In the Cadomian orogenic belt a package of glacigenic sedimentary deposits have been recently described in the Armorican Massif (Normandy, France). The Granville Tillite Member, the middle part of the upper Granville Formation, is late Ediacaran in age. Maximum depositional ages of the pre- and syn-glacial sedimentary deposits obtained by LA-ICP-MS U–Pb detrital zircon dating indicate a maximum age of 561 ± 3 Ma. Combined with geochronological data on the previously described glacial deposits in Cadomia, West Africa, Arabia and Iran, the Granville Tillite Member appears to represent an Upper Ediacaran Glacial Period in northern peri-Gondwana, clearly younger than the c. 580 Ma old Gaskiers glaciation. Detailed mapping and analysis of the depositional regime of two sections near the city of Granville are indicative of two independent glaciomarine lower and upper tillite deposits separated by a distinct conglomeratic marker horizon, evidently a massive gravel beach horizon deposited during an interglacial stage. Age spectra of detrital zircon U–Pb ages constrain the palaeogeographical position of the upper Granville Formation to the periphery of the West African Craton. Post-Gaskiers aged glaciations in Cadomia and in West Africa should be grouped into an Upper Ediacaran Glacial Period dated at c. 565 Ma. This glacial period seems not to be related to the negative δ13C Shuram–Wonoka anomaly. Sedimentary deposits formed during the Upper Ediacaran Glacial Period show a scattered distribution along the marginal orogens of the Gondwana supercontinent independent of palaeolatitude and are coupled most likely to contemporaneous orogenic processes and uplift.

Throughout the Ediacaran Period, variable water-column redox conditions persisted along productive ocean margins due to a complex interplay between nutrient supply and oceanographic restriction. These changing conditions are considered to have influenced early faunal evolution, with marine anoxia potentially inhibiting the development of the ecological niches necessary for aerobic life forms. To understand this link between oxygenation and evolution, the combined geochemical and palaeontological study of marine sediments is preferable. Located in the Yangtze Gorges region of southern China, lagoonal black shales at Miaohe preserve alga and putative metazoans, including Eoandromeda, a candidate total-group ctenophore, thereby providing one example of where integrated study is possible. We present a multi-proxy investigation into water-column redox variability during deposition of these shales (c. 560–551 Ma). For this interval, reactive iron partitioning indicates persistent water-column anoxia, while trace metal enrichments and other geochemical data suggest temporal fluctuations between ferruginous, euxinic and rare suboxic conditions. Although trace metal and total organic carbon values imply extensive basin restriction, sustained trace metal enrichment and δ15Nsed data indicate periodic access to open-ocean inventories across a shallow-marine sill. Lastly, δ13Corg values of between −35‰ and −40‰ allow at least partial correlation of the shales at Miaohe with Member IV of the Doushantuo Formation. This study provides evidence for fluctuating redox conditions in the lagoonal area of the Yangtze platform during late Ediacaran time. If these low-oxygen environments were regionally characteristic, then the restriction of aerobic fauna to isolated environments can be inferred.

Several sag-type basins apparently developed from rift systems, but there is no consensus about how and if these grabens influenced the sedimentation of the post-rift thermal subsidence phase. The Ediacaran Jaibaras Rift Basin is one of the best-exposed sedimentary records among the NE Brazil late Precambrian – early Cambrian rift system, cropping out at the eastern margin of the intracratonic Parnaíba Basin and extending below it towards the west. Here we present detrital zircon U–Pb ages of rocks from the Jaibaras (Aprazível Formation) and Parnaíba (Ipu Formation) basins, in order to understand the provenance patterns, maximum depositional ages (MDA) and age relationship between these units. The MDA for the Aprazível Formation (c. 499 ± 5 Ma) indicates a Cambrian age for the upper part of the Jaibaras Basin. The bulk U–Pb data indicate that the Ipu Formation started to deposit during late Cambrian and/or Early Ordovician time, despite its MDA (c. 528 ± 11 Ma) being older than that of the Aprazível Formation. Detrital zircon provenance suggests that the primary source areas for the early deposits of the Parnaíba Basin were mountains related to the Brasiliano Orogeny to the south and SE (e.g. Rio Preto and Riacho do Pontal metamorphic belts). Finally, our data emphasize the key change in source areas from the rift to the initial deposition of the intracratonic phase, indicating major depositional style changes between both basins after the Gondwana assembly.

Early-middle Ediacaran organic-walled microfossils from the Doushantuo Formation studied in several sections in the Yangtze Gorges area, South China, show ornamented cyst-like vesicles of very high diversity. These microfossils are diagenetically permineralized and observed in petrographic thin-sections of chert nodules. Exquisitely preserved specimens belonging to seven species of Appendisphaera, Mengeosphaera, Tanarium, Urasphaera and Tianzhushania contain either single or multiple spheroidal internal bodies inside the vesicles. These structures indicate reproductive stages, endocyst and dividing cells, respectively, and are preserved at early to late ontogenetic stages in the same taxa. This new evidence supports the algal affiliations for the studied taxa and refutes previous suggestions of Tianzhushania being animal embryo or holozoan. The first record of a late developmental stage of a completely preserved specimen of T. spinosa observed in thin-section demonstrates the interior of vesicles with clusters of identical cells but without any cavity that is diagnostic for recognizing algal cysts vs animal diapause cysts. Various lines of evidence to infer biological affinities of these microfossils – morphology, reproductive characters, spatial arrangement of cells, and biochemical properties of the vesicle wall – are collectively characteristic of algal clades. Recognizing the biological affinities of these microfossils is key to understanding whether animals capable of producing such morphologically complex diapause cysts had an early Ediacaran fossil record (633–610 Ma), or the microfossils were non-animal holozoans or algae as argued herein for Tianzhushania spinosa and other studied microfossils.

New occurrences of flask-shaped and envelope-bearing microfossils, including the predominantly Cambrian taxon Granomarginata, are reported from new localities, as well as from earlier in time (Ediacaran) than previously known. The stratigraphic range of Granomarginata extends into the Cambrian System, where it had a cosmopolitan distribution. This newly reported Ediacaran record includes areas from Norway (Baltica), Newfoundland (Avalonia) and Namibia (adjacent to the Kalahari Craton), and puts the oldest global occurrence of Granomarginata in the Indreelva Member (< 563 Ma) of the Stáhpogieddi Formation on the Digermulen Peninsula, Arctic Norway. Although Granomarginata is rare within the assemblage, these new occurrences together with previously reported occurrences from India and Poland, suggest a potentially widespread palaeogeographic distribution of Granomarginata through the middle–late Ediacaran interval. A new flask-shaped microfossil Lagoenaforma collaris gen. et sp. nov. is also reported in horizons containing Granomarginata from the Stáhpogieddi Formation in Norway and the Dabis Formation in Namibia, and flask-shaped fossils are also found in the Gibbett Hill Formation in Newfoundland. The Granomarginata–Lagoenaforma association, in addition to a low-diversity organic-walled microfossil assemblage, occurs in the strata postdating the Shuram carbon isotope excursion, and may eventually be of use in terminal Ediacaran biostratigraphy. These older occurrences of Granomarginata add to a growing record of body fossil taxa spanning the Ediacaran–Cambrian boundary.

For almost 150 years, megascopic structures in siliciclastic sequences of terminal Precambrian age have been frustratingly difficult to characterize and classify. As with all other areas of human knowledge, progress with exploration, documentation and understanding is growing at an exponential rate. Nevertheless, there is much to be learned from following the evolution of the logic behind the biological interpretations of these enigmatic fossils. Here, I review the history of discovery as well as some long-established core members of widely recognized clades that are still difficult to graft on to the tree of life. These ‘orphan plesions’ occupy roles that were once held by famous former Problematica, such as archaeocyaths, graptolites and rudist bivalves. In some of those cases, taxonomic enlightenment was brought about by the discovery of new characters; in others it required a better knowledge of their living counterparts. Can we use these approaches to rescue the Ediacaran orphans? Five taxa that are examined in this context are Arborea (Arboreomorpha), Dickinsonia (Dickinsoniomorpha), Pteridinium plus Ernietta (Erniettomorpha) and Kimberella (Bilateria?). With the possible exception of Dickinsonia, all of these organisms may be coelenterate grade eumetazoans.

The classical genus of Ediacaran macroorganisms, Dickinsonia, was part of an extensive benthic marine community inhabiting the fields of microbial mats. The remains of Dickinsonia are commonly preserved in the position of adhesion to the habitat substrate. However, these were mobile organisms. In addition to the already known feeding traces of Dickinsonia, structures described as traces of motor activity are reported. Long parallel furrows, extending from the posterior end of the body imprint, are interpreted as imprints of ridges left by an organism moving along the surface of the substrate. Groups of differently shaped grooves laying in the depression that enhalo the Dickinsonia body imprints or accompany their individual areas are interpreted as imprints of ridges and cords of mucous material. They are considered to represent structures of self-determined stretching and lift-off of the body margins from the substrate. The rings and arcs of silt- and sand-sized mineral particles bordering the body imprints are composed of material that was supposedly brushed off from the surface of the microbial mat by Dickinsonia. They are considered traces of the adhesion of these organisms to the substrate. Accumulations of multidirectional pulling and tear-off structures, lacking the body imprint but accompanied by the joint plane passing into the overlying sediment and cutting through the bedding, are interpreted as escape traces. The dual modality of the behaviour (attachment and mobility) could indicate the adaptability of Dickinsonia to life in extremely shallow-water environments.

The recognition of fossiliferous horizons both below and above the classical Ediacara levels of the Flinders Ranges, South Australia, significantly expands the potential of this candidate World Heritage succession. Here we document a small window into the biology and taphonomy of the late Ediacaran seafloor within the new Nilpena Sandstone Member of the Rawnsley Quartzite in Bathtub Gorge, northern Heysen Range. A 1 m2 slab extracted from the gorge, now on permanent display at the South Australian Museum, has a death assemblage dominated by the erniettomorph Phyllozoon hanseni Jenkins and Gehling 1978 and a newly named macroscopic tubular body fossil – Aulozoon soliorum gen. et sp. nov. – on its fine sandstone bed sole. The orientations and juxtaposition of these taxa suggest overprinting of an in situ benthic Phyllozoon community by sand-filled tubes of Aulozoon carried in by a storm wave-base surge. Phyllozoon hanseni is a widespread species that is restricted to the Nilpena Sandstone Member of the Rawnsley Quartzite, whereas Dickinsonia costata ranges from the underlying Ediacara Sandstone Member into the Nilpena Sandstone Member. Fundamental differences in the ways these two vendobiont taxa are constructed and preserved may provide insights into their biology and phylogenetic affinities. In the Nilpena Sandstone Member, D. costata is joined by Dickinsonia rex Jenkins 1992, which appears to be confined to the member, and is here re-described to clarify its taxonomic status and stratigraphic distribution.

Ediacaran rangeomorphs were the first substantially macroscopic organisms to appear in the fossil record, but their underlying biology remains problematic. Although demonstrably heterotrophic, their current interpretation as osmotrophic consumers of dissolved organic carbon (DOC) is incompatible with the inertial (high Re) and advective (high Pe) fluid dynamics accompanying macroscopic length scales. The key to resolving rangeomorph feeding and physiology lies in their underlying construction. Taphonomic analysis of three-dimensionally preserved Charnia from the White Sea identifies the presence of large, originally water-filled compartments that served both as a hydrostatic exoskeleton and semi-isolated digestion chambers capable of processing recalcitrant substrates, most likely in conjunction with a resident microbiome. At the same time, the hydrodynamically exposed outer surface of macroscopic rangeomorphs would have dramatically enhanced both gas exchange and food delivery. A bag-like epithelium filled with transiently circulated seawater offers an exceptionally efficient means of constructing a simple, DOC-consuming, multicellular heterotroph. Such a body plan is broadly comparable to that of anthozoan cnidarians, minus such derived features as muscle, tentacles and a centralized mouth. Along with other early bag-like fossils, rangeomorphs can be reliably identified as total-group eumetazoans, potentially colonial stem-group cnidarians.

Beothukis mistakensis from the Ediacaran System of Newfoundland, Canada demonstrates complex fractal-like morphology through the development of primary-, secondary- and tertiary-order Rangea-like units. The primary-order rangeomorph units observed in B. mistakensis are tightly juxtaposed, show no evidence of being independent of one another and are made up of chamber-like secondary-order – probably mesoglea-filled – units. The growth of these rangeomorph units demonstrates that the frond developed from the tip towards the basal region through ontogeny. The tertiary-order units of Beothukis are considered to represent surface morphology on the secondary-order units. This is in contrast to palaeobiological reconstructions of Beothukis that invoke three-dimensional fractal-like branches with independent units, which has been used to infer an osmotrophic mode of life. It is considered here that the fractal-like morphology of the lower surface of B. mistakensis was an adaptation to increase surface area to volume ratio. The quilted morphology of Beothukis proposed here is consistent with a sessile, reclining, phagocytotic and/or chemosymbiotic mode of life similar to that invoked for the reclining rangeomorph Fractofusus.

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.

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.

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.

Fossils within early Cambrian phosphorites worldwide are often well preserved due to early diagenetic permineralization. Here, we examine the fossil record contained within phosphorites of the Lower Cambrian Pusa Formation (late Fortunian to Cambrian Stage 2) in Fontanarejo, central Spain. The sedimentology and age of these phosphorites have been controversial and are here reviewed and discussed, providing also an updated geological map. The Pusa Formation is composed of fine clastic sediments that are partly turbiditic, with channels of quartz-rich conglomerates and abundant phosphorites in the upper part of the succession. The microfacies and mineralogy of these channel deposits are studied here for the first time in detail, showing that they are mainly composed of subspherical apatite clasts, with minor mudstone intraclasts, quartzite and mica grains. Numerous sponge spicules, as well as entirely preserved hexactinellid sponges and demosponges, were collected within these phosphorites and likely represent stem groups. In addition to sponges, other fossils, such as small shelly fossils (SSF) of the mollusc Anabarella sp., were found. The phosphorites exhibit multiple evidence of intense microbial activity, including diverse fabrics (phosphatic oncoidal-like microbialites, thrombolites, stromatolites and cements) and abundant fossils of filamentous microbes that strongly resemble extant sulphur-oxidizing bacteria. Our findings strongly suggest that microbial processes mediated the rapid formation of most of the Fontanarejo apatite, probably accounting for the exceptional preservation of fragile fossils such as sponge skeletons. The apparent presence of taxonomically diverse hexactinellid and demosponge communities at the lowermost Cambrian further corroborates a Precambrian origin of the phylum Porifera.

The two major structural elements of the Iberian Chains, the Datos and Jarque thrust faults, have been described as occurring in proximity in the area around the village of Codos. The purported Jarque fault corresponds to the axial plane of an anticline known as the Codos anticline, which exposes the oldest stratigraphic unit in this area, i.e. the Codos Bed, a limestone bed bearing skeletal fossils of putative Ediacaran or earliest Cambrian age. Details of the geology of the area and the age of the known fossils are poorly understood or not universally agreed upon. New investigations in the anticline revealed the presence of a normal fault, introduced as the Codos fault, which cross-cuts the course of the alleged Jarque fault. The vertical displacement along the axial plane of the anticline appears to be insignificant, challenging the traditional interpretation of the plane as an equivalent of the Jarque thrust fault. Reinvestigation of the Codos Bed revealed previously unknown skeletal fossils of early Cambrian age, confirming notions that the bed is younger than traditionally assumed. In particular, two helcionelloid molluscs, Anabarella cf. plana and Igorella? sp., allow correlations with Terreneuvian strata of central Spain (Pusa and Fuentepizzara formations) and support previously suggested connections with the Heraultia Limestone of southern France. Former identification of the terminal Ediacaran index-fossil Cloudina in the bed is erroneous. Consequently, the Ediacaran–Cambrian boundary in the Iberian Chains, which has been placed at the top of the formation overlying the Codos Bed, is stratigraphically distinctly lower.

In the Central Iberian Zone, the Cadomian orogenic collapse is represented by chaotic megabreccias, olistostromes and mélange deposits reflecting a drastic change from slope-related deposits, fed by denudation of the Cadomian arc, to offshore-dominant settings episodically punctuated by phosphogenetic processes. In the Ibor and Alcudia anticlines, the pre-rift unconformity is marked by paraconformable to angular discordant contacts separating variable tilted strata of the Ediacaran Lower Alcudian – Domo Extremeño Supergroup and the upper Ediacaran – lower Terreneuvian Ibor Group from the overlying Terreneuvian San Lorenzo and Fuentepizarra formations. The sedimentation of the San Lorenzo Formation reflects two palaeogeographic scenarios: (i) a low-angle stable basement recording shoaling-upward siliciclastic cycles, and (ii) perturbations of basement fault scarps feeding slope-related conglomeratic channels, with NE-directed palaeocurrents, and sourced from topographic palaeohighs controlled by the movement along synsedimentary normal fault systems, such as the so-called El Guijo Fault. The intra-Fortunian age of the pre-rift unconformity is constrained by the ichno- and microfossil content of the succession, and is bracketed between the first occurrence of Treptichnus pedum in the Arrocampo Formation (Ibor Group) and of Anabarella plana in the Fuentepizarra Formation.

Sabellidites cambriensis is a tubular non-mineralized metazoan that appears as compressed ribbon-shaped imprints with transverse wrinkling, thick walls and an even tube diameter of up to 3 mm. The distribution of Sabellidites is investigated in three Ediacaran–Cambrian sections on the Digermulen Peninsula in Arctic Norway, spanning the Manndrapselva Member of the Stáhpogieddi Formation and the lower member of the Breidvika Formation. Here, the Ediacaran–Cambrian boundary is located in the lower part of the upper parasequence (third cycle) of the Manndrapselva Member. Specimens of Sabellidites are rare but consistently present close to the lowest level of Treptichnus pedum and upsection, whereas the taxon is common and abundant in the lower part of the lower member of the Breidvika Formation, with an upper record at c. 55 m above the base. The range is comparable with that of the GSSP section in Newfoundland, Canada, establishing Sabellidites as an index fossil for the lowermost Cambrian. In the Manndrapselva Member, Sabellidites co-occurs with the acritarch Granomarginata, indicative of the lowermost Cambrian Granomarginata Zone, whereas in the Breidvika Formation it co-occurs with Asteridium. Sabellidites is widely distributed in Baltica, through the Rovnian and Lontovan regional stages but confined to the Fortunian global stage. In its lower range, Sabellidites is associated with a Treptichnus pedum trace fossil association and a depauperate leiosphaerid acritarch assemblage, followed by a Granomarginata assemblage. In its upper range, Sabellidites co-occurs with acritarchs of the Asteridium–Comasphaeridium Zone and the tubular foraminiferan Platysolenites. In Baltica, Sabellidites is a useful index fossil.

In northwestern France, the Brioverian series is a thick siliciclastic succession deposited during the Cadomian cycle (c. 750–540 Ma). In the uppermost Brioverian beds, previous studies unravelled an assemblage dominated by simple horizontal trace fossils associated with microbially stabilized surfaces. Here, we report Spirodesmos trace fossils – one-way, irregular and regular horizontal spirals – from Crozon (Finistère, Brittany), Montfort-sur-Meu and St-Gonlay (Ille-et-Vilaine, Brittany). After reviewing the literature on horizontal spiral trace fossils, an Ediacaran–Fortunian Spirodesmos pool is identified from marginal-marine to shelf settings, while an Ordovician–Recent trend formed in the deep-marine realm. These results suggest that an onshore–offshore migration in Spirodesmos took place during Ediacaran–Fortunian to Ordovician time, similar to what happened in graphoglyptids. In addition, the age of the uppermost Brioverian beds (Ediacaran or early Cambrian) is still a pending question. Here, we report two new U–Pb detrital zircon datings from sandstone samples in St-Gonlay, giving maximum deposition ages of 551 ± 7 Ma and 540 ± 5 Ma. Although these results do not discard an Ediacaran age for the uppermost Brioverian beds, a Fortunian age is envisioned because the new dating corroborates previous dating from Brittany, Mayenne and Normandy. However, the intervals of error of the radiometric dating, and the dominance of non-penetrative trace fossils associated with matgrounds (an ecology more typical of the Ediacaran Period), do not allow definitive conclusions on the age of the uppermost Brioverian beds.