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.
6,783
datasets available to search
ShareScore release 0.9.0
Dataset results
6,783 results for “orientator”
Figure 3 in New Angulobaloghia species and records (Acari: Mesostigmata: Rotundabaloghiidae) from the Oriental region
Figure 3 Angulobaloghia badangi sp. nov. female, holotype, A – idiosoma in dorsal view, B – idiosoma in ventral view.
Figure 2 in New Angulobaloghia species and records (Acari: Mesostigmata: Rotundabaloghiidae) from the Oriental region
Figure 2 Angulobaloghia nabau sp. nov. female, holotype, A – leg I in ventral view, B – leg II in ventral view, C – leg III in ventral view, D – leg IV in ventral view.
Figure 1 in New Angulobaloghia species and records (Acari: Mesostigmata: Rotundabaloghiidae) from the Oriental region
Figure 1 Angulobaloghia nabau sp. nov. female, holotype, A – idiosoma in dorsal view, B – idiosoma in ventral view.
Figure 1 in TWO NEW SPECIES OF MONOPELOPIA FITTKAU, 1962 FROM FORESTS IN INDIA ALONG WITH A KEY TO ADULT MALES OF ORIENTAL AND PALEARCTIC SPECIES (DIPTERA: CHIRONOMIDAE) Abstract
Figure 1. Male of Monopelopia (Monopelopia) recta sp. n. A, ultimate antennal flagellomere, scale: 30 µm; B, wing, scale: 1 mm; C, tibial spurs, scale: 10 µm; D, abdomen showing dark bands; E, hypopygium, scale: 100 µm.
Figure 4 in TWO NEW SPECIES OF MONOPELOPIA FITTKAU, 1962 FROM FORESTS IN INDIA ALONG WITH A KEY TO ADULT MALES OF ORIENTAL AND PALEARCTIC SPECIES (DIPTERA: CHIRONOMIDAE) Abstract
Figure 4. Pupal exuvia of Monopelopia (Monopelopia) obscurata sp. n. A, thoracic horn, scale: 100 µm; B, abdominal TI-TVII, scale: 1 mm; C, tergite VIII and anal lobe, scale: 100 µm.
Figure 3 in TWO NEW SPECIES OF MONOPELOPIA FITTKAU, 1962 FROM FORESTS IN INDIA ALONG WITH A KEY TO ADULT MALES OF ORIENTAL AND PALEARCTIC SPECIES (DIPTERA: CHIRONOMIDAE) Abstract
Figure 3. Male of Monopelopia (Monopelopia) obscurata sp. n. A, wing, scale: 1 mm; B, ultimate flagellomere, scale: 30 µm; C, tibial spurs, scale: 10 µm; D, hypopygium, scale: 100 µm.
Figure 2 in TWO NEW SPECIES OF MONOPELOPIA FITTKAU, 1962 FROM FORESTS IN INDIA ALONG WITH A KEY TO ADULT MALES OF ORIENTAL AND PALEARCTIC SPECIES (DIPTERA: CHIRONOMIDAE) Abstract
Figure 2. Neighbor-Joining tree based on the COX1 gene sequences of Monopelopia recta sp. n. and thirteen most similar sequences from NCBI GenBank. Scale: K2P genetic distance.
Figure 1 in A newly recorded species, Sergentia kizakiensis (Tokunaga, 1940) (Diptera: Chironomidae), from Oriental China with DNA barcode
Figure 1. Sergentia (Baicalosergentia) kizakiensis (Tokunaga, 1940). A) wing; B) thorax; scale bar = 100 µm; C) hypopygium.
Asp138 orientation correlates with ligand subsite occupancy.
<p>This directory contains all files required to plot Asp138 orientation against ligand subsite occupancy across all mouse AMCase structures presented in <strong>Figure 3</strong> of <a href="https://www.biorxiv.org/content/10.1101/2023.06.03.542675">Díaz et al.<em> </em>(2023)</a>.</p> <p>Data was analyzed using Graphpad Prism. Figures were compiled using Adobe Illustrator.</p> <p> </p> <p><strong>Figures</strong></p> <p>- contains PDFs of the occupancy at sugar-binding subsite across all mouse AMCase models presented in Díaz et al., (2023).</p> <p> </p> <p><strong>Occupancy.pzfx </strong></p> <p>- contains raw data and plots of ligand occupancy, and Asp138 <em>active</em> conformation occupancy.</p> <p> </p> <p>Contact:<br> Roberto Efraín Díaz, robertoefrain.diaz@ucsf.edu</p> <p>James Fraser, jfraser@fraserlab.com</p>
IODP Expedition 369 Core orientation
<p>Core orientation data were measured downhole during advanced piston corer (APC) coring, either by Minex FlexIT or Icefield MI-5 core orientation tool. These tools measure magnetic strength and orientation, 3-axis accelerometer data, and tool temperature data.</p>
Figure 1 in Four new species of the genera Dryophthoroides Roelofs, 1879 and Nephius Pascoe, 1885 (Coleoptera, Curculionidae) from Oriental and Papuan Regions
Figure 1. Dryophthoroides spp., holotypes: A – D. telnovi sp. nov., habitus, dorsal view; B – D. insularis sp. nov., habitus, dorsal view; C – D. insularis sp. nov., aedeagus, dorsal view; D – D. telnovi sp. nov., habitus, lateral view; E – D. insularis sp. nov., habitus, lateral view; F – D. insularis sp. nov., aedeagus, lateral view. Scale bar = 1.0 mm for A, B, D, El 0.5 mm for C, F.
Figure 2 in Four new species of the genera Dryophthoroides Roelofs, 1879 and Nephius Pascoe, 1885 (Coleoptera, Curculionidae) from Oriental and Papuan Regions
Figure 2. Nephius spp., holotypes, habitus: A – N. continentalis sp. nov., dorsal view; B – N. philippinensis sp. nov., dorsal view; C – N. continentalis sp. nov., lateral view. Scale bar = 1.0 mm.
Figure 1 in New subtribe and genus of the Metrioxenini (Coleoptera, Belidae) from the Oriental Region
Figure 1. Pseudometrioxena decisa, Timor isl.: a – male, habitus, dorsal view; b – male, habitus, ventral view; c – female, habitus, dorsal view; d – male, abdomen; e – male, aedeagus, dorsal view; f – male, aedeagus, lateral view; g – male, tegmen, dorsal view; h – male, eighth tergite, dorsal view. Scale bar = 1.0 mm for a-c, 0.5 mm for d, 0.2 mm for e-h.
Data from: Quantifying the impact of crop coverings on honey bee orientation and foraging in sweet cherry orchards using RFID
<p>Advancements in agricultural production have seen the rapid adoption of protected cropping systems globally. Such systems have been optimised for plant growth and efficiency, with little understanding of the potential impacts on key insect pollinators. Here we investigate the effect of netting and polythene rain covers on the health and performance of honey bees (<em>Apis mellifera </em>L.) during the pollination of sweet cherry crops. Over two consecutive seasons, twelve full-strength colonies were equipped with tagged bees and radio frequency identification (RFID) systems. The colonies were equally divided between open control, netted, and polythene (semi-permanent VOEN in 2019 and retractable Cravo in 2020) groups. Over 1,300 individual bees were monitored for the duration of the commercial pollination period to determine behavioural parameters such as foraging commencement age, number and duration of trips, and overall survival. Bees began foraging within the optimum age range (mean 15.7-24.1 days) under all covering types, with little indication of prolonged stress or increased mortality during the short season. Polythene covers (VOEN & Cravo) were found to significantly increase the total time needed for bees to orientate successfully. Once orientated, bees placed under covers conducted up to 155% more foraging trips, with a longer cumulative duration. Covering type was found to significantly impact the amount and type of pollen collected, with the most restrictive system (VOEN) yielding the highest proportion of cherry pollen. Overall, we found little evidence to suggest that protective covers have a detrimental impact on honey bee foraging in cherry crops.</p>
IODP Expedition 392 Core orientation
<p>Core orientation data were measured downhole during advanced piston corer (APC) coring, either by Minex FlexIT or Icefield MI-5 core orientation tool. These tools measure magnetic strength and orientation, 3-axis accelerometer data, and tool temperature data.</p>
A new method for quantifying flake scar organisation on cores using orientation statistics
<p>Data and R code for reproducing the results presented in 'in “A new method for quantifying flake scar organisation on cores using orientation statistics” by Lin et al.</p>
Population genomic signatures of the oriental fruit moth related to the Pleistocene climates
Open the record for dataset details and reuse information.
Data from: The effect of external flow on 3D orientation of a microscopic sessile suspension feeder, Vorticella convallaria
Open the record for dataset details and reuse information.
Contributions of mirror-image hair cell orientation to mouse otolith organ and zebrafish neuromast function: Part 2/2, Hair cell and afferent physiology from mouse utricle
Open the record for dataset details and reuse information.
Active cell divisions generate fourfold orientationally ordered phase in living tissue
Open the record for dataset details and reuse information.
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.