Petrography and origin of the Lower Ordovician microbial carbonates in the Songzi Area of Hubei Province, middle Yangtze region, China
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This study is the first systematic assessment of the Lower Ordovician microbial carbonates in Songzi, Hubei Province, China. This paper divides the microbial carbonates into two types according to growth patterns, namely nongranular and granular. The nongranular types include stromatolites, thrombolites, dendrolites, leiolites and laminites; the granular types are mainly oncolites and may include a small amount of microbiogenic oolite. According to their geometric features, the stromatolites can be divided into four types: stratiform, wavy, columnar and domal. Additionally, dipyramidal columnar stromatolites are identified for the first time and represent a new type of columnar stromatolite. The thrombolites are divided into three types: speckled, reticulated and banded. The grazing gastropod Ecculiomphalus and traces of bioturbation are observed in the speckled and reticulated thrombolites. This paper considers these two kinds of thrombolites to represent bioturbated thrombolites. These findings not only fill gaps in the field of domestic Ordovician bioturbated thrombolites but also provide new information for the study of thrombolites. Based on the analysis of the sedimentary characteristics of microbialites, the depositional environments of the various types of microbialites are described, and the distribution patterns of their depositional environments are summarized. The relationship between the development of microbialites and the evolution and radiation of metazoans during the Early to Middle Ordovician is discussed. Consistent with the correspondence between the stepwise and rapid radiation of metazoans and the abrupt reduction in the number of microbialites between the late Early Ordovician and the early Middle Ordovician, fossils of benthonic grazing gastropods (Ecculiomphalus) were found in the stromatolites and thrombolite of the study area. It is believed that the gradual reduction in microbialites was related to the rapid increase in the abundance of metazoans. Grazers not only grazed on the microorganisms that formed stromatolites, resulting in a continuous reduction in the number of stromatolites, but also disrupted the growth state of the stromatolites, resulting in the formation of unique bioturbated thrombolites in the study area. Hydrocarbon potential analysis shows that the microbialites in the Nanjinguan Formation represent better source rocks than those in the other formations.
KeywordsMicrobial carbonate Stromatolites Thrombolites Oncolite Lower Ordovician Songzi Area
Microbial carbonate is the main component of microbialites. In the past 20 years, microbialites have been seen to define a depositional construction of carbonate formed by benthic microflora. The term microbialite refers to the precipitation of carbonates caused by benthic microflora through biochemical processes and the trapping and binding of detrital particles (Burne and Moore 1987). This type of deposition has occurred since the Proterozoic and forms reefs and carbonate sediments, including stromatolites, thrombolites, dendrites and oncolites. Many case studies are available in the literature (Golubic 1973, 1976; Zhang and Hofmann 1982; Hofmann 1987; Zhuravlev and Wood 1996; Feldmann and McKenzie 1997; Knoll and Semikhatov 1998; Myrow 2002; Riding 1991, 2000; Riding and Liang 2005; Rowland and Shapiro 2002; Kruse and Zhuravlev 2008; Hicks and Rowland 2009; Adachi et al. 2011). The Lower Ordovician marine carbonate deposits in the Yangtze Plate developed continuously, and the associated microbialites and reefs are widely distributed (Zhu et al. 1990, 1995, 2006; Mei and Lu 1991; Li and Wu 2001; Yang 2018; Xiao et al. 1993, 1995, 2004, 2011; Adachi et al. 2011; Wang et al. 2012). During the Early Ordovician, the middle Yangtze platform was occupied by different types of microorganisms and metazoans at different times. Microorganisms can form reefs alone or in conjunction with metazoans. The formation of microbialites is linked to events such as environmental, climatic and sea-level changes. Researchers in China and elsewhere have undertaken considerable work on the Lower Ordovician microbialites and reefs, especially the latter (Zhu et al. 1990, 1995, 2006; Mei and Lu 1991; Li and Wu 2001; Yang 2018; Xiao et al. 1993, 1995, 2004, 2011; Adachi et al. 2011; Wang et al. 2012). However, the research has mainly focused on macroscopic feature description of stromatolites, and systematic research on stromatolites and other Ordovician microbialites is very rare. There is no systematic classification or detailed study on the microbialites in Lower Ordovician strata, and the successional relationships of microbialites in the strata have not been determined (Zhu et al. 1990, 1995, 2006; Mei and Lu 1991; Li and Wu 2001; Yang 2018; Xiao et al. 1993, 1995, 2004, 2011; Adachi et al. 2011; Wang et al. 2012). Furthermore, there are few studies on the relationship between the evolution of microbialites and the evolution of metazoans. In view of these shortcomings, the authors believe that a systematic study of Ordovician microbialites will not only enrich the understanding of the stratigraphy by better characterizing the microbialites and types of microbialites in China but is also of economic significance for the exploration of Ordovician source rocks. Even more importantly, the results of this study are of great scientific value for exploring the relationship between microbialite development and the radiation of metazoans in the Middle Ordovician.
2 Regional geological background
The lower part of the Fenxiang Formation is mainly composed of gray medium-bedded sparry calcarenite, oncolitic limestone and calcirudite with shale. The upper stratum is composed of interbedded rocks containing muddy bioclastic limestone, biosparite limestone, thick-bedded stromatolitic limestone, etc. There are abundant fossils in the Fenxiang Formation, and the thickness of this formation is 71 m. The trilobite Tungtzeella szechuanensis, T. sp., which is widely distributed, are characteristic fossils of the Fenxiang Formation and its considerable strata in the Yangtze area. The important graptolite fossils in the study area are Acanthograptus sinensis and A. sinensis var. fenhsiangensis. Acanthograptus is widely distributed in the upper part of the Tonglu Formation in Yunnan, Guizhou and Sichuan Provinces. It is a representative fossil of the Fenxiang Formation. Drepanodus arcuatus, Paltodus deltifer and Paroistodus numarcuatus are important conodonts, and Paltodus deltifer is an important fossil that first appears at the bottom of the Fenxiang Formation and disappears at the top of the Fenxiang Formation. Drepanodus arcuatus is an important component of the P. deltifer—Triangulodus proteus zone in the Fenxiang Formation. Paroistodus numarcuatus is an important fossil in the upper Tremadocian stage in Europe. Therefore, the Fenxiang Formation should belong to the late Tremadocian period (Zhu et al. 1995; Xiao et al. 1996, 2016; Xu et al. 2004).
The Honghuayuan Formation is characterized by the development of moderately thick-bedded sparry calcarenite and biogenic reef limestone, with 2–3 beds of yellow–brown shale. The thickness of the formation is approximately 40–55 m. Among the limestones in the Honghuayuan Formation, reefs consisting of Calathium, sponges, blue-green algae, etc., are generally well developed and rich in fossils. The many fossils include Coreanoceras cf. reniformis, Manchuroceras yangtzeense and M. hubeiense, which are characteristic of the Honghuayuan Formation in the Yichang area. These fossils can be compared with the fossils of the Liangjiashan Formation in North China, the Shorin Formation in North Korea, the Upper Canadian Formation in North America, the Tasmanian Stage in Oceania and a Lower Ordovician formation in Siberia. All of these fossils belonged to the early Arenigian period (Zhu et al. 1995; Xiao et al. 1996, 2016; Xu et al. 2004).
3 Microbialite types and characteristics
There are different division schemes for the types of microbialites. Riding divided microbialites into four categories based on their macroscopic components, namely stromatolites, thrombolites, dendrolites and leiolites (Riding 2000), which are basically consistent with Shapiro’s classification of medium structures (Shapiro and Awramik 2006). Mei Mingxiang, a scholar in China, supplemented the classification system of microbialites. He used laminite and oncolite as two types of microbialites (Mei 2007a). Based on the growth form of microbialites, microbialites are divided into two major types in this paper, namely nongranular and granular types. The nongranular type microbialites mainly include stromatolites, thrombolites, dendrolites, leiolites and laminites. The granular types of microbialites are mainly oncolites and may include a small amount of microbiogenic oolite.
3.1 Nongranular types of microbialite
The nongranular microbialites grow in forms that are laminated or nonlaminated. These types formed through the process of the microbial community capturing and binding detrital particles or causing carbonate to precipitate because of biochemical processes. These processes can form a laminated or nonlaminated carbonate deposit. This kind of microbialite includes stromatolites, thrombolites, dendrolites and leiolites; the research area is dominated by the first two.
In terms of microfacies, the speckled thrombolites possess an inhomogeneous internal structure. The dark-colored layers are mainly micritic clots, which are mostly composed of microcrystalline–crystalline calcite, followed by bioclasts and sand grains. The material between the laminae is mainly micritic calcite, followed by bioclasts and arenaceous sediment. Filamentous microorganisms, i.e., Girvanella, are intertwined with each other within thrombolites (Fig. 5b). These microorganisms are mostly surrounded by micritic calcite, with local sparry calcite. The speckled thrombolite is mostly built on sparry calcarenite.
In terms of microfacies, the dark layers of the thrombolite are mostly expressed as clots and are characterized by micritic clusters, in which microcrystalline–crystalline calcite and small amounts of sand grains are occasionally observed. Notably, interwoven filamentous microorganisms, i.e., Girvanella, are present in the dark layer (Fig. 5d). These observations suggest that the formation of these thrombolites has a certain relationship with the activities of microorganisms.
3.2 Granular types of microbialites
The granular type of microbialites mainly includes coated-grain oncolites and a few types of oolites, but this type of microbialite is dominated by the development of oncolites in the research area. This kind of microbialites is characterized by carbonate precipitation caused by the capture and binding of carbonate mud around rolling cores or particles by microorganism communities in middle- to high-energy seawater environments.
The oncolites in the study area were mainly found in the Fenxiang Formation (Fig. 5e, f). They were mostly medium to thick bedded, with a single-layer thickness of 50–80 cm. Oncolitic limestone is mostly interbedded in the strata or interbedded with sparry arenaceous sediment and bioclastic limestone. The oncolites account for approximately 20%–45% of the rock and have diameters of 0.2–1.5 cm (with an average of approximately 1 cm). Sparry cementation shows visible concentric circle structures inside the oncolites, mostly forming 3–9 layers. Furthermore, more Girvanella development, e.g., Oscillatoriopsis, is more visible in the dark layers than in the light layers (Fig. 5f). All these phenomena also illustrate that oncolites are a special type of microbialite.
4 Analysis of the sedimentary environment of the microbialites
4.1 Sedimentary environment of stromatolites
The main feature of stratiform stromatolites is that their laminae are almost horizontal or exhibit only slight waviness, and their developmental lithology is mainly micrite. Only a small amount of fine clastics is present between the dark laminae. The base of the stratified stromatolites is calcarenite or dolomitic limestone, and it can be inferred that the hydrodynamic energy was relatively low; thus, these stromatolites may have formed in the intertidal zone in a fairly shallow environment. The wavy stromatolites are mostly distributed between the stratiform stromatolites and the columnar stromatolites in the transverse direction. Their laminae are wavy and have peaks and troughs. The underlying strata are mostly composed of calcarenite, and the main lithological component is micrite, with a small amount of dolomitic limestone. Small amounts of arenaceous sediment and bioclasts are also visible between the layers, and the color of these stromatolites varies from light gray to dark gray. These observations suggest that the formation of wavy stromatolites requires a certain amount of energy, and the water depth should be slightly greater than that of stratiform stromatolites. Therefore, the sedimentary environment is inferred to have been an intertidal zone environment, possibly in the lower part of the intertidal zone. The lateral distribution of domal stromatolites is relatively limited, and their formation mechanism and environment are similar to those of the wavy stromatolites.
The columnar stromatolites are distributed at the outer edge of the wavy stromatolites and are farther seaward than the other stromatolites. The material between the laminae is mainly micritic calcite, followed by small amounts of bioclasts and arenaceous sediment. The bioclasts are mainly echinoderm fragments (Fig. 4b), followed by brachiopod fragments; additionally, a few clots are observed. The gaps between adjacent columns are filled with numerous bioclasts and arenaceous sediments, which constitute important microfacies within the columnar stromatolite, i.e., interchannel microfacies deposits. This type of bioclastic deposit is mainly composed of stem stalks of stemmed echinoderms, which account for approximately 40%, followed by a small amount of arenaceous sediment. The cement is mostly sparry calcite. These deposits represent interchannel deposits between the reefs of the columnar stromatolites. Most of these stromatolites are built on calcsparite bioclastic limestone. The above observations indicate that the formation of the columnar stromatolites required a higher-energy environment than that of the wavy stromatolites. Based on the above sedimentary characteristics, it is believed that the columnar stromatolites formed in the higher-energy environment from the lower part of the intertidal zone to the upper part of the subtidal zone.
4.2 The depositional environment of clotted limestone
The three types of thrombolites in the study area were all developed on sparry calcarenite or bioclastic limestone, indicating that they formed on shoals with a certain energy. The interior of the clotted limestone possesses a microcrystalline structure, and these limestones are mostly micritic calcite to microcrystalline calcite. The speckled clotted limestone and the stratiform limestone in the Nanjinguan Formation were partially replaced by fine-grained crystalline dolomite, although a small amount of fine-grained clastics and stem debris from echinoderms remain. In addition, Girvanella microflora can be seen in the dark layer of the boundary of the clotted limestone, and most of these organisms live in relatively restricted water. Therefore, the speckled clotted limestone likely formed in a limited intertidal zone with a certain amount of energy. The reticulated clotted limestone in the Fenxiang Formation is mainly composed of microcrystalline calcite, with no dolomite, and is overlain by a fine-grained gray shale, and floating graptolite fossils are present in the shale. The above observations reflect the deepening of the water body. The reticulated clotted limestone is thought to have likely formed in a low-energy environment below the tidal zone based on the internal microfacies and the sedimentary characteristics of the overlying and underlying strata.
4.3 The depositional environment of the oncolite
The oncolites in the study area are found in the strata between the second section of the Nanjinguan Formation and the first section of the Fenxiang Formation. The oncolites are present as a single layer or interlayer or in alternating layers with spararenite and calcsparite bioclastic limestone. The oncolites are mostly ellipsoidal. The cores are mostly covered with bioclastic, calcarenite and calcirudite material, and the oncolites are commonly cemented with sparry calcite, indicating higher energy. Second, in most oncolites, wedge cross-bedding or parallel bedding is observed. In summary, the oncolites in the study area are thought to have formed in a high-energy environment in the intertidal zone or subtidal zone.
5.1 Analysis and discussion of the formation of thrombolites
There is currently no unified understanding of the formation mechanism of clotted limestones. However, in terms of genesis, clotted limestone can be divided into two major types: protogenic and epigenetic. Moreover, it can be further divided into calcified microbial thrombolites, coarse-aggregate agglomerates, bioturbated thrombolites, dendrites, travertine clots and postdepositional secondary clots (Riding 2000; Mei 2007b).
Among the clotted limestones found in this area, speckled clotted limestone and reticulated clotted limestone belong to the bioturbated type of clotted limestone. The evidence is as follows: First, grazing Ecculiomphalus fossils were found in both kinds of clotted limestone. The fossils were present sporadically or pervasively. In a 40 × 40 cm area of the spotted thrombolites, the Ecculiomphalus fossils accounted for approximately 50% of the area (Fig. 5c). In some local areas where the organism is common, the distribution of thrombolites is very irregular because of grazing and disturbance. Therefore, inside areas with high contents of Ecculiomphalus, the thrombolites are very sporadic and feature only a very small number of small circular clots with a diameter of 0.2 cm (Fig. 5c). In the marginal area where the content of Ecculiomphalus gradually decreases, the thrombolites differ in shape due to gnawing and disturbance, and some are round, elliptical and 0.2–0.3 cm in diameter, whereas others feature long curved bands that are 0.2–0.3 cm in width, forming a fine irregular mesh (Figs. 4-3, 5-3). The existence of these patterns is the most direct evidence of bioturbation. Because Ecculiomphalus features a shell that resembles a flat spiral and moves slowly, they generally inhabited shallow marine areas and were extremely prolific in the Early Ordovician. Most of them lived on carbonate rock mounds, and their abundant presence in microbialites indicates that they fed on submarine cyanobacteria (Garrett 1970). Additionally, the gastropod Ecculiomphalus is also found in the reticulated thrombolites, where it is present not only in the gaps in the grid (the lower circle of Fig. 5a) but also in the dark layers in the reticulated thrombolites (the upper circle of Fig. 5a). Due to the grazing and disturbance of Ecculiomphalus, the dark layers of the reticulated thrombolites show a different grid structure, with different thicknesses and an extremely irregular shape. Third, a fine laminar structure is present between the clots developed within the speckled clotted limestone. The characteristics of this laminar structure are similar to those of stromatolites, with the characteristic alternating light and dark laminae. Fourth, the authors found that in a large portion of the study area, the stratum of the speckled clotted limestone was horizontally connected to the strata of the wavy stromatolites. Although some scholars have suggested that the lateral relationship between stromatolites and thrombolites is complicated (Planavsky et al. 2009), a large number of grazing Ecculiomphalus gastropod fossils are found in the thrombolites, so the presence or absence of biological disturbance explains the genesis of the spotted thrombolites. In other words, the spotted thrombolites were formed by bioturbation of stromatolites.
The same situation is also observed in the Shijiachong Formation of the Neoproterozoic Shennongjia Group in Baokangmaqiao area, Hubei Province (Cao 1997; Cao and Yuan 2006). Cao (1997) discovered a variety of thrombolite limestones and morphologic-specific stromatolites that contain a marked “scar” produced by drilling and herbivorous animals. In addition, many stromatolites have been found to gradually transform into clotted limestone and form unusual distributions of stromatolite, clotted limestone and stromatolite–thrombolite combinations. Previous research provided valuable information for the understanding of the bioturbation-related formation mechanism of clotted limestone in the study area. The question of whether there are similar thrombolites in other times and regions requires further study.
It is worth pointing out that no laminar structure is found except for the discovery of a large number of grazing metazoan Ecculiomphalus in the reticulated thrombolites in the Fenxiang Formation. Therefore, is this kind of clotted limestone also formed by the bioturbation of stromatolites? The authors believe that further research and validation may be needed.
5.2 The relationship between the development of microbialite and the great radiation of metazoans
During the Early Ordovician period in the study area, there were three cycles of development of microbialites, namely the three depositional periods of the Nanjinguan, Fenxiang and Honghuayuan Formations. In terms of development characteristics, the number of layers and thicknesses of the microbialites gradually decreases from the bottom up, and the scale gradually decreases. The number, frequency and scale of the development of microbialites were largest during the deposition of the Nanjinguan Formation. There are three types of microbialites: stromatolites, thrombolites and oncolites. In this formation, there are two layers of stromatolite, four layers of oncolitic limestone and five layers of clotted limestone. In the upper part of the formation, the microbialites are smaller in scale, number and single-layer thickness. During the depositional period of the Fenxiang Formation, the frequency, number and scale of the three types of microbialite, namely stromatolite, clotted limestone and oncolite, gradually decreased. The Fenxiang Formation contains one layer of stromatolite and two layers of clotted limestone, and the thickness, scale and number of aggregates in the clotted limestone are smaller than those of the Nanjinguan Formation. The scale, frequency and quantity of microbialites in the Honghuayuan Formation are also significantly reduced, and the content decreases and eventually disappears. Therefore, what do the evolutionary characteristics of the Lower Ordovician microbialites in the study area illustrate? What caused the disappearance of microbialites at the end of the Florian period, and what is the relationship between them and the evolution of macroscopic organisms? These questions are issues about which many scholars think.
In terms of biological diversity, there are three peak periods of biological evolution in the Ordovician (Sepkoski et al. 1981; Sepkoski 1995). However, the most important peak period is the first peak in the Early or Middle Ordovician period. During the Early and Middle Ordovician, marine invertebrates showed large differences and considerable radiation. Sepkoski analyzed the evolution of the diversity of different species in the early Paleozoic from the perspective of global biological evolution data (Sepkoski et al. 1981; Sepkoski 1995). The analysis results show that the diversity of different types of species significantly increased during the Ordovician period, but the starting times of their radiation were not synchronous. For example, trilobites, brachiopods, graptolites, most mollusks and echinoderms began to show significant increases in diversity at the beginning of the Ordovician period. The diversity of other biological groups exhibited dissimilar evolutionary progress; for example, the diversity of coral almost exponentially accelerated, while that of some mollusks and brachiopods increased in steps (Zhang et al. 2009). Therefore, some scholars believe that the gradual decline of thrombolites and stromatolite over the history of the earth has a certain relationship with the increase in the abundance of metazoans. In other words, the reduction in the abundance of clotted limestone and stromatolites is related to the continuous feeding of metazoans on the algae that formed stromatolites and clotted limestone. Reid and Visscher (2000) found numerous traces of internal laminae destroyed by creatures such as clams and sponges in modern stromatolites, and obvious biological traces are preserved in laminae (Reid and Visscher 2000). Chinese scholars, such as Cao and others, have found scars left by the destruction of drilling animals and herbivores in the stromatolites in the Shijiachong Formation of the Shennongjia Group in Baokangmaqiao, Hubei Province (Cao 1997; Cao and Yuan 2006). These scars formed an unusual collection of stromatolites, clotted limestone and stromatolite–thrombolite combinations. These examples are evidence of the increase in the abundance of metazoans and the consequent grazing pressure on stromatolites. Some scholars have suggested that the development and decline of microbialites may have a certain relationship with changes in the chemical properties of the seawater (Riding and Liang 2005). However, the changes in the chemical properties of the Ordovician seawater were not as different as they were after the Ordovician (Yang 2018). Therefore, this situation also needs further research and verification.
From the development and evolution of microbialites in this area, this article agrees with the above view that the main reason for the gradual decline in microbialites over time is the result of the increase in the number of metazoans and their continuous feeding on the algal microbes that formed the microbialites. First, this point can be confirmed from the diversity characteristics of biological evolution; that is, the increase in benthonic metazoans from the Early Ordovician to the initial stage of the Middle Ordovician has a corresponding relationship with the reduction of microbialites. Second, we found benthic grazing Ecculiomphalus mollusk fossils in the majority of stromatolites and clotted limestone in the study area (Fig. 5a, c), and this type of organism is especially clustered in local intervals (Fig. 5c). These organisms fed on the microbial algae that formed the microbialites, causing a continuous decrease in the number of microbialites over time. Moreover, this feeding behavior also caused the microbialites to transition from stromatolites into bioturbated-type thrombolites with or without laminae. Thus, metazoans are the main reason for the formation of bioturbated thrombolites.
6 Hydrocarbon potential analysis
Research shows that the bacterial and algal microbes in modern marine stromatolites reproduce rapidly, so they have high biological productivity (Walter 1994). Therefore, some scholars believe that under certain conditions, microbialites are beneficial to the preservation of organic matter, and they have a certain hydrocarbon generation potential (Gerdes and Krumbein 1987; Yang et al. 2007) and can be treated as carbonate source rocks.
Organic carbon content of Lower Ordovician microbial carbonate in Liujiachang area
Organic carbon, %
The abundance of organic matter is the most basic index for evaluating source rocks. The evaluation criteria for shale source rocks are consistent both in China and internationally, but the criteria for carbonate source rocks differ due to their low organic carbon content (the peak value of organic carbon samples around the world ranges from 0.12% to 0.25%) (Gehman 1962). Scholars in China and elsewhere have also proposed a lower limit of organic carbon abundance and different evaluation criteria for different carbonate rocks (Gehman 1962; Chen et al. 2014). The organic carbon abundance of the microbialites in this area has a tendency to gradually decrease with time, but the average content of organic carbon is up to 0.19%, indicating that the microbialites in this area have a good hydrocarbon generation potential. However, in terms of the stratigraphic development, the organic matter abundance of the microbialites in the Nanjinguan Formation is higher than that of the Fenxiang and Honghuayuan Formations, and the content of the organic carbon in the stromatolites and thrombolites in the Nanjinguan Formation is 0.15%–0.21%. Consequently, the stromatolites and thrombolites in the Nanjinguan Formation represent better source rocks than those in the other formations. The organic carbon contents of the microbialites in the Fenxiang and Honghuayuan Formations are less than 0.15% and represent lower-quality source rocks. This phenomenon may be related to the relatively restricted environment of the Nanjinguan Formation in contrast to the relatively open environments of the Fenxiang and Honghuayuan Formations.
Microbialites were found in the Lower Ordovician Nanjinguan, Fenxiang and Honghuayuan Formations in the study area. Based on the growth forms of the microbialites, the microbialites are divided into two major types, namely nongranular and granular microbialites, in this paper. The nongranular microbialites mainly include stromatolites, thrombolites, dendrolites, leiolites and laminites. The granular microbialites are mainly oncolites but may include a small amount of microbiogenic oolite. In the vertical direction, the microbialites decrease in size, thickness and number.
According to the geometric features, the stromatolites in the study area were divided into stratiform, wavy, columnar and domal stromatolites based on shape. The dipyramidal stromatolite represents a newly discovered and named type. Based on the shapes of the clotted limestone, three types of thrombolites are recognized: speckled, reticulated and banded. Fossils of grazing Ecculiomphalus mollusks and traces of bioturbation are observed in the speckled and reticulated thrombolites. This paper considers that these two kinds of thrombolite represent bioturbated thrombolites. This discovery not only fills gaps in the field of domestic Ordovician bioturbated thrombolites but also provides new information for the study of thrombolites in general.
Based on the analysis of the sedimentary characteristics, the sedimentary environment of various types of microbialites is explained. This article concludes that the stratiform stromatolites, wavy stromatolites, speckled clotted limestone and banded limestone formed in the intertidal zone. The domal stromatolites and columnar stromatolites formed between the lower intertidal zone and the upper subtidal zone. The reticulated thrombolites formed in the low-energy environment of the subtidal zone. The paper summarizes the distributional patterns of the depositional environments.
This article discusses the relationship between the development of microbial carbonate and the radiation of metazoans in the Early to Middle Ordovician. According to the correspondence between stepwise and rapid radiation of metazoans and the abrupt reduction in microbialites from the late Early Ordovician to the early Middle Ordovician, combined with the discovery of the fossils of grazing Ecculiomphalus in stromatolites and clotted limestone in the study area, the authors suggest that the abundance of microbialites gradually decreased over time in response to the rapid increase in the abundance of metazoans. Notably, the grazers not only grazed on the bacteria that formed the stromatolite but also caused a continuous decrease in the number of stromatolites and disrupted the growth state of the stromatolites. As a result, unique bioturbated thrombolites formed in the study area.
Hydrocarbon potential analysis shows that the organic matter abundance of the microbialites in the Nanjinguan Formation is higher than that in the Fenxiang and Honghuayuan Formations and that the content of the organic carbon in the stromatolites and thrombolites in the Nanjinguan Formation is 0.15%–0.21%. As a result, the stromatolites and thrombolites in the Nanjinguan Formation represent better source rocks than those in the other formations.
This research Project was supported by the National Natural Science Fund of China (Grant No. 41572322) and Hubei Innovation Group Fund (Grant No. 2015CFA024). We thank two anonymous reviewers for their constructive reviews that greatly improved the manuscript.
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