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246 results for “Gonyleptoidea”
Figure 17 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 17. Voriax popeye sp. nov., male paratype (MNRJ 17722). Distal part of penis. A, lateral view; B, ventral view; C, dorsal view; D, detail of glans, laterodorsal view. Scale bars = 0.05 mm (A, B, C), 0.01 mm (D).
Figure 20 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 20. Paratricommatus lockei sp. nov., male paratype (MNRJ 7517), from Guapi-Açu. A, left chelicera, mesal view; B, left pedipalpus, mesal view; C, left leg I retrolateral view; D, left leg IV, prolateral view; E, right femur IV, dorsal view. Scale bars = 500 μm (C, D), 200 μm (A, B, E).
Figure 27 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 27. Cryptogeobiidae, appendages: A, Tibangara nephelina (MNRJ 1964), left pedipalpus, mesal view; B, same, detail of stridulatory grate on femur; C, Bissulla paradoxa (MZSP 432), left pedipalpus, mesal view; D, same, detail of stridulatory grate on trochanter and base of femur; E, Gen. sp. O, male (MNRJ 17557), left distitarsus IV, prolateral view; F, Gen. sp. W, male (MNRJ1977) right pedipalpus, ventral view, showing compression and grate. Scale bars = 0.2 mm (A, C), 0.1 mm (D, F), 0.05 mm (B), 0.02 mm (E).
Figure 31 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 31. Cryptogeobiidae, detail of varied styli and flabella of glans penis compared with a Gonyleptidae with true ventral process of glans, varied views. A, Discocyrtoides nigricans (MNRJ 18884). B, Gen. sp. W (MNRJ 1977). C, Gen. sp. Q (MNRJ 7585). D, Gen. sp. AA (MZSP 18090). E, Gen. sp. H (MZSP 15747). F, Gen. sp. AE (MNRJ 4487). G, Gen. sp. M (MNRJ 17687). H, Pseudopachylus nigripes (MNRJ 4768). I, Gen. sp. AD (MNRJ 5592). Scale bars = 0.05 mm (A), 0.2 mm (D, I), 0.1 mm (B, C, F, G, H).
Figure 13 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 13. Voriax popeye sp. nov., male paratype (MNRJ 17722). A, stigmatic area showing 'encased' position of stigma; B, right ozopore, lateral view; C, right pedipalpal tibia-tarsus, ventral view; D, same, detail of mesal tibial setiferous tubercles; E, left leg III whole, prolateral to dorsal views; F, left distitarsomere + claws III, latero-apical view.
Figure 19 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 19. Paratricommatus lockei sp. nov., schematic dorsal scutum, showing the dimorphism in the ocularium. A, B, male holotype (MNRJ 7582); C, D, female paratype (MNRJ 7583), dorsal and lateral views; E, male holotype, sternites, ventral view. Scale bars = 1 mm.
Figure 23 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 23. Zalanodius convexus (Mello-Leitão, 1940). Male neotype (MNRJ 4878). A, right coxa IV and stigmatic area, partial, ventral view; B, same, detail of rod-like ventral apophysis of coxa IV (VA) resting on sternite II (stigmatic area, S2), oblique view; C, left coxa IV, lateroposterior view, showing multiple dorsal apophyses (DA) of coxa IV; D, left trochanter to tibia of leg IV, dorsal view; E, left tarsus of leg I, showing very faint sutures separating pseudo-articles (1, 2, 3) of distitarsus, lateral view; F, left pedipalpus, mesal view. Other abbreviations: Bt, basitarsus; Dt, distitarsus; Mt, metatarsus; TS, tracheal stigma. Scale bars = 0.2 mm (D, F), 0.1 mm (A, C, E), 0.05 mm (B).
Figure 9 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 9. Cladogram depicting proposed phylogenetic relationships for Tricommatinae and Cryptogeobiidae inside Gonyleptoidea (part 4 of 4). The small 'Navajo rugs' at selected branches indicate which of the four analyses supports a given clade. A key to the analyses is given in the set of four squares at the bottom, abbreviated as: 1, implied weights, concavity 1; 3, same, concavity 3; 6, same, concavity 6; E, strict consensus of the analysis under equal weights. Numerals at branches represent absolute Bremer support/standard bootstrap resampling percentage values.
Figure 7 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 7. Cladogram depicting proposed phylogenetic relationships for Tricommatinae and Cryptogeobiidae inside Gonyleptoidea (part 2 of 4). The small 'Navajo rugs' at selected branches indicate which of the four analyses supports a given clade. A key to the analyses is given in the set of four squares at the bottom, abbreviated as: 1, implied weights, concavity 1; 3, same, concavity 3; 6, same, concavity 6; E, strict consensus of the analysis under equal weights. Numerals at branches represent absolute Bremer support/standard bootstrap resampling percentage values.
Figure 6 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 6. Cladogram depicting proposed phylogenetic relationships for Tricommatinae and Cryptogeobiidae inside Gonyleptoidea (part 1 of 4). The small 'Navajo rugs' at selected branches indicate which of the four analyses supports a given clade. A key to the analyses is given in the set of four squares at the bottom, abbreviated as: 1, implied weights, concavity 1; 3, same, concavity 3; 6, same, concavity 6; E, strict consensus of the analysis under equal weights. Numerals at branches represent absolute Bremer support/standard bootstrap resampling percentage values. GG, Greater Gonyleptidae; MI, Microsetata.
Figure 29. Cryptogeobiidae. Left trochanter IV in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 29. Cryptogeobiidae. Left trochanter IV of male, schematic, dorsal view: A, Camarana minor; B, Camarana insignis; C, Tibangara nephelina; D, Gen. sp. AB; E, Gen. sp. L; F, Taquara pilosa; G, Cryptogeobius crassipes; H, Gen. sp. AE. Alpha and Beta apophyses as defined in the descriptions of characters 47 and 48 (Appendix 1).
Figure 4. Cryptogeobiidae. A in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 4. Cryptogeobiidae. A, Tibangara nephelina, male (MNRJ 1964). Opisthosoma, ventral view, schematic, lacking most tubercles and setae. B, Spinopilar armatus, male (MNRJ 4508). Opisthosoma, ventral view, schematic, lacking most tubercles and setae. C, Gen. sp. F (MZSP 10022). Habitus, lateral view. D, Pararezendesius luridus (MNRJ 9000). Same. E, Gen. sp. H (MZSP 15747). Same. Abbreviations: Cx, coxa; FA, interlocking fasciolate apophyses of coxa and trochanter; Fe, femur; OpA, operculum anale (tergite 9); S2−S8, sternites; Tr, trochanter. Scale bars = 1 mm.
Figure 28 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 28. Apophyses of coxa IV of males (schematic). Left dorso-apical apophysis, dorsal view: A, Camarana insignis; B, Gen. sp. S; C, Gen. sp. I; D, Zalanodius convexus; E, Caramaschia singularis; F, Gen. sp. Y; G, Gen. sp. AB. Right ventro-apical apophysis, ventral view: H, Gen. sp. AB; I, Camarana insignis; J, Taquara bicoloripes; K, Tibangara cocaiensis; L, Gen. sp. X; M, Cryptogeobius crassipes; N, Bunostigma singulare; O, Caramaschia singularis. P−V, the same character states (numbered) of ventral apophyses, ultraschematic.
Figure 5 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 5. Cryptogeobiidae. Matching hyaline fasciolate apophyses (FAp), 'alpha shark's fin' of trochanter IV and 'horse's head' of coxa IV. A, Pseudopachylus longipes, male (MNRJ 17649), ventral view of stigmatic area and base of leg IV. B, Tibangara nephelina, male (MNRJ 1964). The same region as preceding illustration, showing 'bundle' structure of both FAp. Scale bars = 1 mm (A), 0.1 mm (B).
Figure 3 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 3. Cryptogeobiidae, distal part of penis, lateral view. A, Taquara bicoloripes, male (MNRJ 2218). B, Gen. sp. P, male (MNRJ 16192). C, Bunostigma singulare, male (MNRJ 7679). D, Gen. sp. AD, male (MNRJ 5592). Scale bars = 0.05 mm (A–C), 0.1 mm (D).
Figure 2. Cryptogeobiidae. A in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 2. Cryptogeobiidae. A, Bunostigma singulare, male (MNRJ 7679), coxae, stigmatic area and sternites, ventral view; B, Gen. sp. P, male (MNRJ 16192) dorsal scutum, dorsal view; C, Spinopilar armatus, male (MNRJ 2251) carapace, coxae I–III, chelicerae, lateral view; D, Bissulla paradoxa, male (MZSP 432) body with chelicera/pedipalp, lateral view.
Figure 22 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 22. Zalanodius convexus (Mello-Leitão, 1940). Male neotype (MNRJ 4878). A, habitus, dorsal view; B, same, lateral view; C, sternal region, coxae, stigmatic area, and sternites, ventral view. Scale bars = 0.5 mm (A, B), 0.1 mm (C, D).
Figure 11 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 11. Eastern Brazil, showing the distribution of the Tricommatinae. Black outlines are Brazilian states. Abbreviations: BA, Bahia; PR, Paraná; SC, Santa Catarina.
Figure 15. Tricommatus brasiliensis Roewer, 1912 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 15. Tricommatus brasiliensis Roewer, 1912, male holotype (SMF RI 220). A, habitus, dorsal view; B, same, lateral view; C, sternal region, coxae, stigmatic area, and sternites, ventral view. Scale bars = 1 mm.
Figure 1 in Why does the Tricommatinae position bounce so much within Laniatores? A cladistic analysis, with description of a new family of Gonyleptoidea (Opiliones, Laniatores)
Figure 1. Cryptogeobiidae. Habitus of several species. A, Gen. sp. S, male (MNRJ 4558), dorsal view; B, Pseudophalangodes unicolor, male (MNRJ 7005), dorsal view; C, Gen. sp. T, male (MNRJ 18237), dorsal view; D, Heteromeloleptes padbergi, male (MNRJ 2243), lateral view; E, Bunostigma singulare, male (MNRJ 7679), dorsal view; F, Same, female. Scale bars = 1 mm.
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