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806 results for “Neotype”
FIGURE 2 in Neotype designation of the Short-tailed Albatross Phoebastria albatrus (Pallas 1769) (Aves: Procellariiformes: Diomedeidae)
FIGURE 2. (A) old and (B) modern museum labels attached to the neotype specimen. The text on the label (A) is translated as "No. 689. museum skin. Phoebastria albatrus (Pall.) male adult. 18.VIII.1845. Okhotsk Sea, between Cape Longdar-Negotni (near port Ayan) and peninsula Nurki at the north turn. Woznesensky". The text on the label (B) is translated as "No. 4388. coll. Woznesensky. 18 August 1845. Okhotsk Sea between Capes Londar-Negotni and Nurki".
FIGURE 1 in Neotype designation of the Short-tailed Albatross Phoebastria albatrus (Pallas 1769) (Aves: Procellariiformes: Diomedeidae)
FIGURE 1. Neotype of Phoebastria albatrus (Pallas, 1769); ZIN 4388. (A) dorsal and (B) ventral views.
FIGURE 4 in Disentangling the Pelodiscus axenaria complex, with the description of a new Chinese species and neotype designation for P. axenaria (Zhou, Zhang & Fang, 1991)
FIGURE 4. Dorsal and ventral aspects of the holotype of Pelodiscus shipian sp. nov. (JNU 20190011, adult female, 100.5 mm CL).
FIGURE 3 in Disentangling the Pelodiscus axenaria complex, with the description of a new Chinese species and neotype designation for P. axenaria (Zhou, Zhang & Fang, 1991)
FIGURE 3. Variation in plastron colouration and pattern in Pelodiscus axenaria. Males above, females below (none collected); all from Longsheng, Guangxi Zhuang Autonomous Region, China. Not to scale.
FIGURE 7 in Disentangling the Pelodiscus axenaria complex, with the description of a new Chinese species and neotype designation for P. axenaria (Zhou, Zhang & Fang, 1991)
FIGURE 7. Genetically verified records for species of the Pelodiscus axenaria complex in central China (compiled from Chen et al. 2005, 2006; Yang et al. 2011; Gong et al. 2018, 2021 and this study). Blue: P. axenaria, red: P. huangshanensis, green: P. shipian sp. nov.
FIGURE 1 in Disentangling the Pelodiscus axenaria complex, with the description of a new Chinese species and neotype designation for P. axenaria (Zhou, Zhang & Fang, 1991)
FIGURE 1. Dorsal and ventral aspects of the freshly dead neotype of Pelodiscus axenaria (JNU 20210001, adult male, 128.7 mm CL).
FIGURE 6 in Disentangling the Pelodiscus axenaria complex, with the description of a new Chinese species and neotype designation for P. axenaria (Zhou, Zhang & Fang, 1991)
FIGURE 6. Variation in colouration and pattern in Pelodiscus shipian sp. nov. Freshly dead paratypes JNU 20210005 (male, top and bottom left), JNU 20210004 (male, top right) and JNU 20210006 (female, bottom right), all from Hunan Province, China. Not to scale.
FIGURE 5 in Disentangling the Pelodiscus axenaria complex, with the description of a new Chinese species and neotype designation for P. axenaria (Zhou, Zhang & Fang, 1991)
FIGURE 5. One of the paratypes of Pelodiscus shipian sp. nov. (JNU 20210002, adult female, 88.2 mm CL) in life.
New taxonomic position and neotype designation for the conoidean gastropod Pleurotoma patagonica d'Orbigny, 1841
<p>Neotype specimen (MACN-In43983) collected alive at Las Grutas, San Antonio Oeste, Río Negro Province,<br> Argentina, in 8 m depth.</p>
FIGURE 1a in Neotype designation, redescription, biology and distribution of Acanthopsyche alstoni Watt & Mann, 1903 (Lepidoptera: Psychidae) from India
FIGURE 1a: ♂ Neotype of Acanthopsyche alstoni currently at STC Thrissur India—magnified view of head and thorax; b: ♂Neotype of Acanthopsyche alstoni at STC Thrissur India—full body view.
FIGURE 4a in Neotype designation, redescription, biology and distribution of Acanthopsyche alstoni Watt & Mann, 1903 (Lepidoptera: Psychidae) from India
FIGURE 4a: ♂ Fore Wing venation, descaled, coloured in Fuchsine, mounted in alcohol; b: ♂ Hindwing Wing, descaled, coloured in Fuchsine, mounted in alcohol; 4c: Wing venation.
Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae & Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser & Carleton (2005), Richardson & Hussain (2006), Stuart (2008). in Muridae
Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae & Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser & Carleton (2005), Richardson & Hussain (2006), Stuart (2008).
FIGURES 9–13. Hercinothrips splendens n in A key to species of Hercinothrips, with one new species, and a neotype designation for H. trilineatus (Priesner)
FIGURES 9–13. Hercinothrips splendens n.sp. (9) Tergites IX–X; (10) Metanotum; (11) Fore wing; (12) Leaf feeding damage on Aloe sp. caused by H. aethiopiae in Holland; (13) Aloe plants attacked by H. splendens in greenhouse in Holland.
FIGURES 14–23 in A key to species of Hercinothrips, with one new species, and a neotype designation for H. trilineatus (Priesner)
FIGURES 14–23. Hercinothrips species. (14) H. jansei pronotum; (15) H. dimidiatus pronotum; (16) H. aethiopiae microtrichia comb VIII; (17) H. tenuis hind tibia; (18) H. splendens tibia; (19) H. brunneus microtrichia comb VIII; (20) H. trilineatus wing; (21) H. trilineatus tibia; (22) H. trilineatus metanotum; (23) H. splendens metanotum
FIGURES 1–8. Hercinothrips splendens n in A key to species of Hercinothrips, with one new species, and a neotype designation for H. trilineatus (Priesner)
FIGURES 1–8. Hercinothrips splendens n.sp. (1) Habitus female; (2) Head; (3) Pronotum; (4) Head and Pronotum; (5) Tergite I; (6) Tergite II; (7–8) Antennal segments III–VIII.
FIGURE. Multilocus phylogenetic tree inferred from Bayesian analysis based on the combined TEF1-α and ACT sequences. Bayesian posterior probabilities are indicated next to the nodes. The tree was rooted with Cladosporium herbarum CBS 121621. The species in this study are indicated in bold. Types of species are indicated after the culture collection number (T = ex-type, ex-epitype, ex-neotype, or reference strain). in Six new species of Cladosporium associated with decayed leaves of native bamboo (Bambusoideae) in a fragment of Brazilian Atlantic Forest
FIGURE. Multilocus phylogenetic tree inferred from Bayesian analysis based on the combined TEF1-α and ACT sequences. Bayesian posterior probabilities are indicated next to the nodes. The tree was rooted with Cladosporium herbarum CBS 121621. The species in this study are indicated in bold. Types of species are indicated after the culture collection number (T = ex-type, ex-epitype, ex-neotype, or reference strain).
FIG. 1 in Canadaphis mordvilkoi, Kononova 1976 (Hemiptera: Sternorrhyncha: Canadaphididae)-redescription and neotype designation
FIG. 1 New specimen of Canadaphis mordvilkoi; a—ventral side of the body; b—dorsal side of the body.
FIGURE 10 in Neotype designation for Plangia graminea (Serville, 1838) and two new Plangia species from Tanzania, East Africa (Orthoptera: Tettigoniidae: Phaneropterinae)
FIGURE 10. Morphological details of female Plangia variacantans n. sp. A. Lateral view on ovipositor. Scale bar 2 mm B. Subgenital plate. Scale bar 1 mm.
FIGURE 9 in Neotype designation for Plangia graminea (Serville, 1838) and two new Plangia species from Tanzania, East Africa (Orthoptera: Tettigoniidae: Phaneropterinae)
FIGURE 9. Morphological details of male Plangia variacantans n. sp. A. Lateral and semilateral (B) view on abdominal apex. Scale bar 2 mm C. Subgenital plate. Scale bar 2 mm D. Stridulatory file on underside of left tegmen. Scale bar 500 µm.
FIGURE 4 in Neotype designation for Plangia graminea (Serville, 1838) and two new Plangia species from Tanzania, East Africa (Orthoptera: Tettigoniidae: Phaneropterinae)
FIGURE 4. Plangia graminea female, in spirit, NM Vienna. South Africa, M. C. Holub, det. Krss. A. Lateral view on ovipositor B. Subgenital plate.
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Allen Brain Atlas
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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.