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227 results for “Assassin bugs”
Figs. 59–64. Ptilocerus kanoi Esaki, 1931, male genitalia. 59–60 in The assassin bug subfamilies Centrocnemidinae and Holoptilinae in Taiwan (Hemiptera: Heteroptera: Reduviidae)
Figs. 59–64. Ptilocerus kanoi Esaki, 1931, male genitalia. 59–60 – left paramere, two different aspects; 61 – phallus, lateral view; 62 – same, ventral view; 63 – endosoma, dorsal view; 64 – articulatory apparatus, anterior view. Legends as in Figs. 15, 22–24. Scales in mm.
Figs. 33–38 in A survey of the saicine assassin bugs of Taiwan (Hemiptera: Heteroptera: Reduviidae)
Figs. 33–38. Polytoxus rufinervis ardens Ishikawa & Yano, 2002, male, Taiwan. 33 – pygophore, dorsal view; 34 – same, lateral view; 35 – superoposterior process of pygophore, lateral view; 36–38 – left paramere, three different aspects. Scales in mm.
Figs. 39–56 in A survey of the saicine assassin bugs of Taiwan (Hemiptera: Heteroptera: Reduviidae)
Figs. 39–56. Polytoxus rufinervis ardens Ishikawa & Yano, 2002, male, Taiwan. 39 – phallus, dorsal view; 40 – same, ventral view, articulatory apparatus omitted; 41 – same, lateral view, from right; 42 – same, from left, articulatory apparatus omitted; 43–56 – endosomal processes in different aspects (43–45 – process 'A'; 46–47 – process 'B'; 48–49 – process 'C'; 50–51 – process 'D'; 52 – process 'E'; 53–54 – process 'F'; 55–56 – process 'G'). Scales in mm.
Figs. 20–32 in A survey of the saicine assassin bugs of Taiwan (Hemiptera: Heteroptera: Reduviidae)
Figs. 20–32. Polytoxus fuscovittatus (Stål, 1860), male, Philippines: Luzon. 20 – phallus, ventral view, articulatory apparatus omitted; 21 – phallus, dorsal view; 22 – same, lateral view; 23–32 – endosomal processes in different aspects (23–25 – process 'A'; 26–28 – process 'B'; 29 – process 'C'; 30–32 – process 'D'). Scales in mm.
Figs. 1–10 in A survey of the saicine assassin bugs of Taiwan (Hemiptera: Heteroptera: Reduviidae)
Figs. 1–10. Polytoxus fuscovittatus (Stål, 1860). 1 – head and thorax, dorsal view; 2 – same, lateral view; 3 – exposed parts of meso- and metanota, dorsal view; 4 – same, dorsolateral view; 5 – left fore wing; 6–10 – variability of the lengths of humeral and mesoscutellar processes, posterior views (6 – Myanmar, male; 7 – Philippines: Luzon, female; 8 – Malaysia: Sarawak, female; 9 – Philippines: Negros, male; 10 – Philippines: Luzon, male). Scales in mm.
Figs. 37-44 in Two new species of the emesine assassin bug genus Ploiaria (Hemiptera: Heteroptera: Reduviidae) from Indonesia
Figs. 37-44. Ploiaria paveli sp. nov.; setae omitted in 37, 38 and 43. 37-38 – pygophore: 37 – lateral view, 38 – ventral view; 39-40 – left paramere: 39 – lateral view, 40 – dorsal view; 41 – phallus, lateral view; 42 – basal plate of phallus, dorsal view; 43 – left valvifer I and valvula I, lateral view; 44 – styloids, dorsal view. Abbreviations: bp = basal plate; bpb = basal plate bridge; nls = narrow longitudinal sclerotized area; re = rounded extension; vf1 = valvifer I; vl1 = valvula I. Scale bars = 0.2 mm.
Figs. 45-47 in Two new species of the emesine assassin bug genus Ploiaria (Hemiptera: Heteroptera: Reduviidae) from Indonesia
Figs. 45-47. Collecting sites of Ploiaria stysi sp. nov. and P. paveli sp. nov. in Bali and Flores; white circle = site of P. stysi, black circle = site of P. paveli, white and black circle = site of both species; lowercase letters correspond with locality names shown in Type material section, see also Material and methods section. 45 – Bali; 46-47 – Flores: 46 – the west, 47 – the east. Scale bar = 20 km.
Figs. 13-18 in Two new species of the emesine assassin bug genus Ploiaria (Hemiptera: Heteroptera: Reduviidae) from Indonesia
Figs. 13-18 – Ploiaria paveli sp. nov., male (holotype). 13 – protibia and protarsus; 14 – profemur; 15 – apical part of mesofemur; 16 – basal part of mesotibia; 17 – apical part of metafemur; 18 – basal part of metatibia. Scale bars = 1.0 mm.
Figs. 24-31 in Two new species of the emesine assassin bug genus Ploiaria (Hemiptera: Heteroptera: Reduviidae) from Indonesia
Figs. 24-31. Ploiaria stysi sp. nov.; setae omitted in 24, 25 and 30. 24-25 – pygophore: 24 – lateral view, 25 – ventral view; 26-27 – left paramere: 26 – lateral view, 27 – dorsal view; 28 – phallus, lateral view; 29 – basal plate of phallus, dorsal view; 30 – left valvifer I and valvula I, lateral view; 31 – styloids, dorsal view. Abbreviations. ans = apically narrowed sclerotized area; bp = basal plate; bpb = basal plate bridge; fp = foliaceous projection; lsp = laterally sclerotized posterior process; vf1 = valvifer I; vl1 = valvula I. Scale bars = 0.2 mm.
Figs. 7-12 in Two new species of the emesine assassin bug genus Ploiaria (Hemiptera: Heteroptera: Reduviidae) from Indonesia
Figs. 7-12. Ploiaria stysi sp. nov., male (holotype). 7 – protibia and protarsus; 8 – profemur; 9 – apical part of mesofemur; 10 – basal part of mesotibiae; 11 – apical part of metafemur; 12 – basal part of metatibia. Scale bars = 1.0 mm.
Figs. 1-6. 1-3 in Two new species of the emesine assassin bug genus Ploiaria (Hemiptera: Heteroptera: Reduviidae) from Indonesia
Figs. 1-6. 1-3 – Ploiaria stysi sp. nov., male (holotype). 1-2 – habitus: 1 – dorsal view, 2 – lateral view; 3 – head and pronotum, lateral view. 4-6 – P. paveli sp. nov., male (holotype). 4-5 – habitus: 4 – dorsal view, 5 – lateral view; 6 – head and pronotum, lateral view. Scale bars = 5.0 mm for 1-2, 4-5; 1.0 mm for 3, 6.
Figs. 19-23 in Two new species of the emesine assassin bug genus Ploiaria (Hemiptera: Heteroptera: Reduviidae) from Indonesia
Figs. 19-23. Ploiaria stysi sp. nov.; setae omitted except for spine-like setae in 21 and 22. 19-20 – head and pronotum: 19 – dorsal view, 20 – lateral view; 21 – left fore leg; 22 – basal part of profemur, ventrolateral view; 23 – right hemelytron. Abbreviation: bss = basal spine-like seta. Scale bars = 1.0 mm.
Fig. 16 in Taxonomic revision of the African assassin bug genus Fusius (Heteroptera: Reduviidae: Peiratinae)
Fig. 16. Distribution of Fusius Stål, 1862.
Fig. 14 in Taxonomic revision of the African assassin bug genus Fusius (Heteroptera: Reduviidae: Peiratinae)
Fig. 14. Intraspecific variation in Fusius rubricosus (Stål, 1855). Scale bar = 2.00 mm.
Figure. Nymph of assassin bug (Harpactorini) preying a Tityus pusillus Pocock, 1893 juvenile. in Predation of a scorpion (Scorpiones: Buthidae) by an assassin bug (Heteroptera: Reduviidae) in the Brazilian Atlantic Forest
Figure. Nymph of assassin bug (Harpactorini) preying a Tityus pusillus Pocock, 1893 juvenile.
Figure 2 in Eating with the enemy? Mimic complex between a stingless bee and assassin bugs
Figure 2. Mimic complex between Tetragona clavipes (model) and three species of Notocyrtus. (A and E) Worker of T. clavipes. (B and F) N. foveatus. (C and G) N. dorsalis. (D and H) N. dispersus. (A-D) dorsal view. (E-H) lateral view. Scale bars: 2 mm.
Figure 1 in Eating with the enemy? Mimic complex between a stingless bee and assassin bugs
Figure 1. Diversity of visitors of extrafloral nectaries of Bauhinia forficata Link.(A) Worker of Camponotus rufipes (Fabricius) (Hymenoptera: Formicidae). (B) Dynamine coenus (Fabricius) (Lepidoptera: Nymphalidae). (C) Worker of Tetragona clavipes (Fabricius) (Hymenoptera: Apidae: Meliponini). (D) Notocyrtus dorsalis (Gray) preying an ant C. rufipes. (E) N. dorsalis feeding on extrafloral nectary.
Data for: Climatic oscillation promoted diversification of spinous assassin bugs during Pleistocene glaciation
<p>Insect speciation is among the most fascinating topics in evolutionary biology; however, its underlying mechanisms remain unclear. Allopatric speciation represents one of the major types of speciation and is believed to have frequently occurred during glaciation periods, when climatic oscillation may have caused suitable habitats to be fragmented repeatedly, creating geographical isolation among populations. However, supporting evidence for allopatric speciation of insects in East Asia during the Pleistocene glaciation remains lacking. We aim to investigate the effect of climatic oscillation during the Pleistocene glaciation on the diversification pattern and evolutionary history of hemipteran insects and to test the hypothesis of Pleistocene species stability using spinous assassin bugs <em>Sclomina</em> (Hemiptera: <span>Reduviidae</span>), a small genus widely distributed in southern China but was lately found to have cryptic species diversity. Here, using the whole mitochondrial genome (mitogenome) and nuclear ribosomal RNA genes, we investigated both interspecific and intraspecific diversification patterns of spinous assassin bugs. Approximate Bayesian computation, ecological niche modeling and demographic history analyses were also applied to understand the diversification process and driven factors. Our data suggest that the five species of <em>Sclomina</em> are highly diverged, despite three of them currently being cryptic. Speciation occurred during Pleistocene when suitable distribution areas were possibly fragmentated. Six phylogeographic groups in the type species <em>S. erinacea</em> were identified, among which two groups underwent expansion during early Last Glacial Period and after Last Glacier Maximum. Our analyses suggest that this genus may have experienced climate-driven habitat fragmentation and post-glacial expansion in the Pleistocene, promoting allopatric speciation and intraspecific diversification. Our results reveal underestimated species diversity in a small insect group and illustrate a remarkable example of allopatric speciation of insects in East Asia promoted by Pleistocene climatic oscillations. These findings provide important insights into the speciation processes and aid the conservation of insect species diversity.</p>
A revised classification of the assassin bugs (Hemiptera: Heteroptera: Reduviidae) based on combined analysis of phylogenomic and morphological data
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Data for: Climatic oscillation promoted diversification of spinous assassin bugs during Pleistocene glaciation
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