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Fig. 2 in Morphological and molecular characterization of Calicophoron raja (N¨asmark, 1937) collected from wild Bovidae in South Africa
Fig. 2. Representative sagittal sections at the level of the terminal genitalium. (A) Whole image. Arrowhead indicates the genital pore. Thickness of sections: 5 μm (A, B), 10 μm (C). (B) A pharynx of the typical Calicophoron type. (C) A terminal genitalium of the typical Raja type. a: acetabulum, p: pharynx, pm: pars musculosa, t: testis, u: uterus. Scale bar: 0.5 mm (A), 0.2 mm (B), and 0.2 mm (C).
Fig. 1 in Morphological and molecular characterization of Calicophoron raja (N¨asmark, 1937) collected from wild Bovidae in South Africa
Fig. 1. Representative sagittal sections of Laurer's canal (A, C, E) and the excretory duct (B, D, F). Arrowheads indicate the orifice of Laurer's canal. Arrows indicate the excretory pore. a: acetabulum, e: excretory bladder, ed: excretory duct, p: pharynx, pm: pars musculosa, t: testis, l: Laurer's canal. Thickness of sections: 5 μm (A, B, D-F), 10 μm (C). Scale bar: 1 mm (A, B) and 0.5 mm (C–F).
Fig. 2 in Remarks on Eimeria spp. (Apicomplexa: Eimeriidae) from Kobus spp. (Bovidae: Reduncini), with supplementary morphological data of Eimeria congolensis Ricci-Bitti et al., 1973 from a new host subspecies, the common waterbuck Kobus ellipsiprymnus ellipsiprymnus (Ogilbyi, 1833)
Fig. 2. Photomicrographs of sporulated oocysts of Eimeria congolensis from common waterbucks Kobus ellipsiprymnus ellipsiprymnus in a safari park of Portugal. Note the inner layer (il) and rough outer layer (rol) of the oocyst wall, micropyle (m), nucleous (n), polar granule (pg), refractile body (rb), sporocyst residuum (sr), Stieda (sb) and sub-stieda (ssb) bodies. Scale bar: 10 μm.
Fig. 1 in Remarks on Eimeria spp. (Apicomplexa: Eimeriidae) from Kobus spp. (Bovidae: Reduncini), with supplementary morphological data of Eimeria congolensis Ricci-Bitti et al., 1973 from a new host subspecies, the common waterbuck Kobus ellipsiprymnus ellipsiprymnus (Ogilbyi, 1833)
Fig. 1. Composite line drawing of the sporulated oocyst of Eimeria congolensis from common waterbucks Kobus ellipsiprymnus ellipsiprymnus in a safari park of Portugal. Scale-bar: 10 μm.
FIGURE 17 in Pleistocene Bovidae (Mammalia) from Malapa, Gauteng Province, South Africa
FIGURE 17. Types of surface modification identified on Malapa bovid limb bones and number of specimens with that modification.
FIGURE 16 in Pleistocene Bovidae (Mammalia) from Malapa, Gauteng Province, South Africa
FIGURE 16. Metapodial (left), UW 88-1247, demonstrating cracking and longitudinal fractures typical of Behrensmeyer (1975) Stage 1 weathering and diagenetic processes. UW 88-1224, (right) metatarsal exhibits longitudinal fractures, cracking, and cortical peeling.
FIGURE 15 in Pleistocene Bovidae (Mammalia) from Malapa, Gauteng Province, South Africa
FIGURE 15. Lingual view of Malapa UW 88-518 and UW 88-519 demonstrating high occlusal relief and sharp cusps.
FIGURE 13. Block 848 bovid BSC II in Pleistocene Bovidae (Mammalia) from Malapa, Gauteng Province, South Africa
FIGURE 13. Block 848 bovid BSC II in situ with femur and tibiae in articulation. Associated right metatarsal, astragalus, naviculocuboid, and distal phalanx are also in the Block.
FIGURE 12 in Pleistocene Bovidae (Mammalia) from Malapa, Gauteng Province, South Africa
FIGURE 12. UW 88-555 horn core fragment of BSC II (left). UW 88-734 partial horn core of a BSC III (right).
FIGURE 4 in Pleistocene Bovidae (Mammalia) from Malapa, Gauteng Province, South Africa
FIGURE 4. Comparison of holotype M 18 (top) and paratype M 19 (center) of T. pricei with Malapa mandible (bottom).
FIGURE 3 in Pleistocene Bovidae (Mammalia) from Malapa, Gauteng Province, South Africa
FIGURE 3. Occlusal surface of Malapa UW 88-518, UW 88-519, and UW 88-1015 refit together. The arrows are illus- trating the mesostylid, paraconid, and parastylid, from left to right.
FIGURE 5 in Pleistocene Bovidae (Mammalia) from Malapa, Gauteng Province, South Africa
FIGURE 5. Malapa specimen UW 88-1299, right maxillary fragment with M2 and M3 (left). Malapa specimen UW 88- 1205, left maxillary fragment with M1 (right).
Table 2 in Demodex bialoviensis sp. nov. (Acariformes, Demodecidae) a new, specific parasite of the European bison Bison bonasus (Artiodactyla, Bovidae)
<p><b>Table 2</b> Morphometric comparison between <i>Demodex bialoviensis</i> sp. nov. and <i>Demodex bisonianus</i>.</p><table><tbody><tr><th>Feature/Species</th><th><i>Demodex bialoviensis</i> sp. nov.</th><th><i>Demodex bisonianus</i></th></tr></tbody><tbody><tr><th>Source</th><td>Present study</td><td></td><td>Kadulski and Izdebska</td></tr><tr><th></th><td></td><td></td><td>(1996)</td><td></td></tr><tr><th>Sex Sample size</th><td>Males (n =12)</td><td>Females (n =</td><td>Males</td><td>Females</td></tr><tr><th></th><td></td><td>34)</td><td>(n =</td><td>(n =20)</td></tr><tr><th></th><td></td><td></td><td>20)</td><td></td></tr><tr><th>Body total length</th><td>176</td><td>239</td><td>517, SD</td><td>534, SD</td></tr><tr><th></th><td>(158–198), SD</td><td>(200–268), SD</td><td>23 a</td><td>20 a</td></tr><tr><th></th><td>13</td><td>15</td><td></td><td></td></tr><tr><th>Body total width</th><td>31 (30–35), SD</td><td>35 (30–40), SD</td><td>63, SD 9</td><td>68, SD 9</td></tr><tr><th></th><td>2</td><td>2</td><td></td><td></td></tr><tr><th>Body length to</th><td>5.6:1</td><td>6.8:1</td><td>8.2:1b</td><td>7.9:1b</td></tr><tr><th>width ratio</th><td>(4.9–6.4:1), SD</td><td>(5.2–7.9:1), SD</td><td></td><td></td></tr><tr><th></th><td>0.6:1</td><td>0.6:1</td><td></td><td></td></tr><tr><th>Opisthosoma</th><td>62 (57–65), SD</td><td>65 (60–69), SD</td><td>68b</td><td>69b</td></tr><tr><th>length to body</th><td>2</td><td>2</td><td></td><td></td></tr><tr><th>length ratio (%)</th><td></td><td></td><td></td><td></td></tr><tr><th>Aedeagus length</th><td>21 (18–29), SD</td><td>–</td><td>33, SD 7</td><td>–</td></tr><tr><th>3</th></tr><tr><th>Vulva length</th><td>–</td><td>12 (10–17), SD</td><td>–</td><td>22, SD 2</td></tr><tr><th></th><td></td><td>2</td><td></td><td></td></tr></tbody></table><p><sup>a</sup> Measurements were rounded to the nearest micrometer with respect to the original results (Kadulski and Izdebska, 1996).</p><p><sup>b</sup> Calculated from measurements of Kadulski and Izdebska (1996).</p>
Fig. 4 in Tetracerus quadricornis (Artiodactyla: Bovidae)
Fig. 4.—Male Tetracerus quadricornis in typical habitat of dry deciduous forest edge, Panna National Park, central India; note inner ear markings that may serve to automimic posterior horns in adult males and enhance threat displays (Guthrie and Petocz 1970). Photograph by K. Sharma.
Fig. 1.—Male Tetracerus quadricornis illustrating the 4 in Tetracerus quadricornis (Artiodactyla: Bovidae)
Fig. 1.—Male Tetracerus quadricornis illustrating the 4 horns typical of adult males of 2 subspecies; note enlarged preorbital gland extending below the eye. Photograph by K. Sharma.
Fig. 2 in Tetracerus quadricornis (Artiodactyla: Bovidae)
Fig. 2.—Dorsal, ventral, and lateral views of skull (British Museum [Natural History] BMNH specimen 1902.8.14.3) and lateral view of mandible (BMNH 1856.9.22.1) of adult male Tetracerus quadricornis. Greatest length of skull is 179 mm.
Fig. 5 in Tetracerus quadricornis (Artiodactyla: Bovidae)
Fig. 5.—Male (left) and female (right) Tetracerus quadricornis associate irregularly and are seen together most often during rut in May–July, Panna National Park, central India. Photograph by K. Sharma.
Fig. 3 in Tetracerus quadricornis (Artiodactyla: Bovidae)
Fig. 3.—Distribution of Tetracerus quadricornis in India and Nepal; densities tend to be highest in central parts of the main range in India (Sharma 2006).
Fig. 6 in Bos grunniens and Bos mutus (Artiodactyla: Bovidae)
Fig. 6.—Nomadic pastoralists were dependent on domestic yaks (Bos grunniens) to move supplies throughout the Tibetan Plateau; trucks now deliver most supplies. Photograph by G. B. Schaller.
Fig. 4 in Bos grunniens and Bos mutus (Artiodactyla: Bovidae)
Fig. 4.—Dorsal, ventral, and lateral views of skull and lateral view of mandible of an adult male domestic yak (Bos grunniens); zoo specimen of unknown origin (National Museum of Natural History, specimen 174734). Greatest length of skull 525 mm.
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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.