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1,334 results for “Himalayas”
Figs 260–277 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 260–277: Zyras morulus (260–265), Z. variolatus (266–270), Z. montanus (271–275), and Z. preangeranus from Java (276–277): forebody (260); antenna (261); abdomen (262); median lobe of aedeagus in lateral and in ventral view (263–264, 266–267, 271–272, 276–277); paramere (265, 268, 273); male tergite VIII (269, 274); male sternite VIII (270, 275). Scale bars: 260–262: 1.0 mm; 263–277: 0.5 mm.
Figs 208–226 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 208–226: Zyras parvicollis (208–211), Z. ambulans (212–215), Z. nitens, holotype (216–221), and Z. gratellus (Malaysia) (222–226): median lobe of aedeagus in lateral and in ventral view (208–213, 216–217, 222–223); paramere (214, 218, 224); male tergite VIII (219, 225); male sternite VIII (220, 226); apical lobe of paramere (215); postero–median portion of male sternite VIII (221). Scale bars: 208–214, 216–220, 222–226: 0.5 mm; 215, 221: 0.1 mm.
Figs 227–244 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 227–244: Zyras parahirtus (227–228, 231–232), Z. matangensis (229–230, 233), Z. gratellus (Sulawesi) (234–238), and Z. densissimus (239–244): median lobe of aedeagus in lateral and in ventral view (227–230, 234–235, 239–241); paramere (231, 236, 242); male tergite VIII (232, 237, 243); male sternite VIII (233, 238, 244). Scale bars: 227–233, 237–238, 243–244: 0.5 mm; 234–236, 239–242: 0.2 mm.
Figs 191–207 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 191–207: Zyras proximus (191–197; 191–192: Thailand; 193–197: India), Z. novinversus (198–202), Z. brevilobatus (203–205), and Z. parvicollis (206–207): median lobe of aedeagus in lateral and in ventral view (191–194, 198–199, 203–204); paramere (195, 200, 205); male tergite VIII (196, 201, 206); male sternite VIII (197, 202, 207). Scale bars: 0.5 mm.
Figs 156–173 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 156–173: Zyras longilobatus (156–160), Z. latilobatus (161–165), Z. alternans (166–169), and Z. hirtus (170–173; 170–171: Sri Lanka; 172–173: South India): median lobe of aedeagus in lateral and in ventral view (156–157, 161–162, 166–167, 170–173); paramere (158, 163); male tergite VIII (159, 164, 168); male sternite VIII (160, 165, 169). Scale bars: 0.5 mm.
Figs 174–190 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 174–190: Zyras gardneri (174–177), Z. hirsutiventris (178–181), Z. luteipes (182–186), and Z. russiceps (187–190): median lobe of aedeagus in lateral and in ventral view (174–175, 178–179, 182–183, 187–188); male tergite VIII (176, 180, 185, 189); male sternite VIII (177, 181, 186, 190); paramere (184). Scale bars: 0.5 mm.
Figs 117–133 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 117–133: Zyras kraatzi (117–120), Z. exasperatus (121–124), Z. pindarae (125–131), and Z. perforatus (132–133): median lobe of aedeagus in lateral and in ventral view (117–118, 121–122, 125–128, 132–133); male tergite VIII (119, 123, 130); male sternite VIII (120, 124, 131); paramere (129). Scale bars: 0.5 mm.
Figs 134–155 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 134–155: Zyras perforatus (134–135), Z. pallipes (136–139), Z. nigroaeneus, holotype (140–141), Z. condignus (142–147), Z. morvani, holotype (148–149), and Z. truncatus (150–155): male tergite VIII (134, 138, 140, 146, 148, 152); male sternite VIII (135, 139, 141, 147, 149, 153); median lobe of aedeagus in lateral and in ventral view (136–137, 142–143, 150–151); paramere (144–145); female tergite VIII (154); female sternite VIII (155). Scale bars: 0.5 mm.
FIGURE 2. A in Swertia kashmirensis, a new species from Bangus Valley of Kashmir Himalaya, India
FIGURE 2. A—Habit of Swertia kashmirensis; B—Rhizome; C—Lower petiolate cauline leaves; D—Series of upper sessile cauline leaves; E—Flower; F—Sepal (ventral side); G—Sepal (dorsal side); H—Petal with pair of fimbriate nectary (ventral side); I—Petal (dorsal side); J—Nectary with fimbriae at base; K—Stamen with obovate and dorsifixed anther; L—Carpel with bifid stigma; M—Fruit formation; N—Capsule and O—Seeds.
FIGURE 3 in Swertia kashmirensis, a new species from Bangus Valley of Kashmir Himalaya, India
FIGURE 3. Comparison of distinguishing characters between Swertia kashmirensis (A–I) and S. thomsonii (J–R): A & J—Cauline leaves; B & K—Flower; C & L—Pedicel; D & M—Corolla lobe; E & N—Pair of fimbriate nectary on corolla lobe; F, G & O, P—Stamen; H & Q—Capsule; I & R—Seeds.
FIGURE 1. A in Swertia kashmirensis, a new species from Bangus Valley of Kashmir Himalaya, India
FIGURE 1. A–—Map showing distribution of Swertia kashmirensis (diamond shape) and S. thomsonii (circle shape) in Kashmir Himalaya; B—Habit and habitat of S. kashmirensis (Bangus, Kupwara); C—Holotype of S. kashmirensis (KASH 4259); D—Habit and habitat of S. thomsonii (Gulmarg, Baramulla); E—Voucher specimen of S. thomsonii (KASH 4258).
Tropical forest restoration in the Eastern Himalaya: Evaluating early survival and growth of native tree species
<p>Asian tropical forests have among the highest rates of forest loss in the world. Ecological restoration is a vital step for biodiversity maintenance and climate change mitigation. For restoration practice, evaluation of species performance at early stages is crucial to avoid failure of the efforts and for screening species suitable to a region. Though the long-term performance of restoration plantings has been well-documented, few studies have evaluated the performance during the establishment of the planted saplings, especially in South and Southeast Asia. Restoration efforts in Northeast India, a region experiencing high forest loss, is limited by the lack of species-specific data on survival and growth. We compared inter-specific variation in seasonal survival and growth rates (diameter and height) for multiple native rainforest species from this region. We planted 3022 saplings of 50 species at a degraded open forest site. After 18 months, sapling survival varied between 9.1–94.3% for 32 species, and only six species showed "excellent" survival after 18 months. Eight out of 17 species that were tested for seasonal variation in survival showed significant differences in survival between seasons. While the diameter growth rate varied for species between seasons, the height growth rate was different between both species and season, but the interaction term between species and season was not significant. Certain animal-dispersed, medium to large-seeded primary forest species performed well and are vital for future restoration efforts in this region.</p>
FIGURE 5 in On two species of Gymnomitrion (Gymnomitriaceae, Marchantiophyta) in the Eastern Sino-Himalaya
FIGURE 5. Gymnomitrion rubidum subsp. subvittatum Vilnet, Bakalin & D.G. Long: A—mat, dorsal view; B—part of leaf base with 'vitta' cells (reddish rusty colored group of cells); C, E—midleaf cells; D—leaf lobe cells. Scales: for A—5 mm; for B–E—50 µm. A, C, D from Long 20655 (E), B, E from Long 34462 (E).
FIGURE 1 in On two species of Gymnomitrion (Gymnomitriaceae, Marchantiophyta) in the Eastern Sino-Himalaya
FIGURE 1. Phylogram obtained in a maximum likelihood calculation for the genus Gymnomitrion based on ITS1-2+trnL-F dataset. Bootstrap support values of maximum likelihood and maximum parsimony analyses more than 50% and Bayesian posterior probabilities more than 0.50 are indicated. The GenBank accession number (ITS1-2/trnL-F) are provided.
FIGURE 9 in On two species of Gymnomitrion (Gymnomitriaceae, Marchantiophyta) in the Eastern Sino-Himalaya
FIGURE 9. Gymnomitrion rubidum (Mitt.) Váňa, Crand.-Stotl. et Stotler subsp. rubidum: A—plant habit, fragment, lateral view; B— plant habit with sporogonium, fragment, lateral view. Scales: for A—1 mm; for B—1 mm. All from isolectotype (JE 04000310).
FIGURE 7 in On two species of Gymnomitrion (Gymnomitriaceae, Marchantiophyta) in the Eastern Sino-Himalaya
FIGURE 7. Gymnomitrion rubidum (Mitt.) Váňa, Crand.-Stotl. et Stotler subsp. rubidum: A—plant habit, fragment, ventral view; B— plant habit, fragment, dorsal view; C—plant habit, fragment, lateral view; D–L—leaves; M—stem cross-section; N—midleaf cells; O— cells in leaf lobe apex; P—leaf margin cells; Q—cells in leaf base. Scales: a—1 mm for A–C; b—1 mm for D–L; c—100 µm for M–Q. All from V-19-6-18 (VBGI).
FIGURE 6 in On two species of Gymnomitrion (Gymnomitriaceae, Marchantiophyta) in the Eastern Sino-Himalaya
FIGURE 6. Gymnomitrion rubidum subsp. subvittatum Vilnet, Bakalin et D.G. Long: A—plant habit in dorsal and ventral views; B, C—lower part of leaf with 'vitta' cells. Scales: for A—1 mm; for B, C—300 µm. A from Long 20655 (E), B, C from Long 34462 (E).
FIGURE 3 in On two species of Gymnomitrion (Gymnomitriaceae, Marchantiophyta) in the Eastern Sino-Himalaya
FIGURE 3. Gymnomitrion sichuanicum Bakalin & Vilnet: A, B—plant habit, fragment, dorsal view; C–F—leaves. Scales: for A, B—500 μm, C–F—300 μm. All from China-4-2-17 (VBGI).
FIGURE 6 in A new species of the genus Platycleis Fieber, 1853 (Orthoptera: Tettigoniidae) from the Western and Trans Himalayas, India
FIGURE 6. Sternites of female (A) Platycleis rahmoiensis sp. nov. and (B) P. kashmira (image adapted from Uvarov, 1930) fig. 2. page no. 402), (C) anal tergite and (D) lateral view of sternites of Platycleis rahmoiensis sp. nov. Arrows indicate tubercles on sternites.
FIGURE 9 in A new species of the genus Platycleis Fieber, 1853 (Orthoptera: Tettigoniidae) from the Western and Trans Himalayas, India
FIGURE 9. Mirror on the left FW of (A) Platycleis kashmira (Uvarov, 1930) (image adapted from OSF database) and (B) P. rahmoiensis sp. nov.
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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)
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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.