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1,039 results for “Satyrinae”
FIGURE 5 in Phylogeny of Amathusiini butterflies based on adult morphology (Lepidoptera, Nymphalidae, Satyrinae)
FIGURE 5. Illustrations of character states, numbers on the figures correspond to the character list. M, male; F, female. a, Taenaris artemis F forewing, Australian New Guinea, Kairiru Islands. b, Enispe euthymius M, India, Assam, Tista Valley. c, Thaumantis noureddin M, Malaysia, Perak. d, Callarge sagitta M, [probably from East China]. e, Taenaris catops M, Dutch New Guinea. f, Elymnias hypermnestra F, Pakistan, Hashnabad, Dacca. g, Taenaris artemis M, Dutch New Guinea, Kairiru Islands. h, Amathuxidia amythaon M, Malaya. i, Thauria aliris M, Formosa [Taiwan].
FIGURE 4 in Phylogeny of Amathusiini butterflies based on adult morphology (Lepidoptera, Nymphalidae, Satyrinae)
FIGURE 4. Comparison of relationships proposed by previous researchers and this study. The top two branching diagrams were drawn by hand based on published texts. Groups of genera are shaded to facilitate comparison, and genera in open boxes are no longer considered members of Amathusiini sensu Chazot et al. (2021). Note that those authors used the genus name Morphotenaris Fruhstorfer, which was synonymized with Taenaris by Stichel (1933).
FIGURE 7 in Phylogeny of Amathusiini butterflies based on adult morphology (Lepidoptera, Nymphalidae, Satyrinae)
FIGURE 7. Illustrations of character states, numbers on the figures correspond to the character list. M, male; F, female. a, Elymnias hypermnestra M, Ceylon. b, Amathuxidia amythaon M, Malaya. c, Amathusia phidippus M, Java. d, Discophora celinde M, India, Assam, Tista Valley. e, Thaumantis odana M, Java. f, Taenaris artemis, Dutch New Guinea, Kairiru Islands.
FIGURE 2 in Phylogeny of Amathusiini butterflies based on adult morphology (Lepidoptera, Nymphalidae, Satyrinae)
FIGURE 2. Type species of Amathusiini genera. Image sets show male (M) in dorsal and ventral views, and female (F) in dorsal view. a, Enispe euthymius M, India, Assam, Tista valley, CMP 02-30; F, India, Assam, CMP 02-31. b, Amathuxidia amythaon M, Malaya, CMP 02-06; F, no data, CMP 02-07. c, Amathusia phidippus M, Java, CMP 01-88; F, [Philippines] Mindanao, Davao, CMP 01-89. d, Zeuxidia luxerii M, [Indonesia] West Java, CMP 02-21; F, [Indonesia] West Java. e, Thauria aliris M, [Borneo] Mt. Dulit, CMP 07-123; F, [Malaysia] Sarawak, Baram District, CMP 07-109.
FIGURE 14 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 14. The Bayesian implementation of the Poisson Tree Processes (bPTP) for delimiting species based on a fragment of COI mitochondrial gene.
FIGURE 11. Adults live and habitats A. M. prattorum udima n in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 11. Adults live and habitats A. M. prattorum udima n. ssp. female, Peru, La Florida —via La Udima. Photo P. Boyer B. M. prattorum udima n. ssp. male, Peru, La Florida —via La Udima. Photo P. Boyer C. Abra de Porculla, view towards Pacific coast, type locality of M. punku. Photo T. Pyrcz
FIGURE 13 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 13. Maximum likelihood tree (ML) reconstructed from a fragment of COI mitochondrial gene. Ultrafast bootstrap support values indicated on nodes.
FIGURE 12 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 12. Bayesian Inference tree (BI) reconstructed from a fragment of COI mitochondrial gene. Posterior probability values indicated on nodes.
FIGURE 8 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 8. Male genitalia (A, B) (top—lateral view, middle—plan view, bottom—aedeagus extracted, lateral view) C. Female genitalia (top—lateral view; bottom—ventral view, detail) A. M. inducta n. sp., Peru, Lagunas Arrebiatadas, prep. genit. MUSA_015149 B. M. huamanii n. sp., Peru, Tres Ríos, prep. genit. MUSA_015150 C. M. prattorum udima n. ssp., Peru, La Florida, prep. genit. KF-1473
FIGURE 9 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 9. Female genitalia (top—lateral view; bottom—ventral view, detail) A. M. ronda n. sp., Peru, Laguna Salahuido, prep. genit. MUSA_015151 B. M. inducta n. sp., Peru, Lagunas Arrebiatadas, prep. genit. MUSA_015152
FIGURE 6 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 6. Male genitalia (top—lateral view, middle—plan view, bottom—aedeagus extracted, lateral view) A. M. granatus n. sp. Peru, Rodríguez de Mendoza, prep. genit. KF-2736 B. M. placida n. sp. Ecuador, Zamora, prep. genit. KW-20-021 C. M. benigni tessmanni, Peru, Alto Río Nieva, prep. genit. KF-H_241 D. M. benigni tessmanni, Ecuador, Río Troya, prep. genit. KF-6282
FIGURE 4 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 4. Adults (left—dorsum, right—venter) A. M. granatus n. sp. ♂ Holotype, Ecuador, Paquisha Alto B. M. granatus n. sp. ♂ Paratype, Peru, Alto Río Nieva C. M. granatus n. sp.♀, Ecuador, San Andrés D. M. placida n. sp. ♂ Holotype, Ecuador, Zamora - Arcoiris
FIGURE 2 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 2. Adults (left—dorsum, right—venter) A. M. prattorum udima n. ssp. ♂ Paratype, Peru, vía Hacienda Udima B. M. prattorum udima n. ssp. ♀ Paratype, Peru, vía Hacienda Udima C. M. inducta n. sp. ♂ Holotype, Peru, Lagunas Arrebiatadas D. M. inducta n. sp. ♀ Paratype, Ecuador, Jimbura —San Andrés road
FIGURE 1 in Solving the cryptic diversity of the genus Manerebia Staudinger in northern Peru description of new species and considerations on the biogeographical role of the Huancabamba Deflection (Nymphalidae: Satyrinae: Pronophilina)
FIGURE 1. Adults (left—dorsum, right—venter) A. M. ronda n. sp.♂ Holotype, Peru, Laguna Salahuindo B. M. ronda n. sp.♀ Paratype, Peru, Laguna Salahuindo C. M. ronda amplia n. ssp. ♂ Holotype, Peru, Kañaris D. M. rufanalis (?) ♂, Peru, Hacienda Udima
Figure 6 in The radiation of Satyrini butterflies (Nymphalidae: Satyrinae): a challenge for phylogenetic methods
Figure 6. Chronogram derived from the BEAST analysis with associated posterior credibility intervals. Numbers at the branches are posterior probability values for the node to the left of the number.
Figure 2 in The radiation of Satyrini butterflies (Nymphalidae: Satyrinae): a challenge for phylogenetic methods
Figure 2. Strict consensus of 12 equally parsimonious trees (29 647 steps; consistency index, CI = 0.13; retention index, RI = 0.44) from the maximum parsimony analysis (MP). Numbers given above branches are Bremer support values and the numbers below the branches are partitioned congruence index (PCI) values for the node to the right of the number.
Figure 4 in The radiation of Satyrini butterflies (Nymphalidae: Satyrinae): a challenge for phylogenetic methods
Figure 4. 'Bipartitions tree' obtained from the Maximum Likelihood (ML) analysis in RaxML. Numbers at the branches are bootstrap values for the node to the right of the number.
Figure 5 in The radiation of Satyrini butterflies (Nymphalidae: Satyrinae): a challenge for phylogenetic methods
Figure 5. Majority-rule cladogram based on Bayesian inference (BI), modelled with a GTR + G model. Numbers at the branches are posterior probability values for the node to the right of the number.
Figure 3 in The radiation of Satyrini butterflies (Nymphalidae: Satyrinae): a challenge for phylogenetic methods
Figure 3. Reduced cladograms from (A) maximum parsimony and (B) model-based methods (Bayesian inference and maximum likelihood), showing the incongruent hypotheses of relationships for the subtribes in the Satyrini.
Figure 7 in The radiation of Satyrini butterflies (Nymphalidae: Satyrinae): a challenge for phylogenetic methods
Figure 7. Results of a dispersal–vicariance analysis (DIVA), using three as the maximum number of ancestral areas in the DIVA. The topology of relationships for the out-groups are taken from Peña & Wahlberg (2008). Many terminals that belong to the same subtribe, and are distributed in the same biogeographical area of Figure 1, appear in one leaf: other Hypocystina, Pronophilina clade 1 and Pronophilina clade 2.
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