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116 results for “ape”

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dryad36/100

OpenApePose: a database of annotated ape photographs for pose estimation

Open the record for dataset details and reuse information.

publicAug 2023View details →
dryad36/100

Data from: Downclimbing and the evolution of ape forelimb morphologies

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publicAug 2023View details →
dryad36/100

Brevity is not a universal in animal communication: evidence for compression depends on the unit of analysis in small ape vocalizations

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publicApr 2020View details →
dryad36/100

Data for: Multiple mechanisms for inbreeding avoidance used simultaneously in a wild ape

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publicSep 2023View details →
zenodo32/100

From smart apes to human brain boxes. A uniquely derived brain shape in late hominins clade: supplementary material

<p>DATA.rda: an RData file containing the phylogenetic tree, the landmark and semilandmark sets used in the analyses of the endocast shape (123 specimens), the semilandmark sets used in the asymmetry analyses (120 specimens), the vector of the corresponding ECV values and a mesh containing the triangulated semilandmark configuration.</p> <p>script.R: the annotated script used to replicate the analyses reported in this study.</p>

opencc-by-4.0May 2020View details →
zenodo32/100

FIGURE 4. Palapedia apeli n in Two new species of Palapedia Ng, 1993 (Crustacea, Decapoda, Brachyura, Xanthidae) from the Persian Gulf

FIGURE 4. Palapedia apeli n. sp. Male holotype (ZMUC CRU-945)), CL = 13.41, CB =15.14 mm: (a) posterior surface of carapace; (b) third maxilliped, outer surface; (c) last ambulatory leg, left; (d) large cheliped, outer surface; (f) small cheliped, outer surface.

opennotspecifiedDec 2015View details →
zenodo32/100

Fig. 5 in Miocene small-bodied ape from Eurasia sheds light on hominoid evolution

Fig. 5. Forelimb long bones. Shown are the humerus, radius, and ulna of the holotype (IPS58443) of Pliobates cataloniae gen. et sp. nov. (A to E) Partial left humerus in medial (A), posterior (B), lateral (C), anterior (D), and distal (E) views. (F to K) Left radius in medial (F), posterior (G), lateral (H), anterior (I), proximal (J), and distal (K) views. (L to O) Proximal half of the left ulna in medial (L), posterior (M), lateral (N), and anterior (O) views. (P to T) Distal fragment of the left ulna in medial (P), posterior (Q), lateral (R), anterior (S), and distal (T) views.

opennotspecifiedDec 2015View details →
zenodo32/100

Fig. 1 in Miocene small-bodied ape from Eurasia sheds light on hominoid evolution

Fig. 1. Cranium and dentition. (A to C) Cranium of the holotype (IPS58443) of Pliobates cataloniae gen. et sp. nov.The main cranial fragments, including the basicranium and the right palate, are shown in basal view (A); details of the right palatal fragment are shown in left-lateral (B) and right-lateral (C) views. (D) Detail of the right postcanine teeth, in occlusal view (mesial is to the right).

opennotspecifiedDec 2015View details →
zenodo32/100

Fig. 4 in Miocene small-bodied ape from Eurasia sheds light on hominoid evolution

Fig. 4. Basicranial morphology. (A) Drawing of the left basicranium of the holotype (IPS58443) of Pliobates cataloniae gen. et sp. nov., as preserved in ventral view.The jugular foramen appears artifactually larger because of the displacement of the temporal and occipital portions along the occipitotemporal suture (corrected in the reconstruction in Fig. 3). The course of the carotid canal is shown with a dashed line, based on CT images. AE, articular eminence; CAF, carotid foramen; COF, condylar fossa; EA, Eustachian aperture; EAM, external auditory meatus; EP, Eustachian process; ET, ectotympanic; FM, foramen magnum; FO, foramen ovale; GF, glenoid fossa; JF, jugular foramen; OC, occipital condyle; OTS, occipitotemporal suture; PGP, postglenoid process. (B to D) Drawings of comparable views (not to scale) in Hylobates sp. (B), Proconsul heseloni KNM RU 2036 [(C), reversed], and Victoriapithecus macinnesi KNM MB 29100a (D) (KNM, Kenyon National Museums; RU, Rusinga; MB, Maboko). Arrows denote the V-shaped, incompletely ossified ventral terminal tip of the tubular ectotympanic in the extinct taxa. [Artwork by M. Palmero]

opennotspecifiedDec 2015View details →
zenodo32/100

Fig. 7 in Miocene small-bodied ape from Eurasia sheds light on hominoid evolution

Fig. 7. Carpal bones. Line drawings of carpal bones in Pliobates cata- loniae gen. et sp. nov. (IPS58443) are shown with those of selected anthropoid genera for comparison. (A to E) Left capitate, in radial (top) and proximal (bottom) views, of Cer- copithecus aethiops (A), Ateles paniscus (B), Pierolapithecus cat- alaunicus (C), Hylobates lar (D), and P. cataloniae (E); gray shading denotes articular areas for the second metacar- pals, and cross-hatching denotes those for the third metacarpal. (F to J) Left hamate, in radial (top) and ulnar (bottom) views, of C. aethiops (F), A. paniscus (G), Pi. catalaunicus (H), H. lar (I), and P. catalo- niae (J). (K to O) Left triquetrum, in proximo- medial (top) and distal (bottom) views, of C. aethiops (K), A. paniscus (L), Pi. catalaunicus (M), H. lar (N), and P. cataloniae (O). Drawings are not to scale.

opennotspecifiedDec 2015View details →
zenodo32/100

Fig. 3 in Miocene small-bodied ape from Eurasia sheds light on hominoid evolution

Fig. 3. Cranial reconstruction. Virtual reconstruction of the holotype (IPS58443) cranium of Pliobates cataloniae gen. et sp. nov., including mirrored fragments, in frontal (A), lateral (B), posterior (C), basal (D), and superior (E) views. Further details are given in fig. S3 and the methods in the text.

opennotspecifiedDec 2015View details →
zenodo32/100

Fig. 6 in Miocene small-bodied ape from Eurasia sheds light on hominoid evolution

Fig. 6. Elbow and wrist morphology. The most diagnostic features of the elbow and wrist joints of Pliobates cataloniae gen. et sp. nov. (IPS58443), denoted by arrows in drawings of the distal humerus, proximal radius, and distal ulna, are shown with those of selected extant and extinct anthropoids for comparison. (A to D) Anterior (top) and distal (bottom) views of the distal humerus in P. cata- loniae (A), Epipliopithecus vindobonensis Individual I [(B), reversed], Dendro- pithecus? sp. KNM MO 17022A (C) (MO, Moruorot), and Hylobates moloch (D). (E to H) Views perpendicular to the radial tuberosity (top) and proximal view (bottom) of the proximal radius in P. cataloniae (E), E. vindobonensis Individual I (F), Simiolus enjiessi KNM MO 63 [(G), reversed)], and H. moloch (H). (I to M) Medial (top) and distal (bottom) views of the distal ulna in P. cataloniae (I), E. vindobonensis Indi- vidual I (J), H. moloch (K), Ateles paniscus (L), and Cercopithecus aethiops (M). 1, absence of entepicondylar foramen; 2, absence of capitular tail; 3, lack of spool-shaped trochlea; 4, well-developed beveled surface for the zona conoidea; 5, small and flat area in the radial head; 6, ulnar fovea; 7, two-faceted, expanded semilunar articular surface in the ulnar head. Specimens are shown as if from the left side and are not to scale. [Artwork by M. Palmero]

opennotspecifiedDec 2015View details →
zenodo32/100

Fig. 2 in Miocene small-bodied ape from Eurasia sheds light on hominoid evolution

Fig. 2. Results of the dental microwear analyses. (A) Pitting incidence (%) of Pliobates, the extant comparative sample, and pliopithecoids and extinct hominoids from Europe and Turkey. (B) Bivariate plot of striation breadth versus pitting incidence. (C) Bivariate plot of the first two canonical axes delivered by the canonical variates analysis, based on three distinct, broad dietary groups: folivores, mixed feeders and frugivores, and hard-object feeders. Colored polygons in (B) and ellipses in (C) illustrate the variability of extant dietary categories. Small black symbols denote the comparative sample of extant anthropoids, whereas large black symbols represent the centroids of each dietary category. Different symbols are employed to distinguish the various extinct species; results for Iberian hominoids and pliopithecoids are shown in red and blue, respectively, whereas those from other localities are shown in yellow and green, respectively.

opennotspecifiedDec 2015View details →
zenodo32/100

APES electron precipitation data from the VISIONS-2 Sounding rocket flight

<p>This is a Matlab save file containting the data from the APES instrument from the VISIONS-2 sounding rocket flight. &nbsp;It contains the precipitating electron flux in both units of number flux and energy flux.</p>

opencc-by-4.0Jun 2024View details →
zenodo32/100

High-res Supplementary Figures: 37 human NAHRwhals sSV loci + apes

<p>Wolfram H&ouml;ps, 27th July 2024</p> <p>This upload contains high-resolution versions of Supplementary Figures S15-S22 and S30-S32 of the manuscript titled "Impact and characterization of serial structural variations across humans and great apes"; H&ouml;ps et al., 2024.&nbsp;</p> <p>Contact: wolfram.hoeps@gmail.com</p>

opencc-by-4.0Jul 2024View details →
zenodo32/100

Data and code for: Discrimination between the facial gestures of vocalizing and non-vocalizing lemurs and small apes using deep learning.

<p>Data and code for: Discrimination between the facial gestures of vocalizing and non-vocalizing lemurs and small apes using deep learning</p>

opencc-by-4.0Sep 2021View details →
dryad32/100

Data from: The effect of foot posture on capacity to apply free moments to the ground: implications for fighting performance in great apes

In contrast to most other primates, great apes have feet in which the heel supports body weight during standing, walking, and running. One possible advantage of this plantigrade foot posture is that it may enhance fighting performance by increasing the ability to apply free moments (i.e., force couples) to the ground. We tested this possibility by measuring performance of human subjects when performing from plantigrade and digitigrade (standing on the ball of the foot and toes) postures. We found that plantigrade posture substantially increased the capacity to apply free moments to the ground and to perform a variety of behaviors that are likely to be important to fighting performance in great apes. As predicted, performance in maximal effort lateral striking and pushing was strongly correlated with free moment magnitude. All else being equal, these results suggest species that can adopt plantigrade posture will be able to apply larger free moments to the ground than species restricted to digitigrade or unguligrade foot posture. Additionally, these results are consistent with the suggestion that selection for physical competition may have been one of the factors that led to the evolution of the derived plantigrade foot posture of great apes.

opencc-zeroDec 2016View details →
zenodo32/100

Figure 6 in Fossil Felidae (Carnivora: Mammalia) from the Yuanmou hominid site, southern China (Late Miocene) and its significance in the living environment of the fossil ape

Figure 6. Comparison of upper dentition of Longchuansmilus with other machairodonts. A, Longchuansmilus xingyongi gen. &amp; sp. nov., HMV87001; B, Longchuansmilus xingyongi gen. &amp; sp. nov., PDYV2522; C, Paramachaerodus maximiliani, PMU-M69, Baode, northern China; D, Paramachaerodus transasiaticus, IVPP V20106, Linxia Basin, northern China; E, Megantereon cf. nihowanensis, IVPP V26878, Sabertooth Cave, Guangxi, southern China; F, Homotherium crenatidens, THP 32067, Nihewan Basin, northern China; G, Homotherium crusafonti, AMNH FM 95297, Douglas Co., North America; H, Nimravides thinobates, UCMP V34512; I, Amphimachairodus palanderi, cast, Baode, northern China; J, Smilodon fatalis, LACMHC2001-3, Rancho La Brea tar pit.

opennotspecifiedApr 2022View details →
zenodo32/100

Figure 9 in Fossil Felidae (Carnivora: Mammalia) from the Yuanmou hominid site, southern China (Late Miocene) and its significance in the living environment of the fossil ape

Figure 9. Comparison of the P4 of selected machairodonts. A, Yoshi minor from Baode, AMNH F:AM China-57-L-548; B, Paramachaerodus transasiaticus from Linxia Basin, V20106, type; C, aff. Yoshi sp., RV2006023, p4, and D6. PDYV2525.1, not same individual; D, aff. Yoshi sp., PDYV2522, p4, D6. PDYV2525.1, not same individual. Not to scale.

opennotspecifiedApr 2022View details →
zenodo32/100

Figure 5 in Fossil Felidae (Carnivora: Mammalia) from the Yuanmou hominid site, southern China (Late Miocene) and its significance in the living environment of the fossil ape

Figure 5. Cranial comparison of Longchuansmilus gen. nov. and related taxa, dorsal view. A, Metailurus major from Baode, PMU M3841; B, Paramachaerodus transasiaticus from Linxia Basin, IVPP V20106; C, Longchuansmilus xingyongi gen. &amp; sp. nov., HMV87001; D, Amphimachairodus horribilis from Baode, IVPP V15642.

opennotspecifiedApr 2022View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record