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Much uncertainty remains as to the temporal relationship between the Ediacaran and Cambrian biotas, yet this is critical to our understanding of the rise of metazoans. Here we present new high-resolution carbon isotope chemostratigraphy and biostratigraphy for a terminal Ediacaran to Cambrian succession on the eastern Siberian Platform, Russia, which shows the presence of a succession of diverse fossil assemblages before the start of the basal Cambrian negative carbon isotope excursion (BACE). Soft-bodied Ediacaran biota (Beltanelliformis) occur before the start of the late Ediacaran positive carbon isotope plateau (EPIP), a mixed Ediacaran and Cambrian skeletal biota (Cloudina, Anabarites, Cambrotubulus) appears within the EPIP, and diverse Cambrian-type small shelly fossils including Protohertzina and other protocondonts, halkieriids, chancelloriids, hyoliths, hyolithelminthes, and the burrowing trace fossil Diplocraterion appear at the beginning of the BACE. These integrated data show that taxa attributed to so-called Ediacaran and earliest Cambrian skeletal biotas in fact overlap without notable biotic turnover, and thus refute the presence of a large isotope excursion coincident with mass extinction of all Ediacaran biota. We propose a new biozone, the Cloudina-Namacalathus-Sinotubulites Assemblage Zone, to precede the known small shelly fossil (SSF) zones. These observations raise doubts as to whether there is any true separation between the Ediacaran and Cambrian skeletal biotas, and suggest that there is a deep root for the Cambrian explosion of metazoans. [ABSTRACT FROM AUTHOR]

The trigger for biomineralization of metazoans in the terminal Ediacaran, ca. 550 Ma, has been suggested to be the rise of oxygenation or an increase in seawater Ca concentration, but geochemical and fossil data have not been fully integrated to demonstrate cause and effect. Here we combine the record of macrofossils with early marine carbonate cement distribution within a relative depth framework for terminal Ediacaran to Cambrian successions on the eastern Siberian Platform, Russia, to interrogate the evolution of seawater chemistry and biotic response. Prior to ca. 545 Ma, the presence of early marine ferroan dolomite cement suggests dominantly ferruginous anoxic "aragonite-dolomite seas", with a very shallow oxic chemocline that supported mainly soft-bodied macrobiota. After ca. 545 Ma, marine cements changed to aragonite and/or high-Mg calcite, and this coincides with the appearance of widespread aragonite and high-Mg calcite skeletal metazoans, suggesting a profound change in seawater chemistry to "aragonite seas" with a deeper chemocline. By early Cambrian Stage 3, the first marine low-Mg calcite cements appear, coincident with the first low-Mg calcite metazoan skeletons, suggesting a further shift to "calcite seas". We suggest that this evolution of seawater chemistry was caused by enhanced continental denudation that increased the input of Ca into oceans so progressively lowering Mg/Ca, which, combined with more widespread oxic conditions, facilitated the rise of skeletal animals and in turn influenced the evolution of skeletal mineralogy. [ABSTRACT FROM AUTHOR]

Namacalathus hermanastes is one of the oldest known skeletal metazoans, found in carbonate settings of the terminal Ediacaran (~550-541 million years ago [Ma]). The palaeoecology of this widespread, goblet-shaped, benthic organism is poorly constrained yet critical for understanding the dynamics of the earliest metazoan communities. Analysis of in situ assemblages from the Nama Group, Namibia (~548-541 Ma), shows that Namacalathus exhibited size variation in response to differing water depths, hydrodynamic conditions and substrate types. In low-energy, inner ramp environments, Namacalathus attains the largest average sizes but grew in transient, loosely aggregating, monospecific aggregations attached to microbial mats. In high-energy mid-ramp reefs, Namacalathus spatially segregated into different palaeoecological habitats with distinct size distributions. In outer ramp environments, individuals were small and formed patchy, dense, monospecific aggregations attached to thin microbial mats. Asexual budding is common in all settings. We infer that variations in size distribution in Namacalathus reflect differences in habitat heterogeneity and stability, including the longevity of mechanically stable substrates and oxic conditions. In the Nama Group, long-lived skeletal metazoan communities developed within topographically heterogeneous mid-ramp reefs, which provided diverse mechanically stable microbial substrates in persistently oxic waters, while inner and outer ramp communities were often ephemeral, developing during fleeting episodes of either oxia and/or substrate stability. We conclude that Namacalathus, which forms a component of these communities in the Nama Group, was a generalist that adapted to various palaeoecological habitats within a heterogeneous ecosystem landscape where favourable conditions persisted, and was also able to opportunistically colonise transiently hospitable environments. These early skeletal metazoans colonised previously unoccupied substrates in thrombolitic reefs and other microbial carbonate settings, and while they experienced relatively low levels of interspecific competition, they were nonetheless adapted to the diverse environments and highly dynamic redox conditions present in the terminal Ediacaran. [ABSTRACT FROM AUTHOR]

A current paradigm accepts the presence of weakly biomineralized animals only, barely above a low metazoan grade of organization in the terminal Neoproterozoic (Ediacaran), and a later, early Cambrian burst of well skeletonized animals. Here we report new assemblages of primarily calcareous shelly fossils from upper Ediacaran (553-542 Ma) carbonates of Spain and Russia (Siberian Platform). The problematic organism Cloudina is found in the Yudoma Group of the southeastern Siberian Platform and different skeletal taxa have been discovered in the terminal Neoproterozoic of several provinces of Spain. New data on the morphology and microstructure of Ediacaran skeletal fossils Cloudina and Namacalathus indicate that the Neoproterozoic skeletal organisms were already reasonably advanced. In total, at least 15 skeletal metazoan genera are recorded worldwide within this interval. This number is comparable with that known for the basal early Cambrian. These data reveal that the terminal Neoproterozoic skeletal bloom was a real precursor of the Cambrian radiation. Cloudina, the oldest animal with a mineralised skeleton on the Siberian Platform, characterises the uppermost Ediacaran strata of the Ust'-Yudoma Formation. While in Siberia Cloudina co-occurs with small skeletal fossils of Cambrian aspect, in Spain Cloudina-bearing carbonates and other Ediacaran skeletal fossils alternate with strata containing rich terminal Neoproterozoic trace fossil assemblages. These finds treated together provide a possibility to correlate transitional Neoproterozoiclower Cambrian strata around the world. Such a correlation concurs with available isotope and radiometric data and indicates that typical Ediacaran shelly fossils have not crossed the Precambrian-Cambrian boundary. [ABSTRACT FROM AUTHOR]

The Ediacaran-Cambrian transition, which incorporates the radiation of animals, lacks a robust global temporal and spatial framework, resulting in major uncertainty in the evolutionary dynamics of this critical radiation and its relationship to changes in palaeoenvironmental geochemistry. We first present a new δ13C carb composite reference curve for the Ediacaran Nama Group of southern Namibia, and we then outline four new possible global age models (A to D) for the interval 551–517 million years ago (Ma). These models comprise composite carbonate‑carbon isotope (δ13C carb) curves, which are anchored to radiometric ages and consistent with strontium isotope chemostratigraphy, and are used to calibrate metazoan distribution in space and time. These models differ most prominently in the temporal position of the basal Cambrian negative δ13C carb excursion (BACE). Regions that host the most complete records show that the BACE nadir always predates the Ediacaran-Cambrian boundary as defined by the first appearance datum (FAD) of the ichnospecies Treptichnus pedum. Whilst treptichnid traces are present in the late Ediacaran fossil record, the FAD of the ichnospecies T. pedum appears to post-date the last appearance datums (LADs) of in situ representatives of the skeletal organisms Cloudina and Namacalathus in all environments with high-resolution δ13C carb data. Two age models (A and B) place the BACE within the Ediacaran, and yield an age of ~538.8 Ma for the Ediacaran-Cambrian boundary; however models C and D appear to be the most parsimonious and may support a recalibration of the boundary age by up to 3 Myr younger. All age models reveal a previously underappreciated degree of variability in the terminal Ediacaran, incorporating notable positive and negative excursions that precede the BACE. Nothwithstanding remaining uncertainties in chemostratigraphic correlation, all models support a pre-BACE first appearance of Cambrian-type shelly fossils in Siberia and possibly South China, and show that the Ediacaran-Cambrian transition was a protracted interval represented by a series of successive radiations. [ABSTRACT FROM AUTHOR]

The author comments on the article "The oldest evidence of bioturbation on Earth" by V. Rogov et al. Rogov et al., found bioturbation fabrics, the preserved depth of which achieved 5 centimeter (cm), from the Ediacaran Khatyspyt Formation of the northern Siberian Platform. The age of the bioturbated beds is estimated at circa (ca.) 555 megaannum (Ma).

The article presents a study which explores the skeletal marine invertebrate phyla appeared during the Cambrian explosion, except for Bryozoa with mineralized skeletons, which first appear in the Early Ordovician. It mentions that skeletal diversity of Early Ordovician bryozoans suggests a preceding interval of diversification.

The article presents research report on ediacaran metazoan reveals lophotrochozoan affinity and deepens root of Cambrian explosion. Topics include morphological data support molecular phylogenies and demonstrates that the origin of modern lophotrochozoan phyla, and their ability to biomineralize, had deep roots in the Ediacaran; and supporting an organic-rich composition and tripartite construction with possible sensory punctae.

The Ediacaran skeletal tubular putative metazoan Cloudina occurs globally in carbonate settings, which both provided lithified substrates and minimized the cost of skeletonization. Habitat and substrate preferences and the relationship of Cloudina to other metazoans have not been fully documented, so we know little as to its ecological demands or community dynamics. In situ Cloudina from the Nama Group, Namibia (ca. 550-541 Ma), formed mutually attached reefs composed of successive assemblages in shallow, high-energy environments, and also communities attached to either stromatolites in storm-influenced deep inner-ramp settings or thin microbial mats in lower-energy habitats. Each assemblage shows statistically distinct tube diameter cohorts, but in sum, Cloudina shows an exponential frequency distribution of diameter size. In reefs, we document a periodicity of size variation, where mean, minimum, and maximum tube diameters vary together and show a systematic increase toward the top of each assemblage. We conclude that most Nama Group Cloudina represent one ecologically generalist taxon with highly variable size, that size was environmentally mediated, and that Cloudina could respond rapidly to periodic environmental changes. While Nama Group skeletal metazoans coexisted with soft-bodied biota, there was no apparent ecological interaction, as they were segregated into lithified carbonate and non-lithified clastic microbial mat communities, respectively. We infer that ecological flexibility allowed Cloudina to form varied communities that colonized diverse carbonate substrates under low levels of interspecific substrate competition. This is in notable contrast to the earliest Cambrian skeletal epibenthos that formed biodiverse reef communities with specialist niche occupancy. [ABSTRACT FROM AUTHOR]