Introduction

It is commonly accepted that fault zones act as hydrothermal fluid conduits within the crust. Fluid transmissive fault zones generate veins (Oliver and Bons 2001) and are important loci of ore deposition in a number of geological environments (e.g., Cowan 2020; Foxford et al. 2000). These faults and their associated veins may show a gamut of textures at the meso- and micro-scales (e.g., Dong et al. 1995) that are dependent on the extensional, hybrid, or shear nature of the fault and on fluid pressure (Bons et al. 2012). There is therefore a close feedback between failure modes of fault zones, their fabric, hydrothermal fluid flow, and vein formation, all of which are mutually dependent and steer ore formation.

Hydrothermal fluids within fault zones may modify the mineralogical, chemical, and textural properties of the protolith during deformation. This modification is carried out by the precipitation of minerals within the zone, which might choke or enhance porosity depending on the type of fluid-fault interaction (Torabi et al. 2020b). Away from a fault zone, fluid-fault interactions may leave cryptic to visible haloes in the protolith (Reed 1997), which can vary along and across fault strike due to the variable composition of fault and wallrock minerals (selvaging: Cathles 1991) or due to distinct fault fluids (Garofalo 2004).

Models were set up as a guide for the evaluation of the structural properties of upper-crustal, brittle fault zones (Caine et al. 1996; Torabi et al. 2020a, and ref. therein). These properties are relevant for the interpretation of the data presented in this study. The architecture of a brittle fault zone (Fig. 1) is ideally made of a fault core and a damage zone, which develop at different times and are made of distinct rocks. The core is a part of a fault that accommodates most of the displacement and that is made of thin slip surfaces, clay-rich gouges, incohesive breccias, and cataclasite/ultracataclasite zones in which the protolith experienced the highest degree of comminution. A damage zone is the heterogeneous part of a fault made of veins, cleavage planes, deformation bands, and other fault rocks that form during multiple episodes of slip. As a general rule, a core develops from a damage zone as a result of deformation and comminution. Its permeability is dominated by grain-scale processes and may show stages of fluid-assisted strain hardening and weakening (e.g., Vignaroli et al. 2020). Fault cores tend to be barriers to fluid flow due to permeability reduction processes, while a damage zone is dominated by the hydraulic permeability of the fracture network (Caine et al. 1996). The presence of a wide damage zone and a relatively thin core causes a brittle fault to act as a conduit for hydrothermal fluid flow, and the presence of a wide core and a thin damage zone generates a localized barrier to flow.

Fig. 1
figure 1

Primary structural and lithological components of a brittle normal fault (mod. after: Torabi et al. 2020a). No scalar relationships are implied between these components

Hence, open questions are the differences between the typical upper crustal faults (Fig. 1) and those that host large hydrothermal fluid flow and ore precipitation in terms of fault architecture, fabric, and textures.

In this study, we combine field data with a multi-technique analytical dataset to constrain the processes in an Au-mineralized upper crustal fault. This fault is hosted by serpentinized lherzolite, is enveloped by a wide carbonate hydrothermal alteration halo whose mineral assemblage resembles that of the listwanite, and shows an association of lithologies and fabrics that indicate a high bulk permeability at the time of failure and fluid flow. We focus our attention on the genesis of an Au-bearing, highly permeable zone, which developed synkinematically and shows a peculiar texture made of circular and concentric dolomite aggregates. We propose a link between the structural evolution of the zone and fluid-fault interaction and Au deposition.

Geology of the Lavagnina Lakes area

The Lavagnina Lakes (Fig. 2) are located near Casaleggio Boiro (Alessandria, Italy). The area occupies the north-eastern boundary of the Voltri Unit, Ligurian Western Alps (Scarsi et al. 2019), and belongs to a region that is known for Au deposits that are documented from the year 1589 to the end of the nineteenth century (Pipino 2001). A more complete account of the historical Au deposits of the area is provided in the Electronic Supplementary Materials (ESM). The Lavagnina Lakes zone belongs to the ophiolitic complex of the Voltri Massif. It consists of serpentinite associated with metagabbro, mafic metavolcanics, metasediments, and lherzolite associated with minor pyroxenite and dunite bodies. The Massif experienced an Alpine tectono-metamorphic history including the ductile and brittle regimes (Capponi and Crispini 2002, and ref. therein), and from high-pressure metamorphic conditions to variable retrogressive greenschist overprints (Scarsi et al. 2018).

Fig. 2
figure 2

Geological sketch map of the Lavagnina Lakes and Bisciarelle fault area (modified after: Pipino 2003; Scarsi et al. 2019)

The most abundant lithologies of the Lavagnina Lakes (Fig. 2) are peridotite of the Voltri Unit (also: Erro-Tobbio Unit), continental breccias, and conglomerates of the Tertiary Piedmont Basin. The peridotite consists mainly of lherzolite with minor dunitic lenses, showing degrees of serpentinization and slices of metagabbro and mafic metavolcanics. In the studied area, serpentinized lherzolite shows a transitional contact with serpentine schists.

The structural evolution of the area is made of several superimposed deformation events, which occurred under a tectonic regime evolving from brittle-ductile to brittle. The oldest Alpine structures of the area can be referred to the ductile D1-D2 deformation stages (Capponi and Crispini 2002). The following stages generated a complex superposition of ductile, brittle-ductile, and brittle structures that developed at higher structural levels and are represented by different sets of folds, reverse shear zones, and fault systems. Upper crustal faults are common in the Lavagnina Lakes zone and form sets of reverse shear zones (RSZ 2) that host Au-mineralized vein networks and associated wall rock hydrothermal alteration (Giorza 2010). The historical Au deposits and the Bisciarelle fault are shear zones that belong to this category.

Methods

Field work was conducted to define the structural elements of the Bisciarelle fault and to collect samples of fault rocks and protolith. Ten samples of the host lherzolite (RB1-RB10, Fig. 3ab) were collected along a 15.6-m profile directed at high angle with respect to the fault strike. A structural log of the fault was constructed based on fabric analysis and thickness measurements (Table 1, ESM). Eighteen samples of core and fault lithologies were used to determine the microstructural properties of the fault, mainly carbonated cataclasite, spherulite levels, breccia, and gouge, which were studied in thirty-four polished thin sections. These samples have been studied combining a petrographic study, morphometric analysis of fault core samples, X-ray powder diffraction analysis, SEM-energy dispersive X-ray spectroscopy, whole-rock chemical analyses, and 1-D scan and 2-D chemical analyses by laser ablation-inductively coupled plasma-time-of-flight mass spectrometry (LA-ICP-TOFMS). This last set of analyses followed an established protocol (Burger et al. 2015; Gundlach-Graham et al. 2015), but with distinct operating parameters that lead to different sensitivities. The 2-D element distribution images were constructed using a single-pulse mode, in which laser spot with a 10-µm diameter, a laser shot repetition rate of 25 Hz, and a line scan speed of 250 µm s−1 were used to build an image from an array of 1000 × 1000 LA shots. The 1-D scan mode was carried out using a hole-drilling mode (25 pulses per spot), a 5 µm laser spot diameter and a faster repetition rate (100 Hz) to improve the limits of detection by ablating more material per LA spot. This improvement was quantified as c. 1 order of magnitude for most of the light elements, and c. ½ order of magnitude for the heavy elements including gold (Fig. S14 of ESM). More details on field documentation, descriptions of the analytical techniques used, and pertinent figures of merit for all analytical measurements are provided in the ESM.

Fig. 3
figure 3

Characteristics of the Bisciarelle thrust fault. a Field appearance of fault and associated hydrothermal alteration halo. The dotted curve marks the contact between protolith and fault. The position of the largest spherulite levels is indicated. The Schmidt stereonet shows the attitude of fault surfaces (red spots: slickenlines; arrows show the top-to-E/NE sense of shear). b Relations between spherulite level, fault gouge, and hydrothermal alteration at the hanging wall of the fault. The blue rectangle marks the position of the photo in panel d. The RB1 to RB10 labels mark the sampling points of the alteration halo. Sample LLM* was used for elemental imaging with LA-ICP-TOFMS. c Detail of the spherulite level at the contact with two adjacent chalcedony shear veins. d Polished slab of the spherulites, chalcedony vein, and secondary shear surfaces

Table 1 Log of the Bisciarelle thrust fault

Mass transfer calculations were based on the multisample, immobile element approach of MacLean and Kranidiotis (1987) and Garofalo (2004; 2012). With this method, the concentrations of rock components are measured along a profile of an alteration zone and plotted in pairs to determine their behavior during alteration. A straight line connecting the origin of binary plots with the least altered sample (protolith) represents the expected trend of a pair of components if both are immobile, i.e., their ratio remains constant within the rock mass. Consequently, the evidence for several pairs of geochemically unrelated components of a rock mass showing linear trends at constant ratios and passing through the origin identifies a set of immobile components (Garofalo 2004, 2012). These components can be subsequently used to calculate mass factors and mass transfers between protolith and altered rocks. In the ten RB1-RB10 samples, mass transfers have been calculated for all rock components using the expression:

$$\Delta Ci= {(C}_{i}^{A} {MF}_{x})- {C}_{i}^{O}$$

where \(\Delta Ci\) is the mass of component i exchanged per unit mass of protolith (reported as g/100 g or g/t), CiA is the mass fraction of i in the considered altered sample, CiO is the mass fraction of i in the protolith (sample RB10), and MFx = CAl2O3O/CAl2O3x. The MFx factor is the ratio between the mass fraction of Al2O3 in the protolith and that of Al2O3 in a given sample x, as Al2O3 has been determined as quasi-immobile. Compositional data and results of mass transfer calculations are reported in the ESM Tables S6 and S7.

Results

Field data

The Bisciarelle thrust (44°36′05″ N, 8°47′03″ E, Fig. 2) strikes NE-SW and outcrops for about 100 m close to the transitional contact between serpentinized lherzolite and serpentinite. It dips to the W-SW at c. 20–25°, and has a top-to-NE sense of shear (Fig. 3a). The serpentinized lherzolite of the hanging wall has a thickness of more than 10 m, but it is visibly altered close to the contact for a thickness of about 4 m. The fault has a measured thickness of c. 16 m and is made of a number of distinct lithologies (Table 1, ESM Fig. S1-S6). Its true thickness is higher considering the lack of exposure of the footwall lherzolite.

The hanging wall serpentinite schists contain three poorly coherent and intensely foliated domains located at about 1, 2.8, and 3.8 m from the fault core. Closer to the fault contact, a system of extensional carbonate veins develops along the schistosity of the altered rock (Fig. 3a; ESM Figs. S1-S2). They strike mostly sub-parallel to the fault, are up to 2–3 cm in thickness, and dip gently to the NW. The 50-cm-thick visible alteration halo is made of an emerald green to reddish-brown, dolomite-serpentine schist that grades into the outer serpentinized lherzolites. This rock is intensely foliated, shows millimetric bands, and its reddish-brown color increases in intensity towards the fault contact, suggesting a coeval development of fault deformation and protolith alteration.

The fault rocks that are adjacent to this gouge show transitional or sharp contacts, and make a complex architecture (Table 1). They are a sequence of (a) cataclasites/ultracataclasites in which serpentinite clasts are set in a crystalline carbonate-rich matrix; (b) hydraulic (cf. Jébrak 1997) and cockade (cf. Genna et al. 1996) breccias made of angular serpentinite clasts set in a carbonate matrix; (c) carbonated serpentinite gouge and saponite-bearing duplex structures; (d) spherulite-bearing zones associated with chalcedony veins and massive and cohesive limestone. The thickness of these fault rocks varies between 20 cm and 3 m, and the clay-rich gouges and duplex structures are located at several positions in the fault architecture.

Towards the footwall, the fault rocks grade into veined serpentinite in which patches of foliated, altered, and brownish schists alternate with patches of less altered serpentinite. Randomly oriented, carbonate-chalcedony extension veins having a thickness of few centimeters and cutting the schistosity, combined with the presence of thin, sigmoidal shear zones, show that this serpentinite represents the footwall damage zone of the thrust fault, and not the undeformed protolith. The lack of footwall protolith makes the evaluation of the true thickness of this damage zone difficult.

The most peculiar rocks of the Bisciarelle fault are two gently dipping dolomitic spherulite-bearing zones, which are c. 70 and 20 cm in thickness, discontinuous along strike (Fig. 3a, ESM Fig. S1b), and in sharp contact with the emerald-green saponite gouge. The spherulites (Fig. 3c, d) are distinctly round and have a concentric texture and are set in a porous, fine grained but crystalline matrix. Chalcedony shear veins have a maximum thickness of 15–20 cm, a milky color, and show a banded textures. They may crosscut the spherulite zones; however, the evidence that individual spherulites are cut by — but also overgrow — chalcedony indicates that spherulite growth was essentially coeval with shear deformation.

Protolith petrographic data

The unaltered lherzolite protolith (Fig. 4a, b) shows a typical orthopyroxene, clinopyroxene, olivine, serpentine, rutile, and ilmenite assemblage. Distinct textural domains are identified, i.e., those in which ortho- and clino-pyroxenes are partially replaced by serpentine from the edges and the cleavage planes (Fig. 4a), domains made of serpentine with mesh textures and olivine core (Fig. 4b), and serpentine-rich domains with bastite texture after ortho- and clino-pyroxene replacement. Serpentine occurs also in secondary veins that cut all the previous textures.

Fig. 4
figure 4

Characteristic textures of the hanging wall protolith at distinct distance from the fault contact. a Sample RB10. Clinopyroxenes replaced by serpentine along the crystal edges, with olivine remnants and secondary serpentine veins that cut all the previous textures (cross-polarized light). b Sample RB10. Serpentine mesh texture with olivine core (cross-polarized light). c Sample RB7. Remnants of pyroxenes rotated along the foliation (cross-polarized light). Extensional antitaxial carbonate vein develop parallel to the foliation. d Sample RB6. Serpentinite with shear zones marked by aggregates of subhedral dolomite and abundant euhedral rutile-ilmenite aligned along the foliation (reflected-light). e Sample RB4. Mylonitic texture formed by serpentine microlithons set within a network of microcrystalline carbonate veins, which are present along the schistosity (cross-polarized light). f Sample RB2. Serpentinite gouge in which angular to sub angular clasts are set within a serpentine matrix (cross-polarized light). The oxides bordering the serpentine clast armor the clast. Mineral abbreviations follow Whitney and Bernard (2010)

At a distance of 6–7 m from the fault contact there is a transition from lherzolite to serpentinite and serpentinite schists. The serpentinite shows a foliation boudinage, along which most of the minerals are oriented. Remnants of ortho- and clino-pyroxenes are rotated along the foliation (Fig. 4c), and so are ilmenite, rutile (Fig. 4d), and newly formed extensional antitaxial carbonate veins (Fig. 4c, up to 0.2 mm in thickness). In this part of the host rock, the modal abundance of ilmenite and rutile increases considerably.

Between about 6.5 and 3 m from the core (RB7-RB4, cf. Fig. 3b), the serpentinite develops a penetrative foliation similar to a mylonitic texture. Serpentine microlithons alternate with a thin network of authigenic microcrystalline carbonate (Fig. 4e), and ortho- and clino-pyroxenes of the metaperidotite are almost completely replaced by serpentine. In this part of the external zone, the microtextural characteristics of the schists are progressively turned into those of a fault gouge. At a distance of c. 1 m from the fault zone contact (RB2, Fig. 4f), the rock becomes a non-cohesive aggregate of angular to sub-angular serpentine clasts. The clasts preserve an intense internal foliation, along which dolomite is associated to rutile, ilmenite, and minor pyrite.

The rock immediately adjacent to the fault core (RB1) is a poorly coherent carbonate zone. It is a cataclasite in which fine-grained, sub-angular to well round, randomly oriented dolomite grains are surrounded by saponite, which forms a dark felt around the dolomite. The foliation of this rock is visible at the meso-scale but is lost at the microscale, as only few dolomite veins mark it. Carbonate veins are randomly oriented, up to 0.3 mm in thickness.

Mass transfer in the damage zone

The chemical composition of the protolith lherzolite (sample RB10) is mostly indistinguishable from that of typical lherzolite of the Voltri Massif (Fig. 5). This is shown mainly by the ratios of the major components (e.g., Al/Ca), which preserve a mantle signature and are identical to those measured in other meta-peridotites (cf. Scambelluri et al. 2001). As a whole, the chemical composition of the undeformed protolith is therefore that of a lherzolite.

Fig. 5
figure 5

Mass fractions of major and minor components of lherzolite RB10 vs. mass fractions of the corresponding components of a typical serpentinized lherzolite from the Erro-Tobbio area (data from: Scambelluri et al. 2001, their Table 1). Mass fractions are scaled to avoid the clustering of data points close to the origin of the axes. The line y = x is independent from the plotted dataset, and shows the good correlation between the bulk composition of the distal lherzolite of Bisciarelle and that of typical lherzolites of Erro-Tobbio. Among the analyzed components, those that do not follow the correlation are Zr and Ce. In sample RB10, Zr mass fraction (85 µg/g) is two orders of magnitude higher than that of the typical lherzolites, and Ce (0.18 µg/g) is three times higher. These features are explained by interaction between the rock and the fault fluid, which introduced the two components within the rock

In the multisample, immobile element analysis carried out here (Fig. 6), we make the hypothesis that the mineralogical and chemical modification of the protolith took place during one event of interaction with the fault fluid. This model is justified by the evidence for the unaltered lherzolite being turned progressively into a serpentine-carbonate-ilmenite-rutile schist (Fig. 4ce) and a serpentinite-saponite fault gouge close to the fault.

Fig. 6
figure 6

Multisample immobility trends of a group of major, minor, and trace components of the 10 protolith samples. a Theoretical immobility trends for two components of a hydrothermally altered rock. These components (A and B: major, minor, or trace) are immobile when their concentration ratio, measured in various samples of the block, is constant. This is shown by an x–y scatter plot in which the mass fractions of A and B plots along a line. bi Scatter plots of rock components of the RB10-RB1 sample set. The numbers next to each symbol identify the RBx sample of the profile

Binary compositional plots show that major, minor, and trace components of RB10-RB1 form irregular trends in most cases, i.e., they have variable compositional ratios. This feature is clearly shown by Fig. 6b, e, and f, in which the mass fractions of SiO2, MgO, and Fe2O3 are plotted against those of Al2O3. Lack of linear trends connecting with the origin for the Al2O3-SiO2, Al2O3-MgO, and the Al2O3-Fe2O3 pairs implies that they were mobile during hydrothermal alteration (cf. Garofalo 2012). Mobility is shown also by CaO (Fig. 6d) and by the majority of minor and trace elements. Interestingly, the pairs Al2O3-SiO2, Al2O3-MgO, and Al2O3-Fe2O3 show trends that correspond quite systematically to large changes in Al2O3 concentrations without corresponding changes in SiO2, MgO, and Fe2O3 concentrations. The only sample not following such trend is RB1 from the saponite-bearing gouge. In contrast, the Al2O3-LOI (Fig. 6c), Al2O3-W (Fig. 6h), Al2O3-Sb, and Al2O3-Sr pairs show trends that plot systematically above the immobility line on the bulk gain side of the diagram. These trends indicate that the mineralogical and chemical modification of the damage zone took place during removals and additions of SiO2, MgO, and Fe2O3 from neighboring portions of the host lherzolite, and during substantial addition of CO2, H2O, W, and Sb from an external fluid. Hence, only a small number of chemical components were consistently added to the host lherzolite by the fault fluid.

Importantly, only Al2O3, TiO2, Y, V, Sc, and heavy REEs show mass fractions that co-vary approaching linear trends. This implies that during hydrothermal alteration, only a handful of chemical elements remained immobile. This is exemplified by the Al2O3-TiO2 (Fig. 6g) and Al2O3-Y (Fig. 6i) plots, which show that a decrease or increase of Al2O3 concentration in the rock was coupled with a proportional decrease/increase of Y and TiO2, respectively. The Al2O3, TiO2, and Y concentrations in RB1-RB10 do not follow exactly a path of progressive increase/decrease. We interpret this as a product of both local mass losses and gains occurring in neighboring sections of the protolith.

Clear departures from immobile behavior are shown by the RB1-RB3 samples at 1–2 m from the fault contact (Fig. 6i). Such departures are explained mostly by the increased abundance of mode-I carbonate veinlets (Fig. 3b, ESM Fig. S2), which correspond to a bulk mass addition from an external fluid during fracturing and mineral precipitation (Reed 1997).

The computed mass transfers based on the evidence for Al2O3 immobility identify the rock components that were gained or lost by a unit mass of lherzolite protolith during fluid-rock interaction. The flat profiles lying on the zero-mass-change line show that the protolith did not experience significant mass transfer during deformation up to c. 10 m from the fault contact. This is the protolith showing clinopyroxene and mesh texture in olivine (Fig. 4ab). Starting from a distance of about 8 m from the contact, the protolith records significant chemical and textural modifications. This is the interval in which SiO2 (Fig. 7a), MgO (Fig. 7d), Fe2O3 (Fig. 7f), CaO (Fig. 7b), and LOI (Fig. 7c) show significant coupled transfers from the fluid to the rock. The sharp gains in SiO2, MgO, and volatiles correspond to the formation of serpentine at the expenses of olivine and pyroxene due to dissolution–precipitation reactions, and the gains in CaO and volatiles correspond to the formation of carbonate veinlets (Fig. 4bc). These gains are quantified between 60 and 140% of the protolith values, and are the best estimate of transfers from the fault fluid to the damage zone. Similar gains are shown also by Sb and W (Fig. 7g, h). This transition between the unaltered and serpentinized/foliated protolith is considered the boundary between the damage zone and the relatively intact protolith. Interestingly, the mass transfer data show that this alteration halo is unlike a listwanite alteration due to the lack of significant K mass transfer in the rock (Halls and Zhao 1995).

Fig. 7
figure 7

Calculated mass transfer profiles of the Bisciarelle fault. The sketches on top of the profiles show the schematic architecture of the fault and its typical fabric, and allow correlation with the calculated profiles

The change of mass transfer regime at ca. 2–3 m from the fault contact corresponds to a fault section in which the network of carbonate veinlets is denser, in which several intensely foliated serpentine domains form, and includes the 0.5-m-thick, carbonated saponite-bearing gouge (Table 1, Fig. 3b; Fig. 4f). These transfers should be considered as semi-quantitative due to the difficulty to calculate mass transfers close to the fault. In these rocks, CaO and volatiles are probably gained substantially (we calculated at a proportion > 100% of protolith mass), whereas SiO2, MgO, Fe2O3, Cr, and Ni show limited mobility. Significant mobility is shown only by Sb (Fig. 7g), Sr, alkalis (Fig. 7e), and in part W (Fig. 7h), which are gained by the rock.

Spherulite zones

Petrographic data

Spherulite zones are made of dolomitic spherulites set in a vuggy, fine-grained matrix (Fig. 3c, d; Fig. 8ac). Individual spherulites are typically not in contact with each other. Morphological analysis demonstrates that large and small spherulites have surprisingly high roundness and circularity, and have an average diameter of 0.5 cm (ESM Fig. S7). A circular shape in found in sections cuts orthogonal and parallel to the slickenlines, indicating that spherulites formed without a preferred orientation with respect to the top-to-NE shear direction of the fault. Single-spot SEM–EDS analyses show that the dolomite has consistently a ferroan dolomitic composition.

Fig. 8
figure 8

Characteristic textures of the spherulite zones. a Transmitted light photomicrograph of large spherulite with carbonatic core and several concentric bands. b Photomicrograph (transmitted light) of small spherulite with a core is made of a carbonated serpentinite fragment. c Vuggy chalcedony cementing a group of spherulites. d SEM-BSE image of the tips of dolomite crystals from a spherulite band terminating with aggregates of chalcedony spheres, one of which contains a dolomite clast. e Photomicrograph (plane polarized light) of a moss recrystallization texture shown by the chalcedony of the spherulite matrix. This texture is made of a round silica core and abutting, radial, and fibrous quartz crystals. f Flamboyant textures made of fibrous and radial chalcedony

Spherulites with a diameter of < 2–3 mm are massive, but larger ones may host up to 9 mm thick and show fibrous layers (Fig. 8a). These layers show densely branched dolomite crystals that grow one onto the other from the core, and alternate regularly with dark massive layers having up to 2 mm in thickness. Spherulite cores cane be made of altered protolith clasts (Fig. 8b), fragments of fault core breccias, or relicts of carbonated serpentinite clasts. Concentric growth is evident at the meso- micro-scale and show successive layers that depart radially from the cores. Dolomite crystals grow out of the cores without a crystal preferred orientation and terminate abruptly onto the thin, dark layers. In places, delicate spherical aggregates of chalcedony grow attached at the terminations of the dolomite crystals of the spherulite zones (Fig. 8d). Radial growth from the inner core is a strong indication of epitaxial growth (e.g., Pashley 1975), and the arrangement of chalcedony spheres and dolomite crystals indicates undisturbed, hetero-epitaxial growth (Gibson 1988). This demonstrates that the spherulites did not grow competitively in contact with each other.

The chalcedony found in the matrix between the spherulites shows several textures, all of which are typical of open space filling (Moncada et al. 2012, and ref. therein). They are moss (Fig. 8e), fibrous radial, flamboyant (Fig. 8f), and wall lining with central jigsaw textures.

A number of observations shows that, in some places, spherulitic growth in the zones was interrupted by events of cataclasis and micro-brecciation along some secondary slip surfaces (Fig. 8a). These formed angular to sub angular clasts, which were subsequently recycled as nuclei by following episodes of spherulite growth. Also, carbonate shear zones are found within individual spherulite zones. They are smooth and in general do not crosscut spherulites. The chalcedony shear veins (Fig. 3d) crosscut spherulite zones, but they also overgrow them. This indicates that spherulite formation was essentially coeval with shear deformation. Millimetric breccia veins made of angular to sub-angular carbonate clasts set in chalcedony and quartz matrix are also present.

Laser Ablation-ICP-Time of Flight Mass Spectrometry

We determined the chemical compositions of spherulite zones and chalcedony by combining line scan analyses of a spherulite by LA-ICP-TOFMS (Fig. 9) with multi-element LA-ICP-TOFMS imaging of a 1 cm2 area of a spherulite sample (Figs. 10 and 11). Both datasets confirm the single-spot SEM–EDS analyses showing relatively constant Ca and Mg mass fractions within the spherulites; however, they reveal a number of minor and trace components whose mass fractions co-vary significantly together with Ca and Mg. The line scan profile of the spherulite shows flat Ca and Mg mass fractions across the dolomitic layers that decrease significantly across the thin, massive layers (layers 1, 2, 3 of Fig. 9a, b). Such decrease is mostly coupled with a significant increase in the mass fractions of Fe (Fig. 9c) and a number of trace components (Al, Mn, Cr, Cu, Sb). These coupled variations suggest that the mineralogical composition of the dark thin layers is made of dolomite and a mixture of other phases, but the relative proportion of dolomite is low due to the concomitant deposition of microcrystalline quartz and oxides (Fig. 8ac). Thus, the thin-massive layers represent stages of spherulite formation in which the epitaxial growth of dolomite was interrupted by the precipitation of a number of metal-rich phases. The evidence for alternation of these deposition stages show that the formation of epitaxial dolomite layers and massive, metal-rich layers repeated cyclically.

Fig. 9
figure 9

Compositional profile of a dolomitic spherulite along a 2670-mm-long LA-ICP-TOFMS line scan. a Reflected light photomicrograph of the analyzed spherulite after completion of line scan (i.e., 534 adjacent laser pulses). Numbers mark the positions of five thin, massive bands of the spherulite. The levels marked with dark bands are those of dolomitic composition. Thin fractures occur at the core of the spherulite and cause scatter of compositional data. b, c Mass fractions of Ca, Mg, Fe, and Si plotted as a function of position in the line scan. In c, the ranges of Si and Fe mass fractions are plotted in different scales and at opposite sides of the panel. d Mass fractions of Au in the spherulite plotted as a function of position in the line scan and compared with the determined LOD. The majority of measurements give Au mass fractions below the LOD (ca. 160 ng/g), but 37 analyses give mass fractions comprised between c. 250 ng/g and 3.5 µg/g

Fig. 10
figure 10

Laser ablation-ICP-TOFMS elemental images of a selection of major, minor, and trace components of a spherulite zone and adjacent chalcedony vein. The numbers at the side of the maps show the dimensions of the scanned area, and the color codes correspond to either wt% oxide or µg/g mass fraction units. The false-color scale of all elemental images span ranges from LOD wt% or µg/g to 99.5% of the maximum value: this scaling provides best image contrast and encompasses most of the mass fraction range

Fig. 11
figure 11

Laser ablation-ICP-TOFMS elemental images of a selection of trace components of a spherulite zone and adjacent chalcedony vein (cf. Figure 10)

In the line scan analyses, Cr, Cu, Rb, Sb, Cs, Ce, Au, and U show mass fractions that are close to the corresponding LODs. These components were determined in a relatively low number of analyses (between c. 10% and 30% of the 534 laser spots across the profile). One of these is Au, which has concentrations within the 0.16–3.5 µg/g range (Fig. 9d). The spatial distribution of Au does not show a systematic occurrence within the dolomite or metal-rich layers. This suggests that Au could be present as micro- (or possibly nano-) inclusions. The high Au mass fractions measured at the end of the scan line profile do not necessarily correspond to spherulite Au, but could set within the microfractures that crosscut the core (Fig. 9a). The high Sb, Co, W, Zn, and Cu mass fractions measured in the same region of the sample are a characteristic of the spherulite banding.

Element imaging by LA-ICP-TOFMS provides a detailed account of the mass fractions of elements within spherulites, matrix, and chalcedony shear veins (cf. Gundlach-Graham et al. 2018; Neff et al. 2020) which provides a gamut of chemical data and a unique complement to mineralogical and petrographic documentation. One striking feature of Figs. 10 and 11 is the presence of a 1-mm-thick fragment of microbreccia at the contact between the spherulite zone and the chalcedony shear vein. This fragment is clearly highlighted by the distribution maps of SiO2, CaO, MgO, FeO, MnO, Na, and Sb (Fig. 10), but is less evident in the petrographic photomicrographs (e.g., Fig. 8a).

The thin concentric texture of the large spherulites generates a systematic spatial distribution of major, minor, and trace elements. The thin and massive layers are consistently enriched in Mn, Sr, Co, Pb, Cs, Cr, Y, Ni, Cu, and to a minor degree in SiO2 and Al2O3, with respect to the thicker and fibrous dolomite layers, which show only higher mass fractions of FeO (Fig. 10) and W (Fig. 11). The chemical composition of the fine-grained spherulite matrix reflects the texture of its constitutive dolomite and chalcedony. Its most important minor and trace components are FeO, Al2O3, Sr, Cr, and Cs. Sodium, Cu, Sb, Pb, and U show distinctly higher mass fractions within the matrix.

The chalcedony shear veins host a number of minor and trace components that are disseminated and therefore either replace Si or are inclusions within the solid. The most abundant are Na2O and Al2O3 (Fig. 10), but Cr, Co, Pb, Y, and U are present with a lower range of mass fractions. We highlight in particular the 4–18 μg/g range of Sb, which is one of the elements that are gained by the fault protolith (Fig. 7g). The REEs mass fractions are mostly < 2 μg/g in chalcedony (e.g., Ce, Fig. 11), and are at least one order of magnitude higher than those of spherulites and matrix.

Discussion

Our data confirm previous works carried out in the Lavagnina Lakes area concluding that the brittle RSZ2 faults hosted the Au deposits of the district (Capponi and Crispini 2002; Federico et al. 2009; Giorza 2010; Spagnolo et al. 2007). Our data provide however a set of additional constraints on the fluid-fault interaction processes.

Permeability structure of the bisciarelle fault zone

At Bisciarelle, both hanging wall and footwall protoliths show carbonate extension veins that are typical of damage zones (e.g., Caine et al. 1996). Spherulite zones, cockade, and hydrothermal breccias are fault rocks that must have developed under conditions of tensile hydraulic fracturing, i.e., at conditions at which Pf ≥ σ3 + To, where Pf: fluid pressure; σ3: least compressive stress, and To: tensile strength of the rock (Cox et al. 2001). These conditions must have generated high permeability in the damage zone, consistent with the intense hydration and carbonation shown by the mass transfer calculations. This fault section developed probably in a tensile overpressure state (Sibson 2017), which in shallow compressional settings like that of Bisciarelle in which σ3 = σv is close to lithostatic.

Considering the measured thickness of the fault rocks (Table 1) and the conceptual model of Caine et al. (1996), we calculate that the maximum ratio between the damage zone width and the total fault width (architectural index) was equal to about 0.6. This value is expected in transmissive faults that develop within clastic rocks dominated by damage zones, in which deformation is accommodated within localized cataclasites and aquitards are sandwiched between aquifers (Caine et al. 1996). Such value must be considered a maximum estimation because of the impossibility to measure in the field the entire fault thickness. Hence, gouges, cataclasites, and ultracataclasites localized the shear strain in the Bisciarelle fault, but spherulite zones and breccias constituted the most transmissive segments.

Fault fluid and spherulite growth

The TP conditions at which deformation took place in the fault cannot be exactly constrained with the data presented here due to the lack of direct geothermometric and geobarometric constraints. However, we follow Giorza (2010) in the hypothesis that the H2O-CO2 fluid inclusions (XCO2: 0.02–0.03) in the vein Fe-dolomite, magnesite, pyrite, sphalerite, chalcopyrite, and galena (type II veins of Giorza) are representative of the RSZ2 faults. For these inclusions, the entrapment conditions were estimated at 250–300 °C and 7.5–15 MPa.

The spherulite genesis is an intriguing aspect of the structural history of the Bisciarelle fault because is rare in upper crustal faults. The high roundness and circularity, the close packing, the evidence for undisturbed epitaxial growth, the rhythmic and concentric texture, and their porous and open-space-filling matrix make the spherulites similar to epithermal sinters (Hamilton et al. 2019). We interpret this to indicate that the spherulite zones formed during a combination of dilatation and top-to-NE shearing (hybrid fault failure) at conditions in which the differential stress and Pf satisfied 4 < (σ1 − σ3)/To < 5.66 and Pf ≥ σ3 + To, respectively. This process must have been cyclic and geologically fast.

Experimental data show that spherulite growth is a fast and non-equilibrium process that is generated by a highly supersaturated fluid (Gránásy et al. 2005; Rodriguez-Blanco et al. 2017). Spherulitic growth proceeds via nucleation of new particles onto a core via non-crystallographic branching, following a process that is called growth front nucleation (Gránásy et al. 2005). The round, densely branched spherulites of Bisciarelle belong probably to the sphere category of spherulites (Rodriguez-Blanco et al. 2017), for which fast crystallization under high fluid supersaturation is proven experimentally (Andreassen et al. 2010).

Notably, fast growth rates were probably not exclusive of spherulite zones, but occurred also in cockade breccias (ESM Fig. S3, Table 1). Cockade breccias are peculiar rocks proposed to form in suspension within a hydrothermal fluid during cycles of seismic failures of faults (Berger and Herwegh 2019). These rocks share some characteristics with the spherulites because they show concentric banding around central clasts, open-space filling textures, and sharp boundaries separating clasts and matrix (Frenzel and Woodcock 2014). However, a fundamental difference is that spherulites have small cores (Figs. 3d; 8c, 9a, 10). Also, they lack geopetal indicators, have nearly spherical shapes, and are closely packed with a small volumetric proportion of matrix. These features suggest that while the cockade breccias form after brittle rock failure, disintegration, suspension in a jet of hydrothermal fluid, settling, and agglutination during the interseismic period (Berger and Herwegh 2019), the spherulite zones likely record a shorter sequence of events. They probably grow under a fast, sustained hydrothermal flow that keep them and other clasts in suspension. The evidence for spherulite brecciation and shearing (Figs. 3d and 10) and for brecciated rock fragments at the core of spherulites (Fig. 8b) suggest that episodes of shear deformation and brecciation preceded and followed spherulite formation.

The LA-ICP-TOFMS elemental imaging provides constraints on the mobility of various metals at the time of fluid-fault interaction. Calcium, Sb, W, Sr, and Na are the major and trace constituents of spherulites and matrix (Figs. 10, 11). These components are those that were added in various proportions to the rock during hydrothermal alteration (Fig. 7), indicating that faulting and fluid-mineral equilibria controlled their transfer from the permeable segments of the fault to the protolith. Gold was probably also one of such metals, as the evidence for its determination within the spherulite (0.16–3.5 µg/g, Fig. 9), coupled with its concentration systematically below the LOD of the protolith (2 ng/g), indicate that its mobility was restricted within the fault.

Dolomite supersaturation in the fluid must have constrained the genesis of the spherulite zones. We propose that the following simultaneous equilibria provide sufficient constraints on dolomite precipitation:

$$\mathrm{CaMg}({\mathrm{CO}}_{3}{)}_{2}\rightleftharpoons {\mathrm{Ca}}_{\left(\mathrm{aq}\right)}^{2+}{\mathrm{Mg}}_{\left(\mathrm{aq}\right)}^{2+}+{{2\mathrm{CO}}_{3}}_{(aq)}^{2-}$$
(1)
$${\mathrm{CO}}_{2(\mathrm{g})}\rightleftharpoons {\mathrm{CO}}_{2(a\mathrm{q})}$$
(2)
$${\mathrm{CO}}_{2(aq)}+ {\mathrm{H}}_{2}{\mathrm{O}}_{(aq)}\rightleftharpoons {\mathrm{HCO}}_{{3}_{(aq)}^{-}}+{\mathrm{H}}_{(aq)}^{+}$$
(3)
$${\mathrm{HCO}}_{{3}_{(aq)}^{-}}\rightleftharpoons {{\mathrm{CO}}_{3}}_{\left(aq\right)}^{2-}+{\mathrm{H}}_{(aq)}^{+}$$
(4)

Important constraints coming from (1) are that dolomite solubility is retrograde with respect to temperature (Fig. 12a), but increases with increasing pressure (Fig. 12b). Thus, a dolomite-saturated fluid at a given T would precipitate dolomite if it is heated or if it decompresses. We conclude that fluid decompression during a combination of dilatation and shearing of the fault could have been one factor controlling dolomite deposition at Bisciarelle.

Fig. 12
figure 12

Dolomite solubility and processes potentially controlling dolomite precipitation. a Experimentally determined solubility of dolomite shown as a function of Mg molality in a H2O-NaCl-CO2 solution (from: Bénézeth et al. 2018). Points are measured solubilities and curve is a best-fit. b Dolomite solubility in pure water calculated as a function of fluid pressure and at 100 and 150 °C (from Li et al. 2018). c Experimentally determined mole fractions of Ca2+ and Mg2+ ions in solution in equilibrium with dolomite + magnesite and dolomite + calcite at T between 275 and 420 °C (from Rosemberg and Holland, 1964). mCa2+ and mMg2+ are the molal concentrations of the Ca2+ and Mg2+ ions in solution, respectively. The grey rectangle marks the required fluid composition of the Bisciarelle fluid. d Predicted solubility of aqueous silica in equilibrium with quartz and a H2O-NaCl-CO2 fluid expressed as a function of CO2 concentration and at low-T hydrothermal conditions (modified from: Akinfiev and Diamond, 2009). The solubility is only qualitatively shown because no experimental data are available at 250–300 °C and low P

A second factor that controlled the precipitation of dolomite in the fault fluid was the Ca/Mg concentration ratio. Experimental data (Rosenberg and Holland 1964) show that in the 250–300 °C interval, dolomite would precipitate from a fluid having mCa2+/(mCa2+  + mMg2+) comprised between about 0.72 and 0.94 (Fig. 12c). This is a broad range, which the hydrothermal fluid of Bisciarelle probably met during its flow despite the compositional changes triggered by the mass transfers with the protolith (Fig. 7b, d).

A third factor that controlled the deformation history of the fault must have been the partitioning of CO2(aq) into the vapor phase of the fluid as CO2(g) (effervescence, or boiling), as described by reaction (2). This partitioning is quantified by the volatility ratio, which is calculated as (Drummond and Ohmoto 1985):

$$\mathrm{VR }= {m}^{V}/ {m}^{L}$$

where mV and mL indicate the molality of the gas species in the vapor and liquid phases, respectively. Between 250 and 300 °C, VR decreases from about 107 to 65, showing that irrespective of the T at which dolomite precipitation took place reaction (2) was driven to the left and that an abundant vapor phase must have been present within the fault. We conclude that at least part of dolomite precipitation at Bisciarelle took place as a result of effervescence of CO2(g) from the aqueous fluid experiencing decompression during hybrid opening of the fault. Depending on the starting T, effervescence must have suddenly decreased proton concentration in the fluid by one or more orders of magnitude. As a consequence, this could have driven reactions (3) and (4) to the left, which forced also equilibrium (1) to the left. Effervescence was probably able to cause dolomite precipitation effectively, probably after only 4–5% of exsolution (Drummond and Ohmoto 1985). This process is conceptually similar to that described for the precipitation of hydrothermal calcite in geothermal systems governed by boiling (Simmons and Christenson 1994).

A final aspect to consider in this model is the silica deposition. Hydrothermal silica deposits are typically formed by boiling solutions (Hedenquist et al. 2000) in a proportion that depends on the fraction of the vapor phase at the given temperature. The occurrence of chalcedony veins that are broadly coeval with the spherulites at Bisciarelle, as well as evidence of chalcedony cementing the spheruliltes, suggests that phase separation could have controlled silica precipitation as well. Experimental data and theoretical considerations for high T hyrothermal fluids show that the addition of CO2 in aqueous electrolyte solutions decreases silica solubility considerably, and this tendency increases as a function of CO2 concentration (Akinfiev and Diamond 2009). In the hypothesis that this process controlled silica solubility also at Bisciarelle (Fig. 12d), the CO2-rich fluid could not transport large amounts of silica in solution. However, after phase separation and spherulite formation, an equilibrium shift to the left of (2) must have caused a rapid increase of silica solubility. This increase allowed deposition of chalcedony in veins and matrix. Because the silica deposited by effervescence was the product between the saturation solubility at 250–300 °C and the fraction of water partitioned to the vapor phase (Drummond and Ohmoto 1985), only a proportion of the total silica available in solution formed the chalcedony veins and spherulite matrix.

Constraints on Au deposition in the Lavagnina Lakes

Our model of the structural evolution of the spherulitic zones of Bisciarelle implies that the damage zone of the fault was the most relevant for hydrothermal fluid flow. This flow occurred during cycles of Pf build-ups, fault opening, and fluid flushing. Such process must have been fast to allow growth front nucleation of the spherulites and was similar to that described by Sibson et al. (1988) for the fluid-activated valve model. Considering these characteristics, Bisciarelle is an example of epizonal orogenic vein (Goldfarb and Groves 2015).

Lack of appropriate outcrops due to exploitation and limited mine documentation complicate a comparison between Bisciarelle and the historical deposits of the Voltri area. However, the evidence for thick carbonate alteration haloes still visible in the field along the historical outcrops (Fig. 2) suggests that the Au deposits of the area were probably highly permeable faults that experienced intense mass transfer with the ultramafic protolith, similar to what is shown at Bisciarelle. Also, previous studies on orogenic vein textures documented a “spherular” growth of vein quartz of the Voltri deposits (Herrington and Wilkinson 1993, their Fig. 3), suggesting an important similarity with the Biscarelle fault. This implies that a crystallization process similar to the spherulitic growth described in this study could have occurred in the other veins of the network.

The spherular texture was interpreted as a product of crystallization of a pristine amorphous silica, which subsequently recrystallized into quartz, and the presence of a thermodynamically stable form of colloidal Au was postulated in the hydrothermal fluid (Herrington and Wilkinson 1993). Such hypothesis contrasts with the evidence for Au being found mostly as small millimetric nuggets within sulfide (Pipino 1976), which rather indicate that in these deposits Au was transported mainly by sulfide complexes (Seward et al. 2014). However, the detection of Au within the dolomitic spherulites (Fig. 9d) shows that this metal was not transported solely by sulfide complexes, and that additional species must have been stable in the Bisciarelle fluid. These species could be the colloidal Au species, which have been proven to form in quartz-carbonate veins of epithermal deposits as a result of strong decompression and vigorous boiling (McLeish et al. 2021). The formation of such species at the conditions described at Bisciarelle confirms indirectly the model presented here. However, it is unlikely that colloidal species transported significant amounts of Au in the entire vein network of the area.

In addition to the geological and textural similarities between Bisciarelle and the neighbor deposits, fault mineralogy suggests some relevant differences. Bisciarelle was an Au-poor fault of the network made of dolomite, chalcedony, and Mn-Sr oxides, while the historical deposits were Au-rich faults made of a dolomite, magnesite, quartz, chalcedony, and sulfides-sulfosalts (pyrite, chalcopyrite, pyrrhotite, sphalerite, galena, and tetrahedrite). These distinct assemblages suggest that the ore deposits were generated by a H2S-bearing ore fluid capable to transport higher concentrations of Au. Thus, Bisciarelle could represent a segment of a larger fault network that developed from a distinct batch of fluid. This segment was presumably isolated or poorly interconnected with the other segments, similar to what shown in other orogenic deposits (Garofalo et al. 2002).

Conclusions

The Bisciarelle fault and the neighbor Au deposits are an example of damage zone-dominated, permeable upper crustal fault zones that experienced an intense interaction with a hydrothermal fluid and that modified substantially their fault rocks and protolith. The final product of such interaction are fault zones whose architectures, textures, and compositions differ substantially from those of typical upper-crustal zones in which cataclasis and comminution take place in fluid-poor conditions. These characteristics are probably typical of epizonal orogenic deposits.

A first result of our work is that the coupled study of protolith alteration and faulting processes defines a coherent dataset that is useful to define the chemical and mineralogical modification of a protolith, the fault architecture, and the genesis of fault-hosted mineralizations. We show that the mineralogical and chemical compositions of fault rocks and wallrock may depend critically on which — and to which degree — chemical components are transferred from the fault fluid to the protolith (and vice versa) during deformation.

The mechanism of spherulite growth is probably a unique process. Our proposed fast spherulite formation via growth front nucleation, which involves a CO2-rich effervescing hydrothermal fluid, implies a close association between spherulites and fault activity and supports the hypothesis that they are syn-kinematic. However, spherulites are new in the geological record, and so is the possibility that hydrothermal fluids within faults may generate undeformed growth structures. The poor documentation of spherulites in field studies suggest that they are either rare, or alternatively, that they received relatively less attention.