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The rhodolithic slope deposits of a Burdigalian carbonate platform in Sardinia near Sedini were analyzed to reconstruct facies and palaeobathymetry. There is a distinct red-algal growth zonation along the platform slope. The clinoform rollover area consists of coralline-algal bindstones, which downslope change into a zone where rhodoliths are locally fused by progressive encrustation. Mid-slope rhodoliths are moderately branched, and downslope rhodoliths have fruticose protuberances, resulting in branching rhodolith growth patterns. There is a sharp change from the rhodolitic rudstones to the basinal, bivalve-dominated rudstones at the clinoform bottomsets. Red-algal genera identified include Sporolithon, Lithophyllum, Spongites, Hydrolithon, Mesophyllum, Lithoporella, Neogoniolithon, and other mastophoroids and melobesioids. Genera and subfamilies show a zonation along the clinoforms, allowing palaeobathymetric estimates. The clinoform rollovers formed at a water depth of around 40 m and the bottomsets around 60 m. Results from geometrical reconstruction show that coral reefs in the inner platform formed at water depths of around 20 m. Therefore, the Sedini carbonate platform is an example of a reef-bearing platform in which the edge or the platform-interior reefs do not build up to sea level.
Upper Thanetian microbialite-coral mounds from the Adriatic Carbonate Platform (SW Slovenia) are described herein for the first time, representing an important case study of extensively microbially-cemented boundstones in the Early Paleogene. The mounds are constructed primarily by microbialites associated to small-sized coral colonies, forming metric bioconstructions in a mid-ramp setting. Detailed macroscopic and microscopic studies show that microbes are the major framework builders, playing a prominent role in the stabilization and growth of the mounds, with corals being the second most important component. Microbial carbonates represent up to 70% of the mounds, forming centimetric-thick crusts alternating with coral colonies. The microbial nature of the crusts is demonstrated by their growth form and internal microfabrics, showing accretionary, binding, and encrusting growth fabrics, often with gravity-defying geometries. Thin sections and polished slabs reveal a broad range of mesofabrics, with dense, structureless micrite (leiolite), laminated crusts (stromatolites), and clotted micritic masses (thrombolites). A first layer of micro- encrusters, including leiolites and thrombolites, occurs in cryptic habitats, whereas discontinuous stromatolites encrust the upper surface of corals. A second encrustation, the major mound construction phase, follows and is dominated by thrombolites, encrusting corals and other micro-encrusters. This sequence represents the basic constructional unit horizontally and vertically interlocked, in an irregular pattern, to form the mounds. The processes, which favored the deposition of these microbial carbonates, were mainly related to in situ precipitation, with minor evidences for grain agglutination and trapping processes. Scleractinian corals comprise moderately diversified community of small (centimetric) colonial, massive, platy encrusting, and branching forms. Coral colonies are distributed uniformly throughout the mounds without developing any ecological zonation. These features indicate that coral development remained at the pioneer stage throughout the mound growth. The spatial relationships between corals and microbialites, as well as the characteristics of microbial crusts and coral colonies, indicate a strong ecological competition between corals and microbes. A model for the evolution of the trophic structures during the mound growth is proposed, with changes in the paleoecology of the main bioconstructors triggered by frequent environmental perturbations. Turbidity and nutrient pressure, interpreted here as related to frequent recurrences of wet phases during the warm, humid climate of the Uppermost Thanetian, might have promoted temporary dominance of microbes over corals, causing rapid environmentally- driven "phase shifts" in the dominant biota.