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A catalogue of microbial structural signatures is presented, based upon the coupling of fundamental biogeochemical–microbial processes and local morphogenetic determinants. It summarizes a collection of sedimentary structures obtained from two modern siliciclastic peritidal environments in different climatic zones (temperate humid: Mellum Island, southern North Sea; subtropical arid: coast of southern Tunisia). Textural geometries reveal a high structural diversity, but their determinants are primarily based upon six major parameters: (1) intrinsic biofactors: structural diversification of sedimentary microbial films and mats inherent in the organisms, i.e. their construction morphology, growth, taxis and behaviour, and local abundance of specific morphotypes. Most prominent are the ensheathed filamentous cyanobacteria Microcoleus chthonoplastes and Lyngbya aestuarii, and the sheathless filamentous cyanobacterium Oscillatoria limosa. (2) Biological response to physical disturbances: sediment supply, erosion and fracturing of surface layers resulting from desiccation cause growth responses of biofilms and microbial mats. (3) Trapping/binding effects: physicobiological processes give rise to grain orientations and wavy to lenticular lamina, lamina‐specific grain arrangements and ‘sucrose’ calcium carbonate accumulations. (4) Secondary physical deformation of biogenic build‐ups: mechanical stresses acting upon sediments overgrown and biostabilized by biofilms and mats produce erosional and overthrust structures. (5) Post‐burial processes: textural fabrics that evolve from mechanical effects of gas formation from decaying mats, and features related to the formation of authigenic minerals (calcium carbonates, calcium sulphates, pyrite). (6) Bioturbation and grazing: post‐depositional structures, such as Skolithos‐type dwellings, traces of burrowing insects, gastropod grazing traces and faecal pellets. In synopsis, the catalogue firstly comprises a sound set of ubiquitous signatures. This uniformity in architectural characteristics is attributed to the presence and local dominance of certain microbes throughout the different settings. The catalogue secondly documents signatures that are extremely sensitive to tidal position, hydrodynamic regime and overall climatic conditions. These kinds of signature indicate narrow facies zones, which often coincide with the activity or dominance zones of certain organisms. An overview of structures of microbial origin from the fossil record underlines the potential of many of the signatures included in this catalogue to become fossilized and provide strong indicators of former siliciclastic tidal settings.

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Newly discovered sedimentary structures produced by ancient microbial mats in Early Archean sandstones of the 3.2 Ga Moodies Group, South Africa, differ fundamentally in appearance and genesis from Early Archean stromatolites and bacterial cell fossils preserved in chert. Wrinkle structures, desiccation cracks, and roll-up structures record the previous existence of microbial mats that effectively stabilized sediment on the earliest known siliciclastic tidal flats. In thin-section, the sedimentary structures reveal carpet-like, laminated fabrics characteristic of microbial mats. Negative ␦ 13 C isotope ratios of ؊20.1 to ؊21.5 ؎ 0.2‰ are consistent with a biological origin for the carbon preserved in laminae. The biogenicity of the sedimentary structures in the Moodies Group is substantiated by comparative studies on identical mat-related features from similar tidal habitats throughout Earth history, including the present day. This study suggests that siliciclastic tidal-flat settings have been the habitat of thriving microbial ecosystems for at least 3.2 billion years. Independently of controversial silicified microfossils and stromatolites, the newly detected microbially induced sedimentary structures in sandstone support the presence of bacterial life in the Early Archean.

Microbially induced sedimentary structures (MISS) result from the response of microbial mats to physical sediment dynamics. MISS are cosmopolitan and found in many modern environments, including shelves, tidal flats, lagoons, riverine shores, lakes, interdune areas, and sabkhas. The structures record highly diverse communities of microbial mats and have been reported from numerous intervals in the geological record up to 3.2 billion years (Ga) old. This contribution describes a suite of MISS from some of the oldest well-preserved sedimentary rocks in the geological record, the early Archean (ca. 3.48 Ga) Dresser Formation, Western Australia. Outcrop mapping at the meter to millimeter scale defined five sub-environments characteristic of an ancient coastal sabkha. These sub-environments contain associations of distinct macroscopic and microscopic MISS. Macroscopic MISS include polygonal oscillation cracks and gas domes, erosional remnants and pockets, and mat chips. Microscopic MISS comprise tufts, sinoidal structures, and laminae fabrics; the microscopic laminae are composed of primary carbonaceous matter, pyrite, and hematite, plus trapped and bound grains. Identical suites of MISS occur in equivalent environmental settings through the entire subsequent history of Earth including the present time. This work extends the geological record of MISS by almost 300 million years. Complex matforming microbial communities likely existed almost 3.5 billion years ago.