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Article Reference The tempo of cetacean cranial evolution
Located in Library / RBINS Staff Publications 2022
Article Reference Three new species of Muricidae (Ocenebrinae, Pagodulinae) from the Gulf of California, Mexico and update of the living muricids from the area
Located in Library / RBINS Staff Publications 2020
Article Reference Description of a new species of the genus Prionus Geoffroy, 1762 from northern Vietnam (Coleoptera: Cerambycidae: Prioninae)
Located in Library / RBINS Staff Publications 2019
Article Reference New fossils, systematics, and biogeography of the oldest known crown primate Teilhardina from the earliest Eocene of Asia, Europe, and North America
Omomyiform primates are among the most basal fossil haplorhines, with the oldest classified in the genus Teilhardina and known contemporaneously from Asia, Europe, and North America during the PaleoceneeEocene Thermal Maximum (PETM) ~56 mya. Characterization of morphology in this genus has been limited by small sample sizes and fragmentary fossils. A new dental sample (n ¼ 163) of the North American species Teilhardina brandti from PETM strata of the Bighorn Basin, Wyoming, documents previously unknown morphology and variation, prompting the need for a systematic revision of the genus. The P4 of T. brandti expresses a range of variation that encompasses that of the recently named, slightly younger North American species ‘Teilhardina gingerichi,’ which is here synonymized with T. brandti. A new partial dentary preserving the alveoli for P1-2 demonstrates that T. brandti variably expresses an unreduced, centrally-located P1, and in this regard is similar to that of T. asiatica from China. This observation, coupled with further documentation of variability in P1 alveolar size, position, and presence in the European type species T. belgica, indicates that the original diagnosis of T. asiatica is insufficient at distinguishing this species from either T. belgica or T. brandti. Likewise, the basal omomyiform ‘Archicebus achilles’ requires revision to be distinguished from Teilhardina. Results from a phylogenetic analysis of 1890 characters scored for omomyiforms, adapiforms, and other euarchontan mammals produces a novel clade including T. magnoliana, T. brandti, T. asiatica, and T. belgica to the exclusion of two species previously referred to Teilhardina, which are here classified in a new genus (Bownomomys americanus and Bownomomys crassidens). While hypotheses of relationships and inferred biogeographic patterns among species of Teilhardina could change with the discovery of more complete fossils, the results of these analyses indicate a similar probability that the genus originated in either Asia or North America.
Located in Library / RBINS Staff Publications 2019
Article Reference Notes on Latest Cretaceous Cirripedes (Crustacea, Thoracica) from Tunisia - Part 1. A new species of Pachyscalpellum Buckeridge, 1991
Located in Library / RBINS Staff Publications 2016
Webpublished Reference An update of the lithostratigraphy of the Ieper Group.
The objective of the present revision is to complement the lithostratigraphy of the Ieper Group published in 2001 (Laga et al., 2001). This last publication reflected the activities in the Tertiary Subcommission at that time. The review published in 2001 framed in an initiative of the National Stratigraphic Commission and was limited to the lithostratigraphy at formation level. The Laga et al (2001) reference document has been the basis for the NCS website until now. The Ieper Group is characterised by clay−dominated sediments overlying, in most situations, the Landen Group strata and, if not outcropping, underlying the sand−dominated Zenne Group sediments. According to Laga et al. (2001) in their reference document for Paleogene and Neogene lithostratigraphy, the Ieper Group consists of the Kortrijk, Tielt and Gentbrugge Formations and ,members in these Formations are only listed. These subdivisions are also used on the 1:50 000 geological maps of Flanders, edited in the last decades of the 20th century. Especially the additional description of the members, and where possible, horizons, identified in the Formations, made the present review necessary and also modifications at the formation level itself arisen since 2001 needed to be integrated in a new synthesis. The present update is based on the earlier description of members in Maréchal & Laga (1988), Geets et al. (2000) and Steurbaut (1998) as far as appropriate. All modifications, discussions and additions are supported by the relevant literature references.
Located in Library / RBINS Staff Publications 2016
Article Reference The 'Demange drawings': known and unknown malacological contributions of Victor Demange (1870-1940)
Located in Library / RBINS Staff Publications 2016
Article Reference Synchronous genetic turnovers across Western Eurasia in Late Pleistocene collared lemmings
Located in Library / RBINS Staff Publications 2016
Proceedings Reference Comparing Gravettian and Epigravettian canids from Europe with Late Pleistocene canids from Yakutia
Located in Library / RBINS Staff Publications 2016
Article Reference Mitochondrial DNA hyperdiversity and its potential causes in the marine periwinkle Melarhaphe neritoides (Mollusca: Gastropoda)
Located in Library / RBINS Staff Publications 2016