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1,104 results for “morphological variation”
FIGURE 8 in Genetic and morphological variation analyses of Glandirana rugosa with description of a new species (Anura, Ranidae)
FIGURE 8. Advertisement call of Glandirana reliquia sp. nov. from Tokyo, Japan, recorded at an air temperature of 20.1°C, showing sonogram (top) and wave form (bottom).
FIGURE 6 in Genetic and morphological variation analyses of Glandirana rugosa with description of a new species (Anura, Ranidae)
FIGURE 6. Dorsal (A) and ventral (B) views of the whole body and ventral view of left hand (C) and foot (D) of the male holotype of Glandirana reliquia sp. nov. (KUHE 64088). Scale bar = 20 mm (A, B)/5 mm (C, D). A lateral view of a nearly topotypic male in life (AUEZ 0843: Kamogawa City, Chiba Prefecture) is shown as well (E).
FIGURE 7 in Genetic and morphological variation analyses of Glandirana rugosa with description of a new species (Anura, Ranidae)
FIGURE 7. Dorsal (A), lateral (B), and ventral (C) views and the oral disc (D) of a tadpole of Glandirana reliquia sp. nov. in stage 35 of Gosner (1960), collected on 9 May 2013 at Sendai City, Miyagi Pref., Japan. Scale bar = 10 mm.
FIGURE 4 in Genetic and morphological variation analyses of Glandirana rugosa with description of a new species (Anura, Ranidae)
FIGURE 4. Plot of first against second canonical 28 morphological variates from CANDISC for male (left) and female (right) samples of Glandirana. Squares: East group of G. rugosa; Open diamonds: G. susurra; Closed diamonds: G. emeljanovi; Circles: Central, North, West, and se-Kyushu groups of G. rugosa.
FIGURE 5 in Genetic and morphological variation analyses of Glandirana rugosa with description of a new species (Anura, Ranidae)
FIGURE 5. Frequencies of four categories of the degree of development of larval ventral glands. Black: state A, dark gray: state B, light gray: state C, and white: state D.
FIGURE 3 in Genetic and morphological variation analyses of Glandirana rugosa with description of a new species (Anura, Ranidae)
FIGURE 3. Results of MIG-seq (Multiplexed ISSR genotyping by sequencing), showing unique position of East group. (A) A RAxML tree based on variable sites picked up from SNPs data. Numbers above branches represent bootstrap supports for ML inference. Number of each sample corresponds with those shown in the supplementary Table 1 deposited in Figshare (DOI: 10.6084/m9.figshare.20290599). Boxed numbers indicate the locality where we found both of West and se-Kyushu group of G. rugosa. (B, C) Plot of first against second (B) and third (C) principal scores of 397 alleles derived from SNPs data. Squares: East group of G. rugosa; Open diamonds: G. susurra; Closed diamonds: G. emeljanovi; Circles: Central, North, West, and seKyushu groups of G. rugosa. (D) Genetic structure in each individual of mitochondrial groups of Glandirana. Two primary genetic demes (K = 2) identified by the STRUCTURE analysis.
FIGURE 1 in Genetic and morphological variation analyses of Glandirana rugosa with description of a new species (Anura, Ranidae)
FIGURE 1. Variation in degree of development of larval ventral glands. (A) State A, (B) State B, (C) State C, and (D) State D.
FIGURE 2 in Genetic and morphological variation analyses of Glandirana rugosa with description of a new species (Anura, Ranidae)
FIGURE 2. RAxML trees based on sequence of mitochondrial 12S and 16S rRNA genes (left) and on sequence of cyt b genes (right) for samples of Glandirana. Numbers above or below branches represent bootstrap supports for ML inference and Bayesian posterior probability (ML-BS/BPP). Accession numbers are shown for the data obtained from GenBank. Number of each sample corresponds with those shown in the supplementary Table 1 deposited in Figshare (DOI: 10.6084/m9.figshare.20290599). Boxed numbers indicate the locality where we found both of West and se-Kyushu group of G. rugosa.
› Figure 22. A, B, Tegenaria capolongoi; C-K, Tegenaria parmenidis; L-S, Tegenaria circeoensis sp. nov. Left male palp in ventral (E, N), retrolateral (F, O), and dorsal views (G, P); epigyne in ventral (A, C, Q, S) and vulva in dorsal view (B, D, R); intraspecific epigynal morphological variation (S); face of male in frontal view (J); spinnerets in ventral view (K); habitus (H) of male in dorsal and sternum in ventral view (I); carapace and abdomen of male in dorsal view (L, M). Scale bars = 0.5 mm (except 1 mm for H). in Phylogeny and taxonomy of European funnel-web spiders of the Tegenaria-Malthonica complex (Araneae: Agelenidae) based upon morphological and molecular data
› Figure 22. A, B, Tegenaria capolongoi; C-K, Tegenaria parmenidis; L-S, Tegenaria circeoensis sp. nov. Left male palp in ventral (E, N), retrolateral (F, O), and dorsal views (G, P); epigyne in ventral (A, C, Q, S) and vulva in dorsal view (B, D, R); intraspecific epigynal morphological variation (S); face of male in frontal view (J); spinnerets in ventral view (K); habitus (H) of male in dorsal and sternum in ventral view (I); carapace and abdomen of male in dorsal view (L, M). Scale bars = 0.5 mm (except 1 mm for H).
The research of River Morphology transition and Sediment variation: Shule River, Northwest of China
<p>The morphological features of the Shule River DFS are summarized based on remote sensing image data. It is fan-shaped and nearly symmetric, with a radius of 59.6 km, arc length of 128 km, chord length of 113 km and fan apex angle of 96°, covering an overall area of 3660 km<sup>2</sup>. According to the differences in geomorphological features, slope and river morphology, the Shule River DFS can be divided into the proximal, medial and distal portions (Fig 2). The proximal portion is geomorphologically characterized by the coverage of gravel Gobi, the medial portion by the presence of psammophytic vegetations, and the distal portion by oasis plain. There is a trend of descending slope from the proximal portion through the medial proportion to distal portion (Fig.2). River morphology grades from large-scale braided at the proximal portion through bifurcating braided at the medial portion to meandering at the distal portion. The differences in type of sedimentary microfacies and sedimentary characteristics allow us to determine the distribution law and distribution model of sedimentary facies under modern branched river system.</p>
Figure 1 in Intraspecific variation in the morphology of Alloxysta fracticornis (Thomson, 1862)(Hymenoptera: Figitidae: Charipinae)
Figure 1. Bayesian tree inferred from the GenBank and FRACTI COI sequences (03 and 04 represent brachypterous specimens; 01 and 02 represent winged specimens). Posterior probability values are shown on branches (only values ≥ 0.95 are included).
Figure 2 in Intraspecific variation in the morphology of Alloxysta fracticornis (Thomson, 1862)(Hymenoptera: Figitidae: Charipinae)
Figure 2. Morphological features of Alloxysta fracticornis (Thomson, 1862), brachyptery form: (a) fore wing, (b) pronotum in dorso-lateral view, (c) propodeum, (d) antennae, (e) lateral habitus.
Figure 1 in Neurostigma xanthopterum New, 1980 (Psocodea: Psocoptera: Epipsocidae): updated diagnosis, description of a female specimen, morphological variations and a checklist of all known species of the genus
Figure 1. Neurostigma xanthopterum. (male I). (1) Lateral view. Scale in mm.
Figure 12 in Neurostigma xanthopterum New, 1980 (Psocodea: Psocoptera: Epipsocidae): updated diagnosis, description of a female specimen, morphological variations and a checklist of all known species of the genus
Figure 12. Distribution of the Neurostigma xanthopterum specimens.
FIGURE 7 in Morphological variation in a conservative structure: the scapulocoracoids in Sympterygia acuta Garman, 1837 and Sympterygia bonapartii Müller & Henle, 1841 (Chondrichthyes: Rajidae)
FIGURE 7. Phylogenetic analysis of Sympterygia species from McEachran (1982). Scapulocoracoid characters are shown within boxes. [7] = scapulocoracoid rectangular and expanded between meso- and metacondyles; [8] = multiple postdorsal foramina or expanded fenestra; [14] = ratio of scapulocoracoid height to length <75%; [15] = postdorsal and postventral fenestrae ḵ3; [25] = ratio of scapulocoracoid height to length <55%; [26] = postdorsal and postventral fenestrae>5.
FIGURE 6 in Morphological variation in a conservative structure: the scapulocoracoids in Sympterygia acuta Garman, 1837 and Sympterygia bonapartii Müller & Henle, 1841 (Chondrichthyes: Rajidae)
FIGURE 6. Scapulocoracoid morphotypes observed in Sympterygia bonapartii. With (A) three, (B) four, (C) five, (D) six, (E) seven, (F) eight, and (G) nine postdorsal fenestrae. Arrows indicate small fenestrae not clearly seen in the image.
FIGURE 4 in Morphological variation in a conservative structure: the scapulocoracoids in Sympterygia acuta Garman, 1837 and Sympterygia bonapartii Müller & Henle, 1841 (Chondrichthyes: Rajidae)
FIGURE 4. NMDS (non-metric multidimensional scaling) graphic from four standardized morphometric variables from scapulocoracoids of males (blue; n = 36) and females (pink; n = 49) of (A) Sympterygia acuta (n = 43) and (B) S. bonapartii (n = 42).
FIGURE 3 in Morphological variation in a conservative structure: the scapulocoracoids in Sympterygia acuta Garman, 1837 and Sympterygia bonapartii Müller & Henle, 1841 (Chondrichthyes: Rajidae)
FIGURE 3. NMDS (non-metric multidimensional scaling) graphic from four standardized morphometric variables of scapulocoracoids of (A) males (n = 36) and (B) females (n = 49) of Sympterygia acuta (green; n = 43) and S. bonapartii (purple; n = 42).
FIGURE 2 in Morphological variation in a conservative structure: the scapulocoracoids in Sympterygia acuta Garman, 1837 and Sympterygia bonapartii Müller & Henle, 1841 (Chondrichthyes: Rajidae)
FIGURE 2. Lateral left side view of scapulocoracoids of (A) Sympterygia acuta and (B) S. bonapartii.
FIGURE 5 in Morphological variation in a conservative structure: the scapulocoracoids in Sympterygia acuta Garman, 1837 and Sympterygia bonapartii Müller & Henle, 1841 (Chondrichthyes: Rajidae)
FIGURE 5. Scapulocoracoid morphotypes observed in Sympterygia acuta. With (A) two, (B) three, (C) four, (D) five, and (E) six postdorsal fenestrae. Arrows indicate small fenestrae not clearly seen in the image.
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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.