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110 results for “Sloth”
Figure 5 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 5. Estimated rate multipliers for anatomical partitions in each model. Partition colours as in Figure 1.
Figure 2 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 2. Diversity through time for sloth genera sampled and its association with geological epochs. Time scale in million years ago.
Figure 1 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 1. Anatomical partitions and partitioning schemes. Coloured anatomical regions in the skeleton of Paramylodon harlani (modified from Stock, 1925) correspond to the maximally partitioned data subsets, as used in model A7, whereas their combinations into composite partitions used in schemes A1 to A6 are indicated by other colours in the table. UN, unpartitioned model.
Figure 4 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 4. Selected trees, with node supports (Poisson boostrap and posterior probabilities), depicting the overall variation in topologies obtained. A, parsimony IW100. B, parsimony IW5. C, Bayesian UN_p. D, Bayesian IW100_e. All topologies and branch lengths for Bayesian trees are available in the Supporting Information (File S9).
Figure 3. A in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 3. A, marginal likelihoods of Bayesian models. B, normalized Robinson–Foulds (nRF) distances among topologies (with IW100_e used as reference). C, distribution of node supports, with posterior probabilities for Bayesian inferences and bootstrap values for maximum parsimony.
Figure 7 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 7. Stratigraphic fit of maximum parsimony and Bayesian topologies evaluated with two metrics, considering fossil age intervals as known ranges or as stratigraphic uncertainty. A, stratigraphic consistency index (SCI). B, gap excess ratio (GER).
Figure 10 in Reassessing the phylogeny and divergence times of sloths (Mammalia: Pilosa: Folivora), exploring alternative morphological partitioning and dating models
Figure 10. Relative rates (median and 95% HPD) of speciation, extinction and fossilization obtained with a skyline fossilized birth-death process for seven consecutive time bins.
Data from: Retroposed elements and their flanking regions resolve the evolutionary history of xenarthran mammals (armadillos, anteaters, and sloths)
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Fine-scale ecological and anthropogenic variables predict the habitat use and detectability of sloth bears in the Churia habitat of east Nepal
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Data from: Neogene sloth assemblages (Mammalia, Pilosa) of the Cocinetas Basin (La Guajira, Colombia): implications for the Great American Biotic Interchange
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Data from: Palaeoproteomics resolves sloth phylogeny
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Data from: Evolutionary adaptation to aquatic lifestyle in extinct sloths can lead to systemic alteration of bone structure
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Data from: The curious case of Bradypus variegatus sloths: populations in threatened habitats are biodiversity components needing protection
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Data from: Resolving the phylogenetic position of Darwin’s extinct ground sloth (Mylodon darwinii) using mitogenomic and nuclear exon data
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Data from: Multi-scale effects of habitat structure and landscape context on a vertebrate with limited dispersal ability (the brown-throated sloth, Bradypus variegatus)
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Data from: Gradual adaptation of bone structure to aquatic lifestyle in extinct sloths from Peru
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Data from: Postcranial anatomy of the extinct terrestrial sloth Simomylodon uccasamamensis (Xenarthra: Mylodontidae) from the Pliocene of the Bolivian Altiplano and its evolutionary implications
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Data from: Phylogeny, macroevolutionary trends and historical biogeography of sloths: insights from a Bayesian morphological clock analysis
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Data from: The late Oligocene Xenarthran fauna of Quebrada Fiera (Mendoza, Argentina) and its implications for sloth origins and the diversity of Paleogene Cingulates
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Table Z in Harpy eagle kill sample provides insights into the mandibular ontogenetic patterns of two-toed sloths (Xenarthra: Choloepus)
<p><b>Table Z:</b> Principal components’ factor loadings of eight mandibular measurements of <i>Choloepus</i> sp.</p><table><tbody><tr><th></th><th><b>PC¹</b></th><th><b>PCZ</b></th><th><b>PCƎ</b></th><th><b>PC4</b></th><th><b>PCS</b></th><th><b>PCƂ</b></th><th><b>PC7</b></th><th><b>PCB</b></th></tr></tbody><tbody><tr><th>BAC</th><td>−0.36419</td><td>−0.03257</td><td>−0.37585</td><td>−0.00685</td><td>0.21989</td><td>0.78839</td><td>0.12241</td><td>0.20027</td></tr><tr><th>BCC</th><td>−0.37306</td><td>−0.05151</td><td>−0.04782</td><td>0.07696</td><td>0.19834</td><td>0.01218</td><td>−0.59374</td><td>−0.67672</td></tr><tr><th>HCA</th><td>−0.33771</td><td>−0.40931</td><td>0.39166</td><td>0.70764</td><td>−0.04241</td><td>−0.03279</td><td>0.01090</td><td>0.24754</td></tr><tr><th>HCC</th><td>−0.35614</td><td>−0.02746</td><td>−0.63993</td><td>0.00627</td><td>−0.09856</td><td>−0.50959</td><td>−0.20713</td><td>0.38803</td></tr><tr><th>LAM</th><td>−0.35690</td><td>0.09563</td><td>0.39899</td><td>−0.44229</td><td>−0.55334</td><td>0.16929</td><td>−0.33608</td><td>0.24672</td></tr><tr><th>LCD</th><td>−0.31297</td><td>0.86221</td><td>0.17765</td><td>0.23890</td><td>0.18636</td><td>−0.10852</td><td>0.14633</td><td>0.04581</td></tr><tr><th>LMS</th><td>−0.35341</td><td>−0.25972</td><td>0.29043</td><td>−0.48950</td><td>0.58561</td><td>−0.26349</td><td>0.25401</td><td>0.08244</td></tr><tr><th>TML</th><td>−0.37024</td><td>−0.08940</td><td>−0.13581</td><td>−0.03065</td><td>−0.46577</td><td>−0.08763</td><td>0.62497</td><td>−0.46940</td></tr></tbody></table><p>See main text for measurement abbreviations.</p>
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