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FIGURE 5 in Macrostomum shenda and M. spiriger, two new brackish-water species of Macrostomum (Platyhelminthes: Macrostomorpha) from China
FIGURE 5. Macrostomum spiriger Wang & Xin, n. sp.: (A) mature living animal, dorsal view; (B) mature living animal (slightly squeezed), ventral view; (C) the tail of the body; (D) seminal bursa and male copulatory apparatus; (E) a part of the female copulatory apparatus; (F–G) different views of the stylet; (H) the distal end of stylet; (I) immature sperm; (J) mature sperm.
FIGURE 9 in Macrostomum shenda and M. spiriger, two new brackish-water species of Macrostomum (Platyhelminthes: Macrostomorpha) from China
FIGURE 9. The phylogenetic tree of 18S rDNA sequences generated with Bayesian-inference method (GTR+I+G).
FIGURE 8 in Macrostomum shenda and M. spiriger, two new brackish-water species of Macrostomum (Platyhelminthes: Macrostomorpha) from China
FIGURE 8. The phylogenetic tree of 18S rDNA sequences generated with Maximum Likelihood method (bootstrap=1000, GTR+F+I+G4).
FIGURE 4 in Macrostomum shenda and M. spiriger, two new brackish-water species of Macrostomum (Platyhelminthes: Macrostomorpha) from China
FIGURE 4. Macrostomum shenda Wang & Xin, n. sp.: (A) whole body, ventral view; (B) profile of the tail; (C) male copulatory apparatus; (D) penis stylet; (E) mature sperm.
FIGURE 6 in Macrostomum shenda and M. spiriger, two new brackish-water species of Macrostomum (Platyhelminthes: Macrostomorpha) from China
FIGURE 6. Macrostomum spiriger Wang & Xin, n. sp.: (A) horizontal whole body section; (B–D) different sections of the seminal bursa and female antrum; (E) the highly lobulate testes; (F–H) longitudinal whole body sections.
FIGURE 3 in Macrostomum shenda and M. spiriger, two new brackish-water species of Macrostomum (Platyhelminthes: Macrostomorpha) from China
FIGURE 3. Macrostomum shenda Wang & Xin, n. sp.: (A) mounted specimen, ventral view; (B) horizontal whole body section; (C–F) longitudinal whole body sections.
FIGURE 2 in Macrostomum shenda and M. spiriger, two new brackish-water species of Macrostomum (Platyhelminthes: Macrostomorpha) from China
FIGURE 2. Macrostomum shenda Wang & Xin, n. sp.: (A) mature living animal (slightly squeezed), ventral view; (B) testes and ovaries; (C) male copulatory apparatus; (D) penis stylet; (E–F) sperm.
FIGURE 10 in Macrostomum shenda and M. spiriger, two new brackish-water species of Macrostomum (Platyhelminthes: Macrostomorpha) from China
FIGURE 10. The phylogenetic tree of 28S rDNA sequences generated with Maximum Likelihood method (bootstrap=1000, TIM3e+I+G4).
FIGURE 11 in Macrostomum shenda and M. spiriger, two new brackish-water species of Macrostomum (Platyhelminthes: Macrostomorpha) from China
FIGURE 11. The phylogenetic tree of 28S rDNA sequences generated with Bayesian-inference method (GTR+I+G).
elliptical eumelanosomes in the feathers near the skull (b, c), neck (d, e), humerus (f, g), and ulna (h, i, j); and large oval and elliptical eumelanosomes in the feathers near the tibiotarsus (k, l). The subspherical phaeomelanosomes in the sheet-like soft tissue (m) appear to be less densely distributed than the melanosomes in the feathers. in A bizarre Jurassic maniraptoran theropod with preserved evidence of membranous wings
elliptical eumelanosomes in the feathers near the skull (b, c), neck (d, e), humerus (f, g), and ulna (h, i, j); and large oval and elliptical eumelanosomes in the feathers near the tibiotarsus (k, l). The subspherical phaeomelanosomes in the sheet-like soft tissue (m) appear to be less densely distributed than the melanosomes in the feathers.
Supplementary material 1 from: Reyes-Puig C, Bittencourt-Silva G, Torres-Sánchez M, Wilkinson M, Streicher J, Maddock S, Kotharambath R, Müller H, Angiolani Larrea F, Almeida-Reinoso D, Ron S, Cisneros-Heredia D (2019) Rediscovery of the Endangered Carchi Andean Toad, Rhaebo colomai (Hoogmoed, 1985), in Ecuador, with comments on its conservation status and extinction risk. Check List 15(3): 415-419. https://doi.org/10.15560/15.3.415
Supplementary material 1 from: Reyes-Puig C, Bittencourt-Silva G, Torres-Sánchez M, Wilkinson M, Streicher J, Maddock S, Kotharambath R, Müller H, Angiolani Larrea F, Almeida-Reinoso D, Ron S, Cisneros-Heredia D (2019) Rediscovery of the Endangered Carchi Andean Toad, Rhaebo colomai (Hoogmoed, 1985), in Ecuador, with comments on its conservation status and extinction risk. Check List 15(3): 415-419. https://doi.org/10.15560/15.3.415
FIGURES 3A–M in Revision of the Ulopinae leafhoppers (Hemiptera: Cicadellidae) of the Indian subcontinent, I. Ulopini genera: Daimachus, Radhades and Ulopsina
FIGURES 3A–M. Species of Ulopini: A–C, Radhades crassus Distant, holotype male, dorsal and lateral views and label data; D–H, Ulopsina (Indoulopa) himalayana sp. nov.: D–E, holotype male dorsal, lateral and ventral view; GH, forewing and hind wing of paratype male; I–M, species of Daimachus, faces: I. D. exemplificatus Distant; J. D. matheranensis sp. nov.; K. D. robustus sp. nov.; L. D. sirsiensis sp. nov.; M. D. sudindicus sp. nov.
FIGURES 37–45. Antennomeres. 37—M in Elateridae (Coleoptera) of Lebanon
FIGURES 37–45. Antennomeres. 37—M. tannourinensis sp. nov., male, holotype; 38—M. lizlerwerneri Mertlik, 2005, male, holotype; 39—M. menetriesi (Reitter, 1890), male, holotype. Prosternal process, lateral view. 40—M. tannourinensis sp. nov., male, holotype; 41—M. lizlerwerneri Mertlik, 2005, male, holotype; 42—M. menetriesi (Reitter, 1890), male, holotype. Aedeagus. 43—M. tannourinensis sp. nov., male, holotype. 44—M. lizlerwerneri Mertlik, 2005 male, holotype. 45—M. menetriesi (Reitter, 1890), male, holotype. Scale bars=0.5 mm (Figs 43–45), 1.0 mm (Figs 37–42).
Supplementary material 5 from: Cabezas MP, Ros M, Santos AM, Martínez-Laiz G, Xavier R, Montelli L, Hoffman R, Fersi A, Dauvin JC, Guerra-García JM (2019) Unravelling the origin and introduction pattern of the tropical species Paracaprella pusilla Mayer, 1890 (Crustacea, Amphipoda, Caprellidae) in temperate European waters: first molecular insights from a spatial and temporal perspective. NeoBiota 47: 43-80. https://doi.org/10.3897/neobiota.47.32408
: Explanation note: A Phylogenetic tree of nuclear 28S rRNA. Unfortunately, this gene could not be amplified in P.tenuis species. In P.pusilla, only two haplotypes were detected, differing only by the presence of an indel. B Phylogenetic tree of nuclear ribosomal internal transcribed spacer (ITS). No variation was observed among P.pusilla sequences. Trees were rooted with Caprelladanilevskii and Caprellaliparotensis. Values at the nodes correspond to ML bootstrap support and Bayesian posterior probabilities, respectively.
Environmentally induced lipidome adaptation in the bacterial model organism M. extorquens
<p>Cells, from microbes to man, adapt their membranes in response to the environment to maintain functionality. How cells sense environmental change/stimuli and adapt their membrane accordingly is unclear. In particular, how lipid composition changes and what lipid structural features are necessary for homeostatic adaptation remains relatively undefined. Here, we examine the simple yet adaptive lipidome of the plant-associated Gram-negative bacterium <em>Methylobacterium extorquens </em>over<em> </em>a range of chemical and physical conditions. Using shotgun lipidomics, we explored adaptivity over varying temperature, hyperosmotic and detergent stress, carbon sources, and cell density. Globally, we observed that as few as 10 lipids, representing ca. 30% of the lipidome, characterized by 9 structural features account for 90% of the total changes. We revealed that variations in lipid structural features are not monotonic over a given range of conditions (e.g. temperature) and are not evenly distributed across lipid classes. Thus, despite the compositional simplicity of this lipidome, the patterns in lipidomic remodeling suggest a highly adaptive mechanism with many degrees of freedom. Our observations reveal constraints on the minimal lipidomic requirements for an adaptive membrane and provide a resource for unraveling the design principles of living membranes.</p>
Göhringer, F., Löhr-Limpens, M., Hesse, C., & Schenk, T. (2019) 'Grasping discriminates between object sizes less not more accurately than the perceptual system.' Vision. DOI 10.3390/vision3030036
<p>This repository contains 6 data files and 1 readme file.</p>
FIGURES 29–36. First and second valvula. 29–32 M in Two new species of the bamboo-feeding subgenus Myittana (Benglebra) from China (Hemiptera: Cicadellidae: Deltocephalinae)
FIGURES 29–36. First and second valvula. 29–32 M. (Benglebra) biflaka sp. nov.; 29. First valvula; 30. Detail of dorsal sculptured area of first valvula; 31. Second valvula; 32. Detail of dorsal sculptured area of second valvula; 33–36 M. (Benglebra) curvata sp. nov.; 33. First valvula; 34. Detail of dorsal sculptured area of first valvula; 35. Second valvula; 36. Detail of dorsal sculptured area of second valvular. Scale bars: 0.2 mm.
FIGURES 25–28. Female sternite VII, ventral view 25. M in Two new species of the bamboo-feeding subgenus Myittana (Benglebra) from China (Hemiptera: Cicadellidae: Deltocephalinae)
FIGURES 25–28. Female sternite VII, ventral view 25. M. (Benglebra) biflaka sp. nov.; 26. M. (Benglebra) curvata sp. nov.; 27. M. (Benglebra) introspina (Chen & Yang); 28. M. (Benglebra) ventrospina (Chen & Yang). comb. nov.. Scale bars: 0.2 mm (25–28).
FIGURES 1–12. M in Two new species of the bamboo-feeding subgenus Myittana (Benglebra) from China (Hemiptera: Cicadellidae: Deltocephalinae)
FIGURES 1–12. M. (Benglebra) biflaka sp. nov., male 1. Male habitus, dorsal view; 2. Male habitus, lateral view; 3. Head and thorax, lateral view; 4. Head and thorax, dorsal view; 5. Face; 6. Style, dorsal view; 7. Valve and subgenital plate, ventral view; 8. Shaft, caudal view; 9. Male pygofer, lateral view; 10. Connective and aedeagus, dorsal view; 11. Connective and aedeagus, lateral view; 12. Male pygofer, ventral view. Scale bars: 0.5 mm (1–5); 0.2 mm (6–12).
FIGURES 13–24. M in Two new species of the bamboo-feeding subgenus Myittana (Benglebra) from China (Hemiptera: Cicadellidae: Deltocephalinae)
FIGURES 13–24. M. (Benglebra) curvata sp. nov., male 13. Male habitus, dorsal view; 14. Male habitus, lateral view; 15. Head and thorax, lateral view; 16. Head and thorax, dorsal view; 17. Face; 18. Style, dorsal view; 19. Valve and subgenital plate, ventral view; 20. Shaft, caudal view; 21. Male pygofer, lateral view; 22. Connective and aedeagus, dorsal view; 23. Connective and aedeagus, lateral view; 24. Male pygofer, ventral view. Scale bars: 0.5 mm (13–17); 0.2 mm (18–24).
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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
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