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Article

Genetic and Sealing Mechanisms of Calcareous Sandstones in the Paleogene Zhuhai–Enping Formations, Panyu A Sag, Pearl River Mouth Basin

1
College of Geosciences, China University of Petroleum, Beijing 102249, China
2
Shenzhen Branch of CNOOC (China) Limited, Shenzhen 518082, China
*
Author to whom correspondence should be addressed.
Minerals 2025, 15(12), 1285; https://doi.org/10.3390/min15121285
Submission received: 3 October 2025 / Revised: 25 November 2025 / Accepted: 4 December 2025 / Published: 7 December 2025

Abstract

Calcareous sandstones, acting as sealing layers, play a crucial role in hydrocarbon accumulation of formations with high sand content (sand content > 80%). However, the genetic mechanisms, sealing mechanisms, and effectiveness of calcareous sandstones remain unclear. This study takes the Zhuhai–Enping formations in the Panyu A Sag as an example. By comprehensively analyzing data from well logs, cores, cast thin sections, elemental geochemical analysis and carbon–oxygen isotopes, the genetic mechanisms, development patterns, and controlling effects on hydrocarbon accumulation of calcareous cement layers are investigated. The main findings are as follows: (1) The calcareous sandstone cements are mainly composed of dolomite, ankerite, and anhydrite. With increasing burial depth, dolomite transitions from micritic dolomite to silt-sized and fine-crystalline dolomite, and finally to coarse-crystalline dolomite. (2) The local transgression provided ions such as Ca2+ and Mg2+, forming the material basis for early dolomite formation. As burial depth increased, the diagenetic environment shifted from acidic to alkaline, leading to the dolomitization of early-formed calcite and the formation of ankerite. (3) The high source-reservoir displacement pressure difference effectively seals hydrocarbon accumulation. Vertically interbedded tight calcareous sandstones and thin marine transgressive mud-stones collectively control efficient hydrocarbon preservation and enrichment. This research addresses the current limits in the study of “self-sealing sandstone layers,” and provides new geological insights and predictive models for hydrocarbon exploration in sand-rich settings.

1. Introduction

Calcareous cement is one of the most widely distributed types of cement in clastic rock reservoirs. Its formation and distribution play a significant controlling role in reservoir physical properties, hydrocarbon migration and accumulation [1,2]. The genetic mechanisms, development patterns, and impact on reservoir heterogeneity of carbonate cementation have been central topics in reservoir geology and diagenetic dynamics research. Previous studies have often approached the precipitation and dissolution mechanisms of carbonates from perspectives such as water–rock interactions, organic-inorganic interactions, and material exchange between sandstones and mudstones, utilizing thermodynamic and geochemical methods [3,4,5]. For instance, Barnes et al. [6] and Taylor and Macquaker [7] emphasized the influence of organic acids and thermochemical sulfate reduction (TSR) on carbonate solubility, while Lynch [8] and Rlykke [9] established temporal evolution models for cement development based on diagenetic sequences. Tan et al. [10] systematically summarized the geochemical characteristics and fluid sources of carbonate cements in different basin settings, pointing out that the sources of calcium ions include the decomposition of bioclasts, the dissolution and alteration of feldspar and other aluminosilicate minerals, as well as calcium ions originally present in depositional water and pore water [11,12,13]. Lee et al. (2021) pointed out the carbonates were close to the densest packing by mechanical compaction at a burial depth of 750 m, and major porosity deviations are associated with dolomitization, dolomitic cementation, aragonite needle-rich mud and non-skeletal grains [14].
In formations with high sand content (sand content > 80%), the lack of mudstone cap rocks and weak lateral sealing capacity of faults make the effective preservation of oil and gas a key challenge in exploration. Calcareous cemented layers often develop as dense, discontinuous interlayers within sand bodies. These layers not only control fluid flow pathways within the reservoir, leading to complex oil-water relationships and the distribution of residual oil [15,16], but may also act as a novel type of “internal cap”, providing local cap rock functionality for hydrocarbon accumulation [17]. Previous studies on diagenesis in the sandstones of the Pearl River Mouth Basin indicate that the development of carbonate cements is a key factor leading to the densification of deep reservoirs in the Zhuhai Formation [18,19]. The distribution of calcareous cementation within sand bodies exhibits significant heterogeneity: sandstones adjacent to mudstones undergo preferential cementation due to intense water–rock reactions, forming dense layers, while conversely preserving the primary porosity of the underlying sand bodies [20]. The development of calcareous interbeds within sand bodies is mainly influenced by both sedimentary and diagenetic processes, with bioclasts serving as the primary source of calcium, supplemented by sources such as feldspar dissolution and silicate mineral hydration [1,16,17]. However, existing research predominantly regards calcareous cemented bodies as heterogeneous elements affecting reservoir quality, while systematic investigation into their sealing capacity as potential cap rocks, their formation mechanisms, spatial distribution, and dynamic effectiveness during accumulation processes remains lacking.
Panyu A Sag is located in the southern part of the Xijiang Sag, Zhu I Depression, and is a typical “small but rich” hydrocarbon-generating sag with high source rock potential. In recent years, significant breakthroughs have been made in drilling the Paleogene Zhuhai–Enping formations (with an overall sandstone content of 80%–95%) in Panyu A Sag, discovering proven in-place reserves exceeding 50 million tons [21]. Exploration practices have revealed that both mudstone and calcareous sandstone serve as two types of seals in the Zhuhai–Enping formations of the Panyu A Sag, with calcareous sandstone playing a critical role in sealing hydrocarbon accumulations. This study focuses on the widely developed dolomitic sandstone and anhydritic sandstone in the Zhuhai–Enping formations of the area. It aims to transcend the traditional perception that views calcareous cement merely as a factor influencing reservoir quality, and instead, delves into its sealing mechanisms and effectiveness in sand-rich settings. By integrating petrological, geochemical, and petroleum geological methods, this research seeks to unravel the genetic mechanisms, distribution patterns, and controlling effects of calcareous cemented layers on hydrocarbon accumulation. The findings are expected to address current research limits in “self-sealing sandstone layers” and provide new geological insights and predictive models for hydrocarbon exploration in sand-rich regions.

2. Regional Geological Background

2.1. Structural Location

The Pearl River Mouth Basin, as one of the most important petroliferous basins, is located on the northern continental margin of the South China Sea and is a Mesozoic-Cenozoic extensional basin [22]. Its formation and evolution are largely controlled by the rifting and spreading processes of the South China Sea. During the Paleocene to Eocene, this region underwent multiple phases of rifting, accompanied by lithospheric extension, fault development, and localized magmatic activity, resulting in the formation of several NE-trending dustpan-shaped sags and half-graben structures [23]. The Pearl River Mouth Basin exhibits a structural framework of “three uplifts and three depressions,” which are divided from north to south into the Northern Fault Zone, Northern Depression Zone, Central Uplift Zone, Central Depression Zone, Southern Uplift Zone, and Southern Depression Zone [24]. The Zhu I Depression, located within the Northern Depression Zone of the Pearl River Mouth Basin, is the most significant oil-producing area in the basin. From west to east, it comprises the Enping Sag, Xijiang Sag, Huizhou Sag, Lufeng Sag, and Hanjiang Sag, which are separated by NW-trending low uplifts (Figure 1a).
The Panyu A Sag is located in the southern part of the Xijiang Sag. Its formation and evolution are controlled by the NE-SW trending boundary faults (Figure 1b). During the Paleogene, it experienced multiple tectonic movements, including the Shenhu tectonic movement, the first episode of the Zhuqiong tectonic movement, the Huizhou tectonic movement, and the second episode of the Zhuqiong tectonic movement [25,26] (Figure 1c). These events led to multiple intense phases of uplift and erosion within the sag, resulting in its current anti-”L” shaped distribution pattern, which is narrow in the NE direction and wide in the SW direction. The Panyu A Sag is bounded by the Dongsha Uplift to the east, adjacent to the Xien Low Uplift to the west, and bordered by the Panyu Low Uplift to the south. It can be further subdivided into the Northern Sub-sag, Southern Sub-sag, and Northwestern Sub-sag (Figure 1b).
Figure 1. Structural unit subdivision of the Pearl River Mouth Basin (a); Basement topography and structural unit subdivision of the Panyu A Sag (b); Stratigraphic column of the Panyu A Sag (c) (Modified from [27]).
Figure 1. Structural unit subdivision of the Pearl River Mouth Basin (a); Basement topography and structural unit subdivision of the Panyu A Sag (b); Stratigraphic column of the Panyu A Sag (c) (Modified from [27]).
Minerals 15 01285 g001

2.2. Stratigraphy

The basin basement consists of Early Cretaceous granite. Overlying the basement, the Cenozoic sedimentary strata from oldest to youngest are as follows: the Eocene Wenchang Formation (E2w) and Enping Formation (E2e), the Oligocene Zhuhai Formation (E3z), the Miocene Zhujiang Formation (N1z), Hanjiang Formation (N1h), and Yuehai Formation (N1y), the Pliocene Wanshan Formation (N2w), and the Quaternary (Q) [21]. Among these, the Wenchang Formation and lower Enping Formation deposited during the rift phase represent continental facies, while the upper Enping Formation and Zhuhai Formation formed during the rift-sag transition phase exhibit marine–terrestrial transitional facies. Strata above the Zhujiang Formation deposited during the sag phase are characterized by marine facies [28]. Within the depression, hydrocarbon source rocks are primarily developed in the Wenchang Formation, while high-quality reservoirs occur in the Enping, Zhuhai, Zhujiang, and Hanjiang Formations. Overall, the petroleum system presents a “source rocks below with reservoirs above” accumulation model [27] (Figure 1c).

2.3. Sedimentary Characteristics

The Enping Formation in the Panyu A Sag is characterized by deltaic sandstone deposits, with locally developed shallow lacustrine depositional systems [29]. In the lower member of the Enping Formation, it inherited the active fault characteristics of the Wenchang Formation, with the depositional center largely consistent with that of the Wenchang period. In the upper member of the Enping Formation, fault activity significantly weakened, marking a transition period from faulting to depression. NW-trending faults along the western margin began to control sedimentation, leading to a gradual migration of the depositional center toward the southwestern side. The thickness of the strata in the depositional center is 3 to 5 times greater than that in the marginal areas [30]. The Zhuhai Formation represents a transitional deposit from terrestrial to marine environments, comprising a sequence of deltaic and coastal deposits, with relatively well-developed sandstones (Figure 1c).
Drilling data reveal that the lower member of the Enping Formation in the Panyu 4 Sag ranges from 131 to 280 m in thickness, with sand content of 89.6%–98.4%. The lithology is dominated by thick-bedded, pebbly medium- to coarse-grained sandstones, with intercalations of calcareous siltstones and thin mudstone layers. The upper member of the Enping Formation exhibits a thickness of 211–213 m and sand content of 78.1%–86.8%, primarily composed of medium- to fine-grained sandstones, calcareous sandstones, and mudstones. The Zhuhai Formation ranges from 429 to 639 m in thickness, with sand content of 65%–78%. Sandstone units consist mainly of thick-bedded, pebbly coarse sandstones, coarse sandstones, medium sandstones, and fine sandstones, interbedded with thin layers of calcareous medium- to fine-grained sandstones.

3. Materials and Methods

A total of 182 core samples from wells PY10-A, PY10-D, and PY10-F were collected for this study, encompassing typical intervals from the third member of the Zhuhai Formation, as well as the upper and lower members of the Enping Formation, with a focus on calcareous sandstones. Petrological and mineralogical analyses were first conducted using polarized light microscopy and scanning electron microscopy (TM4000plus, Hitachi, Tokyo, Japan). A total of 31 samples from Well PY10-A and 18 samples from Well PY10-F were selected for analysis of major and trace elements. Major element analysis was performed using a PANalytical Axios mAX wavelength-dispersive X-ray fluorescence (Bruker Corporation, Berlin, Germany) spectrometer, while trace element analysis was carried out with a NexION 300D inductively coupled plasma mass spectrometer (PerkinElmer, Waltham, MA, USA). Quality control measures included duplicate analyses of selected samples and certified reference materials. The relative standard deviation (RSD) for all elemental measurements was maintained below 10%, with both instrumental results and standard deviations falling within acceptable limits.
Next, 17 sandstone samples with well-developed carbonate cements were selected for further carbon and oxygen isotope analysis. Six samples from well PY10-A underwent in situ carbon–oxygen isotope analysis using laser ablation-stable isotope analyzer (Picarro Inc., Santa Clara, CA, USA). This system consists of a CETAC laser ablation unit coupled with a microscopic imaging system and a Delta isotope mass spectrometer. Additionally, 11 samples from wells PY10-A, PY10-D, and PY10-F were analyzed for bulk rock carbon and oxygen isotope ratios. The measured isotope ratios are reported as δ13C and δ18O values relative to the PDB standard in per mil (‰), with an analytical precision of 0.02‰. Detailed sample information and analytical results are presented in Table 1 and Table 2. The in situ isotope analyses were conducted at the Zhanjiang Laboratory of CNOOC’s Experimental Center, while bulk rock isotope analyses were performed at the National Key Laboratory of Petroleum Resources and Engineering at China University of Petroleum (Beijing).
Three calciferous sandstone samples and 11 reservoir samples were selected for porosity and permeability tests and high-pressure mercury injection analysis. The porosity and permeability were measured from 2.5 cm diameter core plugs from the reservoir intervals using a nitrogen permeameter (Core Laboratories, Houston, TX, USA). The dry and clean core samples were placed in the permeameter and injected with nitrogen at confining pressures of 100 and 400 psi. The high-pressure mercury injection experiment was performed on a PoreMaster PM33-13 mercury porosimeter (Micromeritics, Norcross, GA, USA). Three calcareous sandstone samples and two mudstone samples were selected for breakthrough pressure measurements using the pulse decay method. This technique involves applying a high gas injection pressure at the inlet end that exceeds the rock’s critical breakthrough pressure, enabling rapid gas penetration into the core. During gas injection, the outlet end maintains a constant-volume pressure monitoring chamber. The pressure differential across the core is continuously recorded as gas enters the system. This process displaces pore water into the monitoring chamber, resulting in progressive pressure buildup at the outlet. When the outlet pressure stabilizes, the pressure difference between the two ends represents the critical gas breakthrough pressure measured by the pulse decay method. The porosity and permeability tests, high-pressure mercury injection experiment and pulse decay breakthrough pressure tests were conducted at the National Key Laboratory of Petroleum Resources and Engineering, China University of Petroleum (Beijing).

4. Results

4.1. Petrological Characteristics of Calcareous Sandstones

The calcareous sandstone in the Enping–Zhuhai formations of the study area has a single-layer thickness of 1–3 m. The lithology is predominantly dolomitic medium- to fine-grained feldspathic quartz sandstone and feldspathic lithic sandstone (Figure 2). The quartz content ranges from 44.5% to 80% (avg. 67.6%), feldspar content ranges from 4% to 32% (avg. 15.5%), and lithic fragment content ranges from 4% to 35.5% (avg. 16.9%). The lithic fragments are predominantly volcanic in origin, with content ranging from 2.5% to 33.5% (avg. 13.2%). Grain contacts are mainly point-to-line, and roundness is primarily subangular to subrounded. Overall, pore development is poor, with measured porosity ranging from 4.4% to 9.5% and permeability ranging from 0.02 mD to 0.19 mD. In the southern area, the calcareous sandstone in well PY10-A is mainly cemented by (ferroan) dolomite (content 7.5%–43%), exhibiting various occurrences such as micritic, microcrystalline, fine-crystalline, and coarse-crystalline types. In the northern area, wells PY10-D and PY10-F are primarily cemented by anhydrite (content 6%–32%), which often fills large pores and forms polkilotopic cementation between grains.
Glauconite is abundant in the study area (Figure 3a–c), with a content ranging from 1.5% to 12%. It occurs as green elliptical grains with well-preserved morphology and shows no evidence of plastic deformation (Figure 3c). Microscopic examination reveals diverse bioclasts including echinoderms (Figure 3d–e), foraminifera (Figure 3f–g), and bivalves (Figure 3h–i), with minor preservation of intraparticle pores within bioclasts.

4.2. Calcareous Cement Types and Characteristics

4.2.1. Dolomite

Dolomite remains unstained when treated with a mixed solution of potassium ferricyanide and alizarin red S. It predominantly exhibits basal cementation, with subordinate porous cementation and grain replacement textures. Petrographically, dolomite cements are classified into micritic dolomite, euhedral-subhedral silt-to-fine crystalline dolomite, and anhedral coarse crystalline dolomite.
(1) Micritic Dolomite
Micritic dolomite predominantly developed in the upper section of the Enping Formation in Well PY10-A, with contents ranging from 29% to 32%. It mainly exhibits basal cementation. The micritic dolomite usually forms isopachous micritic envelopes around grains, primarily coating bioclasts and intraclasts (Figure 4a–c). Intense micritization obliterates original internal structures of some bioclasts, forming micritic peloids. This micritic dolomite typically precipitates prior to syntaxial overgrowths on cements and bioclasts, serving as a diagnostic indicator of syngenetic marine seafloor diagenesis. The micritization of carbonate grains represents a key diagenetic feature in stagnant marine phreatic zones and also evidence of relatively slow sediment aggradation rates. Under these conditions, intergranular carbonate cementation is underdeveloped, allowing ample time for algal/fungal perforation [31,32].
(2) Silt to Fine-crystalline Dolomite
Silt to fine-crystalline dolomite is the most widespread dolomite texture in the study area, it occurs as crystalline clusters with interconnected or partially overlapping crystals (Figure 4f). It usually evolves from intergranular micritic dolomite precursors. Progressive burial depth and continuous dolomitizing fluid supply drive crystal overgrowth and structural reorganization of micritic matrix, ultimately developing cohesive clusters of planar-faced euhedral-subhedral dolomite crystals. Petrographic observations reveal dolomite replacement textures affecting quartz and glauconite grains (Figure 4d,e). Both micritic dolomite and euhedral-subhedral silt-sized to fine-crystalline dolomite represent products of shallow-burial dolomitization.
(3) Anhedral Coarse-crystalline Dolomite Anhedral coarse-crystalline dolomite exhibits variable crystal sizes ranging from fine to coarse, with curved anhedral boundaries. Under plane-polarized light, crystal surfaces appear turbid with indistinct zoning, while crossed polars reveal uniform extinction (Figure 4g–i). The coarse-crystalline dolomite can be formed through the recrystallization of pre-existing silt-sized to fine-crystalline dolomite, or through the recrystallization or replacement reactions of micritic dolomite when encountering high-temperature dolomitizing fluids during deep burial stages. Enhanced supersaturation of dolomite in fluids (specifically elevated Mg2+/Ca2+ ratios) drives development of mosaic textures with characteristic curvilinear crystal contacts [33].

4.2.2. Ankerite

Ankerite is defined as a dolomite-group mineral where over 50% of magnesium ions are substituted by iron ions [34,35]. It stains blue when treated with a mixed solution of potassium ferricyanide and alizarin red S. Ankerite develops primarily as porous cementation binding detrital grains (Figure 4j,k), and the rhombohedral ankerite crystals exhibit polikilotopic distribution (Figure 4i) under scanning electron microscopy (SEM). Additionally, authigenic quartz is replaced by ankerite (Figure 4k), suggesting alterations in diagenetic fluid chemistry.

4.2.3. Anhydrite

In the southern area of Panyu A Sag, anhydrite occurred in Wells PY10-A is predominantly developed in the upper member of the Enping Formation and the 3rd Member of the Zhuhai Formation. Conversely, in the northern area of Panyu A Sag, anhydrite occurred in Wells PY10-D and PY10-F ubiquitously across all stratigraphic members.
Anhydrite commonly fills large intergranular pores and occurs as patchy or basal cementation binding detrital grains (Figure 5), with contents ranging from 9% to 26%. Its strongly heterogeneous cementation patterns (Figure 5a,b) compromise its effectiveness as a regional seal. Detrital grains cemented by anhydrite predominantly exhibit point-to-line contacts and point contacts (Figure 5c,d), indicating limited compaction. This reflects anhydrite precipitation during shallow-burial stages (syngenetic to eogenetic periods) within evaporative depositional settings. Petrographic observations reveal anhydrite commonly associated with quartz dissolution (Figure 5e) or replacement of quartz grains (Figure 5f), indicating precipitation in an early-stage alkaline diagenetic environment. According to previous studies, the δ34SV-CDT values of Paleogene anhydrite in the Zhu I Depression range from 18.12‰ to 31.71‰, exhibiting broad variability within the isotopic range of marine evaporite sulfates. This indicates formation in evaporative brines during initial burial [36].

4.3. Geochemical Characteristics

4.3.1. Major Elements

The major elemental contents of the 31 core samples from Well PY10-A are shown in Table 1. The MgO content is 0.4%~4.53% (avg. 1.86%), the CaO content is 0.18%~8.58% (avg. 2.14%), the Al2O3 content is 5.5%~17.9% (avg. 8.87%), the SiO2 content is 61.94%~85.99% (avg. 74.68%), the K2O content is 2.40%~4.97% (avg. 2.95%), the MnO content is 0.008%~0.59% (avg. 0.13%), the Na2O content is 0.39%~1.27% (avg. 0.67%), the TiO2 content is 0.08%~0.77% (avg. 0.36%), and the P2O5 content is 0.007%~0.27% (avg. 0.047%).

4.3.2. Trace Elements

The trace element contents of the 31 core samples from Well PY10-A and 18 core samples from Well PY10-D are shown in Table 2 and Table 3. For samples from Well PY10-A, the Sr/Cu ratio ranges from 0.39 to 30.0 (avg. 11.9), the Sr/Ba ratio ranges from 0.012 to 0.177 (avg. 0.065), the B/Ga ratio ranges from 1.74 to 5.89 (avg. 3.64), the V/(V + Ni) ratio ranges from 0.46 to 0.79 (avg. 0.73), the Zr/Y ratio ranges from 7.25 to 15.14 (avg. 20.39), the Rb/Zr ratio ranges from 0.33 to 0.82 (avg. 0.53) (Table 2). For samples from Well PY10-D, the Sr/Cu ratio ranges from 2.3 to 5.77 (avg. 3.32), the Sr/Ba ratio ranges from 0.003 to 0.013 (avg. 0.006), the B/Ga ratio ranges from 1.48 to 6.92 (avg. 4.13), the V/(V + Ni) ratio ranges from 0.72 to 0.83(avg. 0.77), the Zr/Y ratio ranges from 8.1 to 20.0 (avg. 12.53), the Rb/Zr ratio ranges from 0.44 to 0.75 (avg. 0.61) (Table 3).

4.3.3. Carbon and Oxygen Isotope Data

Through analysis of 19 in situ carbon–oxygen isotopes and 11 whole-rock carbon–oxygen isotopes, the in situ δ13CPDB values of Enping–Zhuhai formations in the study area range from −11‰ to −22‰ (avg. −14.95‰), while δ18OPDB values range from −2.2‰ to −10‰ (avg. −5.49‰) (Table 4). Whole-rock δ13CPDB values range from −10‰ to −11‰ (avg. −10.34‰), and δ18OPDB values range from −8‰ to −13‰ (avg. −10.47‰) (Table 5). There are obvious differences in carbon and oxygen isotopes of different lithologies. The δ13CPDB values of micritic dolomite range from −11.73‰ to −22.01‰ (avg. −16.84‰), and δ18OPDB values range from −2.25‰ to −4.24‰ (avg. −3.20‰). The δ13CPDB values of silt-to-fine crystalline dolomite range from −10.97‰ to −15.37‰ (avg. −13.59‰), and δ18OPDB values range from −5.62‰ to −7.28‰ (avg. −6.72‰). The δ13CPDB values of coarse crystalline dolomite range from −11.93‰ to −13.25‰ (avg. −12.44‰), and δ18OPDB values range from −9.15‰ to −10.02‰ (avg. −9.56‰).

4.4. Displacement Pressure and Breakthrough Pressure

Three calciferous sandstone samples and 11 reservoir samples were selected for high-pressure mercury injection tests. The measured displacement pressures of the samples are shown in Table 6. The displacement pressure of calciferous sandstone ranges from 0.779 MPa to 1.417 MPa, with an average of 1.013 MPa, while that of the sandstone reservoir ranges from 0.035 MPa to 0.901 MPa, with an average of 0.275 MPa. The displacement pressure difference in the reservoir–seal assemblage composed of sandstone and calciferous sandstone is 0.738 MPa. The breakthrough pressure of calciferous sandstone measured using the pulse decay method is 0.5 MPa, and that of mudstone is 1.6 MPa (Figure 6).

5. Discussion

5.1. Genetic Mechanisms and Development Models of Calcareous Sandstones

5.1.1. Local Marine Transgressions

Since the Late Eocene (33 Ma), the Pearl River Mouth Basin has occupied a central position within a composite continental margin magmatic arc. Influenced by differential crustal thinning, the South China Sea region experienced subduction of the Paleo-South China Sea and rifting of the Neo-South China Sea Basin [37,38,39,40]. This differential thinning not only redistributed crustal thickness but also triggered terrace-style basin subsidence, driving progressive marine transgressions. Consequently, the formation of the South China Sea exhibits characteristics of a gradual marginal sea tectonic cycle [40]. Following the rifting of the Neo-South China Sea, marine transgressions advanced progressively across the northern South China Sea from south to north, as well as east to west during the period from 38 Ma to 23 Ma [39].
During the Oligocene, terrigenous detritus was transported via submarine channels to the Baiyun Sag, with the marine transgression progressively extending westward into the Zhu I Depression [41]. Following the interpretation of seismic data and the application of decompaction correction [42,43], the original sedimentary stratigraphic thicknesses for the Early and Late Enping stages were derived. Subsequent reconstruction of the paleotopography for different periods was achieved through 3D visualization employing the “template method.” (Figure 7). Paleogeomorphic reconstructions of the Enping period reveal that seawater advanced northward through a conduit between the Dongsha Uplift and Xi’en Low Uplift, entering the southern subsag of Panyu A Sag (Figure 7). This hydrodynamic regime provided essential conditions for the formation of marine-influenced calcareous sandstones and thin mudstones within deep sand-rich strata of the Panyu A Sag. In the northern area of Panyu A Sag, the topographically higher terrains of Wells PY10-D and PY10-F contrast with the lower-lying area of Well PY10-A in the southern area. This paleogeomorphic configuration resulted in more frequent marine incursions into the PY10-A area, while shallower water depths across the PY10-D and PY10-F areas.
In the study area, the glauconite within the calcareous sandstone is well-preserved in morphology and shows no signs of plastic deformation, indicating minimal transport and an authigenic origin [44]. Some glauconite grains have been subsequently replaced by dolomite (Figure 3c). A variety of bioclasts are observed under the microscope, coexisting with detrital grains (Figure 3d–i), suggesting relatively strong wave action capable of transporting bioclasts to the shallow-water depositional area [45]. Furthermore, the major element oxides CaO, MgO, and Fe2O3 (particularly MgO) from well PY10-A show three distinct peaks within the upper member of the Enping Formation (Table 1 and Figure 8), indicating three large-scale marine transgression events in this region [46].
Trace elements and their concentrations in sedimentary rocks exhibit high sensitivity to variations in aqueous media within depositional environments, providing robust proxies for reconstructing paleoenvironmental and paleoclimatic evolution [47,48]. This study employs Sr/Cu, B/Ga, and V/(V + Ni) ratios to investigate paleoenvironmental changes, with trace element analytical results presented in Table 2 and Table 3 and Figure 9. Well PY10-A in the study area exhibits Sr/Cu ratios predominantly exceeding 5 during the depositional period of the Zhuhai–Enping formations (Figure 9a), indicating a prevailing relatively dry and hot climatic condition. The B/Ga ratio serves as a reliable proxy for paleosalinity reconstruction [49]. Analytical results demonstrate that the Enping Formation predominantly records freshwater to brackish conditions, while the Zhuhai Formation transitions into brackish to saline environments (Figure 9b,e). Both units are interpreted as nearshore depositional settings with intermittent marine influences. Particularly during the late Enping depositional stage, the south-to-north transgression advance resulted in more pronounced marine influence at Well PY10-A in the southern area of Panyu A Sag, leading to elevated salinity levels. Overall, the water column remained poorly stratified, developing anaerobic to sub-reductive conditions that facilitated organic matter preservation and early diagenetic cementation. The data of Well PY10-A exhibits frequent fluctuations in paleoclimatic and paleosalinity conditions. This cyclic variation in hydrological parameters created a unique geochemical environment conducive to dolomite diagenesis. Kinetic modeling reveals that pulsed injections of terrestrial freshwater into marine systems trigger oscillatory variations in ionic activities (e.g., Ca2+, Mg2+) within the water column. Paradoxically, such metastable saturation states facilitate sustained growth of dolomite crystal nuclei [50,51,52].

5.1.2. Burial Diagenesis

Controls of Burial Diagenesis on Dolomite/Ankerite Cementation
Carbon and oxygen isotope data are often used to explain the genesis of dolomite. The carbon and oxygen isotope compositions of dolomite are mainly controlled by the carbon and oxygen isotope compositions of the dolomitized minerals and by the salinity and temperature of the diagenetic fluids [53,54,55].
(1) Paleosalinity
Keith and Weber combined δ13C and δ18O to propose an empirical formula for distinguishing marine from freshwater carbonate rocks [56]. This formula calculates a dimensionless Z-value to determine the nature of the aqueous medium and indicate paleosalinity.
Z = 2.048 × (δ13C + 50) + 0.498 × (δ18O + 50)
In the formula, δ13C and δ18O values are both referenced to PDB standard. The Z-value larger than 120 indicates a marine (seawater-derived) aqueous medium, while the Z-value less than 120 indicates a terrestrial freshwater-derived aqueous medium.
Based on the calculated Z-values (Table 4 and Table 5), the dolomite samples from the Zhuhai Formation exhibit Z-values ranging from 80.632 to 101.471, while those from the Enping Formation range from 82.318 to 101.392. All Z-values are below 120, indicating that the carbonate cements in these samples formed in a freshwater-dominated environment.
Research by Irwin et al. demonstrates that during diagenesis, the carbon and oxygen isotopic compositions of CO2 generated at different stages vary significantly: ① 0–10 m depth: Bacterial sulfate reduction produces CO2 with δ13CPDB value is −25‰ and δ18OPDB values range from 0‰ to −2‰; ② 10–1000 m depth: Bacterial fermentation yields CO2 with δ13CPDB value is +15‰ and δ18OPDB values range from −1.5‰ to −5‰; ③ >1000 m depth: Organic acids from kerogen degradation contribute to CO2 with δ13CPDB value is −20‰ and δ18OPDB values range from −3.5‰ to −7‰ [57]. The carbon and oxygen isotopic composition distribution diagram of carbonate cements (Figure 10a) reveals that the calcareous sandstone cements in the Zhuhai–Enping Formations of Panyu A Sag, predominantly interpreted as diagenetic carbonates formed during burial processes. A subset of data points clusters in Zone III, attributed to carbonate precipitated associated with organic acid decarboxylation.
(2) Paleotemperature
Water temperature is a critical factor controlling the stable isotopic composition of carbonate rocks. Temperature exerts a far greater influence on δ18O values than salinity, while δ13C values show minimal variation with temperature. Consequently, δ18O can serve as a reliable indicator of paleotemperature when salinity remains constant [58]. Numerous scholars have proposed using δ18O to determine paleotemperatures [56,58,59,60]:
1000lnαdolomite-water = 2.73 × 106T−2 + 0.26
In the formula, αdol-w = (1 + (δ18Odol/1000))/(1 + (δ18Ow/1000)), T is temperature in Kelvin (K), δ18OSMOW = 1.03086 × δ18OPDB + 30.86 (Converts PDB-standard values to SMOW), assume δ18OSMOW of modern seawater is 0‰.
In situ oxygen isotope thermometry results indicate that carbonate cements formed at temperatures ranging from 39.76 °C to 95.71 °C (Table 4). In the study area, micritic, silt-crystalline, and fine-crystalline dolomites primarily formed under the influence of diagenetic processes, while coarse-crystalline dolomites and ankerites were partially influenced by organic acid activity (Figure 10a). Dolomite types correspond to distinct developmental stages, with three phases identified. Micritic dolomite formed at 39.76–51.59 °C, representing the eodiagenesis A stage (shallow burial). Silt-fine crystalline dolomite formed at 60.66–72.64 °C, representing the eodiagenesis B stage (moderate burial). Coarse-crystalline & ankerite formed at 79.51–128.21 °C, representing the mesodiagenesis A stage (deep burial) (Figure 10b).
As rock burial depth increases, bacterial activity diminishes, and organic acid decarboxylation driven by thermal catalysis becomes the dominant reaction, generating hydrocarbons and CO2. This CO2 can migrate into reservoirs prior to or concurrently with hydrocarbon migration, leading to elevated CO2 pressure within the diagenetic system and subsequent precipitation as carbonate minerals [61]. Organic acids undergo decarboxylation to produce CO2, which combines with water to form carbonic acid (H2CO3). Subsequent ionization generates ions such as H+, HCO3, and CO32− [62]. Simultaneously, organic acids dissolve feldspar or early-stage bioclasts, and the transformation of certain clay minerals releases Ca2+ ions. When these HCO3 and CO32− ions encounter Ca2+ (or Mg2+/Fe2+) in pore water, they precipitate as ferroan calcite or ankerite [63]. Under the microscope, moldic pores formed by feldspar dissolution can be observed, along with intergranular medium-to-coarse crystalline ankerite spatially associated with feldspar dissolution (Figure 4k).
Controls of Burial Diagenesis on Gypsum/Anhydrite Dolomite Cementation
The ratios of Rb/Zr, Zr/Y, and Yb/La can be used to reflect changes in water depth related to sea-level fluctuations. The Rb/Zr ratio serves as an effective indicator of water depth and hydrodynamic conditions. A higher Rb/Zr value indicates deeper water and weaker hydrodynamic energy [64]. The Zr/Y ratio provides insights into sediment provenance distance and water depth. A lower Zr/Y value suggests a depositional environment farther from the terrigenous source and characterized by deeper seawater [65]. The Yb/La ratio is effective in identifying variations in water depth. In shallow marine settings, seawater is typically enriched in light rare earth elements (e.g., La), whereas deep marine environments are relatively enriched in heavy rare earth elements (e.g., Yb). Thus, a higher Yb/La value indicates deeper water [66]. As shown in Figure 11, well PY10-D in the northern area has Yb/La values <0.075, while well PY10-A in the southern area exhibits Yb/La values consistently >0.075. This indicates shallower water depths in the northern area compared to the south, resulting in stronger evaporation and relatively more developed gypsum deposits.
Overall, during the depositional period of the Zhuhai–Enping Formation in the study area, the environment was characterized by a relatively dry and hot freshwater to brackish nearshore setting, with occasional saline water incursions. This represented an anaerobic to sub-reducing environment with weak water stratification. When the climate shifted to semi-arid or arid conditions, continuous evaporation concentrated the depositional water body until CaSO4 reached supersaturation, leading to the precipitation of gypsum (CaSO4·H2O). Geomorphologically, Wells PY10-D and PY10-F in the northern area are topographically higher than Well PY10-6A in the southern area (Figure 7). Consequently, the northern area exhibits shallower water depths, stronger evaporation, and more extensive gypsum development.

5.2. Development Model of Calcareous Sandstones

Based on the transgression background, developmental characteristics, genetic mechanisms, and diagenetic evolution of calcareous sandstones, a development model for calcareous sandstones of the Zhuhai–Enping Formations in the Panyu A Sag has been established (Figure 12).
During the depositional period, marine transgression events reduced sedimentation rates, facilitating the enrichment of bioclastic materials while providing abundant sources of Ca2+ and Mg2+. Local intermittent transgressions caused dolomite saturation states to oscillate between supersaturation and undersaturation, promoting dolomite formation. In the syndiagenetic to early diagenetic stages, seawater evaporation led to supersaturation of SO42− and Ca2+, precipitating gypsum/anhydrite. Simultaneously, supersaturated Ca2+ and Mg2+ formed early-stage calcite/dolomite. Upon reaching the mesodiagenetic stage, increasing burial depth activated two key carbon sources for carbonate cementation: sulfate reduction and thermal decarboxylation of organic acids. As organic acids became progressively depleted, the diagenetic environment shifted from acidic to alkaline. Concurrently, the transformation of smectite to illite released Fe3+ and Mg2+. This triggered dolomitization of calcite and subsequent formation of ankerite, ultimately resulting in dense sandstone cementation (Figure 12).
During the late Enping period, carbon and oxygen isotope analyses combined with elemental data indicate episodic sea-level rise, leading to water salinization that transitioned the freshwater lake basin into a brackish lacustrine environment. This shift provided the depositional setting essential for calcareous sandstone formation. In the Panyu A Sag along the sag margin, Wells PY10-D and PY10-F developed significant anhydrite deposits due to shallow water depths and intense evaporation. In contrast, Well PY10-A in the southern area experienced seawater incursions that delivered abundant ions, promoting dolomite cementation. Following the transition from continental to marine deposition in the Zhuhai Formation, sustained ion supply coupled with increasing burial depth triggered recrystallization of dolomite, forming anhedral coarse-crystalline (ferroan) dolomite (Figure 12).

5.3. Sealing Mechanisms of Calcareous Sandstones

5.3.1. Sealing Mechanism and Effectiveness Evaluation of Calcareous Sandstones

Hydrocarbon exploration practices demonstrate that calcareous sandstones within the sand-rich sequences of the Zhuhai–Enping Formations in the Panyu A Sag play a critical role as caprocks for hydrocarbon accumulation [21]. The sealing capacity primarily relies on the displacement pressure differential between the caprock and reservoir [67,68,69]. Thus, higher displacement pressure in the caprock correlates with stronger capillary pressure sealing capability, whereas lower pressure results in weaker sealing. This stu dy statistically analyzes displacement pressures of calcareous sandstone caprocks and reservoirs across the research area, calculating the maximum hydrocarbon column height sealed by the caprocks. The results confirm the effectiveness of calcareous sandstones as sealing layers.
The maximum hydrocarbon column height (H) sealed by a caprock occurs when buoyancy equals the displacement pressure difference between the caprock and reservoir. The calculation formula is given by [70]:
H = (PcapPres)/((PwPg) ∗ g)
In the formula, H = Hydrocarbon column height (×103 m); Pcap = Displacement pressure of the caprock (MPa); Pres = Displacement pressure of the reservoir (MPa); ρw = Formation water density (typically 1.0 × 103 kg/m3); ρg = Hydrocarbon density (typically 0.75 × 103 kg/m3); g = Gravitational acceleration (9.8 m/s2).
This study reveals that the displacement pressure differential between calcareous sandstone and sandstone reservoir is 0.738 MPa (Table 6). With calcareous sandstone caprock permeability < 0.3 mD, the average sealed hydrocarbon column height calculated directly from constant-rate mercury injection data reaches 295.2 m. Analysis of displacement pressures via pulse-decay breakthrough pressure tests (Figure 6) and constant-rate mercury injection experiments demonstrates that 2–3 m thick transgressive calcareous sandstone layers can seal oil columns of 234–520 m (Figure 13), confirming their effectiveness as caprocks. The average oil column height sealed by calcareous sandstones of all Upper Enping Formation is 437.90 m. In contrast, mudstone caprocks in the study area exhibit higher breakthrough pressures (predominantly 1.6 MPa; Figure 6b), with a calculated maximum hydrocarbon column height of 640 m, indicating superior sealing capacity compared to calcareous sandstones.

5.3.2. Development Model of Hydrocarbon Accumulation

(1) Reservoir–seal assemblage pattern
During the middle depositional stage of the Enping Formation, the lake basin in the study area expanded rapidly, reaching its maximum extent and forming a maximum flooding surface (MFS) (Figure 14). This period developed a regionally extensive mudstone layer with a thickness of 28 m, serving as the most critical regional seal. In the late Enping period, the lake basin shrank and experienced intermittent marine transgressions, leading to localized water salinization. This resulted in the deposition of interbedded calcareous sandstone, mudstone, and normal sandstone. The upper section of the Enping Formation has a thickness of 211–213 m and a sandstone content of 78.1%–86.8%. The lithology is predominantly composed of medium- to fine-grained sandstone, calcareous sandstone, and mudstone. Sandstones from the braided river delta plain or braided river delta front subfacies are interbedded with lacustrine (marine) flooding mudstones and calcareous sandstones, forming two types of high-quality reservoir–seal assemblages (Figure 14).
(2) Hydrocarbon accumulation model
The Panyu A Sag exhibits a hydrocarbon accumulation model characterized by “fault-efficient migration and near-source dominant accumulation” [21]. Long-active trap-controlling faults extensively connect with high-quality source rocks of Wenchang Formation in the southern subsag. Hydrocarbons migrate along these faults into braided river delta sandstone reservoirs of the Enping and Zhuhai Formations, ultimately accumulating in fault-block traps with favorable lateral sealing capacity under the effective confinement of lacustrine flooding mudstones and calcareous sandstones. The reservoirs feature large-scale efficient charging and multi-strata accumulation. Overall, efficient hydrocarbon preservation and enrichment are controlled by vertically interbedded tight calcareous sandstones with strong cementation (formed by intermittent marine transgressions superimposed with burial diagenesis) and thin marine transgressive mudstones (Figure 15).

6. Conclusions

(1) The calcareous sandstone cements in the Zhuhai–Enping formations of the Panyu A Sag are mainly composed of dolomite, ankerite, and anhydrite. Anhydrite typically fills large intergranular pores and forms polkilotopic cement between grains. With increasing burial depth, dolomite transitions from micritic dolomite to silt-sized and fine-crystalline dolomite, and finally to coarse-crystalline dolomite.
(2) The expansion of the New South China Sea at 33 Ma during the late Eocene led to a local transgression, which provided ions such as Ca2+ and Mg2+, forming the material basis for early dolomite formation. As burial depth increased, organic acids were gradually depleted, and the diagenetic environment shifted from acidic to alkaline, leading to the dolomitization of early-formed calcite and the formation of ankerite. In the northern part of the study area, under strong evaporation conditions, the supersaturation of SO42− and Ca2+ concentrations resulted in the precipitation of gypsum/anhydrite.
(3) The braided river delta distributary channel sandstones, together with lacustrine (marine) flooding mudstones and calcareous sandstones, form two types of high-quality reservoir–seal combinations. Vertically interbedded tight calcareous sandstones and thin marine transgressive mudstones collectively control efficient hydrocarbon preservation and enrichment.

Author Contributions

Conceptualization and methodology, Y.Z.; software, K.W. and W.Z.; formal analysis, K.W.; investigation, Y.Z.; resources, G.P., X.Q. (Xinwei Qiu) and Z.L.; data curation, W.Z.; writing—original draft preparation, K.W.; writing—review and editing, Y.Z.; visualization, W.Z.; supervision, X.Q. (Xiaoming Que) and P.J.; funding acquisition, G.P. 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 (42472178) and the National Key R&D Program of China (2024YFE0114000).

Data Availability Statement

All of the data and models generated or used in the present study are available from the corresponding author upon request.

Acknowledgments

The authors would like to express their sincere thanks to the Shenzhen Branch of CNOOC (China) Limited for their assistance in providing the data, and for their technical input to this work.

Conflicts of Interest

Authors Guangrong Peng, Wenchi Zhang, Xinwei Qiu, Zhensheng Li, Xiaoming Que and Peimeng Jia are employed by the Shenzhen Branch of CNOOC (China) Limited. The remining authors declare that they have no known competing financial interest or personal relationships that might have influenced the work presented in this article.

Abbreviations

The following abbreviations are used in this manuscript:
PPLPlane-polarized light
XPLCross-polarized light
SEMScanning electron microscope
MDMicritic dolomite
S-FDSilt-to-fine-crystalline dolomite
CCDCoarse-crystalline dolomite
AnAnkerite
GpGypsum

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Figure 2. Petrographic composition ternary diagram of calcareous sandstones in the Panyu A Sag.
Figure 2. Petrographic composition ternary diagram of calcareous sandstones in the Panyu A Sag.
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Figure 3. Microstructural Characteristics of Glauconite and Bioclasts in the Zhuhai and Enping Formations, Panyu A Sag. (a) Scattered elliptical green glauconite grains, E3z (Zhuhai Fm. Mb. 2), Well PY10-D, 3130 m, blue epoxy, PPL; (b) Minor elliptical glauconite particles, E3z, Well PY10-D, 3225 m, blue epoxy, PPL; (c) Sparse glauconite grains (partially altered), E2e, Well PY10-F, 3698.95 m, blue epoxy, PPL; (d) Pervasive micritic to fine-crystalline dolomite filling intergranular pores and cementing grains, with minor echinoderm debris, E2e, Well PY10-F, 3697.2 m, blue epoxy, PPL; (e) Isolated echinoderm bioclasts, E2e, Well PY10-F, 3700.95 m, blue epoxy, PPL; (f) Micritic dolomite cementing grains with foraminiferal bioclasts, E2e, Well PY10-A, 3686 m, blue epoxy, PPL; (g) Minor foraminifera fragments, E2e, Well PY10-A, 3703.5 m, blue epoxy, PPL; (h) Abundant bivalve bioclasts retaining body cavities, E2e, Well PY10-F, 3702.2 m, blue epoxy, PPL; (i) Dominant bivalve debris with preserved internal molds, E2e, Well PY10-F, 3703.2 m, blue epoxy, PPL. PPL: plane-polarized light. Abbreviations: CCD: coarse crystalline dolomite.
Figure 3. Microstructural Characteristics of Glauconite and Bioclasts in the Zhuhai and Enping Formations, Panyu A Sag. (a) Scattered elliptical green glauconite grains, E3z (Zhuhai Fm. Mb. 2), Well PY10-D, 3130 m, blue epoxy, PPL; (b) Minor elliptical glauconite particles, E3z, Well PY10-D, 3225 m, blue epoxy, PPL; (c) Sparse glauconite grains (partially altered), E2e, Well PY10-F, 3698.95 m, blue epoxy, PPL; (d) Pervasive micritic to fine-crystalline dolomite filling intergranular pores and cementing grains, with minor echinoderm debris, E2e, Well PY10-F, 3697.2 m, blue epoxy, PPL; (e) Isolated echinoderm bioclasts, E2e, Well PY10-F, 3700.95 m, blue epoxy, PPL; (f) Micritic dolomite cementing grains with foraminiferal bioclasts, E2e, Well PY10-A, 3686 m, blue epoxy, PPL; (g) Minor foraminifera fragments, E2e, Well PY10-A, 3703.5 m, blue epoxy, PPL; (h) Abundant bivalve bioclasts retaining body cavities, E2e, Well PY10-F, 3702.2 m, blue epoxy, PPL; (i) Dominant bivalve debris with preserved internal molds, E2e, Well PY10-F, 3703.2 m, blue epoxy, PPL. PPL: plane-polarized light. Abbreviations: CCD: coarse crystalline dolomite.
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Figure 4. Microstructural characteristics of dolomite/ankerite cementation in the Zhuhai and Enping Formations, Panyu A Sag. (a) Micritic dolomite replacing foraminiferal bioclasts in aggregated form, E2e (Upper Enping Fm.), Well PY10-A, 3703.5 m, blue epoxy-impregnated, PPL; (b) Same view as (a) under XPL; (c) Pervasive micritic dolomite filling intergranular pores and cementing grains, with minor bioclasts (foraminifera, echinoderms, brachiopods, bivalves), E2e, Well PY10-F, 3702.95 m, blue epoxy, PPL; (d) Basal-fill dolomite cementation with micritic texture, E2e, Well PY10-A, 3695.5 m, blue epoxy, PPL; (e) Same view as (d) under XPL; (f) Dominant subhedral silt-to fine-crystalline dolomite cementing grains, E2e, Well PY10-A, 3767 m, blue epoxy, PPL; (g) Dolomite infilling interparticle spaces and cementing grains, showing minor elliptical green glauconite (compressed/deformed, partially altered to clay minerals), E2e, Well PY10-F, 3697.95 m, blue epoxy, PPL; (h) Same view as (g) under XPL; (i) Coarse-crystalline dolomite extensively occupying intergranular pores, with minor glauconite alteration and echinoderm debris, E2e, Well PY10-F, 3696.95 m, blue epoxy, XPL; (j) Ankerite cementing grains through pervasive pore-filling, E2e, Well PY10-D, 3604 m, blue epoxy, PPL; (k) Medium-to coarse-crystalline ankerite cementing grains exhibiting feldspar dissolution, E2e, Well PY10-A, 3686 m, blue epoxy, PPL; (l) Aggregated rhombohedral ankerite (Ank) clusters, E3z, Well PY10-A, 3356 m, SEM. PPL: plane-polarized light; XPL: cross-polarized light; SEM: scanning electron microscope. Abbreviations: MD: micritic dolomite, S-FD: silt-to-fine crystalline dolomite, CCD: coarse crystalline dolomite, Ank: ankerite, F: feldspar.
Figure 4. Microstructural characteristics of dolomite/ankerite cementation in the Zhuhai and Enping Formations, Panyu A Sag. (a) Micritic dolomite replacing foraminiferal bioclasts in aggregated form, E2e (Upper Enping Fm.), Well PY10-A, 3703.5 m, blue epoxy-impregnated, PPL; (b) Same view as (a) under XPL; (c) Pervasive micritic dolomite filling intergranular pores and cementing grains, with minor bioclasts (foraminifera, echinoderms, brachiopods, bivalves), E2e, Well PY10-F, 3702.95 m, blue epoxy, PPL; (d) Basal-fill dolomite cementation with micritic texture, E2e, Well PY10-A, 3695.5 m, blue epoxy, PPL; (e) Same view as (d) under XPL; (f) Dominant subhedral silt-to fine-crystalline dolomite cementing grains, E2e, Well PY10-A, 3767 m, blue epoxy, PPL; (g) Dolomite infilling interparticle spaces and cementing grains, showing minor elliptical green glauconite (compressed/deformed, partially altered to clay minerals), E2e, Well PY10-F, 3697.95 m, blue epoxy, PPL; (h) Same view as (g) under XPL; (i) Coarse-crystalline dolomite extensively occupying intergranular pores, with minor glauconite alteration and echinoderm debris, E2e, Well PY10-F, 3696.95 m, blue epoxy, XPL; (j) Ankerite cementing grains through pervasive pore-filling, E2e, Well PY10-D, 3604 m, blue epoxy, PPL; (k) Medium-to coarse-crystalline ankerite cementing grains exhibiting feldspar dissolution, E2e, Well PY10-A, 3686 m, blue epoxy, PPL; (l) Aggregated rhombohedral ankerite (Ank) clusters, E3z, Well PY10-A, 3356 m, SEM. PPL: plane-polarized light; XPL: cross-polarized light; SEM: scanning electron microscope. Abbreviations: MD: micritic dolomite, S-FD: silt-to-fine crystalline dolomite, CCD: coarse crystalline dolomite, Ank: ankerite, F: feldspar.
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Figure 5. Microstructural characteristics of gypsum/anhydrite cementation in the Zhuhai and Enping Formations, Panyu A Sag. (a) Locally developed poikilotopic anhydrite cementing grains with patchy pore-filling, E2e, Well PY10-F, 3711.92 m, blue epoxy, PPL; (b) Same view as (a) under XPL; (c) Pervasive poikilotopic anhydrite occupying intergranular spaces and cementing grains, E3z, Well PY10-F, 3487 m, blue epoxy, XPL; (d) Tabular gypsum (Gp) crystals cementing grains, E3z, Well PY10-A, 3557.9 m, SEM; (e) Local anhydrite pore-filling with pronounced quartz dissolution, E2e, Well PY10-D, 3775.3 m, blue epoxy, XPL; (f) Extensive quartz grain dissolution with anhydrite cementation and pore-occlusion, E2e, Well PY10-D, 3735.8 m, blue epoxy, XPL. Abbreviations: PPL: plane-polarized light; XPL: cross-polarized light; SEM: scanning electron microscope; Gp: Gypsum, Q: Quartz.
Figure 5. Microstructural characteristics of gypsum/anhydrite cementation in the Zhuhai and Enping Formations, Panyu A Sag. (a) Locally developed poikilotopic anhydrite cementing grains with patchy pore-filling, E2e, Well PY10-F, 3711.92 m, blue epoxy, PPL; (b) Same view as (a) under XPL; (c) Pervasive poikilotopic anhydrite occupying intergranular spaces and cementing grains, E3z, Well PY10-F, 3487 m, blue epoxy, XPL; (d) Tabular gypsum (Gp) crystals cementing grains, E3z, Well PY10-A, 3557.9 m, SEM; (e) Local anhydrite pore-filling with pronounced quartz dissolution, E2e, Well PY10-D, 3775.3 m, blue epoxy, XPL; (f) Extensive quartz grain dissolution with anhydrite cementation and pore-occlusion, E2e, Well PY10-D, 3735.8 m, blue epoxy, XPL. Abbreviations: PPL: plane-polarized light; XPL: cross-polarized light; SEM: scanning electron microscope; Gp: Gypsum, Q: Quartz.
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Figure 6. Measured breakthrough pressure for calcareous sandstone and mudstone cap rock in the Enping–Zhuhai Formations, Panyu A Sag. (a) PY10-D, 3564.91 m, calcareous sandstone; (b) PY10-D, 3816.91 m, mudstone.
Figure 6. Measured breakthrough pressure for calcareous sandstone and mudstone cap rock in the Enping–Zhuhai Formations, Panyu A Sag. (a) PY10-D, 3564.91 m, calcareous sandstone; (b) PY10-D, 3816.91 m, mudstone.
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Figure 7. Restored paleogeomorphology of Panyu A Sag during the Enping depositional stage, the arrows indicate the marine transgression pathways.
Figure 7. Restored paleogeomorphology of Panyu A Sag during the Enping depositional stage, the arrows indicate the marine transgression pathways.
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Figure 8. Major element data profile of the Enping Formation in Well PY10-A, Panyu A Sag. (a) Ankerite exhibiting basal cementation, E2e, Well PY10-A, 3686 m, blue epoxy-impregnated, PPL; (b) Echinoderm bioclasts replaced by ankerite, E2e, Well PY10-A, 3686 m, blue epoxy, PPL; (c) Scattered elliptical green glauconite grains, E2e, Well PY10-A, 3690.93 m, blue epoxy, PPL; (d) Minor elliptical glauconite particles, E2e, Well PY10-A, 3726 m, blue epoxy, PPL. PPL: plane-polarized light.
Figure 8. Major element data profile of the Enping Formation in Well PY10-A, Panyu A Sag. (a) Ankerite exhibiting basal cementation, E2e, Well PY10-A, 3686 m, blue epoxy-impregnated, PPL; (b) Echinoderm bioclasts replaced by ankerite, E2e, Well PY10-A, 3686 m, blue epoxy, PPL; (c) Scattered elliptical green glauconite grains, E2e, Well PY10-A, 3690.93 m, blue epoxy, PPL; (d) Minor elliptical glauconite particles, E2e, Well PY10-A, 3726 m, blue epoxy, PPL. PPL: plane-polarized light.
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Figure 9. Trace element ratio plots vs. depth for Wells PY10-A and PY10-D in the Panyu A Sag. (a) Sr/Cu ratio vs. depth, (b) B/Ga ratio vs. depth, (c) V/(V + Ni) ratio vs. depth for Well PY 10-A and (d) Sr/Cu ratio vs. depth, (e) B/Ga ratio vs. depth, (f) V/(V + Ni) ratio vs. depth for Well PY 10-D.
Figure 9. Trace element ratio plots vs. depth for Wells PY10-A and PY10-D in the Panyu A Sag. (a) Sr/Cu ratio vs. depth, (b) B/Ga ratio vs. depth, (c) V/(V + Ni) ratio vs. depth for Well PY 10-A and (d) Sr/Cu ratio vs. depth, (e) B/Ga ratio vs. depth, (f) V/(V + Ni) ratio vs. depth for Well PY 10-D.
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Figure 10. Characteristics of carbon and oxygen isotopic composition in the PY A Sag. (a) Carbon and oxygen isotopic composition of different dolomite types; (b) Relationship between oxygen isotopes and paleotemperature.
Figure 10. Characteristics of carbon and oxygen isotopic composition in the PY A Sag. (a) Carbon and oxygen isotopic composition of different dolomite types; (b) Relationship between oxygen isotopes and paleotemperature.
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Figure 11. Rare earth element ratio plots vs. depth for Wells PY10-A and PY10-D in the Panyu A Sag. (a) Rb/Zr ratio vs. depth, (b) Zr/Y ratio vs. depth, (c) Yb/La ratio vs. depth for Well PY 10-A and (d) Rb/Zr ratio vs. depth, (e) Zr/Y ratio vs. depth, (f) Yb/La ratio vs. depth for Well PY 10-D.
Figure 11. Rare earth element ratio plots vs. depth for Wells PY10-A and PY10-D in the Panyu A Sag. (a) Rb/Zr ratio vs. depth, (b) Zr/Y ratio vs. depth, (c) Yb/La ratio vs. depth for Well PY 10-A and (d) Rb/Zr ratio vs. depth, (e) Zr/Y ratio vs. depth, (f) Yb/La ratio vs. depth for Well PY 10-D.
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Figure 12. Development model diagram of calcareous sandstones in the Enping–Zhuhai Formations, Panyu A Sag.
Figure 12. Development model diagram of calcareous sandstones in the Enping–Zhuhai Formations, Panyu A Sag.
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Figure 13. Distribution histogram of calcareous sandstone thickness and cap rock capacity in the Enping–Zhuhai Formations, Panyu A Sag.
Figure 13. Distribution histogram of calcareous sandstone thickness and cap rock capacity in the Enping–Zhuhai Formations, Panyu A Sag.
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Figure 14. Development model diagram of reservoir–seal assemblage in the Enping–Zhuhai Formations, Panyu A Sag.
Figure 14. Development model diagram of reservoir–seal assemblage in the Enping–Zhuhai Formations, Panyu A Sag.
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Figure 15. Development model diagram of hydrocarbon accumulation controlled by calcareous sandstone-thin mudstone interbeds in the PY A Sag (Modified from [21]).
Figure 15. Development model diagram of hydrocarbon accumulation controlled by calcareous sandstone-thin mudstone interbeds in the PY A Sag (Modified from [21]).
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Table 1. Major element analysis of Zhuhai–Enping Formation in Well PY10-A.
Table 1. Major element analysis of Zhuhai–Enping Formation in Well PY10-A.
StrataDepth (m)Al2O3
/%
CaO
/%
Fe2O3
/%
K2O
/%
MgO
/%
MnO
/%
Na2O
/%
P2O5
/%
TiO2
/%
SiO2
/%
E3z1300511.9 0.93 4.60 2.66 1.29 0.14 0.43 0.04 0.62 72.7
305511.9 0.28 5.11 2.64 1.20 0.17 0.39 0.03 0.75 71.8
31159.70 0.54 3.02 2.58 1.09 0.02 0.43 0.01 0.52 78.4
315014.8 0.20 4.73 3.11 1.55 0.03 0.58 0.03 0.77 68.3
31959.85 0.50 3.43 2.52 1.19 0.04 0.56 0.02 0.55 77.4
E3z2327012.9 0.50 4.49 3.17 1.67 0.04 0.62 0.13 0.70 71.7
33107.84 0.62 3.28 2.66 1.08 0.06 0.60 0.04 0.37 80.2
33758.51 0.44 2.20 3.02 1.02 0.03 0.76 0.05 0.34 80.3
340510.7 1.39 3.02 3.33 1.41 0.04 0.67 0.04 0.42 74.4
E3z3344010.6 0.69 3.77 3.10 1.74 0.05 0.60 0.06 0.45 75.0
34706.34 2.07 2.00 2.83 1.50 0.08 0.67 0.04 0.16 80.5
35055.84 5.49 3.46 2.72 3.41 0.26 0.65 0.04 0.14 68.7
35257.08 5.47 4.89 2.61 3.59 0.24 0.65 0.09 0.26 67.3
35357.34 0.47 2.47 2.90 1.03 0.02 0.77 0.03 0.29 81.3
356011.9 0.76 4.24 3.06 1.92 0.05 0.62 0.04 0.61 72.3
35658.64 0.38 3.30 3.07 1.21 0.02 0.73 0.05 0.33 78.7
35805.86 0.32 1.50 2.60 0.62 0.01 0.66 0.02 0.15 86.0
36406.30 2.45 1.79 3.18 0.71 0.01 0.74 0.01 0.08 82.7
364517.9 0.18 4.26 3.83 1.80 0.02 0.53 0.01 0.74 65.4
E2e136856.53 6.49 5.13 2.79 4.06 0.38 0.64 0.02 0.18 64.1
36905.71 6.14 5.76 2.49 3.93 0.36 0.57 0.08 0.15 69.3
37005.70 8.34 4.71 2.41 4.53 0.44 0.64 0.06 0.18 64.4
37056.05 8.58 6.70 2.49 4.37 0.59 0.65 0.27 0.20 62.0
37157.24 0.52 3.73 2.57 1.22 0.04 0.65 0.02 0.37 81.1
37209.75 0.63 5.23 3.11 1.57 0.06 0.70 0.07 0.41 76.2
37305.50 6.31 5.13 2.40 3.49 0.51 0.68 0.03 0.17 72.4
37506.62 1.32 2.25 2.74 1.24 0.08 0.83 0.03 0.32 79.8
376010.6 0.40 3.43 3.17 1.38 0.03 0.82 0.05 0.49 76.2
37859.22 0.24 1.75 3.58 0.66 0.01 0.83 0.04 0.32 79.8
E2e239256.08 3.28 1.88 3.07 1.87 0.12 0.69 0.01 0.12 77.6
39455.07 3.54 1.66 2.38 1.68 0.12 0.51 0.00 0.11 79.9
Table 2. Trace element analysis of Zhuhai–Enping Formation in Well PY10-A.
Table 2. Trace element analysis of Zhuhai–Enping Formation in Well PY10-A.
StrataDepth (m)V/
ppm
Ni/
ppm
Cu/
ppm
Ga/
ppm
Rb/
ppm
Sr/
ppm
Y/
ppm
Zr/
ppm
Ba/
ppm
B/
ppm
Sr/CuSr/BaB/GaV/(V + Ni)Zr/YRb/Zr
E3z1300556.018.822.012.9122.69128.6257805252.54.1450.0114.0610.7498.9940.476
305556.916.920.113.41258031.3261811749.93.9700.0103.7230.7718.3310.477
311545.014.416.010.61208626.423911,41639.75.3720.0083.7480.7579.0460.501
315061.820.824.115.94149.37833.8266570865.23.2430.0144.0890.7487.8530.562
319546.614.915.910.58115.06824.0245617154.64.2910.0115.1580.75810.2050.470
E3z2327055.619.417.413.16139.87630.7247528365.14.3740.0144.9460.7418.0200.567
331036.115.415.38.10114.577.921.521610,101375.1030.0084.5040.70110.0680.530
337535.313.913.08.36120.88421.221011,34239.66.5100.0074.7380.7179.9210.575
340543.417.714.810.72141.711621.0228986036.27.8430.0123.3730.71010.8470.621
E3z3344046.617.013.811.01397723.8227787053.65.5670.0104.8770.7339.5380.612
347026.911.210.36.11159416.4187821715.89.0770.0112.5830.70611.4200.615
350530.112.613.75.61056819.2179670916.34.9940.0102.9320.7059.3400.586
352542.720.311.97.21067024.2211672521.95.8990.0103.0280.6788.7310.501
353530.812.211.87.41207419.2199960328.86.2830.0083.8960.71710.4150.603
356049.917.217.712.01326928.6259479770.53.8770.0145.8940.7449.0480.509
356536.113.912.68.50122.77523.7217941425.85.9250.0083.0330.7239.1320.566
358024.79.09.15.71116614.7189680825.27.2430.0104.4220.73412.8480.586
364021.46.631.15.34114.3157.712.417263549.35.0660.0251.7410.76313.8230.666
364565.420.123.718.31717635.9260449660.33.2080.0173.3000.7657.2520.655
E2e1368535.913.29.96.410475.519.8199630914.37.6460.0122.2180.73110.0270.524
369044.514.58.65.89173.421.5184676112.08.5590.0112.0630.7558.5550.493
3700-30.811.09.35.48982.121.1199775912.88.7980.0112.3890.7379.4160.445
370538.114.314.96.08977.124.7195612314.45.1930.0132.4150.7277.8880.456
371532.310.615.27.29563.425.5260669938.14.1750.0095.3240.75310.1990.365
372046.217.614.19.612068.327.7257586845.24.8500.0124.7190.7249.2880.465
373037.312.48.95.58965.917.7208558618.07.3740.0123.2480.75011.7200.429
375034.111.513.66.796119.321.728925,20227.18.7520.0054.0390.74813.3500.332
376042.114.914.510.311583.627.028811,37456.15.7640.0075.4410.73910.6810.400
378530.59.511.48.511798.320.7243990727.88.5950.0103.2730.76211.7610.482
E2e2392522.75.99.35.493127.012.017616,2889.413.5890.0081.7450.79414.6850.531
394523.727.237.64.678.712611.617316,40013.43.3650.0082.9200.46514.8970.455
Table 3. Trace element analysis of Zhuhai–Enping Formation in Well PY10-D.
Table 3. Trace element analysis of Zhuhai–Enping Formation in Well PY10-D.
StrataDepth (m)V/
ppm
Ni/
ppm
Cu/
ppm
Ga/
ppm
Rb/
ppm
Sr/
ppm
Y/
ppm
Zr/
ppm
Ba/
ppm
B/
ppm
Sr/CuSr/BaB/GaV/(V + Ni)Zr/YRb/Zr
E3z1298629.89.956.34.3711479.216244,60326.42.6090.0036.0980.75017.5360.442
309732.68.958.93.97617511.315159,73517.32.9700.0034.4600.78613.2840.506
E3z2319338.512.461.36.48103.516413.818952,93736.82.6730.0035.6750.75613.7060.548
319929.37.755.23.3869.51557.815752,15823.42.8190.0036.9190.79120.0290.443
332238.311.549.97.60130.512716.819433,08748.72.5500.0046.4120.76911.5410.671
E3z3345737.111.659.16.43113.5186.613.617547,535413.1570.0046.3330.76212.8650.646
347232.29.553.65.67110.815212.517047,75822.52.8390.0033.9610.77213.6180.652
E2e1354730.19.748.86.50133.228214.019322,64723.25.7730.0123.5670.75613.7840.691
359841.413.260.76.611217418.216923,71815.52.8730.0072.3580.7589.2790.666
360138.813.450.55.29014616.115631,29119.32.8860.0053.7160.7439.6510.579
364038.512.343.55.29316215.016337,71517.73.7220.0043.4220.75810.8990.571
364931.310.444.74.79421915.515335,64413.04.8960.0062.7960.7519.8460.616
365232.69.835.15.811613313.917010,37619.43.7910.0133.3560.76912.2350.681
365838.112.145.56.310914420.722533,07029.43.1680.0044.6530.75910.8930.486
369439.715.345.98.78144.910623.8193932426.22.3020.0112.9830.7228.1010.752
370031.28.737.36.51149615.618415,78627.12.5620.0064.1910.78111.8020.619
E2e2398854.811.348.914.78169.7142.826.023923,06321.92.9210.0061.4820.8299.1640.711
402424.06.051.05.91022638.915422,23311.25.1580.0121.8930.80117.3080.662
Table 4. In situ Carbon and Oxygen Isotope Test Data of Calcareous Sandstone in the Zhuhai and Enping Formations from Well PY10-A, Panyu A Sag.
Table 4. In situ Carbon and Oxygen Isotope Test Data of Calcareous Sandstone in the Zhuhai and Enping Formations from Well PY10-A, Panyu A Sag.
StrataDepth (m)Measured
Point
Cement Typesδ13CPDB (‰)δ18OPDB (‰)δ18OSMOW (‰)ZPaleo-Temperature (°C)
E3z35181CCD−11.94−9.1621.4498.3287.90
2S-FD−14.38−7.2823.3694.2272.64
3CCD−12.12−9.5221.0697.7291.14
3565.31CCD−17.62−2.6428.1489.9441.98
2S-FD−14.56−6.9223.7494.0669.88
3S-FD−10.98−6.7823.88101.4868.84
4MD−22.01−3.2027.5880.6445.20
E2e3695.51S-FD−12.82−6.5024.1697.8466.86
2S-FD−11.76−7.2423.4099.6272.34
3703.51MD−11.74−3.7826.98101.4048.72
2MD−11.86−4.2426.50100.9051.60
3MD−12.70−4.0426.7099.2850.36
4Ank−13.26−10.0220.5395.1895.72
3731.81S-FD−15.30−6.7123.9492.6268.44
2S-FD−15.38−5.6225.0893.0260.66
3755.81MD−16.72−2.7228.0691.7242.40
2MD−21.42−2.2628.5482.3239.76
3MD−20.54−2.6628.1483.9442.06
4MD−16.98−3.2827.5090.9245.68
Abbreviations: MD: micritic dolomite, S-FD: silt-to-fine crystalline dolomite, CCD: coarse crystalline dolomite, Ank: ankerite.
Table 5. Bulk Rock Carbon and Oxygen Isotope Test Data of Calcareous Sandstone in the Zhuhai and Enping Formations in Panyu A Sag.
Table 5. Bulk Rock Carbon and Oxygen Isotope Test Data of Calcareous Sandstone in the Zhuhai and Enping Formations in Panyu A Sag.
StrataWell NameDepth (m)δ13CPDB (‰)δ18OPDB (‰)δ18OSMOW (‰)ZPaleo-Temperature (°C)
E3zPY10F3371.6−9.98−12.418.08100.69120.07
PY10A3530−9.98−12.8817.58100.45125.56
PY10A3418.5−10.61−12.7617.7199.22124.20
PY10A3424.17−10.11−13.117.36100.07128.21
E2ePY10A3686−11.41−8.6621.9399.6283.72
PY10A3710.3−11.01−10.420.1499.5799.31
PY10D3604−10.14−10.9419.58101.09104.57
PY10 D3631.47−10.94−8.1522.46100.8479.52
PY10 D3796.44−9.79−8.2622.35103.1480.41
PY10 D3798.39−9.75−8.3622.24103.1781.23
PY10 D3799.13−10.1−9.2421.34102.0188.70
Table 6. Displacement pressure data of calcareous sandstone and sandstone reservoirs in the Zhuhai–Enping Formations in Panyu A Sag.
Table 6. Displacement pressure data of calcareous sandstone and sandstone reservoirs in the Zhuhai–Enping Formations in Panyu A Sag.
Well NameDepth (m)LithologyPorosity (%)Permeability
(mD)
Displacement Pressure (MPa)Ave. Displacement Pressure (MPa)
PY10-A3530Calcareous sandstone8.3710.2630.8421.013
3686Calcareous sandstone4.8280.04311.417
PY10-D3604Calcareous sandstone9.9920.1270.779
PY10-A3710.3Sandstone reservoirs10.92.560.1630.275
3671.80Sandstone reservoirs14.54.690.749
3690.93Sandstone reservoirs9.53.260.901
3712.94Sandstone reservoirs19.414.70.242
3726.00Sandstone reservoirs14.2/0.040
3738.00Sandstone reservoirs17.130.70.174
3758.13Sandstone reservoirs13.320.60.187
3788.93Sandstone reservoirs10.99.770.330
3795.17Sandstone reservoirs14.98370.035
3798.93Sandstone reservoirs12.51170.091
3844.00Sandstone reservoirs11.367.70.114
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Zhou, Y.; Peng, G.; Zhang, W.; Qiu, X.; Li, Z.; Wang, K.; Que, X.; Jia, P. Genetic and Sealing Mechanisms of Calcareous Sandstones in the Paleogene Zhuhai–Enping Formations, Panyu A Sag, Pearl River Mouth Basin. Minerals 2025, 15, 1285. https://doi.org/10.3390/min15121285

AMA Style

Zhou Y, Peng G, Zhang W, Qiu X, Li Z, Wang K, Que X, Jia P. Genetic and Sealing Mechanisms of Calcareous Sandstones in the Paleogene Zhuhai–Enping Formations, Panyu A Sag, Pearl River Mouth Basin. Minerals. 2025; 15(12):1285. https://doi.org/10.3390/min15121285

Chicago/Turabian Style

Zhou, Yong, Guangrong Peng, Wenchi Zhang, Xinwei Qiu, Zhensheng Li, Ke Wang, Xiaoming Que, and Peimeng Jia. 2025. "Genetic and Sealing Mechanisms of Calcareous Sandstones in the Paleogene Zhuhai–Enping Formations, Panyu A Sag, Pearl River Mouth Basin" Minerals 15, no. 12: 1285. https://doi.org/10.3390/min15121285

APA Style

Zhou, Y., Peng, G., Zhang, W., Qiu, X., Li, Z., Wang, K., Que, X., & Jia, P. (2025). Genetic and Sealing Mechanisms of Calcareous Sandstones in the Paleogene Zhuhai–Enping Formations, Panyu A Sag, Pearl River Mouth Basin. Minerals, 15(12), 1285. https://doi.org/10.3390/min15121285

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