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.
3,648
datasets available to search
ShareScore release 0.9.0
Dataset results
3,648 results for “induction”
Fig. 7 in Transcriptomic analysis of wound-healing in Solanum tuberosum (potato) tubers: Evidence for a stepwise induction of suberin-associated genes
Fig. 7. RT-qPCR validation of select wound-induced genes. Gene expression values for 14 genes from RT-qPCR (ΔΔCq) and RNA-seq (CPM) analyses were normalized to 0 dpw values, then log2-transformed to generate log2 (foldchange) values. Pearson's correlation coefficients were calculated for log2 (foldchange) values from the two experimental procedures, with α = 0.05 (Supplemental Table 9). The 95% confidence interval was calculated and plotted as 95% confidence bands.
Fig. 13 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 13. Ultrastructure of the reproductive apparatus of Cynipini.(A, B) Volume rendered micrographs of accessory gland of the agamic generation of Disholcaspis quercusmamma confocal images stained with phalloidin (actin), revealing smooth muscles cells, and Hoescht (blue), revealing nuclei. (C)Transmission electron micrograph of a smooth muscle cell on the accessory gland of the agamic generation of Acraspis macrocarpae. (D, E) Confocal images of an accessory gland of D. quercusmamma stained with Hoescht (DNA) and Nile Red (lipid). (F) Transmission electron micrograph of the accessory gland of A. macrocarpae. (G–I) Confocal images of: (G, H) an accessory sac and (I) an oviduct of D. quercusmamma with Hoescht and Nile Red staining. Legend: N: nucleus, f: muscle fiber, m: mitochondria, lv: lipid vesicle.
Fig. 14 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 14. Ovariole anatomy of various Cynipids. Ovarioles of 19 species belonging to five tribes, with insets showing the egg development stage. M: mature egg, D: developing egg, Ga.: galler species, and In.: inquiline species. Square colors correspond to tribe colors introduced in Fig. 2.
Fig. 11 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 11. Relative size of the accessory apparatus in Cynipoids.Accessory sac diameter relative to metasoma length, with the name of the species with the highest ratio.The ratios of (A) accessory sac area over metasoma area and (B) accessory gland length over metasoma length for each species dissected.The dendrogram is adapted from Blaimer et al. (2020).The band indicates the species lifestyle (galler or inquiline) and the generation for Cynipini (sexual, agamic, or unknown). The dot colors in (A) correspond to the cynipoid tribes displayed in the dendrogram in (B).
Fig. 9 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 9. Ultrastructure of Cynipini venom glands. (A) Transversal section of a venom gland of the agamic generation of Disholcaspis quercusmamma, obtained with confocal microscope and stained with Hoechst (DNA) and phalloidin (actin). S: nuclei of secretory cells; L: lumen; white arrow: nuclei of ductule cells. (B, C) Volume rendered micrographs of D. quercusmamma agamic generation venom gland. (B) Secretory cell nuclei (blue) and end apparati (represented by red actin canals), with a subfigure showing the proximity between the nuclei and the secretory region. (C) End apparati of secretory cells, with a subfigure showing the curvature of the secretory region.Yellow: lumen. (D, E) Surface rendered micrographs of A. erinacei agamic generation venom gland obtained by serial block face scanning electron microscopy (D: top view, E: lateral view).The subfigures show the connections between the subcellular elements. Red: end apparatus; green: duct; yellow: lumen; blue: secretory cell nuclei; and purple: ductule cell nuclei.
Fig. 10 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 10. Transmission electron micrographs of the venom gland secretory region of Cynipoids. (A, A′) Disholcaspis quercusmamma agamic generation. (B, B′) Acraspis erinacei agamic generation. (C, C′) Amphibolips confluenta sexual generation. (D, D′, D") Diastrophus nebulosus. (E, E′) Antistrophus laciniatus. (F) Synergus sp. (G) Schematic summarizing the organization of the venom secretory unit inferred from TEM images. The extracellular medium of the 3 tested Cynipini contain high concentrations of nanometric particles. In D. quercusmamma, these particles (P1) are also found in secretory vesicles and seem to assemble into fibers once secreted. In A. erinacei, some secretory vesicles are observed, without particle content, whereas no vesicle are clearly visible in A. confluenta. In this last species, secretory units are surrounded by large granules. In Diastrophus nebulosus, nanometric particles seems to assemble into a 250 nm particle (P2) within secretory vesicles. Once secreted these P2 seem to form larger agglomerations. Lamellar bodies are also secreted in this species. The secretory unit is reduced and surrounded by light vesicles that do not contain any particles in the inquiline Synergus sp. An accumulation of vesicles and granules is observed around the secretory unit of A. laciniatus. In comparison, virus-like particles are secreted in Leptopilina sp. (adapted from Ferrarese et al., 2009). Legend: d: duct, e: extracellular medium, v: vesicle, mv: microvilli, g: granules, P1: 50 nm particle, P2: 250 nm particle, L: lamellar body, VLP: viruslike particle, p40: virus-like particle protein p40. Scale bar = 2 μm.
Fig. 12 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 12. Reproductive apparatus anatomy of various Cynipids. Scale bar = 0.5 mm. Ovaries and accessory glands of 8 species belonging to three tribes, with insets showing the detail of the accessory sacs when necessary. Green arrow: accessory sacs, pink arrow: ovary extremity, and yellow dashed line: accessory gland.
Fig. 8 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 8. Evolutionary pattern of the venom apparatus relative size in Cynipoids. Phenograms depicting the relative size of the venom gland on the left (ratio venom gland length over metasoma length) and the relative size of venom reservoir on the right (ratio venom reservoir area over metasoma area), with indication of the four gall-inducing clades.The phenograms are based on a time calibrated phylogeny of Cynipoidea (Blaimer et al. 2020, Ward et al. 2022), and phylogenetic tree tips are plotted according to their phenotypic value. A: agamic generation, S: sexual generation.
Fig. 7 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 7. Boxplots of the relative size of the venom apparatus in Cynipoids in relation to taxonomic group and life-history traits. This includes (A) lifestyle, (B) tribes, (C) plant tissue attacked among gallers, (D) number of larval chambers in the induced galls (uni- or multilocular), and, among Cynipini, (E) generation. Diplolepidini were excluded due to their absence of fully developed venom apparatus. Bars marked with a different letter indicate significant difference, NS indicates a non-significant difference (Tukey post hoc test, P ≤ 0.05).
Fig. 6 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 6. Divergent appearances of Cynipid wasp venoms.The variable venom coloration in the sexual generation of the genus Amphibolips, ranging from light yellow in most species to dark brown in A. acuminata (first line). Other venom coloration observed in gall wasps (middle line).The agamic generation was dissected for Kokkocynips imbricariae and Atrusca unica. For Callirhytis seminator, A: agamic generation, S: sexual generation, Anti.: Antistrophus.The needle crystals found in the venom reservoir of Andricus robustus (bottom line).
Fig. 5 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 5. Venom apparatus anatomy representative of different Cynipid tribes. Scale bar = 0.5 mm.White arrow: insertion point of the reservoir into the ovipositor; red arrow: insertion point of the gland into the reservoir.The insert for Antistrophus silphii shows the detail of the reservoir morphology, with division between the narrow region (NR) and the large region (LR).
Fig. 4 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 4. Relative size of the venom apparatus in Cynipoids. (A) Venom gland length relative to metasoma length, with the names of the species having the largest venom gland over metasoma ratio indicated. (B) Venom reservoir area relative to metasoma area, with the names of the species having the largest venom reservoir over metasoma ratio indicated. (C) The ratios of venom reservoir area over metasoma area, and venom gland length over metasoma length for each species dissected.The dendrogram is adapted from Blaimer et al. (2020). For venom gland graphs, the dashed lines correspond to the venom gland length equaling the metasoma size, and to the reservoir area equaling 5% of the metasoma area for venom reservoir graphs.The central band indicates the species lifestyle (galler, inquiline, or parasitoid) and the generation for Cynipini (sexual, agamic, or unknown).The colors carry through from (A)–(C) and indicate the cynipoid tribes outlined in (C). Ceropt. = Ceroptrini, Diastrop. = Diastrophini, Diplo. = Diplolepidini, G. = Galler, Inq. = Inquiline, ND = Not dissected.
Fig. 3 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 3. Anatomy of the metasoma of the agamic female of Disholcaspis quercusmamma (Cynipini). (A) Photograph of the adult of the agamic generation. (B) Exocrine and reproductive organs of the metasoma studied in this article. (C–E) Reconstructed internal structures of the metasoma using micro-tomography. (C) Right-lateral view. (D) Detail of the venom apparatus in lateral view. e) Detail of the accessory gland complex in dorsal view. Legend: red arrow: insertion point of the gland into the reservoir; orange, venom gland; purple, venom reservoir; yellow, accessory gland; dark blue, accessory sac; green, ovaries; and light blue, gut. Axis: D, dorsal;V, ventral; A, anterior; P, posterior; L, left; R, right. Scale bar: 1 mm.
Fig. 2 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 2. Examples of oviposition in Cynipidae. Unidentified Cynipini wasps laying eggs (A) in the secondary vein of a red oak (Quercus rubra) and (B) in the bud of a white oak (Quercus alba). (C) Inquiline cynipid wasp (Ceroptres sp.) laying eggs into the petiole gall of the sexual generation of Melikaiella tumifica on Q. rubra. (D) Diplolepis nodulosa (Diplolepidini) ovipositing in a rose bud.
Fig. 1 in Comparative anatomy of venom glands suggests a role of maternal secretions in gall induction by cynipid wasps (Hymenoptera: Cynipidae)
Fig. 1. Diversity of galls induced by Cynipid wasps. Four clades of Cynipidae contain gall-inducing species: the rose-gallers (Diplolepidini), the herb gallers (Aylacini sensu lato), the non-rose Rosaceae gallers (Diastrophini), and the oak gallers (Cynipidini). Cynipidini alternate two generations, sexual and agamic, that differ in their phenotype. Cynipid galls can be induced in various organs (bud, flower, fruit, leaf, root, or stem), and contain one larval chamber (unilocular gall) or several (multilocular gall). Photo credits:Tom Murray (Disholcaspis quercusmamma), Matthew Wills (Acraspis erinacei), Jeremy Collison (Amphibolips confluenta), Bill MacIndewar (Callirhytis quercusfutilis), Jeff Skrentny (Antistrophis silphii), and Erin Faulkner (Diplolepis bicolor).
Flexible Automation and Intelligent Manufacturing 2024, Taiwan - Optimization of Thermal Induction Welding Parameters in LPBFM for Enhanced Adhesion Control
<p>Laser powder bed fusion of metals (LPBFM) is an additive manufacturing process in which powdered alloy is selectively fused together to form near net shape parts. A method for qualifying a model to optimize thermal conduction welding parameters to omit lack of fusion defects is proposed. The approach takes into account: material, geometry and previously experimentally derived, robust process parameters.</p> <p><br>It entails carrying out specific experiments to generate data for calibration and validation of the model for fine-tuning of process parameters to compensate for the changing boundary conditions throughout the build. The objective is to achieve defined adhesion criteria for the meltpools of each laser scan vector.</p> <p><br>The method transforms the build job preparation of LPBFM into an optimization problem by determining the required precision and defining requirements for the model approach to be applicable on the shopfloor. The work contributes to a model-based quality assurance of LPBFM technology.</p>
Arabidopsis guard cell vacuoles imaged after the induction of vacuole fusion
<p>Wild type Arabidopsis thaliana plants from the Columbia-0 ecotype were grown in soil at 22C with a 16 h photoperiod. Leaves from 4-week old plants were cut in the morning and immediately processed to generate epidermal peels. Briefly, a small leaf fragment was applied abaxially to a coverslip coated with medical adhesive and all but the bottommost layers of abaxial cells containing the stomata were scrapped away with a razor. 1 mm thick silicone isolators (GraceBio #664170) were used to create wells around the adhesive for incubations. Epidermal peels were immediately incubated in stomata buffer (MES pH 6.1). To induce stomatal closure, peels were incubated in closing buffer (10 mM MES pH 6.1, 40 mM malate, 5 mM CaCl2, 10 µM BCECF, 50 mM ABA (Sigma Aldrich A1049) at 22C in the dark for two hours. To induce stomatal opening or vacuole fusion, ABA-treated peels were incubated in opening buffer (10 mM MES pH 6.1, 50 mM KCl) supplemented with 10 µM BCECF (Fisher Scientific B1170) and either 3 µM fusicoccin (Sigma F0537) or 33 µM wortmannin (Sigma W3144). Wortmannin-treated peels were kept in the dark, while fusicoccin-treated peels were exposed to the light for up to 1 h. All concentrated stocks were first dissolved in DMSO. Images of leaf epidermal peels were acquired after ABA incubation and after 20, 40 and 60 min of fusicoccin or wortmannin treatments. <br><br>Confocal laser scanning microscopy was carried out in a Zeiss LSM 980 confocal microscope. Images were taken with a 40× FCS water objective (1.1 N.A.). Acquisition of BCECF fluorescence was accomplished with 405 nm laser excitation and 495-550 nm emission filter set. Images were acquired with an Airyscan detector with a pinhole size of 2.5 airy units.</p>
Translucent Event Logs based on the Sepsis Event Log and the Inductive Miner - infrequent
<p>The translucent events logs in this file are based on the Sepsis Event Log (https://data.4tu.nl/articles/dataset/Sepsis_Cases_-_Event_Log/12707639/1) published by Felix Mannhardt. The folders' name specify the threshold setting of the Inductive Miner - infrequent (0.4, 0.6, and 0.8). Details on the generation can be found in https://doi.org/10.1007/978-3-031-70396-6_9.</p>
Translucent Event Logs based on the Road Traffic Fine Management Event Log and the Inductive Miner - infrequent
<p>The translucent events logs in this file are based on the Road Traffic Fine Management Event Log (https://data.4tu.nl/articles/dataset/Road_Traffic_Fine_Management_Process/12683249) published by Massimiliano de Leoni and Felix Mannhardt. The folders' name specify the threshold setting of the Inductive Miner - infrequent (0.4, 0.6, and 0.8). Details on the generation can be found in https://doi.org/10.1007/978-3-031-70396-6_9.</p>
Supplementary data for 'An extreme mutational hotspot in nlpD depends on transcriptional induction of rpoS'
<p>This zip file contains raw data and calculations for each figure of the manuscript "An extreme mutational hotspot in <em>nlpD </em>depends on transcriptional induction of <em>rpoS</em>". Please refer to the README tab of each excel file, or the README txt files in each folder, for a description of each set of data. </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.