Trou Magrite is a cave site located at Pont-à-Lesse in the Lesse Valley, commune of Dinant, Belgium. It has been known since E. Dupont conducted excavations at the site in 1867 [1]. The most recent fieldwork was done by L. Straus and M. Otte in 1991-92 [2]. Trou Magrite yielded rich lithic assemblages, osseous artifacts, mobiliary art, and numerous faunal remains. Several human re- mains were also recovered and identified as Palaeolithic humans by E. Dupont but have been only partially published thus far. The archaeological record covers a broad time range spanning from the Middle and Upper Palaeolithic to the Mesolithic, Neolithic, and Iron Age. An important Middle Palaeolithic collection is present, probably representing several occupation phases during the Late Pleistocene [2]. Unfortunately, although E. Dupont conducted excavations that can be characterized as modern for that time, the materials from the different so-called “fauna-bearing levels” that he defined in the field were mixed post-excavation [3]. In 2015, we initiated a multidisciplinary re-assessment of the human and faunal collections from Trou Magrite in order to update the inven- tory of human remains already identified, check for the presence of human remains that may have been previously overlooked, and verify their chronocultural context. We revised the already known human collection, conducted a systematic sorting of the faunal material, and combined the use of morphometrics, taphonomy, stable isotopes, dating, and genetic analyses to perform taxonomic and chronocultural identifications. Here we present two previously unidentified Neandertal fossils that we isolated from the Trou Magrite faunal material excavated by E. Dupont in the 19th century. They represent two different individuals: an adult/adolescent, represented by an upper right permanent canine, and a neonate, represented by the diaphysis of a left femur. Whereas no endoge- nous DNA was recovered from the tooth, the palaeogenetic analyses of the neonate femur confirmed its Neandertal status and indicate its sex to be male. We will present the biological characteristics and mitochondrial DNA phylogenetic position of the Trou Magrite Neandertals, in particular with regard to the other Northern European Neandertals. Our project adds Trou Magrite to the list of Belgian sites that have yielded Neandertal fossils and helps to emphasize the importance of the Mosan Basin in Neandertal studies.
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RBINS Staff Publications 2019
New coleoid cephalopods, assignable to the order Sepiida, are recorded from the Selandian/Thanetian boundary interval (Middle to Upper Paleocene transition, c. 59.2 Ma) along the southeastern margin (Toshka Lakes) of the Western Desert in Egypt. The two genera recognised, Aegyptosaepia n. gen. and ?Anomalosaepia Weaver and Ciampaglio, are placed in the families Belosaepiidae and ?Anomalosaepiidae, respectively. They constitute the oldest record to date of sepiids with a ‘rostrum-like’ prong. In addition, a third, generically and specifically indeterminate coleoid is represented by a single rostrum-like find. The taxonomic assignment of the material is based on apical parts (as preserved), i.e., guard, apical prong (or ‘rostrum-like’ structure), phragmocone and (remains of) protoconch, plus shell mineralogy. We here confirm the shell of early sepiids to have been bimineralic, i.e., composed of both calcite and aragonite. Aegyptosaepia lugeri n. gen., n. sp. reveals some similarities to later species of Belosaepia, in particular the possession of a distinct prong. General features of the phragmocone and protoconch of the new form are similar to both Belocurta (Middle Danian [Lower Paleocene]) and Belosaepia (Eocene). However, breviconic coiling and the presence of a longer ventral conotheca indicate closer ties with late Maastrichtian–Middle Danian Ceratisepia. In this respect, Aegyptosaepia n. gen. constitutes a link between Ceratisepia and the Eocene Belosaepia. The occurrence of the new genus near the Selandian/Thanetian boundary suggests an earlier origin of belosaepiids, during the early to Middle Paleocene. These earliest known belosaepiids may have originated in the Tethyan Realm. From northeast Africa, they subsequently spread to western India, the Arabian Plate and, probably via the Mediterranean region, to Europe and North America.
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