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Silurian brachiopods of Middle Llandovery (Aeronian) ages are reviewed, and 215 genera are identified here, compared with 109 in the preceding Early Llandovery (Rhuddanian), indicating a recovery‐radiation interval after the end‐Ordovician mass extinction. The chief regions in which they are found are the continents of South China, Avalonia‐Baltica, Laurentia and Siberia, which were all at tropical...
The recent invasion of a naticid predator (Laguncula pulchella) and associated changes in the death assemblages of bivalve prey (Ruditapes philippinarum) provide a baseline for interpreting predator–prey interactions in the fossil record. This article presents quantitative data on size‐frequency distributions (SFDs) of living and death assemblages, prey size selectivity and drillhole site selectivity...
Compared with the fossil record of vascular plants, bryophyte fossils are rare; this circumstance is probably related to a lower preservation potential compared with that of vascular plants. We searched for bryophyte remains in extensive collections of plant‐fossil assemblages from the Triassic of Antarctica and identified three assemblages with surprisingly well‐preserved bryophyte fossils. Although...
Enrolment was a major defensive strategy for trilobites that significantly contributed to their evolutionary success. The ability to enrol also helped to constrain the morphological evolution of trilobites, which in part was driven by the need to improve this capability to encapsulate the soft parts of the body within the mineralized dorsal exoskeleton. Here, we describe a unique example of gut content...
Two morphologies of drillhole, probably attributable to gastropods, have been recognized in specimens of the small extant New Zealand platidiid brachiopod Neoaemula vector, collected from Fiordland, New Zealand. Some of these drillholes have been repaired, and these repairs occur in two different ways. The thin replacement shell has both primary and secondary layers and in some cases is punctate....
Early Jurassic belemnites are of particular interest to the study of the evolution of skeletal morphology in Lower Carboniferous to the uppermost Cretaceous belemnoids, because they signal the beginning of a global Jurassic–Cretaceous expansion and diversification of belemnitids. We investigated potentially relevant, to this evolutionary pattern, shell features of Sinemurian–Bajocian Nannobelus,Parapassaloteuthis...
Exceptionally well‐preserved radulae and lower jaws found both inside the body chamber of Cravenoceras fayettevillae (Mississippian) and in isolated nodules (Mississippian and Pennsylvanian) were analysed using CT scan and synchrotron propagation phase‐contrast tomography. This approach reveals new anatomical details allowing us to investigate wear, preservation and muscle insertion in the buccal...
The shallow carbonate facies at the top of the Yacoraite Formation (Late Cretaceous–Early Palaeocene) in the Metán sub‐basin, Salta Basin (Cretaceous‐Eocene), northern Argentina, have domal stromatolitic boundstones with peculiar cavities, interpreted here as bioclaustrations. The cavities appear to have been produced by organisms that lived within the microbial mat contemporarily with its growth,...
The profound ecological change of the marine benthos that eventually led to the almost complete destruction of the Precambrian matgrounds by benthic grazers and bioturbators (the agronomic revolution) was largely completed in the Tommotian. At that time, burrows produced by bottom‐dwelling animals as shelters against predators were supplemented by burrowing for food by predators and sediment feeders...
The carbonates associated with the Late Ordovician (Katian–Hirnantian) Boda mounds of the Siljan district, Sweden, contain a rich cephalopod fauna. Cephalopods are rare in the micritic stromatactis facies of the Katian Boda Core Member, but are concentrated together with other molluscs and trilobites in synsedimentary fillings of caves and crevices of the lithified mound limestone. More than 60 cephalopod...
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