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Figure 3 in A comparison between affiliative and agonistic behaviours in wild and captive Sapajus libidinosus (Spix, 1823) (Mammalia, Primates, Cebidae)
Figure 3. Relative frequency of social behaviours for each of the ten studied groups (BG = Baixa Grande; JB = Jurubeba; PF = Pedra Furada; OT = Oitenta; GT = Gato; FJZB = Fundação Jardim Zoológico de Brasília; PEDI = Parque Estadual Dois Irmãos; PZT2 = Parque Zoobotânico deTeresina (ilha 2); PZT3 = Parque Zoobotânico de Teresina (ilha 3); PZT1 = Parque Zoobotânico de Teresina (ilha 1). Under free-living conditions, agonistic behaviours were proportionally more frequent than were affiliative behaviours.
Figure 1 in Acoustic analysis of vocalization and the behavioral response associated to sound production of the nine banded armadillo Dasypus novemcinctus (Mammalia, Cingulata, Dasypodidae)
Figure 1. Oscillogram (top) and spectrogram (bottom) of the agonistic vocalizations of Dasypus novemcinctus, HCLP-S 1028, recorded from individual M1. (A) A single vocalization composed of the pattern A-I, A-I, B-I, B-II; (B) A single vocalization composed of the pattern A-I, A-II, B-I, A-II, B-I, B-II.
Figure 2. M1 in Acoustic analysis of vocalization and the behavioral response associated to sound production of the nine banded armadillo Dasypus novemcinctus (Mammalia, Cingulata, Dasypodidae)
Figure 2. M1 (marked with white tape at the middle of its moveable bands) Behavior (A) when cornered after being submitted to the presence of other male subject, (B) at a second moment, when the other animal approaches from its back, and then (C) M1 bends its body left to prevent the contact, with the other male scratching the basis of its tail. In (D) the other male bipedally projects its belly against M1's back, and the latter finally changes its position.
Figure 5 in Comparative morphology of tongue surface in Neotropical aerial insectivore bats (Mammalia: Chiroptera)
Figure 5. The tongue of Vespertilionoidea, family Natalidae, Natalus macrourus: (a) Apex covered by flaky-shaped filiform papillae; (b) Salience (arrow) on mid-dorsal region of the tongue; and (c) Posterior region of the tongue with three circumvallate papillae, one anterior (VA) and two posteriorly placed (VM) and pointed basal filiform papillae (B).
Figure 4 in Comparative morphology of tongue surface in Neotropical aerial insectivore bats (Mammalia: Chiroptera)
Figure 4. Tongues of Noctilionoidea, families Mormoopidae, Thyropteridae, and Furipteridae; (a) Oval and grooved fungiform (F) surrounded by crown filiform papillae (C) in Pteronotus rubiginosus; (b) Globular fungiform (F) surrounded by short and pointed strictly filiform papillae (FL) in Thyroptera wynneae; (c) Posterior region with large medial circumvallate with prominent sulcus (S) and surrounding integument (I), and triangular filiform papillae (T) in Furipterus horrens; and (d) Striclty filiform papillae at the apex in F. horrens.
Figure 3 in Comparative morphology of tongue surface in Neotropical aerial insectivore bats (Mammalia: Chiroptera)
Figure 3. Tongues of Emballonuridae (Emballonuroidea): (a) Circumvallate papillae (V) with the groove and surrounding incipient tegument and fungiform papillae (F) to the left of the circumvallate papillae in Peropteryx kappleri; (b) Lateral fungiform papillae (F) and low basal filiform papillae (B) in P. kappleri; (c) Strictly filiform papillae concentrically arranged at the middle region of the tongue in Rhynchonycteris naso; and (d) Bifid filiform tubular-shaped papillae at the apex in P. kappleri.
Figure 2 in Comparative morphology of tongue surface in Neotropical aerial insectivore bats (Mammalia: Chiroptera)
Figure 2. Types of lingual papillae observed in Neotropical aerial insectivore bats: (a) Circumvallate with remarkable sulcus and integument, surrounded by pointed basal filiform (arrows); (b) Fungiform with notable sulcus (arrow); (c) Bifid filiform; (d) Strictly filiform; (e) Flacky-like filiform, note the layered structure with dentate keratinous plates; (f) Giant filiform (center), note the bigger size than the surrounding papillae; (g) Digitiform filiform; (h) Crown-shaped filiform, note the bulbous base and delicate filamentous projections at the apical edge; (i) Scale-like filiform, note the rectangular-shaped and dorsally concave structure; and (j) Triangular filiform.
Figure 7 in Comparative morphology of tongue surface in Neotropical aerial insectivore bats (Mammalia: Chiroptera)
Figure 7. Constrained bat phylogeny and the fittest distribution of characters and their respective state (in parentheses).The coding of characters among the taxa is inTable 2.
Figure 1 in Comparative morphology of tongue surface in Neotropical aerial insectivore bats (Mammalia: Chiroptera)
Figure 1. Dorsal surface of the tongue showing the general division in three regions to facilitate the description and distribution of the papillae.
Figure 6 in Comparative morphology of tongue surface in Neotropical aerial insectivore bats (Mammalia: Chiroptera)
Figure 6. The tongue of Vespertilionoidea, family Vespertilionidae: (a) Posterior region of the tongue with a pair of circumvallate papillae (V) and the conical basal papillae (B) in Histiotus velatus. Note the naked central portion between circumvallate papillae and the glottis (G); (b) Middle portion of the tongue with remarkable salience covered by scale-like filiform papillae with large fungiform papillae in Eptesicus furinalis; (c) Circumvallate papilla, note the lobed surface of the papilla in Eptesicus brasiliensis; (d) Scale-like filiform papillae on the mid-dorsal salience in H. velatus.
Figure 1 in Bats (Mammalia, Chiroptera) from Yuscarán in Eastern Honduras: Conservation and acoustic characterization for the insectivorous species
Figure 1. Geographic location of the study sites in the Yuscarán Biological Reserve and Municipality of Yuscarán, Department of El Paraíso, Honduras, Central America. Geographic coordinates and other details are in Table 1.
Figure 4 in Bats (Mammalia, Chiroptera) from Yuscarán in Eastern Honduras: Conservation and acoustic characterization for the insectivorous species
Figure 4. Echolocation pulses of aerial insectivorous bats. Spectrograms (bottom) and oscillograms (top) correspond to search calls. X axis milliseconds (ms) and Y axis Kilohertz (kHz). Emballonuridae: (BPl) B. plicata, (PMA) P. macrotis; Molossidae: (MAL) M. alvarezi, (MNI) M. nigricans, (MMO) M. molossus. Mormoopidae: (PFU) P. fulvus, (PGY) P. gymnonotus, (PME) P. mesoamericanus, (PPS) P. psilotis. Vespertilionidae: (NIG) M. nigricans, (BRA) E. brasiliensis, (FUR) E. furinalis, (FUS) E. fuscus.
Figure 3 in Bats (Mammalia, Chiroptera) from Yuscarán in Eastern Honduras: Conservation and acoustic characterization for the insectivorous species
Figure 3. Part of the bat species captured with mist nets, in the Yuscarán Biological Reserve and Municipality of Yuscarán, Department of El Paraíso, Honduras, Central America. (A) M. megalophylla; (B) D. rotundus; (C) L. aurita; (D) P. discolor; (E) A. geoffroyi; (F) G. leachii; (G) G. mutica; (H) C. perspicillata; (I) A. jamaicensis; (J) A. lituratus; (K) C. salvini; (L) D. azteca; (M) D. phaeotis; (N) S. hondurensis; (O) S. parvidens; (P) E. fuscus. Photos: (C) D.J.M.Q.; (A-P) W.N.G.C.
Figure 2 in Bats (Mammalia, Chiroptera) from Yuscarán in Eastern Honduras: Conservation and acoustic characterization for the insectivorous species
Figure 2. Species accumulation curve using mist nets, in the Yuscarán Biological Reserve and Municipality of Yuscarán, Department of El Paraíso, Honduras, Central America.
Figure 1 in Characterization of shelters of the giant otter (Pteronura brasiliensis, Mammalia, Carnivora, Mustelidae) in the pantanal wetlands, state of Mato Grosso, Brazil
Figure 1. Demarcation of shelters (dens and campsites) and latrines of giant otter in Espírito Santo Creek, Natural Heritage Private Reserve, SESC Pantanal, municipality of Barão de Melgaço, northern portion of Pantanal, state of Mato Grosso, Brazil.
FIGURE 3. A in Distinguishing between three modern Ellobius species (Rodentia, Mammalia) and identification of fossil Ellobius from Kaldar Cave (Iran) using geometric morphometric analyses of the first lower molar
FIGURE 3. A) Kaldar Cave location. B) Entrance from the south of Kaldar Cave.
Figure 2 in First occurrence of Duboisia (Bovidae, Artiodactyla, Mammalia) from Thailand
Figure 2. Posterior view (right side) of PPN 01-000109 before preparation.
Fig. 6 in Morphometric And Biochemical Variation And The Distribution Of The Genus Apodemus (Mammalia: Rodentia) In Turkey
Fig. 6. Genetic relationship of Apodemus species based on Nei genetic distance of 10 enzyme loci
Fig. 5 in Morphometric And Biochemical Variation And The Distribution Of The Genus Apodemus (Mammalia: Rodentia) In Turkey
Fig. 5. Morphometric relationship of six Apodemus species based on Mahalanobis distance
Fig. 3. A in Morphometric And Biochemical Variation And The Distribution Of The Genus Apodemus (Mammalia: Rodentia) In Turkey
Fig. 3. A scatterplot of six Apodemus species based on DFA of the Mosiman adjusted data matrix
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.