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Рис. 2. Основные части теΛа и эΛементы окраски Mesobuthus eupeus: I – просома; II – мезосома; III – метасома; a – меΑиаΛьная поΛоса; b – парамеΑиаΛьная поΛоса; с – маргинаΛьная поΛоса; d – поперечная поΛоса; e – пятна. Fig. 2. Main body parts and colour pattern elements of Mesobuthus eupeus: I – prosoma; II – mesosome; III – metasoma; a – medial stripe; b – paramedical stripe; с – marginal stripe; d – transverse stripe; e – spots. in Materials on the colour pattern variability of Mesobuthus eupeus (C.L. Koch, 1839) (Arachnida: Scorpiones) in southeastern Shirvan and Gobustan (Eastern Azerbaijan)
Рис. 2. Основные части теΛа и эΛементы окраски Mesobuthus eupeus: I – просома; II – мезосома; III – метасома; a – меΑиаΛьная поΛоса; b – парамеΑиаΛьная поΛоса; с – маргинаΛьная поΛоса; d – поперечная поΛоса; e – пятна. Fig. 2. Main body parts and colour pattern elements of Mesobuthus eupeus: I – prosoma; II – mesosome; III – metasoma; a – medial stripe; b – paramedical stripe; с – marginal stripe; d – transverse stripe; e – spots.
Рис. 3–20. Варианты окраски Mesobuthus eupeus. 3–7 – Северо-ЗапаΑный Гобустан; 8–10 – Северо-Восточный Гобустан; 11–14 – ЦентраΛьный Гобустан; 15–17 – Юго-Восточный Гобустан; 18–20 – Юго-Восточный Ширван. Figs 3–20. Colour pattern variation in Mesobuthus eupeus. 3–7 – northwestern Gobustan; 8–10 – northeastern Gobustan; 11–14 – central Gobustan; 15–17 – southeastern Gobustan; 18–20 – southeastern Shirvan. in Materials on the colour pattern variability of Mesobuthus eupeus (C.L. Koch, 1839) (Arachnida: Scorpiones) in southeastern Shirvan and Gobustan (Eastern Azerbaijan)
Рис. 3–20. Варианты окраски Mesobuthus eupeus. 3–7 – Северо-ЗапаΑный Гобустан; 8–10 – Северо-Восточный Гобустан; 11–14 – ЦентраΛьный Гобустан; 15–17 – Юго-Восточный Гобустан; 18–20 – Юго-Восточный Ширван. Figs 3–20. Colour pattern variation in Mesobuthus eupeus. 3–7 – northwestern Gobustan; 8–10 – northeastern Gobustan; 11–14 – central Gobustan; 15–17 – southeastern Gobustan; 18–20 – southeastern Shirvan.
Рис. 2. Ширина трофической ниши паукообразных в биотопах трех типов: I – поΛупустынная равнина; II – каменистые скΛоны пΛато; III – ΔоΛина со скопΛениями скаΛьных останцев. Fig. 2. The width of the trophic niche of arachnids in biotopes of three types: I – semidesert plain; II – stony slopes of the plateau; III – valley with clusters of rocks. in Comparison of trophic spectra and hunting strategies of some large arachnids (Arachnida: Scorpiones, Solifugae, Aranei) in semi-desert biocenoses of Gobustan (Eastern Azerbaijan)
Рис. 2. Ширина трофической ниши паукообразных в биотопах трех типов: I – поΛупустынная равнина; II – каменистые скΛоны пΛато; III – ΔоΛина со скопΛениями скаΛьных останцев. Fig. 2. The width of the trophic niche of arachnids in biotopes of three types: I – semidesert plain; II – stony slopes of the plateau; III – valley with clusters of rocks.
Рис. 3. Ритм ночной активности паукообразных Mesobuthus eupeus, Galeodes araneoides, Lycosa praegrandis. Fig. 3. The rhythm of the night activity of arachnids Mesobuthus eupeus, Galeodes araneoides, Lycosa praegrandis. in Comparison of trophic spectra and hunting strategies of some large arachnids (Arachnida: Scorpiones, Solifugae, Aranei) in semi-desert biocenoses of Gobustan (Eastern Azerbaijan)
Рис. 3. Ритм ночной активности паукообразных Mesobuthus eupeus, Galeodes araneoides, Lycosa praegrandis. Fig. 3. The rhythm of the night activity of arachnids Mesobuthus eupeus, Galeodes araneoides, Lycosa praegrandis.
Рис. 21–25. Частота изменчивости основных эΛементов рисунка (меΑиаΛьной, парамеΑиаΛьных и маргинаΛьных поΛос) ΑорсаΛьной поверхности мезосомы Mesobuthus eupeus в посеΛениях кажΑой из выборок. 21 – Северо-ЗапаΑный Гобустан (n = 57); 22 – Северо-Восточный Гобустан (n = 40); 23 – ЦентраΛьный Гобустан (n = 81); 24 – Юго-Восточный Гобустан (n = 103); 25 – Юго-Восточный Ширван (n = 86). По оси абсцисс указаны посеΛения, по оси орΑинат – частота изменчивости. Figs 21–25. Frequency of variability of the main elements of pattern (medial, paramedical and marginal stripes) of dorsal surface of mesosome of Mesobuthus eupeus in conglomerations of each sample. 21 – northwestern Gobustan (n = 57); 22 – northeastern Gobustan (n = 40); 23 – central Gobustan (n = 81); 24 – southeastern Gobustan (n = 103); 25 – southeastern Shirvan (n = 86). Abscissas show conglomerations, ordinates – the frequency of variability. in Materials on the colour pattern variability of Mesobuthus eupeus (C.L. Koch, 1839) (Arachnida: Scorpiones) in southeastern Shirvan and Gobustan (Eastern Azerbaijan)
Рис. 21–25. Частота изменчивости основных эΛементов рисунка (меΑиаΛьной, парамеΑиаΛьных и маргинаΛьных поΛос) ΑорсаΛьной поверхности мезосомы Mesobuthus eupeus в посеΛениях кажΑой из выборок. 21 – Северо-ЗапаΑный Гобустан (n = 57); 22 – Северо-Восточный Гобустан (n = 40); 23 – ЦентраΛьный Гобустан (n = 81); 24 – Юго-Восточный Гобустан (n = 103); 25 – Юго-Восточный Ширван (n = 86). По оси абсцисс указаны посеΛения, по оси орΑинат – частота изменчивости. Figs 21–25. Frequency of variability of the main elements of pattern (medial, paramedical and marginal stripes) of dorsal surface of mesosome of Mesobuthus eupeus in conglomerations of each sample. 21 – northwestern Gobustan (n = 57); 22 – northeastern Gobustan (n = 40); 23 – central Gobustan (n = 81); 24 – southeastern Gobustan (n = 103); 25 – southeastern Shirvan (n = 86). Abscissas show conglomerations, ordinates – the frequency of variability.
Рис. 1. ПреΔпочтитеΛьное отношение паукообразных (1 – Galeodes araneoides, 2 – Lycosa praegrandis, 3 – Mesobuthus eupeus) к объектам питания по способу переΔвижения жертвы: I – Λетающие; II – прыгающие; III – бегающие; IV – хоΔящие; V – поΛзающие; VI – маΛопоΔвижные; VII – непоΔвижные. Fig. 1. Preferred attitude of arachnids (1 – Galeodes araneoides, 2 – Lycosa praegrandis, 3 – Mesobuthus eupeus) to food objects by the method of movement of pray: I – flying; II – jumping; III – running; IV – walking; V – crawling; VI – sluggish; VII – motionless. in Comparison of trophic spectra and hunting strategies of some large arachnids (Arachnida: Scorpiones, Solifugae, Aranei) in semi-desert biocenoses of Gobustan (Eastern Azerbaijan)
Рис. 1. ПреΔпочтитеΛьное отношение паукообразных (1 – Galeodes araneoides, 2 – Lycosa praegrandis, 3 – Mesobuthus eupeus) к объектам питания по способу переΔвижения жертвы: I – Λетающие; II – прыгающие; III – бегающие; IV – хоΔящие; V – поΛзающие; VI – маΛопоΔвижные; VII – непоΔвижные. Fig. 1. Preferred attitude of arachnids (1 – Galeodes araneoides, 2 – Lycosa praegrandis, 3 – Mesobuthus eupeus) to food objects by the method of movement of pray: I – flying; II – jumping; III – running; IV – walking; V – crawling; VI – sluggish; VII – motionless.
Figure 82 in Two new species of the remarkable scorpion genus Megacormus Karsch, 1881 (Scorpiones: Euscorpiidae)
Figure 82. Distribution of Megacormus specimens examined for this review (see Comparative material examined in Methods, Material & Abbreviations section).
Figures 62–65 in Two new species of the remarkable scorpion genus Megacormus Karsch, 1881 (Scorpiones: Euscorpiidae)
Figures 62–65. Hemispermatophores of Megacormus spp. Figure 62. M. orizaba sp. n. 19MD (holotype, No. 1621). Figure 63. M. granosus (No. 2462). Figures 64–65. M. seductus sp. n. 22MA (holotype and paratopotype, Nos. 2460, 2461). Convex views of left hemispermatophores (62, 63) and right hemispermatophores shown in mirror image (64, 65). Scale bars: 500 μm.
Figures 35–42 in Two new species of the remarkable scorpion genus Megacormus Karsch, 1881 (Scorpiones: Euscorpiidae)
Figures 35–42. Megacormus seductus sp. n. Figures 35, 37–39. Male holotype, telson in lateral (35), metasoma and telson in lateral (37), dorsal (38) and ventral (39) views. Figures 36, 40–42. Female paratype, telson in lateral (36), metasoma and telson in lateral (40), dorsal (41) and ventral (42) views. Scale bars: 10 mm (37–39, 40–42).
Figures 78–81 in Two new species of the remarkable scorpion genus Megacormus Karsch, 1881 (Scorpiones: Euscorpiidae)
Figures 78–81. Chromosomes of Megacormus species. 78–79. M. seductus sp. n. (No. 2461) (2n=109). 80. M. segmentatus (No. 1262) (2n=144). 81. M. granosus (No. 2462) (2n=148). Postpachytene (78 and 80), one sister metaphase II (79), ane mitotic metaphase (81). Arrowhead shows trivalent in postpachytene. Scale bar: 10 μm.
Figures 17–26 in Two new species of the remarkable scorpion genus Megacormus Karsch, 1881 (Scorpiones: Euscorpiidae)
Figures 17–26: Megacormus seductus sp. n., female paratype, pedipalp chela dorsal (17), external (18) and ventral (19) views, patella dorsal (20), external (21) and ventral (22) views, femur and trochanter dorsal (23) and ventral (24) views, movable (25) and fixed (26) fingers dentition.
Figures 27–34 in Two new species of the remarkable scorpion genus Megacormus Karsch, 1881 (Scorpiones: Euscorpiidae)
Figures 27–34: Megacormus seductus sp. n. Figures 27–28. Male holotype, carapace and tergites I–IV (27) and coxosternal area and sternites (28). Figures 29–34. Female paratype, carapace and tergites I–IV (29), coxosternal area and sternites (30), and left legs I–IV, retrolateral aspect (31–34).
Figures 3–6 in Two new species of the remarkable scorpion genus Megacormus Karsch, 1881 (Scorpiones: Euscorpiidae)
Figures 3–6: Megacormus seductus sp. n. Figures 3–4. Male holotype in dorsal (3) and ventral (4) views. Figures 5–6. Female paratype in dorsal (5) and ventral (6) views. Scale bars: 10 mm.
Figures 1–2 in Two new species of the remarkable scorpion genus Megacormus Karsch, 1881 (Scorpiones: Euscorpiidae)
Figures 1–2. Megacormus seductus sp. n., male holotype (1) and female paratype with a juvenile (2) in vivo habitus.
Figures 66–77 in Two new species of the remarkable scorpion genus Megacormus Karsch, 1881 (Scorpiones: Euscorpiidae)
Figures 66–77. Hemispermatophore capsules of Megacormus. 66. M. orizaba sp. n. (holotype, No. 1621). 67–68. M. gertschi (Nos. 1619, 1620). 69. M. franckei (paratype, No. 1618). 70–71. M. xichu (Nos. 1617, 1626). 72–73. M. seductus sp. n. (holotype and paratopotype, Nos. 2460–2461). 74. M. segmentatus (No. 1622). 75. M. granosus (No. 2462). 76. M. grubbsi (No. 1623). 77. M. grubbsi (No. 2463). Convex views of left capsules (66, 68–71, 73–75 and 77), and right capsules shown in mirror image (67, 72 and 76). Abbreviations: dpd, distal dentate process; dpp, proximal dentate process; cls, crown-like structure; trd, distal transverse ridge; trp, proximal transverse ridge; tmsd, terminal membrane of the sperm duct. Scale bars: 400 μm.
Fig. 1 in The earliest record of terrestrial animals in Gondwana: A scorpion from the Famennian (Late Devonian) Witpoort Formation of South Africa
Fig. 1. Gondwanan reconstruction with position of the South Pole (star), main latitudes reconstructed for Late Devonian/Early Carboniferous (modified after Scotese & Barrett 1990), and the position of the Waterloo Farm (WF).
Figure 2 in Another new species of Pseudouroplectes Lourenço, 1995 from Madagascar (Scorpiones, Buthidae)
Figure 2. Habitus of Pseudouroplectes maculatus, female paratype. Scale bar = 2 mm.
Figure 28 in The genus Ananteris Thorell, 1891 (Scorpiones, Buthidae) in southeast Brazil, with the description of three new species
Figure 28. Map of distribution of the species of the genus Ananteris in Brazil.
FIG. 2 in The scorpions from the Mitaraka Massif in French Guiana (Scorpiones: Buthidae, Chactidae)
FIG. 2. — Aerial view of the Massif of Mitaraka in French Guiana (photo: Xavier Desmier).
Image 13 in Diversity of scorpion fauna of Saswad-Jejuri, Pune District, Maharashtra, western India
Image 13. Industrialization in scrubland. The most important habitat for arachnids
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