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.
461,131
datasets available to search
ShareScore release 0.9.0
Dataset results
461,131 results for “FIGURES”
Figure 4 in Some new species records of the predatory mite family Phytoseiidae (Acari: Mesostigmata) from The Netherlands
Figure 4. Amblyseius meridionalis Berlese (Female): (A) Idiosoma, dorsal view; (B) Idiosoma, ventral view; (C) Spermatheca; (D) Chelicera; (E) Leg IV.
Figure 10 in Some new species records of the predatory mite family Phytoseiidae (Acari: Mesostigmata) from The Netherlands
Figure 10. Typhlodromus (Anthoseius) kerkirae Swirski & Ragusa (Female): (A) Idiosoma, dorsal view; (B) Idiosoma, ventral view; (C) Spermathecae; (D) Chelicera; (E) Leg IV.
Figure 9 in Some new species records of the predatory mite family Phytoseiidae (Acari: Mesostigmata) from The Netherlands
Figure 9. Typhloseiulus peculiaris (Kolodochka) (Female): (A) Idiosoma, dorsal view; (B) Idiosoma, ventral view; (C) Spermatheca; (D) Leg IV.
Figure 8 in Some new species records of the predatory mite family Phytoseiidae (Acari: Mesostigmata) from The Netherlands
Figure 8. Neoseiulus insularis (Athias-Henriot) (Female): (A) Idiosoma, dorsal view; (B) Idiosoma, ventral view; (C) Spermatheca; (D) Chelicera; (E) Leg IV.
Figure 1 in Some new species records of the predatory mite family Phytoseiidae (Acari: Mesostigmata) from The Netherlands
Figure 1. Kampimodromus florinensis Papadoulis, Emmanouel & Kapaxidi (Female): (A) Idiosoma, dorsal view; (B) Idiosoma, ventral view; (C) Spermathecae; (D) Chelicera; (E) Ventrianal shield, a variation; (F) Leg IV.
Figure 13 in Some new species records of the predatory mite family Phytoseiidae (Acari: Mesostigmata) from The Netherlands
Figure 13. Metaseiulus (Metaseiulus) smithi (Schuster) (Female): (A) Idiosoma, dorsal view; (B) Idiosoma, ventral view; (C) Spermathecae; (D) Chelicera; (E) Leg IV.
Figure 3 in Some new species records of the predatory mite family Phytoseiidae (Acari: Mesostigmata) from The Netherlands
Figure 3. Amblyseius herbicolus (Chant) (Female): (A) Idiosoma, dorsal view; (B) Idiosoma, ventral view; (C) Chelicera; (D) Spermatheca; E – Leg IV.
Figure 2 in Some new species records of the predatory mite family Phytoseiidae (Acari: Mesostigmata) from The Netherlands
Figure 2. Kampimodromus langei Wainstein & Arutunjan (Female): (A) Idiosoma, dorsal view; (B) Idiosoma, ventral view; (C) Spermathecae; (D) Chelicera; (E) Leg IV.
Figure 13 in A taxonomic revision of the members of the Camponotus lateralis species group (Hymenoptera: Formicidae) from Europe, Asia Minor and Caucasia
Figure 13. Classification of Camponotus candiotes (green bars) and C. piceus (red bars) by four exploratory data analyses considering body size and five RAV-corrected shape characters. The error relative to the final species hypothesis is 0 % in NC-Ward, 0 % in NC-NMDSk-means and 0 % in NC-part.hclust. However, as indicated by black bars, 3.5 % of the samples remained unclassified in NC-part.hclust and NC-part.kmeans failed to confirm two separate clusters.
Supporting Data for Figures in "Localized, tidal energy extraction in Puget Sound can adjust estuary resonance and friction, modifying barotropic tides system-wide"
<p>Supporting data for figures in "Localized, tidal energy extraction in Puget Sound can adjust estuary resonance and friction, modifying barotropic tides system-wide" by Preston S. Spicer, Parker MacCready, and Zhaoqing Yang. The manuscript is being considered for publication in Journal of Geophysical Research: Oceans (2024). The article analyzes the effect of a tidal turbine farm on incident and reflected tidal energy fluxes in the Salish Sea. Files are in MATLAB data and .m format with some .txt and shape files. Files named figX.m create the corresponding Figure X using provided .mat and other files. Variable names and units correspond to graphed data of each figure in the journal article.</p>
Figure 1 in Contribution to the knowledge of Parichoronyssus bakeri Morales-Malacara and Guerrero, 2007 (Mesostigmata: Macronyssidae): new locality and host-association records with additional molecular data
Figure 1 Light Microscopy images of the female Parichoronyssus bakeri. A – General view of the ventral idiosoma; B – General view of the dorsal idiosome; C – Close up of sternal shield; D – Close up of genital and anal shields; E – Gnathosoma and coxa of the Leg I, with the black arrow pointed out the spine-like projection; F – Close up of the dorsal shield. Scales: A and B 50µm, C-F 20µm.
Human Psychophysics Dataset on Figure Ground Segregation in Texture Stimuli
<div> <div>The dataset is derived from a psychophysics experiment where 8 participants discriminated the orientation of a rectangular figure within a texture stimulus comprised of Gabor annuli. The figure region differed from the background in its contrast distribution, controlled by two independent variables: Contrast Heterogeneity and Grid Coarseness. Contrast Heterogeneity refers to the range of contrasts exhibited by Gabor annuli. In this experiment, there were five values for Contrast Heterogeneity in the figure: 0.01, 0.2575, 0.505, 0.7525, and 1. The contrast distribution of the background was always maximally heterogeneous with Contrast Heterogeneity equal to 1. Grid Coarseness, on the other hand, refers to the scaling factor that controls the spacing between the Gabor annuli. It determines the density of the grid pattern in the background <em>and</em> the figure region. In this experiment, there were five values for Grid Coarseness: 1, 1.125, 1.250, 1.375, and 1.5. The experiment consisted of 9 sessions, each containing multiple blocks of trials. Each block of trials contained 25 unique stimulus conditions, defined by the combination of Contrast Heterogeneity and Grid Coarseness.</div> <div> <p><strong>Stimuli, Tasks, and Procedure </strong></p> </div> <div> <p>Each texture stimulus consisted of a full-screen irregular grid of non-overlapping Gabor annuli placed on a grey background. The Gabor annuli had a diameter of 0.7°, a spatial frequency of 5.7 cycles/degree, and a mean luminance of 60.76 Cd/m2. Embedded within this texture was a rectangular figure region located in the lower right quadrant of the screen, which differed from the rest of the texture in the contrast distribution of its annuli. For sessions 1-8, the figure center was placed at an eccentricity of (7 ± 1)° but slightly varied in terms of polar angle such that it was completely inside the lower right quadrant. For session 9 (transfer session), the figure was placed in the upper left quadrant. </p> </div> <div> <p>Participants were required to indicate whether the rectangular figure was oriented horizontally or vertically by pressing the right and left arrow keys, respectively. The experiment employed a two-alternative forced-choice design, in which participants had to make a decision about the orientation of the figure in each trial. Responses were given with the middle and index fingers of the right hand. In each trial, the stimulus was presented for 1000 ms or less if the participant lost fixation or provided a response. Participants were required to maintain fixation throughout the presentation of the stimulus. </p> </div> <div> <p>After each trial, participants received feedback on their response. If the response was correct, a green fixation point was presented for 500 ms. If the response was incorrect, a red fixation point was presented for 500 ms. </p> </div> <div> <p>The experiment was conducted in a dimly lit room. A chin and head-rest was used to support the participant's head and to keep eye-screen distance constant at 57 cm. Stimuli were displayed on a 19'' Samsung SyncMaster 940BF LCD monitor. Stimulus representation and response recording were performed using Psychtoolbox-3 for Matlab 64-Bit (Version 3.0.14 - Build date: Apr 6th, 2018) running on a Windows operating system. Fixation was monitored with a desktop-mounted Eyelink 1000 eye-tracker (SR Research Ltd.) with a sampling frequency of 500 Hz or 1000 Hz and a spatial resolution of <0.01° RMS. Eye-movement data were down-sampled to 250 Hz. </p> </div> <div> <p><strong>Procedure for Handling Aborted Trials </strong></p> </div> <div> <p>If a participant's gaze fell outside the fixation window during the fixation period preceding the stimulus, or during stimulus presentation, the trial was aborted. Aborted trials were repeated at a randomly chosen time during the experiment. </p> </div> <div> <p><strong>Parametrization of the Experimental Setup </strong></p> </div> <div> <p>The eye-screen distance was set to 57 cm. The stimulus presentation time was set to 1000 ms. The inter-trial interval was set to 900 ms. Each session consisted of 30 blocks, with 25 trials per block. </p> </div> <div> <p><strong>Transfer Session </strong></p> </div> <div> <p>The transfer session (session 9) was unique in that the rectangular figure was presented in the upper left quadrant of the screen, rather than the lower right quadrant as in sessions 1-8. This was done to test the transfer of learning to a new location. Participants were made aware of the figure displacement but were not told in which quadrant to expect it. </p> </div> <div> <p><strong>Variables </strong></p> </div> <div> <p>The dataset includes identifiers for each participant (SubjectID), session (SessionID), and block of trials (BlockID). For each trial, the dataset includes the condition (Condition), the contrast heterogeneity (ContrastHeterogeneity), the grid coarseness (GridCoarseness), the participant's response (IndicatedOrientation), the actual orientation of the rectangular region (ActualOrientation), and whether the participant's response was correct (Correct). The dataset also includes demographic information comprising their unique identifier (SubjectID), age (Age), and sex (Sex). </p> <p><strong>Ethics</strong></p> <p>After receiving full information about all procedures and about the right to withdraw participation at any time, they provided written informed consent according to the Helsinki Declaration. All procedures were approved by the local Ethical Committee of the Faculty of Psychology and Neuroscience (ERCPN). Participants received<br>monetary reward.</p> </div> </div>
Simulation input scripts for figures in the article "Experimental parameters for plasma wakefield acceleration in a narrow plasma column"
<p>Simulation input scripts for figures in the article "Experimental parameters for plasma wakefield acceleration in a narrow plasma column"</p> <p>Alter line "my_constants.dx_dz= 10e-6" to chage the misalignment degree</p>
Figure 1 in Are fisheries regulations influencing the biology and reproduction of the surmullet Mullus surmuletus Linnaeus, 1758 on the south-eastern coasts of France (NW Mediterranean)?
Figure 1. – Sampling sites in West, AMA (Adjacent Marine Protected Area of Hyères Bay) and East zones on the south-eastern coast of France, NW Mediterranean Sea.
Figure 3 in Diet of the European eel Anguilla anguilla (Linnaeus, 1758) in two transitional waters of Southwestern Mediterranean
Figure 3. – Comparison of the IRI of major items ingested by Anguilla anguilla from Mellah lagoon (in black) and Wadi El Kebir (in gray).
Figure 1 in Diet of the European eel Anguilla anguilla (Linnaeus, 1758) in two transitional waters of Southwestern Mediterranean
Figure 1. – Geographical location of sampling sites (*) of Anguilla anguilla in Mellah lagoon (ML) and Wadi El Kebir (WEK).
Figure 4 in Are fisheries regulations influencing the biology and reproduction of the surmullet Mullus surmuletus Linnaeus, 1758 on the south-eastern coasts of France (NW Mediterranean)?
Figure 4. – Percentages of both sexes and females:males sex-ratio of Mullus surmuletus by zone (A) and season (B).
Figure 3 in Are fisheries regulations influencing the biology and reproduction of the surmullet Mullus surmuletus Linnaeus, 1758 on the south-eastern coasts of France (NW Mediterranean)?
Figure 3. – Mean (± SE) total length (TL, cm) of Mullus surmuletus in West, AMA and East zones. N: number of analyzed individuals per sex in zones. Values with the same post-hoc letters (red for females, blue for males) are not significantly different (p> 0.05).
Figure 2 in First record of the Small-eyed loter Prionobutis microps (Weber, 1907) (Teleostei: Eleotridae: Butinae) in Java, Indonesia
Figure 2. – Map of the known distribution of Prionobutis microps. New record in Java, Indonesia (black star); published records (black circles) are based on Larson (2021).
Figure 1 in First record of the Small-eyed loter Prionobutis microps (Weber, 1907) (Teleostei: Eleotridae: Butinae) in Java, Indonesia
Figure 1. – Collected specimens of Prionobutis microps, EFRM 0003, 19.1 cm TL (A), EFRM 0039, 22.5 cm TL (B), Solo River Estuary, East Java, Indonesia.
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.