The study of active and fossil hydrothermal systems shows clay minerals to be a fundamental tool for the identification and characterization of hydrothermal alteration facies. The occurrence and composition of hydrothermal alteration facies could provide useful information on the physicochemical conditions of the hydrothermal activity affecting a rock volume. In particular, clay minerals (i.e., smectite group, chlorite, illite, kaoline group, pyrophyllite, biotite) are pivotal for extrapolating important parameters that strongly affect the development of water/rock interaction processes such as the temperature and pH of the hydrothermal environment. This work aims to give a general reference scheme concerning the occurrence of clay minerals in hydrothermal alteration paragenesis, their significance, and the information that can be deduced by their presence and chemical composition, with some examples from active and fossil hydrothermal systems around the world. The main mineralogical geothermometers based on chlorite and illite composition are presented, together with the use of hydrogen and oxygen isotope investigation of clay minerals in hydrothermal systems. These techniques provide a useful tool for the reconstruction of the origin and evolution of fluids involved in hydrothermal alteration. Finally, a list of oxygen and hydrogen fractionation factor equations between the main clay minerals and water is also provided.

In this paper we build a subsurface model that helps in visualizing and understanding the structural framework, geology and their interactions with the Mt. Amiata geothermal system. Modelling in 3D provides the possibility to interpolate the geometry of structures and is an effective way of understanding geological features. The 3D modelling approach appears to be crucial for further progress in the reconstruction of the assessment of the geothermal model of Mt. Amiata. Furthermore, this model is used as the basis of a 3D numerical thermo-fluid-dynamic model of the existing reservoir(s). The integration between borehole data and numerical modelling results allows reconstructing the temperature distribution in the subsoil of the Mt. Amiata area.

In the Radicondoli–Travale area of the Larderello geothermal field (Italy) new structural and petrologic data on some metamorphic units, cored from geothermal wells, reveal the existence of a wide complex of hornfels rocks. The development of the complex is related to the emplacement of Neogene magmatic rocks at a shallow depth within a Permo–Triassic terrigenous metasedimentary sequence of a low metamorphic grade. The sequence was subjected to alpine tectonic-metamorphic events. This reconstruction gives new insights in the tectonic setting of metamorphic units below the Tuscan Nappe, in southern Tuscany. Particularly, the medium and high grade metamorphic rocks seem strictly related to the development of Neogene thermal aureoles and do not represent remnants of a Paleozoic basement. Furthermore, in this sector of the Larderello geothermal system, the presence of deep geothermal reservoir at a depth of 3 000 m is mainly linked to the enhanced permeability caused by fracturing in these hornfels rocks. This fracturing is a consequence of the dehydration reaction occurring in the metapelites due to Neogene thermal metamorphism. This mechanism allowed the development of a long-lived hydrothermal system, shown by the secondary mineralogical assemblages. These testify the presence of at least two hydrothermal stages which are well preserved in the less permeable units. © 2000 Editions scientifiques et médicales Elsevier SAS

The quartz-monzonitic intrusion of ‘Botro ai Marmi’ in Tuscany, Italy, can be considered to be a typical example of an intrusion-centred magmatic hydrothermal system. The evolution of hydrothermal fluids in the ‘Botro ai Marmi’ intrusion was investigated using fluid-inclusion analyses to provide suitable physico-chemical constraints on the fluids involved in the late- to post-magmatic hydrothermal activity that affected the intrusion, providing inferences on their origin and variations of temperature and pressure with time. This work demonstrates that the earliest fluids circulating in the ‘Botro ai Marmi’ intrusion were high-temperature brines exsolved directly from the crystallizing magma. This fluid circulated in the intrusion under lithostatic conditions (P > 90 MPa, T > 540°C). A second evolutionary stage of the magmatic hydrothermal system is marked by the transition from lithostatic (>90 MPa) to hydrostatic dominated conditions (50 to 10 MPa). In this stage the fluids are also interpreted to be mainly orthomagmatic in origin but unmixed in a high-salinity brine and in a low-salinity vapour aqueous phase, at a temperature ranging from ~500 to 300°C. These fluids were responsible for the potassic alteration facies. At a later stage of hydrothermal evolution, abundant meteoric dominated fluids entered the system and are associated with propylitic alteration. This event marks the transition from a magmatic-hydrothermal system to a typical hydrothermal (‘geothermal’) system, which can be assumed to be similar to some extent to the nearby active high-enthalpy geothermal system of Larderello. Low-temperature and low-salinity meteoric water-dominated fluids characterize the latest stage of the ‘Botro ai Marmi’ hydrothermal system.

Artisanal and small-scale gold mining (ASGM) poses significant environmental challenges globally, particularly due to mercury (Hg) use. As an example, in Ecuador, Hg use still persists, despite its official ban in 2015. This study investigated the geogenic and anthropogenic contributions of potentially toxic elements (PTEs) in the Ponce Enriquez Mining District (PEMD), a region characterized by hydrothermally altered basaltic bedrock and Au-mineralized quartz veins. To assess local baseline values and identify PTE-bearing minerals, a comprehensive geochemical, mineralogical, and petrographic analysis was conducted on bedrock and mineralized veins. These findings reveal distinct origins for the studied PTEs, which include Hg, As, Cu, Ni, Cr, Co, Sb, Zn, and V. Specifically, Hg concentrations in stream sediments downstream (up to 50 ppm) far exceed natural bedrock levels (0.03–0.707 ppm), unequivocally indicating significant anthropogenic input from gold amalgamation. Furthermore, copper shows elevated concentration primarily linked to gold extraction. Conversely, other elements like As, Ni, Cr, Co, Sb, Zn, and V are primarily exhibited to be naturally abundant in basalts due to the presence of primary mafic minerals and to hydrothermal alterations, with elevated concentrations particularly seen in sulfides like pyrite and arsenopyrite. To distinguish natural geochemical anomalies from mining-related contamination, especially in volcanic terrains, this study utilizes Upper Continental Crust (UCC) normalization and local bedrock baselines. This multi-faceted approach effectively helped to differentiate basalt subgroups and assess natural concentrations, thereby avoiding misinterpretations of naturally elevated element concentrations as mining-related pollution. Crucially, this work establishes a robust local geochemical baseline for the PEMD area, providing a critical framework for accurate environmental risk assessments and sustainable mineral resource management, and informing national environmental quality standards and remediation efforts in Ecuador. It underscores the necessity of evaluating local geology, including inherent mineralization, when defining environmental baselines and understanding the fate of PTEs in mining-impacted environments.

Wide areas of the Southern sector of Ecuador are characterized by Cretaceous mafic volcanic rocks, pervasively altered by a propylitic mineralogical assemblage with epidote, chlorite, and quartz with minor titanite, illite and prehnite. These propylitically altered rocks host significant gold mineralization in veins, deeply exploited in the last decades. Porphyry Au-Cu deposits also occur in the area. This work focuses on the study of this propylitic alteration to assess the genetic conditions and the relation with the distance from the porphyry system, through the chemical composition of the secondary minerals (particularly trace elements in epidote and chlorite) and fluid inclusion data. The aim is to improve knowledge of the trace element geochemistry of secondary minerals in propylitic alteration and their relationship to the causative porphyry systems. The results of this work indicate that alteration affecting the rocks of the Pallatanga Fm. can be related to the propylitic hydrothermal alteration halo of porphyry copper deposits. Fluid inclusion investigation in quartz veins associated with epidote and chlorite evidenced at least two pulses of hydrothermal fluids characterized by temperature around 345°C for the first one and around 305°C for the second one. The salinity of the fluids is always low (around 1.5 wt% NaCl_equiv.) suggesting a dominantly meteoric component. Evidence of boiling processes have not been observed. We hypothesize that the hydrothermally altered “green rocks” of the Ponce Enriquez Mining District could be envisaged as the propylitic halo of the Miocene hornblende-bearing Au-Cu porphyry deposits of Gaby-Papa Grande, and discuss the epidote and chlorite trace element composition in this scenario. The results help improving the general knowledge of the propylitically altered rocks in southern Ecuador and add new data for the use of trace element chemistry of epidote and chlorite in mineral exploration elsewhere.