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.
30,817
datasets available to search
ShareScore release 0.9.0
Dataset results
30,817 results for “type”
Fig. 10 in Type Specimens of Halacarid Mites by Dr. N. G. Makarova Relocated in the Collection of the National Museum of Nature and Science, Tsukuba, Japan
Fig. 10.ɹHalacarellus longus [nomen nudum], ˁ NSMT-Ac 14700. Body (A), genitoanal region (B), gnathosoma (C). Scale bars for A=100 µm, BC=50 µm.
Fig. 7 in Type Specimens of Halacarid Mites by Dr. N. G. Makarova Relocated in the Collection of the National Museum of Nature and Science, Tsukuba, Japan
Fig. 7.ɹThalassarachna aculeata, paratype deutonymph NSMT-Ac 14698 (No. 5). Body (A), genitoanal region (B). Scale bars for A=100 µm, B=50 µm.
Fig. 4 in Type Specimens of Halacarid Mites by Dr. N. G. Makarova Relocated in the Collection of the National Museum of Nature and Science, Tsukuba, Japan
Fig. 4.ɹThalassarachna aculeata, holotype ˁ NSMT-Ac 14695. Body (A), genitoanal region (B), gnathosoma (C). Scale bars for A=100 µm, BC=50 µm.
Fig. 2 in Type Specimens of Halacarid Mites by Dr. N. G. Makarova Relocated in the Collection of the National Museum of Nature and Science, Tsukuba, Japan
Fig. 2.ɹAcanthopalpus hirsutus, holotype ˂ NSMTAc 14693 (A, B, D) and paratype ˂ NSMT-Ac 14694 (C, E). Idiosoma (A), genitoanal region (B), body (C), gnathosoma (D), first leg (E). Scale bars for AC=100 µm, BDE=50 µm.
Fig. 6 in Type Specimens of Halacarid Mites by Dr. N. G. Makarova Relocated in the Collection of the National Museum of Nature and Science, Tsukuba, Japan
Fig. 6.ɹThalassarachna aculeata, paratype deutonymph NSMT-Ac 14697 (No. 4). Body (A), genitoanal region (B). Scale bars for A=100 µm, B=50 µm.
Fig. 8. Antennal s in Types and functions of mole cricket (Orthoptera: Gryllotalpidae) antennal and palpal sensilla
Fig. 8. Antennal s. coeloconicum (type I), located in the cuticular pit (×28k) (A), in contrast to s. ceoloconicum (×25k) (type II) positioned on the antennal surface (B). S. campaniformia, proprioreceptor, can be located on the tip of the segment (× 17k) (C) and at the midsection (× 21k) (D).
Fig. 3 in Types and functions of mole cricket (Orthoptera: Gryllotalpidae) antennal and palpal sensilla
Fig. 3. Sensilla chaetica, the most abundant sensilla on S. vicinus antennae. Antennal surface of S. vicinus with s. chaetica positioned in the flexible sockets (mag- inifaication ×9k) (A), aporous ridged surface of the sensillum (magnification ×6k) (B), antennal segment and different types of sensilla, s. chaetica types I and II (schI and II), arranged into transverse patterns, type III s. chaetica (sch III) are small and evenly distributed on the flagellomere (×600) (C). Row of s. basioconica (sb) and s. trichodea (si) (C) usually observed on the apical portion of the flagellomere.
Fig. 2 in Types and functions of mole cricket (Orthoptera: Gryllotalpidae) antennal and palpal sensilla
Fig. 2. Böhm sensilla (Bs) (SEM, ×1.1k and ×2K) (A, B) on the S. abbreviatus pedicel (×500) (C) and scape (×650) (D).
Fig. 7 in Types and functions of mole cricket (Orthoptera: Gryllotalpidae) antennal and palpal sensilla
Fig. 7. Sensillum trichodium (st) located at the distal part of flagllomere together with s. chaeticum (sch), s. basioconicum (sb) and s. coeloconicum (sc) (×9k) (A); cross-section of s. trichodium (B) showing presence of the sensillum lumen (sl) with dendrites (d) and thick wall (sw) with pores (wp) (C).
Fig. 1 in Types and functions of mole cricket (Orthoptera: Gryllotalpidae) antennal and palpal sensilla
Fig. 1. SEM photos of the flagellum mid-section of N. hexadactyla (A), S. abbreviatus (B), S. vicinus (C) and S. borellii (×140) (D).
Fig. 5 in Types and functions of mole cricket (Orthoptera: Gryllotalpidae) antennal and palpal sensilla
Fig. 5. Transmission electron micrographs (A, B) and the longitudinal section of s. basioconicum (sb), located on the tip of the each segment (C), indicate presence of the wall pore (wp), sensilla lumen (sl) and dendrites (d).
Fig. 6. Short s in Types and functions of mole cricket (Orthoptera: Gryllotalpidae) antennal and palpal sensilla
Fig. 6. Short s. basioconica (×22k and 15k) (sb) (A), arranged in transverse row on the apical part of antennal segment of N. hexadactyla (×900) (B).
Fig. 4 in Types and functions of mole cricket (Orthoptera: Gryllotalpidae) antennal and palpal sensilla
Fig. 4. Transmission electron micrographs of s. chaetica type I and II (A, B) which are not innervated and are dense inside with thick sensillum wall (sw), type III s. chaetica have less dense sensillar lumen (sl) and are innervated with 4 dendrites (d) (C, D).
Fig. 9 in Types and functions of mole cricket (Orthoptera: Gryllotalpidae) antennal and palpal sensilla
Fig. 9. Mole cricket labial and maxillary palps are densely covered with sensilla (× 300) (A). The dominant type is s. chaetica (× 8k) (B), other types include s. coeloconica (×15k) (C) with tip-pore (× 40k) (D), single-wall tip-pore sensilla (× 9k) (E) and club-like s. basioconica (× 11k) (F).
Figs. 6–10. 6. Cerithium magnum Jay, 1836 in Catalog Of Recent Type Specimens In The Division Of Invertebrate Zoology, American Museum Of Natural History. V. Mollusca, Part 2 (Class Gastropoda [Exclusive Opisthobranchia And Pulmonata With Supplements To Gastropoda [Opisthobranchia], And Bivalvia
Figs. 6–10. 6. Cerithium magnum Jay, 1836 (lectotype—AMNH 56067), X 0.75. 7. Conus Bernardi and Crosse, 1861 (syntype—AMNH 47629), X 1.75. 8. Conus pseudoaustini Usticke, (holotype—AMNH 195452), X 2. 9. Cyclostoma maculosa Jay, 1839 (syntype—AMNH 56086), 10. Cyclostoma multilineata Jay, 1839 (syntype—AMNH 56087), X 2.6.
◂Fig. 17 Iberozospeum costulatum n. sp. (a–e) holotype, 1.43 mm height [MNCN 15.05/200128, ex. ZUPV 1952], Mina del Pedreo (Bizkaia: Arcentales; 43.26800 -3.21402, 440 m). (f–g) paratype shells from the type locality [ZUPV 1952, F: juvenile shell, G: shell of 1.51 mm height. (h–i) no paratype shell of 1.48 mm height [ZUPV 3807] from Cueva del Cesáreo (Cantabria: Liérganes: Extremera; 43.32034 -3.72279, 258 m). (j–k) paratype shells from Cueva de Cuvias Negras (Cantabria: Soba: Asón; 43.25132 -3.60688, 250 m) [CSQS·w/o nº]. (l) no paratype shell from Cueva del Cesáreo [CSQS·w/o nº]. Photos a–i by Carlos Prieto; j–l by Sergio Quiñonero and Álvaro Alonso in Molecular investigation and description of Iberozospeum n. gen., including the description of one new species (Eupulmonata, Ellobioidea, Carychiidae)
◂Fig. 17 Iberozospeum costulatum n. sp. (a–e) holotype, 1.43 mm height [MNCN 15.05/200128, ex. ZUPV 1952], Mina del Pedreo (Bizkaia: Arcentales; 43.26800 -3.21402, 440 m). (f–g) paratype shells from the type locality [ZUPV 1952, F: juvenile shell, G: shell of 1.51 mm height. (h–i) no paratype shell of 1.48 mm height [ZUPV 3807] from Cueva del Cesáreo (Cantabria: Liérganes: Extremera; 43.32034 -3.72279, 258 m). (j–k) paratype shells from Cueva de Cuvias Negras (Cantabria: Soba: Asón; 43.25132 -3.60688, 250 m) [CSQS·w/o nº]. (l) no paratype shell from Cueva del Cesáreo [CSQS·w/o nº]. Photos a–i by Carlos Prieto; j–l by Sergio Quiñonero and Álvaro Alonso
Fig. 2 - Mericarps. A, B in Dichoropetalum schottii: examination of the type specimen, distribution and comparison with D. carvifolium-chabraei (Apiaceae)
Fig. 2 - Mericarps. A, B) Dichoropetalum carvifolium-chabraei; C, D) D. schottii; A, C) dorsal side; B, D) commissural side. Scale bars = 1 mm.
Fig. 4 in Dichoropetalum schottii: examination of the type specimen, distribution and comparison with D. carvifolium-chabraei (Apiaceae)
Fig. 4 - Microphotographs of mericarp transections. �) Dichoropetalum carvifolium-chabraei; B) D. schottii. Scale bar = 0.1 mm.
Fig. 3 in Dichoropetalum schottii: examination of the type specimen, distribution and comparison with D. carvifolium-chabraei (Apiaceae)
Fig. 3 - Mericarp transections, schematic. A) mature mericarp of Dichoropetalum carvifolium-chabraei, B) mature mericarp of D. schottii; C) immature mericarp of isolectotype of D. schottii. Scale bar = 1 mm. Abbreviations: cav) cavity, dc) commissural secretory duct, dr) rib secretory duct, dv) vallecular secretory duct, es) endosperm, ex) exocarp, he) hypendocarp, lp) lignified pitted parenchyma, vb) vascular bundle.
Fig. 5 - Fruit micromorphology. Mericarps. A, B in Dichoropetalum schottii: examination of the type specimen, distribution and comparison with D. carvifolium-chabraei (Apiaceae)
Fig. 5 - Fruit micromorphology. Mericarps. A, B) Dichoropetalum carvifolium-chabraei; C, D) D. schottii; A, C) dorsal rib; B, D) vallecula.
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.