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213 results for “Geometric morphometric analysis”
Figure 6 from: Guan K, Su J, Wang J, Yang Y (2015) Significance of hind wing morphology in distinguishing genera and species of cantharid beetles with a geometric morphometric analysis. ZooKeys 502: 11-25. https://doi.org/10.3897/zookeys.502.9191
Figure 6 - Comparisons of centroid size variables among different groups: A Lycocerus, Prothemus and Themus B Lycocerus asperipennis, Lycocerus metallescens and Lycocerus orientalis; Prothemus chinensis, Prothemus kiukiangensis and Prothemus purpuripennis; Themus licenti, Themus coelestis and Themus impressipennis.
Data from: Studying developmental variation with Geometric Morphometric Image Analysis (GMIA)
Open the record for dataset details and reuse information.
Data from: Crowdsourced geometric morphometrics enable rapid large-scale collection and analysis of phenotypic data
Open the record for dataset details and reuse information.
Figure 9 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 9 Species richness and morphological diversity of the elytron at the genus level.
Figure 8 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 8 Species richness and morphological diversity of the pronotum at the genus level.
Figure 1 from: Guan K, Su J, Wang J, Yang Y (2015) Significance of hind wing morphology in distinguishing genera and species of cantharid beetles with a geometric morphometric analysis. ZooKeys 502: 11-25. https://doi.org/10.3897/zookeys.502.9191
Figure 1 - Hind wing of Lycocerus asperipennis showing digitizing landmarks.
Fig. 1 in Functional morphology of the cave bear (Ursus spelaeus) mandible: a 3D geometric morphometric analysis
Fig. 1 Phylogenetic tree of the family Ursidae as used in the present study, based on BinindaEmonds et al. (1999), Hofreiter et al. (2002) and Krause et al. (2008)
Fig. 6. The Bayesian 50 in Several Subspecies or Phenotypic Plasticity? A Geometric Morphometric and Molecular Analysis of Variability of the Mayan Cichlid Mayaheros urophthalmus in the Yucatan
Fig. 6. The Bayesian 50% majority rule tree of M. urophthalmus based on concatenated mitochondrial protein gene fragments (cytb and COI, 1677 bp). Bayesian posterior probability supports are shown at the bases of nodes.
Fig. 5 in Several Subspecies or Phenotypic Plasticity? A Geometric Morphometric and Molecular Analysis of Variability of the Mayan Cichlid Mayaheros urophthalmus in the Yucatan
Fig. 5. Topology of haplotypic relationships of 15 populations of the M. urophthalmus complex inferred at a network based on two concatenated mitochondrial protein gene fragments (cytb and COI, 1677 bp) and showing the north and south components.
Figure 7 in Geometric morphometric analysis of shell shape variation in Conus (Gastropoda: Conidae)
Figure 7. Plot of the results of the canonical variate analysis of scores on principal components 1–4 from landmark analysis.
Figure 1 in The evolution of Metriorhynchoidea (mesoeucrocodylia, thalattosuchia): an integrated approach using geometric morphometrics, analysis of disparity, and biomechanics
Figure 1. Two extinct marine crocodylians, and an ichthyosaur, showing the extensive morphological adaptations to a pelagic lifestyle in metriorhynchids: Platysuchus SMNS 9930 (A), a teleosaurid, displays the comparatively heavier body typical of semi-aquatic teleosaurids, goniopholidids, pholidosaurids and eusuchians; in contrast to the hydrodynamic metriorhynchids, such as Cricosaurus suevicus SMNS 9808 (B). The ichthyosaur Stenopterygius SMNS 81841 (C) has similar adaptations to metriorhynchids, i.e. hydrofoil-like forelimbs, hypocercal tail, and the reduction in limb girdle size. Scale bar = 50 mm.
Figure 11. A in The evolution of Metriorhynchoidea (mesoeucrocodylia, thalattosuchia): an integrated approach using geometric morphometrics, analysis of disparity, and biomechanics
Figure 11. A, relative warps cranial morphology morphospace, delimited by the first two axes. B, shape changes corresponding to the mean shape, and the extremes of both of the first two axes.
Figure 10 in The evolution of Metriorhynchoidea (mesoeucrocodylia, thalattosuchia): an integrated approach using geometric morphometrics, analysis of disparity, and biomechanics
Figure 10. Dorsal view of a generalized metriorhynchid skull, with the landmarks measured shown (see Table 4). Image redrawn from Frey et al. (2002).
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
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.