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Article Reference Description, notes and new records in south american Cerambycidae (Coleoptera)
Located in Library / RBINS Staff Publications 2019
Article Reference Supplementary feeding increases nestling feather corticosterone early in the breeding season in house sparrows
Located in Library / RBINS Staff Publications 2017
Article Reference Finding loci associated to partial resistance to white pine blister rust in sugar pine (Pinus lambertiana Dougl.)
Located in Library / RBINS Staff Publications 2017
Article Reference Pleistocene vertebrate faunas of the Süttő Travertine Complex (Hungary)
Numerous fossil remains (vertebrates, molluscs and plants) were found in more than twenty sites of the Süttő Travertine Complex during the last 150 years. The majority of these remains were recovered from fissures of the travertine, but also from the travertine and an overlying loess–paleosol sequence. The aims of this study were to review the fossil content, to determine the stratigraphical positions of the various vertebrate faunas of Süttő and provide paleoecological interpretation of the periods on the basis of their faunas and floras. In addition, this paper describes new faunas and floras from the sites Süttő 16–20 and provides 14C dates for Süttő 16. On the basis of the new uranium series isotope and optical dating (OSL), the age of the travertine complex is Middle Pleistocene (235 ± 21–314 ± 45 ka, \MIS\ 7–9), while the age of the loess–paleosol sequence in superposition of the travertine is Middle–Late Pleistocene (MIS 2–MIS 6). In contrast, the fossils of the travertine indicated an older, Pliocene–Early Pleistocene age. A fissure (Süttő 17) and a red clay layer (Süttő 19) contained mammal faunas of Early–Middle Pleistocene age. These results indicated the existence of older travertine in certain quarries (Hegyháti quarry, Cukor quarry). Sedimentological and \OSL\ data of well-dated layers of the loess–paleosol sequence (Süttő/LPS) at Süttő allowed a correlation with the layers of Süttő 6. The paleosol layer in the upper part of the sequence of Süttő 6, was correlated with a pedocomplex of the overlying loess–paleosol sequence, which was dated to \MIS\ 5c (upper, dark soil) and \MIS\ 5e (lower, reddish brown soil). The paleoecological analysis of the mammal and mollusc faunas supported the former interpretation of Novothny et al. (2011) inferring warm, dry climate during the sedimentation of the upper layers, and more humid climate for the lower layers). However, the fauna of the lower soil layer indicated cold climate, so an age of \MIS\ 5d is suggested. Dating of the fissure faunas is based on similarity studies. For some faunas, this method cannot be used, because of the low number of species. On the basis of the species compositions and former interpretations, these faunas originated mainly from sediments that were deposited under cold climatic conditions. Other fissure faunas were dated by \AMS\ 14C (Süttő 16), or by correlation with soil layers of Süttő 6. According to these results, most of the fissure faunas can be correlated with different phases of \MIS\ 5. However, there are a younger (MIS 2) and an older (Early–Middle Pleistocene) fissure fauna also.
Located in Library / No RBINS Staff publications
Article Reference Revealing Invisible Beauty, Ultra Detailed: The Influence of Low Cost UV Exposure on Natural History Specimens in 2D+ Digitization
Digitization of the natural history specimens usually occurs by taking detailed pictures from different sides or producing 3D models. Additionally this is normally limited to imaging the specimen while exposed by light of the visual spectrum. However many specimens can see in or react to other spectra as well. Fluorescence is a well known reaction to the ultraviolet (UV) spectrum by animals, plants, minerals etc. but rarely taken into account while examining natural history specimens. Our tests show that museum specimens still fluoresce when exposed to UV light of 395 nm and 365 nm, even after many years of preservation. When the UV exposure is used in the digitization of specimens using our low cost focus stacking (2D+) setup, the resulting pictures reveal more detail than the conventional 2D+ images. Differences in fluorescence using 395 nm or 365 nm UV lights were noticed, however there isn’t a preferred wavelength as some specimens react more to the first, while others have better results with the latter exposure. Given the increased detail and the low cost of the system, UV exposure should be considered while digitizing natural history museum collections.
Located in Library / RBINS Staff Publications 2016
Article Reference The whale barnacle Cryptolepas rhachianecti (Cirripedia: Coronulidae), a phoront of the grey whale Eschrichtius robustus (Cetacea: Eschrichtiidae), from a sandy beach in The Netherlands
Located in Library / RBINS Staff Publications 2016
Article Reference Spondylosis deformans in three large canids from the Gravettian Předmostí site: Comparison with other canid populations
Located in Library / RBINS Staff Publications 2016
Article Reference Evidence for herbivorous cave bears (Ursus spelaeus) in Goyet Cave, Belgium: implications for palaeodietary reconstruction of fossil bears using amino acid δ15N approaches
Located in Library / RBINS Staff Publications 2016
Article Reference Neanderthal and animal karstic occupations from southern Belgium and south-eastern France: Regional or common features?
Located in Library / RBINS Staff Publications 2016
Article Reference Locked in the icehouse: Evolution of an endemic Epimeria (Amphipoda, Crustacea) species flock on the Antarctic shelf
The Antarctic shelf’s marine biodiversity has been greatly influenced by the climatic and glacial history of the region. Extreme temperature changes led to the extinction of some lineages, while others adapted and flourished. The amphipod genus Epimeria is an example of the latter, being particularly diverse in the Antarctic region. By reconstructing a time-calibrated phylogeny based on mitochondrial (COI) and nuclear (28S and H3) markers and including Epimeria species from all oceans, this study provides a temporal and geographical framework for the evolution of Antarctic Epimeria. The monophyly of this genus is not supported by Bayesian Inference, as Antarctic and non-Antarctic Epimeria form two distinct wellsupported clades, with Antarctic Epimeria being a sister clade to two stilipedid species. The monophyly of Antarctic Epimeria suggests that this clade evolved in isolation since its origin. While the precise timing of this origin remains unclear, it is inferred that the Antarctic lineage arose from a late Gondwanan ancestor and hence did not colonize the Antarctic region after the continent broke apart from the other fragments of Gondwanaland. The initial diversification of the clade occurred 38.04 Ma (95% HPD [48.46 Ma; 28.36 Ma]) in a cooling environment. Adaptation to cold waters, along with the extinction of cold-intolerant taxa and resulting ecological opportunities, likely led to the successful diversification of Epimeria on the Antarctic shelf. However, there was neither evidence of a rapid lineage diversification early in the clade’s history, nor of any shifts in diversification rates induced by glacial cycles. This suggests that a high turnover rate on the repeatedly scoured Antarctic shelf could have masked potential signals of diversification bursts.
Located in Library / RBINS Staff Publications 2017