vulture volcano in the Apennines, Italy, whose latest eruption occurred 141 ± 11 kyr ago. The relationship between δ13CCO2 and total dissolved carbon at Mt. Vulture volcano indicates that the emitted CO2 is a mixture of a biogenic end-member with an average δ13CCO2 of about − 17 ‰ and a mantle-derived CO2 end-member with δ13CCO2 values from − 3 ‰ to + 2 ‰ . These values of mantle-derived δ13CCO2 are in the range of those for gas emitted from active volcanoes in the Mediterranean. We calculated the contribution of individual components (CO2 in groundwater, in lakes and from main pools) to the total CO2 budget in the area. We used new measurements of water flow, combined with literature data, to calculate the CO2 flux associated with groundwater, and measured the gas flux from the main pools on the volcanic edifice. Finally, we calculated the CO2 flow in the lakes based on the gradient concentration and eddy diffusivity. The total mantle-derived CO2 budget in the area is 4.85 × 10 8 mol yr − 1 , which is more than double previous estimates. This is higher than those observed in younger volcanic systems elsewhere, thereby supporting the existence of actively degassing mantle melts below Mt. Vulture volcano. A structural map highlights the tectonic control on CO2 flow across the Mt. Vulture volcanic edifice. Indeed, the tectonic discontinuities that controlled the magma upwelling during the most recent volcanic activity are still the main active degassing structures. The new estimate of CO2 budget in the Mt. Vulture area, together with literature data on CO2 budget from historically active and inactive Italian volcanoes, suggests a power-law functional relationship between the age of the most recent volcanic eruption and both total discharged CO2 ( R 2 = 0.73 ) and volcano size-normalized CO2 flux ( R 2 = 0.66 ). This relation is also valid by using data from worldwide volcanoes highlighting that deep degassing can occur over very long time too. In turn, the highlighted relation provides also an important tool to better evaluate the state of activity of a volcano, whose last activity occurred far in time. Finally, our study highlights that in the southern Apennines, an active degassing of mantle-derived volatiles (i.e., He, CO2) occurs indiscriminately from west to east. This is in contrast to the central–northern Apennine, which is characterized by a crustal radiogenic volatile contribution, which increases eastward, coupled to a decrease in deep CO2 flux. This difference between the two regions is probably due to lithospheric tears which control the upwelling of mantle melts, their degassing and the transport of volatiles through the crust.

This paper presents new data on the chemical composition of precipitation in a selected area of the southern Apennines of Italy; these data are used to assess natural and anthropogenic contributions to the precipitation. The town of Potenza was used as a representative urban site, and the major and minor element (Na + , K + , Ca 2 + , Mg 2 + , NH 4 + , Cl − , NO 3 − , SO 4 2 − , and Li + , NO 2 − , F − , Br − , PO 4 3 − ) and trace element (Zn, Fe, Al, Sr, Mn, Ba, Cu, Cr, V, As, Pb, Ni, and Cd) concentrations of bulk precipitation from three different sampling sites within the study area were determined between June 2011 and May 2012. The majority of the collected rainwater has pH values higher than 5.6. The composition of this rainwater was dominated by Ca 2 + the element with the highest total volume-weighted mean concentration (TVWA), followed by Cl − , SO 4 2 − , Na + , NO 3 − , K + , Mg 2 + , and NH 4 + . The TVWA of the trace metals decreased in the order Zn > Fe > Al > Ba > Sr > Mn > Pb > Cu > As. Neutralising factor (NF Xi ) values indicate that Ca 2 + is the dominant neutralising cation within this rainwater, with lower contribution from NH 4 + and Mg 2 + . The precipitation analysed during this study has a negligible marine influence as determined using Cl − concentrations as a proxy for the abundance of sea salts. Precipitation F i values (marine fraction of element i) indicate that Na + is the element with the highest seawater component, and we found partial marine contributions for the SO 4 2 − and Mg 2 + concentrations within this rainwater. Enrichment factors (EF) of selected elements were calculated to identify the sources of non-crustal elements: K + , Mg 2 + , Fe, and Ca 2 + are the only elements dominantly sourced from the crust, whereas Mn and Ba have highly variable EF values (10–100) suggesting that a small proportion of these elements was derived from anthropogenic sources in addition to a more significant crustal contribution. Sr, Cu, Pb, Zn, and As are highly enriched with respect to average crustal compositions, confirming that the concentrations of these elements within precipitation are significantly controlled by human activities.

The Mt Vulture carbonatites are the only carbonatite occurrence in the southern Apennines. We present new trace element data for these rocks in order to evaluate the factors influencing rare earth element (REE) and other trace element fractionations and their REE grade. This study focuses on massive hyalo-alvikites from two lava flows and one dike, which have different relative abundances of silicate and carbonate (i.e. Si/Ca). These differences are also evident from CaO/(CaO + MgO + FeO(T) + MnO) and Sr/Ba ratios. The REE grade of the Mt Vulture carbonatites is very similar to that of the global average for calcio-carbonatites. R-mode factor analysis shows that most of the trace element variance reflects the relative roles of carbonate and silicate minerals in influencing trace element distributions. Silicates largely control heavy rare earth element (HREE), transition metal, Zr, and Th abundances, whereas carbonate minerals control light rare earth element (LREE), Ba, and Pb abundances. In addition, apa...

We report the results of a geochemical study of gas emissions along a NE–SW transect in southern Italy in order to test the hypothesis that the region around Monte Vulture is affected by degassing of mantle-derived fluids through a lithospheric discontinuity. We also investigated lavas from the Monte Vulture volcano displaying 3 He/ 4 He (up to ~ 6.0 Ra) and Sr isotopes that are consistent with an origin in mantle that has had minimal pollution from subducted Adriatic slab. Similar 3 He/ 4 He in fluids from around Mt. Vulture indicate that the deep volcanic system is still degassing. Mantle-derived He occurs in fluids along the length of the Vulture line, reinforcing the hypothesis that it is a deep tectonic discontinuity along which mantle fluids and/or melts advect to the surface. The CO 2 / 3 He ratios are highly variable (2.7 × 10 8 –2.15 × 10 11 ) in response to processes such as gas dissolution into aquifers, addition of crustal gases and degassing fractionation.

Identifying the origin of nitrate is important for the control and management of groundwater quality in aquifer systems. In the southern Apennines (Italy), the Mount Vulture volcanic aquifer is a large and valuable resource of potable and mineral water supply. Unfortunately, signs of anthropogenic impact, especially nitrogen contamination, have recently become evident. In this study, and for the first time, stable isotope ratios (δ15N and δ18O) of NO3− were determined in groundwater to identify their origins and evaluate the presence of transformation processes. The Mount Vulture groundwaters are meteoric in origin, as demonstrated by measurements of δD and δ18O, and can be divided into two distinct areas based on their NO3− content. In the southeastern area, characterized by active agricultural land use, the high NO3− content and the δ15N–NO3 isotopic values are due to anthropogenic contamination (inorganic fertilizer). In groundwaters from the western area, the NO3− contents below 4 mg/L and the δ15N–NO3 values can be associated at organic soil N. Evidence for local denitrification may be assumed in a few groundwater samples of the western area showing relatively heavy δ15N values and low concentrations of nitrate. Finally, the low measured δ18O values indicate that nitrification occurred in both investigated areas.

In this paper we provide a geochemical investigation on 34 groundwater samples in the Mt. Vulture volcanic aquifer representing one of the most important groundwater resources of the southern Italy pumped for drinking and irrigation supply. The present study includes the first data on the abundance and mobility of minor and trace elements and the thermodynamic considerations on water–rock interaction processes in order to evaluate the conditions of alkali basalt weathering by waters enriched in magma-derived CO 2 . The results highlight the occurrence of two hydrofacies: bicarbonate alkaline-earth and alkaline waters deriving from low-temperature leaching of volcanic rocks of Mt. Vulture, and bicarbonate-sulfate-alkaline waters (high-salinity waters) related to prolonged water circulation in alkali and feldspathoids-rich pyroclastic layers interbedded with clay deposits. The Al-normalized relative mobility (RM) of metals in Vulture's aquifer varies over a wide range (10 − 1 4 ), confirming that the basalt weathering is not a congruent and isochemical process. Chemical equilibrium studies show that the bicarbonate alkaline-earth and alkaline waters, having a short interaction with silicate minerals, plot very close to the kaolinite–smectite stability boundary, whereas the high-salinity waters fall in the stability field of smectite and muscovite because of prolonged interaction with alkali and feldspathoids-rich pyroclastic layers. Overall, for the bicarbonate alkaline-earth and alkaline waters, the release of toxic metals in solutions is related to the spatial variation of host-rock geochemistry, the high-salinity waters, collected near urban areas, show values higher than legal limits for Ni and As, likely as a consequence of anthropogenic contribution.

Environmental isotope techniques, hydrogeochemical analysis and hydraulic data are employed to identify the main recharge areas of the Mt. Vulture hydrogeological basin, one of the most important aquifers of southern Italy. The groundwaters are derived from seepage of rainwater, flowing from the highest to the lowest elevations through the shallow volcanic weathered host-rock fracture zones. Samples of shallow and deep groundwater were collected at 48 locations with elevations ranging from 352 to 1,100m above sea level (a.s.l.), for stable isotope (δ18O, δD) and major ion analyses. A complete dataset of available hydraulic information has been integrated with measurements carried out in the present study. Inferred recharge elevations, estimated on the basis of the local vertical isotopic gradient of δ18O, range between 550 and 1,200m a.s.l. The isotope pattern of the Quaternary aquifer reflects the spatial separation of different recharge sources. Knowledge of the local hydrogeological setting was the starting point for a detailed hydrogeochemical and isotopic study to define the recharge and discharge patterns identifying the groundwater flow pathways of the Mt. Vulture basin. The integration of all the data allowed for the tracing of the groundwater flows of the Mt. Vulture basin. Se emplearon técnicas isotópicas ambientales, análisis hidrogeoquímicos y datos hidráulicos para identificar las principales áreas de recarga de la cuenca hidrogeológica del Mt. Vulture, uno de los más importantes acuíferos del sur de Italia. Las aguas subterráneas provienen de la infiltración del agua de lluvia, flujo desde las elevaciones más altas a las más bajas a través de zonas de fracturas someras de rocas reservorio volcánicas meteorizadas. Se recolectaron muestras de aguas subterráneas someras y profundas en 48 sitios con alturas en el intervalo que va de 352 a 1,100 m por sobre el nivel del mar (m s.n.m), para análisis de isótopos estables (δ18O, δD) e iones mayoritarios. Se integró una completa base de datos de la información hidráulica disponible con las mediciones llevadas a cabo en el estudio presente. Las alturas de recarga deducidas, estimadas sobre la base de gradiente isotópico vertical local de δ18O, oscilaron entre 550 y 1,200 m s.NM El patrón isotópico del acuífero Cuaternario refleja la separación espacial de diferentes fuentes de recarga. El conocimiento de la configuración hidrogeológica local fue el punto de partida para un estudio isotópico e hidrogeoquímico detallada para definir el esquema de la recarga y descarga identificando las trayectorias de flujo subterráneo de la cuenca del Mt. Vulture. La integración de todos los datos permitió el seguimiento de los flujos de las aguas subterráneas de la cuenca del Mt. Vulture., Department of Geological Sciences, University of Basilicata, Italia, Department of Chemistry, University of Basilicata, Italia, Unidad de Sevilla, Instituto Geológico y Minero de España, España, Institute of Geological Sciences, Freie Universität Berlin, Alemania, Unit Potsdam, Isotope Laboratory, Alfred Wegener Institute for Polar and Marine Research, Alemania, Department of Structural Engineering, Geotechnical Engineering, Engineering Geology, University of Basilicata, Italia

Geochemical investigations have shown that there is a considerable inflow of gas into both crater lakes of Monticchio, Southern Italy. These lakes are located in two maars that formed 140 000 years ago during Mt. Vulture volcanos last eruptive activity. Isotopic analyses suggest that CO2 and helium are of magmatic origin; the latter displays 3 He ⁄ 4 He isotope ratios similar to those measured in olivines of the maar ejecta. In spite of the fact that the amount of dissolved gases in the water is less than that found in Lake Nyos (Cameroon), both the results obtained and the historical reports studied indicate that these crater lakes could be highly hazardous sites, even though they are located in a region currently considered inactive. This could be of special significance in very popular tourist areas such as the Monticchio lakes, which are visited by about 30 000 people throughout the summer, for the most part on Sundays.

Geochemical investigations carried out at the Campano–Lucano Apennine (Southern Italy) revealed the presence of fluids composed of a mixing between components of shallow and deep origin, where mantle-derived helium is also detectable. For the gas phase, the deep component is represented by both CH4 and CO2-rich gases, while the shallow one is N2-dominated. Coinciding with the 3 April 1996 ML=4.9 earthquake, the CH4-rich component mixed with the shallow, N2-dominated one at the Tramutola well (Val d’Agri), displaying wide variations in mixing proportions. In contrast, no significant modifications occurred in relation to the 1998 ML=5.5 event. According to the collected data, an earthquake-related transient modification of local crustal permeability is suggested for the 1996 event. The different crustal response to the two events may be related to different stress distributions around the epicentres or may suggest a different tectonic connection between the Val d’Agri and the two earthquake locations.

During “Mineral CO2 sequestration” the CO2 is chemically stored in solid carbonates by the carbonations of minerals. The sequestration of CO2 is permanent and safe. Mineral carbonation is an exothermic reaction and occurs naturally in the subsurface as a result of fluid–rock interactions within serpentinite. In situ carbonation aims to promote these reactions by injecting CO2 into porous, subsurface geological formations. In the northern sector of the Pollino Massif (southern Italy) extensively occur serpentinites; they are the subject of a project devoted to their possible use for in situ geological sequestration of CO2.