First Report of Small Shelly Fossils from the Cambrian Miaolingian Limestones (Zhangxia and Hsuzhuang Formations) in Yiyang County, Henan Province of North China

Small Shelly Fossils (SSFs) from the Cambrian are widely distributed and well known across different paleocontinents of the world. However, middle Cambrian SSFs from North China Platform have only rarely been documented until now. In this paper, we presented the first report on SSFs from bioclastic and oolitic limestones of the Zhangxia and Hsuzhuang formations of Henan province, North China. The carbonate-hosted fauna includes brachiopods (Micromitra sp., M. modesta, Eoobolus sp., and Schizopholis sp.), helcionellids (Oelandiellaaccordionata and O. aliciae), hyolithids, Hyolithellus sp., Chancelloriaeros, sponge spicules, echinoderm ossicles, and chancelloriid sclerites. In terms of preservation, the brachiopod shell valves of M. modesta appeared to be homogeneous, consisting of tightly packed phosphate grains. Eoobolus sp. is composed of primary layer and secondary baculate, both of which consist of tightly compacted phosphate grains. Schizopholis sp. has multiple-lamellar phosphatized microstructures that distinctly differ from the other brachiopods recovered from the Longwanggou section. A similar multiple-lamellar microstructure was also revealed in conchs of Hyolithellus, with tightly compacted phosphate grains. The argillaceous shell of Oelandiellaaccordionata and O. aliciae, and the calcitic inner molds of hyolith did not preserve any shell structure. The helcionellids O. accordionata and O. aliciae and the brachiopod M. modesta were reported for the first time from North China. The fauna is most similar to the middle Cambrian faunas of South Australia, in the brachiopod and mollusk components; it is also similar in composition of brachiopods and mollusks to coeval faunas from South China. The new fauna of SSFs in the Yiyang Longwanggou Section indicated that the Hsuzhuang and Zhangxia formations are late Drumian to middle Guzhuangian in age, most likely correlating with the Murrawong Creek Formation of South Australia.


Introduction
Diverse kinds of data are needed for characterizing and global correlation of stratigraphic intervals in the Cambrian across the paleocontinents. The most abundant and diverse biostratigraphic data in early to middle Cambrian successions come from Small Shelly Fossils (SSFs), which are well documented and broadly known from the lower Cambrian of South China [1,2] and North China (Figure 1). In recent years, SSFs from the Xinji Formation have been studied in detail. Among the SSFs, hyoliths and mollusks have a high diversity and disparity and are the typical representatives of SSFs from North China Platform (NCP) [3][4][5][6][7]. Brachiopods, though less abundant, have also been reported recently by Pan et al. from the basal Cambrian of North China [8], in connection with studies of the Shuiyu Section, Shanxi Province. The Longwanggou section is labelled by a red star. Abbreviation: 1 = Chaijiawa section in Yun et al. [26], 2 = Shuiyu section in Pan et al. [8], 3 = Qingxing section in Mei [24], 4 = Mantoushan section in Park et al. [25], 5 = Weifang section in Liu et al. [22], 6 = Xiaomeiyao section in Pan et al. [27].

Geological Background
The Cambrian outcrops occur extensively along the southern margin of NCP from western Shaanxi in the west, through southern Shanxi and Henan provinces in the middle to Shandong province in the east ( Figure 1A). The traditional "Lower" and "Middle" Cambrian chronostratigraphic units officially adopted in North China have been established at stratotype sections mainly located in Jinan City of Shandong province; in ascending order, these are the Mantou, Maozhuang, Hsuzhuang, and Zhangxia formations. In both North China and South China, marine sequences are known in the Henan Province, providing an ideal opportunity to compare the contemporaneous faunal composition. In the Yiyang area, North China type Precambrian-Paleozoic deposits are well exposed and developed in considerable thickness. The well-exposed stratigraphic sequence makes the Yiyang area attractive for new investigations, and they have long been studied by researchers and students from universities around and within the Henan Province.
Longwanggou is one of the type sections that exemplifies the Paleozoic sequences from the lower Cambrian upward to Permian, with the upper part of the Cambrian (Figure 1C), Silurian, Devonian, and most Carboniferous deposits missing. Six formations of the Cambrian have been established in ascending order-the Zhushadong, Mantou, Maozhuang, Hsuzhuang, Zhangxia, and Gushan formations. The well-developed and well-exposed Hsuzhuang Formation is dominated by limestone, bioclastic limestone, and greenish and red mudstone (Figure 2A

Methods and Material
The well-exposed outcrops of the Zhangxia and Hsuzhuang formations at the Longwanggou section contain mostly fossiliferous samples. The Hsuzhuang Formation is composed of a ca. 100 m-thick green shale and limestone, containing skeletal fossils in the limestone, interbedded with shale (samples LWG-11 to LWG-15) ( Figure 2B-D). Acetic acid maceration of the bioclastic limestone and oolitic limestone in the Zhangxia Formation (samples LWG-6 to LWG 10 in Figure 2A) revealed an assortment of abundant skeletal fossils with abundant skeletal and shelly individuals in the level of sample LWG-6, LWG-8, and LWG-9 ( Figure 2A). Phosphatized tubular fossils and brachiopods, calcitic inner-mold, and argillaceous shell were extracted from buffered acetic acid (5%-10%) at the Early Life Institute, Northwest University, Xi'an. SSFs were picked out manually using a ZEISS Stemi 305 microscope at the Early Life Institute, Northwest University, Xi'an, China from the scattered insoluble residues. Most recovered phosphatized tubular fossils, calcitic internal molds, and phosphatic brachiopods are fragile and grayish or grayishwhite in color. Small brachiopod fragments and calcitic internal molds of hyoliths predominate. In spite of the predominance of scattered-shell fragments, some complete individuals of brachiopods were found, some with exquisite preservation of the shell structures and micro-ornaments of the phosphatized shell, which allow identification. The articulated brachiopods were not studied. The interpretation of the SSFs similarities was facilitated by multivariate cluster analysis (based on Jaccard similarity) using the computer program PAST (Version 3.06) [28]. Then, those SSFs were placed on copper plate, gold coated, and were photographed using the Scanning Electron Microscopy facilities at the State Key Laboratory of Continental Dynamics, Northwest University.

Previous Paleontological Work on the Zhangxia and Hsuzhuang Formations of Henan Province
Works on the middle Cambrian of the Henan Province were mainly carried out during the 1960s. The first comprehensive investigation of the paleontology and biostratigraphy of the Henan Province was carried out in the 1990s by the Henan Provincial Bureau of Geology and Mineral Resources and summarized by Pei [29,30]. They described the trilobite fauna from the Zhangxia and Hsuzhuang formations. The Hsuzhuang Formation at the Northwestern Henan Province (e.g., Weihui, Linzhou and Mianchi County) ordinarily contains rich and index fossils of the trilobite Hsuzhuangia, despite the uppermost part yielding the trilobite genera of Bailiella and Lioparia. Three trilobite biozones were identified in the Zhangxia Formation, encompassing the Crepicephalina, Plebiellus, and Tailznia-Poshani trilobite zones (in ascending order) based on the fossil assemblages investigated in Weihui County [29]. However, there were no subsequent studies of brachiopods and other faunas from all of the Henan Province except for the report of sponge by Liu et al. [31]. As mentioned before, the studies of SSFs from NCP are from the Xinji, Suyukou, and Houjiashan formations, lower Cambrian. Nevertheless, the Cambrian trilobite assemblages or biozones in the Longwanggou section and even in the entire Yiyang area remain poorly known at the present time.

Fossil Assemblages
In terms of total species richness, the Zhangxia and Hsuzhuang formations had a comparatively low diversity compared with SSFs from the Xinji Formation, lower Cambrian, NCP [3][4][5]7,8,26,27,[32][33][34][35]. This may be due to the restricted taphonomic conditions preventing the preservation of SSFs in the middle Cambrian of North China. Brachiopods and hyoliths were the most abundant components in the fauna, but with them occurred several other skeletal remains. Hyoliths were the most abundant forms ( Figure  3F; n = 1) were less abundant. In addition, fragments of ptychopterid trilobites ( Figure  3G,H; n = 177) as well as Hyolithellus-like tubular fossils ( Figure 6; n = 129) were also found.
Four species of brachiopod taxa are described (see Section 6 for details), two of them belonging to the Class Paterinata, the rest two belonging to the Class Lingulida of the subphylum Linguliformea [36]. Paterinids are the most abundant, and are here referred to as Micromitra, i.e., M. modesta Lochman, 1940 (Figures 7 and 8;n => 78). The rest of the brachiopod fauna included two species, comprising Eoobolus sp. (Figure 9; n = 565) and Schizopholis sp. (Figure 10; n = 6). Most of the brachiopod shell valves were represented by disarticulated and broken fragments and conjoined shells were lacking.
M. modesta is also known from South Australia [37], Laurentia [38][39][40], and South China [41], and Micromitra has a cosmopolitan distribution. Eoobolus, Schizopholis, and Hyolithellus from the NCP are hard to identify at the species level. Oelandiella aliciae and O. accordionata are mollusks recovered from the Hsuzhuang Formation. O. aliciae is only otherwise known from the Murrawong Creek Formation, South Australia [42]. However, O. accordionata is cosmopolitan and it has been recovered from South Australia [43], New Zealand [44], and South China [45,46]. M. modesta, O. accordionata, and O. aliciae are three typical species from the lower part of the Murrawong Creek Formation in Australia that are also recovered from the Longwanggou Section. The Murrawong Creek Formation is assigned to the late-middle Cambrian (Undillan-Boomerangian equal to late Drumian to early Guzhuangian) [47]. The similarity of the faunas in the Zhangxia and Hsuzhuang formations and the Murrawong Creek Formation prompts us to propose that these can be roughly correlated chronostratigraphically, belonging to the late Drumian to early Guzhuangian.

Global Correlations
Both palaeomagnetic insights and fossil correlation aspects (especially trilobites, brachiopods and other SSFs) have been used to understand the palaeogeographic location of the NCP, during the latest Ediacaran and the early to middle Cambrian [8,26,48,49]. Previous studies point a relatively close palaeogeographic location between the independent NCP continent and the East Gondwana, especially South Australia [8,34]. However, detrital zircon age combined with late Cambrian trilobite biogeography support a relatively closer palaeogeographic location between NCP and northeastern India (West Gondwana) [50]. However, the zircon age by U-Pb and Hf isotopic works imply a close palaeogeographic location of NCP and Northern Australia [51]. Pan et al. [8,34] argued for a close palaeogeographic location of NCP with South Australia based on early Cambrian SSFs. The study of Pang et al. [49] firstly discovered and reported typical fossils from the Qaidam, late Ediacaran, proposing a close palaeogeographic location of North China and Australia, and the controversy is still going on.
As mentioned before, chancelloriids, echinoderm, and sponge make up a very small percentage of the fauna. Trilobite fragments were recovered from the upper part of the Hsuzhuang Formation; most of them are fragmentary and badly preserved, but they probably represent ptychopterids ( Figure 3G,H). The huge amounts of hyoliths without any details on their anatomy structure and shell structure also make them hard to compare with materials from other regions, providing poor support for biostratigraphic correlation.
Linguliform brachiopods are some of the most important components of middle Cambrian skeletal communities, and they are globally distributed in both fine grain siliciclastic and carbonate rocks from the middle Cambrian [1]. As proposed by Zhang et al. [52], both paterinids and linguliforms (reported herein) have a planktonic larval stage, leading to a cosmopolitan distribution [1]. On the other hand, mollusks from the Xinji Formation, North China have previously been successfully used for global palaeogeographic correlation [7]. In this paper, brachiopods and mollusk from the Zhangxia and Hsuzhuang formations were used to shed light on the palaeogeographic reconstructions of NCP.
The SSFs assemblage described here represents the first report of such fauna from middle Cambrian deposits of the region. Despite a relative low diversity of SSFs, some palaeogeographic information still could be achieved. Our cluster analysis using PAST (Figures 11 and 12) showed that the middle Cambrian SSFs assemblage from the Longwanggou section, Central China has the highest similarity with South Australia and a relative high similarity with South China (Figure 8). The helcionellids Oelandiella and some of its species are globally distributed, but O. aliciae has only been reported from Australia. The discovery of O. aliciae from NCP represents its first record outside of Gondwana. The Ediacaran faunas discovered from the Qaidam Basin by Pang et al. [49] also suggest a close palaeogeographic location of Qaidam, South China, North China, and Australia. Besides, North China Platform also has a relatively high similarity with Laurentia, especially in the brachiopod fauna. As proposed by Zhao et al. [48], NCP may link the Laurentia and Australia promoting the exchange of faunas during the middle Cambrian. However, further studies of middle Cambrian faunas from North China are required to determine the more precise palaeogeographic location of NCP.

Systematic Paleontology
All illustrated specimens are housed and catalogued at Northwest University Early Life Institute (ELI), Department of Geology and State Key Laboratory of Continental Dynamics, Northwest University, Xi'an of China. All the specimen numbers and horizontal levels of the collection samples are labelled in Figure 2A.  [37,40,[53][54][55][56][57][58]. A large number of Micromitra have been recovered from both carbonate and mudstone, but the internal structure (e.g., muscle impressions) remains poorly understood.
Well-known occurrences of paterinides (Micromitra and Paterina) are indeed sparse outside Laurentia [59], with some exceptions from the Australasian segment of Gondwana and the Toyonian of Siberia [53,60]   Description. The shell is ventribiconvex, transversely subquadrate to circular in commissural outline (Figure 7). All of the available valves are fragmentary, making it difficult to analyze the length:width ratios. It is ornamented with concentric lines on both valves (Figure 7).
The ventral valve is high and gently convex, subquadrate to circular ( Figure 7A1-A7,B1,B2,C1-C3). The ventral pseudointerarea extends procline with a rounded beak projecting slightly posterior of hinge line and its apex embedded in homeodeltidium. The ventral metamorphic shell is subcircular and the size ranges from 0.5 mm to 1 mm ( Figure  7A1,A2), with a flattened posterior margin and prominent rounded beak ( Figure 7A1). The ventral metamorphic shell has a clearly distinguished protegulum, brephic, and neanic shell. The protegulum is sub-rounded with a diameter of about 0.3 mm ( Figure 7A2). The rounded brephic shell has two pairs of weakly defined, rounded lobes flanking with the width of each lobe about 0.25 mm ( Figure 7A2). The sub-rounded neanic shell has weak irregular concentric lines ( Figure 7A2) and the width of the neanic shell is about 0.15 mm ( Figure 7A2). The remainder of the shell surface is covered by fine, concentric, closely spaced filae, with superimposed weaker radial ridges disrupting and wrinkling the concentric elements ( Figure 7A3). The homeodeltidium is moderate and apical, lacking concentric ornamentation ( Figure 7B1,B2).
A single complete dorsal valve is weakly convex, 9.7 mm in length and 6.0 mm in width. The dorsal shell is low and subquadrate ( Figure 7C1). The dorsal metamorphic shell has one rounded protegulum, one brephic shell (with two paired lobes), and a neanic shell with weak concentric lines ( Figure 7C2,C3). The width of dorsal protegulum is about 0.4 mm ( Figure 7C2, C3). The rounded brephic shell has two pairs of clearly defined lobes, about 0.3 mm in width ( Figure 7C3). The sub-rounded dorsal neanic shell has weak concentric lines, but not as continuous as on the post-metamorphic shell ( Figure 7C2). The width of the neanic shell is about 0.1 mm ( Figure 7C2).
Pitted ornamentation is missing in both the ventral and dorsal metamorphic shell. Both ventral and dorsal valve interiors of available specimens lack well-defined features, leaving one pair of possible muscle scars ( Figure 7B2).
Shell structure. Based on the study of Williams et al. [59], the original shell structure of paterinids (including Micromitra) consists of primary and secondary layers, forming laminar shell structures [62]. The primary layer consists of glycosaminoglycans and spherular apatite, acting as the matrix of later shell lamina. The primary and later secreted laminae constitute the conveyor-belt cycle of the shell secretion [59]. Nevertheless, the shell textures of both ventral and dorsal valves presented in this study are diagentically overprinted ( Figure 7A6). It is hard to get the information on mineral secretion process in the Micromitra shell. Occasionally, the interior of the shell is covered by spherulitic phosphorite ( Figure 7A6,A7) that are thought to be due to the activity of bacteria and decomposition of organic matter [63].
Remark. The external characters of the shell valves closely resemble those of Micromitra. The Yiyang specimens of Micromitra are similar to M. modesta described and illustrated by Lochman in shell outline [64], convexity, and exterior ornamentation. Compared with M. georginaensis [65], the posterior margin of our specimens appears to be thicker, but not as thick as M. nerranubawu [66]. As for the ventral homeodeltidium, the valves discussed here had relatively smaller homeodeltidium as compared with M. nerranubawu, and the Australian species had a larger and extended posterior projection. The new Chinese material differs from M. sculptilis in having distinctly coarser radial costellae, and the minute homeodeltidium and homeochilidium of the new material is clearly different from other species of Micromitra.
Ontogeny. Zhang et al. [52] documented the ontogeny of Eohadrotreta based on materials from the Shuijingtuo Formation, South China and proposed that Eohadrotreta experienced embryo, planktotrophic larva, and post-metamorphically sessile juvenile and adult growth stages. This ontogeny sequence is considered as a plesiomorphic character for most early linguliforms including siphonotretoids, linguloids, mickwitziids, rhynchonelliforms, and paterinates that we discussed herein. The protegulum, brephic shell, neanic shell, and post-metamorphic shell are clearly distinguished based on the M. modesta recovered from the Longwanggou section. M. modesta also experienced embryo, planktotrophic larva, and post-metamorphically sessile (post-metamorphically shell) stages (Figure 7).  Description. The shell is ventribiconvex (Figure 8). All available valves are more or less fragmentary and complete specimens with homeodeltidium and homeochilidium are absent, making the length:width ratios impossible to determine. Both valves have an ornamentation with concentric lines.
The ventral valve is high and gently convex, subquadrate to circular ( Figure 8A1-A4,B). The pseudointerarea profile is procline with a rounded beak, projecting posterior of the hinge line ( Figure 8A1-A4,B). The homeodeltidium is moderate, and clearly defined with evenly spaced concentric fila without fine radial costellae ( Figure 8A2,B). The boundary of the ventral metamorphic shell and ventral post-metamorphic shell is weakly defined ( Figure 8A1-A4,B). The ventral metamorphic shell is characterized by a smooth shell without any ornamentation. The post-metamorphic shell surface is covered by fine, concentric filae without radial ridges ( Figure 8A1,B)). The size of the ventral metamorphic shell ranges from 0.3 mm to 0.5mm ( Figure 8A1-A4,B).
The dorsal valve is weakly convex, and circular ( Figure 8C1). The homeochilidium is small with no ornament ( Figure 8C2). The boundary of the dorsal metamorphic shell is not well defined and the ornamentation is poorly preserved ( Figure 8C2). The interior of both valves is poorly preserved.
Remark. This material from the Hsuzhuang Formation only comprises concentric lamellae without of the radial ridges. It is too poorly preserved to compare with other species.
Remark. Eoobolus is one of the oldest known linguliform brachiopods that co-occurs with the oldest trilobite, Parabadiella huoi [2]. Eoobolus is a globally distributed taxon [2,14,27,[67][68][69][70]. The characters of the metamorphic shell, apical angle in adult ventral valves, and the ornamentations are important diagnostic features for the Eoobolidae [67]. The columnar shell structure is also an important character of Eoobolus.

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Eoobolus sp. Description. The relatively well-preserved valves suggest a biconvex, elongated subcircular shell with a sub-rounded anterior margin.
The outline of ventral valve is elongate subtriangular, and the length is about 110% longer than the width, measured from the relative complete ventral valve ( Figure  9A1,A2). The ventral valve is moderate convex with straight posterolateral margins enclosing an apical angle from 80° to 97° ( Figure 9A1-A3,B). Ventral valve pseudointerarea is orthocline ( Figure 9A3). The raised ventral valve pseudointerarea is sub-triangular in outline, equally divided by a deep pedicle groove, and the lateral margin of the pedicle groove is almost parallel ( Figure 9A3). The ventral valve pseudointerarea overhangs on the valve floor, and is divided by flexure lines which enclose an angle of about 110° (Figure 9B). The length of the pseudointerarea ranges from 1.09 mm to 1.94 mm and the width ranges from 1.53 mm to 3.80 mm, with the average length:width radio around 169%. The metamorphic shell of both the ventral and dorsal shell is not clearly seen due to the lack of preserved ornamentation ( Figure 9A2). The post-metamorphic shell is covered by fine, concentric filae without radial ridges. Impressions of muscles and organs are confined to the visceral area ( Figure 9A2). The paired muscle scars are small and run along the entire length of the visceral area from the distal lateral sides of the pedicle groove to the anterior, posterior margin ( Figure 9B).
The dorsal valve is slightly convex, suboval in outline ( Figure 9C1-C3), and on average 130% longer than the width. The post-metamorphic shell is covered by fine, concentric filae without radial ridges ( Figure 9C2). The width of pseudointerarea is about 300% longer than long, with a broad, shallow median groove ( Figure 9C3). Visceral area is unpreserved; muscle scars are poorly marked.
Shell structure. The shell of the Eoobolus sp. from the Longwanggou section is about 0.5 mm thick in the center ( Figure 9D1). In general, the shell structures consist of primary laminar layers and secondary columnar layers ( Figure 9D2-D4). The primary laminar layers are composed of tightly compacted phosphorite grains, with sizes of about 1 μm (Figure 9D4). The thickness of the primary layers is about 1 μm ( Figure 9D4). The thickness of the secondary columnar layer depends on the length of columns forming the secondary columnar layers. The length of these columnar ranges from 5.5 μm to 83.0 μm ( Figure  9D2,D3). Both the primary and secondary columnar layers consist of the tightly compacted phosphorite grains ( Figure 9D4). The phosphorite grains are about 1μm in length and elongated polyhedral in outline.
The columnar shell structure is well-known in linguloid brachiopods, including Eoobolidae, Linguloidea, Zhanatellidae, Kyrshabaktellidae, and Acrotretidae [71]. The shell of these organophosphatic brachiopods is comprised of an organic periostracum, a mineralized laminar layer (primary layer), and a secondary columnar layer [71]. The secondary shell of Eoobolus examined here appears to be baculite, most likely resembling those seen in lingulide brachiopods. In recent studies, Duan et al. reported the columnar shell structure of acrotretoid from early Cambrian mudstones, South China, representing the best counterpart for columnar shell fabrics from carbonate [18]. The secondary columnar pillars (hollow tube [18]) could have contained unmineralized organic fibers. It is widely accepted that the growth of brachiopods shells mainly depends on the mantle epithelial cells, membrane, and inter-crystalline organic matrix [72][73][74]. Analogously, the biomineralization process of Eoobolus sp. depends on membrane-controlled mechanisms. Although the original minerals are overprinted, the membrane in Eoobolus sp. acts as the template or scaffold for both primary and secondary layers. Then, the bioapatite precipitate near the membrane forms the baculate shell structure as the shell structures seen in acrotretids. The columnar shell structure from mudstone [18] probably represents the original shell textures constrained by the organic epithelial membrane that are replaced by clay minerals during later diagenesis. By contrast, the baculate structures reported herein were slightly intercrossing and with no inner hollow tube inside ( Figure 9D4). Both the primary layer and the secondary columnar layer were constituted with elongated polyhedral grains ( Figure 9D4). The origin of the phosphorite grains are thought to be the secondary diagenesis [2,69]. The decomposition of earlier phosphorite or organic matters may cause the supersaturation of apatite solution, leading to the recrystallization of apatite within the hollow tubes and the primary layers. The coarse-grained preservation and the acetic acid maceration of the bioclastic limestone could make the original membranous laminae disappear, leaving the well oriented, elongated polyhedral grains in both the primary layer and secondary baculate layer.
Remark. The apical angle of adult ventral valves is the most stable character for taxonomic work within Eoobolus. The apical angle of ventral valve from the Zhangxia Formation ranges from 80° to 97°, which is similar to many species of Eoobolus, for example, Eoobolus sp. in Betts et al. [75], E. viridis in Zhang et al. [2], and E. priscus in Poulsen [76]. Due to the lack of complete materials, it is hard to assign this type to any known species. Diagnosis. See Popov et al. [60]. Remark. Schizopholis is a widely distributed brachiopod genus in early and middle Cambrian and it has been recovered from Himalaya, Kazakhstan, Australia, Antarctica, South China, and North China [9]. Popov et al. [60] regard Schizopholis as a key role in the evolutionary lineage of Botsfordia, Schizopholis, Eothele, and Acrothele. The record of Schizopholis from the Zhangxia Formation at Longwanggou section extend the distribution of this genus.

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Schizopholis sp. Description. Shell is ventribiconvex and subcircular in outline ( Figure 10A1-A5,B1-B6). All of the specimens are fragmentary, making it hard to determine the length:width radio. Both ventral and dorsal valves are ornamented with pustulose granules, and with weak concentric growth lines ( Figure 10A1,B1).
The ventral valve is subcircular and convex ( Figure 10A1-A5,B1-B6), and the pseudointerarea is procline and very deep, forming an oval opening ( Figure 10A1,B1). The width of the pedicle groove is about 0.1 mm. The metamorphic shell is oval in outline and about 0.38 mm in length and 0.32 mm in width and with pitted ornaments ( Figure  10A2). There are two protuberances posterolaterally on the ventral valve brephic shell, and one protuberance on the protegulum ( Figure 10A2).
Shell structure. Although Schizopholis has been recovered from many localities [8,9,77], the shell structure of Schizopholis is rarely studied and hard to determine. Schizopholis yorkensis is from east Antarctica, with several photographs showing a lamellar microstructure ( Figure 9S in Claybourn et al. [78]). Two different shell structures were observed in Schizopholis sp. from the Longwanggou section. The first shell structures were lamellar microstructures without any columnar structure occurring around the pustulose granules and pitted ornaments ( Figure 10A3,A4). More than 10 lamellar microstructures were found around the pitted ornaments. The thickness of the single lamellar is about 0.15 μm ( Figure 10A5). The surface of the lamellar microstructures is smooth with no phosphate grains preserved ( Figure 10A5). The other shell structures were tightly compacted, elongated phosphate grains (ca. 0.5 μm in length and 0.2 μm in width) forming a homogeneous shell ( Figure 10B4-B6). This structure could be due to the decomposition and recrystallization of earlier phosphorite [2,69]. The shell structure of Schizopholis sp. distinctly differs from the other brachiopods recovered from the Longwanggou section. This may be due to the different biomineralization templates of Schizopholis that are controlled by the secretion of inter-crystalline organic matrix. Future works are needed to make clear the shell mineralization process of Schizopholis.
Remark. The available fragmentary shells make closer taxonomic discrimination impossible. Species of Schizopholis can be determined, mainly on the morphology of the ventral pseudointerarea, which is not available here. The pitted ornamentation of the shell strongly assigns it to Acrotheloidea and the occurrence of the pedicle groove resembles this specimen to Schizopholis. However, the lack of complete ventral pseudointerarea makes it hard to determine the species. Diagnosis. See Gubanov and Peel [79].
Remark. Latouchella, Oelandiella and Oelandia belong to helcionellids and show great similarities in morphology and ornaments with each other. Gubanov and Peel [79] proposed a detailed taxonomic work about Latouchella, Oelandiella, and Oelandia based on the occurrence of the ribs versus the dorsum. Oelandiella is clearly distinguished from the other two genus by the symmetrical commarginal ribs crossing the dorsum. Latouchella is characterized by the ribbed lateral area and a smooth dorsum. Oelandia differs from them by the asymmetrically arranged ribs. Many studies accepted this taxonomy and Oelandiella was found in some new localities, including South China [45,46].

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Oelandiella accordionata Runnegar and Jell, 1976. Description. Most of the specimens are preserved as interior mound (Figure 4), but broken argillaceous outer mound is rarely found too ( Figure 4F1). Shell is moderate high, cyrtoconic, and characterized by univalves (length ranges from 1-3 mm) with simple, regularly spaced, angular commarginal rugae crossing the whole ridge of the shell ( Figure  4A1,A2,B,C,D1,D2). These commarginal rugae are loosely coiled, forming a whorl-shaped shell. The shell aperture is planar, with an oval to subrectangular outline ( Figure 4E1). Fine radial ornaments are preserved on the argillaceous inner mounds ( Figure 4F1). The inner surface of sub-apical shell wall occurs with a pair of uniformly thin ridges ( Figure  4B,C).
Remark. Specimens occurring as inner and outer mounds in the Hsuzhuang Formation are conspecific with O. accordionata from the Coonigan and Murrawong Creek formations in Australia and the Tsinghsutung and Jialao formations in South China for the tall, compressed cyrtoconic univalves with a subrectangular character. The O. accordionata recovered from the Longwanggou Section, middle Cambrian, represents the first report of O. accordionata as well as Oelandiella from the North China Platform. The size of O. accordionata reported here is smaller than earlier materials from the Murrawong Creek Formation [42].

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Oelandiella aliciae Brock, 1998.  Description. The shell is moderately involute, with robust univalves with a shell length around 3 mm and height around 2 mm ( Figure 4E1,E2). The shell is composed of moderate, coiled commarginal rugae forming a whorl-shaped shell in outline ( Figure  4E2). These rugae are separated by a wide interrugal space. The biggest interrugal spaces on the supra-apical surface decrease to the posterior ( Figure 4E2). The shell aperture is planar, with a subrectangular outline ( Figure 4E1). The pair of narrow ridges occurs on the inner subapical margin ( Figure 4E2). No ornamentation is preserved except for the commarginal rugae.
Remark. Comparing with the other species of Oelandiella, the specimen described here should be assigned to O. aliciae for its sharply angular character. Comparing with the other species of Oelandiella, the distribution of O. aliciae is restricted. In early research, O. aliciae is erected based on specimens from Murrawong Creek Formation, Australia [42]. The O. aliciae found in the Hsuzhuang Formation, at Longwanggou section, Central China, represents the first locality out of the Gondwana, suggesting a relatively close palaeogeographic position of NCP and Australia during the middle Cambrian.  Description. The shell is circle shaped in the cross section, and straight or slightly curved in the longitudinal ( Figure 6A,B1,C1-C3). A few tubes occur with annulate ornamentations ( Figure 6A,B1). In the cross section, the annulate ornaments are actually overlapped lamellar structures and the thickness of each lamellar is about 5 μm ( Figure  6B2,C2). Besides, the lamellar is composed of tightly compacted phosphate grains ( Figure  6C3). On the average, the tube exhibits about 12 annulations per mm with individual annulations varying from 50 to 75 μm ( Figure 6A,B1).
Remark. Hyolithellus represents a tube-like fossil that has remained problematic. These tubes are globally distributed and are commonly seen in a wide range of sedimentary deposits of the early and middle Cambrian. Specimens of Hyolithellus have been found in life position from lower Cambrian dolostone and are regarded as the possible stem group of annelids [80]. However, it is hard to identify species of Hyolithellus only based on the morphology of an individual [80,81]. The new record of Hyolithellus sp. from the Hsuzhuang Formation represents its first report from the NCP, extending its paleogeography distribution. Remark: Hyoliths are the most abundant organisms in acid residues, but all of them are exclusively represented by internal molds of the conical conchs. Those indeterminable hyolithids, preserved as internal molds with subtriangular cross-sections, are common throughout the Zhangxia Formation ( Figure 3A,B,D). The specimen from the Hsuzhuang Formation with a sub-circle cross-section could be another species ( Figure 3C). Better-preserved samples are required to perform taxonomic work, rather than on these calcitic internal molds. Material. Three specimens from the sample LWG-15 from the lower part of the Hsuzhuang Formation.
Stratigraphy and locality. The lower part of the Hsuzhuang Formation, Cambrian Miaolingian in western Henan Province.
Remark. The samples are actually preserved as secondary phosphatic infill of the cavities of echinoderm stereom structure ( Figure 3E1,E2) [81]. It is hard to perform any taxonomic work based on the echinoderm ossicles. Remark. Spicules with three rays diverge at 90° from each other in a single plane. This specimen is preserved as argillaceous with no surface details observed ( Figure 3F). The poor and rare preservation restrict taxonomic evaluation.
Stratigraphy and locality. The lower part of the Zhangxia Formation, Cambrian Miaolingian in western Henan Province.
Remark. Most of the chancelloriid sclerites are fragmentary calcitic internal molds that are identified as single, isolated lateral rays and central, vertical rays ( Figure 5). The relatively well-preserved star-shaped sclerites with a rosette of lateral rays surrounding a central (7 + 1) ray resemble Chancelloria eros Walcott, 1920 ( Figure 5F-H). Chancelloria are a globally distributed genus from the early Cambrian to the late Cambrian. It is not the first discovery of Chancelloriidae in the NCP. Before then, amounts of Chancelloriidae were recovered from the Xinji Formation, lower Cambrian [32]. Chancelloriidae also have been reported from the Mantou, Zhangxia, and Changshan formations at NCP [21].

Conclusions
Middle Cambrian small shelly fossils were described from the Zhangxia and the Hsuzhuang formations at the Longwanggou section. The fauna included brachiopods (Micromitra sp., M. modesta, Eoobolus sp., and Schizopholis sp.), helcionelloid (Oelandiella accordionata and O. aliciae), Hyolithellus, Chancelloria eros, Chancelloriidae sclerites, hyolithid, sponge spicule, and echinoderm ossicles. The shell structures of M. modesta, Eoobolus sp., Schizopholis sp., Oelandiella accordionata, and Hyolithellus were described. The shell structure of M. modesta is composed of a homogeneous layer consisting of tightly compacted phosphate grains. Eoobolus sp. is composed of primary layer and secondary columnar structure, and both of them are composed of tightly compacted phosphate grains. Schizopholis sp. has multiple-lamellar microstructures differing from other coeval brachiopods retrieved from the Longwanggou section. Lamellar excretions of multiple-layer microstructures also occur in Hyolithellus that are preserved with tightly compacted phosphate grains. The argillaceous Oelandiella accordionata and O. aliciae, and the calcitic inner molds of hyolith preserved no clear shell structure. The helcionellid O. accordionata, O. aliciae, and M. modesta were recorded for the first time from the North China Platform. The fauna showed similarities to the middle Cambrian faunas of South Australia and South China, but also to Laurentian faunas. The biological assemblage suggests that the palaeogeographic location of the North China Platform and Australia may have been relatively close in location to South China. The age of the small shelly fauna ranged from late Drumian to middle Guzhuangian and may have a similar age to the Murrawong Creek Formation in South Australia.