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FIGURES 221–223 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 221–223. Phylloteras poculum (Osten Sacken), sexual generation. 221, metasoma, female, lateral view. 222–223, male: 222, mesosoma, dorsal view, 223, mesosoma and metasoma, lateral view.
FIGURES 82–87 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 82–87. Bassettia flavipes (Gillette), asexual generation, female. 82–85, head: 82, frontal view, 83, dorsal view, 84, posterior view, 85, lateral view. 86, antenna. 87, pronotum and propleuron, frontal view.
FIGURES 88–91 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 88–91. Bassettia flavipes (Gillette), asexual generation, female. 88, mesosoma, lateral view, 89–90, mesoscutum and mesoscutellum, dorsal view, 91, metascutellum and propodeum, posterodorsal view.
FIGURES 70–75 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 70–75. Antron quercusnubila (Bassett), sexual generation. 70–72, female: 70, mesosoma, lateral view, 71, mesoscutum and mesoscutellum, dorsal view, 72, forewing, part. 73–75, male: 73, mesosoma, lateral view, 74, mesoscutum and mesoscutellum, dorsal view, 75, metascutellum and propodeum, posterodorsal view.
FIGURES 14–21. Acraspis villosa Gillette, sexual generation. 14–17 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 14–21. Acraspis villosa Gillette, sexual generation. 14–17, head, female: 14, frontal view, 15, dorsal view, 16, posterior view, 17, lateral view. 18–21, head, male: 18, frontal view, 19, dorsal view, 20, posterior view, 21, lateral view.
FIGURES 22–25 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 22–25. Acraspis villosa Gillette, sexual generation, female. 22, antenna. 23, pronotum and propleuron, frontal view. 24, mesosoma, dorsal view. 25, metascutellum and propodeum, posterodorsal view.
FIGURES 56–60 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 56–60. Andricus balanaspis (Weld). 56–57, sexual galls on catkins. 58–60, asexual galls in acorns.
FIGURES 51–55 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 51–55. Andricus balanaspis (Weld), sexual generation, female. 51, pronotum and propleuron, frontal view. 52–53, mesosoma: 52, lateral view, 53, dorsal view. 54, metascutellum and propodeum, posterodorsal view, 55, metasoma, lateral view.
FIGURES 61–69 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 61–69. Antron quercusnubila (Bassett), sexual generation. 61–64, head, female: 61, frontal view, 62, dorsal view, 63, posterior view, 64, lateral view. 65, antenna, female. 66–68, head, male: 66, frontal view, 67, dorsal view, 68, posterior view. 69, antenna, male.
FIGURES 44–50 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 44–50. Andricus balanaspis (Weld), sexual generation. 44–46, head, female: 44, frontal view, 45, dorsal view, 46, posterior view. 47, antenna, female. 48–49, head, male: 48, frontal view, 49, dorsal view. 50, antenna, male.
FIGURES 29–36. Amphibolips spinosa Ashmead, sexual generation. 29–32 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 29–36. Amphibolips spinosa Ashmead, sexual generation. 29–32, head, female: 29, frontal view, 30, dorsal view, 31, posterior view, 32, lateral view. 33, antenna, female. 34–35, male: 34, head, frontal view, 35, antenna. 36, forewing, part, female.
FIGURES 7–11 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 7–11. Acraspis quercushirta (Bassett), sexual female. 7–8, mesosoma: 7, lateral view, 8, dorsal view. 9, metascutellum and propodeum, posterodorsal view. 10, forewing, part. 11, metasoma, lateral view.
FIGURES 37–41 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 37–41. Amphibolips spinosa Ashmead, sexual generation, female. 37–39, mesosoma: 37, lateral view, 38–39, dorsal view. 40, metascutellum and propodeum, posterodorsal view. 41, metasoma, lateral view.
FIGURES 26–28. Acraspis villosa Gillette. 26 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 26–28. Acraspis villosa Gillette. 26, forewing, part, sexual female. 27, asexual gall. 28, sexual gall.
FIGURES 1–6 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 1–6. Acraspis quercushirta (Bassett), sexual female. 1–4, head: 1, frontal view, 2, dorsal view, 3, posterior view, 4, lateral view. 5, antenna. 6, pronotum and propleuron, frontal view.
FIGURE. Distribution of Dicorynia. Physical map of the Amazonian region with all analyzed specimens of Dicorynia. A large amount of point overlays leading to reduced number of visible points is due to the large percentage of materials being old collections that rely only on the name of the municipality or similar. Source: NASA with modifications. Note that almost all specimens are contained in areas with less than 200 m high and the high elevations of the Guiana shield may represent a form of isolation between the two species. in A Taxonomic Revision of the Amazonian Genus Dicorynia (Fabaceae: Dialioideae)
FIGURE. Distribution of Dicorynia. Physical map of the Amazonian region with all analyzed specimens of Dicorynia. A large amount of point overlays leading to reduced number of visible points is due to the large percentage of materials being old collections that rely only on the name of the municipality or similar. Source: NASA with modifications. Note that almost all specimens are contained in areas with less than 200 m high and the high elevations of the Guiana shield may represent a form of isolation between the two species.
FIGURE 1. A in Refining the circumscription of a variable species: epitypification of the name Kalanchoe rotundifolia (Crassulaceae subfam. Kalanchooideae)
FIGURE 1. A. At the epitype locality of Kalanchoe rotundifolia plants are generally glaucous to dull light green. The leaves are variably nearly round to oblong-elliptic to elliptic-obovate in outline. B. The distal part of the corolla tubes and corolla lobes of K. rotundifolia are orangey red. In bud as well as post-anthesis the flowers are apically twisted. C. Post-anthesis, the corolla tubes of K. rotundifolia dry whitish grey. This was also noted by Haworth (1824a: 188) in the protologue of the name K. rotundifolia where he described the flowers, which were already spent, as "[…] Flores parvi albi […]". D. At the likely type locality of K. rotundifolia in the vicinity of Gqeberha and Kariega in South Africa's Eastern Cape province, the species occurs in the undergrowth of the largely impenetrable thickets, here with the skyline dominated by Aloe pluridens Haworth (1824b: 299). All photographs by Gideon F. Smith.
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).
Lophuromys stanley: is member of the L. flavopunctatus species complex and was named during partial revision of the L. aguilus species complex. It is characterized by craniometric and genetic character-istics; its skull proportions are similar to L. laticeps, and molecularly, it is similar to L. margarettae and L. zena (cytochrome-b). Lophuromys stanleyi is one of four endemic species in the Rwenzori Mountains diversity hotspot. Monotypic. Distribution. Rwenzori Mts, E DR Congo and SW Uganda. Descriptive notes. Head-body 113-126 mm, tail 40-80 mm, ear 16-19 mm, hindfoot 22-24 mm; weight 36-55 g. The Rwenzori Brush-furred Rat has a speckled pelage similar to other speciesin the L. flavopunctatus species complex. Tail is short, 50-60% of head-body length. Habitat. Poorly known, but type specimen was collected at an elevation of 3700 m. Food and Feeding. No information. Breeding. No information. Activity patterns. No information. in Muridae
Lophuromys stanley: is member of the L. flavopunctatus species complex and was named during partial revision of the L. aguilus species complex. It is characterized by craniometric and genetic character-istics; its skull proportions are similar to L. laticeps, and molecularly, it is similar to L. margarettae and L. zena (cytochrome-b). Lophuromys stanleyi is one of four endemic species in the Rwenzori Mountains diversity hotspot. Monotypic. Distribution. Rwenzori Mts, E DR Congo and SW Uganda. Descriptive notes. Head-body 113-126 mm, tail 40-80 mm, ear 16-19 mm, hindfoot 22-24 mm; weight 36-55 g. The Rwenzori Brush-furred Rat has a speckled pelage similar to other speciesin the L. flavopunctatus species complex. Tail is short, 50-60% of head-body length. Habitat. Poorly known, but type specimen was collected at an elevation of 3700 m. Food and Feeding. No information. Breeding. No information. Activity patterns. No information.
Lophuromys kilonzoi was recently named as a new species and belongs to the L. flavopunctatus "clade." Some molecular analyses placed it in an Ethiopian-Tanzanian subclade including L. brunneus, L. aquilus, and L. verhageni. Monotypic. Distribution. Usambara and Uluguru Mts, E Tanzania. in Muridae
Lophuromys kilonzoi was recently named as a new species and belongs to the L. flavopunctatus "clade." Some molecular analyses placed it in an Ethiopian-Tanzanian subclade including L. brunneus, L. aquilus, and L. verhageni. Monotypic. Distribution. Usambara and Uluguru Mts, E Tanzania.
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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.