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FIGURE 21. Stasimopus filmeri, n in Cryptic diversity of South African trapdoor spiders: Three new species of Stasimopus Simon, 1892 (Mygalomorphae, Ctenizidae), and redescription of Stasimopus robertsi Hewitt, 1910
FIGURE 21. Stasimopus filmeri, n. sp., ♂ (TMSA 23993). A. Prosoma, dorsal aspect. B. Prosoma, ventral aspect. C. Carapace, lateral aspect. Scale: 2 mm.
FIGURE 14. Stasimopus hewitti, n in Cryptic diversity of South African trapdoor spiders: Three new species of Stasimopus Simon, 1892 (Mygalomorphae, Ctenizidae), and redescription of Stasimopus robertsi Hewitt, 1910
FIGURE 14. Stasimopus hewitti, n. sp., ♀ (TMSA FIGURE 15. Stasimopus hewitti, n. sp., ♀ (TMSA 3154), leg I. A. Tibia, metatarsus, tarsus, prolateral 3154). A. Leg III patella, tibia, metatarsus, tarsus, aspect. B. Tibia, metatarsus, dorsal aspect. C. Tibia, prolateral aspect. B. Leg III tibia, metatarsus, tarmetatarsus, tarsus, retrolateral aspect. D. Spinner- sus, dorsal aspect. C. Leg III patella, tibia, metaets, ventral aspect. Scale: A–C, 1 mm. D, 0.5 mm. tarsus, tarsus, retrolateral aspect. D. Leg IV
FIGURE 11. Stasimopus hewitti, n in Cryptic diversity of South African trapdoor spiders: Three new species of Stasimopus Simon, 1892 (Mygalomorphae, Ctenizidae), and redescription of Stasimopus robertsi Hewitt, 1910
FIGURE 11. Stasimopus hewitti, n. sp., ♀ (TMSA 3154). A. Prosoma, dorsal aspect. B. Prosoma, ventral aspect. C. Carapace, lateral aspect. Scale: 2 mm.
FIGURE 9. Stasimopus robertsi Hewitt, 1910 in Cryptic diversity of South African trapdoor spiders: Three new species of Stasimopus Simon, 1892 (Mygalomorphae, Ctenizidae), and redescription of Stasimopus robertsi Hewitt, 1910
FIGURE 9. Stasimopus robertsi Hewitt, 1910, ♂ (TMSA 3084). A–C. Leg III metatarsus, tarsus. D–F. Leg IV metatarsus, tarsus. A, D. Prolateral aspect. B, E. Ventral aspect. C, F. Retrolateral aspect. Scale: 1 mm.v
FIGURE 12. Stasimopus hewitti, n in Cryptic diversity of South African trapdoor spiders: Three new species of Stasimopus Simon, 1892 (Mygalomorphae, Ctenizidae), and redescription of Stasimopus robertsi Hewitt, 1910
FIGURE 12. Stasimopus hewitti, n. sp., paratype ♂ (TMSA 23989). A. Pedipalp patella, tibia, embolus, prolateral aspect. B. Pedipalp tibia, embolus, ventral aspect. C, D. Leg I patella, tibia, metatarsus, tarsus. C. Prolateral aspect. D. Ventral aspect. E. Leg I metatarsus, tarsus, retrolateral aspect. F. Leg I tarsus, ventral aspect. Scale: A–E, 1 mm. F, 0.5 mm.
FIGURE 8. Stasimopus robertsi Hewitt, 1910 in Cryptic diversity of South African trapdoor spiders: Three new species of Stasimopus Simon, 1892 (Mygalomorphae, Ctenizidae), and redescription of Stasimopus robertsi Hewitt, 1910
FIGURE 8. Stasimopus robertsi Hewitt, 1910, ♂ (TMSA 3084). A. Pedipalp patella, tibia, bulb, prolateral aspect. B. Pedipalp tibia, bulb, ventral aspect. C, D. Leg I patella, tibia, metatarsus, tarsus. C. Prolateral aspect. D. Ventral aspect. E. Leg I metatarsus, tarsus, retrolateral aspect. F. Leg I tarsus, ventral aspect. Scale: A–E, 1 mm. F, 0.5 mm.
FIGURE 7. Stasimopus robertsi Hewitt, 1910 in Cryptic diversity of South African trapdoor spiders: Three new species of Stasimopus Simon, 1892 (Mygalomorphae, Ctenizidae), and redescription of Stasimopus robertsi Hewitt, 1910
FIGURE 7. Stasimopus robertsi Hewitt, 1910, ♀ (TMSA 3226). A. Prosoma, dorsal aspect. B. Prosoma, ventral aspect. C. Carapace, lateral aspect. Scale: 2 mm.
FIGURE 6. Stasimopus robertsi Hewitt, 1910 in Cryptic diversity of South African trapdoor spiders: Three new species of Stasimopus Simon, 1892 (Mygalomorphae, Ctenizidae), and redescription of Stasimopus robertsi Hewitt, 1910
FIGURE 6. Stasimopus robertsi Hewitt, 1910, ♂ (TMSA 3084). A. Prosoma, dorsal aspect. B. Prosoma, ventral aspect. C. Carapace, lateral aspect. Scale: 2 mm.
FIGURE 5 in Cryptic diversity of South African trapdoor spiders: Three new species of Stasimopus Simon, 1892 (Mygalomorphae, Ctenizidae), and redescription of Stasimopus robertsi Hewitt, 1910
FIGURE 5. Four species of Stasimopus Simon, 1892, ocular pattern. A, B. Stasimopus robertsi Hewitt, 1910. A. Paratype ♂ (TMSA 3084). B. ♀ (TMSA 3226). C, D. Stasimopus hewitti, n. sp. C. ♂ (TMSA 23989). D. ♀ (TMSA 3154). E, F. Stasimopus griswoldi, n. sp. E. ♂ (TMSA 23993). F. ♀ (TMSA 23998). G, H. Stasimopus filmeri, n. sp. G. ♂ (TMSA 24000). H. ♀ (TMSA 24001). Scale: 0.5 mm.
FIGURE 3 in Cryptic diversity of South African trapdoor spiders: Three new species of Stasimopus Simon, 1892 (Mygalomorphae, Ctenizidae), and redescription of Stasimopus robertsi Hewitt, 1910
FIGURE 3. Known distributions of Stasimopus robertsi Hewitt, 1910 (squares), Stasimopus hewitti, n. sp. (circles), Stasimopus griswoldi, n. sp. (triangles), and Stasimopus filmeri, n. sp. (crosses), on topography with major urban areas and provincial boundaries indicated. Inset indicates extent of mapped region within South Africa.
FIGURE 2 in Cryptic diversity of South African trapdoor spiders: Three new species of Stasimopus Simon, 1892 (Mygalomorphae, Ctenizidae), and redescription of Stasimopus robertsi Hewitt, 1910
FIGURE 2. Four species of Stasimopus Simon, 1892, habitus in life. A. Stasimopus hewitti, n. sp. B. Stasimopus robertsi Hewitt, 1910. C, D. Stasimopus griswoldi, n. sp. E, F. Stasimopus filmeri, n. sp. A, C, E. ♂. B, D, F. ♀.
FIGURE 1 in Cryptic diversity of South African trapdoor spiders: Three new species of Stasimopus Simon, 1892 (Mygalomorphae, Ctenizidae), and redescription of Stasimopus robertsi Hewitt, 1910
FIGURE 1. Habitats and burrows of Stasimopus Simon, 1892, from Gauteng and North West Provinces, South Africa. A. Stasimopus robertsi Hewitt, 1910, habitat, Faerie Glen Nature Reserve, Gauteng Province, Acacia karroo open woodland on red-structured clay soils. B. Stasimopus hewitti, n. sp., habitat, Roodeplaat Dam Nature Reserve, Gauteng Province, Acacia–Cymbopogon/Setaria open woodland on well-drained, red soils. C. Stasimopus griswoldi, n. sp., habitat, Farm Hartebeestfontein 473, North West Province, Acacia karroo open woodland on red, structured clay soils. D. Stasimopus filmeri, n. sp., habitat, Mokoya Lodge, Gauteng Province, Acacia caffra closed woodland on rocky soils. E, F. S. hewitti, n. sp., burrow entrance with trapdoor, Kameeldrift, Gauteng Province. E. Trapdoor closed. F. Trapdoor open. Scale: 1 cm.
Figure 6 in High molecular and phenotypic diversity in the Merodon avidus complex (Diptera, Syrphidae): cryptic speciation in a diverse insect taxon
Figure 6. Scatterplot of individual scores from the canonical variate analysis (CVA) of female specimens of: A, sympatric populations of Merodon avidus A and M. avidus B from Dubašnica Mt (ADUB, BDUB) and Greece (AGRE, BGRE) (Wilks' L = 0.003; F(48,30) = 3.64; P <0.001); B, allopatric populations of M. avidus A from FYR MACEDONIA (AMKD), Morinj (AMOR), and the Pannonian region (APAN) (Wilks' L = 0.09; F(32,48) = 3.59; P <0.0001); C, allopatric populations of M. avidus B from Durmitor Mt (BDUR), Stara Mt (BSPL), Kopaonik Mt (BKOP), and FYR MACEDONIA (BMKD) (Wilks' L = 0.36; F(32,32) = 0.66; P <0.879); D, allopatric populations of M. avidus A and M. avidus B (Wilks' L = 0.09; F(80,245) = 1.94; P <0.0001). The amount of variation explained by each canonical axis is in parentheses.
Figure 5 in High molecular and phenotypic diversity in the Merodon avidus complex (Diptera, Syrphidae): cryptic speciation in a diverse insect taxon
Figure 5. Scatterplot of individual scores from the canonical variate analysis (CVA) of all specimens (both sexes) of metapopulations: A, Merodon avidus A from Dubašnica Mt (ADUB) (Wilks' L = 0.04; F(48,72) = 3.06; P <0.000); B, M. avidus B from Dubašnica Mt (BDUB) (Wilks' L = 0.10; F(64,174) = 2.18; P <0.000); C, M. avidus B from Durmitor Mt (BDUR) (Wilks' L = 0.10; F(64,174) = 2.21; P <0.000); D, M. avidus A from FYR MACEDONIA (AMKD) (Wilks' L = 0.002; F(112,171) = 2.40; P <0.000); E, M. avidus A from Greece (AGRE) (Wilks' L = 0.009; F(64,53) = 1.93; P <0.007). The amount of variation explained by each canonical axis is in parentheses. The number of misclassified specimens/total number of analysed
Figure 1 in High molecular and phenotypic diversity in the Merodon avidus complex (Diptera, Syrphidae): cryptic speciation in a diverse insect taxon
Figure 1. Origin of the analysed populations using wing geometric morphometrics from the Balkan Peninsula: 1, Pannonian Plain (PAN, Serbia); 2, Dubašnica Mt, E 21°59′, N 44°01′ (DUB, Serbia); 3, Stara Mt, E 22°41′, N 43°20′ (SPL, Serbia); 4, Kopaonik Mt, E 20°40′, N 43°15′ (KOP, Serbia); 5, Durmitor Mt, E 19°00′, N 43°11′ (DUR, Montenegro); 6, Morinj, E 18°40′, N 43°29′30″ (MOR, Montenegro); 7, Former Yugoslav Republic of Macedonia (MKD); 8, Greece (GRE). (Numbers within region are noted sampling sites of populations).
A review of Appalachian Dasycerus Brongniart, and the recognition of cryptic diversity within Dasycerus carolinensis Horn (Coleoptera: Staphylinidae: Dasycerinae)
Open the record for dataset details and reuse information.
Appendix 7 in Morphometry and DNA barcoding reveal cryptic diversity in the genus Enteromius (Cypriniformes: Cyprinidae) from the Congo basin, Africa
Appendix 7. PC loadings of the PCA in Fig. 8. Most important loadings indicated in bold.
Appendix 5 in Morphometry and DNA barcoding reveal cryptic diversity in the genus Enteromius (Cypriniformes: Cyprinidae) from the Congo basin, Africa
Appendix 5. PC loadings of the PCA in Fig. 6. Most important loadings indicated in bold.
Appendix 2 in Morphometry and DNA barcoding reveal cryptic diversity in the genus Enteromius (Cypriniformes: Cyprinidae) from the Congo basin, Africa
Appendix 2. PC loadings of the PCA in Fig. 3. Most important loadings indicated in bold.
Appendix 4 in Morphometry and DNA barcoding reveal cryptic diversity in the genus Enteromius (Cypriniformes: Cyprinidae) from the Congo basin, Africa
Appendix 4. PC loadings of the PCA in Fig. 5. Most important loadings indicated in bold.
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