MICROBIAL MAT SANDWICHES AND OTHER ANACTUALISTIC SEDIMENTARY FEATURES OF THE EDIACARA MEMBER (RAWNSLEY QUARTZITE, SOUTH AUSTRALIA): IMPLICATIONS FOR INTERPRETATION OF THE EDIACARAN SEDIMENTARY RECORD

Abstract: The Ediacara Member of the Rawnsley Quartzite of South Australia hosts some of the most ecologically and taxonomically diverse fossil assemblages of the eponymous Ediacara Biota—Earth's earliest fossil record of communities comprised of macroscopic, complex, multicellular organisms. At the National Heritage Site, Nilpena, fifteen years of systematic excavation and reassembly of bedding planes has resulted in reconstruction of over 400 square meters of Ediacaran seafloor, permitting detailed and sequential sedimentary, paleoecological and taphonomic assessment of Ediacara fossilized communities and the shallow marine settings in which these ecosystems lived. Sedimentological investigation reveals that the Ediacara Member consists of successions of sandstone event beds and a paucity of other lithologies. Moreover, these Ediacara sandstones are characterized by a suite of sedimentary features and style of stratigraphic packaging uncharacteristic of Phanerozoic sandstone successions considered to have been deposited in analogous shallow marine, storm-dominated environments, including: (1) extremely thin (sub-mm- to mm-scale) bed thickness; (2) lateral discontinuity; (3) textural uniformity, including lack of disparity in grain size, between adjacent beds; (4) lack of amalgamation; (5) lack of erosional bed junctions; (6) doubly rippled bedforms defined by rippled bed tops and bases which crisply cast the tops of underlying rippled beds; (7) ubiquity of textured organic surfaces (TOS); (8) positive correlation between body fossil size and abundance and bed thickness; and (9) texturally immature assemblages of sandstone rip-up clasts along bed tops. We interpret these features to reflect the presence of widespread matgrounds, which facilitated seafloor colonization by and ecological development of Ediacara macroorganisms in high-energy environments. Further, we argue that pervasive matgrounds directly mediated the formation and preservation of non-uniformitarian sedimentary features and stratigraphic packaging in the Ediacara Member and were responsible for the anactualistically complete nature of the Ediacara stratigraphic record.

[1]  M. Droser,et al.  The Rise of Animals in a Changing Environment: Global Ecological Innovation in the Late Ediacaran , 2017 .

[2]  J. Counts,et al.  Sedimentological interpretation of an Ediacaran delta: Bonney Sandstone, South Australia , 2016 .

[3]  A. Liu,et al.  Resolving MISS conceptions and misconceptions: A geological approach to sedimentary surface textures generated by microbial and abiotic processes , 2016 .

[4]  M. Droser,et al.  EXCEPTIONAL PRESERVATION OF SOFT-BODIED EDIACARA BIOTA PROMOTED BY SILICA-RICH OCEANS , 2016 .

[5]  N. Planavsky,et al.  Protracted development of bioturbation through the early Palaeozoic Era , 2015 .

[6]  M. Droser,et al.  Paleoecology of the enigmatic Tribrachidium: New data from the Ediacaran of South Australia , 2015 .

[7]  M. Droser,et al.  Dickinsonia liftoff: Evidence of current derived morphologies , 2015 .

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

[9]  M. Droser,et al.  The advent of animals: The view from the Ediacaran , 2015, Proceedings of the National Academy of Sciences.

[10]  M. Droser,et al.  Taphonomy and morphology of the Ediacara form genus Aspidella , 2015 .

[11]  J. Perron,et al.  Microbial shaping of sedimentary wrinkle structures , 2014 .

[12]  M. Zakrevskaya Paleoecological reconstruction of the Ediacaran benthic macroscopic communities of the White Sea (Russia) , 2014 .

[13]  G. Narbonne,et al.  When Life Got Smart: The Evolution of Behavioral Complexity Through the Ediacaran and Early Cambrian of NW Canada , 2014 .

[14]  M. Droser,et al.  Widespread delayed mixing in early to middle Cambrian marine shelfal settings , 2014 .

[15]  M. Droser,et al.  Scratch Traces of Large Ediacara Bilaterian Animals , 2014 .

[16]  M. Allen,et al.  A New Ediacaran Fossil with a Novel Sediment Displacive Life Habit , 2014, Journal of Paleontology.

[17]  M. Droser,et al.  Affirming life aquatic for the Ediacara biota in China and Australia , 2013 .

[18]  M. Droser,et al.  How well do fossil assemblages of the Ediacara Biota tell time , 2013 .

[19]  J. Hagadorn,et al.  Microbial influence on erosion, grain transport and bedform genesis in sandy substrates under unidirectional flow , 2012 .

[20]  M. Droser,et al.  TAPHONOMIC CONTROLS ON EDIACARAN DIVERSITY: UNCOVERING THE HOLDFAST ORIGIN OF MORPHOLOGICALLY VARIABLE ENIGMATIC STRUCTURES , 2010 .

[21]  J. Vinther,et al.  A placozoan affinity for Dickinsonia and the evolution of late Proterozoic metazoan feeding modes , 2010, Evolution & development.

[22]  M. Droser,et al.  Textured organic surfaces associated with the Ediacara biota in South Australia , 2009 .

[23]  N. Noffke The criteria for the biogeneicity of microbially induced sedimentary structures (MISS) in Archean and younger, sandy deposits , 2009 .

[24]  R. Reid,et al.  The Microbial Communities of the Modern Marine Stromatolites at Highborne Cay, Bahamas , 2009 .

[25]  M. Droser,et al.  Synchronous Aggregate Growth in an Abundant New Ediacaran Tubular Organism , 2008, Science.

[26]  D. Bottjer,et al.  Mat growth features , 2007 .

[27]  S. Jensen,et al.  Assemblage palaeoecology of the Ediacara biota: The unabridged edition? , 2006 .

[28]  S. Jensen,et al.  A Critical Look at the Ediacaran Trace Fossil Record , 2006 .

[29]  S. Jensen,et al.  Trace fossil preservation and the early evolution of animals , 2005 .

[30]  B. Waggoner The Ediacaran Biotas in Space and Time1 , 2003, Integrative and comparative biology.

[31]  S. Jensen The Proterozoic and Earliest Cambrian Trace Fossil Record; Patterns, Problems and Perspectives1 , 2003, Integrative and comparative biology.

[32]  S. Jensen,et al.  Trace fossils and substrates of the terminal Proterozoic–Cambrian transition: Implications for the record of early bilaterians and sediment mixing , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[33]  A. Ivantsov,et al.  Giant traces of vendian animals , 2002 .

[34]  J. Gehling Environmental interpretation and a sequence stratigraphic framework for the terminal Proterozoic Ediacara Member within the Rawnsley Quartzite, South Australia , 2000 .

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

[36]  A. Seilacher Biomat-related lifestyles in the Precambrian , 1999 .

[37]  P. Gresse,et al.  Microbial sand chips—a non-actualistic sedimentary structure , 1996 .

[38]  J. D. Aitken,et al.  Ediacaran fossils from the Sekwi Brook area, Mackenzie Mountains, northwestern Canada , 1990 .

[39]  J. Gehling A cnidarian of actinian-grade from the Ediacaran Pound Subgroup, South Australia , 1988 .

[40]  S. Ouchi Response of alluvial rivers to slow active tectonic movement , 1985 .

[41]  P. Sadler Sediment Accumulation Rates and the Completeness of Stratigraphic Sections , 1981, The Journal of Geology.

[42]  T. Crimes The production and preservation of trilobite resting and furrowing traces , 1975 .

[43]  M. Glaessner TRACE FOSSILS FROM THE PRECAMBRIAN AND BASAL CAMBRIAN , 1969 .

[44]  M. Wade PRESERVATION OF SOFT‐BODIED ANIMALS IN PRECAMBRIAN SANDSTONES AT EDIACARA, SOUTH AUSTRALIA , 1968 .