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FIGURES 21–25 in A new species of Alhajarmyia Stuckenberg (Diptera: Vermileonidae), the first wormlion fly described from East Africa and its biogeographical implications
FIGURES 21–25. Female terminalia and distribution of Alhajarmyia spp. 21. Terminalia of A. umbraticola (Stuckenberg & Fisher), lateral view (PT, Oman, NMSA). 22. Same, A. stuckenbergi sp. n. (PT, Kenya, NMKE). 23. Inferred changes to the extent and distribution of forest cover in Africa since the mid-Cretaceous. Shoreline changes are not represented. Changes in the position and orientation of the African continent are due to continental drift (after Clarke 2000). 24. Distribution of A. umbraticola and A. stuckenbergi sp. n. in Africa and the Arabian Peninsula. 25. Collecting localities of A. stuckenbergi sp. n. in the Eastern Arc Mountains of Kenya (Copyright 2015 Google, Data SIO, NOAA, US Navy NGA GEBCO, image Landsat). Figs 21–23 not to scale.
FIGURES 1–8 in A new species of Alhajarmyia Stuckenberg (Diptera: Vermileonidae), the first wormlion fly described from East Africa and its biogeographical implications
FIGURES 1–8. External features of Alhajarmyia spp. 1. Mesonotum of A. umbraticola (Stuckenberg & Fisher), dorsal view (HT, Oman, NMSA). 2. Same, A. stuckenbergi sp. n. (HT, Kenya, NMKE). 3. Head and antenna of A. umbraticola, lateral view (HT, Oman, NMSA). 4. Same, A. stuckenbergi sp. n. (HT, Kenya, NMKE). 5. Male wing of A. umbraticola, dorsal view (HT, Oman, NMSA). 6. Same, female (PT, Oman, NMSA). 7. Male wing of A. stuckenbergi sp. n. (HT, Kenya, NMKE). 8. Same, female (PT, Kenya, NMKE). Not to scale.
FIGURES 13–16 in A new species of Alhajarmyia Stuckenberg (Diptera: Vermileonidae), the first wormlion fly described from East Africa and its biogeographical implications
FIGURES 13–16. Male terminalia of Alhajarmyia spp. 13. Synsternite of A. umbraticola (Stuckenberg & Fisher), ventral view (HT, Oman, NMSA). 14. Same, diagrammatic. 15. Synsternite of A. stuckenbergi sp. n. ventral view (HT, Kenya, NMKE). 16. Same, diagrammatic. Not to scale.
FIGURES 9–12 in A new species of Alhajarmyia Stuckenberg (Diptera: Vermileonidae), the first wormlion fly described from East Africa and its biogeographical implications
FIGURES 9–12. Male terminalia of Alhajarmyia spp. 9. Synsternite of A. umbraticola (Stuckenberg & Fisher), dorsal view (HT, Oman, NMSA). 10. Same, diagrammatic. 11. Synsternite of A. stuckenbergi sp. n. dorsal view (HT, Kenya, NMKE). 12. Same, diagrammatic. Not to scale.
FIGURE 2 in New mayfly genera from the Middle Triassic of Poland and their evolutionary and paleogeographic implications (Ephemerida: Litophlebiidae, Vogesonymphidae)
FIGURE 2. Palegonympha triassica, gen. et sp. nov., holotype, ZPAL V.44.I/309. A. Imprint of nymphal exuviae. B. Holotype, line drawing.
FIGURE 1 in New mayfly genera from the Middle Triassic of Poland and their evolutionary and paleogeographic implications (Ephemerida: Litophlebiidae, Vogesonymphidae)
FIGURE 1. Triassolitophlebia palegica, gen. et sp. nov., holotype, ZPAL V.44.I/308. A. Fore wing. B. Fore wing, line drawing.
FIGURE 2 in An updated list of the plants associated with plant-parasitic Aphelenchoides (Nematoda: Aphelenchoididae) and its implications for plant-parasitism within this genus
FIGURE 2. Number of single and shared associated plant species (left) and families (right) of foliar nematodes (Aphelenchoides). Between brackets is the corresponding number of ferns for each case
FIGURE 3 in An updated list of the plants associated with plant-parasitic Aphelenchoides (Nematoda: Aphelenchoididae) and its implications for plant-parasitism within this genus
FIGURE 3. Possible combinations of other plant-parasitic Aphelenchoides and main foliar nematodes on associated plants. Gray areas indicate a combination of the overlapping foliar nematodes
FIGURE 1 in An updated list of the plants associated with plant-parasitic Aphelenchoides (Nematoda: Aphelenchoididae) and its implications for plant-parasitism within this genus
FIGURE 1. Number of species/varieties of plants associated with foliar nematodes in ferns (Pteridophyta), monocots (Liliopsida), dicots (Magnoliopsida) and other botanical groups
FIGURE 5 in An updated list of the plants associated with plant-parasitic Aphelenchoides (Nematoda: Aphelenchoididae) and its implications for plant-parasitism within this genus
FIGURE 5. Number of records of plant-parasitic Aphelenchoides species per plant host taxon. Data plotted on a supertree made using Mesquite 3.01 based on those by The Angiosperm Phylogeny Group (2009) and Lehtonen (2011). *10 families of Pteridophyta with reports for only A. fragariae were excluded
FIGURE 4 in An updated list of the plants associated with plant-parasitic Aphelenchoides (Nematoda: Aphelenchoididae) and its implications for plant-parasitism within this genus
FIGURE 4. Schematic overview of the phylogeny of Aphelenchoides and related taxa (Laimaphelenchus and Schistonchus) after the topologies provided by Kanzaki et al. 2014a, 2014b, Rybarczyk-Mydłowska et al. 2012 and Ryss et al. 2013 based on SSU sequence analyses; clusters 2a and 2b are consistent in the 4 topologies. Feeding behavior is plotted on the tree. (Tree reconstructed using Mesquite 3.01)
FIGURES 22–37 in The phallic structures in Gryllotalpidae (Orthoptera: Gryllotalpoidea), and its generic implications
FIGURES 22–37. Comparative image of some species of Scapteriscus s. l. (Scapteriscinae). Dorsal view (22, 26, 30, 34). Ventral view (23, 27, 31, 35). View of upper margin (epiphallus) (24, 28, 32, 36). View of lower margin (ectophallus) (25, 29, 33, 37). 22–25. Scapteriscus didactylus. 26–29. Scapteriscus borelli. 30–33. Scapteriscus quadripunctatus. 34–37. Scapteriscus tetradactylus.
FIGURES 15–21 in The phallic structures in Gryllotalpidae (Orthoptera: Gryllotalpoidea), and its generic implications
FIGURES 15–21. Diagrams of the dorsal view of the phallic complex of the main Gryllotalpidae genera. 15. Gryllotalpa hirsuta (after Chopard, 1928). 16. Gryllotalpa africana. 17. Undescribed genus n. sp. 1. 18. Neocurtilla hexadactyla. (Gryllotalpinae). 19. Indioscaptor leptodactylus (after Ingrisch, 1990). 20. Scapteriscus oxydactylus. 21. Scapteriscus tetradactylus. (Scapteriscinae).
FIGURES 9–14 in The phallic structures in Gryllotalpidae (Orthoptera: Gryllotalpoidea), and its generic implications
FIGURES 9–14. Comparison and phallic complex structures in Gryllotalpidae 9–10. Scapteriscus didactylus (Scapteriscinae). 11 –12. Neocurtilla sp. 1. 13–14. Undescribed genus sp 1. (Gryllotalpinae).
FIGURES 1–8. Dissection process and digest the phallic complex Scapteriscus borelli. 1 in The phallic structures in Gryllotalpidae (Orthoptera: Gryllotalpoidea), and its generic implications
FIGURES 1–8. Dissection process and digest the phallic complex Scapteriscus borelli. 1. Post-abdomen in ventral view without dissection. 2a. Post-abdomen with the everted subgenital plate and phallic complex. 2b. Approach of everted subgenital plate and phallic complex. 3–7. Phallic complex freshly dissected with the phallic gland.. 3. Phallic complex in side view. 4. View of lower margin (ectophallus). 5. Ventral view. 6. View of upper margin (epiphallus). 7. Dorsal view. 8. Phallic complex after digestion of KOH (without the phallic gland).
FIGURE 6 in DNA barcoding and regional diversity of understudied Micropeplinae (Coleoptera: Staphylinidae) in Southwest China: phylogenetic implications and a new Micropeplus from Mount Emei
FIGURE 6. Five species of Micropeplinae from China and Vietnam. A–F: three Micropeplus species most closely related to M. jason sp. n., forming the sculptus species-group and inhabiting the Chang Shan Mountain Range (A–B), Mount Gongga (C–D) and the Tam Dao Mountain Range (E–F); G–H: Cerapeplus spp., C. sinensis from the Qin Ling Mountain Range (G) and Cerapeplus sp. from the Tam Dao Mountain Range (H). Phylogenetic position of respective specimens can be found by tracing unique specimen numbers in Fig. 2, except for Micropeplus #0882 from the Cang Shan Mountain Range (A–B), which did not amplify and was not represented in the DNA analysis.
FIGURE 3 in DNA barcoding and regional diversity of understudied Micropeplinae (Coleoptera: Staphylinidae) in Southwest China: phylogenetic implications and a new Micropeplus from Mount Emei
FIGURE 3. Micropeplus jason sp. n. from Mount Emei, Sichuan. A–D: holotype, female, #0907, habitus; E–H: paratype, female, #0906, tergite and sternite 8 with enclosed hemisternites (E), hemisternites (F), tergite (G) and ventrite (H) 8; I–M: paratype, male, #0911, tergite and sternite 8 with enclosed aedeagus (I), aedeagus (J, K), tergite (L) and sternite (M) 8.
FIGURE 7 in DNA barcoding and regional diversity of understudied Micropeplinae (Coleoptera: Staphylinidae) in Southwest China: phylogenetic implications and a new Micropeplus from Mount Emei
FIGURE 7. Adult habitus of representatives of three consecutive sister groups of Micropeplinae, as hypothesised by Newton & Thayer (1995). Body length of Empelus 2.7 mm, Proteinus 2.0 mm and Microsilpha 2.9 mm.
FIGURE 2 in DNA barcoding and regional diversity of understudied Micropeplinae (Coleoptera: Staphylinidae) in Southwest China: phylogenetic implications and a new Micropeplus from Mount Emei
FIGURE 2. Maximum Likelihood inference phylogram of 85 Micropeplinae ingroup specimens from Southwest China and two neighbouring localities using the 658 nt of the mtDNA barcoding CO1 gene fragment. The outgroup clades and terminals are in grey. The nine red terminal clades are those from hyperdiverse Mount Emei. Clades A–G are discussed in the text. The digits at branches separated by a slash (/) are ML and MP bootstrap values, respectively; a dash (-) after a slash denotes five ML clades not recovered in MP analysis. BIN, GDTC and OUT are interim taxonomic clusters explained in Methods. Seven grey boxes indicate mismatches between GDTC and BINs. Insert in the upper left corner shows different backbone tree arrangement recovered in alternative MP analysis.
FIGURE 1 in DNA barcoding and regional diversity of understudied Micropeplinae (Coleoptera: Staphylinidae) in Southwest China: phylogenetic implications and a new Micropeplus from Mount Emei
FIGURE 1. Geographical origin of the ingroup Micropeplinae specimens. Eight sampled localities in Southwest China are in the oval. The red frame denotes hyperdiverse mount Emei with at least ten species of Micropeplinae, including Micropeplus jason sp. n. The number in brackets after the regional names indicates the amount of sifted litter in kilograms, followed by Micropeplinae species diversity of Micropeplus (M) and Cerapeplus (C). We failed to amplify DNA of the single Micropeplus specimen #0882 detected from the Cang Mountain Range and, therefore, the entire locality is not included in the DNA analysis.
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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.