The term "Ediacara biota" has received criticism from some scientists due to its alleged inconsistency, arbitrary exclusion of certain fossils, and inability to be precisely defined.
For macroorganisms, the Cambrian biota appears to have almost completely replaced the organisms that dominated the Ediacaran fossil record, although relationships are still a matter of debate.
[9] Multiple hypotheses exist to explain the disappearance of this biota, including preservation bias, a changing environment, the advent of predators and competition from other life-forms.
Palaeontologist Adolf Seilacher proposed a separate subkingdom level category Vendozoa (now renamed Vendobionta)[15] in the Linnaean hierarchy for the Ediacaran biota.
[16] A 2018 study confirmed that one of the period's most-prominent and iconic fossils, Dickinsonia, included cholesterol,[17] suggesting affinities to animals, fungi, or red algae.
[21] However, since they lay below the "Primordial Strata" of the Cambrian that was then thought to contain the very first signs of animal life, a proposal four years after their discovery by Elkanah Billings that these simple forms represented fauna was dismissed by his peers.
Palaeontologist Martin Glaessner finally, in 1959, made the connection between this and the earlier finds[28][29] and with a combination of improved dating of existing specimens and an injection of vigour into the search, many more instances were recognised.
Misra's discovery of fossiliferous ash-beds at the Mistaken Point assemblage in Newfoundland changed all this as the delicate detail preserved by the fine ash allowed the description of features that were previously undiscernible.
In March 2004, the International Union of Geological Sciences ended the inconsistency by formally naming the terminal period of the Neoproterozoic after the Australian locality.
If too thick a layer of sediment is deposited before they can grow or reproduce through it, parts of the colony will die leaving behind fossils with a characteristically wrinkled ("elephant skin") and tubercular texture.
[38] These communities are now limited to inhospitable refugia, such as the stromatolites found in Hamelin Pool Marine Nature Reserve in Shark Bay, Western Australia, where the salt levels can be twice those of the surrounding sea.
Something about the Ediacaran Period permitted these delicate creatures to be left behind; the fossils may have been preserved by virtue of rapid covering by ash or sand, trapping them against the mud or microbial mats on which they lived.
[42] However, it is more common to find Ediacaran fossils under sandy beds deposited by storms or in turbidites formed by high-energy bottom-scraping ocean currents.
[40] Soft-bodied organisms today rarely fossilize during such events, but the presence of widespread microbial mats probably aided preservation by stabilising their impressions in the sediment below.
Most disc-shaped fossils decomposed before the overlying sediment was cemented, whereupon ash or sand slumped in to fill the void, leaving a cast of the organism's underside.
Their more resistant nature is reflected in the fact that, in rare occasions, quilted fossils are found within storm beds as the high-energy sedimentation did not destroy them as it would have the less-resistant discs.
[40] These disparate morphologies can be broadly grouped into form taxa: Classification of the Ediacarans is inevitably difficult, hence a variety of theories exist as to their placement on the tree of life.
[93] However, more recent discoveries have established that many of the circular forms formerly considered "cnidarian medusa" are actually holdfasts – sand-filled vesicles occurring at the base of the stem of upright frond-like Ediacarans.
[100] Seilacher has suggested that the Ediacaran organisms represented a unique and extinct grouping of related forms descended from a common ancestor (clade) and created the kingdom Vendozoa,[101][102] named after the now-obsolete Vendian era.
[114] Several classifications have been used to accommodate the Ediacaran biota at some point,[115] from algae,[116] to protozoans,[117] to fungi[118] to bacterial or microbial colonies,[58] to hypothetical intermediates between plants and animals.
[11] A new extant genus discovered in 2014, Dendrogramma, which at the time of discovery appeared to be a basal metazoan but of unknown taxonomic placement, had been noted to have similarities with the Ediacaran fauna.
[126] On the early Earth, reactive elements, such as iron and uranium, existed in a reduced form that would react with any free oxygen produced by photosynthesising organisms.
[129] However, the assumptions underlying the reconstruction of atmospheric composition have attracted some criticism, with widespread anoxia having little effect on life where it occurs in the Early Cambrian and the Cretaceous.
Each assemblage tends to occupy its own time period and region of morphospace, and after an initial burst of diversification (or extinction) changes little for the rest of its existence.
[146] In Australia, they are typically found in red gypsiferous and calcareous paleosols formed on loess and flood deposits in an arid cool temperate paleoclimate.
[153] Mattress-like vendobionts (Ernietta, Pteridinium, Rangea) in these sandstones form a very different assemblage from vermiform fossils (Cloudina, Namacalathus) of Ediacaran "wormworld" in marine dolomite of Namibia.
[153] An analysis of one of the White Sea fossil beds, where the layers cycle from continental seabed to inter-tidal to estuarine and back again a few times, found that a specific set of Ediacaran organisms was associated with each environment.
It has been estimated that of 92 potentially possible modes of life – combinations of feeding style, tiering and motility — no more than a dozen are occupied by the end of the Ediacaran.