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1,023 results for “Lepidoptera systematics”
Figures 1–8 in On the systematic position of the genus Proaegeria Le Cerf 1916 (Lepidoptera: Sesiidae) with description of a new species
Figures 1–8. Moths. Proaegeria murzini sp. n.: 1–2. Holotype, male, Sesiidae pictures №№ 0023-0024–2023; 3–4. Paratype, male. Sesiidae pictures №№ 0021-0022–2023; 5–6. Paratype, male. Sesiidae pictures №№ 0025-0026–2023; 7–8. Paratype, female. Sesiidae pictures №№ 0019-0020–2023. Dorsal view (1, 3, 5, 7) and ventral view (2, 4, 6, 8).
Figures 9–14 in On the systematic position of the genus Proaegeria Le Cerf 1916 (Lepidoptera: Sesiidae) with description of a new species
Figures 9–14. Genitalia. Proaegeria murzini sp. n.: 9–14. Paratype, male, genitalia preparation № 010–2023. 9. Tegumen-uncus complex; 10. Valva; 11. Saccus; 12. Juxta, ventral view; 13. Phallus. 14. Paratype, female, genitalia preparation № 011–2023. Scale bar 1.0 mm.
Linked collectors and determiners for: A systematic revision of the genus Gnophopsodos Wehrli, 1945, with description of two new species (Lepidoptera: Geometridae).
Natural history specimen data linked to collectors and determiners held within, "A systematic revision of the genus Gnophopsodos Wehrli, 1945, with description of two new species (Lepidoptera: Geometridae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/9c0bf858-c899-45a8-824d-d6c9252185ea">https://bionomia.net/dataset/9c0bf858-c899-45a8-824d-d6c9252185ea</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/9c0bf858-c899-45a8-824d-d6c9252185ea">https://gbif.org/dataset/9c0bf858-c899-45a8-824d-d6c9252185ea</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Subspecies-level systematics and affinities of Cheimas Thieme - an endemic genus of the subparamo of the Venezuelan Cordillera de Mérida (Lepidoptera: Nymphalidae, Satyrinae).
Natural history specimen data linked to collectors and determiners held within, "Subspecies-level systematics and affinities of Cheimas Thieme - an endemic genus of the subparamo of the Venezuelan Cordillera de Mérida (Lepidoptera: Nymphalidae, Satyrinae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/58d86c58-b7b6-4495-98de-0743c98191de">https://bionomia.net/dataset/58d86c58-b7b6-4495-98de-0743c98191de</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/58d86c58-b7b6-4495-98de-0743c98191de">https://gbif.org/dataset/58d86c58-b7b6-4495-98de-0743c98191de</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: A systematic revision of Charissa, subgenus Pterygnophos Wehrli, 1951, with description of a new species (Lepidoptera: Geometridae).
Natural history specimen data linked to collectors and determiners held within, "A systematic revision of Charissa, subgenus Pterygnophos Wehrli, 1951, with description of a new species (Lepidoptera: Geometridae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/4d265a70-8c63-49bb-8b30-bac7d2f060fc">https://bionomia.net/dataset/4d265a70-8c63-49bb-8b30-bac7d2f060fc</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/4d265a70-8c63-49bb-8b30-bac7d2f060fc">https://gbif.org/dataset/4d265a70-8c63-49bb-8b30-bac7d2f060fc</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Revisiting the taxonomy and molecular systematics of Sesamia stemborers (Lepidoptera: Noctuidae: Apameini: Sesamiina): updated classification and comparative evaluation of species delimitation methods.
Natural history specimen data linked to collectors and determiners held within, "Revisiting the taxonomy and molecular systematics of Sesamia stemborers (Lepidoptera: Noctuidae: Apameini: Sesamiina): updated classification and comparative evaluation of species delimitation methods". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/0dedf555-acec-471d-a197-0a2cfe1a1329">https://bionomia.net/dataset/0dedf555-acec-471d-a197-0a2cfe1a1329</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/0dedf555-acec-471d-a197-0a2cfe1a1329">https://gbif.org/dataset/0dedf555-acec-471d-a197-0a2cfe1a1329</a>. Formatted as a Frictionless Data package.
Figure 2 in Molecular phylogeny and systematics of the Pieridae (Lepidoptera: Papilionoidea): higher classification and biogeography
Figure 2. Klots' (1933) intuitive phylogeny of the Pieridae, reconstructed from his generic revision and systematic classification, and hypothetical chart of evolution of the subfamilies and main stock of the Pierinae. Dashed lines indicate uncertainty in the phylogenetic position of genera or groups of genera.
Figure 8 in Molecular phylogeny and systematics of the Pieridae (Lepidoptera: Papilionoidea): higher classification and biogeography
Figure 8. Historical biogeographical hypothesis of the Pseudopontiinae + Dismorphiinae, with dispersal and extinction events optimized to reconcile the area cladogram. Letters designate speciation events: a, vicariance between Pseudopontiinae (Africa) and Dismorphiinae (South America), following the final break-up of Western Gondwana (Late Cretaceous); b, long-distance dispersal of the ancestor of Dismorphiinae from northern South America to northern Africa (Late Cretaceous), followed by allopatric speciation of Leptidea in northern Africa (Late Cretaceous). Numbers designate major biogeographical events: 1, dispersal (range expansion) of the ancestor of Leptidea from northern Africa to Eurasia, following contact of Africa with Eurasia (early Tertiary); 2, extinction (range contraction) of Leptidea in northern Africa following formation of the Sahara Desert (Quaternary). Once Leptidea reached Eurasia it colonized much of the Palaearctic, the Neotropical Dismorphiinae subsequently spread into Central America, whereas the Pseudopontiinae contracted to central western Africa.
Figure 7 in Molecular phylogeny and systematics of the Pieridae (Lepidoptera: Papilionoidea): higher classification and biogeography
Figure 7. Higher classification of the Pieridae, showing two possible phylogenetic hypotheses according to the combined and all available data analyses of this study (Figs 3, 6). A, consensus tree summarizing nodes that are well supported or that are consistently recovered under different methods of analysis (maximum parsimony, maximum likelihood, Bayesian inference), with a question mark denoting uncertainty in the monophyly of the Colotis group. B, fully resolved tree, with question marks denoting uncertainty among nodes and in the monophyly of the Colotis group. Four subfamilies are recognized, with the subfamily Pierinae comprising four major lineages (two tribes, two informal groups); the tribe Pierini is subdivided into five lineages (three subtribes, two subclades of uncertain status).
FIGURE 24 in Systematics of Schinia cupes (Grote) complex: Revised status of Schinia crotchii (Hy. Edwards) (Lepidoptera: Noctuidae: Heliothinae)
FIGURE 24. Seasonal phenology of Schinia cupes, S. crotchii, and S. deserticola.
Data from: Phylogeny and systematics of the "Pronophila clade", with two new genera to resolve the formerly polyphyletic genus Pseudomaniola (Lepidoptera: Nymphalidae, Satyrinae)
<p>Analysis of a target enrichment molecular dataset confirms the monophyly of the Neotropical montane butterfly group known as the <em>Pronophila</em> Westwood clade, one of two major lineages of the satyrine subtribe Pronophilina. The <em>Pronophila </em>clade comprises 18-20 recognized genera and some 125 species. Within this group, the genus <em>Pseudomaniola</em>Röber appears as paraphyletic, and is split here into three genera, <em>Pseudomaniola </em>sensu novum<em> </em>with six species, including four previously considered as subspecies of <em>P. phaselis </em>(Hewitson), the monobasic <em>Fahraeusia </em>Pyrcz n. gen. for <em>Catargynnis asuba </em>Thieme, n. comb., and <em>Boyeriana </em>Pyrcz, Espeland & Willmott<strong> </strong>n. gen., with nine species. The adults of all three genera can be recognized by their wing colour patterns, but the strongest synapomorphies are found in the genitalia, especially those of the male, supporting the above systematic decisions. Notable differences are also found in scale organization and morphology. A divergence time analysis suggests that <em>Fahraeusia </em>diverged<em> </em>from <em>Pseudomaniola </em>+<em>Boyeriana </em>in the mid-Miocene, around 12 Mya, and the subsequent separation of the last two genera occurred at the start of the Pliocene at around 5 Mya.</p>
Fig. 5 in Phylogenetic analysis and systematics of the Acrapex unicolora Hampson species complex (Lepidoptera, Noctuidae, Noctuinae, Apameini), with the description of Fve new species from the Afrotropics
Fig. 5. Major bioregions, modifed after Linder et al. (2012).
Fig. 4 in Phylogenetic analysis and systematics of the Acrapex unicolora Hampson species complex (Lepidoptera, Noctuidae, Noctuinae, Apameini), with the description of Fve new species from the Afrotropics
Fig. 4. Distribution map of sampled specimens of Acrapex Hampson, 1891.
Fig. 11. Suneve gen. n in Comments On The Systematics And Natural History Of Aveexcrenota, A Genus Of Rare Andean Eumaeine Lycaenidae (Lepidoptera)
Fig. 11. Suneve gen. n. apomorphy (indicated by arrow)
Phylogenetic systematics, diversification, and biogeography of Cerurinae (Lepidoptera: Notodontidae) and a description of a new genus
<p>We present the first dated molecular phylogeny of the Cerurinae moths (Notodontidae), based on sequence data for 666 loci generated by anchored hybrid enrichment. Monophyly of Cerurinae is corroborated, which includes the following genera: <em>Pararethona</em> Janse, <em>Pseudorethona</em> Janse, <em>Oreocerura</em> Kiriakoff, <strong>stat. rev.</strong>, <em>Cerurella</em> Kiriakoff, <em>Notocerura</em> Kiriakoff, <em>Hampsonita</em> Kiriakoff, <em>Afrocerura</em> Kiriakoff, <em>Cerurina</em> Kiriakoff, <em>Neoharpyia</em> Daniel, <em>Furcula</em> Lamarck, <em>Neocerura</em> Matsumura, <em>Americerura</em> St Laurent and Goldstein, <strong>gen. nov.</strong>, <em>Cerura</em> Schrank, and <em>Kamalia</em> Koçak & Kemal. The type species of the Neotropical genus <em>Tecmessa</em> Burmeister, <em>T. annulipes</em> (Berg), which had been incorrectly assigned to Cerurinae, is recovered in Heterocampinae; and <em>Americerura</em> <strong>gen. nov.</strong> is proposed to receive 17 unambiguously cerurine species transferred from <em>Tecmessa</em>. Divergence time estimates recover a crown age of Notodontidae roughly coincident with the K-Pg boundary and a late-Oligocene crown age for Cerurinae. An African origin is inferred for Cerurinae, followed by colonization of the Palearctic, the Americas, Indomalaya, and Australasia during the Miocene. At least three independent colonizations of the Americas are inferred, one in the mid-Miocene associated with ancestral <em>Americerura</em> <strong>gen. nov. </strong>and two in the Pliocene and Pleistocene within <em>Furcula</em>. We hypothesize that the global spread of Cerurinae was enabled by that of its primary caterpillar foodplants in the Salicaceae. State-dependent diversification analyses suggest that cerurines diversified most rapidly in temperate climates.</p>
Phylogenetic systematics, diversification, and biogeography of Cerurinae (Lepidoptera: Notodontidae) and a description of a new genus
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FIGURES 40–42 in On systematic status of Spindasis syama Horsfield, [1829] in Taiwan and the Philippines (Lepidoptera: Lycaenidae: Aphnaeini)
FIGURES 40–42. Ventral view of female genitalia of Spindasis. 40, S. syama lamuae ssp. nov. (Taiwan), 41, S. syama sepulveda (Fruhstorfer, 1912) (Yunnan, China), 42, S. negrita Felder, 1862 (Marinduque, Philippines). Scale bar = 1mm.
FIGURES 21–24 in On systematic status of Spindasis syama Horsfield, [1829] in Taiwan and the Philippines (Lepidoptera: Lycaenidae: Aphnaeini)
FIGURES 21–24. Adults of Spindasis negrita Felder, 1862. 21, upperside of male (Mindanao, Philippines), 22, underside of male (Mindanao, Philippines), 23, upperside of female (Marinduque, Philippines), 24, underside of female (Marinduque, Philippines). Scale bar = 1 cm.
FIGURES 9–12 in On systematic status of Spindasis syama Horsfield, [1829] in Taiwan and the Philippines (Lepidoptera: Lycaenidae: Aphnaeini)
FIGURES 9–12. Adults of Spindasis syama lamuae, ssp. nov., dry season form. 9, upperside of holotype male, 10, underside of holotype male, 11, upperside of paratype female, 12, underside of paratype female. Scale bar = 1 cm.
FIGURES 17–20 in On systematic status of Spindasis syama Horsfield, [1829] in Taiwan and the Philippines (Lepidoptera: Lycaenidae: Aphnaeini)
FIGURES 17–20. Adults of Spindasis syama sepulveda (Fruhstorfer, 1912). 17, upperside of male (Chongqing, China), 18, underside of male (Chongqing, China), 19, upperside of female (Hong Kong), 20, underside of female (Hong Kong). Scale bar = 1 cm.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.