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Search publications of the members of the Royal Belgian institute of natural Sciences

Webpublished Reference Crowdsourcing in Europe: how to share macroseismic data of felt earthquakes ?
https://blogs.egu.eu/divisions/sm/2017/11/20/crowdsourcing-in-europe-how-to-share-macroseismic-data-of-felt-earthquakes/
Inproceedings Reference Incorporating data uncertainty in 3D voxel modelling and the importance in decision making
Geological databases resulting from the merging of various data sources and time periods jeopardize harmonization of data products. Data standardization is already common practice and a first step in avoiding semantic overlap. European marine data management infrastructures provide such standards, e.g., Geo-Seas (http://www.geo-seas.eu/) for geological data and SeaDataNet (https://www.seadatanet.org/) for marine metadata in general. In addition, metadata quality control is important, though data uncertainty is seldom quantified and to be used in modelling. Preliminary uncertainty analyses were worked out to provide an extra dimension to the cross-border 3D voxel models of the geological subsurface of the Belgian and southern Netherlands part of the North Sea (http://odnature.naturalsciences.be/tiles/). Starting from simple quality flagging in geological databases and model uncertainty calculations (probability and entropy) in the 3D modelling, data uncertainty (e.g., related to qualities in positioning, sampling and vintage) is now quantified. Combining all uncertainties remains a challenge, as well as communicating their importance in decision making. A demonstration will be given on the status of the uncertainty analyses and how these are incorporated in a newly developed decision support tool allowing interactive querying of the 3D voxel model, now comprising geological, as well as entropy, probability and data uncertainty attributes (figure 1).
Article Reference Givetian rugose corals from the Zemmour in Mauritania
Article Reference Update of the Devonian lithostratigraphic subdivision in the subsurface of the Campine Basin (northern Belgium)
Article Reference Ecology of Devonian ostracods: application to the Frasnian/Famennian boundary bioevent in the type region (Dinant Synclinorium, Belgium)
Article Reference Ostracod and rock facies across the Emsian/Eifelian boundary at Couvin (Dinant Synclinorium, Belgium)
Article Reference New data on the osteoglossid fishes (Teleostei, Osteoglossiformes) from the Marine Danian (Paleocene) of Landana (Cabinda Enclave, Angola)
Article Reference Comments on the phylogenetic relationships of Pholidorhynchodon malzannii and of Eurycormus speciosus (Teleostei, “Pholidophoriformes”), two Mesozoic tropical fishes.
Article Reference Osteology and relationships of Luxembourgichthys (« Pholidophorus ») friedeni gen. nov. (Teleostei, “Pholidophoriformes”) from the Lower Jurassic of Belgium and the Great Duchy of Luxemburg.
Article Reference On the presence of the plethodid fish Dixonanogmius (Teleostei, Tselfatiiformes) in the marine Upper Cretaceous of Burma (Myanmar), tropical Asia.
Article Reference Osteology and relationships of Signeuxella preumonti (Teleostei, “Pholidophoriformes”, Signeuxellidae) from the continental Middle Jurassic (Stanleyville Formation) of Kisangani (Democratic Republic of Congo)
Article Reference Systematic revision of the Cretaceous actinopterygian fauna from Bernissart, Belgium.
Article Reference Osteology and relationships of Italophiopsis derasmoi gen. and sp. nov. (Halecomorphi, Ionoscopiformes) >From the marine Early Cretaceous of Pietraroja (Campania, southern Italy).
Article Reference Revision of « Chanos » leopoldi (Teleostei, Gonorynchiformes, Chanidae) from the marine Albian (Early Cretaceous) of Pietraroja Campania, southern Italy) and the resurrection of the genus Caeus Costa, 1857.
Article Reference A handful of duck radiuses: Peculiarities of the avifaunal exploitation at the Gravettian site of Maisières‐Canal (Belgium)
Article Reference An enigmatic new ungulate-like mammal from the early Eocene of India
We report a new genus and species of herbivorous mammal, Pahelia mysteriosa, from the early Eocene Cambay Shale Formation, Tadkeshwar Lignite Mine, Gujarat, India. The new taxon, approximately the size of a small phenacodontid (e.g. Ectocion parvus), is represented by three mandibular fragments, the most complete of which documents nearly the entire symphysis and mandibular body plus P3–M3. Pahelia has incipiently selenolophodont molars with strong exodaenodonty, absent paraconids, weak but distinct entolophids, and prominent ectostylids. Molar size increases distally, but M3 does not develop a prominent third lobe. Premolars are simple, with prominent protoconids and short talonids but little development of other trigonid cusps. The mandibular symphysis is strongly fused, and there is an enlarged alveolus for an anterior tooth. The combination of features present in the new taxon does not closely match that of any known mammal, but there are some similarities to a diversity of ungulates from Africa, Asia, Europe and North America. Preserved morphology is insufficient to assess the affinities of the new taxon with confidence, but a link to Quettacyonidae, also endemic to the Indian subcontinent, is morphologically and biogeographically plausible. If this scenario is correct, it suggests that P. mysteriosa could be a part of the endemic mammalian fauna of India prior to its initial faunal contact with Asia.
Article Reference A well-preserved pelvis from the Maastrichtian of Romania suggests that the enigmatic Gargantuavis is neither an ornithurine bird nor an insular endemic
We describe a well-preserved pelvis from the Maastrichtian S^anpetru Formation of the Hat¸ eg Basin in Romania. The fossil closely resembles the pelvis of Gargantuavis philoinos from the Ibero-Armorican Peninsula, but differs in a smaller size and a few morphological features. It constitutes the first record of Gargantuavis outside the Ibero-Armorican Island and is more complete than any of the previously known Gargantuavis pelves. The new fossil allows the recognition of characteristics previously unknown for Gargantuavis. These include the presence of large supratrochanteric processes, the absence of a widened midsection of the synsacrum (which indicates the absence of a glycogen body), and the absence of fusion between the pelvic bones at the level of the acetabulum. The latter two features suggest that Gargantuavis is not closely related to the Ornithurae and the taxon may even fall outside the Ornithothoraces, the clade including Enantiornithes and Ornithuromorpha. Recognition of Gargantuavis in the fauna of the Hat¸ eg Island is of particular significance, because various theropods have been described from the Upper Cretaceous of Romania. The Romanian pelvis is of similar size to Elopteryx nopcsai, which was described as avian and is based on hindlimb elements, and it also shows some similarities to the pelvis of the unusual theropod Balaur bondoc. The new fossil furthermore disproves the hypothesis that the flight capabilities of Gargantuavis were lost in an insular environment of the Ibero-Armorican Island, and raises the possibility that Gargantuavis, Elopteryx, and Balaur belong to a distinctive theropod clade of the Late Cretaceous European archipelago.
Inbook Reference Animal Exploitation in Times of Change: Faunal Remains from Zilum, ca. 600-400 BCE, North-Eastern Nigeria
Article Reference Octet Stream Corrigendum: Diversity of mesopelagic fishes in the southern ocean - A phylogeographic perspective using DNA barcoding [Front. Ecol. Evol, 6, 120 (2018)] doi: 10.3389/fevo.2018.00120
However, we highlight potential (pseudo-)cryptic or unrecognized species in Gymnoscopelus bolini, Lampanyctus achirus, and the non-myctophid genus Bathylagus. A correction has been made to the Discussion, Sub-section Phylogeny and Phylogeography of Southern Ocean Mesopelagic Fishes, Paragraph 6: The available sequences identified as Symbolophorus boops (BOLD references DSFSE476-08 to DSFSE480-08 and DSFSG260-10) cluster apart from the two other Symbolophorus clades resolved in our COI tree (one composed of S. californiensis, S. reversus, S. evermanni, Symbolophorus sp., and S. rufinus and the other composed of S. barnardi and S. veranyi; Figure 2). Instead these sequences settle within the Diaphinae (sensu Martin et al., 2017). Unfortunately we discovered a posteriori that the COI sequences included here as S. boops were likely misidentified on BOLD. These sequences are probably from a Diaphus species (P. A. Hulley, pers. comm.) currently also not present on BOLD, but the specimens are in poor condition, preventing definite identification. The correction has been transmitted to the BOLD database. Other studies that included genetic data proposed that Symbolophorus is closer related to Myctophum, Hygophum, and other genera, as opposed to Diaphinae, but they all lacked specimens of S. boops (Poulsen et al., 2013; Denton, 2014; Martin et al., 2017). Therefore, we highly recommend the collection of further samples/sequences in order to resolve the phylogenetic position of S. boops, and to re-identify the specimens erroneously labeled as Symbolophorus boops. In fact, the entire genus would benefit from a detailed systematic revision as already noted by Wisner (1976). © 2018 Christiansen, Dettai, Heindler, Collins, Duhamel, Hautecoeur, Steinke, Volckaert and Van de Putte.
Article Reference Favartia kanneri, a new species (Gastropoda: Muricidae: Muricopsinae) from the Galapagos Islands, Ecuador
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