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858 results for “Carnivore”
Fig. 5 in Morphological disparity in Plio-Pleistocene large carnivore guilds from Italian peninsula
Fig. 5. Disparity values computed for morphospace of each extant and Plio−Pleistocene large carnivore guild. Lines define 95% confidence interval under 999 randomizations. Extant is for all living taxa (N = 34) while Plio−Pleistocene stand for all fossil taxa (N = 23). Kruger, Africa is for Africa, Gunung Lensung, Indonesia for Indonesia, Otishi for South America,, Yellowstone for North America, Krokonose for Czech Republic. Fossil communities are ordered from the youngest to the oldest: Aurelian, 0.3 Ma; Galerian 3, 0.45 Ma; Galerian 2, 0.6 Ma; Galerian 1, 0.8 Ma; Pirro, 1.1 Ma; Valdi− Chiana, 1.5 Ma; Up Valdarno, 1.9 Ma; Montopoli, 2.6 Ma; Triversa, 3.2 Ma.
Fig. 3 in Morphological disparity in Plio-Pleistocene large carnivore guilds from Italian peninsula
Fig. 3. Scatter plots of RW1 (X axis, scale −0.40 / +0.40) versus RW2 (Y axis, scale −0.40 / +0.40). Each extant large carnivore guild is highlighted by closed circles. The Kruger, Africa guild represents Africa, Krokonose is for Czech Republic, Gunung Lensung, Indonesia Lensung for Indonesia, Otishi for South America and Yellowstone for North America.
Fig. 4 in Morphological disparity in Plio-Pleistocene large carnivore guilds from Italian peninsula
Fig. 4. Scatter plots of RW1 (X axis, scale −0.40 / +0.40) versus RW2 (Y axis, scale −0.40 / +0.40). Each Plio−Pleistocene carnivore guild is highlighted by closed circles. Guild are representative of distinct Paleo−Communities trough time: Triversa, 3.2 Ma; Montopoli, 2.6 Ma; Up Valdarno, 1.9 Ma; ValdiChiana, 1.5 Ma; Pirro, 1.1 Ma; Galerian 1, 0.8 Ma; Galerian 2, 0.6 Ma; Galerian 3, 0.45 Ma; and Aurelian, 0.3 Ma.
Fig. 6 in Morphological disparity in Plio-Pleistocene large carnivore guilds from Italian peninsula
Fig. 6. Scatter plot of log number of artiodactyls vs. large carnivore disparity values. Open circles, extant ecosystems; closed, fossil ecosystems. A linear trendline is placed on extant data points. Open circles represent extant ecosystem including Kruger, Africa, Africa; Gunung Lensung, Indonesia Lensung, Indonesia; Otishi, South America; Yellowstone, North America; Krokonose, Czech Republic. Closed circles are fossil communities: Triversa, 3.2 Ma; Montopoli, 2.6 Ma; Up Valdarno, 1.9 Ma; Valdi− Chiana, 1.5 Ma; Pirro, 1.1 Ma; Galerian 1, 0.8 Ma; Galerian 2, 0.6 Ma; Galerian 3, 0.45 Ma; and Aurelian, 0.3 Ma.
Fig. 2 in Factors influencing Dipylidium sp. infection in a free-ranging social carnivore, the spotted hyaena (Crocuta crocuta)
Fig. 2. The effect of prey abundance in spotted hyaena clan territories on the proportion of juveniles infected with Dipylidium sp.
Fig. 1 in Factors influencing Dipylidium sp. infection in a free-ranging social carnivore, the spotted hyaena (Crocuta crocuta)
Fig. 1. (a) A spotted hyaena communal den. (b) Dipylidium sp. egg capsule obtained from a gravid proglottid collected from a spotted hyaena faeces. (c) Spotted hyaena faeces with Dipylidium proglottids present on the surface.
Fig. 1 in High Trypanosoma cruzi infection prevalence associated with minimal cardiac pathology among wild carnivores in central Texas
Fig. 1. Spatial occurrence and distribution of T. cruzi infected, hunter-harvested wildlife, 2014. Number of infected over total number of that species tested are shown by county.
Fig. 2 in Prevalence of Capillaria plica in Danish wild carnivores
Fig. 2. The prevalence of Capillaria plica infections in red foxes per region of Denmark (positive red foxes/total number of red foxes examined). The origin of five red foxes was unknown.
Fig. 1. A in Prevalence of Capillaria plica in Danish wild carnivores
Fig. 1. A typical barrel-shaped Capillaria plica egg in urine sediment from a red fox. The egg show a slightly pitted shell and two opercules with polar plugs. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Functional plasticity in vertebrate scavenger assemblages in the presence of introduced carnivores
<p>Data for manuscript focusing on the consumption of varying amounts of carrion by coastal scavengers in Queensland, Australia. </p>
Review of Recent Trends in Measuring the Computing Systems Intelligence-Figure 1. Intelligence of different simple living creature (accessed 01.11.2017). 1.1. A carnivorous plants catching an insect (https://phys.org/news/2016-05-colombia-peace-reveal-jungle-species.html); 1.2. A colony of ants solving a very complex task (https://mappingignorance.org/2016/05/27/rafting-ants); 1.3. The collective behaviour of a school of fish (https://simple.wikipedia.org/wiki/Shoaling_and_schooling)
<p>The biological intelligence of different life forms, ranging from very simple (such as plants) to very complex (such as humans) is the subject of many studies and a large amount of research. Frequent studies related to different kind of biological intelligence include: the intelligence of horses (Krueger, & Heinze, 2008; Krueger, Farmer, & Heinze, 2014; Schuetz, Farmer, & Krueger, 2016), intelligence of pigs (Broom, Sena, & Moynihan, 2009), intelligence of dogs (Coren, 1995), intelligence of primates (Reader, Hager, & Laland, 2011) and so one. Figures 1, 2, and 3 present some biological life forms that are frequently considered intelligent. Trewavas (2002; 2005) considered that plants intelligence should be based on principles such as their ability to adjust their morphology, and phenotype accordingly to ensure self- preservation and reproduction. Figure 1.1 presents an intelligent plant (carnivorous) that uses a strategy for catching very fast flying insects. In order to eat the insect, it makes a movement. Figure 1.1 presents the catching of an insect by a carnivorous plant. The intelligence of colonies of ants, termites and other insects that live in large colonies is considered at the colony level (Brady, Fisher, Schultz, & Ward, 2014; Johnson, Borowiec, Chiu, Lee, Atallah, & Ward, 2013). Figure 1.2 presents the coherent intelligent surviving behaviour of a colony of a species of ants. The ants make a structural reorganization in order to move on the surface of the water. Figure 1.3 presents a very large school of fish with an intelligent coherent collective feeding and self-protecting behaviour. Each individual fish has a very simple behavior. Based on this it cannot be considered intelligent. The intelligence in large schools of fish emerges at the collective level (Shaw, 1978; Parrish, Viscedo, & Grunbaum, 2002).</p>
RESTORATION OF TYRANNOSAURUS REX. From the type skeleton, Amer. Mus. No. 973. Many of the vertebrae belong to No. 5866. in Tyrannosaurus, upper Cretaceous carnivorous dinosaur (second communication)
RESTORATION OF TYRANNOSAURUS REX. From the type skeleton, Amer. Mus. No. 973. Many of the vertebrae belong to No. 5866.
Plate 4 in A new carnivorous dinosaur from the Lance Formation of Montana
Plate 4 Comparison of Gorgosaurus skulls Fig. 1. Skull and jaws of Gorgosaurus lancensis. Type. C.M.N.H. No. 7541. Viewed from left side (reversed). Fig. 2. Skull and jaws of Gorgosaurus sternbergi. Type. A.M.N.H. No. 5664. Viewed from the left side. Fig. 3. Skull and jaws of Gorgosaurus libratus. A.M.N.H. No. 5434. Viewed from left side.
Plate 3 in A new carnivorous dinosaur from the Lance Formation of Montana
Plate 3 Skull and jaws of Gorgosaurus lancensis. Palatal view. Type. C.M.N.H. No. 7541. h, hyoid. About 1/4 natural size
Plate 2 in A new carnivorous dinosaur from the Lance Formation of Montana
Plate 2 Skull of Gorgosaurus lancensis viewed from above. Type. C.M.N.H. No. 7541. About 1/4 natural size.
Plate 1 in A new carnivorous dinosaur from the Lance Formation of Montana
Plate 1 Skull and jaws of Gorgosaurus lancensis viewed from the left side. Type. C.M.N.H. No. 7541. p, palatine; v, vomer. About 1/4 natural size
Fig. 8 in Tyrannosaurus, upper Cretaceous carnivorous dinosaur (second communication)
Fig. 8. Humerus of Tyrannosaurus. Amer. Mus. No. 972. To same scale as femur (Fig. 9). a, external view; b, posterior view.
Fig. 1 in Tyrannosaurus, upper Cretaceous carnivorous dinosaur (second communication)
Fig. 1. Skull of Tryrannosaurus. d, dentary; sur, surangular; sq, squamosal; prf,prefrontal; o, orbit; na, anterior nares; 1, 2, 3, antorbital openings. Dotted outlines are from Allosaurus.
Fig. 3 in Tyrannosaurus, upper Cretaceous carnivorous dinosaur (second communication)
Fig. 3. Cervical vertebrm of Tyrannosaurus.,Amer. Mus. No. 5866. hypocentrum of atlas; nph, neuropophysis; 2 supposed axis with its hypocentium; od, odontoid; 3, 9 remaining cervicals; r8, r9, ribs found attached to ribs, 8-9, 10-11, cervico-dorsals; c, capitular facet; t, tubercular facets.
Fig. 2 in Tyrannosaurus, upper Cretaceous carnivorous dinosaur (second communication)
Fig. 2. Skull of Allosaurus in the American Museum of Natural History. To same scale as the skull of Tyrannosaurus.
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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.