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4,585 results for “Scorpion”
Figure 12–13 in Description of a new species of Leiurus Ehrenberg, 1828 (Scorpiones: Buthidae) from Southеastеrn Turkey
Figure 12–13: Leiurus abdullahbayrami sp. nov., coxosternal area. 12. Female paratype (Adıyaman Province). 13. Male holotype.
Figure 1 in New data on distribution and ecology of seven species of Euscorpius Thorell, 1876 (Scorpiones: Euscorpiidae)
Figure 1: Euscorpius (Alpiscorpius) alpha, adult female, Cislano (Lombardy, Italy) (photo by Giorgio Colombo).
Figure 1 in The geographic pattern of distribution of the genus Rhopalurus Thorell, 1876 in the Guayana-Amazon region (Scorpiones: Buthidae)
Figure 1: Presumed dispersal tracks of Rhopalurus spp., between 18,000 and 13,000 years BP. A and B illustrate possible corridors between North-South and East-West savannah formations which coalesced during past dry periods (base map after Ab'Saber, 1977).
Figure 9 in Two new species of the genus Chaerilus Simon, 1877 from Malaysia (Scorpiones: Chaerilidae)
Figure 9: Chaerilus rectimanus Pocock, 1899, male from Malaysia, Bukit Fraser, elev. 1500 m, 1.VIII.1999, leg. J. Hromádka, live.
Figures 5–6 in Two new species of the genus Chaerilus Simon, 1877 from Malaysia (Scorpiones: Chaerilidae)
Figures 5–6: Chaerilus sejnai sp. n.: 5. male holotype, live; 6. female allotype, live with two juveniles before the first ecdysis.
Figures 60-71 in The systematic position of the scorpion genera Heteroscorpion Birula, 1903 and Urodacus Peters, 1861 (Scorpiones: Scorpionoidea)
Figures 60-71: Leg tarsus (left), ventrolateral view, of representative genera of families Hemiscorpiidae and Scorpionidae. Note differences in the tarsus terminus and the number of paired spinoid setae between the two families. 60. Heteroscorpion raselimananai, female holotype. 61. Heteroscorpion goodmani, male paratype. 62. Opisthacanthus lepturus. 63. Liocheles australasiae, Papua. 64. Hadogenes troglodytes. 65. Opisthacanthus asper. 66. Urodacus elongatus. 67. Urodacus yaschenkoi. 68. Scorpio maurus. 69. Heterometrus swammerdami. 70. Opistophthalmus wahlbergi. 71. Nebo hierichonticus.
Figure 72 in The systematic position of the scorpion genera Heteroscorpion Birula, 1903 and Urodacus Peters, 1861 (Scorpiones: Scorpionoidea)
Figure 72: Phylogenies based on Stockwell (1989), Prendini (2000), and the results of our analysis for superfamily Scorpionoidea showing familes and subfamilies. Family-group names are those established in this paper and not necessarily levels used by other authors. For Prendini's (2000: Fig. 2) phylogeny, overall support data is CI/RI = 0.55/0.92, and bootstrap results are shown below the branches and are based on a single sequence of 10,000 pseudoreplicates. For the results of our analysis, all nodes are supported by all (100 %) 992 MPTs. Overall support data for our analysis: CI/RI/G-Fit = 0.6189/0.9310/-93.355; bootstrap values are indicated below the branches and represent the mean value of three 1,000 pseudoreplicate sequences.
Figures 73-74 in The systematic position of the scorpion genera Heteroscorpion Birula, 1903 and Urodacus Peters, 1861 (Scorpiones: Scorpionoidea)
Figures 73-74: Alternative topologies and support for scorpionoid families Scorpionidae and Hemiscorpiidae based on the character state assignments of a single ventromedian (VM) carina found on metasomal segments I–IV (character 95). 73. Subfamilies Urodacinae, Heteroscorpioninae, and Hemiscorpiinae are assigned different state values: Note that for majority-rule consensus of 23,990 MPTs, clades Scorpioninae + Urodacinae and Hemiscorpiinae + Hormurinae show only 59 % and 69 % support, respectively. 74. Subfamily Urodacinae is assigned a different state value than subfamilies Heteroscorpioninae and Hemiscorpiinae: Note that all clades are supported by all (100 %) 992 MPTs, both for strict and majority-rule consensus.
Figures 41-44 in The systematic position of the scorpion genera Heteroscorpion Birula, 1903 and Urodacus Peters, 1861 (Scorpiones: Scorpionoidea)
Figures 41-44: Sterna of genera Heteroscorpion and Urodacus. 41. H. goodmani, male paratype. 42. Heteroscorpion opisthacanthoides, female. 43. Urodacus yaschenkoi, female. 44. U. elongatus, male.
Figures 45-49 in The systematic position of the scorpion genera Heteroscorpion Birula, 1903 and Urodacus Peters, 1861 (Scorpiones: Scorpionoidea)
Figures 45-49: Diagrammatic pattern of denticle edge of chelal movable finger, distal aspect, showing first three denticle groups (DG). 45. Heteroscorpion goodmani. 46. Urodacus yaschenkoi. 47. Urodacus novaehollandiae. 48. Urodacus elongatus. 49. Urodacus armatus.
Figures 13-18 in The systematic position of the scorpion genera Heteroscorpion Birula, 1903 and Urodacus Peters, 1861 (Scorpiones: Scorpionoidea)
Figures 13-18: Diagrammatic trichobothrial pattern of external surface of chela for genus Urodacus showing external accessory trichobothria. 13. Urodacus manicatus. 14. U. novaehollandiae. 15. U. armatus. 16. U. elongatus. 17. U. hoplurus. 18. U. yaschenkoi. Open circles depict orthobothriotaxy, closed circles depict hypothesized external accessory trichobothria. Note, ventral accessory trichobothria located on the extreme basal aspect of the palm are not shown.
Figures 1-4 in The systematic position of the scorpion genera Heteroscorpion Birula, 1903 and Urodacus Peters, 1861 (Scorpiones: Scorpionoidea)
Figures 1-4: Diagrammatic trichobothrial pattern of external surface of patella for genus Heteroscorpion. 1. Heteroscorpion raselimananai. 2. H. goodmani. 3. H. opisthacanthoides (after Vachon, 1974, in part) 4. H. magnus (after Lourenço & Goodman, 2002, in part). Distal ventral trichobothrium number and position depicted as vxx. Open circles depict orthobothriotaxy based on Vachon (1974: Fig. 106), closed circles depict hypothesized accessory trichobothria.
Figure 3 in The sting of Mesobuthus gibbosus (Scorpiones: Buthidae): morphological and ultrastructural characterization
Figure 3: TEM micrographs of transverse sections of sting. A. Epicuticle and exocuticle of the three-layer sting cuticle; a chitin channel in the exocuticle, x1,900. B. Lamellar endocuticle layer and the underlying single row of cuboidal support cells (csc), x3,600. C. Intima, cylindrical support cells, endocuticle, and cuboidal support cells, x1,400. D. Intima and cylindrical support cells covering the intima, x2,900. E. Connective tissue cells filling the gaps within the sting, x2,900.
Figure 144 in Eight new species of the genera Scorpiops Peters, Euscorpiops Vachon, and Chaerilus Simon (Scorpiones: Euscorpiidae, Chaerilidae) from Tibet and Yunnan, China
Figure 144: Map of China (Tibet), showing the type localities of the new species, and the new records of known species for Tibet. Map abbreviations: ▲ –Chaerilus, ■ –Scorpiops, ● –Euscorpiops; S –Sikkim, Bh –Bhutan, Bu –Burma.
Figures 135–143 in Eight new species of the genera Scorpiops Peters, Euscorpiops Vachon, and Chaerilus Simon (Scorpiones: Euscorpiidae, Chaerilidae) from Tibet and Yunnan, China
Figures 135–143: Chaerilus pictus Pocock, 1890, female. 135–136. Chelicera, dorsal and ventral aspects. 137. Disposition of granulations on the dentate margins of the pedipalp chela movable finger. 138. Carapace dorsal aspect. 139–140. Metasomal segment V and telson, ventral and lateral aspects. 141. Sternum, genital operculum and pectines. 142–143. Legs III and IV, lateral and dorsal aspects. 131. Scales = 1 mm.
Figure 1 in The sting of Mesobuthus gibbosus (Scorpiones: Buthidae): morphological and ultrastructural characterization
Figure 1: A. Lateral view of M. gibbosus sting. The venom pore located at the tip of the sting, and several setae situated more basally are visible, x30. B. A cuticular seta, seta base, and a cuticular pit on the sting at higher magnification, x2,200
Figures 118–125 in Eight new species of the genera Scorpiops Peters, Euscorpiops Vachon, and Chaerilus Simon (Scorpiones: Euscorpiidae, Chaerilidae) from Tibet and Yunnan, China
Figures 118–125: Chaerilus tessellatus sp. n., female holotype. 118. Carapace, dorsal aspect. 119–120. Chelicera, ventral and dorsal aspects. 1121–122. Metasomal segment V and telson, ventral and lateral aspects. 123. Lateral ocular region, in detail, dorsal aspect. 124. Sternum, genital operculum and pectines. 125. Dentate margin of the pedipalp chela movable finger. Scales = 1 mm.
Figures 127–134 in Eight new species of the genera Scorpiops Peters, Euscorpiops Vachon, and Chaerilus Simon (Scorpiones: Euscorpiidae, Chaerilidae) from Tibet and Yunnan, China
Figures 127–134: Chaerilus pictus Pocock, 1890, female. 127–129. Chela, dorsoexternal, ventral and internal aspects. 130– 132. Patella, dorsal, external and ventral aspects. 133–134. Femur, dorsal and external aspects. Scale = 1 mm.
Figures 50-59 in The systematic position of the scorpion genera Heteroscorpion Birula, 1903 and Urodacus Peters, 1861 (Scorpiones: Scorpionoidea)
Figures 50-59: Pedipalp patella, dorsal view, comparing the development of the internal projection of select hemiscorpiid genera with that of genus Urodacus. 50. Heteroscorpion raselimananai, female holotype. 51. Heteroscorpion goodmani, male paratype. 52. Opisthacanthus lepturus. 53. Hadogenes troglodytes. 54. Liocheles australasiae, Papua. 55. Urodacus novaehollandiae. 56. Urodacus yaschenkoi. 57. Urodacus hoplurus. 58. Urodacus manicatus. 59. Urodacus armatus. Note, only dorsal trichobothria, d1 and d2, are shown.
Figure 27 in A review of the genus Heterometrus Ehrenberg, 1828, with descriptions of seven new species (Scorpiones, Scorpionidae)
Figure 27: Heterometrus spinifer, dorsal view, male, syntype of Palamnaeus (= Heterometrus) oatesii.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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.