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711 results for “Tibetan”
Phenotypic trait variation of Herminium monorchis in the Qinghai-Tibetan Plateau with grazing intensity and climatic conditions
This data set contains raw data supporting the research entitled “Livestock grazing outweighs climate in driving trait variation of a widespread alpine plant” (currently under peer review), which documents how phenotypic traits of a widespread herbaceous plant in the Qinghai-Tibetan Plateau, Herminium monorchis, vary with grazing intensity and environmental conditions.
Figure 2 in Reproductive ecology of a Tibetan frog Nanorana parkeri (Anura: Ranidae)
Figure 2. Typical habitats used by the frogs, and spatial locations of the hibernation (closed circles) and spawning (open circles) ponds in the study plot (100 × 55 m). Sizes of the circles represent pond area.
A part-of-speech (POS) tagged corpus of Classical Tibetan
<p>This part-of-speech (POS) tagged corpus of Classical Tibetan was prepared in the course of the research project 'Tibetan in Digital Communication' (2012-2015) hosted at SOAS, University of London and funded by the UK's Arts and Humanities Research Council (grant code: AH/J00152X/1). For a description of the tag set see Garrett et al. 2014. and Garrett et al. 2015. This corpus includes the <em>Mdzaṅs blun</em> (9th century, canonical), the <em>Bu ston chos ḥbyuṅ</em> (13th century, ecclesiastical history), the <em>Mi la ras paḥi rnam thar</em> and <em>Mar paḥi rnam thar</em> (15th century, biography).</p>
A rule based Tibetan part-of-speech (POS) tagger for the creation of gold standard training data
<p>This rule based Tibetan part-of-speech (POS) tagger was prepared in the course of the research project 'Tibetan in Digital Communication' (2012-2015) hosted at SOAS, University of London and funded by the UK's Arts and Humanities Research Council (grant code: AH/J00152X/1). For a description of the tag set see Garrett et al. 2014. and Garrett et al. 2015. For a description of the tagger itself see Garrett et al. 2014. Note that the tagger must be used together with a lexicon (for example Hill & Garrett 2017a). One must use one's own script to tag all words with all tags in the lexicon and then apply the tagger to remove incorrect tags.</p> <p>On the associated corpus of 318,230 words (Hill & Garrett 2017b) the lexical tagger (i.e. simply applying all available tags to all words) tags 141,911 words with the correct unique tag, achieves as accuracy of 1.000 (by definition getting the right tag among others for each word) with an ambiguity of 2.73111. In contrast, the Rule Tagger tags 241,256 words with the correct unique tag, achieves an accuracy of 0.99893 and an ambiguity of 1.38577.</p> <p>Because this tagger does not achieve ambiguity 1.000 it is not suitable for tagging large scale corpora, but instead is useful for the creation of gold standard training data.</p> <p>N.B. In some rare cases the tagger removes all POS-tags.</p>
Comparative wordlist of Tibetan dialects
<p>This is a collection of Tibetan dialect material compiled by Roland Bielmeier and his collaborators, mostly from existing sources, but also making use of original fieldwork.</p>
Figure 10 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 10. Species ranges, phyletic relationship, and zoogeographical positions of the Paradicrocerus–Stephanocemas clade. Most of the species ranges are approximate. Phyletic relationship is based on one of the shortest trees in our cladistic analysis, and some indeterminate taxa not included in the cladogram are inserted here based on our estimates of their relationships. The antlers are scaled to their approximate relative size, and dashed lines are mostly our own reconstructions of missing tines.
Figure 9 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 9. Strict consensus of four shortest trees (tree length = 12) of the Paradicrocerus–Stephanocemas clade found by the branch and bound option of the PAUP program on a ten taxa ¥ nine characters data matrix (Table 1).
Figure 8. IVPP V15726 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 8. IVPP V15726, Stephanocemas sp. from IVPP locality CD0406. A, dorsal, and B, ventral views of antler fragment. Scale is for both views.
Figure 6. IVPP V15724 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 6. IVPP V15724, referred specimen of Stephanocemas palmatus sp. nov. A, dorsal, B, ventral, and C, medial views of posterior palm portion of a juvenile antler.
Figure 7. IVPP V15725 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 7. IVPP V15725, Stephanocemas sp. from IVPP locality CD9818. A, stereophoto of dorsal view, B, lateral view, and C, ventral view of partial antler.
Figure 5. IVPP V15723 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 5. IVPP V15723, referred specimen of Stephanocemas palmatus sp. nov. A, dorsal, and B, ventral views of palm portion of antler.
Figure 4. IVPP V15722 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 4. IVPP V15722, left antler without pedicel, holotype of Stephanocemas palmatus sp. nov. from Qaidam Basin, northern Tibetan Plateau. A, medial, and B, ventral views. Left is posterior and right is anterior.
Figure 3 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 3. Stereophoto of dorsal view of IVPP V15722, left antler without pedicel, holotype of Stephanocemas palmatus sp. nov. from Qaidam Basin, northern Tibetan Plateau. Top is posterior and bottom is anterior.
Figure 2 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 2. Satellite image of the Barun Yawula anticline, with key fossil localities and their relative stratigraphical positions indicated. The east–west trending fold is asymmetrical with the south limb dipping more steeply than the north limb. A prominent resistant bed (a dark–light band combination, indicated by black dashed lines) within the rusty green sandstones layers helps to trace stratigraphical relationships between localities in eastern and western ends of the anticline, although multiple faults (with offsets ranging from 50 to 500 m), particularly those in the eastern end, complicate correlations. White lines are the measured section.
Frictional properties of natural granite fault gouge under hydrothermal conditions: A case study of strike-slip fault from Anninghe Fault zone, southeastern Tibetan Plateau
<p>We performed friction experiments on natural granite gouge under hydrothermal conditions to investigate roles of the Anninghe Fault (ANHF) on seismogenesis in the continental crust. In this dataset, we report processed data after correction. Detailed information about the files in the zip-files is given in the explanatory file Lei-et-al-2023-Data-Description.pdf.</p>
FIG. 2. — Sporoschisma lignicola R.J in Two new freshwater hyphomycetous species of Sporoschisma Berk. & Broome (Chaetosphaeriales) from Tibetan Plateau, China
FIG. 2. — Sporoschisma lignicola R.J.Xu & Q.Zhao, sp. nov. (holotype, HKAS 129208): A, colonies on substrate; B, D, conidiophores with conidia; C, conidiophores with setae; E-G, conidia; H, conidiogenous cell; I, culture on PDA. Scale bars: B-D, 50 μm; E-H, 20 μm.
FIG. 1 in Two new freshwater hyphomycetous species of Sporoschisma Berk. & Broome (Chaetosphaeriales) from Tibetan Plateau, China
FIG. 1. — RAxML tree based on analysis of combined ITS, LSU and TEF1-α sequences. Bootstrap support values for maximum likelihood (ML) equal to or greater than 75% were given above the nodes (left). Bayesian posterior probability (PP) equal to or greater than 0.95 were given above the nodes (right) and hyphen (-) were marked as values below 0.95. The tree was rooted to Adautomilanezia caesalpiniae LAMIC 010212. The type strains were shown in bold, and the newly generated isolates were shown in red.
FIG. 3. — Sporoschisma verruculosa R.J in Two new freshwater hyphomycetous species of Sporoschisma Berk. & Broome (Chaetosphaeriales) from Tibetan Plateau, China
FIG. 3. — Sporoschisma verruculosa R.J.Xu & Q.Zhao, sp. nov. (holotype, HKAS 129210): A, B, colony on wood with long conidia chains; C, D, conidiophores with setae; E, conidiophores with conidia; F, G, conidiogenous cell with a conidium; H-M, conidia; N, culture on PDA. Scale bars: C-E, 50 μm; F-M, 20 μm.
Figures 1 in Biogeographical affinities and evolution of terrestrial fauna in the Qinghai-Tibetan Plateau and the Himalayas: a case study of Aphidomorpha
Figures 1. Generalized tracks and nodes based on the global distributions of aphid species in the QTPH. Generalized tracks are indicated by colored lines, and nodes are indicated with orange dots. A generalized track is a summary of replicated distribution patterns of different taxa (species); a node is a distribution area where two or more generalized tracks intersect. Generalized tracks and nodes together indicate biogeographical affinities between aphid faunas in the QTPH and other regions.
Figures 11–18 in Two new species of Eryciini (Diptera: Tachinidae) from the Eastern edge of the Qinghai-Tibetan Plateau, China
Figures 11–18. Lydella gannanensis sp. nov., male. 11–12. Body in dorsal and lateral views. 13–14. Head in anterior and lateral views. 15. Sternite 5. 16–17. Cerci, surstyli and epandrium in lateral and caudal views. 18. Bacilliform sclerite, ejaculatory apodeme, hypandrium, phallapodeme, pregonite, postgonite, basiphallus, distiphallus, epiphphallus, and acrophallus in lateral view. Scale bars: 11–14 = 1.0 mm, 15–18 = 0.2 mm.
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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)
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.