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480 results for “M 15”
FIGURES 15–23. Morphological character variation within P. c a m b o u e i. Figs 15–17 in Revision of the Pachycondyla wasmannii - group (Hymenoptera: Formicidae) from the Malagasy region
FIGURES 15–23. Morphological character variation within P. c a m b o u e i. Figs 15–17: Head in profile showing the shape of the occipital corner. Fig. 15: Normally rounded in form 1; Fig. 16: Protruding as a lobe in form 2; Fig. 17: Hornlike extension in form 3. Figs 18–19: Mesosoma in lateral view showing hairs on propodeal dorsum. Fig. 18: Hairs present in form 1; Fig. 19: Hairs absent in form 4. Figs 20–21: Anterodorsal angles of pronotum. Fig. 20: Bidentate in form 5; Fig. 21: Smoothly rounded in form 6. Figs 22–23: Sculpture and pubescence on fourth abdominal tergite. Fig. 22: Smooth and shiny between large punctures and pubescence absent (form 1); Fig. 23: With closely-spaced small punctures between large punctures and abundant pubescence (form 6).
FIGURES 15–18. 15–16, male abdominal segment VIII. 15, Metecia cornifrons. 16, M. lacustris. 17–18, M in A revision of the South American genus Metecia Snellen (Lepidoptera, Noctuidae, Noctuinae)
FIGURES 15–18. 15–16, male abdominal segment VIII. 15, Metecia cornifrons. 16, M. lacustris. 17–18, M. lacustris male genitalia, uncus (lateral view). 17, uncus apex curved upwards. 18, close up of uncus apex showing dorsal strong small spines.
FIGURES 12–15 in Second highly modified hypogean species of the genus Morimotoidius Habu from western Jiangxi Province, China, with a new locality for M. zhushandong (Coleoptera: Carabidae: Platynini)
FIGURES 12–15. Cave Guanfeng Dong, type locality of M. cavicola sp. n. 12. location of the cave (indicated by arrowhead); 13. entrance; 14. environment of entrance; 15. an adult of M. cavicola sp. n.
FIGURE 15. A in Redescription of the eagle rays Myliobatis hamlyni Ogilby, 1911 and M. tobijei Bleeker, 1854 (Myliobatiformes: Myliobatidae) from the East Indo-West Pacific
FIGURE 15. A) Upper and B) lower tooth plates of Myliobatis tobijei FFNU unregistered (adult, dried jaws only).
FIGURE 15. M in Taxonomic study of the genus Myrmarachne of Borneo (Araneae: Salticidae)
FIGURE 15. M. crassembolus sp. nov., male. A, body, dorsal view; B, maxillae, labium, sternum and coxae; C, body, lateral view; D, chelicera and fang, ventral view; E, palp, ventral view; F, palp, lateral view; G, palpal tibia, dorsal view. (Scales. A–D: 1 mm; E–G: 0.25 mm)
FIGURES 11–15. F. f u m o s a in Isotomidae (Collembola) of Buryat Republic. II. A revision of the genus Folsomia
FIGURES 11–15. F. f u m o s a sp. nov.: 11, habitus of adult male; 12, chaetotaxy; 13, hind corner of Th.II; 14, sensilla of Abd.IV and V; 15, records.
FIGURES 15–26. Fig.15. M. zhengi Li in Two new species and a key to nine species of the genus Mongolotettix Rehn, 1928 from China (Acrididae, Acridoidea, Orthoptera)
FIGURES 15–26. Fig.15. M. zhengi Li & Lian, 1994 body lateral view Ƌ; Fig.16. M. chongqingensis Xie & Li, 2000 body lateral view Ƌ; Fig.17. M. angustiseptus Wan, Ren & Zhang, 1998 epiphallus; Fig.18. M. anomopterus (Caudell, 1921) epiphallus; Fig.19. M. japonicus (Bolívar, 1898) tergum of periproct Ƌ; Fig.20. M. vittatus (Uvarov, 1914) tergum of periproct Ƌ; Fig.21. M. vittatus (Uvarov, 1914) mesosternum Ƌ; Fig.22. M. angustiseptus Wan, Ren & Zhang, 1998 mesosternum and metasternum Ƌ; Fig.23. M. mistshenkoi Chogsomzhav, 1974 mesosternum Ƌ; Fig.24. M. japonicus (Bolívar,1898) mesosternum Ƌ; Fig.25. M. zhengi Li & Lian, 1994 epiphallus; Fig.26. M. japonicus (Bolívar,1898) epiphallus. [Figs.15, 25 after Li et al., 1994; fig. 16 after Xie et al., 2000; figs 17, 22 after Wan, Ren & Zhang, 1998; Fig. 18 after Zhang in Yin et al. 2003; Figs. 19–21, 23–24, 26 after Chogsomzhav, 1974]
FIGURES 13–15. Mniotype, Mniopamea ssp. female genitalia. 13. M in A new Mniotype Franclemont (Lepidoptera, Noctuidae) species from China
FIGURES 13–15. Mniotype, Mniopamea ssp. female genitalia. 13. M. ripa sp. n., female, paratype, China, W. Sichuan, prep. PGY4380f (PGM); 14. M. melanodonta, female, China, Shaanxi, prep. PGY4403f (PGM); 15. M. gandhara, female, Pakistan, Karakoram, prep. PGY4401f (PGM); Figure 16. China, West Sichuan, near Litang, the type locality of M. ripa sp. n.: 4000 m, N29°49.136′, E100°20.576′.
FIGURES 13–16. Tamarixia dahlsteni, female. 13. Head, frontal view. 14. Mesosoma, lateral view. 15. Mesosoma, dorsal view. 16 in Two new species of Ta m a r i x i a (Hymenoptera: Eulophidae) from Chile and Australia, established as biological control agents of invasive psyllids (Hemiptera: Calophyidae, Triozidae) in California
FIGURES 13–16. Tamarixia dahlsteni, female. 13. Head, frontal view. 14. Mesosoma, lateral view. 15. Mesosoma, dorsal view. 16. Propodeum.
FIGURE 15. Antenna, genus Megalothorax. M in Morphological review of the order Neelipleona (Collembola) through the redescription of the type species of Acanthoneelidus, Neelides and Neelus
FIGURE 15. Antenna, genus Megalothorax. M. nigropunctatus (A) posterior side, (B) anterior side modified after Schneider & D'Haese (2013); M. perspicillum (C) posterior side, (D) anterior side modified after Schneider & D'Haese (2013), (E) dorsal side; M. svalbardensis (F) posterior side, (G) anterior side. Scale bar (E) = 10 µm.
FIGURE 15. a in Identification guide to the shallow water (0-200 m) octocorals of the South Atlantic Bight 2599
FIGURE 15. a) Pseudodrifa nigra; b) Nidalia occidentalis (from Bayer, 1961); c) Bellonella rubistella.
Distribution. NW Colombia, between the Rio Atrato and the lower Rio Cauca (W of the Rio Cauca and the Mompos I) and Rio Magdalena (from the Uraba region, W of the Rio Cauca), and NE Choco Department, E of the Rio Atrato, from sea level to ¢.400 m. Small, introduced populations occur in Tayrona National Natural Park (15,000 ha) and on some small Is near Cartagena and in Panama, outside its natural distribution. in Callitrichiade
Distribution. NW Colombia, between the Rio Atrato and the lower Rio Cauca (W of the Rio Cauca and the Mompos I) and Rio Magdalena (from the Uraba region, W of the Rio Cauca), and NE Choco Department, E of the Rio Atrato, from sea level to ¢.400 m. Small, introduced populations occur in Tayrona National Natural Park (15,000 ha) and on some small Is near Cartagena and in Panama, outside its natural distribution.
FIGURES 15–20. Mallomonas voloshkoae and M. pechlaneri. TEM images. FIGURES 15–18 in Mallomonas voloshkoae sp. nov. (Synurales, Chrysophyceae) and distribution of M. pechlaneri in mountain lakes of Siberia
FIGURES 15–20. Mallomonas voloshkoae and M. pechlaneri. TEM images. FIGURES 15–18. Mallomonas voloshkoae sp. nov. Body scales from different habitats. Figure 15. Unnamed lake 1. Figure 16. Unnamed lake 2. Figure 17. Unnamed lake 3. Figure 18. Lake Frolikha. FIGURES 19–20. Mallomonas pechlaneri. Figure 19. Scales with bristles from Teletskoe Lake. Figure 20. Scales with bristles from Ilchir Lake. Scale bars: Figs 15–20: 2 μm.
FIGURES 15–21 in Five new species in the predaceous midge genus Macrurohelea Ingram & Macfie from Argentina, and descriptions of the previously unknown males of M. kuscheli Wirth and M. monotheca Spinelli & Grogan (Diptera: Ceratopogonidae)
FIGURES 15–21. Macrurohelea kuscheli Wirth, male, 15–18. Macrurohelea monotheca Spinelli & Grogan, male, 19–21. 15, 19 head. 16 thorax. 17, 20 wing. 18-21 genitalia. Scale bars = 0.05 mm.
FIGURES 12–15. The Carpathian Mesochorus spp. 12—M in A checklist of the subfamily Mesochorinae (Hymenoptera, Ichneumonidae) from the Ukrainian Carpathians
FIGURES 12–15. The Carpathian Mesochorus spp. 12—M. faciator; 13—M. pictilis; 14—M. atriventris; 15—M. cf. pini.
FIGURES 15–18. Distribution maps for the Metallactus taeniatellus species group. M in Revision of the Metallactus taeniatellus species group (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 15–18. Distribution maps for the Metallactus taeniatellus species group. M. planipennis (15); M. quadrinus (16); M. superbiens (17); M. taeniatellus (18). Striped squares: two possible (alternative) locations for the type locality of M. planipennis due to the ambiguous report in the original description (see text for further information).
Distribution. CE Madagascar, known only from its type locality, the Sahafina Forest (29-230 m above sea level), a lowland rainforest fragment of 15-6 km2, and its surrounding "savoka" (fallow farmland with cultivated trees), about 58 km E of Andasibe-Mantadia National Park and 18 km W of the Indian Ocean. The geographic range is presumably limited to the lowland areas (below 700 m) between the Mangoro River to the S and the Rianila River to the N, an area of about 7600 km?2. in Cheirogaleidae
Distribution. CE Madagascar, known only from its type locality, the Sahafina Forest (29-230 m above sea level), a lowland rainforest fragment of 15-6 km2, and its surrounding "savoka" (fallow farmland with cultivated trees), about 58 km E of Andasibe-Mantadia National Park and 18 km W of the Indian Ocean. The geographic range is presumably limited to the lowland areas (below 700 m) between the Mangoro River to the S and the Rianila River to the N, an area of about 7600 km?2.
Although previously treated as a subspecies of G. dolichurus, G.dryas was later recognized as a good species. Monotypic. Distribution. Restricted to elevations above 1000 m within the Albertine Rift Mts. Descriptive notes. Head-body 100-130 mm, tail 142-177 mm, car 15-21 mm, hindfoot 22-28 mm; weight 30-59 g. Fur of the Albertine Rift Thicket Rat is tawny brown above, becoming brighter orange brown on rump, with sharply demarcated pure white belly bordered by thin orange line. Tail is very long (160% of head-body length), semi-prehensile, tufted, and dark brown. Feet are pale buff, with four digits on forefoot and five on relatively short hindfoot, fifth digit longer and semi-opposable. Females have 0+2 = 2 pairs of nipples. in Muridae
Although previously treated as a subspecies of G. dolichurus, G.dryas was later recognized as a good species. Monotypic. Distribution. Restricted to elevations above 1000 m within the Albertine Rift Mts. Descriptive notes. Head-body 100-130 mm, tail 142-177 mm, car 15-21 mm, hindfoot 22-28 mm; weight 30-59 g. Fur of the Albertine Rift Thicket Rat is tawny brown above, becoming brighter orange brown on rump, with sharply demarcated pure white belly bordered by thin orange line. Tail is very long (160% of head-body length), semi-prehensile, tufted, and dark brown. Feet are pale buff, with four digits on forefoot and five on relatively short hindfoot, fifth digit longer and semi-opposable. Females have 0+2 = 2 pairs of nipples.
Lophuromys medicaudatus, L. woosnami, and L. luteogaster are in subgenus Kivumys and woosnami species group. Monotypic. Distribution. Endemic to the Albertine Rift, occurring around Lake Kivu in E DR Congo and Rwanda and SW Uganda (Bwindi). Descriptive notes. Head—body 92-112 mm, tail 73-95 mm, ear 15-19 mm, hindfoot 18-23 mm; weight 29-43 g. Similar to other species in subgenus Kivumys, the Western Rift Brush-furred Rat has unspeckled pelage, and tail ¢.85% of head-body length. Dorsum is uniform dark brown-olive, and venter is orange. Females have three pairs of mammae. Habitat. Mountain swamps and mountain forests at elevations of 1850-2500 m. Food and Feeding. The Western Rift Brush-furred Rat is omnivorous; diets contain 30-100% arthropods, mollusks, seeds, and fruits. Breeding. Female Western Rift Brush-furred Rats can have 1-2 embryos. Pregnant females were observed in February, April, and July. Activity patterns. The Western Rift Brush-furred Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Vulnerable on The IUCN Red List. The Western Rift Brush-furred Rat has never been found in modified secondary environment and is quite rare. Bibliography. Dieterlen (1976b, 1987 2013g), Kasangaki et al. (2003), Verheyen et al. (1996). in Muridae
Lophuromys medicaudatus, L. woosnami, and L. luteogaster are in subgenus Kivumys and woosnami species group. Monotypic. Distribution. Endemic to the Albertine Rift, occurring around Lake Kivu in E DR Congo and Rwanda and SW Uganda (Bwindi). Descriptive notes. Head—body 92-112 mm, tail 73-95 mm, ear 15-19 mm, hindfoot 18-23 mm; weight 29-43 g. Similar to other species in subgenus Kivumys, the Western Rift Brush-furred Rat has unspeckled pelage, and tail ¢.85% of head-body length. Dorsum is uniform dark brown-olive, and venter is orange. Females have three pairs of mammae. Habitat. Mountain swamps and mountain forests at elevations of 1850-2500 m. Food and Feeding. The Western Rift Brush-furred Rat is omnivorous; diets contain 30-100% arthropods, mollusks, seeds, and fruits. Breeding. Female Western Rift Brush-furred Rats can have 1-2 embryos. Pregnant females were observed in February, April, and July. Activity patterns. The Western Rift Brush-furred Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Vulnerable on The IUCN Red List. The Western Rift Brush-furred Rat has never been found in modified secondary environment and is quite rare. Bibliography. Dieterlen (1976b, 1987 2013g), Kasangaki et al. (2003), Verheyen et al. (1996).
FIGURES 15–16 in Taxonomic review of Manulea (M.) tienmushanica (Daniel), comb. nov., and its allies with descriptions of two new species from mainland China (Lepidoptera Erebidae: Arctiinae)
FIGURES 15–16. Manulea spp.: female genitalia. Depositories of the specimens dissected: 15 in ASV; 16 in MWM/ZSM.
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