Spatial distributions of Tribrachidium, Rugoconites, and Obamus from the Ediacara Member (Rawnsley Quartzite), South Australia

The spatial distribution of in situ sessile organisms, including those from the fossil record, provides information about life histories, such as possible dispersal and/or settlement mechanisms, and how taxa interact with one another and their local environments. At Nilpena Ediacara National Park (NENP), South Australia, the exquisite preservation and excavation of 33 fossiliferous bedding planes from the Ediacara Member of the Rawnsley Quartzite reveals in situ communities of the Ediacara Biota. Here, the spatial distributions of three relatively common taxa, Tribrachidium, Rugoconites, and Obamus, occurring on excavated surfaces were analyzed using spatial point pattern analysis. Tribrachidium have a variable spatial distribution, implying that settlement or post-settlement conditions/preferences had an effect on populations. Rugoconites display aggregation, possibly related to their reproductive methods in combination with settlement location availability at the time of dispersal and/or settlement. Additionally, post-settlement environmental controls could have affected Rugoconites on other surfaces, resulting in lower populations and densities. Both Tribrachidium and Rugoconites also commonly occur as individuals or in low numbers on a number of beds, thus constraining possible reproductive strategies and environmental/substrate preferences. The distribution of Obamus is consistent with selective settlement, aggregating near conspecifics and on substrates of mature microbial mat. This dispersal process is the first example of substrate-selective dispersal among the Ediacara Biota, thus making Obamus similar to numerous modern sessile invertebrates with similar dispersal and settlement strategies.

[1]  P. Wilby,et al.  A crown-group cnidarian from the Ediacaran of Charnwood Forest, UK , 2022, Nature Ecology & Evolution.

[2]  S. Xiao,et al.  A new approach for investigating spatial relationships of ichnofossils: a case study of Ediacaran–Cambrian animal traces , 2022, Paleobiology.

[3]  M. Droser,et al.  What Happens Between Depositional Events, Stays Between Depositional Events: The Significance of Organic Mat Surfaces in the Capture of Ediacara Communities and the Sedimentary Rocks That Preserve Them , 2022, Frontiers in Earth Science.

[4]  M. Droser,et al.  Picking out the warp and weft of the Ediacaran seafloor: Paleoenvironment and paleoecology of an Ediacara textured organic surface , 2022, Precambrian Research.

[5]  Katie M. Maloney,et al.  The Importance of Size and Location Within Gregarious Populations of Ernietta plateauensis , 2021, Frontiers in Earth Science.

[6]  D. Erwin,et al.  Ediacara growing pains: modular addition and development in Dickinsonia costata , 2021, Paleobiology.

[7]  Philip B. Vixseboxse,et al.  Orientations of Mistaken Point fronds indicate morphology impacted ability to survive turbulence , 2021, bioRxiv.

[8]  Mariem Ben-Said Spatial point-pattern analysis as a powerful tool in identifying pattern-process relationships in plant ecology: an updated review , 2021, Ecological Processes.

[9]  P. Donoghue,et al.  The developmental biology of Charnia and the eumetazoan affinity of the Ediacaran rangeomorphs , 2021, Science Advances.

[10]  E. Mitchell,et al.  Facilitating corals in an early Silurian deep‐water assemblage , 2021, Palaeontology.

[11]  D. Erwin,et al.  Developmental processes in Ediacara macrofossils , 2021, Proceedings of the Royal Society B.

[12]  Mark A. James,et al.  Return to sender: The influence of larval behaviour on the distribution and settlement of the European oyster Ostrea edulis , 2020 .

[13]  Simon Harris,et al.  Mortality, Population and Community Dynamics of the Glass Sponge Dominated Community “The Forest of the Weird” From the Ridge Seamount, Johnston Atoll, Pacific Ocean , 2020, Frontiers in Marine Science.

[14]  M. Droser,et al.  BIOLOGICAL AND ECOLOGICAL INSIGHTS FROM THE PRESERVATIONAL VARIABILITY OF FUNISIA DOROTHEA, EDIACARA MEMBER, SOUTH AUSTRALIA , 2020, Palaios.

[15]  M. Droser,et al.  You can get anything you want from Alice's Restaurant Bed: exceptional preservation and an unusual fossil assemblage from a newly excavated bed (Ediacara Member, Nilpena, South Australia) , 2020 .

[16]  M. Droser,et al.  Biostratinomy of the Ediacara Member (Rawnsley Quartzite, South Australia): implications for depositional environments, ecology and biology of Ediacara organisms , 2020, Interface Focus.

[17]  Mary L. Droser,et al.  Discovery of the oldest bilaterian from the Ediacaran of South Australia , 2020, Proceedings of the National Academy of Sciences.

[18]  D. Erwin The origin of animal body plans: a view from fossil evidence and the regulatory genome , 2020, Development.

[19]  E. Sampayo,et al.  Patch size drives settlement success and spatial distribution of coral larvae under space limitation , 2020, Coral Reefs.

[20]  E. Carreño,et al.  Spatial distribution in marine invertebrates in rocky shore of Araucania Region (38° S, Chile). , 2020, Brazilian journal of biology = Revista brasleira de biologia.

[21]  A. Liu,et al.  The influence of environmental setting on the community ecology of Ediacaran organisms , 2019, bioRxiv.

[22]  M. Droser,et al.  La transición ediacárico-cámbrica: facies sedimentarias versus extinción , 2019, Estudios Geológicos.

[23]  M. Droser,et al.  Slime travelers: Early evidence of animal mobility and feeding in an organic mat world , 2019, Geobiology.

[24]  Imran A. Rahman,et al.  Gregarious suspension feeding in a modular Ediacaran organism , 2019, Science Advances.

[25]  M. Fortin,et al.  Disentangling the spatial distributions of a sponge-dwelling fish and its host sponge , 2019, Marine Biology.

[26]  M. Droser,et al.  Piecing together the puzzle of the Ediacara Biota: Excavation and reconstruction at the Ediacara National Heritage site Nilpena (South Australia) , 2017, Palaeogeography, Palaeoclimatology, Palaeoecology.

[27]  A. Liu,et al.  The importance of neutral over niche processes in structuring Ediacaran early animal communities , 2018, bioRxiv.

[28]  K. Stierhoff,et al.  A Status Review of Pinto Abalone (Haliotis kamtschatkana) Along the West Coastof North America: Interpreting Trends, Addressing Uncertainty, and Assessing Risk for a Wide-Ranging Marine Invertebrate , 2018, Journal of Shellfish Research.

[29]  M. Droser,et al.  Ediacaran scavenging as a prelude to predation. , 2018, Emerging topics in life sciences.

[30]  J. Hope,et al.  Ancient steroids establish the Ediacaran fossil Dickinsonia as one of the earliest animals , 2018, Science.

[31]  M. Droser,et al.  Stuck in the mat: Obamus coronatus, a new benthic organism from the Ediacara Member, Rawnsley Quartzite, South Australia , 2018, Australian Journal of Earth Sciences.

[32]  E. Mitchell,et al.  The utility of height for the Ediacaran organisms of Mistaken Point , 2018, Nature Ecology & Evolution.

[33]  Simon Harris,et al.  Revealing rangeomorph species characters using spatial analyses , 2018, Canadian Journal of Earth Sciences.

[34]  C. Bradshaw,et al.  Evidence of sensory-driven behavior in the Ediacaran organism Parvancorina: Implications and autecological interpretations , 2018 .

[35]  N. Butterfield,et al.  Spatial analyses of Ediacaran communities at Mistaken Point , 2018, Paleobiology.

[36]  P. Donoghue,et al.  Ediacaran developmental biology , 2017, Biological reviews of the Cambridge Philosophical Society.

[37]  M. Carrer,et al.  Tree spatial patterns and stand attributes in temperate forests: The importance of plot size, sampling design, and null model , 2018 .

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

[39]  I. Rahman,et al.  Inference of facultative mobility in the enigmatic Ediacaran organism Parvancorina , 2017, Biology Letters.

[40]  M. Droser,et al.  MICROBIAL MAT SANDWICHES AND OTHER ANACTUALISTIC SEDIMENTARY FEATURES OF THE EDIACARA MEMBER (RAWNSLEY QUARTZITE, SOUTH AUSTRALIA): IMPLICATIONS FOR INTERPRETATION OF THE EDIACARAN SEDIMENTARY RECORD , 2017, Palaios.

[41]  S. Bengtson,et al.  The origin of animals: Can molecular clocks and the fossil record be reconciled? , 2017, BioEssays : news and reviews in molecular, cellular and developmental biology.

[42]  Thorsten Wiegand,et al.  An evaluation of the state of spatial point pattern analysis in ecology , 2016 .

[43]  D. Marshall,et al.  Spatial pattern of distribution of marine invertebrates within a subtidal community: do communities vary more among patches or plots? , 2016, Ecology and evolution.

[44]  D. Stoyan,et al.  Envelope tests for spatial point patterns with and without simulation , 2016 .

[45]  M. Laflamme,et al.  Ediacaran distributions in space and time: testing assemblage concepts of earliest macroscopic body fossils , 2016, Paleobiology.

[46]  L. Harris,et al.  The influence of substrate material on ascidian larval settlement. , 2016, Marine pollution bulletin.

[47]  M. Eichhorn,et al.  Too close for comfort: spatial patterns in acorn barnacle populations , 2016, Population Ecology.

[48]  I. Rahman,et al.  Suspension feeding in the enigmatic Ediacaran organism Tribrachidium demonstrates complexity of Neoproterozoic ecosystems , 2015, Science Advances.

[49]  D. Erwin Novelty and Innovation in the History of Life , 2015, Current Biology.

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

[51]  M. Droser,et al.  Depositional and preservational environments of the Ediacara Member, Rawnsley Quartzite (South Australia): Assessment of paleoenvironmental proxies and the timing of ‘ferruginization’ , 2015 .

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

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

[54]  T. Guy‐Haim,et al.  Different settlement strategies explain intertidal zonation of barnacles in the Eastern Mediterranean , 2015 .

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

[56]  A. Metaxas,et al.  Selective settlement by larvae of Membranipora membranacea and Electra pilosa (Ectoprocta) along kelp blades in Nova Scotia, Canada , 2014 .

[57]  H. Mallison,et al.  PHOTOGRAMMETRY IN PALEONTOLOGY – A PRACTICAL GUIDE , 2014 .

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

[59]  Michael Greenacre,et al.  Spatial distribution patterns of the soft corals Alcyonium acaule and Alcyonium palmatum in coastal bottoms (Cap de Creus, northwestern Mediterranean Sea) , 2013 .

[60]  K. Wiegand,et al.  Disentangling facilitation and seed dispersal from environmental heterogeneity as mechanisms generating associations between savanna plants , 2011 .

[61]  J. Franklin,et al.  A spatially explicit census reveals population structure and recruitment patterns for a narrowly endemic pine, Pinus torreyana , 2011, Plant Ecology.

[62]  Fangliang He,et al.  Modeling spatial aggregation of finite populations. , 2010, Ecology.

[63]  I. Sun,et al.  Point patterns of tree distribution determined by habitat heterogeneity and dispersal limitation , 2010, Oecologia.

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

[65]  S. Xiao,et al.  Osmotrophy in modular Ediacara organisms , 2009, Proceedings of the National Academy of Sciences.

[66]  Andreas Huth,et al.  Recruitment in Tropical Tree Species: Revealing Complex Spatial Patterns , 2009, The American Naturalist.

[67]  J. Illian,et al.  Ecological information from spatial patterns of plants: insights from point process theory , 2009 .

[68]  M. Maldonado,et al.  Reproduction in the phylum Porifera: a synoptic overview , 2009 .

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

[70]  Thorsten Wiegand,et al.  Analyzing the spatial structure of a Sri Lankan tree species with multiple scales of clustering. , 2007, Ecology.

[71]  T. Wiegand,et al.  A spatially explicit analysis of seedling recruitment in the terrestrial orchid Orchis purpurea. , 2007, The New phytologist.

[72]  Thorsten Wiegand,et al.  Species Associations in a Heterogeneous Sri Lankan Dipterocarp Forest , 2007, The American Naturalist.

[73]  T. Wiegand,et al.  Spatial ecology of a root parasite – from pattern to process , 2007 .

[74]  J. Castilla,et al.  Roles of larval behaviour and microhabitat traits in determining spatial aggregations in the ascidian Pyura chilensis , 2007 .

[75]  Giles M. Foody,et al.  Investigating spatial structure in specific tree species in ancient semi-natural woodland using remote sensing and marked point pattern analysis , 2007 .

[76]  Thorsten Wiegand,et al.  Extending point pattern analysis for objects of finite size and irregular shape , 2006 .

[77]  S. Jenkins Larval habitat selection, not larval supply, determines settlement patterns and adult distribution in two chthamalid barnacles , 2005 .

[78]  Thorsten Wiegand,et al.  Rings, circles, and null-models for point pattern analysis in ecology , 2004 .

[79]  Pierre Legendre,et al.  SPECIES DIVERSITY PATTERNS DERIVED FROM SPECIES–AREA MODELS , 2002 .

[80]  O. Hoegh‐Guldberg,et al.  Genetic variation of the scleractinian coral Stylophora pistillata, from western Pacific reefs , 2002, Coral Reefs.

[81]  M. Snyder,et al.  Competition for Space Among Sessile Marine Invertebrates: Changes in HSP70 Expression in Two Pacific Cnidarians , 2001, The Biological Bulletin.

[82]  J. Kirschvink,et al.  Age of Neoproterozoic bilatarian body and trace fossils, White Sea, Russia: implications for metazoan evolution. , 2000, Science.

[83]  Kyle E. Harms,et al.  Pervasive density-dependent recruitment enhances seedling diversity in a tropical forest , 2000, Nature.

[84]  B. Boudreau,et al.  Intertidal barnacle distribution : a case study using multiple working hypotheses , 1999 .

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

[86]  T. Hughes,et al.  DENSITY-DEPENDENT DYNAMICS OF SOFT CORAL AGGREGATIONS: THE SIGNIFICANCE OF CLONAL GROWTH AND FORM' , 1996 .

[87]  D. Grazhdankin,et al.  Reconstructions of Biotopes of Ancient Metazoa of the Late Vendian White Sea Biota , 1996 .

[88]  N. Inestrosa,et al.  Settlement of benthic marine invertebrates , 1993 .

[89]  J. Pawlik Chemical ecology of the settlement of benthic marine invertebrates , 1992 .

[90]  N. C. Kenkel,et al.  Pattern of Self‐Thinning in Jack Pine: Testing the Random Mortality Hypothesis , 1988 .

[91]  G. Narbonne,et al.  Ediacaran biota of the Wernecke Mountains, Yukon, Canada , 1987 .

[92]  M. Keough KIN‐RECOGNITION AND THE SPATIAL DISTRIBUTION OF LARVAE OF THE BRYOZOAN BUGULA NERITINA (L.) , 1984, Evolution; international journal of organic evolution.

[93]  G. Schmidt Random and Aggregative Settlement in Some Sessile Marine Invertebrates , 1982 .

[94]  M. Glaessner,et al.  The Late Precambrian fossils from Ediacara, South Australia , 1966 .

[95]  B. Daily,et al.  The geology and late precambrian fauna of the Ediacara fossil reserve , 1959 .