The Ediacaran Subcommission of the International Commission on Stratigraphy is diligently working toward the goal of subdividing the Ediacaran Period into precise and useful chronostratigraphic units. As emphasized by Xiao and colleagues in 2016, one of the most effective tools in this endeavor will be the use of index fossils. Our special issue serves as a presentation of ongoing research efforts aimed at advancing this task and contains explorations into taxonomy, taphonomy, and the diversity of life during the Ediacaran Period.

The terminal Ediacaran Period is signaled worldwide by the first appearance of skeletonizing tubular metazoan fossils, e.g., Cloudina Germs, 1972 and Sinotubulites Chen, Chen, and Qian, 1981. Although recent efforts have focused on evaluating the taxic composition and preservation of such assemblages from the southwestern United States, comparable forms reported in the 1980s from Mexico remain to be re-examined. Here, we reassess the latest Ediacaran skeletal materials from the La Ciénega Formation of the Caborca region in Sonora, Mexico, using a combination of analytical methods: optical microscopy of extracted fossils, thin-section petrography, scanning electron microscopy and energy dispersive X-ray spectroscopy, and X-ray tomographic microscopy. From our examination, we conclude that the La Ciénega hosts a polytaxic assemblage of latest Ediacaran tubular organisms that have been preserved through two taphonomic pathways: coarse silicification and calcareous recrystallization preserving finer details. Further, these fossils show signs that their shells might not have been inflexible or completely mineralized in vivo, and that they might also record tentatively interpreted predation traces in the form of drill holes or puncture marks. This work, along with ongoing efforts around the world, helps to provide a framework for biostratigraphic correlation and possible subdivision of the Ediacaran Period, and further shapes our view of metazoan evolution and ecology in the interval directly preceding the Cambrian explosion.

Since the 1980s, the existence of one or more extinction events in the late Ediacaran has been the subject of debate. Discussion surrounding these events has intensified in the last decade, in concert with efforts to understand drivers of global change over the Ediacaran–Cambrian transition and the appearance of the more modern-looking Phanerozoic biosphere. In this paper we review the history of thought and work surrounding late Ediacaran extinctions, with a particular focus on the last 5 years of paleontological, geochemical, and geochronological research. We consider the extent to which key questions have been answered, and pose new questions which will help to characterize drivers of environmental and biotic change. A key challenge for future work will be the calculation of extinction intensities that account for limited sampling, the duration of Ediacaran ‘assemblage’ zones, and the preponderance of taxa restricted to a single ‘assemblage’; without these data, the extent to which Ediacaran bioevents represent genuine mass extinctions comparable to the ‘Big 5’ extinctions of the Phanerozoic remains to be rigorously tested. Lastly, we propose a revised model for drivers of late Ediacaran extinction pulses that builds off recent data and growing consensus within the field. This model is speculative, but does frame testable hypotheses that can be targeted in the next decade of work.

Proterozoic eukaryotic macroalgae are difficult to interpret because morphological details required for proper phylogenetic studies are rarely preserved. This is especially true of morphologically simple organisms consisting of tubes, ribbons, or spheres that are commonly found in a wide array of bacteria, plants, and even animals. Previous reports of exceptionally preserved Tonian (ca. 950−900 Ma) fossils from the Dolores Creek Formation of Northwestern Canada feature enough morphological evidence to support a green macroalgal affinity. However, the affinities of two additional forms identified on the basis of the size distribution of available specimens remain undetermined, while the presence of three unique algal forms supports other reports of increasing algal diversity in the early Neoproterozoic. Archaeochaeta guncho new genus new species is described as a green macroalga on the basis of its well-preserved morphology consisting of an unbranching, uniseriate thallus with uniform width throughout and possessing an elliptical to globose anchoring holdfast. A larger size class of ribbon-like forms is interpreted as Vendotaenia sp. A third size class is significantly smaller than Archaeochaeta n. gen. and Vendotaenia, but in the absence of clear morphological characters, it remains difficult to assign. As Archaeochaeta n. gen. and Vendotaenia represent photoautotrophic taxa, these findings support the hypothesis of increasing morphological complexity and phyletic diversification of macroalgae during the Tonian, leading to dramatic changes within benthic marine ecosystems before the evolution of animals.

Ecophenotypic variation in populations is driven by differences in environmental variables. In marine environments, ecophenotypic variation may be caused by differences in hydrodynamic conditions, substrate type, water depth, temperature, salinity, oxygen concentration, and habitat heterogeneity, among others. Instances of ecophenotypic variation in modern and fossil settings are common, but little is known about the influences of time averaging and spatial averaging on their preservation. Here we examine the shell morphology of two adjacent populations, both live collected and death assemblages, of the infaunal, suspension-feeding, intertidal bivalve Leukoma staminea from the well-studied Argyle Creek and Argyle Lagoon locations on San Juan Island, Washington. Individuals in the low-energy lagoon are free to burrow in the fine-grained substrate, while clams in the high-energy creek are precluded from burrowing in the rocky channel. Our results demonstrate variation in size and shape between the adjacent habitats. Lagoon clams are larger, more disk-shaped, and have relatively larger siphons than their creek counterparts, which are smaller, more spherical in shape, and have a relatively shallower pallial sinus. This ecophenotypy is preserved among death assemblages, although with generally greater variation due to time averaging and shell transport. Our interpretation is that ecophenotypic variation, in this case, is induced by differing hydrodynamic regimes and substrate types, cumulatively resulting in physiological trade-offs diverting resources from feeding and respiration to stability and shell strength, all of which have the potential to be preserved in the fossil record.

The earliest fossil record of animal biomineralization occurs in the latest Ediacaran Period (c. 550 Ma). Cloudina and Sinotubulites are two important tubular taxa among these earliest skeletal fossils. The evolutionary fate of Cloudina-type fossils across the Ediacaran–Cambrian transition, however, remains poorly understood. Here we report a multi-layered tubular microfossil Feiyanella manica gen. et sp. nov. from a phosphorite interval of the lowest Cambrian Kuanchuanpu Formation, southern Shaanxi Province, South China. This newly discovered fossil is a conical tube with a ‘funnel-in-funnel’ construction, showing profound morphological similarities to Cloudina and Conotubus. On the other hand, the outer few layers, and particularly the outermost layer, of Feiyanella tubes are regularly to irregularly corrugated, a feature strikingly similar to the variably folded/wrinkled tube walls of Sinotubulites. The Feiyanella tubes additionally exhibit two orders of dichotomous branching, similar to branching structures reported occasionally in Cloudina and possibly indicative of asexual reproduction. Owing to broad similarities in tube morphology, tube wall construction and features presumably indicative of asexual reproduction, Cloudina, Conotubus, Sinotubulites and the here described Feiyanella may thus constitute a monophyletic group traversing the Ediacaran–Cambrian boundary. The tube construction and palaeoecological strategy of Feiyanella putatively indicate evolutionary continuity in morphology and palaeoecology of benthic metazoan communities across the Ediacaran–Cambrian transition.

Yuknessia Walcott, 1919 recently was transferred from the green algae to the Phylum Hemichordata on the basis of new details observed for the type species, Y. simplex, from the Burgess Shale Formation (Cambrian Stage 5) of British Columbia. This has prompted reexamination of material attributed to Yuknessia from various Cambrian localities in South China. Findings preclude both a Yuknessia and a hemichordate affinity for all of the Chinese study material, and most of this material is formally transferred to Fuxianospira Chen and Zhou, 1997, a taxon common in the Chengjiang biota. Comparable material from the Cambrian Marjum, Wheeler, and Burgess Shale formations of North America is also assigned to Fuxianospira, and this reassignment expands both the paleogeographic and stratigraphic range of this taxon. All aspects of the study specimens, including details obtained from scanning electron microscopy, are consistent with an algal affinity, as proposed in the original descriptions of the Chinese material.

Ediacara-type fossils are found in a diverse array of preservational styles, implying that multiple taphonomic mechanisms might have been responsible for their preservational expression. For many Ediacara fossils, the “death mask” model has been invoked as the primary taphonomic pathway. The key to this preservational regime is the replication or sealing of sediments around the degrading organisms by microbially induced precipitation of authigenic pyrite, leading toward fossil preservation along bedding planes. Nama-style preservation, on the other hand, captures Ediacaran organisms as molds and three-dimensional casts within coarse-grained mass flow beds, and has been previously regarded as showing little or no evidence of a microbial preservational influence. To further understand these two seemingly distinct taphonomic pathways, we investigated the three-dimensionally preserved Ediacaran fossil Pteridinium simplex from mass flow deposits of the upper Kliphoek Member, Dabis Formation, Kuibis Subgroup, southern Namibia. Our analysis, using a combination of petrographic and micro-analytical methods, shows that Pteridinium simplex vanes are replicated with minor pyrite, but are most often represented by open voids that can be filled with secondary carbonate material; clay minerals are also found in association with the vanes, but their origin remains unresolved. The scarcity of pyrite and the development of voids are likely related to oxidative weathering and it is possible that microbial activities and authigenic pyrite may have contributed to the preservation of Pteridinium simplex; however, any microbes growing on P. simplex vanes within mass flow deposits were unlikely to have formed thick mats as envisioned in the death mask model. Differential weathering of replicating minerals and precipitation of secondary minerals greatly facilitate fossil collection and morphological characterization by allowing Pteridinium simplex vanes to be parted from the massive hosting sandstone.

With the 1859 publication of On the Origin of Species, Charles Darwin posed contention against his synthesis on the history of life. His dilemma specifically regarded that the geologically sudden appearance of complex shelly invertebrates at the Cambrian Explosion followed an incomprehensible absence of a long-standing gradual transition to such forms. Indeed, as quoted from Chapter 10 of the sixth edition, “To the question why we do not find rich fossiliferous deposits belonging to these assumed earliest periods prior to the Cambrian system, I can give no satisfactory answer… the difficulty of assigning any good reason for the absence of vast piles of strata rich in fossils beneath the Cambrian system is very great… The case at present must remain inexplicable; and may be truly urged as a valid argument against the views here entertained” (p. 286–288). In the 155 years since this assertion, paleontologists focusing on the strata of the Ediacaran–Cambrian transition have uncovered a rich evolutionary history prior to the radiation of animals, but our resulting discoveries have neither been without debate nor unraveled the intricacies suggested by Darwin's dilemma. While we are continuing to learn from both geological and paleontological records, the organisms, their expanding ecosystem intricacy, and the increasing complexity of their behaviors during the Ediacaran and Cambrian periods are yet not well understood. With rapidly growing data and ideas, this transition in evolutionary history has become one of the intellectually richest periods in our record of life on Earth.

Fossilized animal embryos from lower Cambrian rocks provide a rare opportunity to study the ontogeny and developmental biology of early animals during the Cambrian explosion. This paper reports possible animal embryos, along with sponge spicules, hyolithelminths, and linguliformean brachiopods, from the upper Shuijingtuo Formation limestone (Cambrian Stage 3) at Changyang, Hubei Province, South China. This limestone unit has carbonate carbon and oxygen isotopic compositions similar to the upper Shuijingtuo limestone in the Yangtze Gorges area. The Shuijingtuo embryo fossils were exposed by physical fracturing, extracted with acetic acid maceration, and observed in thin sections. They were examined using light microscopy, scanning electron microscopy, energy dispersive X-ray spectroscopic elemental mapping, and micro-focus X-ray computed tomography. Most of them are poorly preserved, with a phosphatic envelope (interpreted as a chorion or fertilization envelope) surrounding sparitic calcite. In some specimens, a polygonal pattern is present on the surface, and these are interpreted as multicelled blastula embryos. In others, sets of grooves are present on the surface of a calcitic spheroidal structure, presumably representing the calcitic interior within the chorion; these grooves are superficially similar to annulations of Markuelia embryos, but their biological significance is unknown. Although their phylogenetic and taxonomic placement is largely unconstrained, the Shuijingtuo animal embryos indicate that chorions are taphonomically more robust and are selectively phosphatized. Embryos within the chorions, on the other hand, can be completely lost or entirely replaced by calcite, with only poorly preserved surficial structures. This style of preservation can be explained by a taphonomic switch from early phosphatization to later calcitization. This study illustrates the importance of combining physical fracturing with widely used acid digestion methods in the study of calcitized animal embryos, and it alludes to the possibility that many empty phosphatic vesicles recovered by acid digestion from Cambrian carbonates may be fossilized chorions.

To investigate the phylogenetic affinity of Yuknessia simplex Walcott, 1919, scanning electron microscopy was applied to the Burgess Shale (Cambrian Series 3, Stage 5) type material and to new material from the Trilobite Beds (Yoho National Park) and specimens from the Cambrian of Utah. On the basis of fine-scale details observed using this approach, including banding structure interpreted as fusellae, Yuknessia Walcott, 1919 is transferred from the algae, where it resided for nearly a century, to the extant taxon Pterobranchia (Phylum Hemichordata). Considered as such, Yuknessia specimens from the Trilobite Beds and Spence Formation (Utah) are amongst the oldest known colonial pterobranchs. Two morphs regarded herein as two different species are recognized from the Trilobite Beds based on tubarium morphology. Yuknessia simplex has slender erect tubes whereas Yuknessia stephenensis n. sp., which is also known in Utah, has more robust erect tubes. The two paratypes of Y. simplex designated by Walcott (1919) are formally removed from Yuknessia and are reinterpreted respectively as an indeterminate alga and Dalyia racemata Walcott, 1919, a putative red alga.

This paper addresses the taphonomic processes responsible for fossil preservation in calcium phosphate, or phosphatization. Aside from silicification and rarer examples of carbonaceous compression, phosphatization is the only taphonomic mode claimed to preserve putative subcellular structures. Because this fossilization window can record such valuable information, a comprehensive understanding of its patterns of occurrence and the geochemical processes involved in the replication of soft tissues are critical endeavors. Fossil phosphatization was most abundant during the latest Neoproterozoic through the early Paleozoic, coinciding with the decline of non-pelletal phosphorite deposits. Its temporal abundance during this timeframe makes it a particularly valuable window for the study of early animal evolution. Several occurrences of phosphatization from the Ediacaran through the Permian Period, including Doushantuo-type preservation of embryo-like fossils and acritarchs, phosphatized gut tracts within Burgess Shale-type carbonaceous compressions, Orsten-type preservation of meiofaunas, and other cases from the later Paleozoic are reviewed. In addition, a comprehensive description of the geochemical controls of calcium phosphate precipitation from seawater is provided, with a focus on the rates of phosphate nucleation and growth, favorable nucleation substrates, and properties of substrate tissue and pore-fluid chemistry. It is hoped that the paleontological and geochemical summaries provided here offer a practical and valuable guide to the Neoproterozoic–Paleozoic phosphatization window.