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Fig. 24 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 24. Distribution of the three species of the candezei subgroup.
Fig. 34 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 34. Distribution of the four species of the bridarollii subgroup.
Fig. 27 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 27. Sylvicanthon genieri sp. nov. A. Dorsal view. B. Ventral view.
Fig. 25 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 25. Sylvicanthon candezei (Harold, 1869). A. Dorsal view. B.Ventral view.
Fig. 39 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 39. Sylvicanthon securus (Schmidt, 1920) comb. nov. A. Dorsal view. B. Ventral view.
Fig. 30 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 30. Distribution of the two species of the aequinoctialis subgroup.
Fig. 16 in Taxonomic revision of the genus Arsipoda Erichson, 1842 (Coleoptera, Chrysomelidae) in New Caledonia
Fig. 16. Strict consensus tree with jackknife values (see text).
Fig. 16. Megatrigon nivalis and M in Taxonomic revision of the Afrotropical genus Megatrigon Johnson, 1898 (Diptera: Syrphidae)
Fig. 16. Megatrigon nivalis and M. argenteus species group (subgroup 2), distribution.
Fig. 15 in Taxonomic revision of the Afrotropical genus Megatrigon Johnson, 1898 (Diptera: Syrphidae)
Fig. 15. Megatrigon argenteus species group (subgroup 1), distribution.
Taxonomic revision of Delphinium (Ranunculaceae) in the south-east of European Russia
<p>Morphological and phylogenetic (nrITS barcode) analyses are conducted to clarify the taxonomic status of 10 <i>Delphinium</i> species (<i>D. cuneatum, D. dyctiocarpum, D. duhmbergii</i>, <i>D. elatum, D. litwinowii</i>, <i>D. pubiflorum</i>, <i>D. puniceum, D. sergii</i>, <i>D. subcuneatum, D. uralense</i>) grown in the south-east of European Russia. The morphometric analysis is carried out with 22 quantitative and 32 qualitative parameters. Based on all parameters, the PCoA supports the differentiation of <i>D. puniceum</i>, <i>D. sergii</i>, <i>D. uralense</i> and <i>D. pubiflorum</i> whereas other studied taxa remain undistinguished. Furthermore, the Random forest analysis and the MrBayes phylogenetic analysis of ITS sequences confirm the species independence of <i>D. puniceum</i> belonging to the <i>Diedropetala</i> section and <i>D. elatum</i>, <i>D. uralense</i>, <i>D. dyctiocarpum</i> and <i>D. pubiflorum</i> belonging to the <i>Delphinastrum</i> section. Finally, recursive partitioning is performed to develop the dichotomous key which can be used to differentiate between <i>Delphinium</i> species in the territory under study. In conclusion, we stress that the definition of species belonging to the <i>Delphinastrum</i> section is hindered by the presence of numerous intermediate or hybrid forms, on the one hand, and the impact of climatic conditions on the display of morphological (and specifically, taxonomically significant) traits, on the other.</p>
Fig. 90-91 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
Fig. 90-91: Metatarsus. (90) M. octonotata, ungues. (91) M. octonotata, 4th tarsomere.
Fig. 96 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
Fig. 96: Geographic distribution of Muisca species as listed.
Data from: A taxonomic revision of the whitefish radiation of lakes Brienz and Thun, Switzerland, with descriptions of four new species (Teleostei: Coregonidae)
<p>The alpha taxonomy of the endemic whitefish of lakes Brienz and Thun, Switzerland, is revised. We evaluate the status of seven known species: <em>Coregonus steinmanni </em>sp. nov., <em>Coregonus profundus</em> sp. nov. and <em>Coregonus acrinasus</em> sp. nov. are endemic to Lake Thun; <em>Coregonus brienzii </em>sp. nov. is endemic to Lake Brienz; and <em>C. alpinus, C. albellus,</em> and <em>C. fatioi</em> from lakes Brienz and Thun are redescribed. One of these species, <em>C. alpinus</em>, is revised, since the lectotype for this species is incongruent with the species description given by Kottelat (1997) and Kottelat and Freyhof (2007). The name <em>C. alpinus</em> is thus retained for the lectotype designated by Kottelat (1997) and a new description of this taxon provided. For the species otherwise described by Kottelat (1997) and Kottelat and Freyhof (2007) as C. alpinus the new name C. profundus is designated. <em>Coregonus acrinasus </em>is genetically partially of allochthonous origin, closely related to the radiation of Lake Constance, and we therefore compare it to all recognized species of Lake Constance, <em>C. wartmanni, C. macrophthalmus, C. arenicolus,</em> and <em>C. gutturosus.</em></p>
Species delimitation and taxonomic revision of Oxyopes (Araneae: Oxyopidae) of Taiwan
<p><span><span><span><span><span><span><span><span><span><span><span>This study revised the spider genus <i>Oxyopes</i> Latreille, 1804 in Taiwan and delineated the species boundaries based on morphological and molecular characters. A total of seven <i>Oxyopes</i> spiders were recognized, including two newly described species, <i>O. hasta</i> <b>sp. nov. </b>and <i>O. taiwanensis</i> <b>sp. nov.</b> <i>Oxyopes</i><i> fujianicus</i> Song & Zhu 1993 from Yilan County, Nantou County, and Kaohsuing City, and <i>O. striagatus</i> Song 1999 from New Taipei City, Taichung City, Nantou County, and Kaohsiung City were recorded for the first time in Taiwan. An identification key and a distributional map of Taiwanese <i>Oxyopes</i> species were provided. Partial <i>COI</i> sequences were obtained for molecular phylogenetic and species delimitation analyses. Maximum likelihood and Bayesian phylogenies, and DNA barcoding gap analysis supported morphologically defined species. However, molecular species delimitation based on Automatic Barcode Gap Discovery(ABGD), P<sub>ID</sub> (Liberal), and generalized mixed Yule coalescent (GMYC) were incongruent in species assignment. The results showed that the interspecific genetic divergence between <i>O. sertatus</i> and <i>O. taiwanensis</i> was relatively low (1.28 ± 0.43%), and the intraspecific genetic divergence of <i>O. striagatus</i> was relatively high (1.69 ± 0.35%). Ecological data, additional samples and genetic loci are required to further examine the level of reproductive isolation and patterns of population genetic structure in Taiwanese <i>Oxyopes</i>.</span></span></span></span></span></span></span></span></span></span></span></p>
Data from: Taxonomic revision of the flavopalliata species group of Signiphora (Hymenoptera: Signiphoridae)
The flavopalliata species group of Signiphora Ashmead (Hymenoptera: Signiphoridae) is revised. Twelve species are redescribed: Signiphora aleyrodis Ashmead, S. aspidioti Ashmead, S. borinquensis Quezada et al., S. coquilletti Ashmead, S. fax Girault, S. flavella Girault, S. flavopalliata Ashmead, S. lutea Rust, S. maculata Girault, S. merceti Malenotti, S. perpauca Girault and S. xanthographa Blanchard. Signiphora townsendi Ashmead is synonymized under S. aleyrodis n. syn.; Thysanus insularis Dozier and S. flavopalliata desantisi De Santis are synonymized under S. fax n. syns.; S. basilica Girault, S. euclidi Girault, S. flava Girault, S. caridei Brèthes, S. thoreauini Girault and Thysanus louisianae Dozier are synonymized under S. flavella n. syns.; and S. woolleyi Hayat is synonymized under S. perpauca n. syn. Thirteen new species are described: S. bennetti n. sp., S. biloba n. sp., S. brachyptera n. sp., S. curepensis n. sp., S. dozieri n. sp., S. ehleri n. sp., S. ensifera n. sp., S. falcata n. sp., S. jojobae n. sp., S. longitibia n. sp., S. plaumanni n. sp., S. renuncula n. sp. and S. tridentata n. sp. Lectotypes are designated for S. aleyrodis, S. townsendi, S. fax, S. flavella, S. occidentalis, S. lutea, S. maculata and S. xanthographa.
FIGURE 58 in Taxonomic revision of Stagmatoptera Burmeister, 1838 (Mantodea: Mantidae, Stagmatopterinae)
FIGURE 58. Stagmatoptera indicator, original illustration from Stoll (1787, 1813).
FIGURE 57 in Taxonomic revision of Stagmatoptera Burmeister, 1838 (Mantodea: Mantidae, Stagmatopterinae)
FIGURE 57. Stagmatoptera abdominalis, original illustration from Stoll (1787, 1813).
FIGURE 24 in Taxonomic revision of Stagmatoptera Burmeister, 1838 (Mantodea: Mantidae, Stagmatopterinae)
FIGURE 24. Stagmatoptera biocellata, female holotype of. Not to scale.
FIGURE 9 in A taxonomic revision of the kalshoveni species-group of the genus Nemophora Hoffmannsegg (Lepidoptera, Adelidae), with descriptions of six new species from Indonesia and Papua New Guinea
FIGURE 9. Distribution of Nemophora kalshoveni species-group.
Figure 9 in A taxonomic revision of the Tragulus mouse-deer (Artiodactyla)
Figure 9. Map of the Terutau and Langkawi island groups west of the Malay and Thai peninsula.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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