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502 results for “1832”
Figure 6 from: Gul MA, Soliman AM, Gadallah NS, Al Dhafer HM, Delvare G (2020) The genus Phasgonophora Westwood, 1832 (Hymenoptera, Chalcididae) in Saudi Arabia: re-evaluation of its limits and description of three new species. Journal of Hymenoptera Research 76: 1-38. https://doi.org/10.3897/jhr.76.38340
Figure 6 A−CPhasgonophora baiocchii Soliman & Gul, sp. nov., male (paratype) A head (fronto-lateral view) B antenna C head and mesosoma (dorsal view).
Figure 9 from: Gul MA, Soliman AM, Gadallah NS, Al Dhafer HM, Delvare G (2020) The genus Phasgonophora Westwood, 1832 (Hymenoptera, Chalcididae) in Saudi Arabia: re-evaluation of its limits and description of three new species. Journal of Hymenoptera Research 76: 1-38. https://doi.org/10.3897/jhr.76.38340
Figure 9 A, BPhasgonophora granulis Delvare, sp. nov., female (holotype) A metasoma (dorsal view) B syntergum (lateral view).
Figure 5 from: Gul MA, Soliman AM, Gadallah NS, Al Dhafer HM, Delvare G (2020) The genus Phasgonophora Westwood, 1832 (Hymenoptera, Chalcididae) in Saudi Arabia: re-evaluation of its limits and description of three new species. Journal of Hymenoptera Research 76: 1-38. https://doi.org/10.3897/jhr.76.38340
Figure 5 A−DPhasgonophora baiocchii Soliman & Gul, sp. nov. A, B female (holotype): A metasoma (dorsal view) B syntergum (lateral view) C, D male (paratype): C head (dorsal view) D head (frontal view).
Figure 1 from: Gul MA, Soliman AM, Gadallah NS, Al Dhafer HM, Delvare G (2020) The genus Phasgonophora Westwood, 1832 (Hymenoptera, Chalcididae) in Saudi Arabia: re-evaluation of its limits and description of three new species. Journal of Hymenoptera Research 76: 1-38. https://doi.org/10.3897/jhr.76.38340
Figure 1 Strict consensus tree of the Phasgonophorini achieved from phylogenetic inference using parsimony. Bootstrap support below nodes. A, B, C denote the supported clades; * denote specimens used for the phylogenetic study using the Ultra Conserved Elements (Cruaud et al. 2020); 1, type species of Phasgonophora Westwood; 2, type species of Trigonura Sichel; 3, type species of Chalcidellia Girault.
FIGURE 4 in Dating and publication of the Encyclopédie Méthodique (1782- 1832), with special reference to the parts of the Histoire Naturelle and details on the Histoire Naturelle des Insectes
FIGURE 4. Title page of volume 4 of the Histoire Naturelle. Insectes. Laporte separate edition.
FIGURE 2 in Dating and publication of the Encyclopédie Méthodique (1782- 1832), with special reference to the parts of the Histoire Naturelle and details on the Histoire Naturelle des Insectes
FIGURE 2. Timeline of production for all the dictionnaires of the EM.
FIGURE 36 in Solenoptera Audinet-Serville, 1832 (Coleoptera, Cerambycidae, Prioninae, Solenopterini) in Cuba, with description of a new species
FIGURE 36. Distribution map of Solenoptera zayasi Devesa, Fonseca & Barro in Cuba.
FIGURE 23 in Solenoptera Audinet-Serville, 1832 (Coleoptera, Cerambycidae, Prioninae, Solenopterini) in Cuba, with description of a new species
FIGURE 23. Distribution map of Solenoptera parandroides Lameere.
FIGURE 19 in Taxonomic decision as a compromise: Acasis appensata (Eversmann, 1832) in Central Italy—a case of conflicting evidence between DNA barcode and morphology (Lepidoptera: Geometridae)
FIGURE 19. Type-locality of A. appensata callaina ssp. nov. (Monte Terminillo, Abruzzi, Italy).
FIGURES 4–6 in Solenoptera Audinet-Serville, 1832 (Coleoptera, Cerambycidae, Prioninae, Solenopterini) in Cuba, with description of a new species
FIGURES 4–6. Solenoptera cubana (Zayas): PARATYPE female: 4) dorsal; 5) ventral; 6) lateral.
FIGURES 1–3 in Solenoptera Audinet-Serville, 1832 (Coleoptera, Cerambycidae, Prioninae, Solenopterini) in Cuba, with description of a new species
FIGURES 1–3. Solenoptera cubana (Zayas): HOLOTYPE male: 1) dorsal; 2) ventral; 3) lateral.
FIGURE 11 in Solenoptera Audinet-Serville, 1832 (Coleoptera, Cerambycidae, Prioninae, Solenopterini) in Cuba, with description of a new species
FIGURE 11. Distribution map of Solenoptera cubana (Zayas).
Figs 2a-h in Zur Verbreitung und subspezifischen Gliederung von Bolitobius castaneus (STEPHENS 1832) (Coleoptera, Staphylinidae, Tachyporinae)
Figs 2a-h: (a-c) Bolitobius castaneus castaneus (STEPHENS) und (d-h) B. c. boreomontanicus ssp. nov.: (a, d) Aedoeagus, dorsal; (b, e) Aedoeagus, dorsal, Innenstrukturen; (f) -Sternit VIII; (c, g)
Supplementary material 1 from: Parasram N, Santana W, Vallès Y, Windsor AМ, Vallès H (2024) Morphological and molecular support for Amphithrax verrucosus (H. Milne Edwards, 1832) and Amphithrax aculeatus (Herbst, 1790) (Crustacea, Decapoda, Brachyura) as valid species. Zoosystematics and Evolution 100(1): 15-30. https://doi.org/10.3897/zse.100.109192
Phylogenetic trees of individual datasets of 12S, 16S, and ITS-1 genes
Figure 3 from: Parasram N, Santana W, Vallès Y, Windsor AМ, Vallès H (2024) Morphological and molecular support for Amphithrax verrucosus (H. Milne Edwards, 1832) and Amphithrax aculeatus (Herbst, 1790) (Crustacea, Decapoda, Brachyura) as valid species. Zoosystematics and Evolution 100(1): 15-30. https://doi.org/10.3897/zse.100.109192
Figure 3 Amphithrax aculeatus (Herbst, 1790) adult male (BLSZ 331). A. Habitus, dorsal; B. Ventral view, locality: Barbados; C. Pleonal view of right G1 (BLSZ 222); D. Distal third of the right G1. Scale bars: 20 mm (A, B); 10 mm (C). Photos: Nadeshinie Parasram.
Figure 2 from: Parasram N, Santana W, Vallès Y, Windsor AМ, Vallès H (2024) Morphological and molecular support for Amphithrax verrucosus (H. Milne Edwards, 1832) and Amphithrax aculeatus (Herbst, 1790) (Crustacea, Decapoda, Brachyura) as valid species. Zoosystematics and Evolution 100(1): 15-30. https://doi.org/10.3897/zse.100.109192
Figure 2 A.BI molecular phylogenetic tree for Amphithrax verrucosus, A. aculeatus and other selected species within the family Mithracidae MacLeay, 1838. Based on GTR+G nucleotide substitution model on the concatenated dataset for two mitochondrial (12S, 16S) and one nuclear (ITS-1) genes, represented as a maximum likelihood phylogram with Bayesian posterior probabilities and maximum likelihood bootstrap values (black diamond = ≤ 50% support, * = 16S sequences only). Note: ULLZ's 9148 and 4534, of Windsor and Felder (2014) and 13596 all re-identified as Amphithrax verrucosus (H. Milne Edwards, 1832); B.Amphithrax verrucosus (H. Milne Edwards, 1832), male (CW: 40.7 mm; CL: 29.5 mm), Barbados (BLSZ 218); C.Amphithrax aculeatus (Herbst, 1790), juvenile female (CW: 53.8 mm; CL: 44.0 mm), Barbados (BLSZ 217).
Figure 6 from: Parasram N, Santana W, Vallès Y, Windsor AМ, Vallès H (2024) Morphological and molecular support for Amphithrax verrucosus (H. Milne Edwards, 1832) and Amphithrax aculeatus (Herbst, 1790) (Crustacea, Decapoda, Brachyura) as valid species. Zoosystematics and Evolution 100(1): 15-30. https://doi.org/10.3897/zse.100.109192
Figure 6 Colour in life. Young female of Amphithrax aculeatus (Herbst, 1790) (BLSZ 217), Barbados. A. Habitus dorsal view; B. Ventral view. Adult male of Amphithrax aculeatus (Herbst, 1790) (MNHN-IU-2013-5929), Guadeloupe; C. Habitus, dorsal view; D. Ventral view. Adult male of Amphithrax verrucosus (H. Milne Edwards, 1832) (GIC 072), Venezuela; E. Habitus, dorsal view; F. Ventral view. Female of Amphithrax verrucosus (H. Milne Edwards, 1832) (BLSZ 328), Barbados; G. Habitus, dorsal view; H. Ventral view. Scale bars: 20 mm. Photos: A, B, G, H. Nadeshinie Parasram. C, D. Joseph Poupin. E, F. William Santana.
Figure 5 from: Parasram N, Santana W, Vallès Y, Windsor AМ, Vallès H (2024) Morphological and molecular support for Amphithrax verrucosus (H. Milne Edwards, 1832) and Amphithrax aculeatus (Herbst, 1790) (Crustacea, Decapoda, Brachyura) as valid species. Zoosystematics and Evolution 100(1): 15-30. https://doi.org/10.3897/zse.100.109192
Figure 5 Type specimens. A. Paralectotype of Cancer aculeatus, Herbst, 1790, dry preserved carapace without setae and with most of the spines broken (ZMB Herbst 79), locality: Antilles; B. Holotype of Mithrax plumosus Rathbun, 1901 (USNM 23775), ovig. female (CW: 37.0 mm; CL: 29.0 mm), locality: Puerto Rico; C. Holotype of Mithrax pilosus Rathbun, 1892, setae on carapace removed (USNM 16299), male (CW: 30.0 mm; CL: 28.0 mm), locality: Bahamas; D. Distal third of the right G1 of the holotype of Mithrax pilosus (USNM 16299) in pleonal view. Photos: A Kristina von Rintelen. B, C, D Amanda Windsor.
Figure 4 from: Parasram N, Santana W, Vallès Y, Windsor AМ, Vallès H (2024) Morphological and molecular support for Amphithrax verrucosus (H. Milne Edwards, 1832) and Amphithrax aculeatus (Herbst, 1790) (Crustacea, Decapoda, Brachyura) as valid species. Zoosystematics and Evolution 100(1): 15-30. https://doi.org/10.3897/zse.100.109192
Figure 4 Amphithrax verrucosus (H. Milne Edwards, 1832) adult male (BLSZ 218). A. Habitus, dorsal; B. Ventral view, locality: Barbados; C. Pleonal view of left G1 (BLSZ 228); D. Distal third of left G1. Scale bars: 20 mm (A, B); 10 mm (C). Photos: Nadeshinie Parasram.
Figure 1 from: Parasram N, Santana W, Vallès Y, Windsor AМ, Vallès H (2024) Morphological and molecular support for Amphithrax verrucosus (H. Milne Edwards, 1832) and Amphithrax aculeatus (Herbst, 1790) (Crustacea, Decapoda, Brachyura) as valid species. Zoosystematics and Evolution 100(1): 15-30. https://doi.org/10.3897/zse.100.109192
Figure 1 A. Map of Barbados with sampling locations during this study and position of Barbados (red circle) within the Caribbean region; B. Nearshore rubble habitat (exposed at low tide); C. A cluster of cage crab traps in subtidal habitat. Photos: Nadeshinie Parasram.
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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.