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2,914 results for “replacement”
Figs 48–53 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 48–53. Tipula (Sinotipula) hobsoni EdwaRds, 1928, ♂♂ (CAU). 48. Tergite 9, dorsal view (Yadong City). 49. Hypopygium, ventral view. 50. Tergite 9, rear view (Yadong City). 51. Tergite 9, rear view (Qing Dynasty Customs Site, Yadong City). 52. Outer gonostylus, lateral external view. 53. Inner gonostylus, lateral external view. Scale bars = 0.2 mm.
Figs 38–43 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 38–43. Tipula (Sinotipula) heminga sp. nov., holotype, ♂ (CAU). 38. Tergite 9, dorsal view. 39. Tergite 9, rear view. 40. Hypopygium, ventral view. 41. Outer gonostylus, lateral external view. 42. Adminiculum, ventral view. 43. Inner gonostylus, lateral external view. Scale bars: 38–39, 41–43 = 0.2 mm; 40 = 0.5 mm.
Figs 34–37 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 34–37. Tipula (Sinotipula) heminga sp. nov., holotype, ♂ (CAU). 34. Habitus, lateral view. 35. Head and thorax, dorsal view. 36. Hypopygium, lateral view. 37. Wing. Abbreviations: see Material and methods. Scale bars = 1.0 mm.
Figs 29–33 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 29–33. Tipula (Sinotipula) forcipicauda sp. nov., holotype, ♂ (CAU). 29. Tergite 9, dorsal view. 30. Hypopygium, ventral view. 31. Inner gonostylus, lateral external view. 32. Outer gonostylus, lateral external view. 33. Adminiculum, ventral view. Scale bars = 0.2 mm.
Figs 58–59 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 58–59. Tipula (Sinotipula) longiloba sp. nov., paRatype, ♀ (CAU). 58. Habitus, lateral view. 59. Ovipositor, lateral view. Scale bars: 58 = 2.0 mm; 59 = 1.0 mm.
Figs 14–17 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 14–17. Tipula (Sinotipula) exquisita AlexandeR, 1935, ♂ (CAU). 14. Habitus, lateral view. 15. Head and thorax, dorsal view. 16. Hypopygium, lateral view. 17. Wing. Scale bars = 1.0 mm.
Figs 5–6 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 5–6. Tipula (Sinotipula) drolma sp. nov., paRatype, ♀ (CAU). 5. Habitus, lateral view. 6. Ovipositor, lateral view. Scale bars = 1.0 mm.
Figs 1–4 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 1–4. Tipula (Sinotipula) drolma sp. nov., holotype, ♂ (CAU). 1. Habitus, lateral view. 2. Hypopygium, lateral view. 3. Head and thorax, dorsal view. 4. Wing. Abbreviations: see Material and methods. Scale bars = 1.0 mm.
Figs 18–24 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 18–24. Tipula (Sinotipula) exquisita AlexandeR, 1935, ♂♂ (CAU). 18. Tergite 9, dorsal view (near Zhagu Temple). 19. Tergite 9, dorsal view (Qihankai). 20. Hypopygium, ventral view. 21. Tergite 9, rear view (near Zhagu Temple). 22. Plate of tergite 9, rear view (Qihankai). 23. Outer gonostylus, lateral external view. 24. Inner gonostylus, lateral external view. Scale bars: 18–19, 21–24 = 0.2 mm; 20 = 0.5 mm.
Figs 54–57 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 54–57. Tipula (Sinotipula) longiloba sp. nov., holotype, ♂ (CAU). 54. Habitus, lateral view. 55. Hypopygium, lateral view. 56. Head and thorax, dorsal view. 57. Wing. Abbreviations: see Material and methods. Scale bars: 54, 56–57 = 1.0 mm; 55 = 0.5 mm.
Figs 7–13 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924
Figs 7–13. Tipula (Sinotipula) drolma sp. nov., holotype, ♂ (CAU). 7. Tergite 9, dorsal view. 8. Sternite 9, ventral view. 9. Hypopygium, rear view. 10. Inner gonostylus, lateral external view. 11. Outer gonostylus, lateral external view. 12. Gonostylus, lateral external view. 13. Gonostylus, lateral internal view. Abbreviations: see Material and methods. Scale bars: 7–8 = 1 mm; 9, 12–13 = 0.5 mm; 10–11 = 0.2 mm.
2,5-Furandicarboxaldehyde as a Bio-based Crosslinking Agent Replacing Glutaraldehyde for Covalent Enzyme Immobilization
<p>In the quest for a bio-based and safer substitute for glutaraldehyde, we have investigated 2,5 diformylfuran (DFF) as bifunctional crosslinking agent for the covalent immobilization of glucoamylase on amino-functionalized methacrylic resins. Immobilization experiments and systematic comparison with glutaraldehyde at four different concentrations for the activation step showed that DFF leads to comparable enzymatic activities at all tested concentrations. Continuous flow experiment confirms a similar long term stability of the immobilized formulations obtained with the two crosslinkers. The NMR study of DFF in aqueous solution evidenced a much simpler behaviour as compared to glutaraldehyde, since no enolic forms can form and only a mono-hydrated form was observed. Unlike in the case of glutaraldehyde, DFF reacts covalently with the primary amino groups <em>via</em> imine bond formation only. Nevertheless, the stability of the covalent immobilization was confirmed also at acidic pH (4.5), most probably because of the higher stability of the imine bonds formed with the aromatic aldehydes. In terms of toxicity DFF has the advantage of being poorly soluble in water and, more importantly, poorly volatile as compared to glutaraldehyde, which displays severe respiratory toxicity. We have performed preliminary ecotoxicity assays using <em>Aliivibrio fischeri</em>, a marine bacterium, evidencing comparable behaviour (below the toxicity threshold) for both dialdehydes at the tested concentrations.</p>
ANI matrices for isolates from patients with metagenomic evidence of strain replacement
<p>Matrices of average nucleotide identity (ANI) values for all-vs-all comparisons of isolate genomes of the same species recovered from four participants in the PREMIX study. Genome IDs can be linked to publication by genome metadata found on Emory DataVerse site: <a href="https://doi.org/10.15139/S3/GCV41M">https://doi.org/10.15139/S3/GCV41M</a></p>
"It was recorded on Sunday, morning of the 28th of September as some of the slower runners of the Berlin Marathon made it past Torstrasse near my flat. Iwas out to buy some bread for breakfast, but Iusually bring a camera and my Edirol R-1 recorder whenever Igo out. Since Iwas freshly returned to Berlin Iguess Iwas sensitive to the more antiquated sounds which still survive there, like that of the organ grinder. Iam generally interested in how human beings are replacing the presence of Nature with an artificial environment made entirely by human hands (and thus far more understandable, it is hoped). In this new Human Nature, the sounds of Nature are also Human made. Iwrite about these things, but Ialso use the sounds in my videos and my interactive and generative media work, so generally Iam wandering around building up my archive of media documents for use as material in future works." [Baruch/ gottlieb]17 in Collecting Sounds. Online Sharing of Field Recordings as Cultural Practice
"It was recorded on Sunday, morning of the 28th of September as some of the slower runners of the Berlin Marathon made it past Torstrasse near my flat. Iwas out to buy some bread for breakfast, but Iusually bring a camera and my Edirol R-1 recorder whenever Igo out. Since Iwas freshly returned to Berlin Iguess Iwas sensitive to the more antiquated sounds which still survive there, like that of the organ grinder. Iam generally interested in how human beings are replacing the presence of Nature with an artificial environment made entirely by human hands (and thus far more understandable, it is hoped). In this new Human Nature, the sounds of Nature are also Human made. Iwrite about these things, but Ialso use the sounds in my videos and my interactive and generative media work, so generally Iam wandering around building up my archive of media documents for use as material in future works." [Baruch/ gottlieb]17
Figure 3 in Tooth shape in teleosts and its link to tooth spacing and replacement
Figure 3. - The upper jaw dentition in three different life stages of Eretmodus cf. cyanostictus (lineage A) (A-C) (11.4 mm SL, 23.4 mm SL and 51.0 mm S.L., resp.) and magnifications of an individual tooth in the respective dentition (A'-C'). D: Lower jaw of the specimen used in (B, B'), showing monocuspid teeth, formed extramedullary (arrowhead), at the end of a row of spatulate teeth, displaying intramedullary replacement. D': Detail of the last spatulate tooth (arrow) showing replacement tooth forming intramedullary below (asterisk). Scale bars: A, B', D' = 100 µm; A' = 15 µm; B, C = 500 µm; C', D = 200 µm.
Figure 1. – A in Tooth shape in teleosts and its link to tooth spacing and replacement
Figure 1. – A: Scanning electron micrograph of the pharyngeal dentition of a one month-old zebrafish (10.4 mm SL). Note considerable differences in tooth shape in the different positions, and micro-ornamentations (arrowheads) at the tooth tip. Anterior to the left, dorsal to the top. B: Detail of the micro-ornamentations of the tooth tip. Note major cusp (asterisk), minor cusp (arrow), and basal protuberance (arrowhead). C: Transmission electron micrograph of a developing replacement tooth in a one month-old zebrafish (9 mm S.L.). Note that the minor cusp is developing with just one odontoblast extending into it (arrow). Scale bars: A = 50 µm; B = 10 µm; C = 10 µm.
Physical Therapy and Occupational Therapy After Transcatheter Aortic Valve Replacement
ClinicalTrials.gov study NCT03117296. IPD Sharing: NO. Countries: 1. Publications: 3.
Comparative Effectiveness of Decision Support Strategies for Joint Replacement Surgery
ClinicalTrials.gov study NCT02729831. IPD Sharing: YES. Countries: 1. Publications: 2.
Gene Replacement Therapy Clinical Trial for Participants With Spinal Muscular Atrophy Type 1
ClinicalTrials.gov study NCT03306277. IPD Sharing: YES. Countries: 1. Publications: 2.
Single-Dose Gene Replacement Therapy Using for Patients With Spinal Muscular Atrophy Type 1 With One or Two SMN2 Copies
ClinicalTrials.gov study NCT03837184. IPD Sharing: YES. Countries: 3. Publications: 1.
ScienceDex guides
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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.