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823 results for “attachment”
FIGURE 1 in Redescription of Ceratothoa carinata (Bianconi, 1869) and Ceratothoa oxyrrhynchaena Koelbel, 1878 (Crustacea: Isopoda: Cymothoidae), buccal-attaching fish parasites new to Australia
FIGURE 1. Ceratothoa carinata, ovigerous female (31 mm) (MTQ W30409). A, dorsal view; B, dorsal view of pereonite 1 and cephalon; C, dorsal view of pleotelson; D, lateral view.
FIGURE 5 in Redescription of Ceratothoa carinata (Bianconi, 1869) and Ceratothoa oxyrrhynchaena Koelbel, 1878 (Crustacea: Isopoda: Cymothoidae), buccal-attaching fish parasites new to Australia
FIGURE 5. Ceratothoa oxyrrhynchaena, ovigerous female (20 mm) (MTQ W15730). A, antennule; B, antenna; C, maxillule; D, maxillule tip; E, mandible; F, maxilla; G, maxillab tip; H, maxilliped; I, maxilliped article 3; J, uropod.
FIGURE 2 in Redescription of Ceratothoa carinata (Bianconi, 1869) and Ceratothoa oxyrrhynchaena Koelbel, 1878 (Crustacea: Isopoda: Cymothoidae), buccal-attaching fish parasites new to Australia
FIGURE 2. Ceratothoa carinata, ovigerous female (31 mm) (MTQ W30409). A, antennule; B, antenna; C, maxillule; D, maxillule tip; E, maxilla; F, maxilla tip; G, mandible; H, maxilliped; I, maxilliped article 3; J, uropod.
FIGURE 3 in Redescription of Ceratothoa carinata (Bianconi, 1869) and Ceratothoa oxyrrhynchaena Koelbel, 1878 (Crustacea: Isopoda: Cymothoidae), buccal-attaching fish parasites new to Australia
FIGURE 3. Ceratothoa carinata, ovigerous female (31 mm) (MTQ W30409). A–D, pereopod 1, 2, 6, 7 respectively; E–I, pleopod 1–5 respectively.
FIGURE 4 in Redescription of Ceratothoa carinata (Bianconi, 1869) and Ceratothoa oxyrrhynchaena Koelbel, 1878 (Crustacea: Isopoda: Cymothoidae), buccal-attaching fish parasites new to Australia
FIGURE 4. Ceratothoa oxyrrhynchaena, ovigerous female (20 mm) (MTQ W15730). A, dorsal view; B, dorsal view of pereonite 1 and cephalon; C, dorsal view of pleotelson; D, lateral view.
FIGURE 1. Coral rock with attached brachiopod specimens, ZMB Bra 2235 in Revision of the brachiopod genus Amphithyris (Rhynchonelliformea: Platidiidae) with descriptions of two new species
FIGURE 1. Coral rock with attached brachiopod specimens, ZMB Bra 2235. White crosses indicate the position of specimens of A. cavernicola n. sp. Scale bar = 5 cm.
FIGURE 3 in Review of the buccal-attaching fish parasite genus Glossobius Schioedte & Meinert, 1883 (Crustacea: Isopoda: Cymothoidae)
FIGURE 3. Glossobius impressus (Say, 1818), southern African ovigerous female (32 mm; SAM C345). A, dorsal view of body; B, ventral view of mouthparts; C, antennula; D, antenna; E, ventral view of pleotelson; F, pleopod 1 exopod; G, dorsal view of pleon and pleotelson; H, uropod.
FIGURE 2 in Review of the buccal-attaching fish parasite genus Glossobius Schioedte & Meinert, 1883 (Crustacea: Isopoda: Cymothoidae)
FIGURE 2. Glossobius impressus (Say, 1818), Australian ovigerous female (25 mm; AM P53749). A–F, pereopods 1, 2, 3, 4, 6, 7 respectively; G, dorsal view of pleon and pleotelson; H, ventral view of pleotelson.
FIGURE 1 in Review of the buccal-attaching fish parasite genus Glossobius Schioedte & Meinert, 1883 (Crustacea: Isopoda: Cymothoidae)
FIGURE 1. Glossobius impressus (Say, 1818), Australian ovigerous female (25 mm; AM P53749). A, dorsal view of body; B, dorsal view of pereonites 1, 2 and cephalon; C, ventral view of mouthparts; D, lateral view of cephalon; E, lateral view of body.
Salivary levels of eluents during InvisalignTM treatment with attachments: an in vivo preliminary investigation
<p>Dataset for all analyses.<br><br>Dataset initially made available to editor and peer-reviewers during the peer review phase. After acceptance, the dataset will be made openly available to all without any restrictions.</p>
Mussel attachment geometric models
<p><span>The provided data includes the geometric model files (in STL format) of fouling mussel (<em>Limnoperna fortunei</em>) attachment. The geometric model of an individual adult mussel was generated in Blender. Considering the size of an individual adult mussel (about 20 mm), a 20 cm × 20 cm plane was selected to place a certain density of mussels. The density of the attachment model was set from 500 ind/m2 to 20,000 ind/m2. The location and orientation of each individual mussel was randomly placed on the plane, and three replicates were provided. Besides, the mussel attachment considered the mussel size distributions based on the sampling data from South China and North China. </span></p>
Hydrography from LOPC-attached CTD during PolarFront cruise 2024-01
<p>See the Cruise Report (Daase 2024) for details.</p> <p>Daase, M. (2024). PolarFront January 2024 Cruise Report. Zenodo. <a href="https://doi.org/10.5281/zenodo.10623810" target="_blank" rel="noopener">https://doi.org/10.5281/zenodo.10623810</a></p>
Wideband acoustic transceiver data from probe attached to Frankenstein rosette during PolarFront 2024-01 cruise
<p>See the Cruise Report (Daase 2024) for details.</p> <p>Daase, M. (2024). PolarFront January 2024 Cruise Report. Zenodo. <a href="https://doi.org/10.5281/zenodo.10623810" target="_blank" rel="noopener">https://doi.org/10.5281/zenodo.10623810</a></p>
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.
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.
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.
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.
The Development of the !trumpet [attached video]
<p>Video attached to the article by Nicolas Collins <em>The Development of the !trumpet</em></p>
FIGURE. Fruiting heads and peduncles of C. spongifolia. A. Site WP260; two peduncles have lost heads (arrows 1 and 2), the upper part (male zone) of one spadix lies on ground (arrow 3), and six attached heads all touch ground. B–E. Site WP251; a single, detached immature head with bite marks in upper and lower ends, and torn surface at junction with peduncle (at left in D–E). Scale bars: 10 cm with 1 cm units (main image); 8 cm with 2 cm units (lower right); B–C enlarged, without scale. (Bach Ma NP, 2018). Photos: PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Fruiting heads and peduncles of C. spongifolia. A. Site WP260; two peduncles have lost heads (arrows 1 and 2), the upper part (male zone) of one spadix lies on ground (arrow 3), and six attached heads all touch ground. B–E. Site WP251; a single, detached immature head with bite marks in upper and lower ends, and torn surface at junction with peduncle (at left in D–E). Scale bars: 10 cm with 1 cm units (main image); 8 cm with 2 cm units (lower right); B–C enlarged, without scale. (Bach Ma NP, 2018). Photos: PJM.
FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM.
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.