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.
4,391
datasets available to search
ShareScore release 0.9.0
Dataset results
4,391 results for “cryptic”
Fig. 2 in Integrated morphometrics reveals conservatism in the cryptic yellowstripe scad (Perciformes: Carangidae) lineages from the Tropical Western Pacific
Fig. 2. Overview of the different lineal morphometrics and location of the anatomical landmarks () on S. leptolepis. Landmarks refer to (1) tip of snout, (2) occiput/ posterior end of the cranium, (3) anterior insertion of 1st dorsal fin, (4) anterior insertion of 2nd dorsal fin, (5) upper base of caudal fin, (6) end of caudal peduncle, (7) lower base of caudal fin, (8) anterior base of anal fin, (9) anterior base of pelvic fin, (10) mid-base of the pectoral fin (11) ventral edge of the operculum, (12) posterior point of operculum (13) mid-point of the eye. See Table 2 for additional code definitions (Specimen on photo: KAUM-I16948, SL 114.72 mm).
Luciferase readout: Raw neutralization results for neutralization assays from pseudoparticles containing the SARS-CoV-2 receptor binding domain from a cryptic lineage
<div> <div> <div> <p>Deep sequencing of wastewater to detect SARS-CoV-2 has been used during the COVID- 19 pandemic to monitor viral variants as they appear and circulate in communities. SARS- CoV-2 lineages of an unknown source that have not been detected in clinical samples, referred to as cryptic lineages, are sometimes repeatedly detected from specific locations. We have continued to detect one such lineage previously seen in a Missouri site. This cryptic lineage has continued to evolve, indicating continued selective pressure similar to that observed in Omicron lineages.</p> </div> </div> </div> <p>This file contains the raw neutralization data using pseudoparticles containing a SARS-CoV-2 Spike protein with the RBD from the cryptic lineage detected in Missouri wastewater.</p>
Fig. 3 in A new cryptic species of yellow-eared bat Vampyressa melissa species complex (Chiroptera: Phyllostomidae) from Colombia
Fig. 3.—Dorsal, ventral, and lateral views of the skull and lower jaw of the holotype of Vampyressa voragine sp. nov. (ICN 21938).
Fig. 2 in A new cryptic species of yellow-eared bat Vampyressa melissa species complex (Chiroptera: Phyllostomidae) from Colombia
Fig. 2.—Geographic distribution of the four species of the Vampyressa melissa complex. Stars are V. voragine sp. nov. from Colombia. Pentagons are localities of collection of V. elisabethae from Panama. Squares represent V. sinchi from Colombia. Circles are V. melissa from Colombia, Ecuador, and Peru. Black symbols are the type localities of each species.
Fig. 4 in A new cryptic species of yellow-eared bat Vampyressa melissa species complex (Chiroptera: Phyllostomidae) from Colombia
Fig. 4.—Comparative morphology of Vampyressa melissa (left, ICN 23802♀) and Vampyressa voragine sp. nov. (right, ICN 21938♀). (A and B) Morphology of ethmoturbinal bones with respect to the mesethmoid; and the differences in bilobated morphology and shape of inner upper
Fig. 10 in Messor erwini sp. n., a hitherto cryptic harvester ant in the Iberian Peninsula
Fig. 10. Messor capitatus major (A, C, E, G, H; collection code #19646) and minor (B, D, F, I, J; collection code #19643) workers. Lateral view of body (A, B); dorsal view of body (C, D); head in full-face view (E, F); frontal triangle in larger magnification (G, I); lateral view of petiole in larger magnification (H, J).
Fig. 7 in Messor erwini sp. n., a hitherto cryptic harvester ant in the Iberian Peninsula
Fig. 7. Dendrogram solution for the morphometric data of Iberian Messor species. Sample information in the dendrogram given as follows: final species hypothesis followed by a five-digit sample code applied by the genetic lab separated by a hyphen. Two columns of rectangles represent results of the partitioning algorithms 'hclust' and 'kmeans'. Different colors distinguish species. Messor barbarus: black, M. erwini sp. n.: green, M. capitatus: blue, M. bouvieri: red.
Fig. 5 in Messor erwini sp. n., a hitherto cryptic harvester ant in the Iberian Peninsula
Fig. 5. Phylogenetic analysis based on COI of Messor barbarus, M. bouvieri, M. capitatus, and the hitherto unidentified M. erwini sp. n. with Aphaenogaster iberica, M. lobognathus, and M. chamberlini as outgroups, using the Neighbor-Joining method based on Kimura 2-parameter. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) are shown next to the branches. The analysis was conducted in MEGA 7.0.26 (Felsenstein 1985; Saitou and Nei 1987; Nei and Kumar 2000; Kumar et al., 2016).
Fig. 1 in Messor erwini sp. n., a hitherto cryptic harvester ant in the Iberian Peninsula
Fig. 1. Sampling sites. (A) Iberian peninsula; (B) Catalonia. Occurrences of Messor barbarus (yellow, subclades 1 and 2 as defined by Romiguier et al., 2017), M. bouvieri (red), M. capitatus (blue), and the hitherto unidentified M. erwini sp. n. (green) depicted; at the focal study area Castellbell i el Vilar, M. barbarus, M. bouvieri, and the unidentified Messor co-occur (Google Earth Pro 2019, Data SIO, NOAA, U.S. Navy, NGA, GEBCO, Image Landsat/Copernicus).
Fig. 6 in Messor erwini sp. n., a hitherto cryptic harvester ant in the Iberian Peninsula
Fig. 6. Phylogenetic analysis based on COI of Messor barbarus, M. bouvieri, M. capitatus, and the hitherto unidentified M. erwini sp. n. with Aphaenogaster iberica, M. lobognathus, and M. chamberlini as outgroups, using the Maximum Likelihood method based on the General Time Reversible model. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) are shown next to the branches. The analysis was conducted in MEGA 7.0.26 (Nei and Kumar 2000; Kumar et al., 2016).
Fig. 3 in Messor erwini sp. n., a hitherto cryptic harvester ant in the Iberian Peninsula
Fig. 3. Method of Evanno et al. (2005) implemented on the STRUCTURE output data. L(K): mean ± standard deviation (SD) (left) and DeltaK (right). The analysis was conducted in STRUCTURE Harvester (Earl and von Holdt 2012).
Fig. 9 in Messor erwini sp. n., a hitherto cryptic harvester ant in the Iberian Peninsula
Fig. 9. Messor bouvieri major (A, C, E, G, H; collection code #19624) and minor (B, D, F, I, J; collection code #19620) workers. Lateral view of body (A, B); dorsal view of body (C, D); head in full-face view (E, F); frontal triangle in larger magnification (G, I); lateral view of petiole in larger magnification (H, J).
Fig. 4 in Messor erwini sp. n., a hitherto cryptic harvester ant in the Iberian Peninsula
Fig. 4. Bar plot of the Bayesian cluster analysis based on microsatellites genotyped in 286 individuals. The number of clusters is 4: Messor barbarus (yellow cluster), M. bouvieri (red), M. capitatus (blue), and the hitherto unidentified M. erwini sp. n. (green). The y axis shows the percentage of assignment to a certain cluster. The analysis was conducted in STRUCTURE 2.3.4 (Pritchard et al., 2000).
Fig. 8 in Messor erwini sp. n., a hitherto cryptic harvester ant in the Iberian Peninsula
Fig. 8. Messor barbarus major (A, C, E, G, H; collection code #19610) and minor (B, D, F, I, J; collection code #19612) workers. Lateral view of body (A, B); dorsal view of body (C, D); head in full-face view (E, F); frontal triangle in larger magnification (G, I); lateral view of petiole in larger magnification (H, J).
Fig. 2 in Messor erwini sp. n., a hitherto cryptic harvester ant in the Iberian Peninsula
Fig. 2. Position of morphometric characters on head in frontal view, including scape and frontal triangle, and on mesosoma in lateral and dorsal view; see Table 4 for definition of abbreviations and measurement of characters.
Fig. 11 in Messor erwini sp. n., a hitherto cryptic harvester ant in the Iberian Peninsula
Fig. 11. Messor erwini sp. n. major (A, C, E, G, H; holotype; collection code #19603e) and minor (B, D, F, I, J; paratype; collection code #19603d) workers. Lateral view of body (A, B); dorsal view of body (C, D); head in full-face view (E, F); frontal triangle in larger magnification (G, I); lateral view of petiole in larger magnification (H, J).
Figure 1 in Cryptic diversity of Italian bats and the role of the Apennine refugium in the phylogeography of the western Palaearctic
Figure 1. Minimum (pmin, light) and maximum (pmax, dark) genetic distances of mitochondrial sequence marker detected between bat populations from Italy and the rest of their western Palaearctic ranges measured as uncorrected p-distances. Species codes are as follows: MSC, Miniopterus schreibersii; MAL, Myotis alcathoe; NLE, Nyctalus leisleri; PKU, Pipistrellus kuhlii; REU, Rhinolophus euryale; MEM, Myotis emarginatus; RFE, Rhinolophus ferrumequinum; TTE, Tadarida teniotis; MMS, Myotis mystacinus; PAU, Plecotus auritus; PPI I, Pipistrellus pipistrellus clade I; ESE, Eptesicus serotinus; BBA, Barbastella barbastellus; HSA, Hypsugo savii; MDA, Myotis daubentonii; MBR, Myotis brandtii; MPU, Myotis punicus; MCA, Myotis capaccinii; MMY, Myotis myotis/blythii; MNA I, Myotis nattereri clade I; PPI II, Pipistrellus pipistrellus clade II; MBE, Myotis bechsteinii; MNA II, Myotis nattereri clade II (see also Fig. 2).
Microbial responses to stress cryptically alter natural selection on plants
<p><span>Microbial communities can rapidly respond to stress, meaning plants may encounter altered soil microbial communities in stressful environments. Stress may therefore affect plant natural selection not only directly, but also indirectly via changes to the microbial community. Because stress can cause lasting changes to microbial communities, microbes may also cause legacy effects on plant selection that persist even after the stress ceases.</span></p> <p><span>To explore microbial indirect and legacy effects, we grew plants in stressful (salt, herbicide, or herbivory) or non-stressful conditions with microbes that had experienced each of these environments in the previous generation.</span></p> <p><span>Microbial indirect effects generally counteracted the direct effects of stress on plant selection, thereby weakening the strength of stress as a selective agent. Microbial legacy effects altered plant selection in non-stressful environments, suggesting that stress-induced changes to microbes may continue to affect selection after stress is lifted. </span></p> <p><span>These results suggest that soil microbes may play a cryptic role in plant adaptation to stress, potentially reducing the strength of stress as a selective agent and altering the evolutionary trajectory of plant populations.</span></p>
Fig. 3 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)
Fig. 3. Maximum likelihood tkee based on COI sequences of analyzed specimens of Meloe %Eurymeloe). Only suppokted values of nodes %UFBootstkap, UFB ≥ 95 and SH-aLRT ≥ 80%) ake kepokted %SH-LRT/UFB).;ashes %–) indicate non-suppokted values. Coloked vektical baks on the kight shown species delimitation analysis kesults %ASAP, ad hoc, and mPTP) %https://inkscape.okg/it/).
Fig. 8 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)
Fig. 8. Thkee diffekent pattekns of biogeogkaphic discunction and theik kelative moleculak dating %with the 95%HP; in squake bkackets) obsekved in %A) M. orobates and M. digiuliorum; %B) M. apenninicus and M. rugosus ′ M. cfk. rugosus; and %C) M. b. baudii and M. b. glazunovi %https://inkscape.okg/it/).
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.