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130 results for “gliding”
Vocal range and ultraviolet-induced photoluminescence in gliding mammals and their relatives
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Ice gliding diatoms establish record-low temperature limits for motility in a eukaryotic cell
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How biomechanics, path-planning and sensing enable gliding flight in a natural environment
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Data from: Gliding for a free lunch: biomechanics of foraging flight in Common Swifts (Apus apus)
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Data from: phenology and environmental determinants of explosive breeding in gliding treefrogs: diel timing of rainfall matters
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Data to: Remotely sensed tree height and density explain global gliding vertebrate richness
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Bridging the gap: Optimising connectivity solutions for an arboreal gliding mammal
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Data from: Gliding dragons and flying squirrels: diversifying versus stabilizing selection on morphology following the evolution of an innovation
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Repository for "Activity-induced polar patterns of filaments gliding on a sphere"
<p>Activity-induced polar patterns of filaments gliding on a sphere (Nature Communications)</p> <p>The structure of this repository is as follows:</p> <p>1. Image.zip -- contains confocal images and equirectangular projections </p> <ul> <li> <p>Confocal_Stacks </p> </li> </ul> <p> contains confocal stacks of Movie S1-S8</p> <ul> <li> <p>Epifluorescence_Projections</p> </li> </ul> <p> contains epifluorescence projections of 100, 150, 300, and 600 nM encapsulated actin concentrations for Figure 1&2</p> <ul> <li> <p>Equirectangular_Projections</p> </li> </ul> <p> contains equirectangular projections of Movie S2, S4-6, S8</p> <p>2. Code.zip -- contains python3 codes and data for MSD and optical flow analysis </p> <ul> <li> <p>MSD</p> </li> </ul> <p> contains codes and data for the MSD analysis in Figure 3f&3g and Figure S5</p> <ul> <li> <p>OpticalFlow</p> </li> </ul> <p> contains codes and data for optical flow analysis in Figure 4b&4c</p> <p> </p>
Figure 7 in Glide-leflection symmetly in deutelostomes: an evolutionaly pelspective
Figure 7. Scheme of a hypothetical transformation of gastrulation in deuterostomes that explains the dorsoventral inversion of some parts with retention of left–right polarity. Gastrulae are shown from left-dorso-vegetal side. A* animal pole; V* vegetal pole. Blue* ectodermal border of the blastopore whose lateral sides give rise to paired neural crests of vertebrates; yellow* embryonic area that makes the neural plate of chordates (regarded here as neurendoderm); pink* LRO distinguished by eccentric cilia; brown* notochordal area of the archenteron; grey* original floor of the archenteron. Two evolutionary steps of a single morphogenetic transformation are: animal–vegetal elongation of the blastopore over the embryonic dorsal side in basal deuterostomes* and the shift of LRO from the dorsal lip of the blastopore to the anterior tip of the archenteron in non-chordate deuterostomes* which caused the inversion of the notochordal area of archenteron from the roof to the floor. See further explanations in the text.
Figure 6 in Glide-leflection symmetly in deutelostomes: an evolutionaly pelspective
Figure 6. Tail scaly organ of anomalurid gliding rodents: A* Anomalurus beecrofti; B* C* Anomalurus derbianus; D* Anomalurus pusillus. A* B* D* external view from the ventral side with the tail base at the top of the figure. C* 3D reconstruction from a CT-scan showing part of the skeleton (lumbar* sacral* and tail vertebrae with pelvis) and a patch of scale-bearing ventral skin of the tail from the left side (see Supporting Information* Model S5). Arrowheads point at the tips of individual scales. (A* B* prepared by Aleksandra A. Panyutina; C* D* prepared by Nadezhda V. Kryukova.)
Figure 5 in Glide-leflection symmetly in deutelostomes: an evolutionaly pelspective
Figure 5. Dorsal osteoderms of Saurosuchus galilei PVSJ 32. A* dorsal view of osteoderms belonging to anterior dorsal vertebrae. B* left-side view of the spinous processes (SP#) of the 8th–10th dorsal vertebrae with attached osteoderms; pink arrowheads point at the tips of the left osteoderms* and blue arrowheads at the right ones. Scale bar 10 cm.
Figure 4 in Glide-leflection symmetly in deutelostomes: an evolutionaly pelspective
Figure 4. Details of calcified rings in the notochordal sheath of Chimaera monstrosa ZIN 34419. A* B* the pectoral trunk region just posterior to the synarcuale (also shown in Fig. 3B and Supporting Information* Models S2* S3). C* D* the tail region just anterior (C) and just posterior (D) to the beginning of the anal fin (also shown in Supporting Information* Model S4). Asterisks marks the dorsal suture between the left and right halves of the rings and commissures. A* C* D* schemes of ring halves in posterior view; the planes of mirror-reflection symmetry are indicated by green lines. B* left-posterior view of CT-scan-based 3D reconstruction of spiral commissures between the rings; the commissures are painted in pink (left part) and blue (right part); calcified parts of basidorsal (BD) and interdorsal (ID) elements of the neural arches are shown for orientation.
Figure 3 in Glide-leflection symmetly in deutelostomes: an evolutionaly pelspective
Figure 3. Somitomeric glide-reflection symmetry in chimaeroid fishes. A* dorsal view of synarcuale (SA) and anterior neural arches of alizarin-stained preparation of Chimaera monstrosa MSU; ID1* first pair of interdorsal elements (photo by Vladislav A. Gorin). B* C* Chimaera monstrosa ZIN 34419. B* left-dorsal view of CT-scan-based 3D reconstruction of calcified rings (CR) in the notochordal sheath and calcified parts of basidorsal (BD)* and interdorsal (ID) elements of neural arches of the pectoral trunk region (see Supporting Information* Model S2); the lips of basidorsal elements are indicated which border the outlets for the ventral nerve root. C* ventral view of the spinal canal enclosing the spinal cord (SC) and ventral nerve roots (VNR) of the pre-anal trunk region. D* X-ray dorsal view of Hydrolagus ogilbyi (image by Artem M. Prokofiev). Arrowheads on (A) and (D) point at the left (pink) and the right (blue) foramina in the posterior blades of synarcuale.
Figure 2. Hagfish segmentation. A in Glide-leflection symmetly in deutelostomes: an evolutionaly pelspective
Figure 2. Hagfish segmentation. A* segmental structures of the roof of the abdominal cavity of Myxine glutionosa ZIN 39898 in ventral view. B–E* Eptatretus stoutii ZIN 56859: (B)* (D1)* and (E) belong to the same individual. B* segmental structures of the walls of abdominal cavity dissected along the right side and spread on a plane; C* external orifices of gill sacs and mucous pouches of the left side (skin removed); D1– D3* individual variations of segmentation represented by subcutaneous blood vessels (some marked with arrowheads) on the underside of the skin of the dorsal surface of the cranial part of the body; E* mucous pouches on the ventral side of the tail. GS* gill sac [its orifice in (C)]; MM* myomere; MP* mucous pouch [its orifice in (C)]; NT* notochord; OD* opisthonephric duct (ureter).
Figure 1 in Glide-leflection symmetly in deutelostomes: an evolutionaly pelspective
Figure 1. Hypothesized alignment of myosepta in a swimming amphioxus. The images (A) and (B) show schematic frontal sections through the notochord and parietal musculature of the same part of the body with a lag of half a locomotor cycle between the two. MM* myomere; MS* myoseptum. Active myomeres and tense myosepta are shown in darker colours than the relaxed ones. Parallel hatching of myomeres represents the longitudinal direction of myofibrils within their respective muscular plates. Red arrows are the force vectors of contraction of the active myomeres applied to corresponding myosepta at the boundary with the relaxed ones* and blue arrows are the force vectors of tension in these myosepta produced by the forces of active myomeres. Blue cross-hatching represents spiral collagen fibres in the tunica fibrosa of the notochord* which transmit diagonal forces of tense myosepta between the left and the right sides of the body.
Supplement of the GIF format images for GLIDE modeling
<p><span><span> </span>the raw exhumation evolution results of the GLIDE modeling: both the original set of the 103 subareas and the test set of the 10 randomly selected subareas</span></p>
Supplement of the GIF format images for GLIDE modeling
<p>the raw exhumation evolution results of the GLIDE modeling: both the original set of the 95 subareas and the test set of the 10 randomly selected subareas</p>
Figure 4 in Gliding canopy flatties and relatives from the Selenops banksi group (Araneae: Selenopidae)
Figure 4. (a) Selenops banksi, ex-S. kikay syn. nov., holotype male, palp, retrolateral view, image has been flipped horizontally (MNRJ – destroyed) (b) Selenops banksi, ex-S. kikay syn. nov. holotype male, palpal tibia and RTA retrolateral view, image has been flipped horizontally (MNRJ – destroyed) (c) S. banksi, ex-S. kikay syn. nov. holotype male, palpal tibia and RTA, retrolateral view, left palp (MNRJ – destroyed) (d) S. banksi, palpal tibia and RTA, ventral, Orellana, Ecuador (NMNH) (e) S. banksi, holotype male, palpal tibia and RTA, ventral, Panama (MCZ 20436) (f) S. banksi, palpal tibia and RTA, ventral, Peru, image has been flipped horizontally (MCZ) (g) S. banksi, palpal tibia and RTA, ventral, Guyana (CAS) (h) S. banksi, ex-S. kikay syn. nov., holotype male, palpal tibia and RTA, ventral (MNRJ – destroyed) (i) S. banksi, ex-
Figure 7 in Gliding canopy flatties and relatives from the Selenops banksi group (Araneae: Selenopidae)
Figure 7. (a) Primary forest habitat of Selenops banksi in Costa Rica [where the specimen in Figure 1(b) was photographed] (photo by Gernot Kunz) (b) habitat around Lloró, Chocó, Colombia, where S. curruganja sp. nov. is found (c) exact locality where a specimen of S. curruganja sp. nov. was collected – arrow indicates the guava tree (d) typical dry forest habitat (forest at centre left) of S. micropalpus, St. Lucia; S. micropalpus is also found in wet forests (e) habitat of S. banksi group in Belize. This record extends the range of the group by ~700 km (photo by Athena Lam).
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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.
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.