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575 results for “taxonomic changes”

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FIGURE 9 in Taxonomic changes and new species in Malagasy Euphorbia (Euphorbiaceae)

FIGURE 9. Euphorbia antsingiensis, in Antsingy of Bemaraha, near Antsalova. A. inflorescence; B. detail of cyathium and cyathophylls. Credits: J.Bosser (A and B).

opennotspecifiedMar 2021View details →
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FIGURE. Euphorbia xanthadenia, in situ. A & B. flowering branches near Tsimalahai and Tranomaro; C. Amboasary area. Credits: P.Pavelka (A–C). in Taxonomic changes and new species in Malagasy Euphorbia (Euphorbiaceae)

FIGURE. Euphorbia xanthadenia, in situ. A & B. flowering branches near Tsimalahai and Tranomaro; C. Amboasary area. Credits: P.Pavelka (A–C).

opennotspecifiedMar 2021View details →
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FIGURE. Euphorbia atimovatae in Lavanono area. A. habit; B. young fruit with staminate flower; C. young cyathium. Credits: T.Haevermans (A and C) and I.Kiefer (B). in Taxonomic changes and new species in Malagasy Euphorbia (Euphorbiaceae)

FIGURE. Euphorbia atimovatae in Lavanono area. A. habit; B. young fruit with staminate flower; C. young cyathium. Credits: T.Haevermans (A and C) and I.Kiefer (B).

opennotspecifiedMar 2021View details →
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FIGURE 2. Euphorbia agatheae. A in Taxonomic changes and new species in Malagasy Euphorbia (Euphorbiaceae)

FIGURE 2. Euphorbia agatheae. A. young fruit; B. male cyathium; C. detail of brachyblasts. Credits: T.Haevermans (A and B) and P.E.Berry (C).

opennotspecifiedMar 2021View details →
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FIGURE 4 in Taxonomic changes and new species in Malagasy Euphorbia (Euphorbiaceae)

FIGURE 4. Euphorbia atimovatae in the Lavanono area, young plant showing the thick rootstock and young stems. Credits: T.Haevermans.

opennotspecifiedMar 2021View details →
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FIGURE. Euphorbia agatheae in the type locality (Ifaty, north of Toliary). A. habit; B. detail of the bark. Credits: T.Haevermans (A and B). in Taxonomic changes and new species in Malagasy Euphorbia (Euphorbiaceae)

FIGURE. Euphorbia agatheae in the type locality (Ifaty, north of Toliary). A. habit; B. detail of the bark. Credits: T.Haevermans (A and B).

opennotspecifiedMar 2021View details →
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FIGS 44–46 in Taxonomic changes and review of the genera Tipulamima Holland, 1893 and Macrotarsipodes Le Cerf, 1916 stat. rev. (Lepidoptera: Sesiidae: Sesiinae)

FIGS 44–46. Genitalia structures of Macrotarsipodes. 44–45. M. tricinctus. (44) ♀, South Africa, Natal, Durban. (45) ♂, South Africa, Eastern Cape, East London. 46. M. pedunculata ♂, Nigeria, Ile-Ife. (a) left lateral, right ventral. (b) phallus (twice size as other Figs). Scales 1 mm.

opennotspecifiedFeb 2022View details →
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FIGS 32–43 in Taxonomic changes and review of the genera Tipulamima Holland, 1893 and Macrotarsipodes Le Cerf, 1916 stat. rev. (Lepidoptera: Sesiidae: Sesiinae)

FIGS 32–43. Specimens of Macrotarsipodes. 32–33. M. leptosceles (Bradley, 1968). (32) holotype ♂. (33) paratype ♀. 34–36. M. pedunculata (Hampson, 1910) comb. nov., (34) holotype ♂. (35–36) ♂ Ghana, Gyawale, Kakum. 37–38. M. sexualis (Hampson, 1910) comb. nov. (37) lectotype ♂. (38) paralectotype ♀. 39–43. M. tricinctus Le Cerf, 1916 comb. rev. (39–40) ♂ South Africa, East London. (41) holotype ♂. (42–43) ♀ South Africa, Natal, Durban. Scale 10 mm.

opennotspecifiedFeb 2022View details →
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FIGS 3–14 in Taxonomic changes and review of the genera Tipulamima Holland, 1893 and Macrotarsipodes Le Cerf, 1916 stat. rev. (Lepidoptera: Sesiidae: Sesiinae)

FIGS 3–14. Type specimens of Tipulamima. 3–5. T. flavifrons Holland, 1893. (3–4) holotype ♀. (5) ♀ Uganda, Kawanda. 6–8. T. haugi (Le Cerf, 1917). (6–7) paralectotype ♂. (8) lectotype ♀. 9–14. T. pterotarsa (Meyrick, 1933). (9–10) holotype ♀. (11, 14) ♂ Cameroon, SW slope of Mount Cameroon. (12–13) ♀ Ghana, Central Region, Abrafo village. Scale 10 mm.

opennotspecifiedFeb 2022View details →
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FIGS 1–2 in Taxonomic changes and review of the genera Tipulamima Holland, 1893 and Macrotarsipodes Le Cerf, 1916 stat. rev. (Lepidoptera: Sesiidae: Sesiinae)

FIGS 1–2. Female of Tipulamima pterotarsa (1) resting. (2) egg laying on Clerodendrum paniculatum (arrows).

opennotspecifiedFeb 2022View details →
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FIGS 27–28 in Taxonomic changes and review of the genera Tipulamima Holland, 1893 and Macrotarsipodes Le Cerf, 1916 stat. rev. (Lepidoptera: Sesiidae: Sesiinae)

FIGS 27–28. Genitalia structures of Tipulamima pterotarsa (27a) ♂, Ghana? (27b) ♂, abdominal segment eighth. (28a) ♀, Nigeria, Osun, Ile-Ife. Scale 1 mm. (28b) corpus bursae. Scale 0.5 mm.

opennotspecifiedFeb 2022View details →
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FIGS 15–26 in Taxonomic changes and review of the genera Tipulamima Holland, 1893 and Macrotarsipodes Le Cerf, 1916 stat. rev. (Lepidoptera: Sesiidae: Sesiinae)

FIGS 15–26. Specimens of Tipulamima. 15. T. flammipes (Hampson, 1910), lectotype ♂. 16–17. T. pyrosoma Hampson, 1919, holotype ♀. 18–20. Tipulamima hesperia sp. nov. 18–19. ♂ Guinea, Nimba Mts. (20) ♂ Ghana, Kumasi. 21–23. T. grandidieri (Le Cerf, 1917). (21) holotype ♂. 22–23. ♂ Madagascar Est, Moramanga, Andasibe. 24–26. T. seyrigi Viette, 1955. (24–25) holotype ♀. (26) ♀ Madagascar, Sambirano. Scale 10 mm.

opennotspecifiedFeb 2022View details →
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FIGS 29–31 in Taxonomic changes and review of the genera Tipulamima Holland, 1893 and Macrotarsipodes Le Cerf, 1916 stat. rev. (Lepidoptera: Sesiidae: Sesiinae)

FIGS 29–31. Genitalia structures of Tipulamima. 29. T. flammipes (Hampson, 1910), lectotype ♂. 30. T. grandidieri (Le Cerf, 1917), ♂, Madagaskar, Tolongoina, Mandriandry (left valva removed). 31. T. hesperia sp. nov., holotype ♂, Guinea, Nimba Mts. Scale 1 mm.

opennotspecifiedFeb 2022View details →
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text FIG.2 in Taxonomic changes and review of the genera Tipulamima Holland, 1893 and Macrotarsipodes Le Cerf, 1916 stat. rev. (Lepidoptera: Sesiidae: Sesiinae)

text FIG.2. Phylogenetic analysis (MrBayes using RAxML usertree) of Macrotarsipodes (based on COI barcode sequences, 10 million generations, values are posterior probabilities). Sister groups Macrotarsipus Hampson, [1893], Lepidopoda dasysceles (Bradley, 1968) and two indeterminate Synanthedonini from Cameroon and Tanzania.

opennotspecifiedFeb 2022View details →
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text FIG.1 in Taxonomic changes and review of the genera Tipulamima Holland, 1893 and Macrotarsipodes Le Cerf, 1916 stat. rev. (Lepidoptera: Sesiidae: Sesiinae)

text FIG.1. Phylogenetic analysis (MrBayes using RAxML usertree) of Tipulamima species (based on COI barcode sequences, 10 million generations, values are posterior probabilities). Sister groups Lophoceps abdominalis Hampson, 1919, Pseudalcathoe aspetura Meyrick, 1932 and four indeterminate Synanthedonini from Kenya.

opennotspecifiedFeb 2022View details →
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Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003). in Muridae

Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003).

opennotspecifiedNov 2017View details →
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FIGURES 3–11 in Taxonomic changes in Salyavatinae (Heteroptera: Reduviidae), with an updated generic key

FIGURES 3–11. Various salyavatine species, dorsal habitus: (3) Petalocheirus rubiginosus, adult female; (4) Petalocheirus villiersi, adult female; (5) Platychiria murrayi, adult male; (6) Platychiria umbrosa, adult female; (7) Salyavata mcmahanae, adult female; (8) Valentia apetala, adult female; (9) Lisarda inornata, adult female; (10) Lisarda annularis, adult male; and (11) Lisarda annularis, nymph, same series as Fig. 10. Scale bar = 2 mm.

opennotspecifiedAug 2017View details →
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FIGURE 1 in Taxonomic changes in Salyavatinae (Heteroptera: Reduviidae), with an updated generic key

FIGURE 1. Pronotal armature, dorsal and lateral view, of foliate-legged genera: (a) Alvilla obesa comb. nov. (representing Alvilla); (b) Petalocheirus inimicus (representing Petalocheirus s.s.); (c) Platychiria montana (representing umbrosa group); (d) Platychiria striata (representing murrayi group); and (e) Rhachicephala dilatibia (representing Rhachicephala). Line drawings after Miller (1940) (a), Miller (1950) (b–d), and Truong et al. (2007) (e).

opennotspecifiedAug 2017View details →
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FIGURE 2 in Taxonomic changes in Salyavatinae (Heteroptera: Reduviidae), with an updated generic key

FIGURE 2. Valentia langkawiensis, adult female: (a) dorsal habitus; (b) lateral habitus; (c) left foreleg, lateral view; (d) external genitalia, dorso-caudal view; and (e) idem., caudal view. Scale bar = 2 mm.

opennotspecifiedAug 2017View details →
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FIGURES 10–27. 10–14 in Taxonomic changes of some neotropical species of Arctiini Leach (Lepidoptera: Erebidae: Arctiinae)

FIGURES 10–27. 10–14. Agaraea nigrostriata (Rothschild, 1909). 10. Habitus. 11. Male genitalia. 12. Aedeagus. 13. Coremata. 14. Female genitalia. 15–17. Halysidota infucata Berg, 1882 15. Habitus. 16. Male genitalia. 17. Aedeagus. 18–21. Melese paranensis Dognin, 1911. 18. Habitus. 19. Male genitalia. 20. Aedeagus. 21. Female genitalia. 22–24. Tessellota cancellata (Burmeister, 1878). 22. Habitus. 23. Male genitalia. 24. Aedeagus. 25–27. Tessellota pura Breyer, 1957. 25. Male paratype. 26. Male genitalia. 27. Aedeagus. Scale bar: 10 mm.

opennotspecifiedDec 2017View details →

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behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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