Materials collected on the territory of the southeastern White Sea area, including diversely preserved body imprints, combined body-trace fossils, specimens with signs of intravital damage and regeneration, and extended ontogenetic series, make it possible to significantly widen the data on the body plan and biology of Dickinsonia, the oldest known mobile animal, included in the Late Precambrian taxon of high rank, Proarticulata. A number of reconstructed anatomical features were added to the obvious directly observed features of Dickinsonia, such as a consistent body shape lacking lateral appendages and temporary outgrowths, transverse differentiation, and anterior–posterior polarity. These reconstructed features include dorsoventral polarity, ciliated mucus-secreting epithelium underlain by a basal lamina, two rows of blind food-gathering pockets, absence of a through-gut, nervous system of diffusive type, axial support band and muscle fibres. Such a set of features indicates the affinity of Dickinsonia and Proarticulata as a whole (the only known Ediacaran Metazoa) to Urbilateria, a hypothetical ancestor of bilaterally symmetrical animals.

Palaeopascichnida is a problematic group of extinct organisms that is globally distributed in Ediacaran sequences of Avalonia, Baltica, Siberia, South China and Australia. The fossils related to Palaeopascichnida consist of serially or cluster-like arranged, millimetre- to centimetre-scale globular or allantoid chambers, which are characterized by substantial differences in preservation, leading to no consistent diagnosis for these organisms. Here we integrate morphometric variation, stratigraphic distribution and habitat settings of more than 1200 specimens from all known fossil localities. The results of the morphological analysis demonstrate variation in chamber shape and size, and allow us to recognize six valid species within the group. Statistical analysis of the specimen distribution with respect to sedimentary environments indicates a significant difference in palaeoecological settings between species, making a significant contribution to the evolution and systematic palaeontology of these problematic organisms and perspective on their use in Neoproterozoic biostratigraphy. Our revision and systematic study sheds new light on one of the least studied groups of the late Ediacaran biota.

The relative timing of extinctions and originations is a foundation for reconstructing evolutionary causes. However, there has been a tendency to dismiss reported Ediacaran holdovers in favour of effective extinction around the Cambrian boundary. Here, focusing on the classically Ediacaran frondose biota (Petalonamae), I suggest four main reasons why proposed Ediacaran survivors have previously been denied the acceptance they deserve: denials based on mistaken identity, doppelgängers, a last gasp or dead clades walking. I then point to the lower Cambrian species Stromatoveris psygmoglena as a key example which simultaneously meets these objections. Collectively, Cambrian survivors are a ‘smoking gun’ showing that extinction of the classically Ediacaran frondose biota did not occur until at least 30 Ma after the end of the Ediacaran period, registered by phylogenetic petalonamid Thaumaptilon from the Burgess Shale. Therefore, to paraphrase Mark Twain, reports of their earlier demise have been greatly exaggerated. Causes of their ultimate extinction should instead be sought in their total range and diversity dynamics. Overall, the Ediacaran–Cambrian transition shows extremely low numbers of recorded survivors, but diversity dynamics are dominated by the Cambrian explosion. In this context, recorded occurrences for the classically Ediacaran frondose biota are compatible with at least two extinction events, one within a possible mass extinction near the Cambrian boundary, and later, their ultimate extinction in, or after, the middle Cambrian (Miaolingian Series, Wuliuan Stage). There is, however, no correlative basis for a causal link between the Cambrian transition and the effective or final demise of the classically Ediacaran soft-bodied biota.

In the Ediacaran marine succession of the Cerro Negro Formation (Tandilia System, NE Argentina), abundant microbially induced sedimentary structures indicate general conditions of substrate biostabilization. Numerous discoidal structures in this succession were previously interpreted as moulds of soft-tissue holdfasts of sessile organisms, within the form genus Aspidella. In this study, we performed a detailed re-analysis of some of these features and discuss two alternative hypotheses to explain their genesis: (1) as the result of soft-sediment deformation and fluid injection structures; and (2) as structures of active animal–sediment interaction (i.e. trace fossils). We show that the dome-shaped discs are internally laminated, with a cylindrical to a funnel-shaped vertical tube at their central region. The presence of these downwards vertical extensions and other intricate internal arrangements cannot be explained under the taphonomic spectrum of discoidal fossils, but shows striking similarities to Intrites-like structures and other sand-volcano-like pseudofossils (e.g. Astropolithon). However, some structures are hard to distinguish from vertical dwelling burrows with funnel-shaped apertures and thick-lined walls, commonly produced by suspension- and detritus-feeding invertebrates (e.g. Skolithos isp., Monocraterion isp. and, less likely, Rosselia isp.). Since reliable age constraints are unavailable, and further investigation concerning other palaeobiological indicators is needed, the most parsimonious hypothesis is that of a structure derived from fluid-escape processes. Our study demonstrates the importance of detailed investigation on discoidal structures in either upper Ediacaran or lower Cambrian strata.