Mineralogy, Geochemistry and Genesis of Zeolites in Cenozoic Pyroclastic Flows from the Asuni Area (Central Sardinia, Italy)

Natural zeolite occurrences have been recognized in several Cenozoic pyroclastic deposits in central Sardinia. This study concerns the mineralogical and geochemical characterization of the zeolitized tuffites in the Asuni area (Oristano province) and aims to complement information regarding the zeolitization processes developed in the nearby Allai deposits. Optical and scanning electron microscopy, X-ray powder diffraction, qualitative vs. quantitative microanalyses and bulk-rock geochemistry were performed. Analytical results allow defining the mineral distribution, textural relationships and geochemical features of the zeolite-bearing rocks. The most abundant secondary minerals are Ca-Na mordenites. Contrarily to the most common worldwide clinoptilolite + mordenite paragenesis, mordenite is dominant and occurs in different morphologies, rarely coexisting with clinoptilolite in the studied volcanic tuffites. Glauconite and dioctahedral smectite complete the authigenic assemblages. The primary volcanic components mostly include plagioclase, quartz and glass shards, roughly retaining their original appearance. The tuffites range in composition from dacite to rhyolite. The collected dataset shows that zeolitization is most abundant in coarser-grained deposits and points to a genetic process that mainly involves an open hydrothermal environment governed by aqueous fluids with significant marine component, in post eruption conditions.

Natural zeolites have a peculiar framework structure characterized by channels and cages among the oxygen atoms linking the constituting SiO4 and AlO4 tetrahedra. These cavities have molecular-sizes and are usually occupied by H2O molecules and extra-framework cations [14], resulting in selective properties for circulating substances on dimensional and charge basis.
Here, we focus on the Asuni area, central Sardinia, in order to (1) complete the mineralogical characterization of zeolitized deposits in the province of Oristano, i.e., those developed in the nearby Allai area [30]; (2) propose a possible scenario involving the zeolitization process and (3) give a background for potential exploitation of natural zeolites at a regional scale.
Hence, we have investigated the Asuni zeolite-rich deposits by optical and scanning electron microscopy with energy dispersive spectrometry, X-ray powder diffraction, and bulk-rock geochemistry. We present the mineralogical results of zeolite-bearing rocks as well as their petrographic and geochemical features, with the final aim of describing the textural relationships of the main zeolite types throughout the epiclastic deposits and discussing the minerogenetic models.

Geological Background
The island of Sardinia ( Figure 1) records a long geological history with a Paleozoic basement widespread from SW to NE, dissected from the later rifting phases and the magmatism [38][39][40]. The transtensive-extensional regime followed Eocene-Early Oligocene Alpine compressive phases and caused faulting and rifting thus leading to: (i) formation of the Oligo-Miocene rift system crossing the whole island from North to South and (ii) translation southwards and counterclockwise rotation of the Sardinia-Corsica continental microplate, with coeval opening of the Balearic back-arc basin [41,42]. Based on Cherchi et al. [43] the latest Oligocene (Chattian-Aquitanian) time corresponds to a rapid deepening of the Oligo-Miocene graben. The authors showed that during the rifting stage (Aquitanian, late Miocene), a deep marine trough already existed along the graben system axis, except in areas where the volcanism was particularly important such as in central Sardinia.  [44]), showing the outcrop area of the Oligo-Miocene volcano-sedimentary succession and the studied sites. In the area, the older Variscan basement corresponds with the Nappe Zone that consists of marine silico-clastic successions equilibrated under greenish facies. Sampled sites and labels used hereafter: P, E and I for Pranu; M and N for Asuni; H and F for Pardu.
The Asuni Unit is a dominant epiclastic formation of this period. It belongs to a major volcano-clastic succession of the eastern Sardinian Rift (Fordongianus-Nureci area, central Sardinia). This volcano-sedimentary succession up to ca. 300 m [47,48] includes five pyroclastic ignimbrites. Two of them are rhyolite-rhyodacite ignimbrites of the Luzzana and Allai units, both related to highly explosive phreatomagmatic episodes. These units are lowermost in the succession, overlaid by the sedimentary episclastic terrigenous-tuffaceous complex, and, in turn, by dacite lava domes and flows. The Ruinas Unit, a poorly consolidated to welded dacite ignimbrite, up to 40m thick, starts the sedimentary succession and is buried by the Asuni Unit. This latter Unit, about 50 m thick, consists of poorly welded epiclastites with composition ranging from rhyolite to dacite. It is overlain by an epiclastic arenaceous sequence formed by erosion of previous volcaniclastic formations. The latest pyroclastic products in the area form the Monte Irone Unit, a welded dacitic ignimbrite, ca.10-20 m thick.
The rhyolitic to dacitic volcanoclastic deposits often show evidence of zeolization and welding. However, studies about zeolites in the deposits from central Sardinia, are scarce [26,27,30]. In the Allai deposits, the neoformed zeolites have been related to specific physicochemical conditions (water content, temperature) of fluids circulating in the pyroclastic flows during and just after its emplacement [30]. More information exists for zeolites in the northern Sardinia. For example, in the Logudoro region zeolitization is due to circulation of hydrothermal fluids favored by the fault systems of the area [28]. In the Anglona district, fluids were either percolating groundwaters or trapped volcanic water-gas mixtures [49]. The Bosa region was affected by syn-and postdepositional zeolitization due to the phreatomagmatic fluid components [26,50].

Materials and Methods
Our studies were conducted on a total of 25 samples, representative of the epiclastic deposits of the Asuni Unit, found between the villages of Allai and Laconi ( Figure 1).
The investigated sequences were sampled at different stratigraphic heights in seven outcrop sites (labelled H, F, P, I, E, N, and M in Figure 2), albeit stratigraphic correlation was impossible due to the absence of interbedded paleosols or discontinuities, and recognized marker levels. Sampling was based on different sedimentological and lithological appearances, in order to investigate the possible relationships between the primary volcanological features and the secondary mineral assemblages.
The samples were ground to ca. 5 mm and divided in two halves, similar for texture and lithology. The first half was used to prepare polished sections and stub-positioned portions for optical microscopy (OM), electron microscopy and microanalysis; the second one was pulverized for X-ray diffraction and whole-rock geochemistry.
X-Ray powder diffraction (XRPD) made use of a Panalytical X'Pert PRO PW 3040/60 diffractometer equipped with a pyrolitic graphite analyzer crystal at the "Istituto per i Polimeri, Compositi e Biomateriali", Centro Nazionale delle Ricerche, Pozzuoli, Italy. We used unfiltered CuKα radiation in the following conditions: accelerating voltage 40 kV, tube current 40 mA, 3°-70° 2θ range, steps of 0.02° 2θ, counting time in 30 s/step, 0.5 mm divergence slit, 0.1 mm receiving slit, and a 0.5° anti-scatter slit. Few samples were analyzed at the Dipartimento di Scienze della Terra, dell'Ambiente e delle Risorse (DiSTAR) University of Naples Federico II (Napoli, Italy). In this case, we used a Seifert-GE ID3003 diffractometer (Napoli, Italy), with CuKα radiation, Ni-filtered at 40 kV and 30 mA, in the 3-70° 2θ range, a 0.02° 2θ step scan, time of 10 s/step and the RayfleX (GE) software package (Inspection Technologies, 2004). All powdered samples were side-loaded to minimize eventual preferred orientation effects. The qualitative identifications were carried out through the search-match software and the ICDD PDF2 database (version 2012, Napoli, Italy).
Optical microscopy (OM) on thin sections was performed using a Leica DFC280 microscope (Leica, Wetzlar, Germany) to observe the textural features and the petrographic composition of samples.
A JEOL JSM 5310 scanning electron microscopy (SEM) integrated with an energy dispersion spectrometry (EDS) operating at Dipartimento di Scienze della Terra, dell'Ambiente e delle Risorse, DiSTAR, University of Naples Federico II (Napoli, Italy), was used for micro-morphological and chemical study both on fragments and polished thin sections. Fragments were fixed onto aluminum stubs with double-stick carbon tape, whereas thin sections were positioned on aluminum planar holder after coating by carbon about 10 nm thick under a vacuum evaporator, observed by SEM and analyzed by EDS. The following conditions were adopted: 15 kV electric current, 50-100 μA filament current, variable spot size and 20 mm working distance. EDS based an automated qualitative elemental analysis mode by Oxford (INCA) with ZAF matrix correction, using standards of anorthoclase for Si, Al and Na, diopside for Ca microcline for K, rutile for Ti, fayalite for Fe, olivine for Mg, serandite for Mn, sphalerite for Zn. Detection limits of the analyzed elements are below 0.1%.
Whole-rock geochemistry was carried out at Bureau Veritas Commodities Canada Ltd (Vancouver, Canada). Major elements were determined on dried sample powders mixed with lithium tetraborate/metaborate flux followed by fusion and casting into glass discs, by X-ray fluorescence (XRF; method XF701). Minor elements were determined by inductively coupled plasma-mass spectrometry (ICP-MS) after LiBO2/Li2B4O7 fusion of powdered sample (method LF100; Bureau Veritas Commodities Canada Ltd., Vancouver, Canada). Moisture and loss on ignition (LOI) were determined separately at 105 °C and 1000 °C.  Figure 1, arranged from North-West to South-East and completed by qualitative abundance of secondary minerals. Underlined sample names highlight clinoptilolite and mordenite coexistence. In the legend, the deposits are distinguished based on dominant zeolite. Note: The relative abundance in collected samples allows to infer the vertical trend in the zeolite stratigraphy.

Sedimentological, Petrographic and Mineralogical Descriptions
The sampled sequences of the Asuni Unit are mostly epiclastic tuffites, with an extensive brown-yellowish appearance (Figures 3a,c and 4) and a cohesive to hard consistency (Figure 4a,c). The sequences consist of a series of coarse sandy-to-ashy layers with variable thickness of down to ca. few centimeters, showing planar-to-medium angle lamination and locally characterized by greenish (most common) and blackish or reddish (occasional) tones (Figures 3c and 4c). Coarse (grain size up to dm) dense fragments are widespread in the deposits with an abundance between 25 vol % (upper portion) and 40 vol % (lower portion); the denser blocks are highly to poorly welded ignimbrites, andesite lavas and Paleozoic crystalline basement rocks. Pumices occur in low amounts. They are usually broken and represented by brown to white and light gray colors; elongated vesicles often aligned to a tube structure are also observed. Overall, pumices are coarser in the uppermost levels with size of 1 to 5 mm in diameter. Based on bulk-rock geochemistry of selected samples, the Asuni tuffites are dacites, rhyodacites to rhyolite (Tables 1 and 2).   Note: * ppb. Under the optical microscope, the samples show variable textures and colors, even though they share common features. Their primary crystalline component is represented by fractured and altered plagioclase grains (Figure 5a,b), alkali-felspars, rounded quartz ( Figure 5c) and altered biotite laths (Figure 5d). Rare pyroxene and accessory apatite, hematite and/or magnetite crystals are also recognized. The glassy component is widespread, forming the bulk matrix and the cuspidate shards (Figures 5d,f, and 6a,b). Moreover, the dark brown, greenish and reddish colors of the bulk matrix can be seen, together with other evidence of post-depositional and alteration processes, i.e., (1) zeolite and minor clay minerals growing in the rock cavities (i.e., vesicles, voids, fractures), on the crystals and/or at the expense of glassy component (Figure 5f); (2) pervasive greenish formations running for few mm across the bulk-matrix (Figure 5e) or thinly coating the glass component (Figures 5f and 6f); (3) rock fractures filled by greenish and whitish mineralization (Figure 5g,h); (4) dissolution areas in quartz (Figure 5c). We attribute the above green aggregates within the veins and widespread in the bulk matrix of the samples to glauconite, as constrained by microanalyses performed on well crystallized minerals within fracture (Figure 5g,h). Voids can host small k-feldspar and quartz that coexist with the dominant zeolites and cannot be considered primary but are later secondary phases.  Table 1 reports the mineralogical composition of both primary and secondary minerals derived by combined XRPD analyses and OM-SEM observations. Primary minerals, i.e., plagioclase and quartz, amounts are prevailing phases, associated with a ubiquitous amorphous fraction.
Zeolites are the most important and widespread secondary ore minerals, and are mainly represented by mordenite and subordinate clinoptilolite ( Table 1, Figures 2 and 6).
Zeolite abundance seems to depend on the glass matrix availability. Mordenite forms mostly acicular crystals growing at the expense of the glass components such as shards, cineritic matrix and/or spherical cavities (Figure 6d-f). Despite the low content, euhedral tabular clinoptilolite crystals fill the spherical cavity where they grew upwards (Figure 6a), deeply transforming the cuspate glass shards (Figure 6b) and locally replacing the glassy matrix (Figure 6c). Tabular clinoptilolite can coexist with acicular mordenite, particularly in vugs of coarser aggregates ( Figure  6a). In association with clinoptilolite plats, mordenite appears to determine spherulitic aggregates ( Figure 6a) and is likely a later phase. Clay minerals are subordinate [26].  The occurrence of mordenite and clinoptilolite is variable, both among sequences and inside along a single outcrop. On the basis of the OM and XRPD we observe that (i) the strongly cohesive ignimbrites are unzeolitized; (ii) mordenite is the most abundant zeolite and increases towards the high stratigraphic levels (i.e., sequences N, F, E, M); (iii) clinoptilolite seems to increase proceeding downwards (i.e., sequence N, F); (iv) H and I sequences are characterized by mordenite only; (v) dioctahedral smectite is ubiquitous, but its content is low (see Cappelletti et al. [26]). However, an inverse correlation between the clinoptilolite and mordenite may be observed. Furthermore, the relation is positive considering coarse-grained layers where the authigenic phases are more abundant.

SEM Observations and EDS Microanalysis
Dioctahedral smectite occurs as thin plates along the outer side of the glass shards and precedes the zeolite crystallization, as assumed by textural relationships.
Mordenite displays three main morphologies that coexist in the same sample and, based on observations, we confidently associate with the alteration stage.
The first mordenite type consists of tiny crystals emerging from the glassy component and/or from its substratum smectite coating (Figure 7a). This mordenite can represent an embryonic stage of zeolite growth; it produces limited replacement of the glass phase that still shows the proper primary or early argillification features. The second mordenite type is a stubby fibrous microcrystals that assembly in characteristic ''inter-twinned bundles'' (Figure 7b,c). In this occurrence, mordenite is finely intergrown with smectite, crystallizing at the expense of the clay mineral (Figure 7d). Figure  7b-d displays this second morphological type within vugs of both the pumice and host matrix. The mordenite is rarely covered by plate-like smectite (Figure 7f). The third mordenite (Figure 7g) arranges in tuft and occurs on euhedral clinoptilolite crystals. In this latter case, mordenite has an acicular shape with slender fibers, which can reach up to 40 μm in length. Otherwise, in the first and in the second types, mordenite is very small and rarely reaches 5 μm in length.
Contrarily to mordenite, clinoptilolite always shows a well-developed crystal habit ( Figure  7h,i). In coarse-grained assemblages, clinoptilolite laths reach their largest size of 30 μm along the c axis and thickness of ca. 5 μm, showing characteristics of monoclinic symmetry. When grown on glassy shards, clinoptilolite forms radial arrangements.
Chemical composition of the studied mordenite and clinoptilolite is in Supplementary Materials Tables S1 and S2. Plotted in a (Ca + Mg)-Na-K ternary diagram (Figure 8a,b), these zeolites display wide chemical variations. In particular, the clinoptilolites have (Mg + Ca) in the range 1.69-2.72 (atoms per formula unit, hereafter apfu), Na at 0.48-2.59 apfu, and K at 0.16-0.64 apfu; while the mordenite yielded (Mg + Ca) values of 1.53-4.01 apfu, Na of 0.84-3.77 apfu, and K of 0.28-3.33. Therein, clinoptilolite that was studied here is characterized by a lower K content and a higher Ca/K ratio with respect to mordenite (Ca/K at 0. 44 Mordenites and clinoptilolites measured in the Allai unit [30] and those studied here perfectly overlap in terms of building major oxides (Figure 8d) and extra framework cation contents ( Figure  8a). However, when compared to literature data ( [52][53][54] and reference therein), the Asuni zeolites are characterized by lower Na (Figure 8e,f) and higher Ca + Mg content (Figure 8a). Notably, the Mg cation of clinoptilolite is mostly at around 1apfu (Figure 8f).
Furthermore, the mordenite in sequence I (see envelop by dashed line in Figure 8e) is richest in K (i.e., ca. 3 apfu for those in shards and cavities, respectively). The mordenites occurring in sequence H exhibit a higher Na content (up to 3.77 apfu) compared to others (see envelop by dashed line in Figure 8e). However, the Na cations decrease moving upwards along the sequence (arrow in figure 8f).
Finally, OM and EDS analyses (Figure 5g,h) show glauconite occurring in veins and often in the bulk matrix, as well as being responsible for the greenish color of the studied deposit.   [25,53,55]; the arrow shows main trend along sequence. The plots allow the comparison with literature on clinoptilolite and mordenite chemistry, namely, from Allai Unit [30] and other Si-rich zeolites worldwide. Errors are within symbol size.

Discussion
The XRPD and EDS-SEM results indicate that the Asuni tuffites are altered but moderately zeolitized. The studied deposits contain more than half of the primary mineral components, i.e., plagioclase, quartz and K-feldspars (Table 1). It is also possible to recognize several glass shards with a broad primary structure and characteristic cuspate shapes (Figures 5d and 6b). The authigenic minerals are subordinate (as found by [26]), and mainly represented by mordenite and clinoptilolite, with subordinated smectite and glauconite (Tables 2; Figures 5 and 6). Similarly to other deposits of central Sardinia [9,26,27,30,31], mordenite is the most widespread and can be the sole zeolite phase. Glauconite is instead uncommon in this area.
The Asuni Unit was deposited in a sub-aqueous environment [44,47]. More in detail, Assorgia et al. [47] indicated a lacustrine-type depositional environment for the Asuni Unit, on the basis of sedimentological and stratigraphic evidence. These authors suggest that the unit consists of fluvial-lacustrine sediments that derive from erosion, reworking and short transport of previous volcanoclastic formations. Moreover, Cherchi et al. [44] proposed a detailed Oligo-Miocene chronology of the tectonic and of the sedimentary events, also defining environment and deposition depth based on chrono-biostratigraphical considerations. In specifying the timing of pre-, syn-, and post-rift stages in the Oligo-Miocene graben system of Sardinia, the authors dated the first marine ingression in latest Oligocene and, by further considering seismic reflection profiles, indicating a rapid subsidence and deep-water sedimentation during Oligo-Miocene in central Sardinia. There is substantial textural and mineralogical evidence corroborating these geological and paleo-environmental reconstructions.
Evidence of the sub-aqueous environment is the diffuse greenish color of the studied sequences, both in the field observations and at macro-to-microscale investigations; which also show a characteristic layered arrangement (Figures 3 and 4). OM and EDS microanalyses on thin sections (Figure 5e,g,h) show that these greenish formations contain glauconite. According to literature [56][57][58][59][60], glauconite growth derives from (i) alteration of the clay component through addition of Fe, (2) supply of K to the growing smectites (with glauconite-smectites transformation). The two processes are favored in K-enriched rocks and generally occur in marine or hypersaline aqueous environments. Although oversimplifying, we are confident in recommending that propose that the lacustrine environment basin, in which the Asuni tuffites are deposited, was produced by the marine ingression in the central Sardinia subject to the extensive tectonics. In these regards, Cherchi et al. [44] showed that during the rifting stage (Aquitanian, late Miocene), there was already a deep marine environment in the graben, except for the areas subject to the volcanism-derived sedimentation, like central Sardinia.
The mineralogical data obtained on zeolites provides further evidence for an active hydrothermal system and points to the circulation of fluids depending on permeability over other parameters. As a matter of fact, the type and abundance of zeolites cannot be related to differences in rock components (i.e., lithic clasts, juvenile elements, minerals) that are homogeneously distributed in all the studied Asuni sequences. The zeolite chemistry is independent from bulk-rock compositions (rhyolite, rhyodacite and dacite; Tables 1 and 2) and location (Figures 1 and 2). However, clinoptilolite and mordenite contents are higher in very coarse-grained layers compared to the other, fine-grained, levels ( Figure 4b). Clinoptilolite occurs abundantly in the lowermost and intermediate levels of the stratigraphic sequences, with an apparent increase in clinoptilolite contents moving from top downwards. Contrarily, mordenite occurs more frequently in the upper layers and sometimes tends to disappear towards the bottom, particularly in successions where it coexists with clinoptilolite. The described distribution of zeolites is testified by the sequence E (Pranu Pirastru, Figure 4). Here, the very coarse-grained aggregates, which corresponds to the maximum zeolite content, as confirmed by OM and SEM investigations (in Section 4.1).
In open hydrological systems, the vertical zoning of zeolites is explained in terms of progressive chemical-physical variations of percolating solutions, leading to formation of different zeolite species [61]. This process justifies the vertical zonation of authigenic minerals in the Asuni Unit, supporting the possible formation of zeolite in an open hydrologic system, as also hypothesized by Cappelletti et al. [26]. This type of system also accounts for the cations in the analyzed zeolites that have content too high with respect to those in the bulk epiclastites and the Na trend of zeolite chemistry ( Table 2; Supplementary Materials Tables S1 and S2). In addition, Asuni bulk epiclastites, if compared to those Allai and free-zeolites [62], showed an enrichment in CaO (and K2O) and a depletion in Na2O content (Figure 9a,b), so that three distinct fields can be suggested: Asuni, Allai and free-zeolite. We think that this distribution has a genetic significance and can offer important information to distinguish minerogenesis in various zeolitic rocks. There are few constraints to explore the Ca distribution. The experiments by Wirshing et al. [63] suggest that the kind of calcium zeolites strongly depends on the presence of an open system. In particular, products increasingly rich in calcium required a Ca-rich external reactant solution, which provided available Ca 2+ and thus justified the formation of calcium zeolites.
Our data, therefore, corroborate the hypothesis about a major contribution from external fluids. It is also remarkable that the REE concentrations are higher in Asuni epiclastites with respect the Allai pyroclastic Unit. The Asuni patterns are shifted-upward, even if mutual fractionations among REEs are roughly similar. Rock compositions cannot explain this difference, as the two units are similar in SiO2, Al2O3 and alkali contents (Figure 9b).  Table 2 and [30,62]. Chondrite values from [64].
However, Allai deposits tend to be rich in LREE relative to HREE, contrary to the Asuni rocks that show nearly flat patterns. In our opinion, the REE patterns and the alteration type provide evidence for the limited involvement of primary fluids in the Asuni tuffites which instead was dominant in the Allai pyroclasts. This is in agreement with the lithology of the deposits.
Additional support to the open system model comes from the textures of some zeolites, which form cement around denser and residual mineral fragments in the studied Asuni sequences (Figure  7h,i) and in other volcanic products of central Sardinia affected by a post-depositional alteration [29].
The possible zeolitization sequence for the Asuni Unit is schematized as follows: glass  smectite  mordenite (I-II type) and/or clinoptilolite  mordenite (III type) This sequence of zeolite crystallization is very common in natural open system environments and is in agreement with literature data from Sardinia [28,30,34,65] and elsewhere [52]. At Asuni, it is also supported by morphology of mordenites (e.g., mordenite type in Section 4.2).
The early mordenites are first and second types (e.g., embryonic and fibrous, respectively) which originated as a direct expense of volcanic glasses under the action of alteration fluids ( Figures  7 and 10). In this case, the zeolitization is peripheral to vugs and y-shards, which likely trapped original fluid at the moment of deposit emplacement. By considering previous studies [66][67][68], the Si and (mainly alkalies) cation contents of mordenite depends on the Si and cation contents of the glass and on the pH of the permeating solutions (being at ca. 7 in "open systems") (Figure 10a,b).
The later third mordenite type (tuft morphology) followed the clinoptilolite crystallization and/or the external supply ( Figure 10c). SEM investigations show that web-like fibers of mordenite have grown both on the glassy components (i.e., Figures 6e and 7g) and between clinoptilolite crystals (Figure 7h). Clinoptilolite seems to form in response to the progressive chemical changes of fluids towards higher Ca/K ratios and perhaps the availability of Mg 2+ cations of marine water origin. It rarely forms crystals with traces of dissolution, indicating equilibria condition and/or a relatively small change in the physical condition of the system.

Conclusions
Field observations and analytical investigations on zeolite-bearing epiclastites of Asuni units allow to suggest a mineralogical and genetic model that may have implications for mineral exploration in central Sardinia and paleo-environmental reconstructions as well.
The different types, distribution and abundance of the zeolites can be explained by considering an open hydrologic system, continuously evolving due to water-rock interaction and supply of marine waters after eruption. As result, a different concentration and chemistry of the zeolite minerals occurred at specific levels in the sequences. In particular, we can identify a clinoptilolite enrichment in the lower part of the Asuni Unit, which unlike the higher levels is enriched in mordenite.
The data presented in this study on the Asuni tuffites improves the existing background about the areal distribution of zeolite occurrences in central Sardinia. Considering that this study may contribute to an evaluation of the quality and the reserves of zeolite mineralization, it is aimed at a possible future exploitation and potential use in the Mediterranean area.