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48 results for “Antelope”
Developments in taxonomy could see safari hunters killing 25 types of antelope, instead of the previous 9, to achieve the 'spiral horned grand slam'. in Taxonomy anarchy hampers conservation
Developments in taxonomy could see safari hunters killing 25 types of antelope, instead of the previous 9, to achieve the 'spiral horned grand slam'.
Dataset: Antelope Enterprise Holdings Limited (AEHL) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
Dataset: Antelope Enterprise Holdings Limited (AEHL) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
Fig. 9 in Taxonomic re-assessment and phylogenetic relationships of Miocene homonymously spiral-horned antelopes
Fig. 9. Phylogenetic history of the subtribe Oiocerina at the species level (A) according to the results of the cladistic analysis (Fig. 6) and (B) assuming a morpho−chronological and regional continuum for Samotragus. Grey and white boxes indicate reliably known and questionable chrono−stratigraphic occurrences, respectively. Dashed lines indicate presumed ranges (vertical) or relationships (horizontal). Abbreviations: NKT, Nikiti−1; RZ1, Ravin de Zouaves 1.
Fig. 5. Oiocerin antelope Samotragus from Northern Greece. A, B, E in Taxonomic re-assessment and phylogenetic relationships of Miocene homonymously spiral-horned antelopes
Fig. 5. Oiocerin antelope Samotragus from Northern Greece. A, B, E. Samotragus praecursor Bouvrain and Bonis, 1985 from Ravin de la Pluie (RPl), Axios Valley, late Vallesian (Late Miocene). A. LGPUT RPl−105n, cranium in dorsal (A1) and lateral (A2) views. B. LGPUT RPl−480, holotype cranium in lateral view. E. LGPUT RPl−37, left horncore in lateral view. C, D. Samotragus cf. praecursor Bouvrain and Bonis, 1985 from Ravin des Zouaves 1 (RZ1), Axios Valley, late Vallesian (Late Miocene). C. LGPUT RZ1−11, left horncore in anterior (C1) and lateral (C2) views. D. LGPUT RZ1−17 left horncore in anterior (D1) and lateral (D2) views.
Fig. 3 in Taxonomic re-assessment and phylogenetic relationships of Miocene homonymously spiral-horned antelopes
Fig. 3. Oiocerin antelope Hispanodorcas cf. orientalis Bouvrain and Bonis, 1988 from Nikiti−1 (NKT), Chalkidiki Peninsula, Northern Greece, latest Vallesian. A. LGPUT NKT−231, lateral view of the right basal horncore. B. LGPUT NKT−227, left lateral (B1) and anterior (B2) views of the frontlet. C. LGPUT NKT−232, lateral view of the left distal horncore. The arrow indicates the distal end of the lateral depression and marks the distal "bilobation" of the lateral side of the horncore.
Fig. 8 in Taxonomic re-assessment and phylogenetic relationships of Miocene homonymously spiral-horned antelopes
Fig. 8. Time range, geographic distribution, ecological features, and paleoenvironment of several members of the Oiocerina. Abbreviations: V, Vallesian; T, Turolian; R, Ruscinian; O, open, I, intermediate, and C, closed environment; grass for grazing, scrub for mixed, and tree for browsing diets; sheep for ramming (rm), kudu for wrestling/pushing (ps), eland for wrestling/fencing (fc), and dik−dik for stabbing (st) fighting style (some drawings adopted from Lundrigan 1996).
Fig. 7 in Taxonomic re-assessment and phylogenetic relationships of Miocene homonymously spiral-horned antelopes
Fig. 7. Drawings of the horncores of several Oiocerina in right lateral view, showing the main shared characters. A.?Hispanodorcas pilgrimi from Toril−3, Spain. B. Hispanodorcas orientalis from Dytiko−3, Greece. C. Urmiatherium rugosifrons from Samos (Greece) and Turkey, adult (C1) and juvenile (C2) individual. D. Samotragus crassicornis from Samos, Greece. E. Oioceros rothii (combination of Pikermi, Greece and Maragheh, Iran specimens). F. Urmiatherium polaki from Maragheh, Iran. G. Samotragus cf. praecursor from Ravin des Zouaves 1 (G1) and Samotragus praecursor from Ravin de la Pluie, Greece (G2). H. Paraoioceros wegneri from Samos, Greece.
Fig. 6. Cladograms showing the evolutionary relationships within Oiocerina. A in Taxonomic re-assessment and phylogenetic relationships of Miocene homonymously spiral-horned antelopes
Fig. 6. Cladograms showing the evolutionary relationships within Oiocerina. A. Intrageneric relationships (rooted to Eotragus Pilgrim, 1939), based on available morphological and zoogeographic evidence (see text). B. 75% majority−rule consensus of the four most parsimonious trees (length: 172; CI: 0.46; RI: 0.65) showing the relationships of eight fossil genera of Oiocerina, Gazella Blainville, 1816, Ovibos Blainville, 1816, Hemitragus Smith, 1826, and Turcocerus Köhler, 1987, based on the character matrix of Appendix 1. Outgroup: Eotragus Pilgrim, 1939. Synapomorphies supporting nodes (marked with bold letters) are discussed in the text.
Fig. 2 in Taxonomic re-assessment and phylogenetic relationships of Miocene homonymously spiral-horned antelopes
Fig. 2. Oiocerin antelope Hispanodorcas orientalis Bouvrain and Bonis, 1988, from the late Turolian locality of Dytiko−3 (DKO), Axios Valley, Northern Greece, in lateral (A) and anterior (B) views of the holotype cranium LGPUT DKO−4. The arrow in A indicates an enlarged version of the same view, where the white lines indicate the extent of the lateral depression; the arrows in B mark the trace of the anterior keel.
Fig. 1 in Taxonomic re-assessment and phylogenetic relationships of Miocene homonymously spiral-horned antelopes
Fig. 1. Box−plots of the horncore basal compression index (i.e., TD*100/ ADP) for several species and genera of Oiocerina, showing the medial (horizontal line inside the boxes), the 25–75% quartiles (gray boxes) and the minimum and maximum range of values (short horizontal lines). NKT−1, Nikiti−1; RZ1, Ravin des Zouaves 1.
Fig. 4 in Molecular screening for rickettsial bacteria and piroplasms in ixodid ticks surveyed from white-tailed deer (Odocoileus virginianus) and nilgai antelope (Boselaphus tragocamelus) in southern Texas
Fig. 4. Phylogentic analysis of sca0 (rompA) sequences from putative Rickettsia sp. endosymbionts of Amblyomma maculatum and Ixodes scapularis ticks collected from white-tailed deer in southern Texas. This is a maximum-likelihood tree that is rooted at midpoint. Branch support was assessed with 10,000 replicates of UFBoot bootstrap replication, and bootstrap percentages are indicated at each branch point in the tree. Sequences from GenBank used in the comparative analysis were annotated as rickettsial endosymbionts. Accession numbers and tick species from which sequence was identified are included on the branch label.
Fig. 3 in Molecular screening for rickettsial bacteria and piroplasms in ixodid ticks surveyed from white-tailed deer (Odocoileus virginianus) and nilgai antelope (Boselaphus tragocamelus) in southern Texas
Fig. 3. Phylogentic analysis of Theileria sp. fragments from Anocenter nitens ticks. Representative Type F, Type G, and 'divergent' Theileria sp. sequences were identified from individual A. nitens ticks collected from white-tailed deer and a single nilgai host (bold labels). A maximum-likelihood tree was constructed using Toxoplasma gondii as the outgroup, as it is from a different axpicomplexan class than Theileria. Branch support was assessed with 10,000 replicates of UFBoot bootstrap replication, and bootstrap percentages are indicated at each branch point in the tree. GenBank accession numbers and annotated identification for sequences used in the comparative analysis are indicated on the branch labels. Accession numbers in italics are those T. cervi sequences from white-tailed deer on the East Foundation's San Antonio Viejo Ranch in Starr and Jim Hogg Counties, Texas (Yu et al., 2020).
Fig. 1 in A survey of the parasites of Ural saiga antelopes and Turkmenian kulans of Kazakhstan
Fig. 1. Map of Altyn-Emel National Park, with kulan faecal sample collection locations represented as red diamonds (June–August 2021). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in A survey of the parasites of Ural saiga antelopes and Turkmenian kulans of Kazakhstan
Fig. 2. Map of the Ural saigas antelopes' distribution range, with study location enlarged. Arrows represent migration direction, while the blue circle represents rutting location, and the red square represents calving location. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in Molecular evaluation of Eimeria spp. Infection in the Volga-Ural Saiga antelope population of the Republic of Kazakhstan
Fig. 3. Phylogenetic tree generated by the Maximum Composite Likelihood (MCL) method using partial sequences of the 18S rRNA of the Eimeria species that infect the Saiga tatarica.
Fig. 2 in Molecular evaluation of Eimeria spp. Infection in the Volga-Ural Saiga antelope population of the Republic of Kazakhstan
Fig. 2. Eimeria spp. Oocyst at 40x magnification. The outer (OL) and the inner (IL) layers of the oocyst wall, micropyle (M), micropyle cap (MC), spores (S).
Fig. 1 in Molecular evaluation of Eimeria spp. Infection in the Volga-Ural Saiga antelope population of the Republic of Kazakhstan
Fig. 1. Photomicroscope images showing the oocysts of E. elegans (40х magnification). The outer (OL) and the inner (IL) layers of the oocyst wall, cytoplasmic mass (CM), micropyle (M).
Data from: Experimental defaunation alters foraging behavior of a small antelope in Kenya
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Shipwreck Antelope
The Antelope was built as a steamer and converted to a schooner barge in 1888. It was under tow of the Hiram Sibley enroute to Ashland WI when it sprang a leak and sank off Michigan Island in 320 ft of water. It was found in 2016 by Jerry Eliason and Ken Merryman. The model is a Maya digital model and accurate representation of the site. Source: Objaverse 1.0 / Sketchfab
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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.