Abstract

Diagenetic fluids is one of the most important reservoir modifiers, their differences can result in various petrography, storage capacity, and geochemical characteristics, so clarifying the diagenetic fluids is vital for understanding dolostone origin. Dolomitization is an important genetic type of dolostone reservoir, the fluid properties differ in different dolomitization, which may lead to reservoir storage capacity changes. Therefore, the identification of dolomitization fluid properties is critical for deeply understanding of dolomitization process and predicting storage capacity. Two types of dolostone are developed in submember Ma55 of Majiagou Formation in northwestern Ordos Basin, with obviously different petrological characteristics and reservoir properties. On the basis of petrological studies such as core and casting thin section observation and cathodoluminescence analysis, the diagenetic fluid properties of these two dolostone are characterized by geochemical analytical methods such as major and trace element tests. The results show that Type-1 dolostone is mainly composed of micritic dolomite, showing micritic structure and algae-rich lamina structure, and accompanied by evaporite minerals and moldic pores. This type of dolostone has a various Mn content, weak to medium cathodoluminescence intensity, high contents of TiO2, Al2O3, K2O+Na2O, Li, and U, and lower content of TFe2O3. The type-2 dolostone is composed of fine-grained dolomite with obvious residual texture of primary limestone, clear brim, and cloudy center structure, accompanied by the existence of intergranular pores. Most of this kind of dolostone have medium-strong cathodoluminescence, higher TFe2O3 content and lower TiO2, Al2O3, K2O+Na2O, Li, and U contents. Moreover, both the two types of dolostone have similar Fe/Ca and Mn/Ca ratios, and a low and concentrated CaO content, whose composition is similar to that of stoichiometric dolomite. The comprehensive analysis shows that the diagenetic fluid of Type-1 dolostone is mainly a high salinity fluid existed in plaster and calcareous sediments in a near surface environment with low temperature. The diagenetic fluid of Type-2 dolostone may be a high salinity brine formed by evaporation and concentration of seawater with normal salinity. The research results will provide a significant theoretical basis for the evaluation of dolostone reservoir quality and the prediction of favorable areas of reservoir distribution.

1. Introduction

Carbonate reservoir is of great significance in oil and gas exploration and exploitation; more than 50% of hydrocarbons are produced from these reservoirs globally [1]. Dolostone is one of the most vital gas exploration domains of the Majiagou Formation, Ordos Basin. However, in most cases, carbonate reservoirs have strong heterogeneity in terms of their lithologies and pore structures [26]. The influence of diagenesis on reservoir quality has been reported in numerous studies [712], among which the differences of diagenetic fluids is one of the most significant controlling factors affecting the formation of effective dolostone reservoirs [13].

Since the formation of tight dolostone reservoir experienced a long-term evolution process, the source and properties of diagenetic fluid are also complicated [13]. At present, although a very high daily gas output of over 1 million cubic meters has been achieved in several industrial gas wells in submember Ma55, NW Ordos Basin, different opinions on the dolostone formation mechanism of the Member 5 in the Majiagou Formation still remains unclear, one of the reasons is that there is no unified understanding of the diagenetic fluid properties. For example, there is a definite and closed relationship between penecontemporaneous dolomitization fluids and laminar dolomicrite in the northeastern Ordos Basin [1416] and the central-eastern area [17], but regarding the powder-fine crystalline and medium-crystalline dolomites with a high degree of recrystallization, the source of diagenetic fluids is still up in the air [16], including early mixing of seawater and freshwater [1820] in the central area, evaporated concentrated brine [21, 22] in the northeastern region [15] and central-eastern area [2326], seepage reflux dolomitization fluid extensively superimposed by burial dolomitization fluid in late period [22, 27] in the central-eastern area [23, 25, 26, 28], diagenetic dolomitization and burial dolomitization fluids [22, 29], burial dolomitization fluids [3034] in the northeastern [14, 16] and northwestern areas [35], as well as local hydrothermal dolomitization fluids [36].

Within the entire realm of formation processes related to carbonates, diagenetic fluids is one of the most important reservoir modifiers, different diagenetic fluids can result in various petrography, storage capacity [24], and geochemical characteristics [37, 38], so clarifying the diagenetic fluids is very significant for understanding the dolostone origin.

In view of the above scientific problems, on the basis of drilling core observation, thin section identification, whole rock X-ray diffraction, cathodoluminescence analysis, and other conventional petrological analysis methods, combined with the geochemical analysis of major and trace elements, the main types of dolostone and the properties of diagenetic fluids in submember Ma55 of Majiagou formation in the northwestern Ordos Basin were studied, and the origin of dolostone were discussed. The research results will provide an important theoretical basis for the evaluation of dolostone reservoir quality and prediction of favorable areas of reservoir distribution.

2. Geologic Setting

During the stratigraphic sedimentary period of the Ordovician Majiagou formation, the Ordos Basin as a whole is a structural pattern alternating between depression and uplift (Figure 1(a)) [3941]. The central paleo-uplift located in the southwest of the basin and the northern Shaanxi Depression in the east coexist and influence each other for a long time. This tectonic pattern determines the lithofacies palaeogeographic environment of the basin in this period [42]. A set of marine carbonate formations with a stable distribution was deposited in this region during the Early Paleozoic because the basin entered a stable period of craton development [4345]. According to the characteristics of lithologic changes and sedimentary cycles, the Majiagou formation can be divided into six members from Ma1 to Ma6 from bottom to top, and Member 5 can be divided into 10 submembers from Ma51 to Ma 510 from top to bottom (Figure 1(b)). Among which, submember Ma55 is a set of carbonate rocks mainly composed of limestone and dolostone formed in the process of third-order sea level declining and fourth-order sea level rising.

The study area starts from Wuqi in the west to Jingbian in the east, from well S21 in the north to Zhidan in the south. The submember Ma55 can be divided into three lithologic sections, namely Ma551, Ma552, and Ma553, with a total thickness ranging from 15 to 20 m (Figure 2). A set of dolostone developed in the Ma552 layer formed during a period of fifth-order sea level declining is the object of this study.

3. Materials and Methods

3.1. Samples

The dolostone samples were mainly collected from cores of submember Ma55 in wells S21, S22, Cc1, Y1112, Y1113, Y1165, Y1117, and D48 in the northwestern Ordos Basin. The well locations and sampling points are shown in Figures 1(a) and 2, respectively. The scope of sampling covers southeastern Wushenqi, western Jingbian, and eastern Wuqi; it almost represents the whole study area. The lithology of the tested samples mainly includes micritic dolomicrite and powder-fine crystalline dolostone.

3.2. Whole Rock X-Ray Diffraction

The volume contents of dolomite, calcite, anhydrite, quartz, and pyrite were determined by whole rock X-ray diffraction analysis. This analysis was completed in the State Engineering Laboratory of low permeability Oil and Gas Field Exploration and Development of Changqing Oilfield Company of China National Petroleum Corporation. The test standard is SY/T 6210-1996 with a data accuracy of 0.01% [25, 26, 47].

3.3. Micropetrography Analysis

The rock structure and pore characteristics in the carbonate rock samples were analyzed through core observations and thin section identification. The number of samples involved in the analysis was nearly 100. Before observing the thin sections, a mixed staining solution containing sodium alizarinsulfonate and potassium ferricyanide was applied, and then, a high power DMLP-217400 microscope was used to identify rock structure and pore characteristics. These analyses were conducted at the School of Resources and Environmental Engineering, Hefei University of Technology. The detection standard used was SY/T5368-2000, and all of the samples were analyzed at a room temperature.

3.4. Major and Trace Element Analyses

The testing of magnesium (Mg), calcium (Ca), iron (Fe), manganese (Mn), aluminum (Al), titanium (Ti), sodium (Na), potassium (K), lithium (Li), uranium (U), scandium (Sc), cesium (Cs), and other major and trace elements in the sample were analyzed via inductively coupled plasma mass spectrometry (ICP-MS) at the State Key Laboratory of Marine Geology, Tongji University. The procedure was based on standards DZ/T0223-2001, GB/T 3286.5-1999, and DZG20-05, and the analytical precision of the data is better than 5% [47].

3.5. Electron Probe Microanalysis (EPMA)

Electron probe microanalysis was used to excite photons, backscattering electrons, secondary electrons, and X-rays, and to obtain images. The beam spot diameter of the electron probe varies from 0.4 to 1.5 μm. The detected elements included Ca, Mg, Fe, Al, K, Na, Li, U, and other major elements, and Mn, Sr, Ti, Zn, Ba, Ni, S, P, Si, Cl, Br, I, and other trace elements. The brightness of backscattering image strengthens with the increasing of atomic number. The secondary electron images and the X-ray spectrometer are used to show the microscopic features and detect X-rays, respectively, the purpose of the latter is to identify various element components and determine their content.

This test was completed in the State Key Laboratory of Continental Dynamics, Northwest University, using a JEOL JXA-8100 instrument. The analysis was conducted following standard GB/T15616-2008, and the accuracy of the data is 0.001%.

4. Results

4.1. Rock Type and Petrographic Characteristics of Dolostone

According to the genetic-structural classification scheme for carbonate rocks put forward by Feng et al. [48], dolostone in the submember Ma55 can be divided into Type-1 and Type-2 dolostones, and the specific petrographic characteristics are as follows.

4.1.1. Type-1 Dolostone

Type-1 dolostone is mainly characterized by a dolomite content of greater than 90% and a tight micritic texture. The anhydrite, halite, and other evaporite minerals are common in this kind of dolostone (Figures 3(a) and 3(b)), these minerals usually can be dissolved by surface freshwater to form moldic pores (Figure 3(c)), which is considered to be main pore space of Type-1 dolostone. In addition, some bright and dark laminated algae structures were also observed under plain light (Figure 3(d)).

4.1.2. Type-2 Dolostone

Type-2 dolostone has a dolomite content of greater than 50%, most dolomite exhibits automorphic-hypautomorphic crystals, and the order degree of them varies from 0.7 to 0.85. Under plain light, typical residual texture of primary grainy limestone can be commonly observed (Figure 4(a)), and under cathodoluminescence, cloudy center and clear brim structures (Figure 4(b)) can also be seen in the Type-2 dolostone.

Different from Type-1 dolostone, Type-2 dolostone has better porosity and permeability, this might be contributed to the intercrystalline pores (Figure 4(c)) and some microfractures (Figure 4(d)) developed in this kind of dolostone as they can provide favorable storage space and seepage channels.

4.2. Porosity and Permeability

The measured porosities and permeabilities of nearly 70 samples from submember Ma55 in the study area are significantly different. The porosity ranges from 1.37% to 14.2%, with a mean of 4.68% (Figure 5(a)), and the permeability varies from to , with an average value of (Figure 5(b)). Apart from that, Type-2 dolostone show a relatively better correlation between porosity and permeability than Type-1 dolostone (Figure 5(c)), this may be contributed to the good pore connection of Type-2 dolostone.

4.3. Major and Trace Element Compositions

The major and trace element compositions of dolostone in the study area are shown in Table 1. The MgO content in Type-1 dolostone varies from 11.988% to 19.606%, which is lower than that of Type-2 dolostone (19.771% to 21.075%). CaO concentration of Type-1 dolostone ranges from 25.857% to 39.916%, while that of Type-2 dolostone is between 27.353% and 30.847%. MnO and Fe2O3t contents of Type-1 dolostone also show relatively lower values (0.004% to 0.009% and 0.203% to 0.721%, respectively) than those of Type-2 dolostone (0.007% to 0.056% and 0.134% to 1.974%. Al2O3, TiO2, Na2O+K2O, Li, and U concentrations in Type-1 dolostone are all higher (0.133% to 1.637%, 0.009% to 0.061%, 0.122% to 1.177%, 5.231 to 33.775 ppm, and 1.082 to 1.749 ppm) than those in Type-2 dolostone (0% to 0.042%, 0.002% to 0.006%, 0.066% to 0.100%, 2.556 to 3.955 ppm, and 0.349 to 0.851 ppm, respectively).

5. Discussion

5.1. Element Characteristics of Dolostones

Although the occurrence forms of different major and trace elements in carbonate rocks are diverse, e.g. Fe, Al, K, Sr, Ti, and Mn replace calcium and magnesium ions in calcite or dolomite as isomorphism elements, sodium does not enter the lattice and exists in calcite as a mixture [49], they are sensitive to the changes of diagenetic fluids in carbonate rocks.

In normal seawater environment, Na, I, P, and few Ni, Ba, S, Si, and Al are mainly enriched, while Fe2+, Ti, Mn, Zn, and Br are low. In brine environment with high salinity, Fe2+, Cl, I, and S are enriched, but as salinity decreases gradually, Fe2+, Na, Cl, Ti, Sr, and S decrease synchronously, while the content of Ba, Zn, Si, and Al increases accordingly. Additionally, Na and P decrease significantly in freshwater environment [23].

5.1.1. Magnesium (mg) and Calcium (ca)

According to the relationship between CaO and MgO contents, the CaO contents of most samples are low and concentrated, indicating that all the samples should be metasomatism origin [50]. The compositions of most dolostones are close to that of stoichiometric dolomite (30.4% CaO and 21.7% MgO) (Figure 6), implying that the metasomatism is relatively high. Apart from that, the ranges of CaO and MgO content ranges (Table 1) reveal that the composition of Type-2 dolostone is closer to that of stoichiometric dolomite than Type-1 dolostone, demonstrating that the metasomatism degree of Type-2 dolostone is higher than that of Type-1 dolostone.

5.1.2. Iron (Fe) and Manganese (Mn)

Fe and Mn are the main elements controlling the cathodoluminescence intensity (CI) of carbonate rocks, and freshwater is richer in Fe and Mn contents than seawater [21, 51]. The CI mainly depends on Mn rather than Fe when Mn content is less than 40 ppm, and it has no cathodoluminescence when Mn content is less than 20 ppm. When the Fe content is greater than 5000 ppm, the CI mainly depends on Fe rather than Mn, and it also has no cathodoluminescence when Fe content is greater than 10000 ppm. But when the Mn content is greater than 40 ppm and the Fe content is less than 5000 ppm, the CI generally depends on the Fe/Mn ratio. Specifically, the Fe/Mn>30 corresponds to strong CI (region V), the Fe/Mn<7 corresponds to medium CI (region IV), and intermediate Fe/Mn ratio of 7–30 corresponds to weak CI (region III3) [51, 52].

The plot of Fe versus Mn contents of dolostone in submember Ma55 and their relationship with the CI [52] (Figure 7) reveal that three Type-1 dolostone samples with relatively low Mn contents are in weak CI regions (region III1 and III3), and one sample with a relatively high Mn content is in medium CI region (region IV). This maybe contributed to that the Type-1 dolostone have formed in a near-surface seawater environment and was influenced by atmospheric water because near-surface freshwater is always high in Mn and Fe, and seawater is low in Fe and Mn,

With respect to Type-2 dolostone, three samples have medium CI (region IV) and one sample displays strong CI (region V), this maybe a result of their relative low Fe and high Mn contents in them. Another one exhibits weak CI (region III2) can be contributed to its high Fe content. These all imply a burial, reducing, and high temperature environment, prompting Mn and Fe to enter the dolomite’s crystal lattice [50].

In addition, compared with modern seawater, atmospheric freshwater is richer in Fe and Mn, and the Fe/Ca and Mn/Ca ratios of it are about 1000 times higher than those of modern seawater (Figure 8). In the plot of Fe/Ca versus Mn/Ca, all dolostone samples are close to seawater, and most of them have lower Mn contents than that of modern seawater, indicating that the dolomitization fluids of these samples may have come from Ordovician seawater or a pore fluid equivalent to seawater.

5.1.3. Aluminum (Al), Titanium (Ti), Potassium (K), and Sodium (Na)

Al occurs widely in terrigenous clay minerals, its content in illite, kaolinite, and montmorillonite can reach 13.5%, 21%, and 11%, respectively. While in seawater, Al content is low because it always dissolves in strong acid fluids [53]. Ti is one of the relatively stable iron family elements; its content of seawater is very low because it is only soluble in strongly acidic solutions, which rarely exists in natural environment.

The decrease of K+Na content is mainly associated with the property of diagenetic fluids rather than the changes in crystalline dolomite during diagenetic processes [54, 55].

Based on the histograms showing the distribution of the major and trace elements, Type-1 dolostone display high TiO2, Al2O3, and K2O+Na2O and low Fe2O3t contents (Figure 9), indicating a high salinity fluid, near-surface, seawater environment [50]. While Type-2 dolostone show high Fe2O3t and low TiO2, Al2O3, and K2O+Na2O contents (Figure 9), implying a burial, high-temperature, and reducing environment, in which the dolomitization accelerated the incorporation of Mn and Fe enter into the dolomite’s crystal lattice, reducing the Fe3+ to Fe2+ [16, 50].

5.1.4. Lithium (Li) and Uranium (U)

Since the ionic radii of Fe2+ and Mg2+ are similar to that of lithium (Li), and Li is easily adsorbed by clay minerals to make it tend to have higher Li contents. With respect to Uranium (U) content, it is very stable in seawater, and generally close to 3.2 ppm. The U content of atmospheric precipitation in the mainland is between 0.01 ppm and 2 ppm, with an average of 0.02 ppm, which is much higher than that over the ocean [56]. In addition, clay minerals also have high U contents because of its strong adsorption capacity [53].

All samples in the study area display a relatively low U contents (less than 2 ppm), this is apparently between the U content in seawater and atmospheric precipitation. In addition, the plot of Li versus U contents shows that the Type-1 dolostone has higher U and Li contents than those of Type-2 dolostone (Figure 10), indicating that Type-1 dolostone was influenced by surface freshwater, which carried amount clay minerals to make the Li and U contents increase. In contrast, Type-2 dolostone displays low U and Li contents is mainly contributed to the absence of Li and U sources, indicating that Type-2 dolostone formed in a relatively reducing and enclosed environment.

5.2. Source of Diagenetic Fluids and Genesis of Dolostones
5.2.1. Type-1 Dolostone

Through comprehensive analysis of petrographic and major and trace element characteristics of dolostone, it was found that Type-1 dolostone is mainly composed of micritic dolomite (content of >90%), and it exhibits micritic texture of the primary rock under plain light. The evaporite minerals such as anhydrite and salt coexisting with the micritic dolostone also implicate an evaporative environment, and the presence of moldic pores developed in Type-1 dolostone may demonstrate that atmospheric fresh water is involved in the diagenetic fluid of it.

Three samples are located in weak cathodoluminescence regions have relatively low Mn contents (region III1 and III3) and one sample is located in medium cathodoluminescence region has a relatively high Mn content (region IV) (Figure 7), suggesting diagenetic fluids come from near-surface seawater but were influenced by atmospheric freshwater, which also can be proved by the relationship between Fe/Ca and Mn/Ca ratios (Figure 8).

The high TiO2 and Al2O3 in Type-1 dolostone imply that it formed in a near-surface environment, the high contents of K2O+Na2O maybe implicate that the diagenetic fluid of has high salinity, while the low Fe2O3t content in it demonstrates that the diagenetic fluid is seawater rather than freshwater [50].

The low and concentrated CaO content of most samples is similar to that of stoichiometric dolomite (30.4% CaO and 21.7% MgO), revealing that all of the dolostone samples mainly have a metasomatic genesis [50].

Moreover, Type-1 dolostone has higher U and Li contents than Type-2 dolostone (Figure 10), demonstrating that the former was influenced by surface freshwater [53], which is consistent with the interpretation based on the relationship between Fe/Ca and Mn/Ca ratios.

Based on the above discussion, the diagenetic fluids of Type-1 dolostone can be interpreted as a complex fluids of high-salinity pore fluid and atmospheric freshwater. The genesis of this type of dolostone can be described as follows. During the contemporaneous or penecontemporaneous stage and accompanied by the formation of evaporite minerals resulted from strong evaporation, the salinity of the pore fluid in plaster and calcareous sediments increased, and this type of fluid quickly metasomatized algae-rich aragonite and calcite, then forming micritic dolostone, the high salinity of dolomicrite can also be proved by the result of fluid inclusions data [57]. Through leaching by atmospheric freshwater, the evaporite minerals such as anhydrite and salt dissolved, forming moldic pore. After entering the burial stage, the favorable high-temperature (the homogenization temperature of primary inclusions of dolomicrite is between 82.5 and 138.4°C, and the average value was 112.6°C [57]) and high-pressure conditions furtherly promoted the recrystallization of the micritic dolostone to form a laminated structure.

5.2.2. Type-2 Dolostone

From a petrographic point of view, Type-2 dolostone is mainly composed of powder-fine dolomite, and it exhibits residual texture of the primary rock under plain light. In addition, especially under cathodoluminescence, the cloudy centers and clear brims of dolomite are also petrologic evidence of shallow burial active reflux seepage dolomitization because it actually represents the alternation of Mg2+ to Ca2+ from the nucleus to edge of dolomite crystals. When this dolomitization process is not thorough, part of the limey component will remain in the space between dolomite crystals.

Based on the major and trace element compositions of Type-2 dolostone, the CaO contents of most samples are low and concentrated, indicating metasomatic genesis [50]. The CaO and MgO contents are closer to those of stoichiometric dolomite than those of Type-1 dolostone, indicating that the metasomatism degree of Type-2 dolostone is higher than that of Type-1 dolostone.

With respect to Fe and Mn contents and their relationship with cathodoluminescence, except for one sample with weak cathodoluminescence, most samples have medium-strong cathodoluminescence, implying a burial, reducing, and high temperature environment, which promoted the incorporation of Mn and Fe into the dolomite’s crystal lattice [50]. Furthermore, all samples plot in the region close to seawater on the plot of Fe/Ca versus Mn/Ca, also indicates that the diagenetic fluids of Type-2 dolostone may have come from Ordovician seawater or a pore fluid equivalent to seawater.

Apart from the above, the high Fe2O3t, low TiO2, Al2O3, and K2O+Na2O contents also support the opinion that Type-2 dolostone formed in a burial, high temperature, and reducing environment, in which the dolomitization accelerated the incorporation of Fe2+ into the dolomite’s crystal lattice, reducing the Fe3+ to Fe2+ [16, 43]. This reducing and enclosed environment also resulted in the low U and Li contents of Type-2 dolostone.

Judging from the EPMA data, the element content changes regularly from the nuclei to edges of dolomite crystal (Figure 11(a)), reflecting the changes of diagenetic environment. As an initial alteration product, the crystal nuclei of powder-fine dolomite has high Fe, Sr, and Na contents, demonstrating a high salinity, reducing environment. It also displays high Si and Al contents, indicating the influence of freshwater (Figure 11(b)). The Cl, Zn, Ti, and Ba contents decrease from the crystal nuclei to the inner zone (Figure 11(c)), while the I, S, P, and Ni contents increase from the inner zone to the outer zone of the dolomite crystals (Figure 11(d)). Undoubtedly, this is the result of a change of diagenetic environment from high salinity to normal salinity fluid, and it also indicates that type of dolostone formed in a shallow and variable salinity seawater environment. The residual limey component between the dolomite crystals has low Si and Al contents and high I, Ni, and S contents, suggesting a normal seawater environment that was influenced by freshwater and formation water in the later period.

From the above analysis of petrology and geochemistry, Type-2 dolostone may have formed in a burial, high temperature (the homogenization temperature of primary inclusions of dolomicrite is between 105.7 and 155.8°C, and the average value was 140.8°C [57]), and reducing environment, and the diagenetic fluids maybe normal seawater but influenced by freshwater, with a relatively lower salinity (the average salinity of fluid inclusions is nearly 22.6%) than that of Type-1 dolostone (the average salinity of fluid inclusions is nearly 24.2%) [57]. Its formation mechanism can be described as follows. In the early stage, permeable grainy limestone formed in a normal seawater environment, but after the stratum of submember Ma55 was lifted up and exposed near surface, the seawater began to evaporate and formed Mg2+-rich dolomitization fluid, which refluxed into the underlying grain limestone stratum driven by density and gravity differences. When the stratum was burial again, the formation environment became relatively closed and the temperature increased, and the evaporated seawater was remained in the formation pores, this lead to the pore fluid continued to metasomatize the underlying grainy limestone formation, forming powder-fine crystalline dolostone with residual structure of the primary limestone. But when the dolomitization process was not thorough, some of the limey components could be remained in the spaces between dolomite crystals and were dissolved by the later acidic formation fluids or mixed fluids of seawater and atmospheric freshwater, forming intercrystalline pores and/or intercrystalline dissolution pores.

6. Conclusions

(1)Two types of dolostone were identified in submember Ma55 of the Ordovician Majiagou Formation in the northwestern Ordos Basin. Type-1 dolostone consists mainly of micritic dolomite, and it is characterized by a micritic texture and an algae-rich laminated structure, associated evaporates minerals and moldic pores. Type-2 dolostone consists of powder-fine crystalline dolomite and is mainly characterized by the residual texture of primary rock, a cloudy center and clear brim texture, and intercrystalline pores(2)Various Mn content, weak to medium CI, higher contents of TiO2, Al2O3, K2O+Na2O, Li, and U, and lower content of Fe2O3t demonstrate that the diagenetic fluid of Type-1 dolostone is mainly a high salinity fluid existed in plaster and calcareous sediments but was influenced by freshwater, this formed near surface environment with low temperature. Medium-strong CI, higher Fe2O3t content and lower TiO2, Al2O3, K2O+Na2O, Li, and U contents reflect the formation of Type-2 dolostone is related to a high salinity brine, which formed by evaporation and concentration of seawater with normal salinity

Data Availability

All data that support the conclusions of this study are available from the corresponding author upon reasonable request.

Conflicts of Interest

The authors declare that the paper does not have any conflict of interest with other units and individuals.

Acknowledgments

We are grateful to the Geophysics and the State Key Laboratory of Marine Geology, Tongji University, for the major and trace element analyses and to the State Key Laboratory of Continental Dynamics, Northwest University, for the electron microprobe analyses. We also thank the reviewers for their constructive comments and suggestions. This study was supported by the Fundamental Research Funds for the Central Universities (No. JZ2021HGQB0284), the National Natural Science Foundation of China ( No. 91962218), the National 13th Five-Year Plan for Science and Technology Major Project of China (No.2017ZX05005-002-004), the Science and Technology Project of Hebei Education Department (No. ZD2022057), and the Natural Science Foundation Research Project of Shaanxi Province (No. 2019JQ-151).