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693 results for “mouth”
Data from: Reconciling molecular phylogeny, morphological divergence and classification of Madagascan narrow-mouthed frogs (Amphibia: Microhylidae)
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Data from: Genomic data reveals potential for hybridization, introgression, and incomplete lineage sorting to confound phylogenetic relationships in an adaptive radiation of narrow-mouth frogs
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Data from: Phylogeographic and cross-species transmission dynamics of SAT1 and SAT2 Foot-and-Mouth Disease Virus in Eastern Africa
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Data from: Economic costs and health-related quality of life for hand, foot and mouth disease (HFMD) patients in China
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Data from: Towards understanding the genetic basis of mouth asymmetry in the scale-eating cichlid Perissodus microlepis
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Data for: Nestling mouth colors mediate parental favoritism but minimally influence detectability
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Data from: The history of foot-and-mouth disease virus serotype C: the first known extinct serotype?
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Fig. 6 in A new mouth brooder species of Gymnogeophagus with hypertrophied lips (Cichliformes: Cichlidae)
Fig. 6. Geographic distribution of Gymnogeophagus peliochelynion (yellow; star refers to type-locality), G. cf. peliochelynion (orange) and other species of the Gymnogeophagus gymnogenys clade: G. lipokarenos (blue), G. constellatus (green), G. missioneiro (red), G. tiraparae (white), G. mekinos (black), G. pseudolabiatus (pink) in the río Uruguay basin. Records of Gymnogeophagus lipokarenos and Gymnogeophagus constellatus from Argentina (triangles) are based on Casciotta et al. (2017b) and Říčan et al. (2017), respectively.
Fig. 3 in A new mouth brooder species of Gymnogeophagus with hypertrophied lips (Cichliformes: Cichlidae)
Fig. 3. Pharyngeal tooth plate of Gymnogeophagus peliochelynion, 74.2 mm SL, UFRGS 8076, paratype. Dorsal view; anterior to bottom.
Fig. 5 in A new mouth brooder species of Gymnogeophagus with hypertrophied lips (Cichliformes: Cichlidae)
Fig. 5. Gymnogeophagus peliochelynion: above, paratype, male, ZVC-P 13210, paratype, 76.3 mm SL, río Arapey, Colonia Lavalleja, Paso Elías, Salto, Uruguay; below, female, ZVC-P 13057, 65.3 mm SL, Arroyo Sopas, Paso del Cementerio, Salto, Uruguay. Photographs of live specimens.
Fig. 1 in A new mouth brooder species of Gymnogeophagus with hypertrophied lips (Cichliformes: Cichlidae)
Fig. 1. Anterior portion of dorsal-fin skeleton of Gymnogeophagus peliochelynion (anterior towards left), UFRGS 8076, paratype, 74.2 mm SL. Arrow indicates the anterior spine in the first dorsal pterygiophore. Note the lack of su- praneurals between supraoccipital and first dorsal pterygiophore.
Fig. 4 in A new mouth brooder species of Gymnogeophagus with hypertrophied lips (Cichliformes: Cichlidae)
Fig. 4. Gymnogeophagus peliochelynion: top, holotype, male, ZVC-P 12493, 101.9 SL; bottom, paratype, female, UFRGS 8076, 77.2 SL. Both from arroyo de las Tunas on road 31, tributary of río Arapey Grande, Salto, Uruguay. Photographs taken just after collection and fixation in formalin.
FIG. 1 in First record of the rare Wide-mouth flounder Kamoharaia megastoma (Kamohara, 1936) (Pleuronectiformes, Bothidae) from the western Indian Ocean collected during the ATIMO VATAE expedition to Madagascar "Deep South"
FIG. 1. — Map of geographical distribution of Kamoharaia megastoma (Kamohara, 1936) in the Western Pacific and southeastern Indian Ocean (red, after Hensley & Amaoka (2001)) and the southwestern Indian Ocean off Madagascar (yellow stars).
The effects of LED-mediated photobiomodulation vs no photobiomodulation on extraction space closure in adolescents and young adult patients: A split-mouth, randomized controlled trial.
<p>The aim of this split-mouth trial was is to examine the effects of light emitting diode (LED)-mediated photobiomodulation (PBM) compared to no photobiomodulation on maxillary canine distalization.</p> <p>The dataset is openly provided upon acceptance for publication.</p>
Data from: Too constrained to converse: the effect of financial constraints on word-of-mouth
Existing research demonstrates that financial constraints are widespread and influence consumer attention, preference, choice, and consumption in a variety of ways. Despite the growing knowledge of how financial constraints affect the consumer decision making process, less is known about its impact on post-purchase behavior. This work examines whether financial constraints impact an important post-purchase behavior—word-of-mouth—and in what direction. Seven studies show that financial constraints reduce purchase-related word-of-mouth. This effect emerges across consumers' reported frequencies of discussing their purchases with friends and family, as well as their intentions, desires, and real decisions to engage in online word-of-mouth. This effect is explained by reduced anticipated pleasure of engaging in purchase-related word-of-mouth, which results from financially constrained consumers' belief that rehearsing their monetary expenditures will reinforce negative feelings about their limited financial situation. This effect cannot be similarly explained by other accounts such as impression management or the desire to hoard informational resources. Further, the authors show that the reduction in anticipated pleasure from word-of-mouth is specific to sharing about one's monetary expenditures. Thus, financial constraints reduce purchase-related word-of-mouth, but they do not universally decrease one's propensity to share.
Data from: The impact of anchored phylogenomics and taxon sampling on phylogenetic inference in narrow-mouthed frogs (Anura, Microhylidae)
Despite considerable progress in unravelling the phylogenetic relationships of microhylid frogs, relationships among subfamilies remain largely unstable and many genera are not demonstrably monophyletic. Here, we used five alternative combinations of DNA sequence data (ranging from seven loci for 48 taxa to up to 73 loci for as many as 142 taxa) generated using the anchored phylogenomics sequencing method (66 loci, derived from conserved genome regions, for 48 taxa) and Sanger sequencing (seven loci for up to 142 taxa) to tackle this problem. We assess the effects of character sampling, taxon sampling, analytical methods and assumptions in phylogenetic inference of microhylid frogs. The phylogeny of microhylids shows high susceptibility to different analytical methods and datasets used for the analyses. Clades inferred from maximum-likelihood are generally more stable across datasets than those inferred from parsimony. Parsimony trees inferred within a tree-alignment framework are generally better resolved and better supported than those inferred within a similarity-alignment framework, even under the same cost matrix (equally weighted) and same treatment of gaps (as a fifth nucleotide state). We discuss potential causes for these differences in resolution and clade stability among discovery operations. We also highlight the problem that commonly used algorithms for model-based analyses do not explicitly model insertion and deletion events (i.e. gaps are treated as missing data). Our results corroborate the monophyly of Microhylidae and most currently recognized subfamilies but fail to provide support for relationships among subfamilies. Several taxonomic updates are provided, including naming of two new subfamilies, both monotypic.
THE NOMINATIVE FIELD OF MEANS EXPRESSING THE CONCEPT OF "MOUTH" IN ENGLISH AND UZBEK
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The impact of river mouth evolution on shallow gas behaviors: Insights from the Changjiang (Yangtze River) subaqueous delta
<p>Data used for the plots can be found. The data are saved as .grd, .nc, .png and .dat files.</p> <p>1) <strong>Bathymetry of study area.nc</strong><strong> </strong>is used for producing Figs. 1A, 10, 11 and S2 as bathymetric chart.</p> <p>2) <strong>Data for seismic geomorphology.rar</strong> is the dataset used for producing the maps in Figs. 10, 11 and S2.</p> <p>3) <strong>Figure4</strong><strong>.png</strong><strong> </strong>is used for producing Fig. 4.</p> <p>4) <strong>Figure5A.png </strong>and <strong>Figure5D.png</strong><strong> </strong>is used for producing Fig. 5.</p> <p>5) <strong>Figure6A.png </strong>and <strong>Figure6D.png</strong><strong> </strong>is used for producing Fig. 6.</p> <p>6) <strong>Figure7</strong><strong>.png</strong><strong> </strong>is used for producing Fig. 7.</p> <p>7) <strong>Figure8A.png </strong>and <strong>Figure8C.png</strong><strong> </strong>is used for producing Fig. 8.</p> <p>8) <strong>Full waveform & envolope chirp profile.rar</strong> is used for producing Fig. 2. It includes full-size chirp profile in both full waveform and envolope forms shown in Fig. 2.</p> <p>9) <strong>Full waveform & wiggle.rar</strong> is used for producing Fig. 3. It includes full waveform profiles and the wiggle data.</p> <p>10) <strong>History bathymetry during 1958-2011.dat</strong><strong> </strong>is the bathymetric data analyzed and shown in Fig. S3.</p>
Carbohydrate Mouth Rinse Reduces Perceived Exertion and Mental Fatigue, and Improves Technical Actions during Small-Sided Soccer Games
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Made-up mouths with preen oil reveal genetic and phenotypic conditions of starling nestlings
<p>Animal colouration are due to pigments, nanostructures, or to the cosmetic use of natural products, and plays a central role in social communication. The role of cosmetic colouration has traditionally been focussed on scenarios of sexual selection, but it could also be used in other contexts. Here, by using spotless starling (Sturnus unicolor) as a model system, we explore the possibility that nestlings cosmetically used their intensely yellow coloured uropygial secretion to signal their genetic and/or phenotypic quality to their parents. In agreement with the hypothetical cosmetic use of the uropygial secretion, (i) video recorded nestlings collected secretion with the bill at the age of feathering, (ii) cotton swabs turned to the colour of secretion after rubbing with them nestlings' gape, and (iii) gape and skin colourations correlated positively with that of secretion. Furthermore, we found that (iv) secretion colouration has a genetic component, and (v) associated positively with Vitamin-E supplementation and (vi) with plasma carotenoid concentration, which highlights the informative value of nestling secretion. Finally, (vii) colouration of begging related traits and of secretion of nestlings predicted parental feeding preferences. Consequently, all these results strongly suggest that the cosmetic use of coloured uropygial secretion might also play a role in parent-offspring communication, complementing or amplifying information provided by the flamboyant coloured gapes and skin of nestlings. The use of makeups by offspring to communicate with parents has been scarcely explored and we hope that these results will encourage further investigations in birds and some other taxa with parental care. Keywords: Antioxidants, Begging, Makeup hypothesis, Parent-offspring communication, Uropygium --</p>
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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.