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481 results for “palate”
Palate (p1525)
<b>-- <a href="https://doi.org/10.5281/zenodo.11582199">Documentation</a> --</b><br><br><u>Name</u>: Palate<br><u>musiXplora-ID</u>: p1525<br><u>musiXplora-URI</u>: <a href="https://musixplora.de/mxp/p1525">https://musixplora.de/mxp/p1525</a><br><u>Gender</u>: m<br><u>First Mentioned</u>: 1710<br><u>Last Mentioned</u>: 1750<br><u>Sectors</u>: Instrumentenbau<br><u>Professions (Musical)</u>: Geigenbauer<br><u>Main Place of Activity</u>: Lüttich<br><br><br><u>Titel/Medien:</u><br><table><tbody><tr><th>Role</th><th>Sigel</th><th>Title</th><th>mXp-ID</th></tr><tr><td>Related</td><td>Lütgendorff 1922</td><td>Die Geigen- und Lautenmacher vom Mittelalter bis zur Gegenwart. 2 Bände. Lüt2</td><td><a href="https://musixplora.de/mxp/5002059">5002059</a></td></tr></tbody></table><br><br><u>Changelog</u>:<br> - v0.0.1: Initial Upload.<br>
PALATABILITY OF TWO RODENTICIDE PRODUCTS: FIELD-BASED ASSESSMENT AT PALMYRA ATOLL
This dataset describes the palatability, for the land crab Cardisoma carnifex, of two rodenticide bait products available for conservation use in the U.S.: “25W” containing 25 ppm brodifacoum as the active ingredient, and “D50” containing 50 ppm diphacinone as the active ingredient. Both rodenticide bait products were found to be palatable to rats and crabs when presented alongside three commonly available food items: coconut endosperm (meat), the meristematic tissue of young coconut palms, and the fleshy mesocarp of Pandanus fruit.
FIGURE 10 in Convergent Evolution of a Eusuchian-Type Secondary Palate within Shartegosuchidae
FIGURE 10. Simplified phylogenetic tree mapping the stages in the evolution of the secondary palate in Crocodylomorpha. Palatal bones are colored as follows: maxilla, blue; palatine, pink; ectopterygoid, red; pterygoid, brown; and vomer, yellow.
FIGURE 5 in Convergent Evolution of a Eusuchian-Type Secondary Palate within Shartegosuchidae
FIGURE 5. CT scan cross sections through the pterygoid of Shartegosuchus (IGM 200/50). The blue line demarcates the boundary of the pterygoid. A. anterior to palatal fenestra; B. posterior to palatal fenestra; C. through palatal fenestra; D. through choana. Abbreviations: ch, choana; in cav, internal cavity; pal fen, palatal fenestra.
FIGURE 4 in Convergent Evolution of a Eusuchian-Type Secondary Palate within Shartegosuchidae
FIGURE 4. Digital reconstructions and line drawings of Shartegosuchus asperapalatum (IGM 200/50) in A. left lateral view, B. right lateral view of Shartegosuchus asperapalatum (IGM 200/50). Abbreviations: ang, angular; ant fos, antorbital fossa; d, dentary; ect, ectopterygoid; j, jugal; lac, lacrimal; m, maxilla; n, nasal; pf, prefrontal; pm, premaxilla; pty, pterygoid; sp, splenial.
FIGURE 1. A in Convergent Evolution of a Eusuchian-Type Secondary Palate within Shartegosuchidae
FIGURE 1. A. Map of Mongolia with marker indicating the locality of Shartegosuchus asperapalatum (IGM 200/50). B. Photograph of locality of Shartegosuchus asperapalatum (IGM 200/50) with arrow indicating the position the specimen was recovered from.
FIGURE 8 in Convergent Evolution of a Eusuchian-Type Secondary Palate within Shartegosuchidae
FIGURE 8. The five most parsimonious trees from the analyses (length = 897). Red circles indicate the node Shartegosuchoidea and blue circles indicate the node Shartegosuchidae.
FIGURE 6 in Convergent Evolution of a Eusuchian-Type Secondary Palate within Shartegosuchidae
FIGURE 6. Line drawings of the mandible Shartegosuchus asperopalatum (IGM 200/50) in A. dorsal view, B. left lateral view, and C. right lateral view. Abbreviations: ang, angular; d, dentary; sp, splenial.
Data from: Exploring polymorphism in a palatable prey: Predation risk and frequency-dependence in relation to distinct levels of conspicuousness
<p>Camouflage and warning signals are different anti-predator strategies, which offer an excellent opportunity to study the evolutionary forces acting on prey appearance. Edible prey often escape detection via camouflage, which usually leads to apostatic selection favoring rare morphs. By contrast, defended prey often display conspicuous coloration acting as warning signals to predators, which usually leads to positive frequency-dependence and signal uniformity. However, when two morphs of the same species vary greatly in conspicuousness, the maintenance of both cryptic and conspicuous forms in profitable prey populations remains enigmatic. Using the white and melanic morphs of the invasive box tree moth (<em>Cydalima perspectalis</em>) presented at three different frequencies, we investigate a) the palatability of caterpillars and adult moths to birds, b) predation rates on the less conspicuous melanic morph, and c) the role of frequency-dependence in balancing morph frequencies. Our results show that caterpillars are distasteful for birds but not adult moths, which are fully palatable. We found that the less conspicuous, melanic morph, benefits from reduced predation due to its lower detectability. The more conspicuous, white morph, instead, is more predated and is best off when common, suggesting positive-frequency dependence. These results offer new insights into the evolution of color polymorphism and prey defenses in a polymorphic moth species. Further investigation is required to understand the role of different predation regimes on the maintenance of the polymorphism in this species, and test if additional selection pressures operate in natural populations.</p>
Data for "Impact of early cleft lip and palate surgery on maxillary growth in 5- and 10-Year-old patients with unilateral cleft lip and palate: a cross-sectional study"
<p>Relative frequency in % (absolute frequency is shown above each bar). Frequency of 5YO indices in cleft patients and frequency of GOSLON indices in cleft patients.</p>
Raw Datasets of: "Evaluating the Cost-Effectiveness of Plastic Surgery Based on the Satisfaction with Quality of Life and Nasolabial Appearance in Thai Preteens with Cleft Lip and Palate"
<p>A cross-sectional study with 30 Thai preteen CLP patients aged between 8 to 12-year-old was undertaken between 2017 and 2019 at Tawanchai center. Their satisfaction with QoL was reflected through an interview and a questionnaire with the cooperation of their parents as their caregivers while satisfaction with their nasolabial appearance was from the evaluation of five experts who compared their photos with those of normal faces to determine correlation values of the nasolabial appearance from 5-rating scales using Fleiss’s kappa coefficient scores.</p>
Text-fig. 16. WUSC 4C 33, snout of Kubwachoerus khinzikebirus from Gebel Zelten, Libya. a: palatal view; b: anterior view; c: left lateral view. in New Suoid Fossils (Mammalia, Artiodactyla) From The Miocene Of Moghara, Egypt, And Gebel Zelten, Libya: Biochronological Implications
Text-fig. 16. WUSC 4C 33, snout of Kubwachoerus khinzikebirus from Gebel Zelten, Libya. a: palatal view; b: anterior view; c: left lateral view.
Fig. 4 in Palatability of baits containing (S)-methoprene to Wasmannia auropunctata (Hymenoptera: Formicidae)
Fig. 4. Effects of addition of 0.25% (S)-methoprene and increase in attractiveness of (S)-methoprene baits by the addition of an adjuvant as a masking agent. Treatments with different letters are significantly different (Pp <0.05).
Fig. 1 in Palatability of baits containing (S)-methoprene to Wasmannia auropunctata (Hymenoptera: Formicidae)
Fig. 1. Non-linear regression curve showing the relationship between ant recruitment and proportion of (S)-methoprene in the Hawaii Ant Lab's novel gel bait.
Fig. 2 in Palatability of baits containing (S)-methoprene to Wasmannia auropunctata (Hymenoptera: Formicidae)
Fig. 2. Mean recruitment of ants to baits containing different concentrations of (S)-methoprene. Treatments with different letters are significantly different (P <0.05).
Fig. 80. Stereogenys cromeri Andrews, 1901. BMNH R.3191. Partial braincase and palate. A in Evolution Of The Side-Necked Turtles: The Family Podocnemididae
Fig. 80. Stereogenys cromeri Andrews, 1901. BMNH R.3191. Partial braincase and palate. A, dorsal; B, ventral; C, right lateral; D, anterior; E, left lateral. [C. Wilson, del.]
Fig. 79. Stereogenys cromeri Andrews, 1901. BMNH R.3191. Partial braincase and palate. A in Evolution Of The Side-Necked Turtles: The Family Podocnemididae
Fig. 79. Stereogenys cromeri Andrews, 1901. BMNH R.3191. Partial braincase and palate. A, dorsal; B, ventral; C, right lateral; D, anterior; E, left lateral. [E. Heck, del.]
FIG. 16. Eutretauranosuchus delfsi AMNH FARB 570 in Osteology of a North American goniopholidid (Eutretauranosuchus delfsi) and palate evolution in Neosuchia
FIG. 16. Eutretauranosuchus delfsi AMNH FARB 570. Right hemimandible in lateral view. See appendix 2 for abbreviations.
FIG. 14 in Osteology of a North American goniopholidid (Eutretauranosuchus delfsi) and palate evolution in Neosuchia
FIG. 14. Occiput of Eutretauranosuchus delfsi AMNH FARB 570 in posterior view. Dashed lines indicate reconstructed sutures and surfaces. See appendix 2 for abbreviations.
FIG. 12 in Osteology of a North American goniopholidid (Eutretauranosuchus delfsi) and palate evolution in Neosuchia
FIG. 12. Transverse CT sections through the skull of Eutretauranosuchus delfsi AMNH FARB 570. (A) Tra 574, (B) Tra 770, (C) Tra 878, (D) Tra 936, (E) Tra 1036, (F) Tra 1116. See appendix 2 for abbreviations.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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