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3,630 results for “Forming”
ANOVA test results for Figure 3, as well as tables with post hoc results where all P values are presented in numerical form.
<p>ANOVA test results for Figure 3, as well as tables with post hoc results where all P values are presented in numerical form.</p>
ANOVA test results for Figure 5, as well as tables with post hoc results where all P values are presented in numerical form.
<p>ANOVA test results for Figure 5, as well as tables with post hoc results where all P values are presented in numerical form.</p>
FIGURE11. Life stages of Platynaspis variegata Crotch: a, b, d–i. larva; c. adult, nominate form; j–m. darker variant (Image credits: Dr Rojeet Thangjam, CAU, Imphal). in A review of Platynaspini (Coleoptera: Coccinellidae) of the Indian subcontinent, including description of a new genus from north-eastern India and Bangladesh
FIGURE11. Life stages of Platynaspis variegata Crotch: a, b, d–i. larva; c. adult, nominate form; j–m. darker variant (Image credits: Dr Rojeet Thangjam, CAU, Imphal).
Detection of Ore-forming Elements Migrated from Rock and Soil to Vegetation Leaves using Hyperspectral Data
<p>In this paper we present the detection of ore-forming elements migrated from soil and rock to vegetation leaves using hyperspectral data. The rock, soil (C, B, A layer) and vegetation (root, stem, leaf) samples with the measurements of spectra and element concentrations in the vertical section of the abandoned pits were collected. The wavelet approach is applied to analyze the correlations between spectral features and element concentrations. The results show that the significant correlations are found at a lower order mother wavelets such as Haar. Moreover, the significant correlations are negative between Cu and Mo elements and the wavelet energy vector of the soil and rock to vegetation leaves spectrum. The results also show that ore-forming elements migrated from rock and soil to vegetation leaves can be detected using hyperspectral data in the study area.</p>
Trypanosoma brucei bloodstream form tagging: plate R7852 (replicate dated 20180328)
<p>Trypanosoma brucei bloodstream form tagging protein localisation data. Widefield epifluorescence microscope images of protein subcellular localisation in the bloodstream form life cycle stage of the unicellular eukaryotic pathogen <em>Trypanosoma brucei</em> by endogenous tagging with mNeonGreen (mNG). Raw microscopy data and per-cell line localisation annotation for plate R7852, replicate dated 20180328.</p>
Trypanosoma brucei bloodstream form tagging: plate R7854 (replicate dated 20180403)
<p>Trypanosoma brucei bloodstream form tagging protein localisation data. Widefield epifluorescence microscope images of protein subcellular localisation in the bloodstream form life cycle stage of the unicellular eukaryotic pathogen <em>Trypanosoma brucei</em> by endogenous tagging with mNeonGreen (mNG). Raw microscopy data and per-cell line localisation annotation for plate R1566, replicate dated 20180201.</p>
Trypanosoma brucei bloodstream form tagging: plate R7856 (replicate dated 20180612)
<p>Trypanosoma brucei bloodstream form tagging protein localisation data. Widefield epifluorescence microscope images of protein subcellular localisation in the bloodstream form life cycle stage of the unicellular eukaryotic pathogen <em>Trypanosoma brucei</em> by endogenous tagging with mNeonGreen (mNG). Raw microscopy data and per-cell line localisation annotation for plate R7856, replicate dated 20180612.</p>
Trypanosoma brucei bloodstream form tagging: plate R1566 (replicate dated 20180201)
<p>Trypanosoma brucei bloodstream form tagging protein localisation data. Widefield epifluorescence microscope images of protein subcellular localisation in the bloodstream form life cycle stage of the unicellular eukaryotic pathogen <em>Trypanosoma brucei</em> by endogenous tagging with mNeonGreen (mNG). Raw microscopy data and per-cell line localisation annotation for plate R1566, replicate dated 20180201.</p>
Different forms of Scientific Literacy Predict Vaccine Hesitancy and COVID-19 Risk Perception
<p>This is a data set that accompanies a manuscript that is yet to be published. The data set includes demographic information for 461 participants, and their responses to four surveys: one on scientific methodology, one on scientific facts, one on vaccine hesitiancy, and one on risk estimates related to COVID-19. </p>
FIG. 6 in Cranial shape and diet variation in Myotis species (Chiroptera: Vespertilionidae): testing the relationship between form and function
FIG. 6. Fitted regression line and data points for Procrustes distances between configurations of the mandibular process region and the stretch factor of the masseter muscle. FP = facultative piscivorous species. P = piscivorous species, I = insectivorous species. The regression equation is presented
FIG. 3 in Cranial shape and diet variation in Myotis species (Chiroptera: Vespertilionidae): testing the relationship between form and function
FIG. 3. Ordination plots of the first two canonical axes from two skull modules among dietary groups. A — Ordination plot of the first two canonical axes from parieto-occipital region (skull module 1) with deformation grids derived of each the canonical axis. The horizontal arrow indicated the direction of change in M. vivesi with respect to the consensus shape. The vertical arrow indicated the directions of change in insectivores with respect to the consensus shape; B — Ordination plot of the first two canonical axes from frontal-maxillary region (skull module 2) with deformation grids derived of each the canonical axis. The vertical arrow indicated the direction of change in M. vivesi with respect to the consensus shape. The horizontal arrow indicated the directions of change in facultative piscivores with respect to the consensus shape. Three diets were compared: insectivorous species (×), and facultative piscivorous species (●) and piscivorous species (é)
FIG. 2 in Cranial shape and diet variation in Myotis species (Chiroptera: Vespertilionidae): testing the relationship between form and function
FIG. 2. Image of an articulated skull and mandible used to measure the origin (Ot) and insertion (It) of the temporal muscle, and the origin (Om) and insertion (Im) of the masseter muscle. The angles between origin and insertion distances for temporal (OIt) and masseter muscles (OIm) were drawn
FIG. 4 in Cranial shape and diet variation in Myotis species (Chiroptera: Vespertilionidae): testing the relationship between form and function
FIG. 4. Ordination plots of the first two canonical axes from two mandibular modules among dietary groups. A — Ordination plot of the first two canonical axes from mandibular process area with deformation grids derived of each the canonical axis. The direction of changes in M. vivesi with respect to the consensus shape was indicated for the horizontal arrow. The directions of change in facultative piscivorous and insectivorous species with respect to the consensus shape were indicated for the vertical arrows; B — Ordination plot of the first two canonical axes from the alveolar region with deformation grids derived of each the canonical axis. The directions of change in M. vivesi and facultative piscivores with respect to the consensus shape were indicated for the double-headed arrow. Three dietary groups were compared: insectivorous species (×), facultative piscivorous species (●), and piscivorous species (ì)
FIG. 5 in Cranial shape and diet variation in Myotis species (Chiroptera: Vespertilionidae): testing the relationship between form and function
FIG. 5. Stretch factors of the masticatory muscles within genus Myotis. A — Stretch factors for the masseter muscle in each dietary group; B — Stretch factor for the temporal muscle in each dietary group. Data were presented with median, interquartile 25–75%, and minimum–maximum values indicated in box plots. Sample sizes appear below each box plot. Letters indicate differences among groups
FIG. 1 in Cranial shape and diet variation in Myotis species (Chiroptera: Vespertilionidae): testing the relationship between form and function
FIG. 1. Four configurations of points drew to register the shape of two skull and two mandibular characters in 22 Myotis species. A — Parieto-occipital region with 32 points, 1–32, lateral view; B — Frontal-maxillary region with 20 points, 1–20, lateral view; C — Mandible process area with 22 points, 1–18, 33–36, in lateral view. D — Alveolar region with 14 points, 19–32, lateral view
Fig. 4 in Taxonomic status of the nominal forms assigned to Necromys lactens (Rodentia, Cricetidae) as revealed by molecular and morphometric evidence
Fig. 4.—Individual specimen scores based on log-transformed values of 20 cranial measurements (Mosimann shape variables), projected onto the first and second principal components of the "size-free" Principal Component Analysis (PCA) extracted from A) analysis of specimens (all age classes, n = 49) of the three nominal forms assigned to Necromys lactens: Akodon lactens (black circles, n = 24), A. orbus (dark gray triangles, n = 14), and Bolomys negrito (light gray squares, n = 11); B) analysis of specimens (all age classes, n = 88) of the two main clades recovered for N. lactens: northern clade (NC, black circles, n = 20) and southern clade (SC, light gray triangles, n = 68); C) analysis of specimens (all age classes, n = 88) of the four subclades recovered for N. lactens: northernmost clade (NNC, closed black circles, n = 4), southernmost clade (SSC, open light gray squared, n = 25), central-northern clade (CNC, open black circles, n = 16), and centralsouthern clade (CSC, open dark gray triangles, n = 43). Character loadings and the variance explained by each of the first two principal components appear in Table 3 and Supplementary Data SD1.
Fig. 3 in Taxonomic status of the nominal forms assigned to Necromys lactens (Rodentia, Cricetidae) as revealed by molecular and morphometric evidence
Fig. 3.—Majority rule consensus tree obtained in the Bayesian analysis of 31 cytochrome-b gene sequences of specimens of Necromys lactens (plus sequences of other species of the genus used as outgroup). Numbers indicate posterior probability values of the adjacent nodes. Each terminal is labeled with the institution and catalog number (see acronyms in "Materials and Methods") of the specimen, GenBank accession number (of previously published sequences), and locality data (see complete details in Appendix II). Arg = Argentina; Bo = Bolivia.
Fig. 2 in Taxonomic status of the nominal forms assigned to Necromys lactens (Rodentia, Cricetidae) as revealed by molecular and morphometric evidence
Fig. 2.—Toothwear age classes of Necromys. Age class 1: M3 incompletely erupted or unworn; age class 2: M3 fully erupted and exhibits moderate wear, M1–2 unworn; age class 3: M3 well worn, its occlusal surface is flat or concave, M1–2 exhibit moderate wear; age class 4: M3 heavily worn, being generally concave, M1–2 have worn and flattened cusps, M2 with no trace of the paraflexus; age class 5: M1–3 are all worn and concave; most details of the occlusal topography are obliterated.
Fig. 1 in Taxonomic status of the nominal forms assigned to Necromys lactens (Rodentia, Cricetidae) as revealed by molecular and morphometric evidence
Fig. 1.—Map of southern Bolivia and northwestern Argentina, showing the geographic localities of specimens used in this study. A) Collection localities of the sequenced specimens of Necromys (white circles) and the type localities (white stars) of Akodon lactens (León), A. orbus (Otro Cerro), and Bolomys negrito (Las Pavas). B) Collection localities for specimens of Necromys used in morphometric analyses assigned to Akodon lactens (white triangles), A. orbus (white squares), and Bolomys negrito (white circles). C) Collection localities for specimens of Necromys used in morphometric analyses assigned to the two main clades: northern clade (NC, white circles) and southern clade (SC, white squares). D) Collection localities for specimens of Necromys used in morphometric analyses assigned to the four subclades: northernmost clade (NNC, white circles), central-northern clade (CNC, white circles with a midpoint), central-southern clade (CSC, white squares with a midpoint), and southernmost clade (SSC, white squares). Gray shading corresponds to areas above 2,000 m elevation.
Figure 1. A in The limpet form in gastropods: evolution, distribution, and implications for the comparative study of history
Figure 1. A, external and internal views of Haliotis varia (Linnaeus, 1758) (Haliotidae), Kinabohutan, north-east Sulawesi, Indonesia; Vermeij collection. B, external and internal views of Cranopsis Dall, 1914 (Fissurellidae), off Iceberg Point, Lopez Island, Washington State, USA; Vermeij collection. C, external and internal views of Patelloidea saccharina (Linnaeus, 1758) (Lottiidae), Ngerdis Cove, Arakabesan, Palau; Vermeij collection. Note the strong radial ribs that extend beyond the shell margin. D, external and internal views of Concholepas concholepas (Lamarck, 1801) (Muricidae: Ralpaninaek), Montemar, Chile; Vermeij collection. E, external and internal views of Theodoxus vespertinus (Sowerby, 1849) (Neritidae), near the mouth of Wainiha River, Kauai, Hawaii; Vermeij collection. Note the internal septum and the wing-like sides of the limpet-like shell. F, external and internal views of Crepidula lessonii (Broderip, 1834) (Calyptraeidae), Playa Venado, Pacific coast of Panama; Vermeij collection. Note the internal septum, and the external sculpture of imbricated lamellae. G, external and internal views of Siphonaria gigas (Sowerby, 1825) (Siphonariidae), Playa de Panam� a, Pacific coast of Costa Riica; Vermeij collection. Note the convergence with Patelloida saccharina. H, external view of Delminiella soklici Kochansky-Devide & Sli� skovi� c, 1972, Vu� cipolje near Tomislavgrad, Bosnia and Herzegovina, late early Miocene. Holotype, stored in the National Museum of Bosnia and Herzegovina, Sarajevo (MG3631). Figured from Harzhauser et al. (2016), fig. 3A). Photograph provided by T. A. Neubauer. I, Valenciennius reussi (Neumayr in Neumayr & Paul, 1875), Tirol (=Konigsgnad), Romania, late Miocene (Pannonian). Specimen stored in the Natural History Museum Vienna (NHMW 1900/0009/0005). Photograph provided by T. A. Neubauer.
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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.