Post-fossilization processes and their implications for understanding Ediacaran macrofossil assemblages

Abstract Fossil assemblages from Newfoundland's Avalon Peninsula preserve diverse examples of the enigmatic Ediacaran macrobiota, offering some of the earliest evidence for large and complex multicellular life. These fossils are exposed on extensive coastal bedding planes in extraordinary abundances, permitting palaeoecological studies based on census data from spatially extensive palaeocommunities. Such studies have been used to constrain the reproductive strategy and phylogenetic placement of Ediacaran organisms. Geological mapping and stratigraphic correlation in the Mistaken Point Ecological Reserve reveal that some fossil-bearing surfaces can be tracked over distances of several kilometres. These laterally extensive surfaces reveal that the modern processes by which the sediment overlying a fossil surface is removed may impose important controls on the observed composition of fossil assemblages. Weathering and erosion – along with factors associated with tectonics, metamorphism and discovery – are here grouped as ‘post-fossilization processes’ and introduce biases that are often not explicitly accounted for in palaeoecological studies. Specifically, post-fossilization processes may differentially influence the preservational fidelity of individual specimens on a given surface and generate features that could be mistaken for original morphological characters. We therefore recommend that post-fossilization processes must be considered when undertaking palaeoecological studies in Ediacaran successions in Newfoundland and, potentially, elsewhere.

[1]  S. Dufour,et al.  Ediacaran pre-placozoan diploblasts in the Avalonian biota: the role of chemosynthesis in the evolution of early animal life , 2016, Special Publications.

[2]  A. Liu FRAMBOIDAL PYRITE SHROUD CONFIRMS THE ‘DEATH MASK' MODEL FOR MOLDIC PRESERVATION OF EDIACARAN SOFT-BODIED ORGANISMS , 2016, Palaios.

[3]  Sara J. Mason,et al.  Two new Ediacaran small fronds from Mistaken Point, Newfoundland , 2016, Journal of Paleontology.

[4]  D. McIlroy,et al.  The Beothukis/Culmofrons problem and its bearing on Ediacaran macrofossil taxonomy: evidence from an exceptional new fossil locality , 2016 .

[5]  J. Antcliffe,et al.  A new ecological model for the ∼565 Ma Ediacaran biota of Mistaken Point, Newfoundland , 2015 .

[6]  R. Wilby,et al.  Role of low intensity environmental disturbance in structuring the earliest (Ediacaran) macrobenthic tiered communities , 2015 .

[7]  D. Erwin,et al.  Biotic replacement and mass extinction of the Ediacara biota , 2015, Proceedings of the Royal Society B: Biological Sciences.

[8]  A. Liu,et al.  Reconstructing the reproductive mode of an Ediacaran macro-organism , 2015, Nature.

[9]  A. Liu,et al.  Remarkable insights into the paleoecology of the Avalonian Ediacaran macrobiota , 2015 .

[10]  D. McIlroy,et al.  The arrangement of possible muscle fibres in the Ediacaran taxon Haootia quadriformis , 2015, Proceedings of the Royal Society B: Biological Sciences.

[11]  A. J. Kaufman,et al.  A unifying model for Neoproterozoic–Palaeozoic exceptional fossil preservation through pyritization and carbonaceous compression , 2014, Nature Communications.

[12]  D. McIlroy,et al.  Haootia quadriformis n. gen., n. sp., interpreted as a muscular cnidarian impression from the Late Ediacaran period (approx. 560 Ma) , 2014, Proceedings of the Royal Society B: Biological Sciences.

[13]  M. Clapham,et al.  Population structure of the oldest known macroscopic communities from Mistaken Point, Newfoundland , 2013, Paleobiology.

[14]  D. McIlroy,et al.  Evidence for Cnidaria-like behavior in ca. 560 Ma Ediacaran Aspidella , 2013 .

[15]  J. Antcliffe,et al.  The architecture of Ediacaran Fronds , 2012 .

[16]  J. Schiffbauer,et al.  EXPERIMENTAL FORMATION OF A MICROBIAL DEATH MASK , 2012 .

[17]  M. Laflamme,et al.  Ecological Tiering and the Evolution of a Stem: The Oldest Stemmed Frond from the Ediacaran of Newfoundland, Canada , 2012, Journal of Paleontology.

[18]  J. Schiffbauer,et al.  Microbial biofilms and the preservation of the Ediacara biota , 2011 .

[19]  D. McIlroy,et al.  Effaced preservation in the Ediacara biota and its implications for the early macrofossil record , 2011 .

[20]  D. Bottjer,et al.  Taphonomy: Bias and Process Through Time , 2011 .

[21]  M. Clapham Ordination Methods and the Evaluation of Ediacaran Communities , 2011 .

[22]  G. Retallack First evidence for locomotion in the Ediacara biota from the 565 Ma Mistaken Point Formation, Newfou , 2010 .

[23]  D. McIlroy,et al.  First evidence for locomotion in the Ediacara biota from the 565 Ma Mistaken Point Formation, Newfoundland , 2010 .

[24]  G. Narbonne,et al.  New Ediacaran Rangeomorphs from Mistaken Point, Newfoundland, Canada , 2009, Journal of Paleontology.

[25]  M. Laflamme,et al.  Reconstructing a Lost World: Ediacaran Rangeomorphs from Spaniard's Bay, Newfoundland , 2009 .

[26]  J. Antcliffe,et al.  Evolutionary relationships within the Avalonian Ediacara biota: new insights from laser analysis , 2009, Journal of the Geological Society.

[27]  G. Narbonne,et al.  Taphonomy and ontogeny of a multibranched Ediacaran fossil: Bradgatia from the Avalon Peninsula of Newfoundland , 2008 .

[28]  J. Ogg,et al.  The Concise Geologic Time Scale , 2008 .

[29]  G. Narbonne,et al.  Growth and Ecology of a Multi-branched Ediacaran Rangeomorph from the Mistaken Point Assemblage, Newfoundland , 2008, Journal of Paleontology.

[30]  M. Fedonkin The Rise of Animals: Evolution and Diversification of the Kingdom Animalia , 2008 .

[31]  H. Hofmann,et al.  Ediacaran Biota on Bonavista Peninsula, Newfoundland, Canada , 2008, Journal of Paleontology.

[32]  D. McIlroy Lateral variability in shallow marine ichnofabrics: implications for the ichnofabric analysis method , 2007, Journal of the Geological Society.

[33]  J. Gehling,et al.  Spindle-shaped Ediacara fossils from the Mistaken Point assemblage, Avalon Zone, Newfoundland , 2007 .

[34]  M. Laflamme,et al.  Morphology and taphonomy of an Ediacaran frond: Charnia from the Avalon Peninsula of Newfoundland , 2007 .

[35]  G. Narbonne THE EDIACARA BIOTA: Neoproterozoic Origin of Animals and Their Ecosystems , 2005 .

[36]  M. Clapham,et al.  THECTARDIS AVALONENSIS: A NEW EDIACARAN FOSSIL FROM THE MISTAKEN POINT BIOTA, NEWFOUNDLAND , 2004, Journal of Paleontology.

[37]  M. Laflamme,et al.  MORPHOMETRIC ANALYSIS OF THE EDIACARAN FROND CHARNIODISCUS FROM THE MISTAKEN POINT FORMATION, NEWFOUNDLAND , 2004 .

[38]  G. Narbonne Modular Construction of Early Ediacaran Complex Life Forms , 2004, Science.

[39]  D. Wood,et al.  Paleoenvironmental analysis of the late Neoproterozoic Mistaken Point and Trepassey formations, southeastern Newfoundland , 2003 .

[40]  M. Clapham,et al.  Paleoecology of the oldest known animal communities: Ediacaran assemblages at Mistaken Point, Newfoundland , 2003, Paleobiology.

[41]  M. Clapham,et al.  Ediacaran epifaunal tiering , 2002 .

[42]  J. Gehling Microbial mats in terminal Proterozoic siliciclastics; Ediacaran death masks , 1999 .

[43]  W. Gibbons,et al.  Precambrian , 2019, Geological Society, London, Memoirs.

[44]  A. Seilacher Vendobionta and Psammocorallia: lost constructions of Precambrian evolution , 1992, Journal of the Geological Society.

[45]  Mark Wilson,et al.  PALEOSCENE #9. Taphonomic Processes: Information Loss and Information Gain , 1988 .

[46]  S. Kidwell,et al.  Taphonomy's contributions to paleobiology , 1985, Paleobiology.

[47]  H. Williams,et al.  Trepassey map area, Newfoundland , 1979 .

[48]  James W. Valentine,et al.  Evolutionary Paleoecology of the Marine Biosphere , 1974 .

[49]  M. M. Anderson,et al.  Fossils found in the Pre-Cambrian Conception Group of South-eastern Newfoundland , 1968, Nature.

[50]  D. R. Lawrence Taphonomy and Information Losses in Fossil Communities , 1968 .

[51]  H. W. Wellman,et al.  Salt Weathering, a Neglected Geological Erosive Agent in Coastal and Arid Environments , 1965, Nature.

[52]  T. Ford PRE-CAMBRIAN FOSSILS FROM CHARNWOOD FOREST , 1958 .