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1,334 results for “Himalaya”

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zenodo36/100

Fig. 22 in Notes on the Nebria subgenus Epinebriola K. DANIEL, 1904 with the description of Barbonebriola subgen. nov. and 13 new species from the Himalaya-Tibet orogen (Coleoptera, Carabidae, Nebriini)

Fig. 22: Nebria (Epinebriola) montisanimae sp. nov. Male paratype.

opencc-by-4.0Jul 2017View details →
zenodo36/100

Fig. 30 in Notes on the Nebria subgenus Epinebriola K. DANIEL, 1904 with the description of Barbonebriola subgen. nov. and 13 new species from the Himalaya-Tibet orogen (Coleoptera, Carabidae, Nebriini)

Fig. 30: Nebria (Epinebriola) delicata sp. nov. Holotype. Scale bar = 5 mm.

opencc-by-4.0Jul 2017View details →
zenodo36/100

Fig. 14 in Notes on the Nebria subgenus Epinebriola K. DANIEL, 1904 with the description of Barbonebriola subgen. nov. and 13 new species from the Himalaya-Tibet orogen (Coleoptera, Carabidae, Nebriini)

Fig. 14: Nebria (Barbonebriola) kagmara sp. nov. Paratype. Scale bar = 5 mm.

opencc-by-4.0Jul 2017View details →
zenodo36/100

Fig. 12 in Notes on the Nebria subgenus Epinebriola K. DANIEL, 1904 with the description of Barbonebriola subgen. nov. and 13 new species from the Himalaya-Tibet orogen (Coleoptera, Carabidae, Nebriini)

Fig. 12: Nebria (Barbonebriola) tenuisulcata sp. nov. Holotype. Scale bar = 5 mm.

opencc-by-4.0Jul 2017View details →
zenodo36/100

Fig. 32 in Notes on the Nebria subgenus Epinebriola K. DANIEL, 1904 with the description of Barbonebriola subgen. nov. and 13 new species from the Himalaya-Tibet orogen (Coleoptera, Carabidae, Nebriini)

Fig. 32: Gonocoxae of Nebria (Epinebriola) delicata sp. nov., in caudal view.

opencc-by-4.0Jul 2017View details →
zenodo36/100

Fig. 7 in Notes on the Nebria subgenus Epinebriola K. DANIEL, 1904 with the description of Barbonebriola subgen. nov. and 13 new species from the Himalaya-Tibet orogen (Coleoptera, Carabidae, Nebriini)

Fig. 7: Nebria (Barbonebriola) rubostipes sp. nov. Holotype. Scale bar = 5 mm.

opencc-by-4.0Jul 2017View details →
zenodo36/100

Data from: Influence of Check Dams on the Activity Pattern and Morphometric Traits of Overwintering Tadpoles in the Western Himalaya

<p>Dataset for the paper: Influence of Check Dams on the Activity Pattern and Morphometric Traits of Overwintering Tadpoles in the Western Himalaya. See readme.txt for details.</p>

opencc-by-4.0Mar 2022View details →
zenodo36/100

Glacier_inventory_debris_cover_ice_thickness_dataset_Chandra_Bhaga_basin_Himalaya

<p>This is a multitemporal glacier dataset over ChandraBhaga basin in western Himalaya which includes glacier inventory (for 251 glaciers with area &gt; 0.5 km<sup>2</sup>) for year 1993, 2000, 2010 and 2019 (.shp files);&nbsp;debris cover&nbsp;for year 1993 and 2019 (.tif files) and ice thickness&nbsp;(.tif&nbsp;files). Details of files are included in data_description.docx. These datasets form part of manuscript submitted to Earth Systems and Science Data.</p>

opencc-by-4.0May 2022View details →
dryad36/100

Global warming pushes the distribution range of the two alpine 'glasshouse' Rheum species north- and upwards in the Eastern Himalayas (EH) and the Hengduan Mountains (HM)

<p><span>Alpine plants' distribution is being pushed higher towards mountaintops due to global warming, finally diminishing their range and thereby increasing the risk of extinction. Plants with specialized 'glasshouse' structures have adapted well to harsh alpine environments, notably to the extremely low temperatures, which makes them vulnerable to global warming. </span><span>How</span><span>ever, their response to global warming is quite unexplored. Therefore, by compiling occurrences and several environmental strata, we utilized multiple ensemble species distribution modeling (eSDM) to estimate the historical, present-day, and future distribution of two alpine 'glasshouse' species <em>Rheum nobile</em> Hook. f. &amp; Thomson and <em>R. alexandrae</em> Batalin. <em>Rheum nobile</em> was predicted to extend its distribution from the Eastern Himalaya (EH) to the Hengduan Mountains (HM), whereas <em>R. alexandrae</em> was restricted exclusively in the HM. Both species witnessed a northward expansion of suitable habitats followed by a southerly retreat in the HM region. Our findings reveal that both species have a considerable range shift under different climate change scenarios, mainly triggered by precipitation rather than temperature. The model predicted northward and upward migration for both species since the last glacial period which is mainly due to expected future climate change scenarios. Further, the observed niche overlap between the two species presented that they are more divergent depending on their habitat, except for certain regions in the HM. However, relocating appropriate habitats to the north and high elevation may not ensure the species' survival, as it needs to adapt to the extreme climatic circumstances in alpine habitats. Therefore, we advocate for more conservation efforts in these biodiversity hotspots.</span></p>

opencc-zeroAug 2022View details →
zenodo36/100

Thermochronology dataset for Himalaya

<p>Dataset from the Himalaya comprises 1785 thermochronologic ages compiled from papers published through July 2022; full data sources are provided in the associated file. We have excluded some reported ages from the Siwaliks (Sub-Himalayan fold-thrust belt), as that sedimentary unit commonly yields unreset ages. We have also excluded the western and eastern syntaxis regions, where extremely rapid exhumation is driven by processes that are different from those in the main part of the Himalaya (Zeitler et al., 2014; Butler, 2019). Finally, we exclude any pre-Himalayan ages (&gt; 60 Ma), as these are not directly linked to exhumation during Himalayan mountain building. The dataset comprises 345 white mica <sup>40</sup>Ar/<sup>39</sup>Ar&nbsp;ages, 236 ZFT ages, 783 AFT ages, 281 ZHe ages, and 140 AHe ages. Data are provided in an Excel worksheet.</p>

opencc-by-4.0Sep 2022View details →
dryad36/100

Elevational range of mammals, birds, and amphibians in the Himalayas

<p><span>The lowest and highest elevations known for each species are used to delineate its elevational limits. We assume that species potentially exist between their elevational limits. For species that have a single elevational distribution record (resulting in an elevational range of zero) as well as those with elevational ranges less than 200 m, we adjusted their elevation ranges to 200 m. We verified all data for accuracy by experts within the region and any dubious outlying records were removed. Elevational limits were given for 1,488 species, including 314 mammals, 1027 birds, and 147 amphibians in the Himalayas.</span></p>

opencc-zeroDec 2021View details →
zenodo36/100

Fig. 6 in Ichthyofaunal Diversity Of A Ramsar Site In Kashmir Himalayas - Wular Lake

Fig. 6. Graphical representation of Diversity indices.

opencc-by-4.0Jun 2024View details →
zenodo36/100

Figure 6 in Morphometric studies of subgenus Bombus (s. str.) (Hymenoptera: Apidae) from Indian Himalaya

Figure 6. Comparative morphometric parameters of legs of Bombus tunicatus and Bombus jacobsoni.

opencc-by-4.0Dec 2022View details →
zenodo36/100

Figure 3 in Morphometric studies of subgenus Bombus (s. str.) (Hymenoptera: Apidae) from Indian Himalaya

Figure 3. Morphometric parameters of Bombus tunicatus.

opencc-by-4.0Dec 2022View details →
zenodo36/100

Figure 1 in Morphometric studies of subgenus Bombus (s. str.) (Hymenoptera: Apidae) from Indian Himalaya

Figure 1. Map showing the survey areas in Union Territory of Jammu and Kashmir.

opencc-by-4.0Dec 2022View details →
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Figure 4 in Morphometric studies of subgenus Bombus (s. str.) (Hymenoptera: Apidae) from Indian Himalaya

Figure 4. Morphometric parameters of Bombus jacobsoni.

opencc-by-4.0Dec 2022View details →
zenodo36/100

Figure 5 in Morphometric studies of subgenus Bombus (s. str.) (Hymenoptera: Apidae) from Indian Himalaya

Figure 5. Comparative morphometric parameters of wings of Bombus tunicatus and Bombus jacobsoni.

opencc-by-4.0Dec 2022View details →
zenodo36/100

Figure 2 in Morphometric studies of subgenus Bombus (s. str.) (Hymenoptera: Apidae) from Indian Himalaya

Figure 2. Map showing the survey areas of Himachal Pradesh.

opencc-by-4.0Dec 2022View details →
zenodo36/100

Figure 3. Camera trap 2 in Evidence of presence of Marbled Cat Pardofelis marmorata (Martin, 1837) in Neora Valley National Park, Central Himalaya, India

Figure 3. Camera trap 2 recording the second individual.

opencc-by-4.0Dec 2019View details →
zenodo36/100

Figure 3 in First photographic evidence of Panthera tigris from Neora Valley National Park, Central Himalayas, India

Figure 3. Recorded tiger left view at Kattus Dara, Neora Valley National Park.

opencc-by-4.0Dec 2020View details →

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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.

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Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

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Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

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Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record