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Figs 43–48 in Revision of the genus Callipia Guenée, 1858 (Lepidoptera, Geometridae), with the description of 15 new taxa
Figs 43–48. Adult moths (a = dorsal view; b = ventral view). 43. Callipia constantinaria Oberthür, 1881, ♂, lectotype (NHM). 44. C. constantinaria Oberthür, 1881, ♂ (C-0085, COI data). 45. C. rougeriei sp. nov., ♂, paratype (C-0070, COI data). 46. C.rougeriei sp. nov., ♀, holotype. 47. C.rougeriei sp. nov., ♂, paratype (C-0192, COI data). 48. C. occulta Warren, 1904 stat. rev., ♂, holotype of C. hamaria Sperry, 1951 (AMNH).
Figs 94–101 in Revision of the genus Callipia Guenée, 1858 (Lepidoptera, Geometridae), with the description of 15 new taxa
Figs 94–101. Adult moths (a = dorsal view; b = ventral view). 94. Callipia sihvoneni sp. nov., ♂, holotype (C-0418, COI data). 95. C. sihvoneni sp. nov., ♀, paratype (C-0396, COI data). 96. C. wojtusiaki wojtusiaki sp. nov., ♂, holotype (C-0046, COI data). 97. C. wojtusiaki wojtusiaki sp. nov., ♀, paratype (C-0040, COI data). 98. C. wojtusiaki septentrionalis subsp. nov., ♂, holotype (C-0012, COI data). 99. C.wojtusiaki septentrionalis subsp. nov., ♂, paratype (C-0013, COI data). 100. C.milleri sp. nov., ♂, holotype (C-0370, COI data). 101. C.milleri sp. nov., ♂, paratype (C-0008, COI data).
Figs 49–58 in Revision of the genus Callipia Guenée, 1858 (Lepidoptera, Geometridae), with the description of 15 new taxa
Figs 49–58. Adult moths (a = dorsal view; b = ventral view). 49. Callipia occulta Warren, 1904 stat. rev., ♂, holotype (NHM). 50. C. occulta Warren, 1904 stat. rev., ♂ (C-0159, COI data). 51. C. occulta Warren, 1904 stat. rev., ♂ (C-0084, COI data). 52. C. hiltae sp. nov., ♂, holotype (C-0153, COI data). 53. C. aurata Warren, 1904, ♂, holotype (NHM). 54. C.aurata Warren, 1904, ♂ (C-0087, COI data). 55. C.brenemanae Sperry, 1951, ♂, holotype (C-0129). 56. C.brenemanae Sperry, 1951, ♀, paratype (C-0130). 57. C. brenemanae Sperry, 1951, ♂, paratype (NHM; C-0131). 58. C. brenemanae Sperry, 1951, ♂ (C-0084, COI data).
BRAIN Journal-Participative Teaching with Mobile Devices and Social Networks for K-12 Children-Figure 15. Social media visits
<p>We also point out the following the advantages of Google+: - Google+ is a more user-friendly than other social environments and very suitable for use by school children than other blogging environments (e.g. Wordpress); thus it stimulated the play-like learning. - Google+ is more customizable than other social environments; - By allowing teachers to post questionnaires and to share images and videos or links to content on the Time Maps website, the Google+ page acted as an aggregator of information and a for scaffolding the learning process. After different stages of experimentation, we produced different statistical analysis of our results: concerning the most accessed social media. It indicated that Panoramio was the most visited (Figure 15)</p> <p>The statistics indicate that the different social networks had different levels of impact on the children and that in the future developments the focus should be on those more frequently accessed. </p>
Fig. 15 in Genus Profundiconus Kuroda, 1956 (Gastropoda, Conoidea): Morphological and molecular studies, with the description of five new species from the Solomon Islands and New Caledonia
Fig. 15. Profundiconus neocaledonicus sp. nov. A. Holotype, 45.9 × 21.7 mm. B. Paratype 1, 61.3 × 28.1 mm. C. Paratype 2, 52.6 × 24.7 mm. D. Paratype 4, 71.8 × 37.0 mm. E. Paratype 5, 92.0 × 42.0 mm. F. Paratype 1, enlargement of the spire. G. Paratype 3, 46.7 × 20.4 mm. H. Paratype 6, 40.0 × 16.8 mm. I. Paratype 7, 54.5 × 25.4 mm. J. Paratype 8, 67.3 × 33.0 mm. Scale bars = 1 mm unless otherwise indicated.
BRAIN Journal-Swarm Robotics with Circular Formation Motion Including Obstacles Avoidance-Figure 15: third obstacle with 100 robots before passing any robot
<p>The swarm movement and obstacle avoidance are shown in Figures 8, 9 and 10 for the first obstacle. Figures 11, 12 and 13 are to present the second obstacle and its avoidance. Figures 14, 15, 16 and 17 are to present the third obstacle and its avoidance. Figures 18, 19, 20 and 21 are to present the fourth obstacle and its avoidance. Figures 22, 23, 24 and 25 present the fifth obstacle and its avoidance.</p>
Fig. 15 in A revision of the genus Pochytoides Berland & Millot, 1941 (Araneae: Salticidae), with descriptions of six new species
Fig. 15. Pochytoides spiniger sp. nov., paratypes, ♀. A–C. Epigyne. D. Internal structure of epigyne. Scale bars: 0.2 mm.
Fig. 15 in Three new species of Entomobrya (Collembola: Entomobryidae) from China
Fig. 15. Entomobrya dingi sp. nov. A. Anterior face of ventral tube. B. Posterior face of ventral tube. C. Lateral flap of ventral tube. D. Plaque of manubrium. E. Distal part of dens and mucro. Scale bars: A–E = 20 μm.
Underwater hyperspectral scan from India, scene 15
<p>Underwater hyperspectral scan from India, scene 15</p> <p>Used previously in publication Zimmermann, Nevala, Yoshimatsu et al., 2018, Current Biology, in press.</p>
The Prediction of the Rate of the Dropout of the Primary Schools Students by Using the Genetic Algorithm-Figure 15. Drawing of autocorrelation function and partial correlation of the residues for males and females primary stage students
<p>After diagnosing and evaluating the models, the accommodating and the sufficiency of the models must be checked for males and females of primary stage students, through applying the compute (Ljung-Box Q) to check the model accommodation on the Function level 0.05 so the Q value occurs of males and females of primary stage students: Ljung-Box Q' = 1.10306, With p-value = P(Chi-square(1) > 1.10306) = 0.2936 Note that the Tabulated value equals 3.841 while the Q value is less than Tabulated value, so it takes the Null Hypothesis which manifests that the emptiness of the evaluated model out of the contrast in accordance trouble. It's possible to notice that the two parameters functions (Autocorrelation and Partial correlation Functions) of the residues for male females primary stage, in which the residues value is located within confidence interval limits, which means the residues series is random and the evaluated model is good and convenient as it is presented.</p>
A Genetic Algorithm Approach to Regenerate Image from a Reduce Scaled Image Using Bit Data Count-In Figure 15 we were able to generate the symbol H without any help from a small image we used only for row and column data
<p>In Figure 15 we were able to generate the symbol H without any help from a small image we used only for row and column data.</p>
Figs 14–15 in Studies on neotropical Phasmatodea XVII: Revision of Phantasca Redtenbacher, 1906, with the descriptions of six new species (Phasmatodea: Diapheromeridae: Diapheromerinae)
Figs 14–15. Phantasca amabilis sp. nov. Holotype, ♂. 14. Habitus, dorsolateral view. 15. Habitus, dorsal view.
Fig. 15 in Laophontodes typicus T. Scott (Copepoda, Harpacticoida, Laophontodinae) - discovering a species complex by morphology
Fig. 15. Laophontodes gertraudae sp. nov., allotype, ♂ (SMF 37115/1–9). A. A1. A'. Segments 3, 4, 5 and 6 of A1, drawn from counterpart (fourth segment marked with asterisk *). B. Md. C. Mxl. D. Mx. E. Mxp. F. P3 enp. G. P5. Scale bar = 50 µm.
Fig. 15 in Ballomma, a new Afrotropical genus in the Cryptothelinae (Araneae, Zodariidae): eyes on the run
Fig. 15. Predicted distribution of Ballomma gen. nov. calculated in DIVA-GIS on the base of all climatic data as default in the software. Black dots present known localities of Balloma gen. nov. Dark green areas have expected occurrence with the 5–95 percentile; pale green with 2.5–97.5 percentile.
Fig. 15 in A new genus of Theraphosid spider from Mexico, with a particular palpal bulb structure (Araneae, Theraphosidae, Theraphosinae)
Fig. 15. Magnacarina moderata Locht, Mendoza & Medina sp. nov. A–E. ♀, paratype (CNAN-T1004). A. Carapace, dorsal view. B. Prosoma, ventral view. C. Opisthosoma, dorsal view. D. Ocular tubercle, dorsal view. E. Spermatheca, ventral view. F. ♀, paratype (AMNH), spermatheca, ventral view. Scale bars: A–C = 2 mm; E–F = 1 mm; D = 0.5 mm.
Figs 2–15. Live specimens. 2–4 in Evolution of genital asymmetry, exaggerated eye stalks, and extreme palpal elongation in Panjange spiders (Araneae: Pholcidae)
Figs 2–15. Live specimens. 2–4. Pa. lanthana, Mt. Isarog, Ƌ, ♀ with eggsac, and penultimate Ƌ. 5. Pa. malagos Huber sp. nov., Ƌ. 6–7. Pa. casaroro Huber sp. nov., ƋƋ. 8–10. Pa. camiguin Huber sp. nov. 8. ♀ with parasitized eggsac, from Camiguin Island. 9. Ƌ from Bohol Island. 10. Ƌ from Camiguin Island. 11–13. Pa. dinagat Huber sp. nov., Ƌ, ♀ with eggsac, and penultimate Ƌ. 14–15. Pa. marilog Huber sp. nov., ƋƋ showing color variation.
Fig. 15 in A revision of dragon millipedes III: the new genus Gigaxytes gen. nov., with the description of three new species (Diplopoda, Polydesmida, Paradoxosomatidae)
Fig. 15. Gigaxytes parvoterga Srisonchai, Enghoff & Panha gen. et sp. nov., ♂ paratype. A. Anterior body part. B. Body rings 8–10. C. Posteriormost body rings and telson. D. Head and antenna. E. ♂ leg 5 (right). F. ♂ leg 6 (right). G. ♂ leg 7 (right). H. ♂ leg 13 (right). I. Midbody ring.
Fig. 15 in A revision of dragon millipedes II: the new genus Nagaxytes gen. nov., with the description of three new species (Diplopoda, Polydesmida, Paradoxosomatidae)
Fig. 15. Nagaxytes erecta Srisonchai, Enghoff & Panha gen. et sp. nov. (paratype, CUMZ-pxDGT00002), right gonopod. A. Mesal view. B. Dorsal view. C. Lateral view. D. Ventral view.
Figs 15-21. Smeryngolaphria pallida Bromley. 15-17 in Afrotropical Asilidae (Diptera) 18. The genus Smeryngolaphria Hermann, 1912 (Laphriinae)
Figs 15-21. Smeryngolaphria pallida Bromley. 15-17. ♂ (Nigeria, IIIaro Forest). 15. Lateral. 16. Dorsal. 17. Ventral. 18-19. ♀ (Central African Republic, La Maboke). 18. Dorsal. 19. Ventral. 20-21. Egg. 20. Outline shape. 21. Reticulated surface (diagrammatic). Note: Aspects do not take rotation into account. Scale = 1 mm.
Figs 15 in Two new remarkable genera and two new species of Gyponini (Hemiptera: Cicadellidae: Iassinae) from Brazil
Figs 15─22. Acuthana transgressa gen. et sp. nov., paratype, ♀ (DZUP 215370), terminalia. 15. Sternite VII and pygofer, ventral view. 16. Pygofer and valvulae, lateral view. 17. First valvifer and first valvula, lateral view. 18. Apex of first valvula, lateral view. 19. Second valvula, lateral view. 20. Apex of second valvula, lateral view. 21. Second valvifer and gonoplac, lateral view. 22. Apex of gonoplac. Scale bars: 15–16 = 1.0 mm; 17, 19, 21 = 0.5 mm; 18, 20, 22 = not to scale.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.