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The Ediacaran rangeomorph Fractofusus misrai is the most common and best-preserved of the E Surface fossil assemblage in the Mistaken Point Ecological Reserve of southeastern Newfoundland, Canada. Fractofusus has been interpreted as a fusiform epifaunal soft-sediment recliner, and like other rangeomorphs it has a self-similar, fractal-like branching morphology. The rangeomorph branching of Fractofusus has been considered to be identical on the upper and lower surfaces; however, study of specimens with complex biostratinomic histories suggests clear differences between the upper and lower surfaces. The first-order branches grew downwards into the sediment from a high point near the midline but grew above the sediment–water interface at their lateral and distal margins. Our new three-dimensional appreciation of rangeomorph branching in Fractofusus explains many of the taphomorphs of Fractofusus including straight, curved, kinked and tousled forms. The three-dimensional morphology, mode of life, taphonomy and palaeoenvironmental interactions of F. misrai are discussed along with a new three-dimensional reconstruction.

Fossils from the deep-sea Ediacaran biotas of Newfoundland are among the oldest architecturally complex soft-bodied macroorganisms on Earth. Most organisms in the Mistaken Point–type biotas of Avalonia—particularly the fractal-branching frondose Rangeomorpha— have been traditionally interpreted as living erect within the water column during life. However, due to the scarcity of documented physical sedimentological proxies associated with fossiliferous beds, Ediacaran paleocurrents have been inferred in some instances from the preferential orientation of fronds. This calls into question the relationship between frond orientation and paleocurrents. In this study, we present an integrated approach from a newly described fossiliferous surface (the “Melrose Surface” in the Fermeuse Formation at Melrose, on the southern portion of the Catalina Dome in the Discovery UNESCO Global Geopark) combining: (1) physical sedimentological evidence for paleocurrent direction in the form of climbing ripple cross-lamination and (2) a series of statistical analyses based on modified polythetic and monothetic clustering techniques reflecting the circular nature of the recorded orientation of Fractofusus misrai specimens. This study demonstrates the reclining rheotropic mode of life of the Ediacaran rangeomorph taxon Fractofusus misrai and presents preliminary inferences suggesting a similar mode of life for Bradgatia sp. and Pectinifrons abyssalis based on qualitative evidence. These results advocate for the consideration of an alternative conceptual hypothesis for position of life of Ediacaran organisms in which they are interpreted as having lived reclined on the seafloor, in the position that they are preserved.

The Ediacara biota include macroscopic, morphologically complex soft-bodied organisms that appear globally in the late Ediacaran Period (575-542 Ma). The physiology, feeding strategies, and functional morphology of the modular Ediacara organisms (rangeomorphs and erniettomorphs) remain debated but are critical for understanding their ecology and phylogeny. Their modular construction triggered numerous hypotheses concerning their likely feeding strategies, ranging from micro-to-macrophagus feeding to photoautotrophy to osmotrophy. Macrophagus feeding in rangeomorphs and erniettomorphs is inconsistent with their lack of oral openings, and photoautotrophy in rangeomorphs is contradicted by their habitats below the photic zone. Here, we combine theoretical models and empirical data to evaluate the feasibility of osmotrophy, which requires high surface area to volume (SA/V) ratios, as a primary feeding strategy of rangeomorphs and erniettomorphs. Although exclusively osmotrophic feeding in modern ecosystems is restricted to microscopic bacteria, this study suggests that (i) fractal branching of rangeomorph modules resulted in SA/V ratios comparable to those observed in modern osmotrophic bacteria, and (ii) rangeomorphs, and particularly erniettomorphs, could have achieved osmotrophic SA/V ratios similar to bacteria, provided their bodies included metabolically inert material. Thus, specific morphological adaptations observed in rangeomorphs and erniettomorphs may have represented strategies for overcoming physiological constraints that typically make osmotrophy prohibitive for macroscopic life forms. These results support the viability of osmotrophic feeding in rangeomorphs and erniettomorphs, help explain their taphonomic peculiarities, and point to the possible importance of earliest macroorganisms for cycling dissolved organic carbon that may have been present in abundance during Ediacaran times.

Impressions of soft-bodied Ediacaran megafossils are common in deep-water slope deposits of the June beds at Sekwi Brook in the Mackenzie Mountains of NW Canada. Two taphonomic assemblages can be recognized. Soles of turbidite beds contain numerous impressions of simple (Aspidella) and tentaculate (Hiemalora, Eoporpita) discs. A specimen of the frond Primocandelabrum is attached to an Aspidella-like holdfast, but most holdfast discs lack any impressions of the leafy fronds to which they were attached, reflecting Fermeuse-style preservation of the basal level of the community. Epifaunal fronds (Beothukis, Charnia, Charniodiscus) and benthic recliners (Fractofusus) were most commonly preserved intrastratally on horizontal parting surfaces within turbidite and contourite beds, reflecting a deep-water example of Nama-style preservation of higher levels in the community. A well-preserved specimen of Namalia significantly extends the known age and environmental range of erniettomorphs into deep-water aphotic settings. Infaunal bilaterian burrows are absent from the June beds despite favorable beds for their preservation. The June beds assemblage is broadly similar in age and environment to deep-water Avalonian assemblages in Newfoundland and England, and like them contains mainly rangeomorph and arboreomorph fossils and apparently lacks dickinsoniomorphs and other clades typical of younger and shallower Ediacaran assemblages. Fossil data presently available imply that the classically deep- and shallow-water taxa of the Ediacara biota had different evolutionary origins and histories, with sessile rangeomorphs and arboreomorphs appearing in deep-water settings approximately 580 million years ago and spreading into shallow-water settings by 555 Ma but dickinsoniomorphs and other iconic clades restricted to shallow-water settings from their first known appearance at 555 Ma until their disappearance prior to the end of the Ediacaran.

The presumed affinities of the Terminal Neoproterozoic Ediacara biota have been much debated. However, even in the absence of concrete evidence for phylogenetic affinity, numerical paleoecological approaches can be effectively used to make inferences about organismal biology, the nature of biotic interactions, and life history. Here, we examine the population structure of three Ediacaran rangeomorph taxa (Fractofusus, Beothukis, and Pectinifrons), and one non-rangeomorph taxon (Thectardis) across five fossil surfaces around the Avalon Peninsula, Newfoundland, through analysis of size-frequency distributions using Bayesian Information Criterion (BIC). Best-supported models resolve communities of all studied Ediacaran taxa at Mistaken Point as single cohorts with wide variance. This result is best explained in terms of a “continuous reproduction” model, whereby Ediacaran organisms reproduce aseasonally, so that multiple size modes are absent from preserved communities. Modern benthic invertebrates (both as a whole and within specific taxonomic groups) in deeper-water settings reproduce both seasonally and aseasonally; distinguishing between biological (i.e., continuous reproductive strategies) and environmental (lack of a seasonal trigger) causes for this pattern is therefore difficult. However, we hypothesize that the observed population structure could reflect the lack of a trigger for reproduction in deepwater settings (i.e., seasonal flux of organic matter), until the explosive appearance of mesozooplankton near the base of the Cambrian.

We report new high-resolution laser scanning of the type material for the earliest, complex Ediacaran genera Charnia, Bradgatia, Charniodiscus and Ivesheadia from Charnwood, UK, and compare these with Beothukis mistakensis gen. et sp. nov. and the recently described taxa Charnia wardi, Charnia antecedens and Fractofusus spp. from broadly coeval strata in Newfoundland. We use the laser and other techniques to map the similarities and differences in morphology between these Ediacaran rangeomorphs. Key features are suggested to include the number of growth axes, the number and placement of growth tips, the presence of radiating or subparallel axes for the first- and higher-order branches, the extent of displayed or undisplayed leaf-like \"rangeomorph\" architecture, and the extent of furling of the margins of these leaf-like elements. These features are then used to propose suggested homologies between these taxa, leading to a preliminary phylogenetic hypothesis for the evolution of the Avalonian Ediacara biota.

The Mistaken Point assemblage of the Ediacara fossils is dominated by rangeomorphs with homologous fractal branching elements. The most distinctive are the fusiform fossils, herein named Fractofusus misrai n. gen., and n. sp., and Fractofusus andersoni n. gen., and n. sp. Although endemic to the Newfoundland portion of the Avalonia terrane, they dominated deep sea-floor communities below the photic zone, in the mid-Ediacaran Period (ca. 575-560 Ma). Their biological affinities remain uncertain, but their architecture suggests a phylogenetic position near the base of the Metazoa.