...Kaedan O’Brien; Randall B Irmis; Joan Brenner Coltrain; Daniel Martin Dalmas; Katrina M Derieg; Thomas Evans; Eric S Richards; Fumiko M Richards; Eric A Rickart; J Tyler Faith; Kevin Rowe In this study, we seek to highlight the value of Holocene cave skeletal assemblages as a tool for establishing...

...Jianguo Xiong; Yuezhi Zhong; Caicai Liu; Qingri Liu; Huiping Zhang; Chenglong Deng; Youli Li Geomorphology Environmental magnetism Tectonics and climatic interactions Holocene Chinese Loess Plateau Chinese Academy of Sciences 10.13039/501100002367 National Natural Science Foundation...

... mitogenomic results, and demonstrate ancient gene flow from roan into blue antelope. We show that blue antelope genomic diversity was much lower than in roan and sable antelope, indicative of a low population size since at least the early Holocene. This supports observations from the fossil record documenting...

... parapatry; where historical dispersal was asymmetric, we observed abrupt parapatry; and finally, where historical dispersal was symmetric, we observed narrow sympatry. biogeography climatic niche coexistence dispersal Holocene North American monsoon Pleistocene species distribution models Parapatry...

...Xinxia Li; Guoqiao Xiao; Shan Lin; Xiaoke Qiang; Hong Ao Abstract Asia contains more than half the world’s population, and their lives are significantly related to summer monsoon moisture supply. Here, we investigate features and dynamics of late Pleistocene–middle Holocene Asian summer monsoon...

... the presence of red deer sensu lato in south-eastern Europe and western Asia during the Last Glacial Maximum. ancient DNA Cervus elaphus cytochrome b Holocene Last Glacial Maximum Late Pleistocene mtDNA phylogenetic phylogeography postglacial recolonization National Science...

...-gatherer groups to environmental fragmentation, caused by increased aridity during the Mid-Holocene and the consequent loss of productive habitats in the region ( Yacobaccio et al., 2017 ). During this period, hunter-gatherer groups adopted a logistic strategy, reducing their residential mobility...

... sections ( Fig. 1 ). Excavations in Callao Cave by the National Museum of the Philippines began in 1979 ( Cuevas 1980 ), and further excavations during 2003–2011 yielded vertebrate remains that range in age from the Late Pleistocene to Late Holocene ( Mijares 2005 ; Mijares et al. 2010 ). Additional...

...Lara-Sophie Dey; Martin Husemann; Axel Hochkirch; Marianna V P Simões ecological niche modelling Last Glacial Maximum mid-Holocene outlier detection Palaearctic species distribution modelling Corresponding author. E-mail: [email protected] 26 10 2020 21 12 2020 25 12...

...Zhonglou Sun; Pablo Orozco-terWengel; Guotao Chen; Ruolei Sun; Lu Sun; Hui Wang; Wenbo Shi; Baowei Zhang; Yanping Wang Figure 3. Species distribution models of Chinese muntjac at ( A ) the Last Interglacial, ( B ) the Last Glacial Maximum, ( C ) the Middle Holocene, and ( D ) the Current. Color...

... flujo genético heterogeneidad genética microsatélites mitocondrias oso de anteojos Tremarctos ornatus Colombian Andean Cordilleras gene flow genetic heterogeneity microsatellites mitochondrial genes Pleistocene and Holocene demographic changes spatial autocorrelation spectacled bear...

...), with dates ranging from Late Pleistocene to Holocene ( Faure et al. 1999 ; but see Hubbe et al. 2013 ). For comparative purposes, we examined samples (including topotypes) belonging to the living species Bibimys torresi Massoia, 1980 , Bibimys chacoensis ( Shamel, 1931 ), and Bibimys...

... the sampling localities for ancient badger remains. See the map in Figure 3 for the modern distribution of Meles leucurus and Meles meles and the key geographical features, such as the Ural Mountains and the Volga River. A, Late Holocene epoch (2500–100 BP); B, Middle Holocene (8000–2500 BP...

... with the differences measured between the late Pleistocene and Holocene rabbits or between rabbits in, say, the Paris region and Andalucía, we may ignore sex-related differences. Sexual dimorphism of the bones considered here could be studied for several of the modern samples comprising many individuals. Since 2000...

... for Cancer (Arges) parallelus De Haan, 1833 , a fossil crab first described from Japan during the 19th century. The neotype of this species from the Holocene (about 9,000–5,000 ybp) Nanyo Formation of Ise Bay, central Japan, is herein designated. The monotypic genus Arges De Haan...

...: [email protected] marine deep biosphere organic matter diagenesis Glacial-Holocene transition microbial necromass biomass turnover times D:L-amino acid model protein repair Protein-L-isoaspartate(D-aspartate) O-methyltransferase...

...Ondřej Korábek; Adam Petrusek; Lucie Juřičková Our primary focus was the species natural spread during the Holocene. However, large parts of the present range of H. pomatia were colonized only with human aid and often by deliberate introductions (see Supporting Information, Appendix S1...

... of the only fossil records of the genera known to date, whereas the fossil hermit crab remains from the Holocene of Antigua represent the second record of fossil Coenobita worldwide. ( Fig. 1H–J ) Material examined: Two short, disarticulated, fragmented dactyli and pollices, USNM 618303...

... remains of 14 cimicids (Hemiptera: Cimicidae) were recovered during archaeological investigations of the Paisley Five Mile Point Cave site (35LK3400), an exceptionally well-dated (n = 229 radiocarbon dates) late Pleistocene–early Holocene rock shelter site in south-central Oregon. Nine...

... (Halichoerus grypus; Klimova et al., 2014 ) in the North Atlantic. For the southern elephant seal (SES) in particular, de Bruyn et al. ( 2009 ) found evidence for population abundance and dynamics being impacted by climate cycles over a much shorter time frame, during the Holocene...