The siliciclastic succession of the late Neoproterozoic Vendian Group in the White Sea area demonstrates a wide range of lithofacies, some recurring in a vertical succession. Significantly, each lithofacies contains a distinct assemblage of Ediacaran fossils that represents in situ benthic paleocommunities smothered in life position. These lithofacies define (1) a monospecific Inaria as semblage, restricted to the lower-shoreface muds; (2) a Charnia assemblage, within the middle-shoreface graded siltstone-shale couplets; (3) a Dickinsonia-Kimberella assemblage, confined to the interstratified sandstone and shale of prodelta; and (4) a Onegia-Rangea assemblage, preserved within channelized sandstone beds of the distributary-mouth bar. In the White Sea area a strong correlation exists between taxonomic composition, biostratinomic features, and paleoecological context of the Ediacaran fossil assemblages. Facies-controlled distri bution is also evident in other Ediacaran localities, demonstrating the recurrence of similar facies relationships on a global scale. This pattern is interpreted as representing Ediacaran biofacies with Avalon-type biotas distributed in deep marine habitats, Ediacara-type biotas inhabiting microbial biofilms in shallow marine prodeltaic settings, and infaunal Nama-type biotas found in distribu tary-mouth bar shoals. This in turn reveals a marked degree of environmental sensitivity and eco logical specialization. Correspondence between depositional environment and taxonomic compo sition speaks against any obvious biogeographic provinciality of the Ediacaran biotas, and also casts doubt on claims of substantial evolutionary change.

When each of the Avalon-, Ediacara-, and Nama-type fossil assemblages are tracked through geological time, there appear to be changes in species composition and diversity, almost synchronized between different sedimentary environments, allowing a subdivision of the late Ediacaran into the Redkinian, Belomorian and Kotlinian geological time intervals. The Redkinian (580–559 Ma) is characterized by first appearance of both eumetazoan traces and macroscopic organisms (frondomorphs and vendobionts) in a form of Avalon-type communities in the inner shelf environment, whereas coeval Ediacara-type communities remained depauperate. The Belomorian (559–550 Ma) is marked by the advent of eumetazoan burrowing activity in the inner shelf, diversification of frondomorphs, migration of vendobionts from the inner shelf into higher energy environments, and appearance of tribrachiomorphs and bilateralomorphs. Ediacaran organisms formed distinctive ecological associations that coexisted in the low-energy inner shelf (Avalon-type communities), in the wave- and current-agitated shoreface (Ediacara-type communities), and in the high-energy distributary systems (Nama-type communities). The Kotlinian (550–540 Ma) witnessed an expansion of the burrowing activity into wave- and current-agitated shoreface, disappearance of vendobionts, tribrachiomorphs and bilateralomorphs in wave- and current-agitated shoreface, together with a drop in frondomorph diversity. High-energy distributary channel systems of prodeltas served as refugia for Nama-type communities that survived until the end of the Ediacaran and disappeared when the burrowing activity reached high-energy environments. This pattern is interpreted as an expression of ecosystem engineering by eumetazoans, with the Ediacaran organisms being progressively outcompeted by bilaterians.

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A uranium-lead zircon age for a volcanic ash interstratified with fossil-bearing, shallow marine siliciclastic rocks in the Zimnie Gory section of the White Sea region indicates that a diverse assemblage of body and trace fossils occurred before 555.3 +/- 0.3 million years ago. This age is a minimum for the oldest well-documented triploblastic bilaterian Kimberella. It also makes co-occurring trace fossils the oldest that are reliably dated. This determination of age implies that there is no simple relation between Ediacaran diversity and the carbon isotopic composition of Neoproterozoic seawater.