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364 results for “Late Pleistocene”
Figure 11 in Osteology and ecology of Megantereon cultridens SE311 (Mammalia; Felidae; Machairodontinae), a sabrecat from the Late Pliocene - Early Pleistocene of Senéze, France
Figure 11. Rib elements of Megantereon cultridens SE311.
Aligned and curated mtDNA sequences from: Ancient DNA of narrow-headed voles reveals common features of the Late Pleistocene population dynamics in cold-adapted small mammals
<p><span>Narrow-headed vole, together with collared lemming and common vole, was the most abundant small mammal species across Eurasian Late Pleistocene steppe-tundra environments. Previous ancient DNA studies of </span><span>the latter</span><span> </span><span>two</span><span> revealed dynamic past population histories shaped by climatic fluctuations. To investigate the extent to which species with similar adaptations share common evolutionary </span><span>histories,</span><span> we generated a dataset comprising mitochondrial genomes of 139 ancient and 6 modern narrow-headed voles from multiple sites across Europe and north-</span><span>western</span><span> Asia and covering the last ca. 100 thousand years (ka). We inferred Bayesian time-aware phylogenies using 11 </span><span>radiocarbon-dated</span><span> samples for calibration of the molecular clock. We found that across the three </span><span>species,</span><span> divergence of the main mtDNA lineages occurred during Marine Isotope Stages (MIS) 7 and MIS 5, suggesting a common response </span><span>of species adapted to open habitat to the interglacial environments. </span><span>In European narrow-headed voles, we identified multiple </span><span>time-structured</span><span> mtDNA lineages, implying lineage turnovers. Timing of some of these turnovers was synchronous across all three </span><span>species,</span><span> allowing us to identify the main drivers of the Late Pleistocene dynamics of steppe- and cold-adapted species.</span></p>
Global biome patterns of the Middle and Late Pleistocene
<p class="Maintext">Our primary aim was to assess the hypothesis that distinctive features of the patterns of vegetation change during successive Quaternary glacial–interglacial cycles reflect climatic differences arising from forcing differences. We addressed this hypothesis using 207 half-degree resolution global biome pattern simulations, for time slices between 800 ka and 2 ka, made using the LPJ-GUESS dynamic global vegetation model. Simulations were driven using ice-core atmospheric CO<sub>2</sub> concentrations, Earth's obliquity, and outputs from a pre-industrial and 206 palaeoclimate experiments; four additional simulations were driven using projected future CO<sub>2</sub> concentrations. Climate experiments were run using HadCM3. Using a rule-based approach, above-ground biomass and leaf area index of LPJ-GUESS plant functional types were used to infer each grid cell's biome. The hypothesis is supported by the palaeobiome simulations.</p> <p class="Indentedmaintext">To enable comparisons with the climatic forcing, multivariate analyses were performed of global vegetation pattern dissimilarities between simulations. Results showed generally similar responses to glacial–interglacial climatic variations during each cycle, although no two interglacials or glacials had identical biome patterns. Atmospheric CO<sub>2</sub> concentration was the strongest driver of the dissimilarity patterns. Dissimilarities relative to the time slice with the lowest atmospheric CO<sub>2</sub> concentration show the log–linear relationship to atmospheric CO<sub>2</sub> concentration expected of an index of ecocarbon sensitivity.</p> <p class="Indentedmaintext">For each simulation, extent and total above-ground biomass of each biome were calculated globally and for three longitudinal segments corresponding to the major continental regions. Mean and minimum past extents of forest biomes, notably Temperate Summergreen Forest, in the three major continental regions strongly parallel relative tree diversities, hence supporting the hypothesis that past biome extents played an important role in determining present diversity.</p> <p class="Indentedmaintext">Albeit that they reflect the climatic consequences only of the faster Earth system components, simulated potential future biome patterns are unlike any during the past 800 ky, and likely will continue to change markedly for millennia if projected CO<sub>2</sub> concentrations are realised.</p>
Data from: First 87Sr/86Sr Isotope data for the extinct sloth Lestodon armatus: Insights into the spatial ecology of South American Late Pleistocene Megafauna
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Data from: Did Late Pleistocene climate change result in parallel genetic structure and demographic bottlenecks in sympatric Central African crocodiles, Mecistops and Osteolaemus?
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Data from: Osteology of Crocodylus palaeindicus from the late Miocene–Pleistocene of South Asia and the phylogenetic relationships of crocodyloids
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Data from: A late Pleistocene marine glacial refugium in the south-west of Hainan Island, China: Phylogeographical insights from the brown alga Sargassum polycystum
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Late Pleistocene cave bear from Niedźwiedzia Cave (Poland): its fate and preservation inferred from taphonomy, pathology, and geochemistry
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Aligned and curated mtDNA sequences from: Ancient DNA of narrow-headed voles reveals common features of the Late Pleistocene population dynamics in cold-adapted small mammals
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Global biome patterns of the Middle and Late Pleistocene
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Data from: Multiple late-Pleistocene colonisation events of the Antarctic pearlwort Colobanthus quitensis (Caryophyllaceae) reveal the recent arrival of native Antarctic vascular flora
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Data from: Late Pleistocene range expansion of North American topminnows accompanied by admixture and introgression.
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Data from: Cranial remains of Ramsayia magna from the Late Pleistocene of Australia and the evolution of gigantism in wombats (Vombatidae; Marsupialia)
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Late Pleistocene stickleback environmental genomes reveal the chronology of freshwater adaptation
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Data from: The latest freshwater giants: a new Peltocephalus (Pleurodira: Podocnemididae) turtle from the Late Pleistocene of the Brazilian Amazon
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Fig. 4. Bivariate graphs for the Smilodon populator specimen MNHN-P 957. A in An extremely large saber-tooth cat skull from Uruguay (late Pleistocene -early Holocene, Dolores Formation): body size and paleobiological implications
Fig. 4. Bivariate graphs for the Smilodon populator specimen MNHN-P 957. A, PM3 transverse diameter (PM3ML) versus PM3 anteroposterior diameter (PM3AP); B, PM4 transverse diameter (PM4ML) versus PM4 anteroposterior diameter (PM4AP). Data from different sources (see Material and methods).
Figure 3. Bivariate graphs for the Smilodon populator specimen MNHN-P 957. A in An extremely large saber-tooth cat skull from Uruguay (late Pleistocene -early Holocene, Dolores Formation): body size and paleobiological implications
Figure 3. Bivariate graphs for the Smilodon populator specimen MNHN-P 957. A, zygomatic width (ZW) versus condylobasal length (CBL); B, canine transverse diam- eter (CML) versus canine anteroposterior diameter (CAP). Data from different sources (see Material and methods).
FIGURE 21 in Late Pleistocene Red Sea Mollusca: 1. Polyplacophora
FIGURE 21. Craspedochiton sp. A. Erythrea, Massawa North, Abd-el-Cader, 2 valves (intermediate and tail) figured by Selli (1973: pl. 11, figs 6-7) as Craspedochiton (Notoplax) involutus (Carpenter in Pilsbry, 1893). B–E. Egypt, Hurghada, Late Pleistocene (last interglacial MIS5e). B–C. MZB 50561, head valve (St. 14bis), width 1.4 mm, dorsal views. D–E. MZB 50562, intermediate valve (St. 16), width 3 mm, dorsal views.
FIGURE 20. Acanthochitona interglacialis n in Late Pleistocene Red Sea Mollusca: 1. Polyplacophora
FIGURE 20. Acanthochitona interglacialis n. sp. A–C. Saudi Arabia, Gulf of Aqaba, Ash Shaykh Humayd (St. 8), Late Pleistocene (last interglacial MIS5e), Holotype MZB 50560, intermediate valve, width 1.6 mm, dorsal view, detail of tegmentum surface of pleural area and frontal view. Scale bar: 100 µm (B).
FIGURE 14. Lucilina aegyptiaca n in Late Pleistocene Red Sea Mollusca: 1. Polyplacophora
FIGURE 14. Lucilina aegyptiaca n. sp. A–H. Egypt, Hurghada (St. 13), Late Pleistocene (last interglacial MIS5e). A–D. Holotype, MZB 50546, intermediate valve, width 4 mm, dorsal view (A), detail of tegmentum surface of pleural area (B), ventral (C) and frontal (D) views. E–H. Paratype, MZB 50547, tail valve, width 3 mm, dorsal, ventral, lateral and posterior views. I–L. Present-day, Zabargad Island, st. 13/30, MZB 50548, intermediate valve, width 3.8 mm, dorsal view (I), detail of tegmentum surface of pleural area (J), of lateral areas (K) and frontal view (L). Scale bar: 100 µm (B, K).
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.