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1,023 results for “Lepidoptera systematics”
Fig. 9 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 9. Adults of Melitaea timandra timandra Coutsis & van Oorschot, 2014. A–H. UPS. I–P. UNS. A–D. ♂, Turkmenistan, Sary-Yazy, alt. 300 m. E–H. ♀, Turkmenistan, Sary-Yazy, alt. 300 m. I–L. ♂, Turkmenistan, Sary-Yazy, alt. 300 m. M–P. ♀, Turkmenistan, Sary-Yazy, alt. 300 m.
Fig. 27 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 27. Biotope, host plant, and adult of Melitaea shahvarica sp. nov. in nature. A. Shahvar Mt., E Elburs Ridge. B. Biotope with Phlomoides molucelloides (Bunge) Salmaki. C. Host plant Ph. molucelloides. D. Female on Ph. molucelloides.
Fig. 21 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 21. Adults of Melitaea shahvarica sp. nov. A–H. UPS. I–P. UNS. A, I. Holotype, ♂ (SDM). B–H, J–P. Paratypes (EDMSU). A–C. ♂. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mt., alt. 2200–2400 m. D. ♂. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mt., Tohar v. vicinity, alt. 2200 m. E–H. ♀. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mt., alt. 2200– 2400 m. I–K. ♂. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mt., 2200–2400 m. L. ♂. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mts, Tohar v. vicinity, alt. 2200 m. M–P. ♀. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mt., alt. 2200–2400 m.
Fig. 25. I–IV in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 25. I–IV instar caterpillars of Melitaea shahvarica sp. nov. (a = view from above; b = lateral view). A. First instar caterpillar after hatching. B. First instar caterpillar before molting. C. Second instar caterpillar. D. Third instar caterpillar. E. Fourth instar caterpillar.
Fig. 26. V–VI in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 26. V–VI instar caterpillars of Melitaea shahvarica sp. nov. (a = view from above; b = lateral view). A. Fifth instar caterpillar. B. Sixth instar caterpillar. C. Sixth instar caterpillar, head capsule, front view. D. Sixth instar caterpillar, head capsule, lateral view.
Fig. 20 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 20. Eggs of Melitaea timandra binaludica subsp. nov., Iran, Kuh-e-Binalud Mts. A–C. Lateral view. D–F. View from above. G–I. Micropile area.
Fig. 19. Male genitalia and harpe. A–C in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 19. Male genitalia and harpe. A–C. Melitaea timandra timandra Coutsis & van Oorschot, 2014. D–I. M. timandra binaludica subsp. nov. A–C. Turkmenistan, Sary-Yazy, alt. 300 m. D–F. Iran, Rezavi Khorassan Prov., Kuh-e-Binalud Mts, Dorrud v. vicinity, alt. 2430 m. G. Afghanistan, Bamian Prov., Band-e-Amir, alt. 3200 m. H. Afghanistan, Bamian Prov., Band-e-Amir, Dzhudoi-Kvak Gorge, alt. 3200 m. I. Afghanistan, Band-e-Amir, Hazarajat.
Fig. 10 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. 10. Maximum likelihood tree resulting from the analysis of the combined dataset carried out with IQ-TREE. Support of major nodes is displayed as BV (only BV> 50% are shown). On the right, corresponding adult habitus (for species belonging to the A. unicolora species group) are also included for illustrative purposes. Results of PTP analyses are fgured using coloured branches and vertical side bars. Putative molecular species clusters are indicated using transitions between blue-coloured branches to red-coloured branches (vertical bars are also informative).
Fig. 8 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. 8. Adults of species of Acrapex. – A–D. A. parvaclara Berio, 1973. A. ♂, upper side. B. ♂, under side. C. ♀, upper side. D. ♀, under side. – E–F. A. simillima le Ru sp. nov. E. ♀, upper side. F. ♀, under side. – G–J. A. unicolora (Hampson, 1910). G. ♂, upper side. H. ♂, under side. I. ♀, upper side. J. ♀, under side. Scale bars = 10 mm.
Fig. 9. Last instar larva. A 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. 9. Last instar larva. A. Acrapex simillima le Ru sp. nov. B. A. unicolora (Hampson, 1910). Scale bar = 10 mm.
Fig. 7 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. 7. Adults of species of Acrapex. – A–E. A. mediopuncta (Bowden, 1956). A. ♂, upper side. B. ♂, under side. C. ♀, upper side. D. ♀, under side. E. ♀, original labels from BMNH. – F–G. A. miscantha le Ru sp. nov. F. ♀, upper side. G. ♀, under side. Scale bars = 10 mm.
Fig. 6 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. 6. Adults of species of Acrapex. – A–B. A. kavumba le Ru sp. nov. A. ♂, upper side. B. ♂, under side. – C–F. A. kiakouama le Ru sp. nov. C. ♂, upper side. D. ♂, under side. E. ♀, upper side. F. ♀, under side. – G–I. A. malagasy Viette, 1967. G. ♂, upper side. H. ♂, under side. I. ♂, original labels from MNHH. Scale bars = 10 mm.
Fig. 3 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. 3. Female genitalia of species of Acrapex. A. A. cuprescens (Hampson, 1910). B. A. kafula le Ru sp. nov. C. A. kiakouama le Ru sp. nov. D. A. mediopuncta (Bowden, 1956). E. A. miscantha le Ru sp. nov. F. A. parvaclara Berio, 1973. G. A. simillima le Ru sp. nov. H. A. unicolora (Hampson, 1910). Scale bars = 1 mm.
Fig. 1 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. 1. Adults of species of Acrapex. – A–F. A. cuprescens (Hampson, 1910). A. ♂, upper side. B. ♂, under side. C. ♂, original labels from BMNH. D. ♀, original labels from BMNH. E. Upper side. F. Under side. – G–J. A. kafula le Ru sp. nov. G. ♂, upper side. H. ♂, under side. I. ♀, upper side. J. ♀, under side. Scale bars = 3 mm.
Fig. 2 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. 2. Male genitalia of species of Acrapex. – A, I. A. cuprescens (Hampson, 1910). – B, J. A. kafula le Ru sp. nov. – C, K. A. kavumba le Ru sp. nov. – D, L. A. kiakouama le Ru sp. nov. – E, M. A. malagasy Viette, 1967. – F, N. A. mediopuncta (Bowden, 1956). – G, O. A. parvaclara Berio, 1973. – H, P. A. unicolora (Hampson, 1910). Scale bars = 0.5 mm.
Fig. 9 in Comments On The Systematics And Natural History Of Aveexcrenota, A Genus Of Rare Andean Eumaeine Lycaenidae (Lepidoptera)
Fig. 9. Female genital ductus of eumaeine lycaenids in ventral aspect: a = Aceexcrenota anna (DRUCE, 1907) (gen. prep. BÁLINT, HNHM 998), b = Evenus regalis (CRAMER, 1775) (gen. prep. BÁLINT, HNHM 886), c = Theritas mavors HÜBNER, 1818 (gen. prep. BMNH 5792), d = Denivia hemon (CRAMER, 1775) (gen. prep. BÁLINT, HNHM 1087), e = Suneve coronata (HEWITSON, 1865) (gen.
Fig. 10 in Comments On The Systematics And Natural History Of Aveexcrenota, A Genus Of Rare Andean Eumaeine Lycaenidae (Lepidoptera)
Fig. 10. Hypothetical cladogram for the Evenus genus group. Characters are listed and discussed in the text
Figs 7–8. 7 in Comments On The Systematics And Natural History Of Aveexcrenota, A Genus Of Rare Andean Eumaeine Lycaenidae (Lepidoptera)
Figs 7–8. 7 = Spectral reflectance of various eumane lycaenids: a = Aveexcrenota from Colombia (black) and from Peru (red); b = Denivia hemon (CRAMER, 1775) from Peru, San Martin (black) and Loreto (green), Costa Rica, Bugaba (red); c = Thecloxurina chachapoya BÁLINT et WOJTUSIAK, 2003 individuals from Peru, Amazonas, 3000 m (black and red) and Apurímac (green); d = species from genera Aveexcrenota (anna), Denivia (deniva, hemon), Evenus (regalis) and Theritas (paupera, triquetra). 8 = Male hind wing ventral androconia in Eumaeini: a = Theritas mavors HÜBNER, 1818,
Figs 1–6 in Comments On The Systematics And Natural History Of Aveexcrenota, A Genus Of Rare Andean Eumaeine Lycaenidae (Lepidoptera)
Figs 1–6. Recently collected Aveexcrenota anna (DRUCE, 1907) individuals. 1–2: male individual from Cali, Colombia (CHD), 1= in dorsal, 2= in ventral aspects. 3–4: female individual from Caldas, Colombia (CJS), 3 = in dorsal, 4 = ventral aspects (the individual is dissected; see fig. 9). 5–6: male
Fig. 12 in Comments On The Systematics And Natural History Of Aveexcrenota, A Genus Of Rare Andean Eumaeine Lycaenidae (Lepidoptera)
Fig. 12. Monthly distribution of male Aveexcrenota anna (DRUCE, 1907) individuals collected near Cali, Colombia
ScienceDex guides
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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)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.