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Figure 26 in A new trichobothrial character for the high-level systematics of Buthoidea (Scorpiones: Buthida)
Figure 26: Position of continental plates in early Jurassic period (195 Mya) (after Scotese, 2001, in part).
Figures 3-12 in A new trichobothrial character for the high-level systematics of Buthoidea (Scorpiones: Buthida)
Figures 3-12: Pedipalp patella, dorsal view, showing the alignment of trichobothrium d3 with respect to the dorsomedian (DMc) carina. In the buthoid figures d3 is situated internal to or on the DMc carina. 3. Pseudochactas ovchinnikovi (after Soleglad & Fet, 2003b, in part) Note, DMc carina is absent as well as trichobothria d2 and d4. 4. Androctonus bicolor. 5. Razianus zarudnyi. 6. Mesobuthus caucasicus (after Soleglad & Fet, 2003b, in part). 7. Liobuthus kessleri. 8. Orthochirus scrobiculosus. 9. Compsobuthus matthiesseni. 10. Anomalobuthus rickmersi. 11. Buthacus yotvatensis. 12. Microbuthus sp. Note, trichobothrium d3 bifurcates the DMc carina and trichobothrium d2 is absent. Only trichobothria i and d1-d5 are shown in these figures.
Figure 204 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figure 204: General distribution of scorpion subfamily Syntropinae (tribe Syntropini, subtribe Thorelliina) in North America with the ranges of genera Kochius and Thorellius delineated.
Figure 205 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figure 205: General distribution of scorpion subfamily Vaejovinae in North America with the ranges of genera Franckeus and Vaejovis "nigrescens" group delineated.
Figure 203 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figure 203: General distribution of scorpion subfamily Syntropinae (tribe Syntropini, subtribe Syntropina) in North America with the ranges of genera Hoffmannius and Syntropis delineated.
Figure 197 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figure 197: General distribution of scorpion subfamily Smeringurinae in North America with the ranges of genera Paravaejovis (tribe Paravaejovini) and Smeringurus, Paruroctonus, and Vejovoidus (tribe Smeringurini) delineated.
Figure 202 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figure 202: General distribution of scorpion subfamily Syntropinae (tribe Stahnkeini) in North America with the ranges of genera Stahnkeus, Serradigitus, Gertschius, and Wernerius delineated.
Figure 196 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figure 196: Phylogram showing the three current subfamilies of family Vaejovidae based on the results of this study. * Note, subfamily Vaejovinae (shaded), the default nominotypic subfamily for Vaejovidae, has not yet been revised and therefore only reflects the remaining taxa and their relationships as suggested by Stockwell (1989) and/or Soleglad & Fet (2005).
Figure 195 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figure 195: Morphometric ratios contrasting metasomal segments (length/width) for species in tribe Syntropini (female). Variance analysis p-values depicted in rectangles, Hoffmannius as compared to Kochius. Statistically significant p-values (i.e., very small) indicated with black arrow. See Fig. 1 for explanation of histogram components.
Figure 218 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figure 218: Trichobothrial pattern of Kochius kovariki, sp. nov., female holotype, Durango, Durango, Mexico.
Figure 193 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figure 193: Histogram showing maximized morphometric ratios of species (male) in genera Hoffmannius, Kochius, and Thorellius. See Figure 192 for data on female and Table 6 for additional data. Variance analysis p-values depicted in rectangles, Hoffmannius as compared to Thorellius and Kochius on left, and Kochius as compared to Thorellius on right. Statistically significant p-values (i.e., very small) indicated with black arrow. See Fig. 1 for explanation of histogram components.
Figure 192 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figure 192: Histogram showing maximized morphometric ratios of species (female) in genera Hoffmannius, Kochius, and Thorellius. See Figure 193 for data on male, and Table 6 for additional data. Variance analysis p-values depicted in rectangles, Hoffmannius as compared to Thorellius and Kochius on left, and Kochius as compared to Thorellius on right. Statistically significant p-values (i.e., very small) indicated with black arrow. See Fig. 1 for explanation of histogram components.
Figure 194 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figure 194: Morphometric ratios contrasting metasomal segments (length/width) for species in tribe Syntropini (male). Variance analysis p-values depicted in rectangles, Hoffmannius as compared to Kochius. Statistically significant p-values (i.e., very small) indicated with black arrow. See Fig. 1 for explanation of histogram components.
Figures 209–217 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figures 209–217: Kochius kovariki, sp. nov., female holotype. 209. Leg III tarsus, ventral view, showing median spinule row and four pairs of distal spinules. 210. Metasomal segment V, ventral view, showing narrowly bifurcated ventromedian carina. 211. Chelal movable fingers showing dentition pattern and position of trichobothria ib–it, fixed finger left and movable finger right. 212. Carapace with close-up of lateral eyes. 213. Stigma. 214. Chelicerae, ventral, external, and dorsal views. 215. Pecten. 216. Metasomal segments IV–V and telson, lateral view. 217. Telson, ventral view.
Figures 160–169 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figures 160–169: Metasomal segment IV, lateral and dorsal views, showing development of the terminus of the dorsal (D) and dorsolateral (DL) carinae for the three subfamilies of Vaejovidae. Subfamily Smeringurinae: 160. Paruroctonus stahnkei, male, Mesa, Arizona, USA. 161. Smeringurus aridus, male, ABDSP, California, USA. 162. Vejovoidus longiunguis, male, Las Bombas, Baja California Sur, Mexico. 163. Paravaejovis pumilis, male, Ciudad Constitución, Baja California Sur, Mexico. Subfamily Syntropinae: 164. Stahnkeus subtilimanus, ABDSP, California, USA. 165. Kochius punctipalpi punctipalpi, female, Cabo San Lucas, Baja California Sur, Mexico. 166. Hoffmannius viscainensis, male, Las Bombas, Baja California Sur, Mexico. 167. Hoffmannius gravicaudus, female, Santa Rosalia, Baja California Sur, Mexico. Subfamily Vaejovinae: 168. Vaejovis solegladi, female, Cuicatlan, Oaxaca, Mexico. 169. Pseudouroctonus reddelli, male, Comal Co., Texas, USA. AC = articulation condyle, td1 = terminal denticle of dorsal carina, td2 = terminal denticle of dorsolateral carina. After Soleglad & Fet (2003b), in part.
Figures 170–181 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figures 170–181: Telson, lateral view, of representative Syntropini species. 170. Kochius hirsuticauda, female, Indian Gorge Canyon, ABDSP, California, USA. 171. K. bruneus loretoensis, male, Loreto, Baja California Sur, Mexico. 172. K. punctipalpi punctipalpi, female, Cabo San Lucas, Baja California Sur, Mexico. 173. K. punctipalpi punctipalpi, male, Los Aripes, Baja California Sur, Mexico. Note the significant sexual dimorphism in this species. 174. K. cazieri, male, Cuatro Ciénegas, Coahuila, Mexico. 175. K. russelli female, Deming, New Mexico, USA. 176. Thorellius atrox, female, Colima, Colima, Mexico. 177. T. cristimanus, male, Autlán, Jalisco, Mexico. 178. Hoffmannius globosus, female, Zacatecas, Zacatecas, Mexico. 179. H. eusthenura, male, Cabo San Lucas, Baja California Sur, Mexico. 180. Syntropis williamsi, female holotype, Los Aripes, Baja California Sur, Mexico. 181. S. macrura, female, Isla Carmen, Baja California Sur, Mexico. (Figs. 180, 181 after Soleglad et al., 2007, in part).
Figures 182–190 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figures 182–190: Base of telson vesicle, dorsal view, showing development of vesicular "tabs" (pointed to by arrow) in subfamilies Syntropinae and Smeringurinae. Note the reduced tabs, the sharp granules essentially obsolete, in Smeringurus, Paravaejovis, and Vejovoidus, whereas in Paruroctonus and subfamily Syntropinae, the spine is distinct and well developed. 182. Hoffmannius waeringi, male, Indian Gorge Canyon, ABDSP, California, USA. 183. Kochius punctipalpi punctipalpi, female, Cabo San Lucas, Baja California Sur, Mexico. 184. Stahnkeus subtilimanus, female, Split Mountain, ABDSP, California, USA. 185. Paruroctonus becki, male, Cottonwood Springs, Joshua Tree National Monument, California, USA. 186. Paruroctonus silvestrii, Chihuahua Road, ABDSP, California, USA. 187. Paruroctonus luteolus, male, Palo Verde Wash, ABDSP, California, USA. 188. Smeringurus mesaensis, female, Palo Verde Wash, ABDSP, California, USA. 189. Paravaejovis pumilis, male, Ciudad Constitución, Baja California Sur, Mexico. 190. Vejovoidus longiunguis, female, Las Bombas, Baja California Sur, Mexico.
Figures 152–159 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figures 152–159: Diagrammatic view of chelal palm, proximal aspect, showing digital carinae (D1–D5). In particular, this perspective shows the profiled development of the subdigital (D2) carina and its relative position with respect to D1 and D3. See Figs. 140–145 for lateral view of D2 carina showing its relative length as compared to chelal palm length. 152. Kochius punctipalpi punctipalpi, female, Cabo San Lucas, Baja California Sur, Mexico. 153. K. bruneus loretoensis, male, Loreto, Baja California Sur, Mexico. 154. K. hirsuticauda, female, Indian Gorge Canyon, ABDSP, California, USA. 155. K. cazieri, male, Cuatro Ciénegas, Coahuila, Mexico. 156. K. russelli, female, Deming, New Mexico, USA. 157. Thorellius intrepidus, male, Mexico. 158. T. cristimanus, male, Autlán, Jalisco, Mexico. 159. T. atrox, female, Colima, Colima, Mexico. D1 = digital carina, D2 = subdigital carina, D3 = dorsosecondary carina, D4 = dorsomarginal carina, D5 = dorsointernal carina.
Figures 140–151 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figures 140–151: Chela, external view, of representative Kochius, Thorellius, Hoffmannius, and Syntropis species, showing carination and trichobothria pattern. In particular note the well developed subdigital (D2) carina, the mid-palm position of trichobothrium Dt, and location of Db dorsal of the digital (D1) carina. 140. Kochius punctipalpi punctipalpi, female, Cabo San Lucas, Baja California Sur, Mexico. 141. K. hirsuticauda, female, Indian Gorge Canyon, ABDSP, California, USA. 142. K. bruneus loretoensis, male, Loreto, Baja California Sur, Mexico. 143. K russelli, female, Deming, New Mexico, USA. 144. Thorellius intrepidus, male, Mexico. 145. T. atrox, female, Colima, Colima, Mexico. 146. Hoffmannius eusthenura, male, Cabo San Lucas, Baja California Sur, Mexico. 147. H. gravicaudus, female, Santa Rosalia, Baja California Sur, Mexico. 148. H. globosus, female, Zacatecas, Zacatecas, Mexico. 149. H. puritanus, male, Jasper Trail, ABDSP, California, USA. 150. H. viscainensis, female, Las Bombas, Baja California Sur, Mexico. 151. Syntropis williamsi, male paratype, Los Aripes, Baja California Sur, Mexico (after Soleglad et al., 2007: fig. 13, in part).
Figure 191 in Contributions to scorpion systematics. III. Subfamilies Smeringurinae and Syntropinae (Scorpiones: Vaejovidae)
Figure 191: Metasomal segment (I–IV) proportions for subfamily Smeringurinae (ratios = segment width / segment length). Data include both adult males and females combined. These data show that Smeringurus segments are significantly thinner than in the other three genera, not only showing complete separation between standard error ranges, but for all data points. Statistical difference between Smeringurus and Paruroctonus is indicated by significant standard error separation and the negligible variance analysis value (p-value). In addition, segment III is at least twice as long as wide (indicated by 0.500 triangle marker) and segment IV is in general three times as long as wide (indicated by 0.333 triangle marker). The other genera cluster together, with Vejovoidus and Paravaejovis exhibiting the most stocky metasoma. The data, which encompass all species currently defined in Smeringurinae, were gathered from measurements calculated in this study as well as published measurements, primarily from those sources where the species were originally described (i.e., most measurements are from type specimens). See Fig. 1 for explanation of histogram components.
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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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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.