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1,029 results for “altitude”
Analysis of Transcriptional Responses to Altitude-Induced Hypoxia in Bronchial Epithelium, Bronchio-Alveolar Cells, and Blood Reveals Differences Between Smokers and Nonsmokers [blood]
GEO Series GSE120906. Homo sapiens. 153 samples. Type: Expression profiling by array.
Intermittent short-duration reoxygenation protects against simulated high altitude-induced pulmonary hypertension in rats
GEO Series GSE160926. Rattus norvegicus. 12 samples. Type: Expression profiling by high throughput sequencing.
Circulating microRNAs as a signature predicting the occurrence of Acute Mountain Sickness before exposure to high altitude
GEO Series GSE90500. Homo sapiens; Mus musculus; Rattus norvegicus. 22 samples. Type: Non-coding RNA profiling by array.
Transcriptomic Modifications in Developmental Cardiopulmonary Adaptations to Chronic Hypoxia Using a Murine Model of Simulated High Altitude Exposure
GEO Series GSE140146. Rattus norvegicus. 54 samples. Type: Expression profiling by high throughput sequencing.
Whole transcriptomic landscape and regulatory network of High-Altitude Pulmonary Edema
GEO Series GSE260910. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
FIGURE 3. A–B in Qorimayus, a new genus of relictual, high-altitude harvestmen from western Argentina (Arachnida, Opiliones, Gonyleptidae) reveals trans-Andean phylogenetic links
FIGURE 3. A–B: Qorimayus alticola (Ringuelet, 1962) comb. nov., holotype ♂ (MACN), A: right leg IV (coxa to tibia), prolateral view. B: Left tibia and patella IV, retrolateral view. Scale bars: 1 mm. C–E: schematic representation (not at scale) of characters #30 (coxa III, length relative to coxa II) and #31 (relative length of apical Cx II projected onto Cx III width). Dashed vertical lines: projection of landmarks X and Y, as referred to in the characters list (Table 2), the portion of coxa III surpassing X is shaded. Arc (α): projection of the apical coxa II onto coxa III width. C: Tricommatus brasiliensis Roewer, 1912 (from Kury 2014), #30=0, #31=2; D: Eusarcus hastatus Sørensen, 1884, #30=0, #31=2; E: Cynorta conspersa (Perty, 1833) (from Kury et al. 2007), #30=2, #31=1.
deodara and permafrost soil data set of high altitude
<p>This is 16s rRNA amplicon sequences obtained by Dr. Ashwani Kumar</p>
UDWA:UAV Dataset with Altitude Part2
<p>A high-resolution UAV dataset with altitude</p>
Subspecies and Distribution. L. t. timidus Linnaeus, 1758 — Scandinavia S to 59° N, N Russia (S to 57° N to 58° N) to E of Ural Mts, Estonia, perhaps Poland, and Altai and Beita Mts in N Xinjiang (China); from Sweden extending in hybrid zones with the subspecies sylvaticus to S coast of Norway and W Latvia. L. t. abet Kuroda, 1938 — Kurile Is (Russia). L. t. ainu Barrett-Hamilton, 1900 — Hokkaido (Japan). L. t. begitschevi Koljuschev, 1936 — Taimyr Peninsula (Russia). L. t. gichiganus J. A. Allen, 1903 — C Yakutia, Kamchatka and Okhotsk Sea coast (Russia). L. t. hibernicus Bell, 1837 — Ireland. L. t. kolymensis Ognev, 1922 — NE Siberia (Russia). L. t. kozhevnikovi Ognev, 1929 — C Russia from 57° to 58°N, whereit intergrades with the nomonotypical timidus S to 53° N. The W boundary is unclear. L. t. lugubris Kastschenko, 1899 — Siberian Altai Mts (Russia). L. t. mordeni Goodwin, 1933 — Russian Far East (Ussuri Valley and lower and middle Amur River) and Heilongjiang (China). L. t. ori Kuroda, 1928 — Sakhalin (Russia). L. t. scoticus Hilzheimer, 1906 — Scotland. L. t. sibiricorumJohansen, 1923 — W & SW Siberia (Russia), N Kazakhstan, and Tacheng Mts in N Xinjiang (China). L. t. sylvaticus Nilsson, 1831 —S Sweden, extending in hybrid zones with nominotypical timidus to S coast of Norway and W Latvia. L. t. transbaikalicus Ognev, 1929 — Trans-Baikal region in E Siberia (Russia) and E Inner Mongolia (= Nei Mongol, China). L. t. varronis Miller, 1901 — at high altitudes in the Alps, C Europe. in Leporidae
Subspecies and Distribution. L. t. timidus Linnaeus, 1758 — Scandinavia S to 59° N, N Russia (S to 57° N to 58° N) to E of Ural Mts, Estonia, perhaps Poland, and Altai and Beita Mts in N Xinjiang (China); from Sweden extending in hybrid zones with the subspecies sylvaticus to S coast of Norway and W Latvia. L. t. abet Kuroda, 1938 — Kurile Is (Russia). L. t. ainu Barrett-Hamilton, 1900 — Hokkaido (Japan). L. t. begitschevi Koljuschev, 1936 — Taimyr Peninsula (Russia). L. t. gichiganus J. A. Allen, 1903 — C Yakutia, Kamchatka and Okhotsk Sea coast (Russia). L. t. hibernicus Bell, 1837 — Ireland. L. t. kolymensis Ognev, 1922 — NE Siberia (Russia). L. t. kozhevnikovi Ognev, 1929 — C Russia from 57° to 58°N, whereit intergrades with the nomonotypical timidus S to 53° N. The W boundary is unclear. L. t. lugubris Kastschenko, 1899 — Siberian Altai Mts (Russia). L. t. mordeni Goodwin, 1933 — Russian Far East (Ussuri Valley and lower and middle Amur River) and Heilongjiang (China). L. t. ori Kuroda, 1928 — Sakhalin (Russia). L. t. scoticus Hilzheimer, 1906 — Scotland. L. t. sibiricorumJohansen, 1923 — W & SW Siberia (Russia), N Kazakhstan, and Tacheng Mts in N Xinjiang (China). L. t. sylvaticus Nilsson, 1831 —S Sweden, extending in hybrid zones with nominotypical timidus to S coast of Norway and W Latvia. L. t. transbaikalicus Ognev, 1929 — Trans-Baikal region in E Siberia (Russia) and E Inner Mongolia (= Nei Mongol, China). L. t. varronis Miller, 1901 — at high altitudes in the Alps, C Europe.
FIGURES 1‑3 in Bolivian Rhinotragini Vii: Provisional Report Of Higher Altitude Species (Coleoptera, Cerambycidae) With Descriptions Of New Taxa
FIGURES 1‑3: 1, Acyphoderes amboroensis sp. nov.: A = male holotype. 2, Isthmiade mariahelenae sp. nov.: A = male holotype, B = female paratype. 3, Chrysaethe lazzoi sp. nov.: A = male holotype, B = female paratype, C = male paratype (colour variety).
Fig. 2 in Age and body size of Salamandrella keyserlingii (Caudata: Hynobiidae): a difference in altitudes, latitudes, and temperatures
Fig. 2 Frequency distribution of body size for each sex or age class. Snout–posterior vent length (SPVL) was provided for body size of 175 first captures to ensure independence of data: 70 metamorphs (less than one year old), 43 juveniles (over one year old), 29 unsexed individuals, 18 adult males, and 15 adult females. Population structure analysis revealed two distinct groups with a first large peak by numerous metamorphs due to postmetamorphic emigration/dispersal resulted from early metamorphosis
FIG. 5 in A New Species of Silverside of the Genus Odontesthes (Atheriniformes: Atherinopsidae) with Hypertrophic Lips from a High-Altitude Basin in Southern Brazil
FIG. 5. Pectoral girdle in dorsal view. (Left) Odontesthes humensis, left side, anterior to left, UFRGS 22497, 130.3 mm SL; (Right) Odontesthes crossognathos, right side, anterior to left, paratype, UFRGS 28830, 134.6 mm SL. Arrows indicate the dorsomedial wing surpassing the suture between scapula (S) and coracoid (C). Scale bar ¼ 2 mm.
Fig. 2 in New Genus and Species of High-Altitude Flightless Diestotini from the West Indies (Coleoptera: Staphylinidae: Aleocharinae)
Fig. 2. Aleomallus yaque, new genus and species. a) Female, sternite VII, b) Female, sternite VIII, c) Female, tergite VII, d) Female, tergite VIII, e) Male, sternite VII, f) Male, sternite VIII, g) Male, tergite VII, h) Male, tergite VIII. Scale bars = 0.1 mm.
Fig. 3 in New Genus and Species of High-Altitude Flightless Diestotini from the West Indies (Coleoptera: Staphylinidae: Aleocharinae)
Fig. 3. Aleomallus yaque, new genus and species. a) Dorsal aspect of labrum, b) Ventral aspect of labrum (epipharynx), c) Ventral aspect of labium and mentum, d) Ventral aspect of left mandible, e) Ventral aspect of right mandible, f) Ventral aspect of maxilla. Scale bars = 0.1 mm.
Fig. 2 in Ex-situ cultivation at lower altitude and evaluation of Swertia chirayita, a critically endangered medicinal plant of Sikkim Himalayan region, India
Fig. 2. Projected yield of Swertia chirayita mature plant from niche environment and oneyear-old ex-situ cultivated plant at the lower altitude with their respective swertiamarin content.
FIGURE 9 in The Cladocera (Crustacea: Branchiopoda) of six high altitude water bodies in the North Chilean Andes, with discussion of Andean endemism 2430
FIGURE 9. Macrothrix atahualpa, thoracic limbs of adult parthenogenetic female from Laguna Chungará, Chile. A–C. Distal portion of limb II and two smallest setae of its inner distal lobe; D. Limb I, anterior view; E–G. Stiff setae on inner portion of limb I; H–I. Limb II and distal armature of its gnathobase, posterior view; J–K. Limb III and its inner portion, posterior view; L. Limb IV, posterior view; M. Limb V, posterior view. Scale bars 0.1 mm.
FIGURE 10 in The Cladocera (Crustacea: Branchiopoda) of six high altitude water bodies in the North Chilean Andes, with discussion of Andean endemism 2430
FIGURE 10. Pleuroxus fryeri sp. nov., adult parthenogenetic female from Crater Lake, Licancabur Volcano, Chile- Bolivia border. A–B. Lateral and ventral view; C. Head, lateral view; D. Head shield; E. Tip of rostrum; F–G. Dorsal head pores; H–J. Labrum, labral keel and its apex; K. Antenna I; L. Antenna II; M. Apical seta of antenna II. Scale bars 0.1 mm.
FIGURE 2 in The Cladocera (Crustacea: Branchiopoda) of six high altitude water bodies in the North Chilean Andes, with discussion of Andean endemism 2430
FIGURE 2. Daphnia paggii sp. nov., female from Salar de Lagunillas, Chile. A–B. Antenna I, lateral view; C. antenna I, distal view; D. Antenna II, anterior view; E. Sensory setae at coxal portion of antenna II; F–G. Distal segments of antennal exopod and endopod; H. Apical swimming seta of antenna II; I–J. Ephippial female, lateral and posterior view; K. Dorsal portion of ephippium; L. Sculpture in central portion of ephippium. Scale bars 1 mm for I–J; 0.1 mm for A–H, K–L.
Figure 30 in Antikuna, a new genus with seven new species from Peru (Araneae: Theraphosidae: Theraphosinae) and the highest altitude record for the family
Figure 30. Antikuna urayrumi sp. nov., male holotype (MUSM-ENT 0511875) from Peru, Junín, Tarma. (a). Right palpal tibia, prolateral view. (b). Right palpal tibia, retrolateral view. (c). Right tibia I, prolaterally ventral view. Scale bar = 1 mm. Photo by N. Ferretti.
Figure 18 in Antikuna, a new genus with seven new species from Peru (Araneae: Theraphosidae: Theraphosinae) and the highest altitude record for the family
Figure 18. (a). Antikuna cyanofemur sp. nov., female (MUSM ENT 0513575) from Peru, Junín, Huancayo, Waytapallana. Spermathecae with two separated seminal receptacles, dissected from a dried exuvia, ventral view. (b). Antikuna cyanofemur sp. nov., immature female (car. 6.7) (MUSM ENT 0513576) from Peru, Junín, Huancayo, Waytapallana. Spermathecae with two separated seminal receptacles, dissected from exuvia. (c–f). Antikuna cyanofemur sp. nov., female paratype (MUSM ENT 0513574) from Peru, Junín, Huancayo, Waytapallana. Spermathecae with two separated seminal receptacles. (c, d). Dissected from exuvia. (c). Ventral view. (d). Dorsal view. (e–f). Dissected from specimen in alcohol. (e). Ventral view. (f). Dorsal view. (g–h). Antikuna cyanofemur sp. nov., female paratype (MUSM ENT 0513575) from Peru, Junín, Huancayo, Waytapallana. Spermathecae with two separated seminal receptacles, dissected from specimen in alcohol. (g). Ventral view. (h). Dorsal view. Arrows show inner basal extension. Scale bar = 1 mm. Photo by R. Kaderka.
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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.