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360 results for “Artiodactyla”
Fig. 4 in Choeropsis liberiensis (Artiodactyla: Hippopotamidae)
Fig. 4.—An adult female Choeropsis liberiensis in Taï National Park, Côte d'Ivoire. Image used with permission of the photographer, Mark-Oliver Rödel, Museum für Naturkunde, Berlin, Germany.
Fig. 3 in Choeropsis liberiensis (Artiodactyla: Hippopotamidae)
Fig. 3.—Geographic distribution of Choeropsis liberiensis and C. heslopi. Map prepared by Flora Ihlow, Zoological Research Museum Alexander Koenig, based on International Union for Conservation of Nature and Natural Resources Red List map data (Ransom et al. 2015).
Fig. 2 in Kobus vardonii (Artiodactyla: Bovidae)
Fig. 2.—Dorsal, ventral, and lateral views of skull and lateral view of mandible of an adult male Kobus vardonii (MfN [Museum für Naturkunde] Berlin, Germany, specimen ZMB_mam_68238) collected at "Sofi, Ulanga Plains" (today Sofi, Ulanga District, Morogoro Region, Tanzania) by Paul Fromm on 5 July 1908. Occipitonasal length is 305.2 mm. Photographs by Vera Rduch. Used with permission and under the copyright of the Museum für Naturkunde, Leibniz-Institut für Evolutions- und Biodiversitätsforschung, Invalidenstrasse 43, 10115 Berlin, Germany.
Fig. 2 in Choeropsis liberiensis (Artiodactyla: Hippopotamidae)
Fig. 2.—Dorsal, ventral, and lateral views of skull and lateral view of mandible of an adult female Choeropsis liberiensis (ZFMK [Zoological Research Museum Alexander Koenig] MAM 1965.0570) from Côte d'Ivoire. Greatest length of skull is 339 mm. Images used with permission of the photographer Georg Oleschinski.
Fig. 1 in Choeropsis liberiensis (Artiodactyla: Hippopotamidae)
Fig. 1.—An adult female Choeropsis liberiensis, at the Center for Conservation of Tropical Ungulates. Photo by Gabriella Flacke.
Fig. 3 in Beatragus hunteri (Artiodactyla: Bovidae)
Fig. 3.—Geographic distribution of Beatragus hunteri. The black outline represents estimated historical distribution (ca. 1886–1960s) and the solid black polygon represents known native distribution based on an aerial survey in May 1996. Information on Somalia range is not available for security reasons when the survey was conducted. Map adaptation drawn with information from Butynski (2000).
Fig. 2 in Beatragus hunteri (Artiodactyla: Bovidae)
Fig. 2.—Dorsal, ventral, and lateral views of skull and lateral view of mandible of an adult male Beatragus hunteri (Powell-Cotton Museum at Quex Park, specimen NH.SOM2.2). Collected 10 miles north of Afmadow, Jubaland, Somalia 0°8′N, 41°55′E by Miss Diana PowellCotton on 12 April 1934. Occipitonasal length is 349 mm. Photographs are used with permission of the photographer Mr. H. Basford and are copyrighted under Powell-Cotton Museum, Birchington CT7 0BH, Kent, United Kingdom.
Fig. 1 in Beatragus hunteri (Artiodactyla: Bovidae)
Fig. 1.—An adult female Beatragus hunteri from the Ishaqbini Conservancy in Ijara, Kenya, August 2012. Used with permission of photographer A. H. Ali.
FIGURE 2 in Fleas (Insecta: Siphonaptera) with public health relevance in domestic pigs (Artiodactyla: Suidae) from Argentina
FIGURE 2. Geographical distribution in Argentina of Ctenocephalides felis felis (x) and Pulex irritans (●) (Lareschi et al. 2016): 1— Tucumán, 2—Santiago del Estero, 3—Gran Chaco, Chaco, 4—Los Yngleses, Buenos Aires, 5—Ajó, Buenos Aires, 6—La Pampa, 7—Orán (Isla de Cañas), Salta, 8—El Quebrachal, Salta, 9—Formosa, 10—Tucumán, 11—Chumbicha, Catamarca, 12—Quines, San Luis, 13—San Luis capital, 14—Las Catitas, Mendoza, 15—La Paz, Mendoza, 16—San Rafael, Mendoza, 17—Los Molles, Mendoza, 18-Malargüe, Mendoza, 19—Santa Eufemia, Córdoba, 20—Cañada Mariano, Buenos Aires, 21—Ajó (General Lavalle), Buenos Aires, 22—Bahía Blanca, Buenos Aires, 23—Pilcaniyeu, Río Negro, 24—Lago Epuyén, Chubut.
FIGURE 1. Locations and pig production. A in Fleas (Insecta: Siphonaptera) with public health relevance in domestic pigs (Artiodactyla: Suidae) from Argentina
FIGURE 1. Locations and pig production. A) Geographical locations of the studied farms: 1—Mariano Benítez (33°42'43"S; 60°35'16"W), 2—Ayerza (33°50'17"S; 60°34'48"W), 3—Fontezuela (33°57'37"S; 60°28'34"W), 4—Pinzon (33°59'22"S; 60°45'21"W), 5—Junín (34°34'10"S 60°57'35"W), 6—General Viamonte (34°56′00″S; 61°10′00″W), and 7—Azul (36°45'03.3"S; 59°53'38.8"W). B) Illustrative images of extensive production system "to field", in farms from Buenos Aires Province.
Fig. 1. Artiodactyla from Mahmutgazi. A-L – Samotherium major. A in Late Miocene large mammals from Mahmutgazi, Denizli province, Western Turkey
Fig. 1. Artiodactyla from Mahmutgazi. A-L – Samotherium major. A: left mandible Ma3 (A1: occlusal view; A2: lateral view of the rostral part). B, maxilla with P3-M2 Ma2-Gips29. C-D: tibiae in anterior view (C: MA2-Gips16; D: Ma2- Gips11). E: distal humerus n°54, anterior view. F-H: metacarpals in anterior view (F: Ma2-Gips17; G, H: Ma2-Gips20). I: cubonavicular Ma1-Gips10, distal view, to show the absence of plantar metatarsal facet. J: astragalus Ma1-Gips10, anterior view. K: upper deciduous tooth-row Ma1-Gips3. L: lower dp3-dp4 Ma1-Gips11. M – Tragoportax sp., right upper tooth row. N: Miotragocerus (Pikermicerus) gaudryi, left lower tooth-row. Scale bar = 5 cm for Figs. M, N, 10 cm for Figs. A, B, and I-L, 25 cm for Figs. C-H.
Fig. 1. Artiodactyla from Mahmutgazi. A-L – Samotherium major. A in Late Miocene large mammals from Mahmutgazi, Denizli province, Western Turkey
Fig. 1. Artiodactyla from Mahmutgazi. A-L – Samotherium major. A: left mandible Ma3 (A1: occlusal view; A2: lateral view of the rostral part). B, maxilla with P3-M2 Ma2-Gips29. C-D: tibiae in anterior view (C: MA2-Gips16; D: Ma2- Gips11). E: distal humerus n°54, anterior view. F-H: metacarpals in anterior view (F: Ma2-Gips17; G, H: Ma2-Gips20). I: cubonavicular Ma1-Gips10, distal view, to show the absence of plantar metatarsal facet. J: astragalus Ma1-Gips10, anterior view. K: upper deciduous tooth-row Ma1-Gips3. L: lower dp3-dp4 Ma1-Gips11. M – Tragoportax sp., right upper tooth row. N: Miotragocerus (Pikermicerus) gaudryi, left lower tooth-row. Scale bar = 5 cm for Figs. M, N, 10 cm for Figs. A, B, and I-L, 25 cm for Figs. C-H.
Fig. 3 in A phylogeographic framework for the conservation of Saharan and Arabian Dorcas gazelles (Artiodactyla: Bovidae)
Fig. 3 Statistical parsimony network based on (a) a 412 bp fragment (73 sequences) and (b) the complete cytochrome b gene (57 sequences). Each circle represents a different haplotype, whereby circle size is proportional to the number of individuals in our data set
Fig. 2 in A phylogeographic framework for the conservation of Saharan and Arabian Dorcas gazelles (Artiodactyla: Bovidae)
Fig. 2 Phylogeny based on the complete cytochrome b gene, Bayesian analyses of 83 sequences under the GTR + Γ + I parameters. Posterior probability values larger than 0.9 are reported. Dorcas gazelles are gray shaded except for one presumed G. dorcas sample
TABLE 2 in Systematic revision of the family Hoplitomerycidae Leinders, 1984 (Artiodactyla: Cervoidea), with the description of a new genus and four new species
<p><b>TABLE 2.</b> Dental measurements (L=length, W=width; in mm) of the mandibular (above) and maxillar fragments (below) from Scontrone, mandibular premolar/molar ratio and body mass estimation (BM in kg) based on lower molar row length after Damuth (1990) for selenodont browsers. * alveolar measurements. The specimens are sorted according to increasing size. Dental measurements from Mazza & Rustioni (2011, 1999, 1996).</p><table><tbody><tr><th>Mandible fragments</th><th>species</th><th>Lp2–m3</th><th>Lm1–m3</th><th>Lm1 / Wm1 Lm2 / Wm2</th><th>Lm3 / Wm3</th><th>p/m ratio</th><th>BM</th></tr></tbody><tbody><tr><th>SCT88</th><td><i>S. apulicus</i></td><td>53.9</td><td>35</td><td>10.2 / 7 11.6 / 7.7</td><td>14.7 / 7.8</td><td>0.54*</td><td>18.2</td></tr><tr><th>SCT77</th><td><i>S. minutus</i></td><td>-</td><td>36.7</td><td>10.3 / 7 11.8 / 8</td><td>16.1 / 8</td><td>-</td><td>21.3</td></tr><tr><th>SCT76</th><td><i>S. apulicus</i></td><td>-</td><td>36.9</td><td>10.6 / - 11.3 / -</td><td>14.3 / -</td><td>-</td><td>21.7</td></tr><tr><th>SCT177</th><td><i>S. falcidens</i></td><td>56.8</td><td>38.4</td><td>10.1 / 8.2 8.3 / 7*</td><td>13.8 / 6.1*</td><td>0.48</td><td>24.8</td></tr><tr><th>SCT60</th><td><i>S. minutus</i></td><td>-</td><td>38.9</td><td>10.4 / 6.8 11.7 / 7.6</td><td>16.3 / 7.8</td><td>-</td><td></td></tr><tr><th>SCT155</th><td><i>S. minutus</i></td><td>58</td><td>39</td><td>10.2 / 6.4 11.9 / 8.2</td><td>17.2 / 8.6</td><td>0.48</td><td>26.2</td></tr><tr><th>SCT72</th><td><i>S. mazzai</i></td><td>-</td><td>-</td><td>- -</td><td>17.6 / 9.3</td><td>-</td><td></td></tr><tr><th>SCT50</th><td><i>S. apruthiensis</i></td><td>-</td><td>40.3</td><td>10.2 / - 12.5 / 7.7</td><td>18.1 / 7.8</td><td>-</td><td>29.2</td></tr><tr><th>SCT51</th><td><i>S. apruthiensis</i></td><td>-</td><td>-</td><td>10.9 / 8? -</td><td>-</td><td>-</td><td></td></tr><tr><th>SCT16</th><td><i>S. apruthiensis</i></td><td>-</td><td>41.5</td><td>11.5 / - 12 / -</td><td>18 / -</td><td>-</td><td>32.3</td></tr><tr><th>SCT81</th><td><i>S. apruthiensis</i></td><td>-</td><td>41.9</td><td>11.7 / 9.7 12.3 / 10.1</td><td>18.7 / 9.6</td><td>-</td><td>33.3</td></tr><tr><th>SCT102</th><td><i>S. apruthiensis</i></td><td>-</td><td>42.7</td><td>10.5 / 7.6 12.7 / 8.8</td><td>19.5 / 7.9</td><td>-</td><td>35.6</td></tr><tr><th>SCT29</th><td><i>S. apruthiensis</i></td><td>-</td><td>43.4</td><td>10.8 / 7.2 13.1 / 7.5</td><td>19 / 7.5</td><td>-</td><td>37.6</td></tr><tr><th>SCT71</th><td><i>S. apruthiensis</i></td><td>-</td><td>-</td><td>- -</td><td>19.6 / 8</td><td>-</td><td>-</td></tr><tr><th>SCT58+SC T67</th><td><i>S. apruthiensis</i></td><td>-</td><td>-</td><td>- 14.0 / 7.9</td><td>-</td><td>-</td><td>-</td></tr><tr><th>SCT89</th><td><i>S. apruthiensis</i></td><td>-</td><td>-</td><td>12.2 / 7.1 14.1 / 7.3</td><td>-</td><td>-</td><td>-</td></tr><tr><th>SCT20</th><td><i>S. magnus</i></td><td>-</td><td>47.8</td><td>15 / 9.6 15.5 / 9.7</td><td>20 / 10.1</td><td>-</td><td>52.1</td></tr><tr><th>SCT80</th><td><i>S. mazzai</i></td><td>-</td><td>-</td><td>- -</td><td>20.1</td><td>-</td><td></td></tr><tr><th>Maxilla fragments</th><td></td><td>LM1 / WM1</td><td>LM2 / WM2</td><td>LM3 / WM3</td><td></td><td></td><td></td></tr><tr><th>SCT70</th><td><i>S. falcidens</i></td><td>-</td><td>9.3 / 11.5</td><td>11.2 / 10</td><td></td><td></td><td></td></tr><tr><th>SCT59</th><td><i>S. apruthiensis</i></td><td>10.3 / 11.9</td><td>13 / 12</td><td>15.8 / -</td><td></td><td></td><td></td></tr><tr><th>SCT86</th><td><i>S. magnus</i></td><td>15.2 / 16.5</td><td>-</td><td>-</td><td></td><td></td><td></td></tr><tr><th>SCT18</th><td><i>S. magnus</i></td><td>16.1 / -</td><td>13.3 / -</td><td>-</td><td></td><td></td><td></td></tr></tbody></table>
Figure 2 in Global phylogeography of the genus Capreolus (Artiodactyla: Cervidae), a Palaearctic meso-mammal
Figure 2. Phylogeny of Capreolus obtained from the Bayesian analysis of 54 mtDNA haplotypes (925 nt) under the TIM3 model of sequence evolution. Branch length units are expected substitutions per site. Bayesian posterior probability and bootstrap values for NJ, MP and ML, respectively, are shown for the main haplogroups (inner nodes) shared by all trees. Only values over 50% are indicated. A mitochondrial CR sequence of Cervus elaphus was used as an outgroup.
Figure 1. Distribution ranges for C. capreolus and C in Global phylogeography of the genus Capreolus (Artiodactyla: Cervidae), a Palaearctic meso-mammal
Figure 1. Distribution ranges for C. capreolus and C. pygargus, and the area of putative current sympatry between the rivers Volga and Don (Hewison & Danilkin, 2001). The question mark indicates the area of further putative presence of C. pygargus. Collection sites are as follows: (FRA) France, (SWE) Sweden, (DEN) Denmark, (AUS) Austria, (ITA) Central-southern Italy, (E-AL) Eastern Italian Alps, (N-SP) Northern Spain, (CS-SP) Central-southern Spain, (GRE) Greece, (ROM) Romania, (POL) Poland, (LIT) Lithuania, (CRI) Crimea, (W-RUS) Western Russia, (KYR) Kyrgyzstan, (NE-CH) North-eastern China, (CE-CH) Central-eastern China, (E-RUS) Eastern Russia. Multiple sampling sites for one population are indicated by the same acronym. See Table 1 for details on precise sampling locations and sample sizes.
Figure 3 in Global phylogeography of the genus Capreolus (Artiodactyla: Cervidae), a Palaearctic meso-mammal
Figure 3. Median-joining network based on the data set of C. capreolus and C. pygargus haplotypes. Branch lengths are approximately scaled to the number of nucleotide substitutions occurring along the branches. White circles represent missing haplotypes. The main haplogroups are indicated by curved lines. The number of mutations are reported only for the main haplogroups.
Figure 3 in Evolution and functional morphology of the frontal sinuses in Bovidae (Mammalia: Artiodactyla), and implications for the evolution of cranial pneumaticity
Figure 3. Digital reconstructions and computed tomography (CT) slices of bovid skulls, illustrating the frontal sinuses and related anatomy, in Nanger granti (A–C; YPM 11526), Cephalophus leucogaster (D, F; AMNH 52802), and Raphicerus campestris (E, G; YPM 10276). In C, note the distinct frontal sinus that invades the trabecular bone, is bounded by cortical bone on all sides, and is distinctly separated from the olfactory turbinals below. This contrasts with the condition in E, in which a distinct recess above the olfactory turbinals is pressed into the frontal bone, but does not actually invade the trabecular bone. In D, no recess exists at all, and the space beneath the frontals is entirely occupied by turbinals. The dashed lines in A, F, and G indicate the approximate positions of the coronal CT slices in C, D, and E, respectively. The boxed areas in A and B indicate the region of the skull that has been rendered partially transparent in order to visualize the anatomy of the frontal sinuses. Scale bars: 5 cm.
Figure 6 in Evolution and functional morphology of the frontal sinuses in Bovidae (Mammalia: Artiodactyla), and implications for the evolution of cranial pneumaticity
Figure 6. Digital reconstructions from computed tomography (CT) scan data of the skulls of Bubalus depressicornis (A–B; AMNH 152684), Bison bison (C–D; YPM 9023), and Budorcas taxicolor (E–F; AMNH 110476), illustrating frontal sinuses and related anatomy. Skulls are shown in lateral (B, C, E) and dorsal (A, D, F) views. The boxed areas indicate the region of the skull that has been rendered partially transparent in order to visualize the anatomy of the frontal sinuses. The horns have been truncated in C–F. Scale bars: 5 cm.
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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.