Facies distribution of the Lower Cambrian cryptic microbial and epibenthic archaeocyathan‐microbial communities, western Anti‐Atlas, Morocco

Marine microbial communities recorded in the Moroccan Anti‐Atlas were unaffected across the Neoproterozoic–Cambrian transition. A stromatolite‐dominated consortium was replaced at the beginning of the Atdabanian (ca 20 Myr after the Neoproterozoic–Cambrian boundary) by shelly metazoan and thromboid consortia, which contain the oldest biostratigraphically significant fossils of the Moroccan Cambrian. The associated collapse of microbial mat (stromatolitic) growth appears to coincide with a change from pre‐Atdabanian shallow‐water restricted conditions into Atdabanian deeper, open‐sea conditions. It is postulated that this environmental change led to an episode of improved water circulation over carbonate platform interiors, promoting shelly metazoan immigration into the region. The Tiout/Amouslek lithostratigraphic contact in the early Atdabanian marks the end of an episodically unstable seafloor as suggested by the abundance of slumping and sliding structures, and synsedimentary microfaults and cracks recorded in the underlying Tiout Member. Concurrent with the transition is the occurrence of a network of cryptic fissures and cavities that provided habitats for a coelobiontic chemosynthetic–heterotrophic microbial community composed of stromatolitic crusts, Renalcis–Epiphyton–Girvanella intergrowths, and Kundatia thalli. In the overlying Amouslek Formation, archaeocyathan–thromboid reefs were constrained by substrate stability, water depth and subsidence rate. Four reef geometries are distinguished: (i) patch reefs surrounded by shales, (ii) bioherms in which flank beds intercalate laterally with carbonate and shale inter‐reef sediments, (iii) biostromes or low‐relief structures formed as a result of lateral accretion of patch reefs, and (iv) kalyptrate complexes that nucleated because of a marked tendency for aggregation, and in which patch reefs and bioherms occur stacked together bounded by clay–marl–silt seams.

[1]  J. J. Álvaro,et al.  Palaeogeographical controls on the Cambrian trilobite immigration and evolutionary patterns reported in the western Gondwana margin , 2003 .

[2]  A. Perejón,et al.  Early Cambrian coelobiontic communities in tectonically unstable crevices developed in Neoproterozoic andesites, Ossa‐Morena, southern Spain , 2003 .

[3]  R. Riding Structure and composition of organic reefs and carbonate mud mounds: concepts and categories , 2002 .

[4]  S. Westrop The Ecology of the Cambrian Radiation , 2001 .

[5]  A. Perejón,et al.  Sedimentary patterns across the Lower–Middle Cambrian transition in the Esla nappe (Cantabrian Mountains, northern Spain) , 2000 .

[6]  J. J. Álvaro,et al.  Biostratigraphic significance and environmental setting of the trace fossil Psammichnites in the Lower Cambrian of the Montagne Noire, France , 1999 .

[7]  S. Kershaw Classification and geological significance of biostromes , 1994 .

[8]  J. Kirschvink,et al.  Precambrian/Cambrian boundary problem: Carbon isotope correlations for Vendian and Tommotian time between Siberia and Morocco , 1991 .

[9]  J. Kirschvink,et al.  The Precambrian-Cambrian boundary: Magnetostratigraphy and Carbon Isotopes resolve correlation problems between Siberia, Morocco, and South China , 1991 .

[10]  G. Geyer Revised Lower to lower Middle Cambrian biostratigraphy of Morocco , 1990 .

[11]  R. Riding,et al.  Fossil evidence for the location of the Precambrian/Cambrian boundary in Morocco , 1990, Nature.

[12]  H. Posamentier,et al.  An Overview of the Fundamentals of Sequence Stratigraphy and Key Definitions , 1988 .

[13]  D. R. Kobluk Cryptic faunas in reefs; ecology and geologic importance , 1988 .

[14]  S. Rowland,et al.  Structure and paleoecology of Lower Cambrian reefs , 1988 .

[15]  G. Narbonne,et al.  A candidate stratotype for the Precambrian-Cambrian boundary, Fortune Head, Burin Peninsula, southeastern Newfoundland , 1987 .

[16]  A. Zhuravlev Evolution of archaeocyaths and palaeobiogeography of the Early Cambrian , 1986, Geological Magazine.

[17]  A. Rozanov,et al.  The stage scale of the Cambrian System , 1986, Geological Magazine.

[18]  M. Tucker Carbon isotope excursions in Precambrian/Cambrian boundary beds, Morocco , 1986, Nature.

[19]  N. Clauer,et al.  Geochronology of sedimentary and metasedimentary Precambrian rocks of the West African craton , 1982 .

[20]  K. Sdzuy The Precambrian–Cambrian boundary beds in Morocco (Preliminary Report) , 1978, Geological Magazine.

[21]  D. R. Kobluk,et al.  Lower Cambrian patch reefs and associated sediments: southern Labrador, Canada , 1978 .

[22]  E. Cumings Reefs or Bioherms , 1932 .

[23]  A. Gorbushina,et al.  Biofilm, Biodictyon, Biomat Microbialites, Oolites, Stromatolites Geophysiology, Global Mechanism, Parahistology , 2003 .

[24]  R. Shapiro,et al.  Reef Patterns and Environmental Influences in the Cambrian and Earliest Ordovician , 2002 .

[25]  E. Flügel,et al.  The Precambrian/Cambrian boundary in the Anti-Atlas (Morocco) discussion and new results , 1988 .

[26]  W. Van An overview of the fundamentals of sequence stratigraphy and key definition. Sea level change-An integrated approach. , 1988 .

[27]  M. Leblanc,et al.  Interprétation géodynamique du domaine pan-africain (Précambrien terminal) de l'Anti-Atlas (Maroc) à partir de données géologiques et géochronologiques , 1980 .

[28]  Jean-pierre Houzay Empreintes attribuables à des Méduses dans la série de base de l'Adoudounien (Précambrien terminal de l'Anti-Atlas, Maroc) , 1979 .