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2,679 results for “softness”

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zenodo32/100

Figs 1–10 in Protopectinus pseudoparatinus - a new genus and species of soft winged flower beetle of the tribe Apalochrini (Coleoptera: Malachiidae) from East Africa

Figs 1–10. Protopectinus pseudoparatinus Tshrernyshev gen. et sp.n., holotype, male: 1 — external appearance, dorsal view; 2 — external appearance, lateral view; 3 — left antenna; 4 — left anterior tarsus; 5 — tibia and tarsus of left intermediate leg; 6 — femur of right intermediate leg; 7 — pygidium; 8 — ultimate abdominal ventrite; 9 — aedeagus, dorsal view; 10 — tegmen. Scale bars: 0.5 mm. Рис. 1–10. Protopectinus pseudoparatinus Tshrernyshev gen. et sp.n., голотип, самец: 1 — внеШний вид, дорЗально; 2 — внеШний вид латерально; 3 — левый усик; 4 — леваЯ переднЯЯ лапка; 5 — голень и лапка левой средней ноги; 6 — бедро правой средней ноги; 7 — пигидий (апикальный тергит); 8 — восьмой терминальный абдоминальный вентрит (апикальный стернит); 9 — Эдеагус, дорЗально; 10 — тегмен. МасШтаб: 0,5 мм.

opennotspecifiedMar 2020View details →
zenodo32/100

Data: relation between soft tissue energy dissipation and leg stiffness in running at different step frequencies

<p>Data set - paper:&nbsp; <span>Relation between soft tissue energy dissipation and leg stiffness in running at different step frequencies </span></p>

opencc-by-4.0Apr 2024View details →
zenodo32/100

Repository for "Direct simulation and machine learning structure identification unravel soft martensitic transformation and twinning dynamics"

<p>These files contain data and generation codes for figures, a numerical code for the analysis of structure factors, and a numerical code for the simulation, in an article "Direct simulation and machine learning structure identification unravel soft martensitic transformation and twinning dynamics".</p>

opencc-by-4.0Nov 2024View details →
zenodo32/100

Mindfulness, Psychological Capital, Soft Skills, and Refugees' Psychological Wellbeing

<p>The data concerns the role of positive psychological attributes in the wellbeing of refugees in the context of a less developed country in Africa</p>

opencc-by-4.0Nov 2024View details →
zenodo32/100

Mechanoreceptive soft robotic molluscoids made of granular hydrogel-based organoelectronics

Open the record for dataset details and reuse information.

opencc-by-4.0Nov 2024View details →
zenodo32/100

Modelling the growth of biofilms on soft substrates

Open the record for dataset details and reuse information.

opencc-by-4.0Nov 2024View details →
zenodo32/100

Figure 1 in Air sac attachments or tendon scars: the distinction between soft tissue traces in archosaur bone

Figure 1. Lamellar bone fibres in an anhanguerid pterosaur ulna (DGEO-CTG-UFPE 7516; A-F) and in a spinosaurine theropod tibia (LPP-PV-0042; G-L). Note that these fibres are only visible at high magnifications (100×; arrowheads). Silhouettes in A and G indicate sampled elements (not to scale; art by Felipe A. Elias). All polarized light. Crossed nicols in A-E and G-L. Parallel nicols in F. Compensator in A-D, G-I and L. The relative angle to the cortical surface is approximately 80° in A, B; 340° in C; 290° in D-F; 120° in G-L. Scale bar in A, H = 250 µm; in B, I = 50 µm; G = 500 µm; in C-F, J-L = 10 µm.

opennotspecifiedMar 2023View details →
zenodo32/100

Figure 4 in Air sac attachments or tendon scars: the distinction between soft tissue traces in archosaur bone

Figure 4. Side-by-side comparison between lamellar bone fibres A, pneumosteum B and Sharpey's fibres C, all indicated by arrowheads. A, an anhanguerid pterosaur ulna (DGEO-CTG-UFPE 7516). B, a megaraptoran theropod caudal vertebra (MPMA 08-003-94). C, a dorsal vertebra of Arrudatitan (MPMA 12-0001-97-1024). Magnifier indicates microscope magnification. All polarized light and crossed nicols. Compensator in B. The relative angle to the bone surface is approximately 290° in A; 320° in B; 150° in C. Scale bar in A = 10 µm; in B = 50 µm; in C = 300 µm.

opennotspecifiedMar 2023View details →
zenodo32/100

Figure 3 in Air sac attachments or tendon scars: the distinction between soft tissue traces in archosaur bone

Figure 3. Pneumosteum in saurischian dinosaurs. A-C, a megaraptoran theropod caudal vertebra (MPMA 08-003-94). D-F, a cervical vertebra of the lithostrotian titanosaur Uberabatitan (CPPLIP-1024). G-I, a dorsal vertebra of the saltasaurid titanosaur Ibirania (LPP-PV-0200). Pneumosteum is distinguished from regular lamellar bone due to the presence of an array of tiny asbestiform densely packed fibres (usually shorter than 60 µm; arrowheads). These feature low optical relief and undulose extinction. Silhouettes in A, D and G indicate sampled elements (not to scale; art by Felipe A. Elias). All polarized light. Crossed nicols in A-E and G-I. Parallel nicols in F. Compensator in A-D, G-I, and L. The relative angle to the bone surface is approximately 320° in A-B; 220° in C-D; 105° in E-F; 290° in G; 80° in H-I. Scale bar in A, D = 250 μm; in C, E = 100 μm; in B, F, H, I = 50 μm; in G = 200 μm.

opennotspecifiedMar 2023View details →
zenodo32/100

Figure 2 in Air sac attachments or tendon scars: the distinction between soft tissue traces in archosaur bone

Figure 2. Sharpey's fibres in a dorsal vertebra of Arrudatitan (MPMA 12-0001-97-1024; A-F) and in a spinosaurine theropod tibia (LPP-PV-0042; G-I). Note that these fibres are visible at low magnifications (5×; arrowheads). G, H show a cross pattern of Sharpey's fibres. Silhouettes in A and G indicate sampled elements (not to scale; art by Felipe A. Elias). All polarized light. Crossed nicols in A-F. Parallel nicols in. Compensator in G, H. The relative angle to the bone surface is approximately 150° in A-C; 90° in D; 70° in E; 120° in F; 90° in G-I. Scale bar in A = 300 µm; in D, I = 250 µm; in B, C, E, F = 100 µm; in G, H = 500 µm.

opennotspecifiedMar 2023View details →
zenodo32/100

Upgrading and extending the lifecycle of soft robots by in-situ freeform liquid three-dimensional printing

<p>The data is associated with the research article titled '<em>Upgrading and extending the lifecycle of soft robots by in-situ freeform liquid three-dimensional printing</em>', published in <em>Science Robotics</em> journal.</p>

opencc-by-4.0Dec 2024View details →
zenodo32/100

Dataset for Effects Effects of Soft Tissue Mobilization with TECAR Therapy Using Bracelet Electrodes in Women with Chronic Non-specific Neck Pain

<p>This dataset contains anonymized data from a randomized controlled trial (RCT) evaluating the effectiveness of combining Soft Tissue Mobilization Techniques (STMT) with Capacitive and Resistive Electric Transfer Therapy (TECAR) in women with Chronic Non-Specific Neck Pain (CNSNP). Data include assessments at baseline, the 5th week, and the 6th-month follow-up for variables related to pain intensity, disability, and range of motion (ROM).</p>

opencc-by-4.0Dec 2024View details →
zenodo32/100

Figure 3 in Osteological characters of birds and reptiles are more congruent with molecular phylogenies than soft characters are

Figure 3. Differences in pooled average character transition ages in millions of years between morphological partitions in all bird and squamate datasets. Dashed lines indicate mean ages of osteological (older) and non-osteological (younger) characters. Data is coloured by partition, with osteological data in purple and non-osteological data in green.

opennotspecifiedJul 2021View details →
zenodo32/100

Figure 2 in Osteological characters of birds and reptiles are more congruent with molecular phylogenies than soft characters are

Figure 2. Ensemble retention index between cranial and postcranial partitions for birds and squamates. Cranial partitions have relatively greater higher molecular consistency in datasets falling below the x = y line. Colour corresponds to clade and dot size is proportional to dataset size (in number of total osteological characters).

opennotspecifiedJul 2021View details →
zenodo32/100

Figure 1 in Osteological characters of birds and reptiles are more congruent with molecular phylogenies than soft characters are

Figure 1. Ensemble retention index between osteological and non-osteological partitions for birds and squamates. Osteological partitions have relatively higher molecular consistency in datasets falling below the x = y line. Colour corresponds to clade and dot size is proportional to dataset size (in number of total characters).

opennotspecifiedJul 2021View details →
zenodo32/100

Buy Light Pink Soft Woolen Scarfs Online

<p>Double-sided handmade soft wool scarf. Special fastening allows scarves to wear in different ways. All scarves are different and unique. Feel the comfort and coziness with Invisible Touch. For more details, you can visit <a href="https://invisibletouch.lt/product/light-pink-soft-wool-wider-invisible-touch-scarf/">https://invisibletouch.lt/product/light-pink-soft-wool-wider-invisible-touch-scarf/</a></p>

opencc-by-4.0Jan 2022View details →
zenodo32/100

Raw data movie-file for the analysis of dynamics in the location of the large sphere under crowding condition with hard and soft boundaries.

<p>The raw data movie-file indicate that time-dependent change in the location of large sphere under differrent degrees of crowding of numbers small spheres with hard and soft boundaries.</p>

opencc-by-4.0Jan 2022View details →
dryad32/100

A new marrellomorph arthropod from southern Ontario: A rare case of soft tissue preservation on a late Ordovician open marine shelf

<p>Ordovician open marine lagerstätten are relatively rare and widely dispersed, producing a patchy picture of the diversity and biogeography of non-mineralized marine organisms, and challenging our understanding of the fate of Cambrian groups. Here, for the first time, we report soft-bodied fossils, including a well-preserved marrellomorph arthropod, fragmentary carapaces, and macroalgae, from the late Ordovician (Katian) Upper Member of the Kirkfield Formation near Brechin, Ontario. The unmineralized elements and associated exceptionally preserved shelly biota were entombed rapidly in storm deposits that smothered the shallow, carbonate-dominated shelf. The marrellomorph, <em>Tomlinsonus dimitrii</em> gen. et sp. nov., is remarkable for its ornate, curving cephalic spines and pair of hypertrophied appendages, suggesting a slow-moving, benthic lifestyle. Re-evaluation of marrellomorph phylogeny using new data favours an arachnomorph affinity, though internal relationships are robust to differing outgroup selection. Clades Marrellida and Acercostraca are recovered, but the monophyly of Marrellomorpha is uncertain. The new taxon is recovered as sister to the Devonian <em>Mimetaster</em>, and, as the second youngest known marrellid, bridges an important gap in the evolution of this clade. More generally, the Brechin biota represents a rare window into Ordovician open marine shelf environments in Laurentia, representing an important point of comparison with contemporaneous lagerstätten from other paleocontinents, with great potential for further discoveries.</p>

opencc-zeroFeb 2022View details →
zenodo32/100

micro-CT data and segmentation files for "The ant abdomen: the skeletomuscular and soft tissue anatomy of Amblyopone australis workers (Hymenoptera: Formicidae)"

<p>Two compressed (.zip) files are included. One (Amblyopone_australis_CASENT0753222_CT.zip) contains a directory of 2149 .tif files comprising the micro-CT dataset used in the study. The other (Amblyopone_australis_CASENT0753222_Segmentation.zip) contains a .ORSSession (ORS Dragonfly) file with the dataset and all segmentation labels created in the study. The segmentation labels are organized into multi-regions of interest (multiROIs) for organizational purposes.</p>

opencc-by-4.0Oct 2021View details →
zenodo32/100

On following pages: 52. Angolan Soft-furred Fruit Bat (Lissonycteris angolensis); 53. Little Collared Fruit Bat (Myonycteris torquata); 54. Sao Tome Collared Fruit Bat (Myonycteris brachycephala); 55. Sierra Leone Collared Fruit Bat (Myonycteris leptodon); 56. Bergmans's Collared Fruit Bat (Myonycteris relicta); 57. Broad-faced Fruit Bat (Plerotes anchietae); 58. Hammer-headed Fruit Bat (Hypsignathus monstrosus); 59. Franquet's Epauletted Fruit Bat (Epomops franqueti), 60. Buttikofer's Epauletted Fruit Bat (Epomops buettikoferi); 61. Veldkamp's Epauletted Fruit Bat (Nanonycteris veldkampii); 62. Gambian Epauletted Fruit Bat (Epomophorus gambianus); 63. Peters's Epauletted Fruit Bat (Epomophorus crypturus); 64. Angolan Epauletted Fruit Bat (Epomophorus angolensis); 65. Little Epauletted Fruit Bat (Epomophorus labiatus); 66. Minor Epauletted Fruit Bat (Epomophorus minor); 67. Ansell's Epauletted Fruit Bat (Epomophorus ansell)); 68. Wahlberg's Epauletted Fruit Bat (Epomophorus wahlbergi); 69. Dobson's Epauletted Fruit Bat (Epomophorus dobsoni; 70. Sanborn's Epauletted Fruit Bat (Epomophorus grandis); 71. Lesser Epauletted Fruit Bat (Epomophorus pusillus); 72. Hayman's Epauletted Fruit Bat (Epomophorus intermedius). in Pteropodidae

On following pages: 52. Angolan Soft-furred Fruit Bat (Lissonycteris angolensis); 53. Little Collared Fruit Bat (Myonycteris torquata); 54. Sao Tome Collared Fruit Bat (Myonycteris brachycephala); 55. Sierra Leone Collared Fruit Bat (Myonycteris leptodon); 56. Bergmans's Collared Fruit Bat (Myonycteris relicta); 57. Broad-faced Fruit Bat (Plerotes anchietae); 58. Hammer-headed Fruit Bat (Hypsignathus monstrosus); 59. Franquet's Epauletted Fruit Bat (Epomops franqueti), 60. Buttikofer's Epauletted Fruit Bat (Epomops buettikoferi); 61. Veldkamp's Epauletted Fruit Bat (Nanonycteris veldkampii); 62. Gambian Epauletted Fruit Bat (Epomophorus gambianus); 63. Peters's Epauletted Fruit Bat (Epomophorus crypturus); 64. Angolan Epauletted Fruit Bat (Epomophorus angolensis); 65. Little Epauletted Fruit Bat (Epomophorus labiatus); 66. Minor Epauletted Fruit Bat (Epomophorus minor); 67. Ansell's Epauletted Fruit Bat (Epomophorus ansell)); 68. Wahlberg's Epauletted Fruit Bat (Epomophorus wahlbergi); 69. Dobson's Epauletted Fruit Bat (Epomophorus dobsoni; 70. Sanborn's Epauletted Fruit Bat (Epomophorus grandis); 71. Lesser Epauletted Fruit Bat (Epomophorus pusillus); 72. Hayman's Epauletted Fruit Bat (Epomophorus intermedius).

opennotspecifiedOct 2019View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record