Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
382
datasets available to search
ShareScore release 0.9.0
Dataset results
382 results for “high elevation”
FIGURE 9. Polystichum oblongipinnarum Li Bing Zhang, M.Q in Eight new species of Polystichum (subg. Haplopolystichum; Dryopteridaceae) from limestone caves in Guangdong and Yunnan, China, with reference to species diversity in the karst terrains at high elevations in subtropical areas
FIGURE 9. Polystichum oblongipinnarum Li Bing Zhang, M.Q.Han & Yan Liu.—A. Habitat and plant.—B. Abaxial view of lamina.—C. Adaxial view of lamina.—D. Portion of lamina.—E, F. Outside and inside views of the cave where the new species was discovered.
FIGURE 8. Polystichum malipoense Li Bing Zhang, M.Q in Eight new species of Polystichum (subg. Haplopolystichum; Dryopteridaceae) from limestone caves in Guangdong and Yunnan, China, with reference to species diversity in the karst terrains at high elevations in subtropical areas
FIGURE 8. Polystichum malipoense Li Bing Zhang, M.Q.Han & Yan Liu.—A. Two leaves.—B. Portion of abaxial lamina.
FIGURE 7. Polystichum malipoense Li Bing Zhang, M.Q in Eight new species of Polystichum (subg. Haplopolystichum; Dryopteridaceae) from limestone caves in Guangdong and Yunnan, China, with reference to species diversity in the karst terrains at high elevations in subtropical areas
FIGURE 7. Polystichum malipoense Li Bing Zhang, M.Q.Han & Yan Liu.—A. Habitat and plant.—B. Adaxial view of leaves.—C. Abaxial view of lamina.—D. Portion of abaxial lamina.—E. Adaxial view of pinna.—F. Portions of petioles.—G. Portion of pinna.—H, K. Polar and equatorial views of spores with and without perispores under SEM.—J. Inside view of the cave where the new species was discovered.
FIGURE 6. Polystichum hanmengqii Li in Eight new species of Polystichum (subg. Haplopolystichum; Dryopteridaceae) from limestone caves in Guangdong and Yunnan, China, with reference to species diversity in the karst terrains at high elevations in subtropical areas
FIGURE 6. Polystichum hanmengqii Li Bing Zhang & Yan Liu.—A. Two leaves.—B. Portion of adaxial lamina.—C. Portion of abaxial lamina.
FIGURE 5. Polystichum hanmengqii Li in Eight new species of Polystichum (subg. Haplopolystichum; Dryopteridaceae) from limestone caves in Guangdong and Yunnan, China, with reference to species diversity in the karst terrains at high elevations in subtropical areas
FIGURE 5. Polystichum hanmengqii Li Bing Zhang & Yan Liu.—A. Adaxial view of lamina.—B. Abaxial view of lamina.—C. Portion of lamina.—D. Abaxial view of pinna.—E. Portion of rachis with pinna.—F. Portion of pinna.—G. Portion of rachis with portion of pinna.—H, K. Equatorial view of spore under SEM.—J. Outside view of the cave where the new species was discovered.
FIGURE 1. Polystichum deltatum Li Bing Zhang, M.Q in Eight new species of Polystichum (subg. Haplopolystichum; Dryopteridaceae) from limestone caves in Guangdong and Yunnan, China, with reference to species diversity in the karst terrains at high elevations in subtropical areas
FIGURE 1. Polystichum deltatum Li Bing Zhang, M.Q.Han & Yan Liu.—A. Habitat and plant.—B, G. Portions of rachises with pinnae.— C. Lamina.—D. Portion of lamina.—E. Indusium under SEM.—F. Portions of petioles.—H. Portion of pinna.—J, L. Polar views of spores with and without perispores under SEM.—K. Outside view of the cave where the new species was discovered.
FIGURE 4. Polystichum gejiuense Li Bing Zhang, M.Q in Eight new species of Polystichum (subg. Haplopolystichum; Dryopteridaceae) from limestone caves in Guangdong and Yunnan, China, with reference to species diversity in the karst terrains at high elevations in subtropical areas
FIGURE 4. Polystichum gejiuense Li Bing Zhang, M.Q.Han & Yan Liu.—A. Habit.—B. Portion of abaxial lamina.
FIGURE 3. Polystichum gejiuense Li Bing Zhang, M.Q in Eight new species of Polystichum (subg. Haplopolystichum; Dryopteridaceae) from limestone caves in Guangdong and Yunnan, China, with reference to species diversity in the karst terrains at high elevations in subtropical areas
FIGURE 3. Polystichum gejiuense Li Bing Zhang, M.Q.Han & Yan Liu.—A. Habitat and plant.—B, C, E. Portions of lamina.—D, F. Portions of rachises with pinnae.—G, K. Polar and equatorial views of spores with and without perispores under SEM.—H. Indusium.—J. Inside view of the cave where the new species was discovered.
FIGURE 2. Polystichum deltatum Li Bing Zhang, M.Q in Eight new species of Polystichum (subg. Haplopolystichum; Dryopteridaceae) from limestone caves in Guangdong and Yunnan, China, with reference to species diversity in the karst terrains at high elevations in subtropical areas
FIGURE 2. Polystichum deltatum Li Bing Zhang, M.Q.Han & Yan Liu.—A. Habit.—B. Portion of abaxial lamina.
FIGURES 11–15 in How high can trumpet moths occur: documentation of mountainous leaf-mining Tischeriidae, featuring a species from record-high elevations
FIGURES 11–15. Male genitalia of Astrotischeria parapallens Diškus & Stonis, 3,320 m (a new elevation record), non-type specimen, genitalia slide no. AD1140 (MfN). 11, genitalia capsule with phallus removed, focused on the ventral view; 12, same, focused on the dorsal view; 13, anellus; 14, phallus; 15, basal processes of valvae.
FIGURES 34–42 in How high can trumpet moths occur: documentation of mountainous leaf-mining Tischeriidae, featuring a species from record-high elevations
FIGURES 34–42. Male genitalia of Astrotischeria andina Diškus & Stonis, sp. nov., 3,595–3,600 m. 34, phallus, paratype, genitalia slide no. AD748 (MfN). 35, same, holotype, genitalia slide no. AD1160 (MfN); 36–39, details of genitalia capsule, holotype, genitalia slide no. AD1160 (MfN); 40, dentate dorsal lobe of valva, paratype, genitalia slide no. AD748 (MfN); 41, 42, general view of genitalia capsule with phallus removed, holotype, genitalia slide no. AD1160 (MfN).
FIGURES 16–23 in How high can trumpet moths occur: documentation of mountainous leaf-mining Tischeriidae, featuring a species from record-high elevations
FIGURES 16–23. Male genitalia of Astrotischeria peruanica Diškus & Stonis, sp. nov., 2,110 m. 16–19, holotype, genitalia slide no. AD1180 (MfN); 20–23, paratype, with phallus (23) removed, genitalia slide no. AD1172 (MfN).
FIGURES 47–52 in How high can trumpet moths occur: documentation of mountainous leaf-mining Tischeriidae, featuring a species from record-high elevations
FIGURES 47–52. Bionomics of mountainous Astrotischeria species. 47, habitat of A. parapallens Diškus & Stonis and A. montivaga Diškus & Stonis, sp. nov., Ayacucho, Huamanga Province, Peru, 3,320 m; 48, unidentified host plant of A. peruanica Diškus & Stonis, sp. nov., possibly Baccharis trinervis Pers., Asteraceae, 2,110 m; 49, 50, leaf mines with feeding larvae of Astrotischeria peruanica Diškus & Stonis, sp. nov.; 51, 52, Baccharis salicifolia (Ruiz & Pav.) Pers., Asteraceae, a host plant of Astrotischeria viscacha Diškus & Stonis, sp. nov., Pisac, Calca Province, Peru at an elevation of 2,990 m.
FIGURES 53–59 in How high can trumpet moths occur: documentation of mountainous leaf-mining Tischeriidae, featuring a species from record-high elevations
FIGURES 53–59. Bionomics of Astrotischeria andina Diškus & Stonis, sp. nov. 53, 54, habitat, Saqsaywaman, Cusco, Peru, 3,595–3,600 m; 55–57, host plant Baccharis buxifolia (Lam.) Pers., Asteraceae; 58, 59, leaf mines.
FIGURES 4–10 in How high can trumpet moths occur: documentation of mountainous leaf-mining Tischeriidae, featuring a species from record-high elevations
FIGURES 4–10. Adults of mountainous Astrotischeria species. 4, A. viscacha Diškus & Stonis, sp. nov., 2,990 m, male holotype; 5, 6, same, female paratype; 7, A. andina Diškus & Stonis, sp. nov., male holotype, 3,595–3,600 m; 8, same, male paratype; 9, 10, same, female paratype (MfN).
FIGURES 43–46 in How high can trumpet moths occur: documentation of mountainous leaf-mining Tischeriidae, featuring a species from record-high elevations
FIGURES 43–46. Female genitalia of mountainous Astrotischeria species. 43, 44, A. viscacha Diškus & Stonis, sp. nov., 2,990 m, paratype, genitalia slide no. AD1176 (MfN); 45, 46, A. andina Diškus & Stonis, sp. nov., 3,595–3,600 m, paratype, genitalia slide no. AD1179 (MfN).
FIGURES 29–33 in How high can trumpet moths occur: documentation of mountainous leaf-mining Tischeriidae, featuring a species from record-high elevations
FIGURES 29–33. Male genitalia of Astrotischeria viscacha Diškus & Stonis, sp. nov., 2,990 m, holotype, genitalia slide no. AD1177 (MfN). 29, 30, uncus, 31, genitalia capsule with phallus removed, focused on valvae; 32, 33, phallus.
FIGURES 24–28 in How high can trumpet moths occur: documentation of mountainous leaf-mining Tischeriidae, featuring a species from record-high elevations
FIGURES 24–28. Male genitalia of Astrotischeria montivaga Diškus & Stonis, sp. nov., 3,320 m. 24, genitalia capsule with phallus removed, holotype, slide no. AD1185 (MfN); 25, 26, same, paratype, genitalia slide no. AD746 (MfN); 27, same, phallus; 28, same, holotype, genitalia slide no. AD1185 (MfN).
FIGURES 1–3 in How high can trumpet moths occur: documentation of mountainous leaf-mining Tischeriidae, featuring a species from record-high elevations
FIGURES 1–3. Adults of mountainous Astrotischeria species. 1, A. parapallens Diškus & Stonis, 3,320 m, non-type specimen, a new elevation record; 2, A. peruanica Diškus & Stonis, sp. nov., holotype, 2,110 m; 3, A. montivaga Diškus & Stonis, sp. nov., paratype, 3,320 m (MfN).
FIGURES 61–63. Tischeriidae occurrence across different elevations. 61 in How high can trumpet moths occur: documentation of mountainous leaf-mining Tischeriidae, featuring a species from record-high elevations
FIGURES 61–63. Tischeriidae occurrence across different elevations. 61, based on the current data of the global fauna (192 species), with the record-high altitudes for Tischeriidae compared with the record-high altitude reported for Nepticulidae; 62, Tischeriidae in the tropical regions (97 species) showing Astrotischeria andina sp. nov. as a species discovered at record-high altitudes; 63, Tischeriidae in non-tropical regions (105 species) showing the species discovered at record-high altitudes in nontropical regions. *Note that the distribution of some species overlaps across different altitudes, and some species have been discovered in both tropical (Fig. 62) and non-tropical regions (Fig. 63). The total current number of Tischeriidae species is still 192 (not 97+105). Note that this illustrative representation of the diversity of ecosystems, conveyed by J. R. Stonis, is presented in a stylized and idealized manner, without relying on precise depiction of the actual components.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.