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66 results for “Nepal Himalayas”
Major ions in Trambau ice core, Nepal Himalaya
<p>An 81.2-m-long ice core was drilled in November 2019 at 5862m a.s.l. of Trambau Glacier, Rolwaling region, Nepal Himalaya (27.919° N, 86.545° E). This data set contains the concentrations of major ions and tritium concentrations in the ice core.</p> <p>The data set contains Depth in snow/ice (m), Depth in water equivalent (m w.e.), Date (digit year), Na (ppb), Cl (ppb), NH4 (ppb), K (ppb), Mg (ppb), Ca (ppb), NO3 (ppb), SO4 (ppb), T_rough (TU), T_fine (TU)</p>
Seismic and meteorological records from Trakarding-Trambau Glacier system, Nepal Himalaya (October 21 - November 9, 2017)
<p>The following geophysical field data (collected between October 21 and November 9, 2017) at Trakarding-Trambau Glacier system in Nepal Himalaya is provided in this dataset: </p> <p> </p> <p>(1) Hourly air-temperature measured at four sites (AWS, T1, T2 and T3). Units are degrees Celcius. Local time.</p> <p>[file name] Hourly_Air_temperature_AWS_T1_T2_T3_degC.csv</p> <p> </p> <p>(2) Hourly wind speed measured at the AWS site. Units are meters per second. Local time.</p> <p>[file name] Hourly_Wind_speed_AWS_MperS.csv</p> <p> </p> <p>The aforementioned stations had the following dGPS-derived coordinates:</p> <p>{Station, lat [deg], lon [deg], elevation [m] }</p> <p>AWS, 27.84356265, 86.4867231, 4805.582206</p> <p>T1, 27.84575824, 86.49189978, 4591.4429</p> <p>T2, 27.82976456, 86.51989785, 4768.8465</p> <p>T3, 27.855872, 86.531197, 5390.48</p> <p> </p> <p>(3) Raw seismic data (vertical component) recorded at five locations (DAM, C1, C2, C3, and C4) by four data-loggers (AKX, AKS, AKT, AKU) with a sampling frequency of 400 Hz. The file format (*.pri0) corresponds to a standard [.mseed]-format. Units are counts representing velocity. UTC time.</p> <p> </p> <p>The aforementioned stations had the following dGPS-derived coordinates:</p> <p>{StationName-Logger, lat [deg], lon [deg], elevation [m] }</p> <p> </p> <p>DAM-AKX, 27.870954, 86.463243, 4375.030762</p> <p>C1-AKS, 27.84546885, 86.49247316, 4594.0462</p> <p>C2-AKT, 27.82939476, 86.52001441, 4777.5211</p> <p>C3-AKU, 27.83593425, 86.53248327, 5288.3311</p> <p>C4-AKX, 27.87962877, 86.542076, 5555.2085</p>
Figures 3–8 in A new erigonine genus from the Nepal Himalayas (Araneae, Linyphiidae)*
Figures 3–8. Left palp details of Parbatthorax unicornis sp. nov., holotype. 3, 4- Palp, retrolateral and prolateral views, respectively; 5, 6- Embolic division and distal suprategular apophysis, prolateral and retrolateral views, respectively; 7- Palpal tibia, dorsal view; 8- Paracymbium, lateral view. Scale bar = 0.1 mm.
Figures 1 and 2 in A new erigonine genus from the Nepal Himalayas (Araneae, Linyphiidae)*
Figures 1 and 2. Male body of Parbatthorax unicornis sp. nov., holotype. 1- Lateral view; 2- Dorsal view. Scale bar = 0.5 mm.
Digital elevation models, ortho images and outlines of Yala Glacier, Langtang Valley, Nepal Himalaya
<p>Datasets related to article "Up-glacier propagation of surface lowering of Yala Glacier, Langtang Valley, Nepal Himalaya". The data includes three digital elevation models (DEM), two ortho images and five outlines of Yala Glacier between 1981 and 2015.<br> </p> <p>Description of files:<br> 1) DEM and ortho image</p> <p>- 1981Yala_dem_20_-10_bias_cor.tif: 10 m resolution digital elevation model derived from a map that was generated using ground phogogrammetry images that were acquired in 1981 (Yokoyama, 1984; Fujita and Nuimura).</p> <p>- 2007Yala_dem_0_-4_bias_cor.tif: 2 m resolution digital elevation model derived from 14 oblique photographs that were acquired by a private jet with handheld cameras in 2007.<br> - 2007Yala_ortho.tif: an ortho images derived by the same data in 2007.</p> <p>- 2015Yala_dem_0_0_bias_cor.tif: 1 m resolution digital elevation model derived from 519 photographs that were acquired by a UAV-based photogrammetric survey in 2015.<br> - 2015Yala_ortho.tif: an ortho images derived by the same data in 2015.<br> <br> 2) Glacier boundary (shapefile Files)</p> <p>- Yala_area_1981: <br> - Yala_area_2007:<br> - Yala_area_2009:<br> - Yala_area_2012:<br> - Yala_area_2015:<br> <br> <br> Please see the related journal article for details on datasets.<br> <br> Sunako, S., Fujita, K., Izumi, T., Yamaguchi, S., Sakai, A., & Kayastha, R. (2023). Up-glacier propagation of surface lowering of Yala Glacier, Langtang Valley, Nepal Himalaya. Journal of Glaciology, 69(274), 425-432. doi:10.1017/jog.2022.118<br> </p>
Eocene Metamorphism and Anatexis in the Kathmandu Klippe, central Nepal: Implications for early crustal thickening and initial rise of the Himalaya
<p><strong>Rock samples were collected in Kathmandu Nepal in summer of 2016 and 2017. The monazite trace elements and ages data were analyzed at the Institute of Geology and Geophysics, Chinese Academy of Sciences by Gautam Prashad Khanal and Jia-Min Wang in 2019.</strong></p>
Data from: Flower colour and phylogeny along an altitudinal gradient in the Himalaya of Nepal
1. Both the phylogenetic structure and trait composition of flowering plant communities may be expected to change with altitude. In particular, floral colours are thought to vary with altitude because Hymenoptera typically decline in importance as pollinators while Diptera and Lepidoptera become more important at higher elevations. Thus, ecological filtering among elevation zones and competitive processes among co-occurring species within zones could influence the floral chromatic cues present at low and high elevations. 2. We collected data from 107 species of native flowering plants in the Himalaya mountains of central Nepal over an elevation range of 900-4100 m, which includes habitat ranging from subtropical to subalpine within a relatively small geographical area. 3. There was significant phylogenetic clustering in the communities as a result of monocots, particularly orchids, which were found overwhelmingly at lower elevations. Phylogenetic signal for floral colours indicated that related species had colours that were more disparate than expected under Brownian motion evolution. Floral colours were significantly more diverse in the higher elevation subalpine zone than in the subtropical zone. However, the chromatic cues at both elevations were consistent with the hue discrimination abilities of the trichromatic hymenopteran visual system. 4. Synthesis. Flower colour is not highly differentiated between subtropical and subalpine vegetation due to differences in the available orders of insect pollinators, or by the rate or direction of color evolution in the lineages composing the two communities. Differences in colour diversity between zones may reflect differences in the ecologically available morphospace based on pollinator species richness and the constancy of their foraging behaviour. The chromatic signals present in Nepali species are similar to the signals found in insect-pollinated floras of other regions of the world.
FIGURES 24–29 in Pristosia Motschulsky, 1865 from the Nepal Himalaya: Taxonomy and Biogeography (Coleoptera: Carabidae: Sphodrini)
FIGURES 24–29. Pristosia spp., aedeagal median lobe, dorsal view (Figs. 24, 26, 28) and left lateral view (Figs. 25, 27, 29, the internal sac is figured only in dorsal view). Figs. 24, 25, P. s i m i l a t a sp. n., Paratype. Figs. 26, 27, P. a trema (Andrewes, 1926), Holotype. Figs. 28, 29, P. a t re m a (Andrewes, 1926), non-type, India, Pindar Valley. Scale bar = 1 mm.
FIGURES 5–15. Pristosia spp., pronotum. Fig. 5, P. dahud polita ssp. n in Pristosia Motschulsky, 1865 from the Nepal Himalaya: Taxonomy and Biogeography (Coleoptera: Carabidae: Sphodrini)
FIGURES 5–15. Pristosia spp., pronotum. Fig. 5, P. dahud polita ssp. n., Paratype, male. Fig. 6, P. dahud Morvan, 1994, non-type, male, Rara Lake. Fig. 7, P. dahud Morvan, 1994, non-type, male, Maharigaon. Fig. 8, P. dahud Morvan, 1994, non-type, male, Khari Lagna (transitional form). Fig. 9, P. dahud Morvan, 1994, non-type, male, Khari Lagna (typical form). Fig. 10, P. similata sp. n., Paratype, male. Fig. 11, P. glabella sp. n., Paratype, male. Fig. 12, P. amaroides (Putzeys, 1877), non-type, female, India, Darjeeling. Fig. 13, P. a t re m a (Andrewes, 1926), Holotype. Fig. 14, P. nepalensis sp. n., Paratype, male. Fig. 15, P. championi (Andrewes, 1934), Holotype. Scale bar = 2 mm.
FIGURES 36–41 in Pristosia Motschulsky, 1865 from the Nepal Himalaya: Taxonomy and Biogeography (Coleoptera: Carabidae: Sphodrini)
FIGURES 36–41. Pristosia spp., aedeagal median lobe, dorsal view (Figs. 36, 38, 40) and left lateral view (Figs. 37, 39, 41, the internal sac is figured only in dorsal view). Figs. 36, 37, P. dahud Morvan, 1994, non-type, Maharigaon. Figs. 38, 39, P. dahud Morvan, 1994, non-type, Rara Lake. Figs. 40, 41, P. glabella sp. n., Holotype. Scale bar = 1 mm.
FIGURES 16–23 in Pristosia Motschulsky, 1865 from the Nepal Himalaya: Taxonomy and Biogeography (Coleoptera: Carabidae: Sphodrini)
FIGURES 16–23. Pristosia spp., aedeagal median lobe, dorsal view (Figs. 16, 18, 20, 22) and left lateral view (Figs. 17, 19, 21, 23, with exception of P. crenata, the internal sac is figured only in dorsal view). Figs. 16, 17, P. championi (Andrewes, 1934), Holotype. Figs. 18, 19, P. nepalensis sp. n., Paratype. Figs. 20, 21, P. crenata (Putzeys, 1873), nontype, Nepal, Dailekh. Figs. 22, 23, P. amaroides (Putzeys, 1877), non-type, Nepal, Deorali to Sheldoti. Scale bar = 1 mm.
FIGURES 30–35 in Pristosia Motschulsky, 1865 from the Nepal Himalaya: Taxonomy and Biogeography (Coleoptera: Carabidae: Sphodrini)
FIGURES 30–35. Pristosia spp., aedeagal median lobe, dorsal view (Figs. 30, 32, 34) and left lateral view (Figs. 31, 33, 35, the internal sac is figured only in dorsal view). Figs. 30, 31, P. dahud polita ssp. n., Paratype. Figs. 32, 33, P. dahud Morvan, 1994, non-type, Khari Lagna (transitional form). Figs. 34, 35, P. dahud Morvan, 1994, non-type, Khari Lagna (typical form). Scale bar = 1 mm.
FIGURES 1–4. Pristosia spp., habitus. Fig. 1, P in Pristosia Motschulsky, 1865 from the Nepal Himalaya: Taxonomy and Biogeography (Coleoptera: Carabidae: Sphodrini)
FIGURES 1–4. Pristosia spp., habitus. Fig. 1, P. crenata (Putzeys, 1873), non-type, male, Nepal, Dailekh. Fig. 2, P. amaroides (Putzeys, 1877), non-type, female, India, Darjeeling. Fig. 3, P. glabella sp. n., Paratype, female. Fig. 4, P. nepalensis sp. n., Paratype, male. Scale bar = 5 mm.
FIGURE 2 in Koponenius gen. nov., a new genus of the millipede family Haplodesmidae from the Himalayas of India and Nepal (Diplopoda: Polydesmida)
FIGURE 2. Koponenius unicornis sp. nov., male paratype. A, D, E, H, Q: anterior body part, lateral, ventral, ventral, dorsal and ventral views, respectively. B, F, I: midbody segments, lateral, ventral and dorsal views, respectively. C, G, J, K: posterior body part, lateral, ventral, dorsal and dorsal views, respectively. L: head, ventral view. M: cross-section of a midbody segment. N–P: tergal texture, dorsal views. R: midbody leg, subventral view. Scale bars: B, C, F, G, I, M, 0.5 mm; A, D, E, H, J–L, 0.2 mm; P–R, 0.1 mm; N, 0.05 mm; O, 0.02 mm.
FIGURE 1 in Koponenius gen. nov., a new genus of the millipede family Haplodesmidae from the Himalayas of India and Nepal (Diplopoda: Polydesmida)
FIGURE 1. Habitus of Koponenius unicornis sp. nov., male paratype. A: dorsal view. B: lateral view. Pictures by K. Makarov, not taken to scale.
FIGURE 8 in Koponenius gen. nov., a new genus of the millipede family Haplodesmidae from the Himalayas of India and Nepal (Diplopoda: Polydesmida)
FIGURE 8. Koponenius biramus sp. nov., male paratype. A: leg 6, lateral view. B: left gonopod, submesal view. Scale bar: 0.2 mm. Designations explained in text.
FIGURE 4 in Koponenius gen. nov., a new genus of the millipede family Haplodesmidae from the Himalayas of India and Nepal (Diplopoda: Polydesmida)
FIGURE 4. Koponenius unicornis sp. nov., male paratype. A: leg 7, lateral view. B: left gonopod, mesal view. Scale bar: 0.3 mm. Designations explained in text.
FIGURE 5 in Koponenius gen. nov., a new genus of the millipede family Haplodesmidae from the Himalayas of India and Nepal (Diplopoda: Polydesmida)
FIGURE 5. Habitus of Koponenius biramus sp. nov., male paratype, lateral view. Picture by K. Makarov, not taken to scale.
FIGURE 3 in Koponenius gen. nov., a new genus of the millipede family Haplodesmidae from the Himalayas of India and Nepal (Diplopoda: Polydesmida)
FIGURE 3. Koponenius unicornis sp. nov., male paratype. A–D: gonopods, lateral, ventral, lateral and mesal views, respectively. Scale bars: B, 0.5 mm; D, 0.2 mm; A, C, 0.1 mm. Designations explained in text.
FIGURE 6 in Koponenius gen. nov., a new genus of the millipede family Haplodesmidae from the Himalayas of India and Nepal (Diplopoda: Polydesmida)
FIGURE 6. Koponenius biramus sp. nov., male paratype. A, D, G, J: anterior body part, dorsal, lateral, ventral and frontoventral views, respectively. B, E, H: midbody segments, dorsal, lateral and ventral views, respectively. C, F, I: posterior body part, dorsal, lateral and ventral views, respectively. K: cross-section of a midbody segment. L: tergal texture, dorsal view. M: ozopore region, dorsolateral view. Scale bars: H, 0.5 mm; A–G, I–L, 0.2 mm; N, 0.05 mm; L, 0.02 mm.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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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.