Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
144
datasets available to search
ShareScore release 0.9.0
Dataset results
144 results for “North Asia”
Subspecies and Distribution. R m. mehelyi Matschie, 1901 - S Europe (S Iberian Peninsula, Sardinia, E Sicily, SE Italy, S Albania, E Serbia, S Romania, E North Macedonia, Bulgaria, and Greece), SW Asia (Caucasus, Anatolia, N Iraq, and Zagros Mts in W Iran), and N Africa (N Morocco, N Algeria, and N Tunisia); possibly a record from SE France, and there are apparently records from Afghanistan, although exact localities are uncertain. R m. judaicus K. Andersen & Matschie, 1904 - Levant in Cyprus, N Syria, W Jordan, Israel, NE Egypt (including NW Sinai based on echolocation), and NE Libya. in Rhinolophidae
Subspecies and Distribution. R m. mehelyi Matschie, 1901 - S Europe (S Iberian Peninsula, Sardinia, E Sicily, SE Italy, S Albania, E Serbia, S Romania, E North Macedonia, Bulgaria, and Greece), SW Asia (Caucasus, Anatolia, N Iraq, and Zagros Mts in W Iran), and N Africa (N Morocco, N Algeria, and N Tunisia); possibly a record from SE France, and there are apparently records from Afghanistan, although exact localities are uncertain. R m. judaicus K. Andersen & Matschie, 1904 - Levant in Cyprus, N Syria, W Jordan, Israel, NE Egypt (including NW Sinai based on echolocation), and NE Libya.
Data from: Physconia labrata, a new species from western North America and Asia
A new species belonging to the lichen genus Physconia is described from Alaska and the Canadian and American Rocky Mountains and adjacent forested regions. It is also reported from China, Nepal, India and Siberia. The new species, Physconia labrata, is superficially similar to P. perisidiosa, but can be distinguished by having a blackened, corticate lower surface and a paraplectenchymatous upper cortex.
FIGURES 8–13 in A new species of Gamasiphis Berlese (Acari: Ologamasidae) from North Asia, with a key to the Eurasian species
FIGURES 8–13. Gamasiphis angaridis sp. n. Male. 8. Lateral (antiaxial) view of chelicera: A–B; 9. Corniculi; 10. Palpa; 11. Ventral idiosoma; 12. Leg IV; 13. Leg II.
FIGURES 1–7 in A new species of Gamasiphis Berlese (Acari: Ologamasidae) from North Asia, with a key to the Eurasian species
FIGURES 1–7. Gamasiphis angaridis sp.n. Female. 1. Lateral (antiaxial) view of chelicera; 2. Epistome: A–B variations of shape; 3. Hypostome; 4. Corniculi; 5. Dorsal idiosoma; 6. Ventral idiosoma; 7. Spermatheca.
FIGURE 11 in A new tribe and species of Clastopterinae (Hemiptera: Cercopoidea: Clastopteridae) from Africa, Asia and North America
FIGURE 11. Second valvulae of Taphrotylus (A), Sepullia (M–P) and Tremapterus subgenera Nyanja (B–G), Selenion (H), Tremiziana (J–L), and subgenus Abbalomba (Q–R). A, Taphrotylus insignificans, holotype; B, Tremapterus bimaculatus; C, T. humilis; D, T. perfasciatus; E, T. indecisus; F, T. scutellatus; G, T. virididorsum; H, T. longicaudatus, holotype; J, T. araneosus, paratype; K, T. scapulatus, paratype; L, T. oxythymus, paratype; M, Sepullia fuscolimbata; N, S. viridicollis; O, S. abyssinia; P, S. murrayi; Q, T. typicus; R, T. facialis. Scale line: 1 mm.
FIGURE 10 in A new tribe and species of Clastopterinae (Hemiptera: Cercopoidea: Clastopteridae) from Africa, Asia and North America
FIGURE 10. Second valvulae of Clastopterinae: Iba (A–C), Clastoptera (D–E), Tremapterus nominate subgenus (F–K) and subgenus Patriziana (L–P). A, Iba cuneata (holotype of C. bakeri); B, I. venosa sp. nov., holotype; C, I. (Parahindoloides) lumuana, lectotype; D, Clastoptera laevigata sp. nov., holotype; E, C. laenata Fowler, syntype; F, Tremapterus rufus; G, T. pluto, holotype; H, T. nigropunctatus; J, T. centonis; K, T. palimpsestus; L, T. combae, holotype; M, T. turneri, holotype; N, T. brunneus; O, T. janus; P, T. fuscus. Scale line: 1 mm.
FIGURES 12–18 in A new tribe and species of Clastopterinae (Hemiptera: Cercopoidea: Clastopteridae) from Africa, Asia and North America
FIGURES 12–18. Male genitalia of Beesoniella (12–14), Grellaphia (15–16), Tremapterus (17) and Sepullia (18). 12, B. cyclops sp. nov.; 13, B. forceps sp. nov.; 14, B. sylvestris; 15, G. costalis; 16, G. ro b u s t a sp. nov.; 17, T. dregei holotype; 18, Sepullia murrayi. A, genital capsule, lateral aspect (smaller scale than other figures); B, right pygofer process, ventral aspect, tip upwards; C, lateral aspect of connective, phallobase, theca and (17–18) endotheca; D, caudal aspect of theca and endotheca (when present). Scale line: 0.1 mm.
FIGURE 9 in A new tribe and species of Clastopterinae (Hemiptera: Cercopoidea: Clastopteridae) from Africa, Asia and North America
FIGURE 9. Dorsal aspects of the nominate subgenus of Tremapterus (A–F) and Sepullia (G–Q). A, Tremapterus blennus, lectotype; B, T. centonis sp. nov.; C, T. nigropunctatus, lectotype; D, T. palimpsestus sp. nov.; E, T. pluto, holotype; F, T. rufus; G, Sepullia abyssinia sp. nov., male paratype; H, same, female holotype; J, S. sankisiensis, holotype; K–M, colour varieties of S. fuscolimbata; N, S. tricolor sp. nov., holotype; O, S. umzilla, holotype; P–Q, colour varieties of S. viridicollis. Scale line: 1 mm.
FIGURE 2 in A new tribe and species of Clastopterinae (Hemiptera: Cercopoidea: Clastopteridae) from Africa, Asia and North America
FIGURE 2. Sepulliini from South Africa on Malvaceae, a close relative of the one with similar habits identified as Patriziana somalicus (Lallemand 1930), with nymphs that construct short tubes (A–B) from dried spittle masses on Grewia monticola (B) that are filled with sap and small bubbles (C–D). The nymph (E) resembles that of Machaerotinae (Woodward et al. 1970, fig. 26.27B) but has a shorter head and humped back like that of Clastoptera (Fig. 1G). The adult (F), found at the same location a few days later, is Tremapterus izzardi sp. nov. Photographs and data from Lee Gutteridge, Hoedspruit near Kruger National Park in northeastern South Africa.
FIGURE 1 in A new tribe and species of Clastopterinae (Hemiptera: Cercopoidea: Clastopteridae) from Africa, Asia and North America
FIGURE 1. Sepulliini (A–B) and Clastopterini (C–G). A–B, Beesoniella spittle masses and adults photographed at Madpur in Madikeri (Coorg) in Sept. 2009 (H.M. Yeshwanth); C, Clastoptera octonotata, photographed at Durham, North Carolina, USA on Feb. 5, 2014 (Dorothy E. Pugh, USA); D, C. laevigata, photographed at Great Falls Park, Montgomery County, Maryland, USA, on Aug. 20, 2009 (Ashley Bradford, USA); E, Spinola's drawing of C. maculipennis (Spinola), comb. nov.; F spittle mass of C. obtusa photographed at Harvard, Massachusetts, USA, June 26, 2005 (Tom Murray, USA); G, nymph of C. xanthocephala photographed at Assumpink WMA, Monmouth County, New Jersey, USA, June 29, 2008 (Tam Stuart). Photographs used by permission.
FIGURE 8 in A new tribe and species of Clastopterinae (Hemiptera: Cercopoidea: Clastopteridae) from Africa, Asia and North America
FIGURE 8. Dorsal aspects of Tremapterus subgenera Patriziana (A–K) and Tremiziana (L–Q). A, Tremapterus janus; B, T. expurgatus sp. nov., holotype; C, T. wardi sp. nov., holotype; D, T. peregrinus; E, T. atalanta, holotype; F, T. brunneus; G, T. splendens sp. nov., holotype; H, T. izzardi sp. nov., holotype; J, T. turneri sp. nov., holotype; K, T. combae sp. nov., holotype; L, T. arenosus sp. nov., male holotype; M, T. caccabatus sp. nov., male holotype; N, T. oxythymus sp. nov., male holotype; O, same, female paratype; P, T. scapulata sp. nov., male holotype; Q, same, female paratype. Scale line: 1 mm.
FIGURE 7 in A new tribe and species of Clastopterinae (Hemiptera: Cercopoidea: Clastopteridae) from Africa, Asia and North America
FIGURE 7. Dorsal aspects of Grellaphia costalis (A), G. robusta sp. nov. (B) and (at slightly larger scale) Tremapterus subgenus Abbalomba (C–D) and T. subgenus Nyanja (E–Q): C, Tremapterus schoutedeni; D, T. facialis; E, T. viduus, female lectotype; F, same, male paralectotype; G, T. perfasciatus sp. nov., male holotype; H, same, female; J, T. virididorsum sp. nov., holotype; K, T. indecisus sp. nov., holotype; L, T. scutellatus sp. nov., holotype; M, T. humilis sp. nov., holotype; N, T. muiri; O, T. bukamensis, lectotype; P, T. johannae, lectotype; Q, T. bimaculatus, lectotype. Scale line: 1 mm.
FIGURES 3–6 in A new tribe and species of Clastopterinae (Hemiptera: Cercopoidea: Clastopteridae) from Africa, Asia and North America
FIGURES 3–6. Comparison of face (3–4A), tegmen (3–5B), hind wing (3–5C), lateral aspect of head, pronotum and scutellum (6A–M) and dorsal aspect (N–O) in genera of Clastopterini (3–4), Machaerotinae (5), Sepullini (6A–L, O) and Aphrophorinae (6M–N): 3A, Clastoptera atrapicata; 3B–C, Clastoptera globosa Fowler; 6A, Clastoptera achatina; 4B–C, Iba (s.s.) venosa; 5B–C, Aphrosiphon bauhiniae, from China (1935), 6B, Iba (Parahindoloides) lumuana, lectotype, 6C, Beesoniella sylvestris; 6D, Sepullia fuscolimbatus; 6E, Tremapterus (Patriziana) somalicus; 6F, Tremapterus (s.s.) nigropunctatus, lectotype; 6G, Tremapterus (s.s.) palimpsestus sp. nov.; 6H, Tremapterus (Abbalomba) schoutedeni, holotype; 6J, Tremapterus (Abbalomba) facialis, lectotype; 6K, Tremapterus (Abbalomba) typicus; 6L, Grellaphia costalis; 6O, Sepullia viridicollis var. curtula; 6M– N, Witteella major (M–O from Jacobi 1910, with hind legs of Sepullia corrected to place spines on outer surface).
Distribution. Wide distribution in the Palearctic: from Europe to Russian Far East, North and South Korea, and Japan; also N Africa, Middle East, C Asia, Sub-Himalayan zone, S India, Sri Lanka, C, E & S China, Taiwan, Indochina, and Sumatra. in Mustelidae
Distribution. Wide distribution in the Palearctic: from Europe to Russian Far East, North and South Korea, and Japan; also N Africa, Middle East, C Asia, Sub-Himalayan zone, S India, Sri Lanka, C, E & S China, Taiwan, Indochina, and Sumatra.
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest. in Suidae
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest.
Subspecies and Distribution. M.c.coypusMolina,1782—Chilemainland. M.c.bonariensisE.GeoffroySaint-Hilaire,1805—Bolivia,Paraguay,NArgentina,SEBrazil,andUruguay. M.c.melanopsOsgood,1943—ChiloéI(CChile). M. c. santacruzae Hollister, 1914 — Argentina, from the Chaco S to Patagonia. Introduced widely into N South America, S North America, Europe, Central Asia, and East Africa. in Echimyidae
Subspecies and Distribution. M.c.coypusMolina,1782—Chilemainland. M.c.bonariensisE.GeoffroySaint-Hilaire,1805—Bolivia,Paraguay,NArgentina,SEBrazil,andUruguay. M.c.melanopsOsgood,1943—ChiloéI(CChile). M. c. santacruzae Hollister, 1914 — Argentina, from the Chaco S to Patagonia. Introduced widely into N South America, S North America, Europe, Central Asia, and East Africa.
FIGURE 6 in Out of Southeast Asia: A new species of thick-thumbed bat (Chiroptera: Vespertilionidae: Glischropus) from Meghalaya, north-eastern India
FIGURE 6. Dorsal and right lateral views of the baculum of (A) G. meghalayanus n. sp. (ZSIS V/M/ERS/682); (B) G. bucephalus (HNHM 2006.34.4.); and (C). G. tylopus (HNHM 2009.52.1.). Scale = 2 mm.
FIGURE 3 in Out of Southeast Asia: A new species of thick-thumbed bat (Chiroptera: Vespertilionidae: Glischropus) from Meghalaya, north-eastern India
FIGURE 3. Lateral view of skull of the holotypes of (A) G. meghalayanus n. sp. (ZSIS V/M/ERS/682); (B) G. bucephalus (HNHM 2006.34.49.); (C) Glischropus aquilus (MZB 35030); (D) G. tylopus (NHMUK 70.2.10.2); and (E) G. javanus (RMNH 15323). Scale= 5 mm.
FIGURE 2 in Out of Southeast Asia: A new species of thick-thumbed bat (Chiroptera: Vespertilionidae: Glischropus) from Meghalaya, north-eastern India
FIGURE 2. (A) lateral; (B) dorsal; (C) ventral view of cranium; (D) lateral; and (E) ventral view of mandible of the holotype of G. meghalayanus n. sp. (ZSIS V/M/ERS/682).
FIGURE 1 in Out of Southeast Asia: A new species of thick-thumbed bat (Chiroptera: Vespertilionidae: Glischropus) from Meghalaya, north-eastern India
FIGURE 1. External traits of Glischropus meghalayanus n. sp. from Meghalaya (A) habitus; (B) lateral aspect showing fur colouration of the holotype (ZSIS V/M/ERS/682); (C) thumb pad; (D) callosities on the sole; and (E) ventral view of the penis of the paratype (ZSIS V/M/ERS/683) (pictures not to scale).
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.