Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
16
datasets available to search
ShareScore release 0.9.0
Dataset results
16 results for “face individuation”
Explanation of Plate I. Figure 1.—Left tibia of Ornithomimus velox, Marsh; A, front view; b, distal end; c, transverse section. Figure 2.—Left metatarsals of same specimen; A, front view; b, proximal ends; c, transverse section; d, distal ends. Figure 3.—Phalanges of second digit of same foot; front view, a, first phalange; b, second phalange; c, third, or terminal phalange. Figure 4.—Left metacarpals of same species, perhaps of smaller individual; front view. Figure 5.—Left tibia of young Ostrich (Struthio camelus, Linn.); a, front view; b, distal end. The separate calcaneum was first observed by the writer's assistant, Dr. G-. Baur, who prepared the specimen. Figure 6.—Left metatarsals of young turkey (Meleagris gallipavo, Linn.); a, front view; b, proximal ends. a, astragalus; as, ascending process of astragalus; c, calcaneum; f, fibula; f' face for fibula; II, second metatarsal; III, third metatarsal; iv, fourth metatarsal. Figures 1-4 are one-third natural size, and figures 5 and 6, one-half natural size. in Description of new dinosaurian reptiles
Explanation of Plate I. Figure 1.—Left tibia of Ornithomimus velox, Marsh; A, front view; b, distal end; c, transverse section. Figure 2.—Left metatarsals of same specimen; A, front view; b, proximal ends; c, transverse section; d, distal ends. Figure 3.—Phalanges of second digit of same foot; front view, a, first phalange; b, second phalange; c, third, or terminal phalange. Figure 4.—Left metacarpals of same species, perhaps of smaller individual; front view. Figure 5.—Left tibia of young Ostrich (Struthio camelus, Linn.); a, front view; b, distal end. The separate calcaneum was first observed by the writer's assistant, Dr. G-. Baur, who prepared the specimen. Figure 6.—Left metatarsals of young turkey (Meleagris gallipavo, Linn.); a, front view; b, proximal ends. a, astragalus; as, ascending process of astragalus; c, calcaneum; f, fibula; f' face for fibula; II, second metatarsal; III, third metatarsal; iv, fourth metatarsal. Figures 1-4 are one-third natural size, and figures 5 and 6, one-half natural size.
Adjudicating between face-coding models with individual-face fMRI responses: Data and analysis software
<p>Computational model fits to human neuroimaging data. Please see included readme.txt file.</p>
Dataset from 'Billino, J., van Belle, G., Rossion, B., & Schwarzer, G. (2018). The nature of individual face recognition in preschool children: Insights from a gaze-contingent paradigm. Cognitive Development, 47, 168-180. DOI: 10.1016/j.cogdev.2018.06.007
<p>The folder contains a data file and a description file providing column labels.</p> <p>For further questions, please contact:<br> jutta.billino[at]psychol.uni-giessen.de</p>
The risk faced by the early bat: individual plasticity and mortality costs of the timing of spring departure after hibernation
<p>Hibernation is a widespread adaptation in animals to seasonally changing environmental conditions. In the face of global anthropogenic change, information about plastic adjustments to environmental conditions and associated mortality costs are urgently needed to assess population persistence of hibernating species. Here, we used a five-year data set of 1,047 RFID-tagged individuals from two bat species, Myotis nattereri and Myotis daubentonii that were automatically recorded each time they entered or left a hibernaculum. Because the two species differ in foraging strategy and activity pattern during winter, we expected species–specific responses in the timing of hibernation relative to environmental conditions, as well as different mortality costs of early departure from the hibernaculum in spring. Applying mixed-effects modelling, we were able to disentangle population-level and individual-level plasticity in the timing of departure. To estimate mortality costs of early departure, we used both a capture mark recapture analysis and a novel approach that takes into account individual exposure times to mortality outside the hibernaculum. We found that the timing of departure varied between species as well as among and within individuals, and was plastically adjusted to large-scale weather conditions as measured by the NAO (North Atlantic Oscillation) index. Individuals of M. nattereri, which can exploit milder temperatures for foraging during winter, tuned departure more closely to the NAO index than individuals of M. daubentoniid which do not hunt during winter. Both analytical approaches used to estimate mortality costs showed that early departing individuals were less likely to survive until the subsequent hibernation period than individuals that departed later. Overall, our study demonstrates that individuals of long-lived hibernating bat species have the potential to plastically adjust to changing climatic conditions, although the potential for adjustment differs between species.</p>
The risk faced by the early bat: individual plasticity and mortality costs of the timing of spring departure after hibernation
Open the record for dataset details and reuse information.
Distribution. Angola, DR Congo, Malawi, Mozambique, Tanzania, and Zambia. Description. Head-body 46:5-47-8 cm (males), 44-45-5 cm (females), tail 40-43 cm (males), 38-39 cm (females), hindfoot 8:7-9-8 cm (males), 8-9 cm (females), ear 4-7-5-4 cm (males), 5-1-5-8 cm (females); weight 1-3-2 kg. The coat color is pale ocher, with brownish or grayish tones; melanistic individuals are quite common. The throat and chest are blackish, and the ventral pelage varies from creamy white to dirty white. The stripes and spots on the body vary from different hues of brown to black. The nuchal stripes run as two parallel lines from the nape to the shoulders, where they diverge and enlarge towards the elbows; they are not so conspicuously marked as in other genet species. Below them, a pair of thinner stripes and small spots are scattered on the shoulders and sides of the neck. A third pair of thinner, parallel stripes runs down the neck between the nuchal stripes, extending to about one fourth of the mid-dorsal line, where they vanish or diverge as the first row of flank spots. The black mid-dorsal line is continuous and is flanked on each side by four rows of oblong to squared spots, and by a few small-scattered spots below. There is a dorsal erectile crest. The face has a dark mask and a pair of white sub-ocular spots. The tail has seven to nine black rings, alternating with pale rings; the intervening white spaces are pigmented with a brownish tinge on the dorsal midline. The width of the pale rings relative to the dark rings in the middle of the tail is 50-75%; the tip of the tail is dark. The hindlimbs and forelimbs are black; there are white hairs on the metacarpals and metatarsals. [he posterior parts of the feet are dark. There are two pairs of teats. The posterior chamber of the auditory bulla is not ventrally inflated and has a continuous curve line on the external side. The ratio between the inter-orbital constriction and frontal width is 1-00 + 0-12. Dental formula: 13/3, C1/1,P 4/4, M 2/2 = 40. in Viverridae
Distribution. Angola, DR Congo, Malawi, Mozambique, Tanzania, and Zambia. Description. Head-body 46:5-47-8 cm (males), 44-45-5 cm (females), tail 40-43 cm (males), 38-39 cm (females), hindfoot 8:7-9-8 cm (males), 8-9 cm (females), ear 4-7-5-4 cm (males), 5-1-5-8 cm (females); weight 1-3-2 kg. The coat color is pale ocher, with brownish or grayish tones; melanistic individuals are quite common. The throat and chest are blackish, and the ventral pelage varies from creamy white to dirty white. The stripes and spots on the body vary from different hues of brown to black. The nuchal stripes run as two parallel lines from the nape to the shoulders, where they diverge and enlarge towards the elbows; they are not so conspicuously marked as in other genet species. Below them, a pair of thinner stripes and small spots are scattered on the shoulders and sides of the neck. A third pair of thinner, parallel stripes runs down the neck between the nuchal stripes, extending to about one fourth of the mid-dorsal line, where they vanish or diverge as the first row of flank spots. The black mid-dorsal line is continuous and is flanked on each side by four rows of oblong to squared spots, and by a few small-scattered spots below. There is a dorsal erectile crest. The face has a dark mask and a pair of white sub-ocular spots. The tail has seven to nine black rings, alternating with pale rings; the intervening white spaces are pigmented with a brownish tinge on the dorsal midline. The width of the pale rings relative to the dark rings in the middle of the tail is 50-75%; the tip of the tail is dark. The hindlimbs and forelimbs are black; there are white hairs on the metacarpals and metatarsals. [he posterior parts of the feet are dark. There are two pairs of teats. The posterior chamber of the auditory bulla is not ventrally inflated and has a continuous curve line on the external side. The ratio between the inter-orbital constriction and frontal width is 1-00 + 0-12. Dental formula: 13/3, C1/1,P 4/4, M 2/2 = 40.
Re-identification of Individuals in Genomic Datasets Using Public Face Images
<p>Image-genome pairs in these synthetic datasets were created by combining a subset of the publicly available face image dataset, CelebA, and genotypes from OpenSNP. The genome in a given pair does not correspond to the individual in the image (taken from CelebA), but comes instead from an individual with the same set of phenotypes (taken from OpenSNP). Artificial genotypes were created for each image (genotype refers only to the small subset of SNPs we are interested in) using all available data from OpenSNP where self-reported phenotypes are present.</p> <p>In the Synthetic-Ideal dataset, to each image, we assigned a genotype from OpenSNP that corresponds to an individual with the same phenotypes, such that the probability of the selected phenotypes is maximized, given the genotype. In other words, we picked the genotype from the OpenSNP data that is most representative of an individual with a given set of phenotypes.</p> <p>In the Synthetic-Realistic dataset, to each image, we assigned a genotype from OpenSNP that corresponds to an individual with the same phenotypes, but at random according to the empirical distribution of phenotypes for particular SNPs in our data.</p> <p>Since CelebA does not have labels for all considered phenotypes, 1000 images from this dataset were manually labeled by one of the authors. After cleaning and removing ambiguous cases, the resulting datasets consist of 456 records.</p>
The Effect of Web-Based and Face-to-Face Education Based on the Health Promotion Model on Foot Care Behavior in Individuals With Type 2 Diabetes
ClinicalTrials.gov study NCT06780631. IPD Sharing: NO. Countries: 1. Publications: 5.
Effects of Online Pilates and Face-To-Face Pilates on Healthy Individuals
ClinicalTrials.gov study NCT05309486. IPD Sharing: Not stated. Countries: 1. Publications: 7.
Data from: Orientation-invariance of individual differences in three face processing tasks
Numerous studies have reported impairments in perception and recognition, and, particularly, in part-integration of faces following picture-plane inversion. Whether these findings support the notion that inversion changes face processing qualitatively remains a topic of debate. To examine whether associations and dissociations of the human face processing ability depend on stimulus orientation, we measured face recognition with the Cambridge Face Memory Test (CFMT), along with experimental tests of face perception and selective attention to faces and non-face objects in a sample of 314 participants. Results showed strong inversion effects for all face-related tasks, and modest ones for non-face objects. Individual differences analysis revealed that the CFMT shared common variance with face perception and face-selective attention, however, independent of orientation. Regardless of whether predictor and criterion had same or different orientation, face recognition was best predicted by the same test battery. Principal component decomposition revealed a common factor for face recognition and face perception, a second common factor for face recognition and face-selective attention, and two unique factors. The patterns of factor loadings were nearly identical for upright and inverted presentation. These results indicate orientation-invariance of common variance in three domains of face processing. Since inversion impaired performance, but did not affect domain-related associations and dissociations, the findings suggest process-specific but orientationgeneral mechanisms. Specific limitations by constraints of individual differences analysis and test selection are discussed.
Data from: Orientation-invariance of individual differences in three face processing tasks
Open the record for dataset details and reuse information.
The Effects of Online Mat Pilates and Face-to-Face Equipment-Based Pilates on Pain, Kinesiophobia, and Balance in Individuals With Non-Specific Low Back Pain
ClinicalTrials.gov study NCT06946966. IPD Sharing: NO. Countries: 1. Publications: 0.
Oxytocin Effect on Attentional Bias Towards Emotional Expression Faces in Individuals With High and Low Autistic Traits: A Functional Magnetic Resonance Imaging (fMRI) Study
ClinicalTrials.gov study NCT02741063. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Effects of Face Masks on Cardiopulmonary Capacity in Healthy Individuals
ClinicalTrials.gov study NCT04785781. IPD Sharing: NO. Countries: 1. Publications: 0.
The Effect Of Face-To-Face and Online-Education Provided To İndividuals With Atrial Fibrillation On Medication Adherence and Satisfaction
ClinicalTrials.gov study NCT06233721. IPD Sharing: NO. Countries: 1. Publications: 0.
Telerehabilitation and Face-to-Face Clinical Pilates-Based Exercise in Individuals With Axial Spondyloarthritis
ClinicalTrials.gov study NCT05006690. IPD Sharing: NO. Countries: 1. Publications: 0.
ScienceDex guides
Understand access before you commit
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.