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1,968 results for “morphological taxonomy”
FIGURE 3 in Molecular phylogeny, morphology and taxonomy of Moroccan Triops granarius (Lucas, 1864) (Crustacea: Notostraca), with the description of two new species
FIGURE 3. Phylogenetic relationships of A, Triops samples obtained in a combined analysis of three molecular markers (12 S, 16 S, 28 S) and B, western Moroccan Triops granarius samples as inferred from 12 S sequences (best scoring trees obtained in RAxML are shown). ML bootstrap support / Bayesian posterior probabilities are given for selected nodes. Provisional taxon labels of previously discovered lineages correspond to those used in Korn et al. (2013). Symbols correspond to those used in Fig. 1.
FIGURE 2 in Molecular phylogeny, morphology and taxonomy of Moroccan Triops granarius (Lucas, 1864) (Crustacea: Notostraca), with the description of two new species
FIGURE 2. Schematic drawing of A, a detail of the right lateral margin of the telson of a Triops granarius specimen in dorsal view, showing how the length of the largest furcal spine was measured (dotted line), and B, the endopodite of the second trunk limb in anterior view, demonstrating how the length of the endopodite was measured (dotted line). C, a detail of the row of digging spines positioned at the margin of the endopodite showing three examples of length measurements (dotted lines; note that in the present example the largest spine cannot be identified easily so that several rather large spines have to be measured in order to obtain a value for the length of the largest spine) and the position of subsidiary lines used for measurements of spine lengths (dashed lines). D, the distal part of the endopodite showing the distal claw and three of the digging spines. The point where the dashed line (drawn from the base of the distal claw) meets the dotted line (median line of the distal claw) was used as the starting point for length measurements of the endopodite (in the present study the base of the distal claw was defined as the point where the distalmost digging spine diverges from the endopodite). Grey bars (directed approx. in a right angle to measured lines) indicate where measured lines start and end. Abbreviations: C, distal claw; DS, digging spines; SP, largest furcal spine; SPL, length of largest furcal spine; TE, telson; F, furcal ramus.
FIGURE 1. A in Molecular phylogeny, morphology and taxonomy of Moroccan Triops granarius (Lucas, 1864) (Crustacea: Notostraca), with the description of two new species
FIGURE 1. A, map indicating the geographical position of the study area (marked in black). B, map showing the geographical distribution of studied populations of Triops granarius. Symbols used to mark study sites refer to phylogenetic lineages (see Table 1, Fig. 3; population no. 6 was determined morphologically by DFA in this study). Open square: ‘ Triops granarius 8 ’; filled asterisk: ‘ Triops granarius 10 ’.
Figs 25–28 in ON SPLITTING OF THE GENUS NOTOCUPES (COLEOPTERA: ARCHOSTEMATA): NEW DATA ON MORPHOLOGY AND TAXONOMY
Figs 25–28. Elytron venation types of five investigated genera of Archostemata. 25, 26 – Zygadenia alexrasnitsyni Strelnikova et Yan, 2021: 25 – photograph; 26 – interpretative
Figs 14–23 in ON SPLITTING OF THE GENUS NOTOCUPES (COLEOPTERA: ARCHOSTEMATA): NEW DATA ON MORPHOLOGY AND TAXONOMY
Figs 14–23. Integuments of extant Archostemata. 14, 16, 19, 20, 22 – Omma stanleyi Newman, 1839: 14 – abdominal sternite, tomography image; 16 – SEM–micrography of
Fig. 13 in ON SPLITTING OF THE GENUS NOTOCUPES (COLEOPTERA: ARCHOSTEMATA): NEW DATA ON MORPHOLOGY AND TAXONOMY
Fig. 13. Size and density of cuticular tubercles in species studied of ancient Rhabdocupes, Conеxicoxa, Notocupes, Brachilatus, Odontomma, Zygadenia and some extant Omma and Distocupes. Tubercles of Odontomma sulcatum were examined from photographs in Kirejtshuk (2020). Yellow – Triassic species; Red – Early Jurassic; Blue – Middle to Late Jurassic; Green – Cretaceous. Here and further orange columns represent density of small
Figs 9–12 in ON SPLITTING OF THE GENUS NOTOCUPES (COLEOPTERA: ARCHOSTEMATA): NEW DATA ON MORPHOLOGY AND TAXONOMY
Figs 9–12. Odontomma patula (Ponomarenko, 1985). 9 – photograph of the print; 10 – photograph of the counterprint; 11 – interpretative linedrawing of the print; 12 – interpretative linedrawing of the counterprint. Cuticular tubercles depicted in a square frame. Scale bar = 1 mm.
Fig. 11 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 11. Male genitalia of Viuria acadia sp. nov., paratype (DZ 47.183). A–D. Uncus and tegumen. A. Dorsal view. B. Ventral view. C. Right lateral view. D. Left lateral view. E. Valva, left lateral inner view. F. Valva, right lateral inner view. Scale bar: 500 µm.
Fig. 10 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 10. Male genitalia of Viuria acadia sp. nov., paratype (DZ 47.183). A. Left lateral view. B. Right lateral view. C. Dorsal view. D. Ventral view. E. Aedeagus, dorsal view. F. Aedeagus, lateral view. Scale bar: 500 µm.
Fig. 9 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 9. Male genitalia of Viuria innana sp. nov., paratype (DZ 47.172). A–D. Uncus and tegumen. A. Dorsal view. B. Ventral view. C. Left lateral view. E. Valva, left lateral inner view. F. Valva, right lateral inner view. Scale bar: 500 µm.
Fig. 8 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 8. Male genitalia of Viuria innana sp. nov., paratype (DZ 47.172) A. Left lateral view. B. Right lateral view. C. Dorsal view. D. Ventral view. E. Aedeagus, dorsal view. E. Aedeagus, lateral view. Scale bar: 500 µm.
Fig. 7 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 7. Male genitalia of Viuria lista (Evans, 1953) (OM 4.507). A–D. Uncus and tegumen. A. Dorsal view. B. Ventral view. C. Left lateral view. D. Right lateral view. E. Valva, left lateral inner view. F. Valva, right lateral inner view. Scale bar: 500 µm.
Fig. 13 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 13. Patches of modified scales in DHW of species of Viuria Grishin, 2019. A–D. Viuria lista (Evans, 1953). E–F. Viuria licisca (Plötz, 1882). A. Overall view. B. Detail of the modified greyish scales in the swollen vein Sc+R1. C. Details of the creamy scales near the base of the swollen veins Rs and M1. D–F. Same sequence with diaphanized wings.
Fig. 5 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 5. Male genitalia of Viuria licisca (Plötz, 1882) (OM 43.281). A–D. Uncus and tegumen. A. Dorsal view. B. Ventral view. C. Left lateral view. D. Right lateral view. E. Valva, left lateral inner view. F. Valva, right lateral inner view. Scale bar: 500 µm.
Fig. 4 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 4. Male genitalia of Viuria licisca (Plötz, 1882) (OM 43.776). A. Left lateral view. B. Right lateral view. C. Dorsal view. D. Ventral view. E. Aedeagus, lateral view. F. Aedaegus, dorsal view. Scale bar: 500 µm.
Fig. 2 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 2. Male genitalia of Viuria herophile (Harward, 1914) (DZ 9.681). A. Left lateral view. B. Right lateral view. C. Dorsal view. D. Ventral view. E. Aedeagus, dorsal view. F. Aedeagus lateral view. Scale bar: 500 µm.
Fig. 3 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 3. Male genitalia of Viuria herophile (Harward, 1914) (DZ 9.677). A–D. Uncus and tegumen. A. Dorsal view. B. Ventral view. C. Left lateral view. D. Right lateral view. E. Valva, left lateral inner view. F. Valva, right lateral inner view. Scale bar: 500 µm.
Fig. 1 in Viuria Grishin, 2019 (Lepidoptera: Hesperiidae): taxonomy, description of two new species, and remarks on the morphology of secondary sexual organs of males
Fig. 1. Species of Viuria Grishin, 2019, dorsal and ventral views. A–D. V. herophile (Harward, 1914). A–B. ♂, Peru, Madre de Dios, Parque Manu, Pakitza (DZ 52.466). C–D. ♀, Brazil, Acre, 50 km NO of Bujari (DZ 47.221). E–H. V. licisca (Plötz, 1882). E–F. ♀, Costa Rica, San José, Ciudad Colón (OM 26.945). G–H. ♂, Mexico, Oaxaca, Candelaria Loxicha (DZ 47.162). I–L. V. lista (Evans, 1953). I–J. ♀, Brazil, Rondônia, 58 km W of Ariquemes (OM 14.507). K–L. ♀, Brazil, Rondônia, 58 km W of Ariquemes, (OM 14.504). M–P. V. inanna sp. nov. M–N. ♂, holotype (DZ 52.489), Brazil, Paraná, Fênix. O–P. ♀ (DZ 52.492), Brazil, Paraná, Fênix. Q–T. V. acadia sp. nov. Q–R. ♂, holotype (DZ 52.520), Brazil, Mato Grosso, 31 km NO of Barra do Bugres. S–T. ♀ (DZ 52.517), Brazil, Mato Grosso, 31–35 km NO of Barra do Bugres.
Figure S1 in New Insights into the Taxonomy of Myotis Bats in China Based on Morphology and Multilocus Phylogeny
Figure S1. Phylogenetic trees reconstructed based on 123 mitochondrial Cytb haplotypes. Values on the branches represent posterior probability obtained with MrBayes (A) and bootstrap percentage obtained with IQ-TREE (B). Geometries of different colors and shapes represent Myotis species. The information on mitochondrial haplotypes was described in Table S3.
Figure 2 in New Insights into the Taxonomy of Myotis Bats in China Based on Morphology and Multilocus Phylogeny
Figure 2. Principal component analysis based on five morphological characteristics. The first two principal components explained 88.77% and 6.77% of the total variance, respectively. Geometries with different colors and shapes represent Myotis species.
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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)
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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.