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450 results for “hooks”
SQLite3 DB of npm package versions using install hooks
<p>SQLite3 database containing reduced metadata for all versions using at least one of the available install hooks</p> <p>Compressed using zstandard. You can decompress on Linux using these commands:</p> <pre><code class="language-bash">zstd -d npm_registry.db.zst</code></pre> <p> </p>
Figs 121–126 in Sem Study Of Hooks In The Acanthocephala With Emphasis On Structural-Functional Relationships
Figs 121–126. Proboscis and hooks of Paratrajectura longcementglandatus (Transvenidae): 121 — proboscis of P. longcementglandatus with longer anterior hooks; 122 — shorter and more deeply embedded posterior hooks. Note sensory pore just posterior to basal hooks; 123, 124 — a Gallium-cut longitudinal sections of a middle and a more posterior hook, respectively, showing consistent solid core and thin cortical layers continuous with roots; 125 — a partially vacuolated core of another hook in a Gallium cut cross section; 126 — an unusually branched hook in middle of proboscis.
Figs 103–108 in Sem Study Of Hooks In The Acanthocephala With Emphasis On Structural-Functional Relationships
Figs 103–108. Proboscis and hooks of Pallisentis (Pallisentis) nandai (figs 103–107) and Pallisentis (Pallisentis) paranandai (fig. 108) (Quadrigyridae): 103 — an apical view of the proboscis of P. nandai showing the hook arrangement and the proboscis bumps; 104 — an anterior hook with latero-ventral serrations; 105 — a higher magnification of the base of an anterior hook at indented insertion in elevated proboscis ring; note the latero-ventral serrations; 106–107 — a Gallium-cut longitudinal and cross sections of anterior hooks showing the proportion of cortical and core layers and continuity with root elements. These hooks had very high levels of calcium and sulfur but negligible levels of phosphorous; 108 — anterior and middle hooks of P. paranandai also showing elevated serrations at their base.
Figs 97–102 in Sem Study Of Hooks In The Acanthocephala With Emphasis On Structural-Functional Relationships
Figs 97–102. Proboscis and hooks of Acanthogyrus (Acanthosentis) kashmirensis (figs 97–99), Acanthogyrus (Acanthosentis) fusiformis (fig. 100), and Pallisentis (Brevitritospinus) indica (figs 101–102)(Quadrigyridae):97—proboscisof A. kashmirensis showing hook arrangement and sensory pore at its base; 98 — profile of anterior and middle hooks showing their emaciated appearance; 99 — the appearance of the hooks in fig. 98 is explained by their hollow core; see this figure of a Gallium-cut cross section of an anterior hook; 100 — the unusual shape of the proboscis of A. fusiformis with the smaller hooks on the anterior constricted part of the proboscis; 101 — the proboscis of P. indica showing proboscis bumps and sensory pore at its posterior end; 102 — a middle hook showing its angle and relative dimensions.
Figs 73–78 in Sem Study Of Hooks In The Acanthocephala With Emphasis On Structural-Functional Relationships
Figs 73–78. SEM of proboscis and hooks of Nephridiacanthus major (Oligacanthorhynchidae): 73 — hook arrangement and prominent neck of N. major; 74 — a dorso-lateral view of proboscis showing slightly elevated surface of apical organ; 75 — dorsal view of a short posterior hook; 76 — a Gallium-cut section of a hook near its base with prominent ventral expansion similar to that in M. hirudinaceus with almost no cortical layer seen; 77 — a perfectly spherical Gallium cut cross section of another hook near its terminal end; 78 — a lateral Gallium-cut section of another hook showing the same core-cortical relationships as in figs 76 & 77. Note the continuity with the elaborate root.
Figs 49–54 in Sem Study Of Hooks In The Acanthocephala With Emphasis On Structural-Functional Relationships
Figs 49–54. SEM of proboscis and hooks of Moniliformis Saudi (figs 49–50) and Moniliformis kalahariensis (figs 51–54) (Moniliformidae): 49 — apical end of a proboscis of M. Saudi also had 2 sensory pores like M. cryptosaudi; 50 — a middle hook with high levels of calcium and phosphorous; 51 — the proboscis of M. kalahariensis; hooks gradually decrease in size posteriorly; 52 — undeveloped hooks from cockroach; 53 — developing hooks in a juvenile beginning to develop lateral grooves; 54 — fully developed hooks in an adults with completely formed lateral grooves. Hooks of M. kalahariensis, also had high levels of calcium and phosphorous like hooks of M. saudi.
Figs 79–84 in Sem Study Of Hooks In The Acanthocephala With Emphasis On Structural-Functional Relationships
Figs 79–84. SEM of proboscis and hooks of Pachysentis canicola (Oligacanthorhynchidae) (figs 79–82) and Corynosoma strumosum (Polymorphidae) (figs 83, 84): 79 — the proboscis of a female P. canicola showing hook arrangement and sensory pores at posterior proboscis and neck; 80 — an anterior hook deeply recessed in thick cuticular fold; 81 — a posterior hook also deeply recessed in a boat-like cuticular fold; 82 — a Gallium-cut cross section of a hook near its base showing the ventral protrusion as seen in other oligacanthorhynchid genera: Macracanthorhynchus and Nephridiacanthus; 83 — the proboscis of a specimen of C. strumosum showing its bare apical end and larger hooks at the bulge; 84 — a high magnification of a hook showing micropores.
Figs 91–96 in Sem Study Of Hooks In The Acanthocephala With Emphasis On Structural-Functional Relationships
Figs 91–96. Proboscis and hooks of Southwellina hispida (Polymorphidae): 91 — a proboscis of a juvenile S. hispida showing the long anterior hooks, the shorter and thicker middle hooks at swelling, and the smaller posterior hooks; 92 — a few anterior hooks; 93 — shorter and more robust middle hooks at swelling; 94–95 — variations on the degree of vacuolation of the core of hooks with relatively thick cortical layer; 96 — a Gallium-cut section of a middle hook showing a thin cortical layer and solid core.
Figs 31–36 in Sem Study Of Hooks In The Acanthocephala With Emphasis On Structural-Functional Relationships
Figs 31–36. SEM and microscope image of proboscis and hooks of Intraproboscis sanghae (figs 31–34) and SEM of Mediorhynchus africanus (figs 35, 36) (Gigantorhynchidae): 31 — anterior and posterior proboscis of I. sanghae; 32 — a microscope black and while image of proboscides showing the dark receptacle within the posterior proboscis; 33 — the flat apical end of the anterior proboscis with hooks; 34 — a higher magnification of an anterior hook showing the lamellar texture of the lateral and ventral surface; 35 — proboscis of M. africanus showing the divide between anterior hooks and posterior spine-like hooks; 36 — face view of anterior hooks of M. africanus showing proboscis swelling at insertion.
Figs 7–12 in Sem Study Of Hooks In The Acanthocephala With Emphasis On Structural-Functional Relationships
Figs 7–12. SEM of proboscides and hooks of Parhadinorhynchus magnus (Cavisomidae) (figs 7–9) and Centrorhynchus globirostris (Centrorhynchidae) (figs 10– 12): 7 — long cylindrical proboscis with gradually decreasing hook size posteriorly; 8 — a ventral hook; note its curvature and robust base; 9 — a Gallium-cut cross section of a middle hook showing in thick core with high phosphorous and calcium content, and thin cortical layer; 10 — the globular proboscis of C. globirostris showing the separation line between the larger anterior hooks and the smaller posterior spine-like hooks where the anterior end of the receptacle inserts; 11 — an anterior hook showing the ribbed surface found on all hooks; 12 — a Gallium-cut longitudinal section of a hook showing its thick core and marginal cortical layer.
Figs 25–30 in Sem Study Of Hooks In The Acanthocephala With Emphasis On Structural-Functional Relationships
Figs 25–30. SEM of proboscis and hooks of Echinorhynchus cinctulus (figs 25–28) and Echinorhynchus gadi (figs 29–30) (Echinorhynchidae): 25–27 — anterior hooks in some specimens of E. cinctulus with a variety of spines or thorns mostly on the dorsal side of hooks; 28 — the welldeveloped core and thinner cortical layer of a Gallium-cut longitudinal section of a middle hook; 29 — a proboscis of an E. gadi specimen with 15 hooks per row and elevated anterior hooks; 30 — a high magnification of depressed posterior hooks on the same proboscis in fig. 29.
Figs 1—6 in Sem Study Of Hooks In The Acanthocephala With Emphasis On Structural-Functional Relationships
Figs 1—6. SEM of proboscides and hooks of Heterosentis holospinus (Arythmacanthidae) (figs 1—3) and Cavisoma magnum (Cavisomidae) (figs 4–6): 1 — proboscis of H. holospinus with very long anterior hooks and spiny anterior trunk with spine-free anterior cone; 2 — high magnification of posterior spines; 3 — a Gallium-cut longitudinal section of an anterior hook showing thin cortical layer and thick solid core with high levels of calcium and phosphorous; 4 — a partially retracted proboscis of C. magnum showing the gradual reduction in hook size posteriorly; 5 — a high magnification of a middle hook showing its shallow serrated surface; 6 — a Gallium-cut cross section of a middle hook showing its moderately thick cortical layer and core with high sulfur content.
Figs 109–114 in Sem Study Of Hooks In The Acanthocephala With Emphasis On Structural-Functional Relationships
Figs 109–114. Proboscis and hooks of Leptorhynchoides polycristatus (fig. 109), Rhadinorhynchus oligospinosus (figs
Figs 55–60 in Sem Study Of Hooks In The Acanthocephala With Emphasis On Structural-Functional Relationships
Figs 55–60. SEM of proboscis and hooks of Neoechinorhynchus ponticus (figs 55, 56) and Neoechinorhynchus personatus (figs 57–60) (Neoechinorhynchidae): 55 — proboscis of N. ponticus with a sensory pore at level of posterior hooks; 56 — anterior hook showing angle of projection and external serrations; 57 — posterior hook ofN. personatus showing serrations; 58 — a high magnification showing pattern of serrations on an anterior hook; 59 — outermost layer of a hook showing detail of longitudinal serrations in cross section; 60 — a part of a Gallium-cut section of an anterior hook showing its thin cortical layer and dense core, and its articulation vs. the root of the same core density.
Chrysolepis chrysophylla (Douglas ex Hook.) Hjelmq. (BR0000024488099)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Cephalotaxus fortunei Hook. (BR0000024497497)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Cephalotaxus fortunei Hook. (BR0000024497480)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Cephalotaxus fortunei Hook. (BR0000009239296)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Cephalotaxus fortunei Hook. (BR0000024497473)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Cephalotaxus fortunei Hook. (BR0000024497503)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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International Brain Laboratory public data
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OpenNeuro
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