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23 results for “external structure”
Fig. 3 in External Sex Specific Signs In The Structure Of Derivatives Of Sterlet (Acipenser Ruthenus, Linnaeus, 1758) Corium
Fig. 3. Typical dorsal scutes of males (upper) and females (lower) sterlet larvae. Age - 3 months. The average length is 70.3 ± 3.6 mm.
Fig. 1 in External Sex Specific Signs In The Structure Of Derivatives Of Sterlet (Acipenser Ruthenus, Linnaeus, 1758) Corium
Fig. 1. Typical contours of dorsal scutes of males (upper) and females (lower) of adult sterlet. Age - 3 years. The second stage of gonad maturity. The average length is 61.2 ± 1.3 cm.
Figure 1. (a) Part of the acrylic structure where the patient is enclosed to avoid external stimulus; (b) Chin rest, corresponding proportions and measurements.-Design of a Novel Servo-motorized Laser Device for Visual Pathways Diseases Therapy
<p>The device consists mainly of an acrylic semi-spherical structure (Figure 1(a)) where visual<br> stimuli will be shown, according to a pre-designed therapy. Four servomotors will drive the lasers,<br> two inside the structure (short distances drive the lasers, two inside the structure (short distance<br> therapies) and two outside (middle-long distance therapies). A chin-rest must be used to have a<br> better line of sight fixation. A webcam with infrared light will catch the Purkinje-Sanson images to<br> identify the sight line (Borah, 2006; Halswanter, 2011; Pambakian et al., 2000). LabVIEW software<br> is used to control the device, including an audio stimulus along with an image-processing pipeline.<br> Finally a microcontroller is used to control the servo movements, laser beams and buzzers.</p>
Data from: Label-free imaging of intracellular structures in living mammalian cells via external apodization phase-contrast microscopy
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FIGURE 5. M. nigribasis. A. Male external genitalic structures, lateral view. B. Male external genitalic structures, posterior view. C. Male internal genitalic structures, lateral view. D. Male sternite 5, ventral view. E in Revision of the new world fauna of Mesembrina Meigen (Diptera: Muscidae) with the description of a new neotropical species
FIGURE 5. M. nigribasis. A. Male external genitalic structures, lateral view. B. Male external genitalic structures, posterior view. C. Male internal genitalic structures, lateral view. D. Male sternite 5, ventral view. E. Female apical portion of ovipositor, dorsal view. F. Female apical portion of ovipositor, ventral view. G. Female spermatheca.
FIGURE 4. M. latreillii. A. Male external genitalic structures, lateral view. B. Male external genitalic structures, posterior view. C. Male internal genitalic structures, lateral view. D. Male sternite 5, ventral view. E in Revision of the new world fauna of Mesembrina Meigen (Diptera: Muscidae) with the description of a new neotropical species
FIGURE 4. M. latreillii. A. Male external genitalic structures, lateral view. B. Male external genitalic structures, posterior view. C. Male internal genitalic structures, lateral view. D. Male sternite 5, ventral view. E. Female apical portion of ovipositor, dorsal view. F. Female apical portion of ovipositor, ventral view. G. Female spermatheca.
FIGURES 82–83. Fig. 82 in External egg structure of the Pentatomidae (Hemiptera: Heteroptera) and the search for characters with phylogenetic importance
FIGURES 82–83. Fig. 82. Most parsimonious tree (L = 63) in the analysis of the genus Nezara resulting from analysis under equal weighting of characters with 40 characters, six of which were egg characters. Fig. 83. Stric consensus of 10 most parsimonious trees (L = 104.493) of the Chinavia obstinata group resulting from analysis under equal weighting of characters with 45 characters, five of which were egg characters.
FIGURES 73–81 in External egg structure of the Pentatomidae (Hemiptera: Heteroptera) and the search for characters with phylogenetic importance
FIGURES 73–81. Eggs of the Pentatomidae viewed with SEM. Fig. 73. Serdia apicicornis Stål, detail of AMP. Figs. 74–76. Thoreyella maracaja Bernardes, Schwertner & Grazia. Fig. 74. Lateral view. Fig. 75. Anterior view. Fig. 76. Magnification of anterior pole, showing the AMP. Figs. 77–81. Capivaccius bufo Distant. Fig. 77. Anterior view. Fig. 78. Magnification of the lateral wall. Fig. 79. Magnification of anterior pole, showing the eclosion line and the AMP. Fig. 80. Detail of anterior pole. Fig. 81. Detail of AMP. Abbreviations: amp—aero-micropylar process, ec–eclosion line.
FIGURES 37–48 in External egg structure of the Pentatomidae (Hemiptera: Heteroptera) and the search for characters with phylogenetic importance
FIGURES 37–48. Eggs of the Pentatomidae viewed with SEM. Figs. 37 and 38. Euschistus (Lycipta) riograndensis Weiler & Grazia. Fig. 37. Magnification of the lateral wall. Fig. 38. Detail of the lateral wall, showing the AMP. Figs. 39–42. Euschistus (Mitripus) paranticus Grazia. Fig. 39. Lateral view. Fig. 40. Anterior view. Fig. 41. Magnification of anterior pole, showing the AMP. Fig. 42. Detail of AMP. Figs. 43–46. Mormidea cornicollis Stål. Fig. 43. Lateral view. Fig. 44. Anterior view. Fig. 45. Magnification of anterior pole. Fig. 46. Detail of AMP. Figs. 47 and 48. Chinavia armigera (Stål). Fig 47. Lateral view. Fig. 48. Anterior view. Abbreviations: amp–aero-micropylar process, lw–lateral wall.
FIGURES 1–12 in External egg structure of the Pentatomidae (Hemiptera: Heteroptera) and the search for characters with phylogenetic importance
FIGURES 1–12. Eggs of the Pentatomidae viewed with stereomicroscopy. Fig. 1. Podisus nigrispinus (Dallas), egg mass, anterior view. Fig. 2. Euschistus (Lycipta) riograndensis Weiler & Grazia, lateral view. Fig. 3. Euschistus (Mitripus) paranticus Grazia, lateral view. Figs. 4 and 5. Mormidea cornicollis Stål. Fig. 4. Newly laid eggs, anterior view. Fig. 5. Fertile eggs, anterior view. Fig. 6. Chinavia armigera (Stål), fertile eggs, anterior view. Fig. 7. Chinavia aseada (Rolston), lateral view. Fig. 8. Chinavia brasicola (Rolston), anterior view. Fig. 9. Chinavia runaspis (Dallas), anterior view. Fig. 10. Banasa induta Stål, lateral view. Fig. 11. Serdia apicicornis Stål, anterior view. Fig. 12. Thoreyella maracaja Bernardes, Schwertner & Grazia, lateral view. Scale bar = 1 mm.
FIGURES 25–36 in External egg structure of the Pentatomidae (Hemiptera: Heteroptera) and the search for characters with phylogenetic importance
FIGURES 25–36. Eggs of the Pentatomidae viewed with SEM. Fig. 25. Catulona pensa Rolston, detail of anterior pole, showing the AMP and the granulated area. Figs. 26–30. Dichelops (Diceraeus) furcatus (Fabricius). Fig. 26. Lateral view. Fig. 27. Anterior view. Fig. 28. Magnification of the lateral wall. Fig. 29. Magnification of anterior pole, showing the eclosion line and the AMP. Fig. 30. Detail of AMP. Figs. 31–35. Euschistus (Euschistus) heros (Fabricius). Fig. 31. Lateral view. Fig. 32. Anterior view. Fig. 33. Magnification of the lateral wall, showing the AMP. Fig. 34. Magnification of AMP, showing connector sheets (asterisks). Fig. 35. Detail of AMP surface. Fig. 36. Euschistus (Lycipta) riograndensis Weiler & Grazia, anterior view. Abbreviations: amp–aero-micropylar process, ec–eclosion line, ga–granulated area, lw–lateral wall.
FIGURES 49–60 in External egg structure of the Pentatomidae (Hemiptera: Heteroptera) and the search for characters with phylogenetic importance
FIGURES 49–60. Eggs of Chinavia spp. viewed with SEM. Figs. 49–51. Chinavia armigera (Stål). Fig. 49. Magnification of the lateral wall, showing the polygonal cells projected inward in a funnel. Fig. 50. Detail of the anterior pole. Fig. 51. Detail of the anterior pole, showing the eclosion line, the AMP, and the connector sheets (asterisks). Figs. 52–55. Chinavia aseada (Rolston). Fig. 52. Lateral view. Fig. 53. Anterior view. Fig. 54. Magnification of the lateral wall, showing the AMP and the connector sheets (asterisks). Fig. 55. Magnification of anterior pole, showing the eclosion line, the AMP, and the connector sheets (asterisks). Figs. 56–59. Chinavia brasicola (Rolston). Fig. 56. Lateral view. Fig. 57. Anterior view. Fig. 58. Magnification of the lateral wall, showing the AMP and the connector sheets (asterisks). Fig. 59. Magnification of anterior pole, showing the eclosion line and the AMP. Fig 60. Chinavia runaspis (Dallas), lateral view. Abbreviations: amp—aeromicropylar process, ec—eclosion line, lw—lateral wall.
FIGURES 13–24 in External egg structure of the Pentatomidae (Hemiptera: Heteroptera) and the search for characters with phylogenetic importance
FIGURES 13–24. Eggs of the Pentatomidae viewed with scanning electron microscopy (SEM). Figs. 13–17. Podisus distinctus (Stål). Fig. 13. Lateral view. Fig. 14. Anterior view. Fig. 15. Magnification of the lateral wall. Fig. 16. Magnification of anterior pole, showing the eclosion line and the aero-micropylar processes (AMP). Fig. 17. Detail of AMP. Figs. 18–22. Podisus nigrispinus (Dallas). Fig. 18. Lateral view. Fig. 19. Anterior view. Fig. 20. Magnification of the lateral wall. Fig. 21. Magnification of anterior pole, showing the eclosion line and the AMP. Fig. 22. Detail of AMP. Figs. 23 and 24. Catulona pensa Rolston. Fig. 23. Lateral view. Fig. 24. Anterior view. Abbreviations: amp–aero-micropylar process, ec–eclosion line.
FIGURES 61–72 in External egg structure of the Pentatomidae (Hemiptera: Heteroptera) and the search for characters with phylogenetic importance
FIGURES 61–72. Eggs of the Pentatomidae viewed with SEM. Figs. 61–65. Chinavia runaspis (Dallas). Fig. 61. Anterior view. Fig. 62. Magnification of anterior pole. Fig. 63. Magnification of the lateral wall, showing the eclosion line and the AMP. Fig. 64. Detail of AMP and connector sheets (asterisks). Fig. 65. Detail of AMP surface. Figs. 66–69. Banasa induta Stål. Fig. 66. Lateral view. Fig. 67. Anterior view. Fig. 68. Magnification of anterior pole, showing the AMP. Fig. 69. Detail of AMP surface. Figs. 70–72. Serdia apicicornis Stål. Fig 70. Lateral view. Fig. 71. Anterior view. Fig. 72. Magnification of the lateral wall, showing the eclosion line and the AMP. Abbreviations: amp—aero-micropylar process, ec—eclosion line, lw—lateral wall.
Figure 13. Oedothorax paludigena Simon, 1926. A–E, male left palp. A, retrolateral view. B, prolateral view. C, dorsal view. D, ventral view. E, apical view. F, G, epigyne. F, ventral view. G, external morphology. H, male spinnerets. I, female left spinnerets. Scale bar 0.1 in Evolution of nuptial-gift-related male prosomal structures: taxonomic revision and cladistic analysis of the genus Oedothorax (Araneae: Linyphiidae: Erigoninae)
Figure 13. Oedothorax paludigena Simon, 1926. A–E, male left palp. A, retrolateral view. B, prolateral view. C, dorsal view. D, ventral view. E, apical view. F, G, epigyne. F, ventral view. G, external morphology. H, male spinnerets. I, female left spinnerets. Scale bar 0.1 mm.
FIGURE 4. Piezura pardalina ssp. pardalina Rondani. A. Male genitalia external structures, posterior. B. Male mesolobus, variant form. C. Female spermatheca. D. Female genitalia, ventral. E. Male sternite 5 in A taxonomic revision of Piezura Rondani (Diptera: Fanniidae)
FIGURE 4. Piezura pardalina ssp. pardalina Rondani. A. Male genitalia external structures, posterior. B. Male mesolobus, variant form. C. Female spermatheca. D. Female genitalia, ventral. E. Male sternite 5, ventral.
FIGURE 3. Piezura nigrigenus Nishida. A. Male genitalia external structures, posterior. B. Male sternite 5 in A taxonomic revision of Piezura Rondani (Diptera: Fanniidae)
FIGURE 3. Piezura nigrigenus Nishida. A. Male genitalia external structures, posterior. B. Male sternite 5, ventral.
FIGURE 2. Piezura nearctica Chillcott. A. Male genitalia external structures, posterior. B. Female spermatheca. C. Female genitalia, ventral. D. Male sternite 5 in A taxonomic revision of Piezura Rondani (Diptera: Fanniidae)
FIGURE 2. Piezura nearctica Chillcott. A. Male genitalia external structures, posterior. B. Female spermatheca. C. Female genitalia, ventral. D. Male sternite 5, ventral.
Structural control within flawed rock specimens under external loading as visualized through repeating nucleation on multiple sites by acoustic emission (AE) [DATA]
<p>Data for article: Structural control within flawed rock specimens under external loading as visualized through repeating nucleation on multiple sites by acoustic emission (AE).</p>
Fig. 2 in External Sex Specific Signs In The Structure Of Derivatives Of Sterlet (Acipenser Ruthenus, Linnaeus, 1758) Corium
Fig. 2. Typical dorsal scutes of males (upper) and females (lower) of young sterlet. Age - 1 year. The average length is 24.8 ± 1.5 cm.
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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.