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360 results for “Artiodactyla”
FIG. 9 in Mammalian Diversity And Matses Ethnomammalogy In Amazonian Peru Part 2: Xenarthra, Carnivora, Perissodactyla, Artiodactyla, And Sirenia
FIG. 9. Dorsal views of mandibles of Bradypus variegatus infuscatus (A, AMNH 76497) and B. v. variegatus (B, AMNH 95105).
FIG. 13 in Mammalian Diversity And Matses Ethnomammalogy In Amazonian Peru Part 2: Xenarthra, Carnivora, Perissodactyla, Artiodactyla, And Sirenia
FIG. 13. Ventral views of adult skulls of Atelocynus microtis (A, AMNH 98639) and Speothos venaticus (B, AMNH 98560). Note the absence of M2 in Speothos.
FIG. 5. Matses woman butchering a in Mammalian Diversity And Matses Ethnomammalogy In Amazonian Peru Part 2: Xenarthra, Carnivora, Perissodactyla, Artiodactyla, And Sirenia
FIG. 5. Matses woman butchering a long-nosed armadillo (Dasypus sp.) on the upper Quebrada Chobayacu, ca. 1975 (photo by Steven Romanoff).
FIG. 8 in Mammalian Diversity And Matses Ethnomammalogy In Amazonian Peru Part 2: Xenarthra, Carnivora, Perissodactyla, Artiodactyla, And Sirenia
FIG. 8. Lateral views of skulls and mandibles of Bradypus variegatus infuscatus (A, AMNH 76497) and B. v. variegatus (B, AMNH 95105).
FIG. 6 in Mammalian Diversity And Matses Ethnomammalogy In Amazonian Peru Part 2: Xenarthra, Carnivora, Perissodactyla, Artiodactyla, And Sirenia
FIG. 6. Cut-away diagram illustrating how Dasypus pastasae is captured by Matses hunters (see text for explanation).
Figure 18 in A taxonomic revision of the Tragulus mouse-deer (Artiodactyla)
Figure 18. Sundashelf islands in the South China Sea. Thick solid line indicates the coastline during the last glacial maximum. Dotted lines indicate the main Sundashelf river systems during the last glacial maximum (after Voris, 2000).
Figure 10 in A taxonomic revision of the Tragulus mouse-deer (Artiodactyla)
Figure 10. Discriminant analysis of adult T. javanicus-like specimens, with corresponding correlation matrix.
Figure 4 in New data on the Cainotheriidae (Mammalia, Artiodactyla) from the early Oligocene of south-western France
Figure 4. Caenomeryx cf. procommunis. A & B, occlusal view. A, right P2/-P3/ (PCT 420). B, left P/2-M/2 (PCT 951). C. filholi. C & D, occlusal view. C, left P2/-P4/ (PCT 417). D, left P/2-M/1 (PCT 933). Cainotherium sp. E, left P2/-M3/ (PCT 416). Scale bar = 1 mm.
Figure 5 in New data on the Cainotheriidae (Mammalia, Artiodactyla) from the early Oligocene of south-western France
Figure 5. Chronological extension of the early Oligocene Cainotheriidae lineages. MP: Mammalian Palaeogene reference levels from Schmidt-Kittler (1987). Numerical ages follow Odin (1994).
Figure 10. A in The phylogeny and taxonomy of Hippopotamidae (Mammalia: Artiodactyla): a review based on morphology and cladistic analysis
Figure 10. A new phylogeny for the Hippopotamidae. Geographical distribution: anot Eastern African, but from Abu Dhabi, the Arab United Emirates, the Arabic Peninsula (see Gentry, 1999); bknown in Eastern Africa but also in Oubeidiyeh, Israel (see Faure, 1986) and maybe in Algeria (Geraads, 1980); cknown in Africa but also in continental Europe (see Mazza, 1995).
Figure 9 in The phylogeny and taxonomy of Hippopotamidae (Mammalia: Artiodactyla): a review based on morphology and cladistic analysis
Figure 9. Mandibular anatomy within the Hippopotamidae. This figure shows the new taxonomic divisions of the family Hippopotamidae and, for each discussed taxon, some of the mandibular characters that provided additional support to the clades identified in the parsimony analysis (boxes in this figure). These features include: the general shape of the mandible, with expansion of the canine processes and relative length of the symphysis (seen in the dorsal outlines); the shape of the symphysis sagittal cross section; the length of the premolar row relative to the length of the molar row. The figure shows the following features for the taxa listed under each genus name: Saotherium, very inclined symphysis with thin cross-section and poorly developed canine processes; Archaeopotamus, relatively long and shallow symphysis with poorly developed canine processes and longer premolar rows than in any other clade; Hexaprotodon, wide symphysis but with poorly differentiated canine processes, very robust symphysis in cross section; Choeropsis, very short symphysis globular in cross section and poorly developed canine processes; Hippopotamus and aff. Hippopotamus, short symphysis globular in crosssection (lacking a projected incisor alveolar process) and strong extension of the canine processes – the latter feature being not salient in the Afar species (aff. Hip. coryndoni, aff. Hip. afarensis) and aff. Hip. cf. protamphibius from Kanapoi.
Figure 8 in The phylogeny and taxonomy of Hippopotamidae (Mammalia: Artiodactyla): a review based on morphology and cladistic analysis
Figure 8. An example of convergence in the Hippopotamidae: orbit elevation. From bottom to top, right lateral views of the neuro-crania: KNM-WT 19633, Hippopotamus gorgops from the Nachukui Formation, West Turkana, Kenya, housed at the NMK, Nairobi; 36824, Hexaprotodon palaeindicus from the Narbada beds, Central India, housed at the NHM, London; KNM-ER 798, holotype of Hex. karumensis, from the Koobi Fora Formation, East Turkana, Kenya, housed at the NMK, Nairobi. The elevated orbit is related to an aquatic way of life (Mazin & Buffrénil, 2001), indicating a preferential position at the air/water interface. These three species belong to three different lineages and evolved from forms with much lower orbits.
Figure 5. Dental character states. A in The phylogeny and taxonomy of Hippopotamidae (Mammalia: Artiodactyla): a review based on morphology and cladistic analysis
Figure 5. Dental character states. A, upper canine cross section (from left to right: in Anthracokeryx ulnifer, in Hippopotamus amphibius, in Hexaprotodon bruneti, in Hex. harvardi). B, outline of the P1/alveolus (bottom: in Hex. protamphibius, top: in Hex. sivalensis). C, occlusal view of the P3/ (left: in Hex. bruneti, right: in Hex. protamphibius). D, occlusal view of the P4/ (left: in Hex. harvardi, right: both in Hex. protamphibius). E, occlusal view of the P/4 (left: in Hex. mingoz, right: in Hex. aethiopicus).
Figure 4. Mandibular character states. A in The phylogeny and taxonomy of Hippopotamidae (Mammalia: Artiodactyla): a review based on morphology and cladistic analysis
Figure 4. Mandibular character states. A, dorsal view of Hexaprotodon aff. sahabiensis mandible. B, dorsal view of Hippopotamus amphibius mandible. C, dorsal view of Hex. karumensis mandible. D, sagittal cross section (at the I/1-I/1 diastema) of the symphysis (bottom: in Hex. sivalensis, top: in Hip. amphibius); E, three schematic anterior views of the symphysis (from left to right: in Hex. mingoz, in some Hex. protamphibius, in Hex. bruneti). F, three schematic lateral views of the vertical ramus (from bottom to top: in Hip. amphibius, in Hex. sivalensis, in Anthracokeryx ulnifer).
Figure 2. Cranial character states. A in The phylogeny and taxonomy of Hippopotamidae (Mammalia: Artiodactyla): a review based on morphology and cladistic analysis
Figure 2. Cranial character states. A, ventral view of a Hippopotamus amphibius skull. B, ventral view of a Hexaprotodon liberiensis skull. C, Schematic view of Hex. harvardi tympanic bulla area. D, Schematic view of A. ulnifer glenoid articular area. E, Three dorsal views of different bone contacts in the lachrymal area (from bottom to top: in Hex. harvardi, in Hex. protamphibius, in Hip. amphibius). A1 and A2 are Hex. liberiensis autapomorphies (see text).
Figure 11 in The phylogeny and taxonomy of Hippopotamidae (Mammalia: Artiodactyla): a review based on morphology and cladistic analysis
Figure 11. Comparison of mandibular symphysis measurements between the 'narrow muzzled' hippos and other hippopotamids (only adult specimens were included): bivariate plot of sagittal length of symphysis vs. width between lower canines (all adult specimens). Legend: ¥, Archaeopotamus lothagamensis from Lothagam, Kenya; +, A. aff. lothagamensis from Abu Dhabi, United Arab Emirates; Ł, A. harvardi from Lothagam, Kenya; Δ, A. aff. harvardi from Rawi, Kenya; K, UMP 6202, Hexaprotodon? cf. imagunculus from Kazinga Channel, Uganda; Ɨ, other fossil hippopotamids; Z Choeropsis liberiensis, extant; O, Hippopotamus amphibius, extant. Broken line: regression line for the genus Archaeopotamus; unbroken line: regression line for all the other individuals.
Figure 7 in The phylogeny and taxonomy of Hippopotamidae (Mammalia: Artiodactyla): a review based on morphology and cladistic analysis
Figure 7. Second of the three most parsimonious tree obtained from the cladistic analysis. The bold numbers indicate the nodes. The numbered boxes indicate the ACCTRAN character state changes (white boxes indicate reversions and convergences).
Figure 1 in The phylogeny and taxonomy of Hippopotamidae (Mammalia: Artiodactyla): a review based on morphology and cladistic analysis
Figure 1. Synthesis of recent phylogenies (Harrison, 1997; Weston, 2000) for the family Hippopotamidae. The genus Hexaprotodon is shown to be paraphyletic, and Hippopotamus being related to the derived species Hex. protamphibius. The important position of Hex. harvardi and the early divergence of the Hex. liberiensis lineage can be also noted.
Figure 1 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 1. Map of Qaidam Basin showing surrounding mountains and major vertebrate fossil localities.
Figure 9 in A taxonomic revision of the Tragulus mouse-deer (Artiodactyla)
Figure 9. Map of the Terutau and Langkawi island groups west of the Malay and Thai peninsula.
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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.