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CLDF dataset derived from Chacon's "A revised proposal of Proto-Tukanoan consonants and Tukanoan family classification" from 2014
<p>Cite the source of the dataset as:</p> <blockquote> <p>Thiago Chacon. (2014). A revised proposal of Proto-Tukanoan consonants and Tukanoan family classification. Journal of American Linguistics 80.3, pp. 275–322. doi: https://doi.org/10.1086/676393</p> </blockquote>
Figs 98-106 in Classification, Natural History, and Evolution of the Subfamily Peloniinae O (Coleoptera: Cleroidea: Cleridae). Part IX. Taxonomic revision of the New World genus Muisca S
Figs 98-106: Phalli. (98) Muisca dilatata. (99) M. insigna. (100) M. apicalis. (101) M. dozieri. (102) M. irrorata. (103) M. hirtula. (104) M. togata. (105) M. xanthura. (106) M. fera.
Figs 82-83 in Classification, Natural History, and Evolution of the Subfamily Peloniinae O (Coleoptera: Cleroidea: Cleridae). Part IX. Taxonomic revision of the New World genus Muisca S
Figs 82-83: Various organs. (82) M. octonotata, head, ventral view. (83) M. octonotata, forebody, ventral view.
Figs 2-13 in Classification, Natural History, and Evolution of the Subfamily Peloniinae O (Coleoptera: Cleroidea: Cleridae). Part IX. Taxonomic revision of the New World genus Muisca S
Figs 2-13: Various structures of Muisca testacea. (2) Head, frontal view. (3) Head, ventral view. (4) Head, dorsal view. (5) Prothorax, ventral view. (6) Antenna, male. (7) Spicular fork. (8) Maxilla. (9) Labrum. (10) Metendosternite. (11) Mandible. (12) Labium. (13) Metathoracic wing.
Figure 10. Simple setae. A in Revising the definition of the crustacean seta and setal classification systems based on examinations of the mouthpart setae of seven species of decapods
Figure 10. Simple setae. A, typical simple setae from the mandibular palp of Panulirus argus. No outgrowths are seen. B, terminal pore (arrow) from simple seta. C, simple setae situated on the basis of maxilla 2 of Carcinus maenas. Abbreviation: Si, simple setae.
Figure 5. Pappose setae. A in Revising the definition of the crustacean seta and setal classification systems based on examinations of the mouthpart setae of seven species of decapods
Figure 5. Pappose setae. A, overview of two typical pappose setae from Cherax quadricarinatus. Note random arrangement of setules. B, tips of pappose setae from Stenopus hispidus. Setules get smaller closer to the tip (arrow). C, serration on the setules (arrows) from pappose seta. D, pappose setae on the exopod of maxilliped 1 of Carcinus maenas. E, pappose setae on the mandibular palp of Ca. maenas. F, pappose setae on the coxa of maxilliped 1 of Pagurus bernhardus. Abbreviation: Pa, pappose setae.
Figure 4 in Revising the definition of the crustacean seta and setal classification systems based on examinations of the mouthpart setae of seven species of decapods
Figure 4. Substructures of setae. A, infracuticular articulation with the general cuticle. Arrow indicates deep socket. B, supracuticular articulation (arrows) with the general cuticle. C, annulus seen as a ring in the cuticle (arrow). D, two rows of denticles arranged distally on a seta. E, large setule displaying articulation (arrow) with setal shaft. F, small setule with weak articulation (arrows). G, stitched picture showing gradual change from setule (arrow) to denticle (arrowhead) on the same seta. H, subterminal pore (arrow) from seta with denticles. I, terminal pore (arrow) from seta with denticles.
Figure 7. Serrulate setae. A, typical serrulate setae from maxilliped 1 in Revising the definition of the crustacean seta and setal classification systems based on examinations of the mouthpart setae of seven species of decapods
Figure 7. Serrulate setae. A, typical serrulate setae from maxilliped 1 of Pagurus bernhardus. Setules are small and only present on the distal half of the seta. B, middle part of serrulate seta with setules in three rows. C, setules from serrulate seta arranged randomly along the shaft. Note strong serration. D, small setules with weak articulations (arrows). E, scalelike setules from serrulate seta of Palaemon adspersus. Note serration on distal rim (arrows). F, terminal pore (arrow) from serrulate seta. G, serrulate setae on the coxa of maxilla 1 of Penaeus monodon. Abbreviation: Su, serrulate setae.
Figure 9. Papposerrate setae. A, typical papposerrate seta from maxilliped 1 in Revising the definition of the crustacean seta and setal classification systems based on examinations of the mouthpart setae of seven species of decapods
Figure 9. Papposerrate setae. A, typical papposerrate seta from maxilliped 1 of Cherax quadricarinatus, with long, randomly arranged setules on proximal part and denticles in two rows on distal part. B, transition region between long setules and denticles. Abbreviations: D, denticles; LS, long setules; SS, short setules.
Figure 8. Serrate setae. A in Revising the definition of the crustacean seta and setal classification systems based on examinations of the mouthpart setae of seven species of decapods
Figure 8. Serrate setae. A, typical serrate setae from the endopod of maxilla 1 of Cherax quadricarinatus. Denticles in two strict rows on the distal half. B, serrate seta with setules (arrow). Arrowhead indicates denticles. C, tip of serrate seta with terminal pore (arrow). No denticles, only scale-like setules near the tip (arrowhead). D, partial (arrows) and complete fusion of denticles on serrate seta from Penaeus monodon. E, serrate setae on the dactylus of maxilliped 3 of Palaemon adspersus. F, serrate setae on the dactylus of maxilliped 2 of Pe. monodon. Abbreviation: Se, serrate setae.
Figure 2 in Revising the definition of the crustacean seta and setal classification systems based on examinations of the mouthpart setae of seven species of decapods
Figure 2. Types of projections found on the general cuticle. A, type I projection, a seta, is an elongate circular projection, which is articulated with the general cuticle (arrow). It is the most common type of projection. B, type II projection, a seta, from maxilla 1 of Pagurus bernhardus with a more or less direct transition into the general cuticle. In the other species articulated setae are situated in the same place (compare with Fig. 11A). They may have small outgrowths (arrows). C, type III projections, denticles, from maxilliped 1 of Panulirus argus. Arrows indicate direct transition into general cuticle without an articulation. D, type IV projections, setules, from the paragnath of Stenopus hispidus. Arrows indicate serration and arrowheads indicate articulation with the general cuticle. Note the flattened shape at the base.
Figure 11. Cuspidate setae. A in Revising the definition of the crustacean seta and setal classification systems based on examinations of the mouthpart setae of seven species of decapods
Figure 11. Cuspidate setae. A, Typical cuspidate setae from the basis of maxilla 1 of Cherax quadricarinatus. Note clear articulation with general cuticle (arrowheads) and compare with Figure 2B. B, cuspidate seta with teeth-like outgrowths in two rows (arrows). C, subterminal pore (arrow) from cuspidate seta with debris in pore. D, cuspidate setae on the dactylus of maxilliped 2 of Carcinus maenas. One is lacking articulation (arrow). E, cuspidate setae on the endopod of maxilla 2 of Penaeus monodon. Abbreviation: Cu, cuspidate setae.
Figure 6. Plumose setae. A in Revising the definition of the crustacean seta and setal classification systems based on examinations of the mouthpart setae of seven species of decapods
Figure 6. Plumose setae. A, Typical plumose setae from the exopod of maxilliped 2 of Panulirus argus. Arrows indicate supracuticular articulations. B, basal part of setule. No articulation is seen (arrows). C, setule (inserted in a groove) from plumose seta. Note absence of serration. D, plumose seta with pseudo articulations (arrows) from an exopod flagellum. E, plumose setae on the exopod flagellum of maxilliped 2 of Pan. argus. Abbreviations: Endo, endopod; Exo fla, flagellum of exopod; Pl, plumose setae.
Figure 2 Sphecodini male genital capsule. A in A revised genus-level classification for the Neotropical groups of the cleptoparasitic bee tribe Sphecodini Schenck (Hymenoptera, Apidae, Halictinae)
Figure 2 Sphecodini male genital capsule. A) Austrosphecodes sp., B) Microsphecodes sp., C) Melissocleptis capriciosa, D) Ptilocleptis tomentosa. Abbreviations: gs = gonocoxite striations, isp = gonostylus internal setose patch, vp = ventral prong. All images under the same scale.
Figure 3 in A revised genus-level classification for the Neotropical groups of the cleptoparasitic bee tribe Sphecodini Schenck (Hymenoptera, Apidae, Halictinae)
Figure 3 Nesosphecodes depressus sp. nov. Female Holotype. A) habitus, B) head in frontal view, C) mesosoma in dorsal view, D) metasoma in dorsal view. B and C under the same scale.
Figure 5 in A revised genus-level classification for the Neotropical groups of the cleptoparasitic bee tribe Sphecodini Schenck (Hymenoptera, Apidae, Halictinae)
Figure 5 Nesosphecodes depressus sp. nov. Male Paratype. A) T6, B) S7 and S8, C) genital capsule, ventral view, D) genital capsule, dorsal view. All images under the same scale.
Figure 4 in A revised genus-level classification for the Neotropical groups of the cleptoparasitic bee tribe Sphecodini Schenck (Hymenoptera, Apidae, Halictinae)
Figure 4 Nesosphecodes depressus sp. nov.Male Paratype. A) habitus, B) head in frontal view, C) mesosoma in dorsal view, D) metasoma in dorsal view.B and C under the same scale.
Figure 1 Melissocleptis gen. nov. and Austrosphecodes. A in A revised genus-level classification for the Neotropical groups of the cleptoparasitic bee tribe Sphecodini Schenck (Hymenoptera, Apidae, Halictinae)
Figure 1 Melissocleptis gen. nov. and Austrosphecodes. A) Melissocleptis capriciosus, female head, colored bars indicating the scape and frons length, B) M. capriciosus male head, F1–3 colored; C) M. capriciosa male metasoma, pygidial plate indicated in blue; D) Austrosphecodes brasiliensis, female head, colored bars indicating the scape and frons length, E) A. brasiliensis male head, F1–3 colored; F) A. brasiliensis male metasoma, pygidial plate indicated in blue. All images under the same scale.
A revised phylogenetic classification for Viola (Violaceae)
<p>The genus <em>Viola</em> (Violaceae) is among the 40–50 largest genera among angiosperms, yet its taxonomy has not been revised for nearly a century. In the most recent revision, by Wilhelm Becker in 1925, the then known 400 species were distributed among 14 sections and numerous unranked groups. Here we provide an updated, comprehensive classification of the genus, based on data from phylogeny, morphology, chromosome counts, and ploidy, and based on modern principles of monophyly. The revision is presented as an annotated global checklist of accepted species of <em>Viola</em>, an updated multigene phylogenetic network and an ITS phylogeny with denser taxon sampling, a brief summary of the taxonomic changes from Becker’s classification and their justification, a morphological binary key to the accepted subgenera, sections and subsections, and an account of each infrageneric subdivision with justifications for delimitation and rank including a description, a list of apomorphies, molecular phylogenies where possible or relevant, a distribution map, and a list of included species. We distribute the 664 species accepted by us into 2 subgenera, 31 sections, and 20 subsections. We erect one new subgenus of <em>Viola</em> (subg. <em>Neoandinium</em>, a replacement name for the illegitimate subg. <em>Andinium</em>), six new sections (sect. <em>Abyssinium</em>, sect. <em>Himalayum</em>, sect. <em>Melvio</em>, sect. <em>Nematocaulon</em>, sect. <em>Spathulidium</em>, sect. <em>Xanthidium</em>), and seven new subsections (subsect. <em>Australasiaticae</em>, subsect. <em>Bulbosae</em>, subsect. <em>Clausenianae</em>, subsect. <em>Cleistogamae</em>, subsect. <em>Dispares</em>, subsect. <em>Formosanae</em>, subsect. <em>Pseudorupestres</em>). Evolution within the genus is discussed in light of biogeography, fossil record, morphology, and particular traits. <em>Viola</em> is among very few temperate and widespread genera that originated in South America. The biggest identified knowledge gaps for <em>Viola</em> concern the South American taxa, for which basic knowledge from phylogeny, chromosome counts, and fossil data is virtually absent. <em>Viola</em> has also never been subject to comprehensive anatomical study. Study on seed anatomy and morphology is required to understand the fossil record of the genus.</p>
Figure 3 in Revised classification design of the Anatolian species of Nannospalax (Rodentia: Spalacidae) using RFLP analysis
Figure 3. Neighbor-joining and span tree showing genetic relationships among populations, based on Nei's genetic distance measure.
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