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The Cambrian coral Cambroctoconus occurs selectively in the crypts of calcimicrobe Epiphyton reefs of the Zhangxia Formation (Miaolingian) in Shandong Province, North China. These cryptobionts preferentially grow laterally and/or downward, in some cases showing pendent growth from the ceilings of the reef framework. The upside‐down growth is clearly shown by the downward‐oriented aperture and the presence of fork‐like holdfasts at its base. The coral aggregations reveal two cryptic growth strategies: one involves the prevalence of far smaller individuals in vertically narrow spaces; the other involves the predominance of modular individuals in large cavernous spaces. Offset individuals frequently appear projecting downward and are connected to each other in a chain‐like fashion. Individuals often undergo rejuvenescence laterally and downward, when the growth directions may change. Therefore, the size and modularity of individuals and the direction of budding depend largely upon the cryptic microenvironments available at the time. The cryptobionts make the best use of vacant spaces by modifying the location of budding and altering their growth directions through rejuvenescence. The cryptic growth strategies found in Cambroctoconus indicate a certain degree of morphological variability in the modules. More importantly, they indicate that the individuals flexibly and exquisitely utilized the microbial crypts that were still predominant even during the middle Cambrian. These modes of cryptic growth demonstrate the age‐specific exploitation of niches by sessile skeletal organisms that was facilitated by the development of a firm attachment structure. [ABSTRACT FROM AUTHOR]

The Cambrian–Ordovician interval was an intriguing period of geologic time, when reef transitions occurred along with important biodiversification events. This study examines the secular reef transitions in North and South China during the Cambrian and Ordovician in terms of changes in reef construction and related geobiological changes. Microbial reefs in the Terreneuvian have not been well documented in South China. The Cambrian Series 2 interval saw the almost simultaneous appearance of reef-building skeletal archaeocyaths and calcimicrobes. The widely developed archaeocyath–calcimicrobe reefs had totally disappeared by the middle of Series 2 in South China and were followed by purely calcimicrobial reefs. During the Miaolingian and Furongian, skeletal-reef builders were commonly thought to have been inhibited owing to elevated sea-water temperature, which caused lowered oxygen. However, microbial reefs containing lithistid sponges and keratosan sponges were more common in this interval in North China than previously thought. The first skeletal-dominated reefs were established during the Early Ordovician, coincident with a decline in stromatolite reefs in the central Yangtze Platform. During the Middle and Late Ordovician interval, a variety of skeletal reef-builders with diversified calcimicrobes contributed markedly to reef construction in limited areas of both North and South China. The appearance and increase of skeletal-dominated reefs are considered to have been related to lowering global sea-water temperature. Recently reported Late Ordovician cement-rich reefs in both North and South China may contain further evidence of global cooling; however, from an ecological perspective, the novel niches and biological interactions created by early skeletal-dominated reefs may have promoted the further development of reef-building organisms. Cambrian and Ordovician reef successions in North and South China are distributed discontinuously; however, integrating information from both North and South China could yield improved understanding of reef evolution and background environments through these intervals. • Four intervals of Cambrian–Ordovician reef transitions in China are identified. • Calcimicrobial diversity changed dramatically throughout the intervals. • Stromatolite decline coincided with increasing diversity of metazoans. • Data from North and South China will improve understanding of reef succession. [ABSTRACT FROM AUTHOR]

Abstract: The Lower Ordovician records a transition from microbial- to metazoan-dominant reefs immediately prior to the Great Ordovician Biodiversification Event. The Hunghuayuan Formation (late Tremadocian-early Floian) of the Jianxin section in Anhui Province, South China, includes well-preserved reefs, which consist of a combination of microbial boundstones and microbial-lithistid sponge-receptaculitid boundstones. The microbial boundstones are characteristically made up of nodular or columnar stromatolites produced by an irregular alternation of Girvanella-rich layers and thick micrite layers in which the filamentous calcimicrobe Girvanella and bioclasts occur sporadically. Microbial biofilms, including the filamentous microbes, may have trapped and bound lime mud and/or precipitated micrite during their growth and metabolic activities. These activities contemporaneously contributed to substrate stabilisation, encrustation, and the construction of microbialite frameworks (stromatolites). In contrast, the microbial-lithistid sponge-receptaculitid boundstones are characterised by more micritic constituents than skeletal reef-building constituents. Thin and/or domal crusts produced by peloid and dense micrite, together with various proportions of Girvanella, occur upon bioclastic sediments and reef-building skeletal organisms. These micritic crusts with Girvanella therefore played roles as binders and stabilisers, and as consolidators by encrusting reef-building skeletal organisms. In the boundstones, it is remarkable that the degradation of lithistid sponges, due to microbial decay, produced micrite in the sponge bodies. As a result, lithistid sponges played an apparently inconspicuous but potentially significant role as micrite producers as well as automicrite framework constructors. These Lower Ordovician reefs, in which microbialites (e.g., stromatolites) dominate but coexist with metazoans (e.g., sponges), were widespread at the time. They provide excellent examples for understanding reefal palaeoecology during the transition from microbe-dominant reefs to reefs enriched in metazoans. [Copyright &y& Elsevier]

Peloids are major contributors to modern and ancient limestones, although their origins are not yet comprehensively understood. Upper Permian to Lower Triassic carbonate successions are well preserved at the Bangeng area in Guizhou Province, South China, where microbialites (thrombolites), coccoidal microbes and peloids are preserved together. These peloids are classified into three types (Peloid-A, B, C) that typically occur together along with coccoidal microbes and restricted bioclasts in a variety of microenvironments. Peloid-A is most common and exhibits close relationship with coccoidal microbes. Peloid-A1 has spherical grain and a size range typical for coccoidal microbes (10–60 μm in diameter), whereas Peloid-A2 is marked by larger spherical and subrounded grains with diffuse margins, ranging from 70 to 200 μm in diameter. Peloid-A1 is in part produced by the complete micritic filling in coccoidal microbes by their metabolic activities, whereas Peloid-A2 is related to the calcification of a colony of coccoidal microbes by their metabolic activities, or simply to the aggregation of individual peloids and coccoidal microbes. Peloids of this type might also originate from other carbonate precipitation processes. Peloid-B is derived merely by micrite filling in ostracodes and gastropods skeletons, whereas Peloid-C is of micritized-bioclast origin. These peloidal origins do not explain those of all environments and ages. Peloids are polygenetic in origin, irrespective of the presence of coccoidal microbes. However, it is emphasized that the peloids formed after the end-Permian extinction are dominated by microbes related ones. Those kinds of peloids might have occurred repeatedly and predominantly, especially in severely deteriorated environments such as those after the end-Permian mass extinction. [Copyright &y& Elsevier]

Calcimicrobes together with archaeocyaths became significant in reef construction during the early Cambrian; however, purely calcimicrobial reefs have not been as well documented as archaeocyath-bearing reefs. Here we describe the age-specific features of calcimicrobial reefs of the Zhushadong Formation (Cambrian Series 2, Stage 4) at the Sunmayu and Jinhe sections in Shandong Province, North China. The calcimicrobial reefs of the Sunmayu section are constructed mainly by Epiphyton , Kordephyton , and tubiform microbes. The reefs are in some cases dominated by Amgaina , passing from a framework of Kordephyton , Epiphyton , and tubiform microbes to dendritic growth of Epiphyton , and finally to aggregations of Amgaina. Calcimicrobial reefs in the Jinhe section are likewise constructed mainly by Epiphyton , Kordephyton , and tubiform microbes, but with subordinate Tarthinia and Bija. Epiphyton and Kordephyton as well as Amgaina were thus the main framework builders in the Zhushadong calcimicrobial reefs. Tubiform microbes contributed as encrusters, enhancing the framework rigidity, whereas Tarthinia and Bija played subordinate roles as encrusters and consolidators. Interreef deposits of the Sunmayu reefs are of peloidal or ooidal grainstone; these reefs are inferred to have formed in a high-energy shoal setting. In contrast, interreef deposits of the Jinhe reefs are of peloidal and intraclastic wackestone or grainstone with bioclasts such as trilobites and hyoliths. Tubular cavities, possibly representing burrows, are common in the spaces among frameworks. These calcimicrobial reefs are interpreted to have formed in a subtidal setting, where the water energy was lower than that in the Sunmayu section. In North China, reefs of Cambrian Epoch 2 are limited, as development of the carbonate platform began only toward the end of that epoch. The reefs of the Zhushadong Formation are therefore among the earliest on the North China Platform. The calcimicrobial reefs contain various kinds of calcimicrobes, and the calcimicrobial assemblages are similar to or more diverse than those of coeval archaeocyath-bearing reefs during this period of archaeocyath decline. Calcimicrobes thus flourished at that time and contributed greatly to the construction of reefs. These purely calcimicrobial reefs provide further information on the spatial and temporal changes in calcimicrobial diversity and reef construction during the period before and after the extinction of archaeocyaths. • Zhushadong reefs in the Jinhe and Sunmayu sections contain various calcimicrobes. • The Jinhe reefs developed in a lower-energy setting than the Sunmayu reefs. • Calcimicrobes contributed to the construction of reefs without archaeocyaths. • The reefs are some of the oldest calcimicrobial reefs in North China. • The reefs show calcimicrobial diversity around the time of archaeocyath extinction. [ABSTRACT FROM AUTHOR]