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.
789
datasets available to search
ShareScore release 0.9.0
Dataset results
789 results for “display”
Text-fig. 9. Progyrolepis heyleri POPLIN, 1999. a: right dentalosplenial of adult specimen in lateral view, GMC 1, scale bar 5 mm; b: left dentalospelenial and suboperculum in medial view, GMC 1, scale bar 5 mm; c: set of bones of the right side of the cheek displaying maxilla, preoperculum, hyomandibula, left and right ceratohyal, epibranchial and neural spine from the axial skeleton, G 123, scale bar 5 mm; d: drawing of the right frontal in dorsal view, GMC 81, scale bar 5 mm; e: right operculum in lateral view, GMC 10, scale bar 5 mm. Abbreviations: Cbr – ceratobranchial, Cer – ceratohyal, Ds – dorsal spine, Hy – hyomandibula, Md – mandible, Mx – maxilla, Op – operculum, Pop – preoperculum. in New Actinopterygians From The Permian Of The Brive Basin, And The Ichthyofaunas Of The French Massif Central
Text-fig. 9. Progyrolepis heyleri POPLIN, 1999. a: right dentalosplenial of adult specimen in lateral view, GMC 1, scale bar 5 mm; b: left dentalospelenial and suboperculum in medial view, GMC 1, scale bar 5 mm; c: set of bones of the right side of the cheek displaying maxilla, preoperculum, hyomandibula, left and right ceratohyal, epibranchial and neural spine from the axial skeleton, G 123, scale bar 5 mm; d: drawing of the right frontal in dorsal view, GMC 81, scale bar 5 mm; e: right operculum in lateral view, GMC 10, scale bar 5 mm. Abbreviations: Cbr – ceratobranchial, Cer – ceratohyal, Ds – dorsal spine, Hy – hyomandibula, Md – mandible, Mx – maxilla, Op – operculum, Pop – preoperculum.
Text-fig. 3. Juglandaceae. Carya (a–x). Scale bars = 1 cm. a–e: USNM PAL 772346. Micro-CT scan surface rendering. a, b: Lateral, c: apical, d: basal views. e: Virtual equatorial transverse section. f–n: USNM PAL 772347. f: Lateral view, reflected light, showing path of saw cut for transverse section of (i). g: Basal view, reflected light. h: Apical view, micro-CT surface rendering. i: Physical transverse section displaying locule and cellular preservation of parts of wall. j–n: Virtual sections from micro-CT scan data. j: Transverse section at apical 1/3 of nut. Note narrow lacunae (arrows). k: Longitudinal section parallel to primary septum, traversing one of the cotyledon lobes and showing secondary septum at base. l: Longitudinal section in plane at right angles to (k) in plane of primary septum, showing divergent placental bundles arising from base of nut (arrows). m: Equatorial transverse section showing two lobes of locule separated by primary septum. n: Transverse section near base of nut showing primary and secondary septa, creating four basal lobes of locule; note diverging placental bundles (arrows). o–x: USNM PAL 772351. o: Lateral view of broken nut with exposed locule cast, reflected light. p: Same orientation of nut, micro-CT surface rendering. q: Same specimen lateral view, rotated 90° from (p), micro-CT surface rendering. r: Apical view, reflected light. s–x: Virtual sections from micro-CT in The Early Middle Eocene Wagon Bed Carpoflora Of Central Wyoming, U.S.A.
Text-fig. 3. Juglandaceae. Carya (a–x). Scale bars = 1 cm. a–e: USNM PAL 772346. Micro-CT scan surface rendering. a, b: Lateral, c: apical, d: basal views. e: Virtual equatorial transverse section. f–n: USNM PAL 772347. f: Lateral view, reflected light, showing path of saw cut for transverse section of (i). g: Basal view, reflected light. h: Apical view, micro-CT surface rendering. i: Physical transverse section displaying locule and cellular preservation of parts of wall. j–n: Virtual sections from micro-CT scan data. j: Transverse section at apical 1/3 of nut. Note narrow lacunae (arrows). k: Longitudinal section parallel to primary septum, traversing one of the cotyledon lobes and showing secondary septum at base. l: Longitudinal section in plane at right angles to (k) in plane of primary septum, showing divergent placental bundles arising from base of nut (arrows). m: Equatorial transverse section showing two lobes of locule separated by primary septum. n: Transverse section near base of nut showing primary and secondary septa, creating four basal lobes of locule; note diverging placental bundles (arrows). o–x: USNM PAL 772351. o: Lateral view of broken nut with exposed locule cast, reflected light. p: Same orientation of nut, micro-CT surface rendering. q: Same specimen lateral view, rotated 90° from (p), micro-CT surface rendering. r: Apical view, reflected light. s–x: Virtual sections from micro-CT
Text-fig. 6. Cornaceae. Alangium (a–e), Mastixia (f–r). a–e: Alangium, DMNH EPI.47806. Scale bar = 1 cm. b, e: Reflected light, palladium coated. a, c, d: Micro-CT scan surface rendering. a: Locule cast, face view of slightly larger locule. b: Face view of slightly smaller locule. c: Lateral view of the endocarp, the slightly enlarged left carpel separated from the smaller carpel by a longitudinal septal groove; the faint pitting in the groove suggestive of the septal vasculature. d, e: Views of either end of the endocarp, illustrating the size difference between the two carpels and the pitting in the septal groove suggestive of the septal vasculature. f–k: Mastixia USNM PAL 772362. Scale bar = 1 cm. f, g, j, k: reflected light, palladium coated; h, i: micro-CT scan surface rendering. f: Lateral view of endocarp, inferred dorsal germination valve groove facing the viewer. Note irregular, rugose, longitudinal ridges. g: Lateral view of endocarp, inferred germination valve with median longitudinal groove to left. h: Lateral view of endocarp reoriented with the same longitudinal groove to the right. i: Lateral view, rotated to ventral surface. j: View of one end of the endocarp, germination valve groove up. k: Opposite end view, with prominent radial ridges and intervening grooves, germination valve groove up. l–r: Mastixia USNM PAL 772363. Scale bar = 1 cm. l: View of one face of endocarp, displaying a groove that may represent the surficial expression of the dorsal infold of a Mastixia-like germination valve. Surface badly eroded, reflected light, palladium coated. m: Opposite face of endocarp displaying extensive erosion and a central hole interpreted as feeding damage. n: Lateral view; m, n micro-CT scan surface renderings. o: A view of one end, displaying the prominent groove, reflected light, palladium coated. p: Opposite end to (o). q: View as in (o); p, q micro-CT scan surface renderings. r: Virtual transverse section showing curved locule (arrows). in The Early Middle Eocene Wagon Bed Carpoflora Of Central Wyoming, U.S.A.
Text-fig. 6. Cornaceae. Alangium (a–e), Mastixia (f–r). a–e: Alangium, DMNH EPI.47806. Scale bar = 1 cm. b, e: Reflected light, palladium coated. a, c, d: Micro-CT scan surface rendering. a: Locule cast, face view of slightly larger locule. b: Face view of slightly smaller locule. c: Lateral view of the endocarp, the slightly enlarged left carpel separated from the smaller carpel by a longitudinal septal groove; the faint pitting in the groove suggestive of the septal vasculature. d, e: Views of either end of the endocarp, illustrating the size difference between the two carpels and the pitting in the septal groove suggestive of the septal vasculature. f–k: Mastixia USNM PAL 772362. Scale bar = 1 cm. f, g, j, k: reflected light, palladium coated; h, i: micro-CT scan surface rendering. f: Lateral view of endocarp, inferred dorsal germination valve groove facing the viewer. Note irregular, rugose, longitudinal ridges. g: Lateral view of endocarp, inferred germination valve with median longitudinal groove to left. h: Lateral view of endocarp reoriented with the same longitudinal groove to the right. i: Lateral view, rotated to ventral surface. j: View of one end of the endocarp, germination valve groove up. k: Opposite end view, with prominent radial ridges and intervening grooves, germination valve groove up. l–r: Mastixia USNM PAL 772363. Scale bar = 1 cm. l: View of one face of endocarp, displaying a groove that may represent the surficial expression of the dorsal infold of a Mastixia-like germination valve. Surface badly eroded, reflected light, palladium coated. m: Opposite face of endocarp displaying extensive erosion and a central hole interpreted as feeding damage. n: Lateral view; m, n micro-CT scan surface renderings. o: A view of one end, displaying the prominent groove, reflected light, palladium coated. p: Opposite end to (o). q: View as in (o); p, q micro-CT scan surface renderings. r: Virtual transverse section showing curved locule (arrows).
Data and code for "Uncertainty Displays Using Quantile Dotplots or CDFs Improve Transit Decision-Making" (CHI 2017)
<p>This repository contains data and analysis code for the following paper:</p> <p>Michael Fernandes, Logan Walls, Sean Munson, Jessica Hullman, and Matthew Kay. "Uncertainty Displays Using Quantile Dotplots or CDFs Improve Transit Decision-Making", Proceedings of the 2018 CHI Conference on Human Factors in Computing Systems - CHI 2018. DOI: 10.1145/3173574.3173718<br> </p>
Data from: Coyotes display minimal response to Cougar scent at experimental carcass sites
<p>Interactions among predators can have cascading impacts on communities and ecosystems. These interactions often occur around carrion, where the carrion provides a food reward, but also a risk of encountering other, potentially dominant, predators. Understanding how predators balance risk and reward at carrion, and how perceived risk changes in response to carcass origins and conditions, provides valuable insight into intraguild interactions. We investigated Coyote (Canis latrans) behavior at carrion simulated as cache sites treated with Cougar (Puma concolor) scent versus carrion used as control sites to better understand how Coyotes assess risk while feeding on carrion. Coyotes displayed similar behavior between sites treated and untreated with Cougar scent, suggesting that the presence of Cougar scent did not alter perceived risk by coyotes in our study. Instead, coyote behavior responded to carcass age, elevation, and whether avian scavengers had visited the carcass. Coyotes spent more time feeding, more time on camera, and touched carcasses quicker as carcass age increased. Avian scavengers appeared to compete with Coyotes, and while the presence of avian scavengers reduced time to carcass detection by Coyotes, it also decreased time spent feeding. These results suggest that carcass condition is a more important indicator of risk and reward than the presence of dominant predator scent to Coyotes. Predator scent may be an unreliable cue of immediate predator presence. Alternatively, all carcasses may be risky because dominant predators also scavenge carrion, creating similar risk regardless of previous visitation by dominant predators. These results provide insights into predator interactions and can also inform the use of scent cues in wildlife management.</p>
Figure 2. Salopella australis displaying parallel parent axes dichotomising into much shorter daughter axes that are terminated with elongate sporangia, delineated with a in Early land plants from the Lower Devonian of central Victoria, Australia, including a new species of Salopella
Figure 2. Salopella australis displaying parallel parent axes dichotomising into much shorter daughter axes that are terminated with elongate sporangia, delineated with a constriction just above dark sporogeneous region. All from Wilson Creek Shale on Frenchmans Spur track, 10 km west of Matlock. A, erect parent axes parallel to each other, dichotomising into two elongate sporangia from Wilson Creek Shale. Re-photographed here; originally published in Tims and Chambers (1984: pl. 32, fig. 4) and Tims (1980: fig. 4.1.9). Specimen NMV P50014. B, forked dichotomy terminated by sporangia from Wilson Creek Shale. And to the right hand side of the forked axis is another long axis, which based on its orientation may also be part of the same plant. Constriction at arrow, lower arrow at dichotomy and double arrow at two aligned axes. Specimen NMV P33219. C, close-up of fructification in A, sporangia barely extend beyond the confines of their subtending axes, with slight constriction present above sporogeneous region (at arrow). Specimen NMV P50014. D, E, holotype, part and counterpart. On part, constriction at arrow in sporangium. On counterpart, both parent axes are parallel to each other (at dotted arrow). Re-photographed here, originally published in Tims and Chambers (1984: pl. 32, figs. 1, 2). Specimens NMV P50008.1 and NMV P50008.2, respectively. F, Gen. et sp. indet. – short daughter axes terminated in elongate sporangia. The cortex may be absent from subtending axes, with only the central line visible. The lack of cortex prevents assigning to S. australis as width of subtending axis to sporangial width is required. Originally photographed by Tims (1980: fig. 4.1.13). Specimen NMV P50010.2. G, S. australis, with two short daughter axes, with constriction at arrow of the sporangium, which is the same width as its subtending axis. Specimen NMV P202886.
Figure 13. Argonauta nouryi shell displaying a in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 13. Argonauta nouryi shell displaying a single change in shell formation type: a–d, four perspectives of shell #37 (65.5 mm shell length, SBMNH 345766) displaying a single change from Type 1 (T1) to Type 2 (T2) shell formation; a, left lateral view; b, oblique left lateral view; c, close-up oblique left lateral view; d, posterior keel view. Scale bar = 1 cm.
Figure 12. Repaired shell displaying components consistent with Argonauta nouryi and A in Recognising variability in the shells of argonauts (Cephalopoda: Argonautidae): the key to resolving the taxonomy of the family
Figure 12. Repaired shell displaying components consistent with Argonauta nouryi and A. cornutus: a–d, four perspectives of a single shell (52.3 mm shell length, SBMNH 357476) displaying an initial component consistent with A. nouryi Lorois, 1854 ("nouryi") followed by a subsequent component consistent with A. cornutus Conrad, 1854 ("cornutus"); a, right lateral view; b, oblique right lateral view; c, anterior aperture view; d, oblique ventral keel view. Dashed line represents repair line separating two visually different components. Scale bar = 1 cm.
figure 5 in The sawFIsh (Rhinopristiformes, Pristidae) rostrum displayed in the "Basilica Santuario del Carmine Maggiore" in Naples, Italy: A long story of legends and taxonomic errors
figure 5 Alignment of coi (A) and nd2 (B) sequences obtained for the rostrum of the bscm (indicated by a pink box) and those available in GenBank for sawfish species (see main text for details and Accession numbers). nd 2 haplotypes for P. pectinata from Faria et al. (2013) are indicated as HapC, HapD, HapE. Unrooted neighbor-joining tree (C) constructed using coi + nd2 sequences and displaying only>50% percentage bootstrap scores.
figure 1 in The sawFIsh (Rhinopristiformes, Pristidae) rostrum displayed in the "Basilica Santuario del Carmine Maggiore" in Naples, Italy: A long story of legends and taxonomic errors
figure 1 (A) Picture of the sawfish rostrum kept in the bscm and (B) illustration of the "miraculous event" in which it allegedly took part; note the fish tail protruding from the leak circled in white (from page 81; Bacco, 1605). (C) The original lacquer wax stamp present on the rostrum (central) compared to the logo of the Roman Curia of the Carmelite Order (left) and the logo of the Carmelite fathers of Naples (right). The logo of the Roman Curia of the Carmelite Order was downloaded from https://fraticarmelitani.wixsite.com/fraticarmelitani and, the Downloadedlogo of fromtheBrill.com 06/21/2024 06:27:30PM via Open Access . This is an open access article distributed under the terms Carmelite fathers of Naples was photographed by N. Maio . of the CC BY 4.0 license . https://creativecommons.org/licenses/by/4.0/
Dataset: Universal Display Corporation (OLED) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
Fig. 3 in Cluster Analysis of Non-conserved Proteins of Trypanosoma cruzi Reference Strains Displays Parity between these Groupings (Peptidemes) and the Consensually Accepted Parasite Lineages
Fig. 3. Phenogram of the peptidemes (P) of eight Trypanosoma cruzi reference strains obtained using the SM coefficient and the UPGMA clustering algorithm, based on data from non-conserved proteins, as seen in SDS-PAGE analysis. The major peptidemes are indicated as mP 1 and mP 2. Their subgroups are identified on the right (P II, P VI, P I), and were numbered following their respective genetic types (TcII, TcVI, TcI), as currently used.
Fig. 1 in Cluster Analysis of Non-conserved Proteins of Trypanosoma cruzi Reference Strains Displays Parity between these Groupings (Peptidemes) and the Consensually Accepted Parasite Lineages
Fig. 1. Total protein profiles of eight Trypanosoma cruzi reference strains separated in 10% SDS-PAGE at 250 V, 25 mA, 90 min, and stained by Coomassie brilliant blue. The position of some conserved proteins is indicated on the right. M: molecular mass markers. (kDa) are indicated on the left.
Fig. 2 in Cluster Analysis of Non-conserved Proteins of Trypanosoma cruzi Reference Strains Displays Parity between these Groupings (Peptidemes) and the Consensually Accepted Parasite Lineages
Fig. 2. Diagrammatic representation of the twenty-two protein bands not shared by all Trypanosoma cruzi reference strains (nonconserved proteins), as visualized in SDS-PAGE. These bands were coded and analyzed by numerical taxonomy procedures. At the top is indicated the number of the major groups they belong, as identified by different approaches. The bands that were exclusive of one or more strains were highlighted with rectangles. M: molecular mass markers. (kDa) are indicated on the left.
Agricultural landscape simplification affects wild plant fitness indirectly through herbivore-mediated changes in floral display
<p>As natural landscapes are modified and converted into simplified agricultural landscapes, the community composition and interactions of organisms persisting in these modified landscapes are altered. While many studies examine the consequences of these changing interactions for crops, few have evaluated the effects on wild plants. Here, we examine how pollinator and herbivore interactions affect fitness for wild resident and phytometer plants at sites along a landscape gradient ranging from natural to highly simplified. We tested the direct and indirect effects of landscape composition on plant traits and fitness mediated by insect interactions. For phytometer plants exposed to herbivores, we found that greater landscape complexity corresponded with elevated herbivore damage, which reduced total flower production but increased individual flower size. Though larger flowers increased pollination, the reduction in flowers ultimately reduced plant fitness. Herbivory was also higher in complex landscapes for resident plants, but overall damage was low and therefore did not have a cascading effect on floral display and fitness. This work highlights that landscape composition directly affects patterns of herbivory with cascading effects on pollination and wild plant fitness. Further, the absence of fitness consequences for resident plants suggests that they may be adapted to their local insect community. </p>
Fig. 1 Histogram displaying A in Evolution of chromosome number in grasshoppers (Orthoptera: Caelifera: Acrididae)
Fig. 1 Histogram displaying A: the distribution of chromosome numbers across Caelifera and B: chromosome numbers across the different subfamilies of Acrididae. Chromosome numbers are shown as relative frequencies in percent; here, just subfamilies with more than ten records are shown as separated units. Subfamilies with lower sam-
Figure 10b. The control loop's information displayed by the controller-Designing a Growing Functional Modules "Artificial Brain"
<p>Once performed the design and configuration, the controller and the local application are<br> executed by pressing the corresponding button. In case of a local simulation, two terminal windows<br> are generated. The first one, localized on the left side of the screen (figure 10.a), displays the<br> behavior of the simulation; the second one, localized on the right side of the screen (figure 10.b),<br> displays the behavior of the controller. Both application run concurrently and their respective<br> contents allow the user to observe and monitor the control session. The last text line of figure 10.b<br> displays the set of commands at cycle 201.</p>
Figure 10.a. Simulation's display: The characters "\__/" represents the front part of the car that should pass through the string "....==..=.==..==" representing the range of obstacles-Designing a Growing Functional Modules "Artificial Brain"
<p>Once performed the design and configuration, the controller and the local application are<br> executed by pressing the corresponding button. In case of a local simulation, two terminal windows<br> are generated. The first one, localized on the left side of the screen (figure 10.a), displays the<br> behavior of the simulation; the second one, localized on the right side of the screen (figure 10.b),<br> displays the behavior of the controller. Both application run concurrently and their respective<br> contents allow the user to observe and monitor the control session. The last text line of figure 10.b<br> displays the set of commands at cycle 201.</p>
Figure 4. (a) Therapy player software screen, where a) is the stimuli time, b) is the total therapy time, c) is the file path, d) displays the numeric values of each sequence of the therapy, e) shows the current value, and f) shows the current lag angle for zenith and azimuth values; (b) USB mechanism for conversion, where a) USB-UART converter, and b) USB-Zigbee converter.-Design of a Novel Servo-motorized Laser Device for Visual Pathways Diseases Therapy
<p>Where tt time expended by the servomotors to point the laser to a given position and execute<br> a laser beam sequence; tspin is the time that a servomotor needs to spin one degree; ttol is a given the<br> tolerance time; θservo is the addition of degrees that both servos in a laser driver need to spin point<br> the laser in a given position; tstimuli is the time expended in execute a laser beam, between 250 and<br> 605 ms (Weiskrantz et al., 1991); T is the total time of all repetitions in a therapy, suggested<br> between 20 and 60 minutes and N is the number of repetitions in a therapy.</p>
BRAIN Journal-ANNSVM: A Novel Method for Graph-Type Classification by Utilization of Fourier Transformation, Wavelet Transformation, and Hough Transformation-Figure 1. Example displaying two scatter plots with different characteristics and patterns
<p>In addition to this introductory section, the remainder of this paper is organized as follows. In Section 2, we present previous work related to our present study. In Section 3, we describe details regarding the methodology used in this study. In Section 4, we describe our experiments and results, then discuss our findings. Finally, we summarize the key content of our study in Section 5. </p>
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.