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14,185 results for “phylogenies”
Figs 213–218 in Revision, phylogeny, and microhabitat shifts in the Southeast Asian spider genus Aetana (Araneae, Pholcidae)
Figs 213–218. Aetana omayan group, female genitalia, part 1 (cf. Figs 234–242); untreated in ventral view, cleared in ventral and dorsal views. 213–215. A. abadae Huber, sp. nov. 216–218. A. omayan Huber, 2005.
Figs 243–248 in Revision, phylogeny, and microhabitat shifts in the Southeast Asian spider genus Aetana (Araneae, Pholcidae)
Figs 243–248. Male gonopores and ALS. — 243–244. Khorata khammouan Huber, 2005. — 245– 246. K. dupla Yao & Li, 2013. — 247–248. K. circularis Yao & Li, 2013. Scale lines: 243 = 50 µm; 244, 246, 248 = 10 µm; 245 = 40 µm; 247 = 60 µm.
Figs 155–162 in Revision, phylogeny, and microhabitat shifts in the Southeast Asian spider genus Aetana (Araneae, Pholcidae)
Figs 155–162. Aetana indah Huber, sp. nov. 155–156. Left palp, prolatero-distal and retrolaterodistal views. 157. Left procursus, retrolatero-distal view. 158. Detail of left procursus (and trochanter apophysis), prolateral view. 159. Left embolus (arrow points at sperm duct opening). 160–161. Left male cheliceral apophyses, oblique frontal and frontal views. 162. Male gonopore. b = genital bulb; e = embolus; f = femur; p = procursus; ti = tibia; tr = trochanter. Scale lines: 155–156 = 200 µm; 157 = 100 µm; 158–160 = 60 µm; 161 = 80 µm; 162 = 30 µm.
Figs 113–117 in Revision, phylogeny, and microhabitat shifts in the Southeast Asian spider genus Aetana (Araneae, Pholcidae)
Figs 113–117. Aetana lambir Huber, sp. nov. 113–114. Left male palp, prolateral and retrolateral views. 115. Male chelicerae, frontal view. 116–117. Cleared female genitalia, ventral and dorsal views (arrow points at membranous pocket). b = genital bulb; e = embolus; rp = retrolatero-ventral process; rt = retrolateral trichobothrium; vl = ventral lamina. Scale lines: 113–114 = 0.5 mm; 115–117 = 0.3 mm.
Figs 111–112. Aetana kinabalu Huber, 2005 in Revision, phylogeny, and microhabitat shifts in the Southeast Asian spider genus Aetana (Araneae, Pholcidae)
Figs 111–112. Aetana kinabalu Huber, 2005. Cleared female genitalia, ventral and dorsal views (arrow in Fig. 112 points at membranous pocket). ip = internal sclerotized pocket. Scale line: 0.5 mm.
Fig. 1 in Revision, phylogeny, and microhabitat shifts in the Southeast Asian spider genus Aetana (Araneae, Pholcidae)
Fig. 1. Single most parsimonious cladogram resulting from analyses of the matrix in Appendix 1. For characters and character states see Appendix 3. Only unambiguous character changes are shown. See Cladistic analysis section for further details.
Fig. 18 in Uncovering hidden diversity: phylogeny and taxonomy of Physoderinae (Reduviidae, Heteroptera), with emphasis on Physoderes Westwood in the Oriental and Australasian regions
Fig. 18. Ventral habitus images for species of Physoderes Westwood, 1845 (partial). Scale bars = 2 mm.
Fig. 15 in Uncovering hidden diversity: phylogeny and taxonomy of Physoderinae (Reduviidae, Heteroptera), with emphasis on Physoderes Westwood in the Oriental and Australasian regions
Fig. 15. Dorsal habitus images for species of Physoderes Westwood, 1845 (partial). For an explanation of the colored arrows, see key on page 66. Scale bars = 2 mm.
Fig. 13 in Uncovering hidden diversity: phylogeny and taxonomy of Physoderinae (Reduviidae, Heteroptera), with emphasis on Physoderes Westwood in the Oriental and Australasian regions
Fig. 13. Distribution map for species of Nanophysoderes gen. nov., Paraphysoderes Villiers, 1962 and Physoderes Westwood, 1845 (in part).
Fig. 16 in Uncovering hidden diversity: phylogeny and taxonomy of Physoderinae (Reduviidae, Heteroptera), with emphasis on Physoderes Westwood in the Oriental and Australasian regions
Fig. 16. Dorsal habitus images for junior synonym holotypes of species in Physoderes Westwood, 1845 (except P. minor = paratype). Scale bars = 2 mm.
Fig. 10 in Uncovering hidden diversity: phylogeny and taxonomy of Physoderinae (Reduviidae, Heteroptera), with emphasis on Physoderes Westwood in the Oriental and Australasian regions
Fig. 10. Dorsal habitus images for species of Macrophysoderes gen. nov. and Nanophysoderes gen. nov. For an explanation of the colored arrows, see key on page 37. Scale bars = 2 mm.
Fig. 4 in Uncovering hidden diversity: phylogeny and taxonomy of Physoderinae (Reduviidae, Heteroptera), with emphasis on Physoderes Westwood in the Oriental and Australasian regions
Fig. 4. Dorsal habitus images for species of Breviphysoderes gen. nov. For an explanation of the colored arrows, see key on page 17. Scale bars = 2 mm.
Fig. 14 in Uncovering hidden diversity: phylogeny and taxonomy of Physoderinae (Reduviidae, Heteroptera), with emphasis on Physoderes Westwood in the Oriental and Australasian regions
Fig. 14. Dorsal habitus images for species of Paraphysoderes Villiers, 1962 and Physoderes Westwood, 1845 (partial). For an explanation of the colored arrows, see keys on page 63 and 66. Scale bars = 2 mm.
Fig. 3 in Uncovering hidden diversity: phylogeny and taxonomy of Physoderinae (Reduviidae, Heteroptera), with emphasis on Physoderes Westwood in the Oriental and Australasian regions
Fig. 3. Dorsal habitus images of other specimens examined for morphological coding. Images by Jean-Michel Berenger, except Leptophysoderes sarapiqui Davranoglou, Hwang & Weirauch, 2015 and Aradomorpha crassipes Champion, 1899. Scale bars = 2 mm.
Fig. 11 in Uncovering hidden diversity: phylogeny and taxonomy of Physoderinae (Reduviidae, Heteroptera), with emphasis on Physoderes Westwood in the Oriental and Australasian regions
Fig. 11. Ventral habitus images for species of Macrophysoderes gen. nov. and Nanophysoderes gen. nov. Scale bars = 2 mm.
Fig. 8 in Uncovering hidden diversity: phylogeny and taxonomy of Physoderinae (Reduviidae, Heteroptera), with emphasis on Physoderes Westwood in the Oriental and Australasian regions
Fig. 8. Dorsal view of the male pygophore in species of Breviphysoderes gen. nov., Macrophysoderes gen. nov., Paraphysoderes Villiers, 1962 and Physoderes Westwood, 1845. For an explanation of the colored arrows, see keys on pages 37 and 66.
Fig. 2 in Uncovering hidden diversity: phylogeny and taxonomy of Physoderinae (Reduviidae, Heteroptera), with emphasis on Physoderes Westwood in the Oriental and Australasian regions
Fig. 2. Phylogeny of Physoderinae based on 57 morphological characters for 57 taxa analyzed using parsimony on TNT. Open white circles denote homoplastic characters, black circles denote characters that are not homoplastic. Numbers above the circles refer to character number (Table 1) and numbers below the circles refer to the character states (Table 3). Numbers in bold indicate symmetric resampling values.
Fig. 1 in Uncovering hidden diversity: phylogeny and taxonomy of Physoderinae (Reduviidae, Heteroptera), with emphasis on Physoderes Westwood in the Oriental and Australasian regions
Fig. 1. In situ images of Physoderes curculionis China, 1936 in Singapore on mossy substrate (left) and vegetation debris (right).
Data to Richter et al. 2020 Comparative analysis of worker head anatomy of Formica and Brachyponera (Hymenoptera: Formicidae) in Arthropod Systematics & Phylogeny
<p>This dataset contains the ant head µCT-Sanning Datasets used for the article "Comparative analysis of worker head anatomy of <em>Formica</em> and <em>Brachyponera</em> (Hymenoptera: Formicidae)" by Richter et al. published in <em>Arthropod Systematics & Phylogeny </em>2020. In addition, the image plates from that article (in highest resolution as TIF files) and a series of supplementary 3D-volume render video files are deposited.</p> <p>The datasets for CASENT0709409, CASENT0709411 and CASENT0790267 are deposited as they were used in this study (with transformation to adjust the orientation of the ant head to the global axes and cropped to reduce file size) while CASENT0709419 is deposited as the original scanning result as it was not modified for the work in this article.</p> <p>Scanning details can be found in the materials and methods section of the article. Scanning parameters were as follows:</p> <p>Power (W): 3W all specimens</p> <p>Voltage (kV): 40kV all specimens</p> <p>Voxel Size: CASENT0709409: 1,1557 µm<sup>3</sup>; CASENT0709419: 1,2244 µm<sup>3</sup>; CASENT0709411: 2,5527µm<sup>3 </sup>; CASENT0790267: 2,8337 µm<sup>3</sup> </p> <p>Exposure Time (s): CASENT0709409: 25 s; CASENT0709419: 15 s; CASENT0709411: 7 s<sup> </sup>; CASENT0790267: 5 s</p> <p>Source Distance (mm): CASENT0709409: -9,5038 mm; CASENT0709419: -9,5321 mm; CASENT0709411: 10,038 mm<sup> </sup>; CASENT0790267: 13,0037 mm</p> <p>Detector Distance (mm): CASENT0709409: 46 mm; CASENT0709419: 43,0166 mm; CASENT0709411: 16,5043 mm<sup> </sup>; CASENT0790267: 18,0015 mm</p>
Fig. 4 in Integrative redescription of Hypsibius pallidoides Pilato et al., 2011 (Eutardigrada: Hypsibioidea) with the erection of a new genus and discussion on the phylogeny of Hypsibiidae
Fig. 4. Hypsibius pallidoides Pilato, Kiosya, Lisi, Inshina & Biserov, 2011. A. Lateral view of the head region, white arrowhead indicates the anterior porous area, black arrowhead indicates the elliptical sensory organ, SEM. B. Enlarged view of the lateral surface of the head, white arrowhead indicates the anterior porous area, white arrow indicates the muscle attachment zone, SEM. C. Mouth opening with peribuccal lobes, SEM. D. Mouth opening with anterior ring of teeth, SEM. E. Dorsal sculpture of the juvenile, SEM. F. Bucco-pharyngeal apparatus (SPbU 251(82)), PhC. G. Dorsal view of the buccal cavity, black arrowhead indicates the circumoral elliptical structures (SPbU 251(82)), PhC. H. Ventral view of the buccal cavity, black arrowhead indicates the circumoral elliptical structures (SPbU 251(82)), PhC. Scale bars: A, F–H = 5 µm; B–C = 2 µm; D = 1 µm; E = 10 µm.
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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.