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86 results for “evolutionary tree”
Figure 3. Phylogenomic tree estimated from a in Comparative genomics reveals the evolutionary history of the unicellular eukaryote class Litostomatea and its adaptive evolution based on biochemical metabolic capacity
Figure 3. Phylogenomic tree estimated from a concatenated dataset of 1680 orthogroups of 28 litostomateans and two spirotricheans
Figure 3. Phylogenomic tree estimated from a in Comparative genomics reveals the evolutionary history of the unicellular eukaryote class Litostomatea and its adaptive evolution based on biochemical metabolic capacity
Figure 3. Phylogenomic tree estimated from a concatenated dataset of 1680 orthogroups of 28 litostomateans and two spirotricheans by maximum likelihood (ML) and Bayesian inference (BI) methods. Sequences from the present study are in bold. Ŋe numbers at the nodes are the bootstrap values of ML out of 1000 pseudoreplicates and the posterior probability of Bayesian analysis* respectively. Ŋe black dots represent full support values both in the ML and in the BI trees. º* subclass ºrichostomatia; H* subclass Haptoria; R* subclass Rhynchostomatia.
Fig. 12. Tree 1 in Ultrastructure of attachment specializations of hexapods (Arthropoda): evolutionary patterns inferred from a revised ordinal phylogeny
Fig. 12. Tree 1 of three minimum length cladograms obtained after successive reweighting, adhesive pad characters included, unambiguous apomorphies (accelerated and delayed transformation) mapped on trees; asterisks indicate nonhomoplasious changes. Thysanoptera are placed as sistergroup of Hemiptera in tree 2 and as sistergroup of the remaining Paraneoptera in tree 3
Figure 3. Strict consensus trees from the constrained analyses. First constrained analysis forcing a in Taxonomic, palaeobiological and evolutionary implications of a phylogenetic hypothesis for Ornithischia (Archosauria: Dinosauria)
Figure 3. Strict consensus trees from the constrained analyses. First constrained analysis forcing a monophyletic Silesauridae apart from the 'traditional ornithischians'. Abbreviations: Aphan, Aphanosauria; Herrer, Herrerasauridae. Silhouettes are based on artwork by Márcio L. Castro, Gabriel Lio, Rodrigo T. Müller, Maurício S. Garcia, John Sibbick and Douglas M. Heman.
Figure 16 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 16. Synapomorphies common to all the most parsimonious trees mapped on the implied weighting consensus topology. The six new characters (223-228) described in the present study are mapped. See main text for descriptions of characters and states.
Figure 13 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 13. Endocranial surfaces of two sirenian skulls. A, Kaupitherium bronni (sketch based on Voss & Hampe, 2017: figs 4, 11). B, Protosiren fraasi (sketch based on Sickenberg, 1934: plate I, fig. 4). For abbreviations, see the Material and Methods section.
Figure 14 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 14. Comparison of basicranial region of various Eocene sirenian skulls. A, Prorastomus sirenoides (sketch based on holotype BMNH 44897). B, Sobrarbesiren cardieli (MPZ 2017/1). C, Eotheroides aegyptiacum (sketch based on Abel, 1913: table (II) XXXI, fig. 2). D, 'Halitherium' taulannense (sketch based on holotype RGHP D040). E, Protosiren fraasi (sketch based on the BMNH skull cast PV M 9367). For abbreviations, see the Material and Methods section.
Figure 9 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 9. Bones of the ear region of Sobrarbesiren cardieli. A, right periotic of the paratype skull MPZ 2017/2 in ventral view. B, C, MPZ 2020/607, right pars temporalis (= tegmen tympani) in ventral (B) and dorsal (C) views. D, E, right tympanic of the holotype skull MPZ 2017/1 in lateral (D) and medial (E) views. Dashed areas denote broken surfaces. For abbreviations, see the Material and Methods section.
Figure 8 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 8. Isolated squamosals and jugal of Sobrarbesiren cardieli. A–E, MPZ 2020/603, right isolated squamosal; cranial portion in lateral view (A), interpretive sketch (B), and in posterior view (C); and zygomatic process in lateral (D) and ventral (E) views. F–K, MPZ 2020/604, right isolated juvenile squamosal in lateral (F), ventral (G) and medial (H) views, and interpretative sketches (I–K, respectively). L–O, MPZ 2020/606, left partial jugal in lateral (L) and medial (N) views, and interpretative sketches (M, O, respectively). Dashed lines indicate incomplete bones, and dashed areas denote broken surfaces. For abbreviations, see the Material and Methods section.
Figure 4 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 4. Skulls of Sobrarbesiren cardieli in dorsal view. A, paratype skull MPZ 2017/2. B, interpretative sketch of the paratype skull. C, holotype skull MPZ 2017/1. D, skull MPZ 2020/591. Sutures are marked with continuous lines. Dashed lines indicate incomplete bones, and dashed areas denote broken surfaces. For abbreviations, see the Material and Methods section.
Figure 2 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 2. Skulls of Sobrarbesiren cardieli in ventral view. A, paratype skull MPZ 2017/2. B, interpretative sketch of the paratype skull. C, holotype skull MPZ 2017/1. D, skull MPZ 2020/591. Sutures are marked with continuous lines. Dashed lines indicate incomplete bones, and dashed areas denote broken surfaces. For abbreviations, see the Material and Methods section.
Figure 5 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 5. Frontal bones assigned to immature individuals of Sobrarbesiren cardieli. A–F, MPZ 2020/593, left frontal in dorsal (A), ventral (B) and lateral (C) views, and interpretative sketches (D–F, respectively). G–I, MPZ 2020/592, left frontal in dorsal (G), ventral (H) and lateral (I) views. J–L, MPZ 2020/594, left frontal in dorsal (J), ventral (K) and lateral (L) views. Dashed lines indicate incomplete parts. For abbreviations, see the Material and Methods section.
Figure 7 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 7. Skulls of Sobrarbesiren cardieli in posterior view. A, paratype skull MPZ 2017/2. B, interpretative sketch of the paratype skull. C, holotype skull MPZ 2017/1. Sutures are marked with continuous lines. Dashed lines indicate incomplete bones, and dashed areas denote broken surfaces. For abbreviations, see the Material and Methods section.
Figure 11 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 11. Mandibular fragment of Sobrarbesiren cardieli (MPZ 2020/608) in dorsal (A) and medial (B) views. For abbreviations, see the Material and Methods section.
Figure 10 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 10. Schematic drawings of tympanic bones of various sirenian taxa. A, Sobrarbesiren cardieli, right tympanic of the holotype skull MPZ 2017/1. B, Prorastomus sirenoides, right tympanic BMNH 44897. C, Eotheroides lambondrano, left tympanic (from Samonds et al., 2009: fig. 6B). D, Metaxytherium albifontanum, right tympanic (from Vélez-Juarbe & Domning, 2014: fig. 8A). E, Trichechus senegalensis, right tympanic (from Robineau, 1969: fig. 11, not to scale). For abbreviations, see the Material and Methods section. Measurements: APL, Anteroposterior length; DVH, Dorsoventral height; ID, Internal diameter.
Figure 3 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 3. Isolated right nasal process of the premaxilla of Sobrarbesiren cardieli (MPZ 2017/3) in dorsal (A) and medial (B) views. For abbreviations, see the Material and Methods section.
Figure 1 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 1. Skulls of Sobrarbesiren cardieli in lateral view. A, paratype skull MPZ 2017/2. B, interpretative sketch of the paratype skull. C, holotype skull MPZ 2017/1. D, skull MPZ 2020/591. Sutures are marked with continuous lines. Dashed lines indicate incomplete bones, and dashed areas denote broken surfaces. For abbreviations, see the Material and Methods section.
Figure 6 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 6. Endocranial structures of Sobrarbesiren cardieli. Skull roof of skull MPZ 2020/591 (A) and MPZ 2017/2 (B) in ventral view. C–F, MPZ 2020/598, parietal–supraoccipital skullcap of a juvenile individual in posterior (C) and ventral (E) views, and interpretative sketches (D, F, respectively). For abbreviations, see the Material and Methods section.
Figure 12 in Neurocranial bones are key to untangling the sea cow evolutionary tree: osteology of the skull of Sobrarbesiren cardieli (Mammalia: Pan-Sirenia)
Figure 12. Isolated teeth of Sobrarbesiren cardieli. A, B,?I1 (MPZ 2017/4) in occlusal (A) and labial (B) views. C, D,?I3 (MPZ 2017/5) in occlusal (C) and lateral (D) views. E–G, P2 (MPZ 2020/610) in occlusal (E), labial (F) and lingual (G) views. H–J,?P3–4 (MPZ 2020/611) in occlusal (H), labial (I) and lingual (J) views. K–M, deciduous premolar (MPZ 2020/614) in occlusal (K), labial (L) and lingual (M) views.
Evolutionary adaptation of trees and modelled future larch forest extent in Siberia. Code and simulation data
<p>Code and datset used for the publication: "Evolutionary adaptation of trees and modelled future larch forest extent in Siberia" 2023 Gloy et al.</p>
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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)
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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.