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Figure 48 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 48. Left adductor mandibulae and associated structures of the tetragonurid Tetragonurus cuvieri (Tetragonuridae: MZUSP 123241) in lateral (A) and medial (B) view. Scale bar: 5 mm.
Figure 44 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 44. Dorsal (A) and left lateral (B) views of the basipterygium of the stromateid Peprilus triacanthus (Stromateidae: USNM 302441). Arrow in A indicates point of fusion between basipterygia. Arrow in B indicates the posteriorly oriented pelvic spiny process. Scale bar: 3 mm.
Figure 36 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 36. Micro-computed tomography scan of the branchial and pharyngeal-sac skeleton of the ariommatid Ariomma bondi (MZUSP 86717) in dorsal (A) and left lateral (B) view. Scale bar: 4 mm.
Figure 34 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 34. Left hyopalatine arch, opercular series and associated musculature of the paralichthyid Paralichthys isosceles (MZUSP 72323) in lateral (A) and medial (B) view. Scale bar: 10 mm.
Figure 12 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 12. Radiographs of the occipital region and anteriormost vertebrae of the latid Lates niloticus (MZUSP 123243; A) and the centropomid Centropomus parallelus (MZUSP 108244; B) in left lateral view. Scale bars: 4 mm.
Figure 2 in New phenotypic synapomorphies delimit three molecular-based clades of New World direct-developing frogs (Amphibia: Anura: Brachycephaloidea)
Figure 2. Ventral view of hands showing the comparative size of discs on fingers I and II in frogs of the superfamily Brachycephaloidea. A, Yunganastes mercedesae (Lynch & McDiarmid, 1987) (UTA 53291). B, Tachiramantis douglasi (Lynch, 1996) (ICN 15405). C, Craugastor spatulatus (Smith, 1939) (KU 137466). D, Craugastor aurilegulus (Savage et al., 1988) (KU 209010). E, Niceforonia dolops (Lynch & Duellman, 1980) (KU 165868). F, Strabomantis anomalus (Boulenger, 1898) (KU 177631). The shaded areas represent fingers I and II. Scale bars = 2 mm.
Figure 5 in New phenotypic synapomorphies delimit three molecular-based clades of New World direct-developing frogs (Amphibia: Anura: Brachycephaloidea)
Figure 5. Optimization of the relative size of disc on finger I in Pristimantis and related groups. The phylogenetic hypothesis for Pristimantis is that of Padial et al. (2014). Species groups were collapsed, but complete distribution of character states is shown in Table 1. Character numbers are given beneath the square, with primitive-derived character states inside the square (see text and Table 1 for character definitions). Colour-coding: red = untransformed, homoplastic.
Dataset related to article "Emerging Variants, Unique Phenotypes, and Transcriptomic Signatures in COASY-Associated Diseases"
<p>The database contains the raw data included in the article at title.</p>
GWAS Phenotype Data
Open the record for dataset details and reuse information.
Fig. 8 in Tracking the variability of phenotypic traits on a molecular phylogeny: an example from scolopendrid centipedes in peninsular India
Fig. 8 Presence of a lateral spine on the coxopleuron (on one side) mapped onto phylogeny of Indian Digitipes
Fig. 3 in Tracking the variability of phenotypic traits on a molecular phylogeny: an example from scolopendrid centipedes in peninsular India
Fig. 3 Number of glabrous antennal articles mapped onto phylogeny of Indian Digitipes. Taxonomic identifications from Joshi and Edgecombe (2013). CES codes refer to specimen registration numbers
Fig. 2 in Phenotypic influences on the reproductive strategy of the facultative sexual rotifer Brachionus rubens (Monogononta)
Fig. 2 Relationship between either the number of asexual offspring (a) or the production of at least one sexual offspring (b) with the lifetime reproduction for all females. The dashed line in a indicates total investment into asexual offspring. In b, the number of individuals with a given lifetime reproduction and producing either sexual (state 1) or asexual (state 0) offspring is represented by the diameter of the filled circle (see insert). Data in b were fitted ignoring the minor influence of food quality and temperature (see Results)
Fig. 5 a 95 in Using haplotype networks, estimation of gene flow and phenotypic characters to understand species delimitation in fungi of a predominantly Antarctic Usnea group (Ascomycota, Parmeliaceae)
Fig. 5 a 95% probability haplotype network for the U. sphacelata group based on a combined dataset of ribosomal IGS and ITS and protein-coding RPB1 sequences. The 3-step nesting level is shown. Haplotypes are represented by colored circles according to the sample localities. The circle size is proportional to the number of sequences sharing a haplotype, except for haplotype H5 comprising too many
Fig. 3 in Phenotypical plasticity and homoplasy complicate species delimitation in the Cladonia gracilis group (Cladoniaceae, Ascomycota)
Fig. 3 Results of PTLPT analysis, actual tree length compared to the tree lengths for 1,000 artificially recombined
Fig. 1 in Phenotypical plasticity and homoplasy complicate species delimitation in the Cladonia gracilis group (Cladoniaceae, Ascomycota)
Fig. 1 Phylogeny of the C. gracilis group. 50% Majority Rule Bayesian tree based on a combined data set including ITS rDNA, IGS and RPB2. Branches supported with posterior probability ≥0.95 and
Fig. 4 in Evolutionary insights into the eco-phenotypic diversification of Dysdera spiders in the Canary Islands
Fig. 4 Morphological variation of the chelicerae visualized by principal component analysis (PCA) for the three cheliceral parameters and 48 Dysdera species. The first (horizontal) axis explains 42%, and the two first axes together explain 77% of the variability in the data. Only the parameters directly related to the particular grasping tactics, i.e., the relative chelicera length (associated with the "pincers" tactic), fang flatness (associated with the "key" tactic), and concavity of the basal segment (associated with the "fork" tactic) were analyzed. Species abbreviations: ale – D. alegranzaensis, amb – D. ambulotenta, and – D. andamanae, ara – D. arabisenen, ban – D. bandamae, bre – D. breviseta, brp – D. brevispina, cal – D. calderensis, chi – D. chioensis, cri – D. cribellata, cur – D. curvisetae, eng – D. enghoffi, esq – D. esquiveli, gib – D. gibbifera, gol – D. gollumi, gom – D. gomerensis, gua – D. guayota, her – D. hernandezi, hir – D. hirguan, igu – D. iguanensis, ins – D. insulana, lab – D. labradaensis, lan – D. lancerotensis, lev – D. levipes, lio – D. liostetha, lon – D. longa, mac – D. macra, mad – D. madai, mah – D. mahan, min – D. minutissima, mon – D. montanetensis, nes – D. nesiotes, nsp – D. n. sp., ora – D. orahan, pau – D. paucispinosa, ram– D. ramblae, rat – D. ratonensis, rug – D. rugichelis, san – D. sanborondon, sib – D. sibyllina, sil – D. silvatica, sim – D. simbeque, spi – D. spinidorsa, til – D. tilosensis, ung – D. unguimmanis, ver – D. verneaui, vol – D. volcania, ygu – D. yguanirae
Fig. 1 a in Evolutionary insights into the eco-phenotypic diversification of Dysdera spiders in the Canary Islands
Fig. 1 a The chelicera of Dysdera (dorsal view) with measured cheliceral parameters. b, c The measurements used for the calculation of the concavity of the basal cheliceral segment. Abbreviations: BL – basal segment length, BW – section where the basal segment width was measured, CO – concavity of the frontal side of the basal cheliceral segment
Fig. 2 in Evolutionary insights into the eco-phenotypic diversification of Dysdera spiders in the Canary Islands
Fig. 2 Phylogenetic tree with the projected trophic strategy, capture tactic, body size (the larger the body, the fuller the circle), habitat, and cheliceral type (symbols at terminals) of each species. Gray rectangles mark the sister species that occur on the different islands and could
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.
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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.