The advent of mineralized skeletons in Neoproterozoic Metazoa—new fossil evidence from the Gaojiashan Fauna

The terminal Neoproterozoic (Ediacaran) Dengying Formation in southern Shaanxi, China, hosts two types of conical fossils: one is the so‐called Conotubus, found in siliciclastic rocks in the lower and middle part of the Gaojiashan Member; the other is the renowned Cloudina in carbonate rocks of the upper Gaojiashan Member and succeeding Beiwan Member. Conotubus are conical and gently curved tubular fossils, with a variable rate of expansion. They are built of multiple thin, steep, eccentrically nested funnels set one within the next. A detailed comparison of the two conical fossils suggests that the organic tubes of Conotubus may be the precursor of the mineralized Cloudina tubes; this inference is consistent with their similarities in both wall structure and life style. Our research thus suggests that the organic skeleton preceded the rise of the mineralized skeleton in Cloudina‐like fossils. Sophisticated hypotheses have been advocated, some linking the skeletal genesis to increasing levels of Ca2+ in the seas, others to the enlargement of body sizes of animals. Yet our findings have supported the ‘arms race’ hypothesis: skeletons evolved primarily through selective predation pressure. Copyright © 2007 John Wiley & Sons, Ltd.

[1]  Hua Hong,et al.  Pyritization in the Gaojiashan Biota , 2007 .

[2]  B. Cohen Not armour, but biomechanics, ecological opportunity and increased fecundity as keys to the origin and expansion of the mineralized benthic metazoan fauna , 2005 .

[3]  S. Xiao,et al.  Skeletogenesis and asexual reproduction in the earliest biomineralizing animal Cloudina , 2005 .

[4]  Wei Wang,et al.  U-Pb Ages from the Neoproterozoic Doushantuo Formation, China , 2005, Science.

[5]  K. Simkiss Biomineralization and detoxification , 1977, Calcified Tissue Research.

[6]  Maoyan Zhu,et al.  Lower Cambrian Small Shelly Fossils of northern Sichuan and southern Shaanxi (China), and their biostratigraphic importance , 2004 .

[7]  Maoyan Zhu,et al.  Sinian-Cambrian stratigraphic framework for shallow- to deep-water environments of the Yangtze Platform: an integrated approach , 2003 .

[8]  B. Pratt,et al.  Borings in Cloudina Shells: Complex Predator-Prey Dynamics in the Terminal Neoproterozoic , 2003 .

[9]  J. Grotzinger,et al.  Extinction of Cloudina and Namacalathus at the Precambrian-Cambrian boundary in Oman , 2003 .

[10]  M. Fedonkin The origin of the Metazoa in the light of the Proterozoic fossil record , 2003 .

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

[12]  J. Grotzinger,et al.  Proterozoic Modular Biomineralized Metazoan from the Nama Group, Namibia , 2002, Science.

[13]  Zhe Chen,et al.  Preservation and morphologic interpretation of Late Sinian Gaojiashania from southern Shaanxi , 2002 .

[14]  E. Mountjoy,et al.  Namacalathus-Cloudina assemblage in Neoproterozoic Miette Group (Byng Formation), British Columbia: Canada's oldest shelly fossils , 2001 .

[15]  A. Knoll,et al.  Eumetazoan fossils in terminal proterozoic phosphorites? , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[16]  J. Banner,et al.  Evolution of the Sr and C Isotope Composition of Cambrian Oceans , 2000 .

[17]  A. Knoll,et al.  Testate amoebae in the Neoproterozoic Era: evidence from vase-shaped microfossils in the Chuar Group, Grand Canyon , 2000, Paleobiology.

[18]  A. Knoll,et al.  Calcified metazoans in thrombolite-stromatolite reefs of the terminal Proterozoic Nama Group, Namibia , 2000, Paleobiology.

[19]  S. Carroll,et al.  Early animal evolution: emerging views from comparative biology and geology. , 1999, Science.

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

[21]  E. Savazzi Functional morphology of the invertebrate skeleton , 1999 .

[22]  A. Knoll,et al.  Three-dimensional preservation of algae and animal embryos in a Neoproterozoic phosphorite , 1998, Nature.

[23]  Geerat J. Vermeij,et al.  A Natural History of Shells , 2021 .

[24]  Derek E. G. Briggs,et al.  Decay and preservation of polychaetes: taphonomic thresholds in soft-bodied organisms , 1993, Paleobiology.

[25]  S. Bengtson,et al.  Predatorial Borings in Late Precambrian Mineralized Exoskeletons , 1992, Science.

[26]  G. Vermeij The origin of skeletons , 1989 .

[27]  K. Simkiss Biomineralisation in the context of geological time , 1989, Earth and Environmental Science Transactions of the Royal Society of Edinburgh.

[28]  G. Vermeij Evolution and Escalation , 1987 .

[29]  G. Vermeij Unsuccessful Predation and Evolution , 1982, The American Naturalist.

[30]  James F. Kitchell,et al.  Prey Selection by naticid gastropods: experimental tests and application to the fossil record , 1981, Paleobiology.

[31]  A. Knoll,et al.  Late Proterozoic vase-shaped microfossils from the Visingsö Beds, Sweden , 1980 .

[32]  S. Stanley Fossil data and the Precambrian-Cambrian evolutionary transition , 1976 .

[33]  G. Germs New shelly fossils from Nama Group, South West Africa , 1972 .