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Article

Discovery of Pseudomorph Scapolite and Diagenetic Indication from the Permian Volcaniclastic Rocks in Western Sichuan (SW China)

1
School of Geoscience and Technology, Southwest Petroleum University, Chengdu 610500, China
2
Research Institute of Petroleum Exploration and Development, PetroChina, Beijing 100083, China
3
Exploration and Development Research Institute, PetroChina Southwest Oil & Gas Field Company, Chengdu 610041, China
*
Author to whom correspondence should be addressed.
Minerals 2024, 14(2), 200; https://doi.org/10.3390/min14020200
Submission received: 31 October 2023 / Revised: 12 February 2024 / Accepted: 13 February 2024 / Published: 15 February 2024
(This article belongs to the Section Mineral Geochemistry and Geochronology)

Abstract

:
Volcaniclastic rocks are important unconventional oil and gas reservoirs from which it is difficult to determine the protolith due to strong metasomatic alteration. Intensive alteration has occurred in much of western China, but few robustly documented examples are known from which to assess the alteration processes. Further recognition from the petrological and mineralogical record is essential to quantify the diagenetic environment, the degree of alteration, and its impacts. Permian volcanic rocks are widely developed in the western Sichuan Basin (southwestern China), with a thickness of more than 200 m. The thickness of volcaniclastic rocks in the Permian Emeishan Basalt Formation is up to 140 m, with a 5600~6000 m burial depth. In this study, we demonstrate an approach to recognizing hydrothermal alteration by the occurrence of scapolite megacryst mineral pseudomorphs (SMMPs) in Permian volcaniclastic rocks in the Sichuan Basin (southwestern China). The results show that SMMPs in the Permian volcaniclastic rocks in the western Sichuan Basin mainly occur in the lower part of the Permian basalts as intragranular minerals and rock inclusions. Scapolite is transformed into quartz and albite, and only the pseudomorph is preserved, indicating secondary hydrothermal fluid metasomatic alteration. Scapolite is formed after microcrystalline titanite and is the product of the high-temperature pneumatolytic metasomatism of plagioclase from the mafic protolith during the post-magmatic stage. The mixing of meteoric water and barium-rich hydrothermal fluid leads to the precipitation of barite; additionally, the pores are filled with barite and halite after the alteration of scapolite. The silicification and hydrothermal dissolution of scapolite and the albitization of sodium-rich matrix minerals increase the pore volume, which is conducive to the later recharge by hydrothermal fluids. The discovery of SMMPs can serve as an indicator of the high-temperature pneumatolytic metasomatism and mixing of meteoric water and deep hydrothermal fluid.

1. Introduction

Volcanic rocks are important unconventional reservoirs with a wide distribution [1,2,3,4]. Among them, volcaniclastic rocks (especially tuff) have drawn significant attention from the oil and gas exploration community; tight oil resources have been found in low-permeability tuff reservoirs in many oil- and gas-bearing basins [5]. In addition, tuff has specific features such as, a small particle size, complex alteration pathway, and intricate reservoir space, making it difficult to study volcaniclastic rocks [6,7,8].
Volcanic rocks, particularly volcaniclastic rocks, are prone to weathering and hydrothermal alteration; temperature, pressure, and hydrothermal fluid composition are key parameters. Alteration not only changes the mineralogical composition and structure of the primary rocks, but also changes their geochemical characteristics [9,10,11]. Some studies have suggested that the geochemical characteristics of volcanic rock minerals are not always significantly changed during the process of alteration. For example, in the case of the hydrothermal alteration of rhyolite, the geochemical characteristics of the new minerals are not significantly different from those of primary rocks [12]; for example, the heavy rare-earth element (HREE) contents of whole rocks in the Sm-Nd isotopic system remained consistent in the Lala Fe-Cu-REE deposit [13]. Generally, however, alteration changes the characteristics of protoliths. During hydrothermal alteration, the concentration of aluminum, iron, manganese, and magnesium in a hydrothermal solution gradually decreases, while the concentration of calcium gradually increases, and carbonate minerals are formed [14,15]. The alteration minerals in basalts are mainly chlorite, quartz, montmorillonite, calcite, zeolite, and pyrite [14,15,16]. Moreover, apatite mineral chemistry studies show an enrichment in light rare earth elements (LREEs) and negative Eu anomalies via hydrothermal alteration [17]. Tuff alteration also changes the geochemical characteristics of primary rocks [18]. Furthermore, in the process of mineral alteration, changes in mineralogy affect the density and volume of rocks. More specifically, changing the volume of surrounding rocks affects the seal integrity of fractures, further impacting the physical properties of volcanic rock reservoirs [19]. Some mineral alteration leads to an increase in the surrounding rock volume, which blocks fluid conduits and hinders further reactions. For example, the presence of chlorite [20] and the precipitation of quartz [11] lead to a decrease in rock density and an increase in rock volume, greatly reducing the porosity and permeability of the reservoir. Conversely, feldspar sericitization (clay alteration) is an alteration process that reduces volume, creates reservoir space, and improves the reservoir properties [18,21].
Permian volcanic rocks are widely distributed in the western Sichuan Basin (southwestern China), with a thickness of more than 200 m, and have great exploration potential. Among them, the volcaniclastic rocks in the Chengdu–Jianyang area on the northern margin of the Emeishan Large Igneous Province (EMLP) are widely distributed. The thickness of volcaniclastic rocks in the Permian Emeishan Basalt Formation is up to 140 m, with a 5600~6000 m burial depth [22,23,24,25]. Previous studies have indicated that the effects of the volcanic environment, lithofacies, reservoir physical properties, and diagenesis on volcaniclastic rocks are crucial [24]. Shimizu (2021) and Somarin and Lentz (2008) showed that the formation of new minerals via alteration can provide information regarding the diagenetic environment. For example, quartz, pyrite, epidote, chlorite, and calcite often occur in low-temperature hydrothermal systems [26,27]. However, it is often difficult to determine the lithology of the protolith due to strong metasomatic alteration, which further affects the analysis of its genetic mechanism [7,28,29,30]. In addition, the effect of metasomatic alteration on the reservoir can be very important, in which minerals maintain their original crystal morphology. Therefore, it is helpful to analyze the composition of primary and alteration minerals, identify the lithology of protoliths, and reconstruct fluid–rock interactions under the condition of strong alteration according to the pseudomorphic characteristics and chemical composition changes in metasomatic minerals [31,32]. In this study, our main objectives were to (1) specify the timing and the process of scapolitization, (2) propose a conceptual model of hydrothermal alteration, and (3) investigate the origin of scapolite.

2. Geological Setting

The western Sichuan Basin (southwestern China), located in the western region of the Yangtze paraplatform (Figure 1a), is a composite superimposed basin with multicycle evolution [33]. This basin is a late Mesozoic–Cenozoic foreland basin overlying a Precambrian–Middle Mesozoic passive margin [34] that experienced strong compressive tectonic deformation after the Permian. During the Jinning tectonic activity and Chengjiang tectonic activity, the basement structure was established and separated by a central uplift of brittle lithologies [35]. Thereafter, the basin experienced several significant tectonic episodes, including the Tongwan, Caledonian, Yunnan, Dongwu, Indosinian, Yanshanian, and Himalayan [36,37]. The study area (Jianyang) is located in the western Sichuan Basin, which is situated on the border of Chengdu and Suining counties (Figure 1a,b), restricted by the Longquanshan Fault. The Permian Emeishan Basalt Formation lies within the eastern part of the Emeishan Large Igneous Province, which developed as a result of Hercynian orogeny and ranges in age from 261 to 257 Ma [38].
Emeishan basalt is widely distributed in the western and southwestern Sichuan Basin, and has an exposed area greater than 25 × 104 km2 [40]. Volcanic rocks comprise the main continental eruption, and partly interbedded volcanic rocks and limestone indicate a marine eruption in the early stage [39,41]. The thickness of the Emeishan Basalt Formation (P2β) in the southwestern Sichuan Basin is up to 1400 m, with a 500–6000 m burial depth, and at least eight eruptive cycles are recognized [42]. Unconformable contacts lie between the Emeishan Basalt Formation (P2β) and the underlying Middle Permian Maokou Formation (P2m) and the overlying Permian Longtan Formation (P2l). The underlying Maokou Formation interval is mainly composed of gray thin-to-medium limestone with thin dark calcareous mudstone interlayers, representing a relatively shallow and mid-energy marine environment during the sea-level fall. The upper part of the Maokou Formation was mostly eroded during the Dongwu movement. The overlying Longtan Formation interval is mainly composed of black thin mudstone and silty mudstone, locally containing carbonaceous shale and coal, which belong to the coastal marsh facies. The Longtan Formation comprises subordinate source rocks for oil and gas exploration, whilst Cambrian shales are primary source rocks [42].
Several wells (YS1, YT1, TF2) have been drilled into the Permian Emeishan basalt interval in the Jianyang area of the western Sichuan Basin. Well YT1, located in the Jianyang area of the western Sichuan Basin, is the first key risk exploration well in the Permian volcaniclastic rock reservoir and produced 225,000 m3/d of gas during the test. Previous studies have shown that the distribution of the volcaniclastic rocks in well YT1 is obviously controlled by the Longquanshan basement fault (Figure 1a). The volcaniclastic rock section has a thickness of almost 100 m and consists of deposits of alkaline basalt rock fragments (Figure 2a,b). It is widely recognized that the reservoir space type is dominated by secondary nano-micropores, and the volcanic reservoir is a high-quality porous natural gas reservoir [22,41,43,44,45]. It is also recognized that the volcanic eruption environment, lithology, and lithofacies are the basis for the formation of volcaniclastic rock reservoirs, while a series of alteration processes that volcanic rocks undergo when they condense are the key factors for the formation of reservoirs [46,47]. The alteration processes include hydrothermal alteration, weathering, and burial dissolution. Notably, a series of actions related to hydrothermal fluid activities contribute greatly to the formation of reservoir pore space. In addition, the hydrothermal fluid activities also formed particular mineral paragenesis assemblages, e.g., the hydrothermal accessory minerals chlorite and albite [39,46].
Some hydrothermal accessory minerals such as titanite, apatite, monazite, and zircon can be found in the upper part of the volcaniclastic rocks (5645.76–5646.25 m). A unique altered form of the mineral scapolite, referred to as scapolite megacryst mineral pseudomorphs (SMMPs), can also be found. SMMPs occur as large and elongated crystal forms, with lengths ranging from 1 to 5 cm, and belong to the megacryst–pegmatitic mineral group. This alteration pseudomorph is blue-gray in hand specimens (Figure 3a–d) and colorless and transparent in thin sections. It is composed of quartz, albite, titanite, calcite, barite, and chlorite. Additionally, secondary minerals such as tourmaline and anthophyllite are found in the lower part of volcaniclastic rock sections.

3. Sampling and Methodology

Twenty cores from well YT1 and four cores from well TF2 were collected in order to document the petrological characteristics of the volcanic rocks. One hundred doubly polished and blue epoxy-impregnated thin sections were produced to determine lithological components, porosity, and alteration minerals. Four samples were prepared for fluid inclusion analysis. Thin-section, electron probe, and fluid inclusion investigations were all carried out at the Natural Gas Geology Key Laboratory of Sichuan Province, Southwest Petroleum University, China. Firstly, the rock was ground into 0.03 mm thin sections, and these were examined with an Olympus BX53M microscope (Shinjuku-ku, Tokyo Japan, Olympus). Bulk and clay mineral analyses based on X-ray diffraction (two samples) were accomplished at the National Key Laboratory of Oil and Gas Reservoir Geology and Exploitation, Southwest Petroleum University, in which selected samples rich in SMMPs were ground into 200-mesh powder and tested for bulk mineral composition using an X-ray diffractometer (X Pert PRO MPD, PANalytical B.V., Almelo, The Netherlands). Particles smaller than 2 μm were further extracted for separate determination of clay mineral types and contents [48]. The standard minerals were calculated using an Excel (2009) spreadsheet designed by Kurt Hollocher and using the Le Maitre (1976) method to adjust iron oxide according to volcanic rocks. Oxides were converted to 100% after removing H2O-, etc. The standard minerals were represented by the weight percentage content. Other parameters were as follows: combination index (σ): σ43 = (Na2O + K2O) ^2/(SiO2-43) (Wt%); differentiation index (DI) = Qz + Or + Ab + Ne + Lc + Kp. The A/NK-A/CNK diagram of volcanic rocks and the chemical type discrimination were taken from Mania and Piccoli (1989): A/NK = Al2O3/(Na2O + K2O) (mol); A/CNK = Al2O3/(CaO + Na2O + K2O) (mol); and alkalinity rate (AR) = [Al2O3 + CaO + (Na2O + K2O)]/[Al2O3 + CaO − (Na2O + K2O)] (Wt.%).
Electron probe microanalyzer (EPMA) analysis (YT1 well, 5645.76 m, 5645.98 m, 5646.41 m) was carried out on polished sections 500 μm thick that were cut from the same blocks as thin sections. EPMA analyses were performed using a JXA-8230 electron probe micro-analyzer (Showima, Tokyo, Japan, JEOL) combined with a backscattered electron (BSE) detector, energy spectrometer (EDS) and wavelength dispersive spectrometer (WDS) (London, UK, Oxford Instruments). The accelerating voltage was 15.0 kV, the beam current was 20 nA, the beam diameter was 5 µm, and the peak counting time was 10 s. The spectral analysis accuracy was better than 1% (main element content > 5%) and 5% (secondary element content 1%–5%); the detection limit was 0.01 wt.%. EDS surface scanning was used to scan the local area of the scapolite and obtain the distribution of nine main elements: Si, Al, K, Na, Ba, Ca, Ti, Fe, and Mg. Authigenic minerals and micropores were observed using a Quanta 650 FEG scanning electron microscope (SEM) (Brno-Kralovo Pole, Czech Rep, FEI Czech Republic S.R.O) with backscatter electron (BSE) imaging in the State Key Laboratory of the Southwest Petroleum University.
Fluid inclusion was investigated at the Southwest Petroleum University with a Linkam THMSG600 system (Salfords, Surrey, UK, Linkam Scientific Instruments). The composition of the fluid inclusion was measured using a Renishaw inVia-Qontor microconfocal Raman spectrometer (Waltham, MA, US, America Thermo Scientific) laser with a wavelength of 532 nm and a grating size of 1800 L/mm. The exposure time was 2 s, laser power was 10%, and accumulation number was 3. The measurement range of the hot and cold stage was −196~600 °C, and the heating–freezing rate was reduced to 1–10 °C/min. When the temperature was close to the phase transition temperature, the heating–freezing rate was reduced to 0.2–1 °C. During the cooling process, the measurement accuracy was ±0.1 °C when the temperature was less than 30 °C, and the measurement accuracy was ±1 °C when the temperature was between 30 °C and 300 °C. The analysis was carried out in the laboratory at room temperature (25 °C) and 50% humidity.

4. Results

4.1. Petrology and Mineralogy

The core observation results show that SMMPs mainly occur at a depth of 5645.76–5745.98 m in well YT1 (also an important reservoir interval), consisting mainly of breccia lava. In addition to SMMPs, there are basaltic and other intermediate-basic rock fragments, plastic magma fragments, plastic rock debris, and feldspar crystal fragments (Figure 3a–d). The rock samples display a massive structure and common dark mineral network veinlets, likely corresponding to fluid migration conduits (Figure 3d). According to the results of the major and trace element analyses, the SiO2 content ranges from 51.5 to 57.1 wt.%, and the Na2O + K2O content ranges from 6.7 to 8.9 wt.%. The rock samples belong to the intermediate-basic alkaline igneous rock series. The Chemical Index of Alteration (CIA) ranges from 58.1 to 59.3, Alteration index (AI) ranges from 9.56 to 17.29, and Loss on ignition (LOI) ranges from 2.01 to 3.27 wt.% (Table 1) [49,50]. The TiO2 content ranges from 4.2 to 4.4 wt.%, the Sr content ranges from 129 to 141 ppm, and the Ba content ranges from 35.5 to 49.2 ppm; the Sr/Ba ratio ranges from 2.87 to 3.63 (Table 1). The total rare earth element content (ΣREE) ranges from 202.95 to 320.32 ppm, and LREE/HREE ranges from 6.96 to 8.86 (Table 2) [39]. The X-ray diffraction analyses show that albite and chlorite are the most abundant minerals, together constituting more than 90 wt.% of the rocks. Quartz and titanite are the other two important minerals but are present in low concentrations, from 1 to 3 wt.% and from 5 to 7 wt.%, respectively (Figure 4).
The CIPW normative composition calculated for rock samples (Table 3) includes albite (75.80 wt.%), anorthite (7.09%), titanite (2.85 wt.%), diopside (2.24 wt.%), and iron-rich minerals such as ilmenite (5.91 wt.%) and hematite (2.79 wt.%). However, XRD did not detect minerals such as Ca-rich plagioclase, diopside, ilmenite, and hematite. The minerals consist of alteration minerals and primarily include albite, titanite, and chlorite, subordinated by quartz (<1 wt.%), indicating a very high degree of alteration (Figure 4).
Dark reticular veins are composed of subhedral to anhedral microcrystals of titanite; the enclosed breccia is characterized by directional features that obviously indicate flow. Additionally, hematite fills the dark mineral dissolution pores (Figure 5a). The SMMPs are mainly subhedral and bypass or locally transect the titanite veins, indicating that the pseudomorphs formed slightly later than the titanite (Figure 5b). The SMMPs could have two possible origins: (1) replacement of scapolite by quartz, albite, titanite, barite, calcite, and chlorite; (2) complete dissolution of scapolite, the generated pores being filled later by the same secondary minerals (Figure 5c,d). Further, hornblende, calcium-rich plagioclase (dissolved tabular albite, titanite, and reprecipitated), basalt (Figure 5c,f), and other minerals or rock inclusions are clearly visible (Figure 5e,f).
Metasomatic alteration of the scapolite produced and formed much of the quartz, and there are few quartz crystals in the matrix (Figure 5c,f). Quartz is suggested to mainly result from the interaction between the fluid and the scapolite. In addition, amygdaloidal structures present in the altered rock are filled with albite (Figure 5d).
Moreover, xenomorphic granular barite is present between quartz and other minerals. In the electron probe backscattering image, barite can be distinguished from other minerals with higher brightness; the rim is often enclosed by subhedral and euhedral granular quartz, and there may be a small amount of lath albite mineral inclusions inside (Figure 6a,b). Barite is almost invisible in the matrix, except that it is present inside and outside the scapolite crystal, suggesting that the precursor is derived from the decomposition products of scapolite minerals.
The matrix is mainly composed of albite, microcrystalline titanite, and chlorite. Microporosity in the matrix is abundant and is associated with volcanic glass devitrification (Figure 7a–c). In addition, euhedral granular halite crystals fill the matrix pores (Figure 7d).

4.2. Composition of Altered Minerals

The SMMPs formed due to mineral replacement or dissolved-refilling by quartz, albite, titanite, barite, calcite, and chlorite. The electron probe analysis shows that the quartz that replaced scapolite generally contains a small amount of CaO (0.46–1.99 wt.%), FeO (0.09–0.22 wt.%), and Al2O3 (0.01–0.07 wt.%) (Table 4). The microcrystalline titanite occurs in bands, and titanite fills the pores resulting from feldspar dissolution; both contain components such as Al2O3, ranging from 1.34 to 2.16 wt.%, FeO, ranging from 0.67 to 1.76 wt.%, and BaO, ranging from 0.18 to 0.31 wt.%. However, the pore-filling titanite contains relatively low amounts of TiO2 and more Al2O3 (Table 5). The albite filling the pores and pseudomorph analcime are both pure albite (Ab) with more than 99 wt.% albite, containing only small amounts of orthoclase (Or) and anorthite (An) components (Table 3). The barite generally contains small amounts of components such as SrO, ranging from 2.85 to 3.59 wt.%, FeO, ranging from 0.02 to 0.27 wt.%, and SiO2, ranging from 0.08 to 0.41 wt.%, and thus showing relatively high levels of these substitution elements (Table 6).

4.3. Fluid Inclusions

To determine the properties of diagenetic fluids, we measured the homogenization temperatures and freezing temperatures of fluid inclusions in the quartz that replaced the scapolite crystals and analyzed the composition of the fluid. As shown in Figure 8, the fluid inclusions in the quartz mainly occur in isolation, with a round to elliptical shape. The size is between 4 and 6 μm, and these are mainly brine inclusions with a gas–liquid ratio between 5% and 10%. In the area of study, all the fluid inclusions from quartz have homogenization temperatures (Th) greater than 200 °C (averaging 207 °C), and freezing temperatures (Tm ice) ranging from −2 to −1.4 °C. The salinities of the fluid inclusions range from 24.1 to 33.9 g/l and are therefore slightly lower than the average salinity of seawater (35 g/l) (Table 7). The results of the homogenization temperatures of the fluid inclusions in quartz are consistent with the formation temperature results calculated from the Si/Al ratio of the chlorite; the temperature of authigenic chlorite is higher than at least 200 °C (even surpassing 300 °C) [39,51].
In addition, fluid inclusion components were detected via laser Raman spectroscopy. The test results show that the inclusions not only have distinctive peaks of bitumen, CH4, SO2, alkanes, and water, but also SO42−, CO32−, and other components, indicating the complexity of the fluid properties and the influence of hydrothermal events on early hydrocarbon charging (oil starts to crack gradually at temperatures above 120 °C) [53,54] (Figure 8).

5. Discussion

5.1. Origin of Scapolite

Scapolite comprises a group of volatile-rich, calcium, sodium, aluminum, tectosilicate minerals that includes two endmembers, marialite (Na4Al3Si9O24Cl) (Ma) and meionite (Ca4Al6Si6O24CO3) (Me). In addition, scapolite is the product of high-temperature gas metasomatism of plagioclase in mafic protoliths (the components of precursor basalt is replaced by albite; Figure 5d and Figure 6a,b), and storage for most of the early (high temperature) volatiles (such as Cl, CO2, and SO3). The wide stability range that characterizes scapolite and the presence of a variety of important volatile components make it a good indicator of mineralizing fluid components [55,56,57]. Scapolite can be altered into epidote, albite, zeolite, and mica through hydrothermal action. During the later low-temperature period or through pressure reduction, the sulfuric volatile components released can form pyrite. However, F, Cl can enter the mineral or escape along fractures [58,59,60]. In the Jianyang area, the secondary tourmaline and anthophyllite that occur in the lower basalt section constitute pneumatolytic hydrothermal minerals rich in volatile components such as B, OH, and F. Tourmaline and anthophyllite can indicate high-temperature magma–hydrothermal and medium-high metamorphic environments, revealing a temperature range of 650 °C [61]. The emergence of scapolite in the volcaniclastic rocks and secondary tourmaline and anthophyllite in the lower basalt indicates a higher ambient temperature on the one hand, and the presence of a large number of volatiles on the other hand [62,63]. In other words, their occurrence and later evolution not only provide evidence for hydrothermal events after the higher temperature magmatic period of volcanic rocks, but also provide a research basis for studying the influence of the post-magmatic process on volcaniclastic reservoirs in this area. More specifically, the occurrence of scapolite may represent evaporite sequences, and the morphology of evaporites can be greatly changed or even completely changed [64,65,66,67]. This is consistent with previous results, which showed that the diagenetic evolution of volcanic minerals is affected by sodium-rich and high-salinity fluids [39].
Microscopic observation and electron probe analysis show that the main mineral components in the lower unaltered basalt are plagioclase (An = 49–57, Ab = 40–48) and augite (Wo = 41–45, En = 31–35, Fs = 19–25), together with ilmenite as an accessory mineral (Figure 7). Considering these minerals and the rock fragments observed in the scapolite, the scapolite is inferred to be the product of the interaction between volatile components in the magmatic gasification–hydrothermal stage and the high-salinity water at the sedimentary stage with the plagioclase in the basal protolith (Figure 5 and Figure 9). In contrast, the microcrystalline titanite was cut by scapolite and occurs in belts; this is readily interpreted as the result of hydration and oxidation of Fe-Ti oxides (ilmenite, Ti-bearing pyroxene, etc.) during the post-magmatic alteration stage. The replacement by sodium-rich hydrothermal fluids led to a large loss of calcium within plagioclase, and the lost calcium was involved in the generation of titanite [39,68]. In addition, the main calcium-rich minerals in the volcaniclastic rocks are titanite (CaTi [SiO4] (O, OH, Cl, F)) rather than calcite (CaCO3). It is implied that in addition to CO2–NaCl–H2O, there may be an exogenous SiO2 input into the alteration system before and after the formation of the scapolite.

5.2. Evolution of Scapolite and Alteration Environments

The quartz occurring as a pseudomorph of scapolite should be the product of alteration by secondary hydrothermal fluids, while the halite and barite in the pores are suggested to be products of Cl and SO3 volatile components released via the alteration of scapolite, and the combination of Na+ and Ba2+, respectively. Because the content of barium in seawater is much lower than that of strontium, when affected by meteoric water, Ba2+ in meteoric water and SO42− in seawater are more prone to precipitating BaSO4 [69,70]. In addition, the presence of hematite related to weathering in the Permian volcaniclastic rocks [71] indicates that the high content of Ba and barites in rocks may be related to the mixing of meteoric water and sodium-rich hydrothermal fluids [72].
The homogenization temperature and salinity analysis results of the quartz fluid inclusions show that high-temperature–low-salinity magmatic hydrothermal fluid will continue to react with scapolite after its formation [73]. In the quartz fluid inclusions, a large number of hydrocarbons were detected, suggesting that the time the scapolite underwent alteration is consistent with the expulsion of mature hydrocarbons from the Cambrian-interval source rock [54]. The scapolite was affected by hydrothermal fluid and atmospheric meteoric water after its formation, as revealed by its petrography (Figure 10).
Possible reactions of scapolite, titanite, quartz, and other minerals follow:
CaAl2Si2O8 + Na+ + Si4+ = NaAlSi3O8 + Ca2+ + Al3+;
FeTiO3 + Ca2+ + Fluid = CaTiSiO5;
Plagioclase An17 + NaCl + CaCO3 ≥ Scapolite Me35.85:
3.17Na0.84Ca0.16Al1.26Si2.84O8 + 0.61NaCl + 1.12CaCO3 =
Na2.47Ca1.47Al4Si8O24(Cl)0.61(CO3)0.29 + SiO2 + 0.83CO2 +0.80Na+ + 0.16Ca2+.
As mentioned above, there may have been input from allochthon SiO2 in the system when the scapolite was formed. The input of allochthon SiO2 fluids not only causes the formation of calcium-rich silicate minerals such as titanite, but also a large number of hydrothermal zircons in the alkaline volcaniclastic rocks [47]. Radiochronometric analyses results for hydrothermal zircon reveal that the Jianyang area has undergone two phases of hydrothermal events related to magmatic action, corresponding to the Indosinian movement during the Early and Middle Triassic (260~225 Ma) and the Yanshanian movement during the Late Jurassic (158.0 ± 0.54 Ma), respectively. Furthermore, the first phases of the event were accompanied by episodic hydrocarbon charging and the formation of microcrystalline titanite, scapolite, and quartz. In addition, the second-phase hydrothermal event was mainly manifest in the reservoir space [46,74,75].
Since these events, the upper section of the Permian volcaniclastic rocks near the fault zone in the Jianyang area has undergone multistage and multisource hydrothermal fluid alteration. During volcanic eruptions, the volcaniclastic rocks were mainly influenced by sodium-rich and high-salinity seawater. During the solidification period, volcaniclastic rocks were comprehensively affected by (1) the volatiles released via pressure reduction during the ascent of alkaline magma, (2) the deep high-temperature hydrothermal fluid that formed bottom to top along the fault, (3) the charging by hydrocarbon fluids released from maturating Lower Cambrian source rocks, and (4) the circulation of atmospheric meteoric water. In the late diagenesis stage, the rocks were altered by deep hydrothermal fluids and hydrocarbon circulations.
Therefore, the silicification of scapolite and hydrothermal dissolution and albitization of sodium-rich matrix minerals increased the overall pore volume. These processes are beneficial to entry by hydrothermal fluids in later stages. In addition, volcaniclastic reservoirs with micropores (Figure 6) as the main reservoir space were formed by multistage and multisource hydrothermal fluid alteration.

6. Conclusions

(1) Scapolite minerals are present in Permian volcaniclastic rocks in the Jianyang area (SW China) and formed after the microcrystalline titanite; they are products of plagioclase in the mafic protolith altered by high-temperature pneumatolytic metasomatism during the post-magmatic period.
(2) The scapolite was altered by multiple episodes of hydrothermal fluids and finally transformed into quartz and albite, retaining only the precursor pseudomorphs. Halite and barite in the pores are intimately associated with the alteration of scapolite. The precipitation of barite depends on the mixing of meteoric water and barium-rich hydrothermal fluids.
(3) The silicification of scapolite and hydrothermal dissolution of sodium-rich matrix minerals increase the pore volume, which enhances the later entry by hydrothermal fluids. In terms of volcaniclastic reservoirs in hydrocarbon exploration, the common presence of micropores is ascribed to multistage and multisource hydrothermal fluid alteration.
(4) In areas with strong metasomatic alteration, restoration of the protolith based on petrological and mineralogical indicators can provide decisive evidence for further research on volcaniclastic rocks.

Author Contributions

Conceptualization, X.L. and Y.L.; methodology, X.L.; software, Z.C.; validation, X.L. and M.F.; formal analysis, X.L.; investigation, Y.L.; resources, J.C.; data curation, C.T.; writing—original draft preparation, X.L.; writing—review and editing, Y.L.; visualization, H.J.; supervision, M.F.; project administration, M.X.; funding acquisition, X.L. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the National Natural Science Foundation of China (NSFC), “Mechanism of Multiple Authigenic Mineral Symbiosis in Volcanic Reservoirs and Implications for Fluid Tracing” (Grant No. 41202109); National Science and Technology Major Project, “Study of Permian and Triassic Tectonics, Sedimentary Evolution and Reservoir Formation Mechanism in Sichuan Basin” (Grant No. 2016ZX05007004-001); the Major Science and Technology Projects of PetroChina, “Study on main controlling factors of natural gas enrichment in deep clastic and volcanic rocks in Sichuan Basin”. (Grant No. 2021DJ0204) and the Fundamental and Forward-looking Major Science and Technology Project of the PetroChina Company, Limited. "Study on Formation Evolution and Dynamic Mechanism of Middle-Lower Combination in Superposition Basin" (Grant No. 2023ZZ0201).

Data Availability Statement

Data that support the findings of this study are available from the corresponding author upon reasonable request.

Acknowledgments

The manuscript was much improved by the careful reviews of three anonymous reviewers.

Conflicts of Interest

Cong Tan, Zhenglin Cao, Hui Jin, and Maolong Xia are employees of PetroChina. The paper reflects the views of the scientists and not the company.

References

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Figure 1. Simplified geological maps and location of Sichuan Basin. (a) Simplified geological map in the western Sichuan Basin, southwest China; (b) Distribution map of Permian volcanic rocks facies in Sichuan basin [39]. Red dotted box is the study area and YS1, YT1, TF2 are the exploratory wells. P1, P2, P3 are the locations corresponding to Figure 2a.
Figure 1. Simplified geological maps and location of Sichuan Basin. (a) Simplified geological map in the western Sichuan Basin, southwest China; (b) Distribution map of Permian volcanic rocks facies in Sichuan basin [39]. Red dotted box is the study area and YS1, YT1, TF2 are the exploratory wells. P1, P2, P3 are the locations corresponding to Figure 2a.
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Figure 2. Comprehensive histogram of Sichuan Basin. (a) Comprehensive histogram of stratigraphy along the NW-SE section across western and central part of Sichuan Basin; (b) stratigraphic column of Permian in Jianyang area (western Sichuan). Line P1–P3 corresponds to Figure 1a.
Figure 2. Comprehensive histogram of Sichuan Basin. (a) Comprehensive histogram of stratigraphy along the NW-SE section across western and central part of Sichuan Basin; (b) stratigraphic column of Permian in Jianyang area (western Sichuan). Line P1–P3 corresponds to Figure 1a.
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Figure 3. Core photographs of scapolite megacrysts minerals pseudomorph (SMMPs) in volcaniclastic rocks from the Permian Formation. (a) Breccia lava with plastic magma fragment and scapolite giant crystal pseudomorph, YT1 well, 5645.76–5645.98 m; (b) Breccia lava with plastic magma fragments and SMMPs, YT1 well, 5645.98–5646.24 m; (c) Breccia lava with plastic magma fragments and SMMPs, YT1 well, 5645.98–5645.24 m; (d) Breccia lava with feldspar pieces, basalt breccia, altered breccia and dark reticular veins, YT1 well, 5645.76–5645.98 m.
Figure 3. Core photographs of scapolite megacrysts minerals pseudomorph (SMMPs) in volcaniclastic rocks from the Permian Formation. (a) Breccia lava with plastic magma fragment and scapolite giant crystal pseudomorph, YT1 well, 5645.76–5645.98 m; (b) Breccia lava with plastic magma fragments and SMMPs, YT1 well, 5645.98–5646.24 m; (c) Breccia lava with plastic magma fragments and SMMPs, YT1 well, 5645.98–5645.24 m; (d) Breccia lava with feldspar pieces, basalt breccia, altered breccia and dark reticular veins, YT1 well, 5645.76–5645.98 m.
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Figure 4. X-ray diffraction analysis results of volcaniclastic rocks from the Permian Formation, Well YT1; 5645.98m; Detect limitation: 1%. Ab-Albite; Ttn-titanite; Chl-Chlorite; Q-Quartz.
Figure 4. X-ray diffraction analysis results of volcaniclastic rocks from the Permian Formation, Well YT1; 5645.98m; Detect limitation: 1%. Ab-Albite; Ttn-titanite; Chl-Chlorite; Q-Quartz.
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Figure 5. Photomicrographs of the Permian volcaniclastic rocks and SMMPs in the western Sichuan Basin. (a) Microcrystalline titanites are arranged in a directional manner around the breccia to form a dark reticular vein, dark mineral dissolution pore in the hematite, well YT1, 5645.76 m, blue casting, plane polarized light; (b) The SMMPs is subhedral, growing around dark mesh veins, well YT1, 5645.98 m, plane polarized light; (c) The scapolite is replaced by quartz and barite, and a chlorite inclusion is also seen, well YT1, 5645.98 m, crossed polarized light; (d) The SMMPs is composed of quartz, albite, chlorite, and barite, and titanites are transected by SMMPs, well YT1, 5645.98 m, plane polarized light, amygdaloidal structures–red circle; (e) Mineral or rock inclusions such as amphibole, plagioclase feldspar (now converted into albite and titanite), and basalt rock fragment are found in the SMMPs that is replaced by quartz, well YT1, 5645.98 m, plane polarized light; (f) Photo (e) crossed polarized light. Scp–Scapolite; Q–Quartz; Ab–Albite; Ttn–Titanite; Brt–barite; Chl–chlorite; Amp–Amphibolite; Hem–Hematite; Cal–Calcite.
Figure 5. Photomicrographs of the Permian volcaniclastic rocks and SMMPs in the western Sichuan Basin. (a) Microcrystalline titanites are arranged in a directional manner around the breccia to form a dark reticular vein, dark mineral dissolution pore in the hematite, well YT1, 5645.76 m, blue casting, plane polarized light; (b) The SMMPs is subhedral, growing around dark mesh veins, well YT1, 5645.98 m, plane polarized light; (c) The scapolite is replaced by quartz and barite, and a chlorite inclusion is also seen, well YT1, 5645.98 m, crossed polarized light; (d) The SMMPs is composed of quartz, albite, chlorite, and barite, and titanites are transected by SMMPs, well YT1, 5645.98 m, plane polarized light, amygdaloidal structures–red circle; (e) Mineral or rock inclusions such as amphibole, plagioclase feldspar (now converted into albite and titanite), and basalt rock fragment are found in the SMMPs that is replaced by quartz, well YT1, 5645.98 m, plane polarized light; (f) Photo (e) crossed polarized light. Scp–Scapolite; Q–Quartz; Ab–Albite; Ttn–Titanite; Brt–barite; Chl–chlorite; Amp–Amphibolite; Hem–Hematite; Cal–Calcite.
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Figure 6. The back-scattered electron image (of EPMA) characteristics of SMMPs. (a) Large number of xenomorphic granular barites, irregular titanite, flaky chlorites, etc. are scattered in the SMMPs composed of quartz minerals, and the matrix is mainly composed of albite with the morphology of analcime and albite after devitrification of volcanic glass. Titanites (black line) are obviously transected by SMMPs, and partly (yellow polygon) remain pseudomorphs of hornblende. The yellow thick dashed line shows the boundary between the matrix and SMMPs. In the matrix, the yellow dotted circles show an amygdaloidal structure filled by albite, and the red polygon shows plagioclase replaced by albite, well YT1, 5645.98 m, the boundary of SMMPs and matrix is clearly visible (dotted yellow line); (b) The enlargement of the area enclosed by the white rectangle in white rectangle in (a), well YT1, 5645.98 m. Q–Quartz; Ab–Albite; Ttn–Titanite; Brt–barite; Chl–Chlorite; O Ka1, Si Ka1, Al Ka1, Na Ka1-2, Ba La1, Ca Ka1,Ti Ka1, Fe Ka1 and Mg Ka1-2 are O, Si, Al, Na, Ba, Ca, Ti, Fe, Mg. The higher the brightness in the image, the higher the element content.
Figure 6. The back-scattered electron image (of EPMA) characteristics of SMMPs. (a) Large number of xenomorphic granular barites, irregular titanite, flaky chlorites, etc. are scattered in the SMMPs composed of quartz minerals, and the matrix is mainly composed of albite with the morphology of analcime and albite after devitrification of volcanic glass. Titanites (black line) are obviously transected by SMMPs, and partly (yellow polygon) remain pseudomorphs of hornblende. The yellow thick dashed line shows the boundary between the matrix and SMMPs. In the matrix, the yellow dotted circles show an amygdaloidal structure filled by albite, and the red polygon shows plagioclase replaced by albite, well YT1, 5645.98 m, the boundary of SMMPs and matrix is clearly visible (dotted yellow line); (b) The enlargement of the area enclosed by the white rectangle in white rectangle in (a), well YT1, 5645.98 m. Q–Quartz; Ab–Albite; Ttn–Titanite; Brt–barite; Chl–Chlorite; O Ka1, Si Ka1, Al Ka1, Na Ka1-2, Ba La1, Ca Ka1,Ti Ka1, Fe Ka1 and Mg Ka1-2 are O, Si, Al, Na, Ba, Ca, Ti, Fe, Mg. The higher the brightness in the image, the higher the element content.
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Figure 7. The SEM of the Permian volcaniclastic rocks, well YT1, 5645.98 m. (a) Quartz, chlorite, basalt (yellow line) and albite occur in SMMPs and the boundary of SMMPs and matrix is clearly visible (dotted yellow line). (b) Quartz, albite, chlorite, barite and micropore occur in SMMPs. (c) Micro-porosity in the matrix is abundant (d) Euhedral granular halite crystals which filling the matrix pores. Q–Quartz; Ab–Albite; Chl–Chlorite.
Figure 7. The SEM of the Permian volcaniclastic rocks, well YT1, 5645.98 m. (a) Quartz, chlorite, basalt (yellow line) and albite occur in SMMPs and the boundary of SMMPs and matrix is clearly visible (dotted yellow line). (b) Quartz, albite, chlorite, barite and micropore occur in SMMPs. (c) Micro-porosity in the matrix is abundant (d) Euhedral granular halite crystals which filling the matrix pores. Q–Quartz; Ab–Albite; Chl–Chlorite.
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Figure 8. Photomicrographs and laser Raman spectroscopy of fluid inclusions of quartz in the SMMPs. (a) Typical fluid inclusions in quartz; (b) Laser Raman spectroscopy of three fluid inclusions of quartz; (ce) Typical fluid inclusions in quartz. 5645.76 m. D-Bitumen peak D; G-Bitumen peak G; red circle-fluid inclusion in quartz.
Figure 8. Photomicrographs and laser Raman spectroscopy of fluid inclusions of quartz in the SMMPs. (a) Typical fluid inclusions in quartz; (b) Laser Raman spectroscopy of three fluid inclusions of quartz; (ce) Typical fluid inclusions in quartz. 5645.76 m. D-Bitumen peak D; G-Bitumen peak G; red circle-fluid inclusion in quartz.
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Figure 9. Conceptual model of the formation and evolution of SMMPs in the Permian volcanic rocks in the Jianyang area. (a) Volcanic material formed; (b) Early mineral alteration; (c) Scapolite formation; (d) Scapolite euhedral crystal; (e) Scapolite dissolved along cleavage; (f) Pseudomorph metasomatic scapolite.
Figure 9. Conceptual model of the formation and evolution of SMMPs in the Permian volcanic rocks in the Jianyang area. (a) Volcanic material formed; (b) Early mineral alteration; (c) Scapolite formation; (d) Scapolite euhedral crystal; (e) Scapolite dissolved along cleavage; (f) Pseudomorph metasomatic scapolite.
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Figure 10. Paragenetic sequence of hydrothermal minerals in Permian volcaniclastic rocks.
Figure 10. Paragenetic sequence of hydrothermal minerals in Permian volcaniclastic rocks.
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Table 1. The major and trace element analysis of Permian volcaniclastic rocks in well YT1.
Table 1. The major and trace element analysis of Permian volcaniclastic rocks in well YT1.
Sample
Number
DepthAl2O3CaOK2OBaOSrONa2OSiO2MgOSrBaSr/BaLOICIAAI
mwt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%ppmppm
YT1-15645.7616.024.240.070.030.026.6751.092.21129.035.53.633.2763.9117.29
YT1-35645.9817.033.410.070.040.028.8057.091.22141.049.22.872.0161.619.56
LOI- Loss on ignition; AI-alteration index; CIA-chemical index of alteration.
Table 2. The REE contents of Permian volcaniclastic rocks in well YT1.
Table 2. The REE contents of Permian volcaniclastic rocks in well YT1.
Sample
Number
DepthLREEHREEΣLREEΣHREEΣREE LREE/HREE
LaCePrNdSmEuGdTbDyHoErTmYbLu
mppmppmppmppm
YT1-15645.7654.7131.516.3566.714.54.0912.251.718.591.644.110.553.180.45287.8432.48320.328.86
YT1-35645.9822.981.611.3347.810.653.189.441.347.031.283.270.442.360.33177.4625.49202.956.96
Table 3. CIPW results of volcaniclastic rocks from the Permian Formation, well YT1, 5645.98 m.
Table 3. CIPW results of volcaniclastic rocks from the Permian Formation, well YT1, 5645.98 m.
CIPW
Calculation
Mineral
(Matrix)
QAnAbOrDiHyOlIlHmApZrCmTtnThTotal
wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%
0.07.0975.780.422.240.491.115.912.791.180.070.022.850.09100.04
DI = 76.2H2O = 1.25A/NK = 1.17A/CNK = 0.821AR = 2.53σ43 = 5.35
Above data is calculated from the major and trace element of matrix component (Table 1) (YT1-3, 5645.98 m). Q-Quartz; An-Anorthite; Ab-Albite; Or-Orthoclase; Di-Diopside; Hy-Hypersthene; Ol-Olivine; Il-Ilmenite; Hm-Hematite; Ap-Apatite; Zr-Zircon; Cm-Chromite; Ttn-Titanite; Th-Thenardite; Chl-Chlorite.
Table 4. The EPMA data of silicate minerals in SMMPs in the Well YT1.
Table 4. The EPMA data of silicate minerals in SMMPs in the Well YT1.
Sample
Number
DepthSiO2TiO2Al2O3FeOCr2O3MnOMgOCaONa2OK2OBaOTotalSample PointsMineral
mwt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%
YT1-1-A5645.7699.290.000.040.100.020.000.000.630.020.000.00100.10Q-1MQ
YT1-1-B5645.7698.650.020.060.090.000.000.011.230.000.030.00100.09Q-2MQ
YT1-3-C5645.9899.790.000.040.150.020.010.000.460.010.000.00100.49Q-3MQ
YT1-3-D5645.9897.700.060.010.170.000.020.001.890.030.000.0099.87Q-4MQ
YT1-4-E5646.4199.940.050.070.220.030.000.000.460.050.000.00100.82Q-5MQ
YT1-4-F5646.4197.430.000.010.150.010.000.011.990.000.000.0099.60Q-6MQ
YT1-4-G5646.4169.580.0019.680.040.030.000.000.0311.700.090.00101.15Ab1-1MA(Ab = 99.36)
YT1-1-H5645.7667.190.0319.060.070.050.010.010.0512.160.080.0098.70Ab1-2MA(Ab = 99.34)
YT1-3-I5645.9869.430.0019.580.060.050.020.000.0511.770.090.00101.05Ab1-3MA(Ab = 99.27)
YT1-4-J5646.4167.540.0119.310.080.040.010.020.0912.130.070.0099.29Ab2-1EA(Ab = 99.25)
YT1-4-K5646.4168.700.0619.710.080.140.010.020.0712.090.070.00100.96Ab2-2EA(Ab = 99.32)
YT1-4-L5646.4168.400.0319.300.020.090.000.000.0511.840.060.0099.78Ab2-3EA(Ab = 99.44)
YT1-4-M5646.4168.080.0019.610.030.110.000.010.0312.370.060.00100.30Ab2-4EA(Ab = 99.58)
Q–Quartz; Ab–Albite; MQ-metasomatic quartz; MA-metasomatic albite; EA-euhedral albite.
Table 5. The EPMA data of titanite in the Well YT1.
Table 5. The EPMA data of titanite in the Well YT1.
Sample
Number
DepthSiO2TiO2CaOAl2O3FeOFCr2O3Na2OBaOK2OMgOTotalSample PointsMineral
mwt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%
YT1-1-Q5645.7631.5634.6727.852.161.740.340.050.100.270.020.0298.65Ttn1-1ET
YT1-1-R5645.7631.4934.7928.002.091.760.440.050.090.290.000.0298.84Ttn1-2ET
YT1-3-S5645.9831.0636.1928.081.381.180.470.010.070.180.050.0598.71Ttn2-1MT
YT1-3-T5645.9831.4437.0727.371.360.670.250.000.040.290.200.1498.82Ttn2-2MT
YT1-4-U5646.4131.0536.8527.331.561.690.270.040.070.310.050.0999.33Ttn2-3MT
YT1-4-V5646.4131.6636.2427.771.340.770.370.020.050.270.060.0498.58Ttn2-4MT
ET-euhedral titanite; MT-microcrystalline titanite.
Table 6. The EPMA data of barite in the Well YT1.
Table 6. The EPMA data of barite in the Well YT1.
Sample
Number
DepthBaOSO3SrONa2OK2OCaOSiO2Al2O3FeOMnOMgOTotalSample PointsMineral
mwt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%wt.%
YT1-1-N5645.7659.1735.233.180.090.020.040.410.070.020.010.0098.24Brt-1barite
YT1-3-O5645.9861.1836.032.850.140.050.040.330.050.050.040.01100.77Brt-2barite
YT1-4-P5646.4160.3735.513.590.070.010.240.080.020.270.010.00100.14Brt-3barite
Table 7. Result of microthermometric study of fluid inclusions (average values).
Table 7. Result of microthermometric study of fluid inclusions (average values).
Sample
Number
MineralSizeVapor Liquid RatioFI TypeThTm IceSalinity
μm%°C°Cg/lwt.% NaCl eq
YT1-2-AQuartz410Pr210−1.424.12.41
YT1-2-BQuartz66Pr205−1.729.02.90
YT1-2-CQuartz55Pr208−1.830.63.06
YT1-2-DQuartz48Pr205−2.033.93.39
Note: Salinity calculation formula according to Bodnar, 1993 [52].
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Liu, X.; Li, Y.; Tan, C.; Cao, Z.; Jin, H.; Feng, M.; Xia, M.; Chen, J. Discovery of Pseudomorph Scapolite and Diagenetic Indication from the Permian Volcaniclastic Rocks in Western Sichuan (SW China). Minerals 2024, 14, 200. https://doi.org/10.3390/min14020200

AMA Style

Liu X, Li Y, Tan C, Cao Z, Jin H, Feng M, Xia M, Chen J. Discovery of Pseudomorph Scapolite and Diagenetic Indication from the Permian Volcaniclastic Rocks in Western Sichuan (SW China). Minerals. 2024; 14(2):200. https://doi.org/10.3390/min14020200

Chicago/Turabian Style

Liu, Xiaohong, Yue’e Li, Cong Tan, Zhenglin Cao, Hui Jin, Mingyou Feng, Maolong Xia, and Junlang Chen. 2024. "Discovery of Pseudomorph Scapolite and Diagenetic Indication from the Permian Volcaniclastic Rocks in Western Sichuan (SW China)" Minerals 14, no. 2: 200. https://doi.org/10.3390/min14020200

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