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The geographic and temporal origins of the domestic dog remain controversial, as genetic data suggest a domestication process in East Asia beginning 15,000 years ago, whereas the oldest doglike fossils are found in Europe and Siberia and date to >30,000 years ago. We analyzed the mitochondrial genomes of 18 prehistoric canids from Eurasia and the New World, along with a comprehensive panel of modern dogs and wolves. Themitochondrial genomes of all modern dogs are phylogeneticallymost closely related to either ancient or modern canids of Europe. Molecular dating suggests an onset of domestication there 18,800 to 32,100 years ago. These findings imply that domestic dogs are the culmination of a process that initiated with European hunter-gatherers and the canids with whom they interacted.

Ancient DNA analyses have provided enhanced resolution of population histories in many Pleistocene taxa. However, most studies are spatially restricted, making inference of species-level biogeographic histories difficult. Here, we analyse mitochondrial DNA (mtDNA) variation in the woolly mammoth from across its Holarctic range to reconstruct its history over the last 200 thousand years (kyr).We identify a previously undocumented major mtDNA lineage in Europe, which was replaced by another major mtDNA lineage 32–34 kyr before present (BP). Coalescent simulations provide support for demographic expansions at approximately 121 kyr BP, suggesting that the previous interglacial was an important driver for demography and intraspecific genetic divergence. Furthermore, our results suggest an expansion into Eurasia fromAmerica around 66 kyr BP, coinciding with the first exposure of the Bering Land Bridge during the Late Pleistocene. Bayesian inference indicates Late Pleistocene demographic stability until 20–15 kyr BP, when a severe population size decline occurred.

The large faunal sample from Spy, a Belgian cave site famous for its Neandertal remains, is for the first time studied in detail. Some 11,600 bones were examined. A wide spectrum of Pleistocene species is present. Horse, cave hyena, mammoth, woolly rhinoceros and reindeer are the primary taxa. Hyena scavenging activities are indicated by the gnawed mammoth and rhinoceros postcranial bones and cervid antlers. Bears used the cave as a hibernation den evidenced by remains of cubs, and of female and male adult bears. Indications of human manipulation (cut marks, ochre traces, worked bone/tooth) occur especially on remains from foxes, mammoth and deer. The age profile of the mammoth is dominated by calves. This selective mortality suggests that they were hunted by prehistoric people. AMS dates range from c. 44,400 BP to c. 25,700 BP. The Spy bone assemblage therefore accumulated through a series of agents over a long period of the Pleniglacial.

Cave bears are among the most well known extinct Pleistocene mammals. Their biogeography and taxonomy, along with the factors that led to their extinction, have been subject to long-standing controversy. Here, we reconstruct the phylogeography as well as the temporal and spatial population dynamics of cave bears across their range using mitochondrial DNA control region sequences from 77 published as well as 65 new cave bear samples, Our analyses reveal a dramatic loss of genetic diversity in cave bear populations after 30,000 years before present and provide evidence for a range decline from east to west towards the onset of the last glacial maximum. Our results also suggest that the three major haplogroups within cave bears, which may correspond to distinct species, were previously more widespread, with relict populations in remote and alpine areas still harbouring haplotypes that have disappeared from most of their previous range. Applying a phylogenetic dating approach, we estimated the age of the oldest of our samples, originating from the Yana River region in north-eastern Siberia, to be around 178,000 years, which confirms a previous estimate of a Middle Pleistocene age based on its stratigraphic position. Our results extend our knowledge about the evolutionary history of cave bears, but they also show that to unravel the complexities of cave bear evolution future ancient DNA studies on this Pleistocene species will need to go beyond short mitochondrial DNA fragments, including full mitochondrial genomes as well as nuclear DNA sequences.

Anatomical, systematic, and paleobiogeographical data on the Devonian antiarchs from Belgium are reviewed, updated and completed thanks to new data from the field and re-examination of paleontological collections. The material of Bothriolepis lohesti Leriche, 1931 is enhanced and the species better described. An undetermined species of Bothriolepis is recorded from the Famennian of Modave (Liège Province), one species of Asterolepis redescribed from the Givetian of Hingeon and another one described from the Givetian of Mazy (Namur Province). Grossilepis rikiki sp. nov. is recorded from the Famennian tetrapod-bearing locality of Strud (Namur Province) and from the Famennian of Moresnet (Liège Province). It is the first occurrence of Grossilepis after the Frasnian and on the central southern coast of the Euramerican continent. Its occurrence in the Famennian of Belgium may be the result of a late arrival from the Moscow Platform and the Baltic Depression, where the genus is known from Frasnian deposits. Remigolepis durnalensis sp. nov. is described from the Famennian of Spontin near Durnal (Namur Province). Except for the doubtful occurrence of Remigolepis sp. in Scotland, this is the first record of this genus in Western Europe. Its occurrence in Belgium reinforces the strong faunal affinities between Belgium and East Greenland and the hypothesis of a hydrographical link between the two areas during the Late Devonian.

This abstract is not available in English. Résumé La stratigraphie des dépôts appartenant au Pleistocène supérieur de Belgique se base - tout comme c'est souvent le cas dans le nord de l'Europe - sur la présence dans le nord-ouest de la Belgique de formations fluviomarines d'âge eemien. Ces dernières sont caractérisées par la présence de Tapes senescens var. eemiensis ("Senescens Sande"). Leur passage latéral au sol de Rocourt a été observé. Ailleurs, les dépôts appelés "Tourbe et gravier" sont indiqués comme eemiens à la suite de leurs caractéristiques floristiques. Dans les dépôts appartenant à la dernière Glaciation ou Weichsel, les unités litho-stratigraphiques suivantes ont été distinguées: sable et gravier, limon et sable grossier, formations limono-tourbeuses formant le Pléniglaciaire A (conditions de sédimentation froid-humide); sables entrecroisés, sable ou limon de couverture 1 ou 2, formant le Pléniglaciaire B (conditions de sédimentation froid-sec) et finalement sable de couverture récent 1 ou 2 datant du Tardiglaciaire. Il existe plusieurs horizons périglaciaires importants: cailloutis 1 à petites fentes de gel se situant à la limite supérieure du dépôt limon et sable grossier; cailloutis 2 à fines fentes de gel à la limite supérieure des formations limono-tourbeuses et cailloutis 3 à grandes fentes de gel à la limite supérieure des sables ou limons de couverture 1. Il existe aussi des horizons pédologiques, caractéristiques: le sol de Rocourt datant de la fin de l'Eemien; le sol de Warneton datant de la période de sédimentation du limon et sable grossier; l'horizon pédologique cryoturbé (Kesselt - Zelzate -Paudorf), datant de la fin du Pléniglaciaire A; le sol de Stabroek datant du début du Tardiglaciaire. Nous sommes arrivés à la conclusion que la période du Weichsel est caractérisée par une sédimentation bicyclique: d'une part le Pléniglaciaire A caractérisé par des conditions de milieu froid-humide avec dominance de processus de solifluction et d'autre part l'ensemble Pléniglaciaire B-Tardiglaciaire caractérisé par des conditions de milieu froid-sec avec dominance de sédimentation éolienne. Les deux cycles sont en outre divisés par une période d'extrême froid (déflation) résultant respectivement dans l'établissement du cailloutis 1 à petites fentes de gel et du cailloutis 3 à grandes fentes de gel. Samenvatting De stratigrafie van de Boven-Pleistocene afzettingen in België sluit rechtstreeks aan bij deze van het Noord-Europese ruim. Deze bewering is gesteund op het voorkomen in het noordwesten van België van fluvio-marine Eem afzettingen met Tapes senescens (die de meest zuidelijk gekende uitbreiding vormen van de "Senescens Sande") en de rechtstreekse laterale correlatie van de interglaciale Rocourt bodem met deze marine formaties. Elders werden aan afzettingen, aangeduid als "Veen en grind", eveneens een Eem ouderdom toegekend op grond van palynologische bevindingen. De afzettingen behorende tot de Laatste Glaciatie periode of Weichsel worden in de volgende litho-stratigrafische eenheden onderverdeeld : zand en grind, leem en grof zand, (venige) leem afzettingen gezamenlijk het Pleniglaciaal A (koud-vochtige sedimentatie omstandigheden) opbouwend; kris-kras gelaagde zanden, dekzand en dekleem 1 of 2, gezamenlijk het Plenigla-ciaal B (koud-droge sedimentatie omstandigheden) opbouwend; laat dekzand 1 of 2 behorend tot het Laat-Glaciaal. Merkwaardige periglaciale horizonten vormen: keienvloer 1 met kleine vorstscheuren aan de bovengrens van de leem en grof zand afzetting; keienvloer 2 met fijne vorstscheuren aan de bovengrens van de (venige) leem afzettingen en keienvloer 3 met grote vorstscheuren aan de bovengrens van de dekzand of dekleem 1 afzettingen. Merkwaardige bodem-vegetatie horizonten treden op: op het einde van het Eem, de Rocourt bodem; tijdens de afzetting van het leem en grof zand, de Warneton bodem en op het einde van het Pleniglaciaal A, het cryoturbaat bodem horizont (Kesselt-Zelzate - Paudorf horizont); verder een Stabroek bodem bij de aanvang van het Laat-Glaciaal. Hieruit vloeit voort dat de Weichselperiode door een bi-cyclische sedimentatie wordt gekenmerkt: eensdeels de fase van het Pleniglaciaal A, gekenmerkt door koud-vochtige milieu omstandigheden met dominerend solifluctie processen en anderdeels de fase van het Pleniglaciaal B - Laat-Glaciaal, gekenmerkt door koud-droge milieu omstandigheden met overheersend eolische sedimentatie. Beide cycli worden verder gekenmerkt door het optreden van een extreem koude (deflatie) fase respectievelijk de keienvloer 1 met kleine vorstscheuren en de keienvloer 3 met grote vorstscheuren.

Dental remains of land mammals are sometimes discovered in shallow marine Paleogene deposits of the North Sea Basin. Such is the case for eleven specimens we describe here from the Early Eocene Egemkapel Clay Member in the middle part of the Tielt Formation, found in Ampe quarry at Egem in Northwestern Belgium. The small fauna consists of 6 taxa, including the neoplagiaulacid multituberculate Ectypodus, the erinaceomorph insectivore Macrocranion, the nyctitheriid Leptacodon, an eochiropteran bat possibly belonging to a palaeochiropterygid, an unidentified perissodactyl possibly belonging to an equoid, and a new species of the peradectid marsupial Armintodelphys. The latter represents the first European occurrence of the genus, which was previously only known from the North American late Early and early Middle Eocene of the Wind River and Green River basins in Wyoming and the Uinta Basin in Utah. Biogeographic and biostratigraphic analyses of peradectid marsupials suggest that Armintodelphys dispersed between North America and Europe around the time of the Early Eocene Climatic Optimum. The Egemkapel Clay Member has been dated as middle NP12, early late Ypresian, whereas the Egem mammal fauna can be correlated to the fauna of Avenay from the Paris Basin, which is the international reference-level MP8+9 of the mammalian biochronological scale for the European Paleogene.

One of the earliest basal carnivoraforms, Miacis latouri, previously known by only two teeth from the earliest Eocene of Dormaal, Belgium, is here described based on about 280 new specimens from Dormaal, allowing illustration of almost the entire deciduous and permanent dentition and thus giving information on the dentition of an early basal carnivoraform species and its variability. Based on the dental features, we refer the species to a new genus, Dormaalocyon. We identify possible sexual dimorphism in D. latouri that is less pronounced than in Uintacyon rudis. We also describe for the first time the tarsal bones (calcaneum and astragalus) of D. latouri; these indicate arboreal capabilities for this species. In order to ascertain the position of Dormaalocyon among basal carnivoraforms, we performed a phylogenetic analysis of the carnivoramorphans. Among basal carnivoraforms, three groups are recovered: the Uintacyon group, Oodectes group, and the Vulpavus group. Dormalocyon is one of the most primitive carnivoraforms and is closely related to North American Vulpavus and Miacis species. We propose that the two latter genera are North American with an ancestry that involves the European Dormaalocyon; this implies a dispersal of carnivoraforms from Europe to North America near the Paleocene-Eocene boundary. Finally, the topology of the phylogenetic tree supports a Paleocene radiation of the carnivoraforms, which is presently unknown.