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959 results for “GeoMetre”
Figure 2 in Chondrocranial differences in Bufotes variabilis (Anura: Bufonidae): geometric morphometric comparison with two anuran species
Figure 2. Larval chondrocranium in different species. A) B. variabilis, stage 31; B) R. macrocnemis, stage 29; C) H. orientalis, stage 34. ct, cornu trabeculae; lop, larval otic process; cqo, commissura quadratoorbitalis; sc, suprarostral cartilage.
Figure 1 in Chondrocranial differences in Bufotes variabilis (Anura: Bufonidae): geometric morphometric comparison with two anuran species
Figure 1. The suprarostral cartilages in different species. A) B. variabilis, stage 28; B) R. macrocnemis, stage 35; C) H. orientalis, stage 31. cc, central corpus; la, lateral ala.
Figure 3 in Chondrocranial differences in Bufotes variabilis (Anura: Bufonidae): geometric morphometric comparison with two anuran species
Figure 3. Hyobranchial skeleton in different species. A) B. variabilis, stage 45; B) R. macrocnemis, stage 46; C) H. orientalis, stage 44. alp, anterolateral process; c, corpus; h, hyale; plp, posterolateral process; pmp, posteromedial process.
Fig. 2 in Sexual dimorphism and population differentiation in the Chilean Neotropical moth Macaria mirthae (Lepidoptera, Geometridae): a wing geometric morphometric example
Fig. 2. Benítez et al. (2015), representation of the 13 morphological landmarks identified in the forewings of Macaria mirthae.
Fig. 3 in Sexual dimorphism and population differentiation in the Chilean Neotropical moth Macaria mirthae (Lepidoptera, Geometridae): a wing geometric morphometric example
Fig. 3. PCA analysis of the sexual shape dimorphism of Macaria mirthae: the figure shows the first two orthogonal PC components' axes that represent the shape space dimensions, also a decomposition of shape variation between sexes. *Each point represents a different shape.
Fig. 5 in Sexual dimorphism and population differentiation in the Chilean Neotropical moth Macaria mirthae (Lepidoptera, Geometridae): a wing geometric morphometric example
Fig. 5. Multivariate regression of the wing shape on the wing centroid size of Macaria mirthae. Grey points represent female wings and black points represent male wings.
Fig. 1 in Sexual dimorphism and population differentiation in the Chilean Neotropical moth Macaria mirthae (Lepidoptera, Geometridae): a wing geometric morphometric example
Fig. 1. Graphical scheme of the location of the two Valleys in Atacama Desert in the north of Chile.
Figure 6 in Discrimination of the sister hedgehog species Erinaceus concolor and E. roumanicus (Erinaceomorpha: Mammalia): a geometric morphometric approach
Figure 6. Multivariate regression analysis of shape variables vs centroid size of the dorsal cranium (closed circle: E. concolor, n = 39; open circle: E. roumanicus, n = 10).
Figure 4 in Discrimination of the sister hedgehog species Erinaceus concolor and E. roumanicus (Erinaceomorpha: Mammalia): a geometric morphometric approach
Figure 4. PCA scatter plot graphics showing the variations in the mandible (closed circle: E. concolor, n = 54; open circle: E. roumanicus, n = 14) with warped outline drawings describing shape changes along the PC1 axis for each species.
Figure 5 in Discrimination of the sister hedgehog species Erinaceus concolor and E. roumanicus (Erinaceomorpha: Mammalia): a geometric morphometric approach
Figure 5. Histograms of the crossvalidation results. a. Dorsal surface of crania, b. Right side of mandible. Red bars: E. concolor; blue bars: E. roumanicus.
Figure 3 in Shape variation in head scales of species of the genus Ophiomorus DUMÉRIL & BIBRON, 1839 in Iran, a geometric morphometrics approach
Figure 3. Photos of the species of the genus Ophiomorus in Iran: O. tridactylus (A), O. brevipes (B), O. nuchalis (C), O. persicus (D), O. blanfordii (E), and O. streeti (F).
Figure 1. The genus Ophiomorus currently comprises 12 in Shape variation in head scales of species of the genus Ophiomorus DUMÉRIL & BIBRON, 1839 in Iran, a geometric morphometrics approach
Figure 1. The genus Ophiomorus currently comprises 12 extant species and distribution from southeastern Europe (mainland of Greece) to western India (Camaiti et al., 2019).
Figure 6 in Shape variation in head scales of species of the genus Ophiomorus DUMÉRIL & BIBRON, 1839 in Iran, a geometric morphometrics approach
Figure 6. Above wireframe graph in PC2 and scatter plot resulting from the between-group principal components analysis on specimens of the genus Ophiomorus.
Figure 5 in Shape variation in head scales of species of the genus Ophiomorus DUMÉRIL & BIBRON, 1839 in Iran, a geometric morphometrics approach
Figure 5. Landmarks that were used on the intersection of dorsal head scales in Ophiomorus. For detailed definitions of each landmark see Appendix 2.
Fig. 1 in Differentiation of Trichuris species eggs from non-human primates by geometric morphometric analysis
Fig. 1. Trichuris sp. eggs collected from the samples. A. Macaque (Macaca sylvanus) B. Colobus (Colobus guereza kikuyensis). C. Grivet (Chlorocebus aethiops. D. Brazza's monkey (Cercopithecus neglectus). The bar represents 20 μm.
Fig. 2 in Differentiation of Trichuris species eggs from non-human primates by geometric morphometric analysis
Fig. 2. Trichuris sp. egg lineal measurements. L1: maximum width of polar opercula, L2: minimum width of polar opercula, L3: base width of polar opercula, L4: length of polar opercula, measured from exterior midpoint to the narrow midpoint, L5: total length of polar opercula, measured from the exterior midpoint to the base midpoint, L6: wall thickness at its midpoint, L7: wall thickness in contact with polar opercula, L8: interior length of the egg.
Fig. 5. Ordination plot for principal components 1 and 2 in Evaluating sexual dimorphism in the ambrosia beetle Xyleborus affinis (Coleoptera: Curculionidae) using geometric morphometrics
Fig. 5. Ordination plot for principal components 1 and 2 representing elytra shape variation between sexes of Xyleborus Affinis: deformation grids describing variation between sexes on the 2 first principal components are presented.
Fig. 4 in Evaluating sexual dimorphism in the ambrosia beetle Xyleborus affinis (Coleoptera: Curculionidae) using geometric morphometrics
Fig. 4. Boxplots for the body structure centroid size in Xyleborus affinis: (A) elytra centroid size; (B) pronotum centroid size. The line within each box represents the median, and the height of each box represents first and third quartiles (75% of all data). The lines correspond to the observed minimum and maximum values and dots are outliers
Fig. 2 in Evaluating sexual dimorphism in the ambrosia beetle Xyleborus affinis (Coleoptera: Curculionidae) using geometric morphometrics
Fig. 2. Allometric regression of shape on centroid size for each sex: (A) predicted elytra shapes (Predline) to each centroid size; (B) predicted pronotum shapes (Predline) to each centroid size.
Fig. 1 in Evaluating sexual dimorphism in the ambrosia beetle Xyleborus affinis (Coleoptera: Curculionidae) using geometric morphometrics
Fig. 1. Configuration of landmarks and semi-landmarks used to register 1 side of the 2 body structures (elytra and pronotum) of Xyleborus affinis: (A) configuration of 3 landmarks (1, 9, 10) and 7 semi-landmarks (2–8) describing elytra shape; (B) configuration of 3 landmarks (1, 2, 8) and 5 semi-landmarks (3–7) describing pronotum shape.
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
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International Brain Laboratory public data
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OpenNeuro
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