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”
Distribution. Known only confidently from holotype in NE part of N Peninsula of Sulawesi; there are apparently records from Tolai and Rurukan, N Sulawesi, and two other specimens from Tobelo, N Sulawesi, which are all located near type locality, but all of these specimens need to be reexamined to determine whether or not they truly represent this species. in Vespertilionidae
Distribution. Known only confidently from holotype in NE part of N Peninsula of Sulawesi; there are apparently records from Tolai and Rurukan, N Sulawesi, and two other specimens from Tobelo, N Sulawesi, which are all located near type locality, but all of these specimens need to be reexamined to determine whether or not they truly represent this species.
Dataset for "Glycaemic control is associated with SARS-CoV-2 breakthrough infections in vaccinated patients with Type 2 diabetes"
<p>Dataset for "Glycaemic control is associated with SARS-CoV-2 breakthrough infections in vaccinated patients with Type 2 diabetes"</p>
FIGURE 10 in Revision of the type species of some cheilostome bryozoan genera in the collection of the Swedish Museum of Natural History
FIGURE 10. Terwasipora complanata (Norman, 1864), Holotype SMNH-Type-1772, Ireland. A. General view of the colony. B. Label on the underside of the rock substrate. Scale bars: A = 1 mm; B = 3 cm.
FIGURE 9 in Revision of the type species of some cheilostome bryozoan genera in the collection of the Swedish Museum of Natural History
FIGURE 9. Stenopsella fenestrata (Smitt, 1873), Holotype SMNH-Type-1800, Tortugas, United States, here proposed as Gigantopora fenestrata comb. nov. A. General view of the colony. B. Group of zooids some in frontal and other in lateral view. C. Close-up of some zooids in lateral view, showing the development of the peristome, a variable position of the avicularium in relation to the spiramen, and the prickly appearance of the frontal shield. D. Close-up of a zooid with broken peristome and showing the primary orifice. E. Close-up of the adventitious, peristomial avicularium with complete crossbar. Scale bars: A = 1 mm; B, C = 500 µm; D = 300 µm; E = 100 µm.
FIGURE 7 in Revision of the type species of some cheilostome bryozoan genera in the collection of the Swedish Museum of Natural History
FIGURE 7. Fedorella minima Silén, 1947, Anguilla. A–C. Lectotype (designated here) SMNH-128088a. A. General view of the colony. B. Group of zooids, showing avicularian variability, the shape of the orifice and opercula. C. Close-up of a zooid with paired giant avicularia and lateral view of an ovicell. D. Paralectotype SMNH-128088b, group of ovicellate zooids showing the triangular opening of the ooecium. E, F. Paralectotype SMNH-128088c. E. Close-up of two zooids with only one or completely lacking avicularia; the orifice of the zooid on the left shows signs of repetitive intramural budding. F. Close up of an orifice with closure plate. Scale bars: A = 500 µm; B, D = 300 µm; C, E = 200 µm; F = 100 µm.
FIGURE 8 in Revision of the type species of some cheilostome bryozoan genera in the collection of the Swedish Museum of Natural History
FIGURE 8. Cheilopora sincera (Smitt, 1868), Lectotype (designated here) SMNH-Type-1733, northern Norway. A. Group of zooids, most ovicellate. B. Close-up of an ovicell, orifice with operculum, and paired latero-oral avicularia with semielliptical mandibles. C. Close-up of an autozooidal orifice lacking avicularia. D. Close-up of two zooids with single avicularium and a closure plate. Scale bars: A = 1 mm; B, C = 200 µm; D = 300 µm.
FIGURE 5 in Revision of the type species of some cheilostome bryozoan genera in the collection of the Swedish Museum of Natural History
FIGURE 5. Lepraliella contigua (Smitt, 1868), Hammerfest, Norway. A, B. Paralectotype SMNH-Type-1695b. C–E. Lectotype (designated here) SMNH-Type-1695a. F. Paralectotype SMNH-Type-1695c. A, C, F. General view of the three colony fragments. B. Group of zooids, showing a variable number of oral spine bases, either due to spreading of calcification during ontogeny or to the development of ovicells. D. Close-up of zooids with suboral avicularium and developing ooecia. E. Close-up of a zooid showing the eye-shaped secondary orifice and the wrinkled to nodular surface of the frontal shield. Scale bars: A, C = 1 mm; B, D, E = 300 µm; F = 2 mm.
FIGURE 2 in Revision of the type species of some cheilostome bryozoan genera in the collection of the Swedish Museum of Natural History
FIGURE 2. Floridina antiqua (Smitt, 1873), Lectotype (designated here) SMNH-Type-1835a, Florida, United States. A. Portion of the colony including about 80 zooids and three vicarious avicularia. B. Group of autozooids, ovicellate zooids (note the ooecium formed by both the vicarious avicularium and the distal zooid, see asterisk), and vicarious avicularia with raised rostrum showing the smooth gymnocyst. C. Group of autozooids, ovicellate zooids (with ooecium formed by the distal zooid, see asterisk), and vicarious avicularia. D. Group of autozooids and vicarious avicularium with an unusual rectangular rostrum. E. Close-up of zooids, those ovicellate with ooecium formed by one (black asterisk) or two (white asterisk) distal zooids, avicularium with undulate, raised, triangular rostrum, and zooid showing signs of intramural budding (arrowed). F. Putative kenozooids. G. Group of zooids, vicarious avicularia and putative kenozooid with reduced opesia (asterisk). H. Group of zooids and vicarious avicularia, one zooid irregularly shaped and with reversed polarity (asterisk). Scale bars: A = 1 mm; B–D, F–H = 500 µm; E = 400 µm.
FIGURE 6 in Revision of the type species of some cheilostome bryozoan genera in the collection of the Swedish Museum of Natural History
FIGURE 6. Fedorella minima Silén, 1947, Anguilla. A, B. Paralectotype SMNH-Type-8734a. A. General view of the colony. B. Close-up of a zooid with paired avicularia, one small and triangular, the other one giant and spathulate. C. Paralectotype SMNH-Type-8734b, general view of the colony with zooids having single avicularium. D. Paralectotype SMNH-Type-8734c, group of zooids, some with paired distolateral, oral spine bases (arrowed) and a kenozooid (asterisk). Scale bars: A, C = 500 µm; B = 200 µm; D = 300 µm.
FIGURE 4 in Revision of the type species of some cheilostome bryozoan genera in the collection of the Swedish Museum of Natural History
FIGURE 4. Smittipora americana (Canu & Bassler, 1928), catalogued as SMNH-Type-1786 of S. abyssicola, Florida, United States. A. Close-up of two zooids with opercula and vicarious avicularium with leaf-shaped, pointed mandible. B. Group of zooids, showing the opesia with indentations, vicarious avicularia and ovicells. Scale bars: A = 400 µm; B = 500 µm.
FIGURE 1 in Revision of the type species of some cheilostome bryozoan genera in the collection of the Swedish Museum of Natural History
FIGURE 1. Doryporella spathulifera (Smitt, 1868), Lectotype (designated here) SMNH-Type-1729a, Hinlopen Strait, Svalbard, Norway. A. General view of the fan-shaped colony with subsequent generations of zooids budded only distally from the ancestrula. B. Close-up of the tatiform ancestrula and periancestrular zooids. C. View of colony growing edge showing paired distal pore chamber windows. Asterisks indicate kenozooidal ovicells. D. Group of ovicellate zooids showing ovicells produced either by a kenozooid (asterisks) or the distal autozooid, the suboral spatula-like spine and triangular avicularia mandibles. Scale bars: A = 2 mm; B–D = 500 µm.
FIGURE 3 in Revision of the type species of some cheilostome bryozoan genera in the collection of the Swedish Museum of Natural History
FIGURE 3. Smittipora abyssicola (Smitt, 1873). A. Paralectotype SMNH-Type-9104, off Cojima, Cuba. General view of the small colony encrusting a phidoloporid bryozoan. B–F. Lectotype (designated here) SMNH-Type-1815, Florida, United States. B. General view of the colony with encrusting base and two starting erect branches, encrusting a solitary coral. C. Group of zooids and vicarious avicularia (with triangular mandibles, see asterisk) at the encrusting base and at the start of an erect branch. D. Close-up of the ancestrula (asterisk) and periancestrular zooids and avicularia. E. Group of zooids and vicarious avicularia rising from the encrusting base to form an erect branch. F. Close-up of an autozooid and two vicarious avicularia. Scale bars: A–C = 2 mm; D, E = 1 mm; F = 400 µm.
Data from: Multiple types of genomic variation contribute to adaptive traits in the mustelid subfamily Guloninae
<p>Species of the mustelid subfamily Guloninae inhabit diverse habitats on multiple continents, and occupy a variety of ecological niches. They differ in feeding ecologies, reproductive strategies and morphological adaptations. To identify candidate loci associated with adaptations to their respective environments, we generated a de novo assembly of the tayra (<em>Eira barbara</em>), the earliest diverging species in the subfamily, and compared this with the genomes available for the wolverine (<em>Gulo gulo</em>) and the sable (<em>Martes zibellina</em>). Our comparative genomic analyses included searching for signs of positive selection, examining changes in gene family sizes, as well as searching for species-specific structural variants (SVs). Among candidate loci associated with phenotypic traits, we observed many related to diet, body condition and reproduction. For example, for the tayra, which has an atypical gulonine reproductive strategy of aseasonal breeding, we observe species-specific changes in many pregnancy-related genes. For the wolverine, a circumpolar hypercarnivore that must cope with seasonal food scarcity, we observed many changes in genes associated with diet and body condition. All types of genomic variation examined (single nucleotide polymorphisms, gene family expansions, structural variants) contributed substantially to the identification of candidate loci. This strongly argues for consideration of variation other than single nucleotide polymorphisms in comparative genomics studies aiming to identify loci of adaptive significance.</p>
FIGURE 2 in Notes on the genus Micromorphus Mik (Diptera: Dolichopodidae) and the uncertain identity of its type species, M. albipes (Zetterstedt)
FIGURE 2. Micromorphus caudatus (Aldrich): a, male habitus, left lateral; b, male postabdomen, left lateral; c, female habitus, dorsal; M. micidus Parent; d, female postabdomen, dorsal; e, male habitus, left lateral; f, male wing, dorsal.
FIGURE 1 in Notes on the genus Micromorphus Mik (Diptera: Dolichopodidae) and the uncertain identity of its type species, M. albipes (Zetterstedt)
FIGURE 1. Micromorphus caudatus (Aldrich): a, male postabdomen, ventral; b, male postabdomen, left lateral. M. micidus Parent: c, male postabdomen, left lateral. Legend: cer, cercus; el, epandrial lobe; epand, epandrium; hyp, hypandrium; ph, phallus; st, sternite, tg, tergite; vsur, ventral surstylus. Arrows indicate position of diagnostic setae.
Distribution. Known only from SE Ecuador (Cordillera del Condor, Zamora Chinchipe Province) and type locality in SC Peru. in Phyllostomidae
Distribution. Known only from SE Ecuador (Cordillera del Condor, Zamora Chinchipe Province) and type locality in SC Peru.
Distribution. Known only from two localities, one in C Costa Rica (Cartago Province) and the other in W Panama (type locality). in Phyllostomidae
Distribution. Known only from two localities, one in C Costa Rica (Cartago Province) and the other in W Panama (type locality).
Distribution. Known only from type locality in Yavari-Ucayali interfluvial region of NE Peruvian Amazon. in Phyllostomidae
Distribution. Known only from type locality in Yavari-Ucayali interfluvial region of NE Peruvian Amazon.
Distribution. Colombia, Venezuela, the Guianas, N, W, S & SE Brazil, Ecuador, Peru, Bolivia, and NW Argentina resulting in arc-type distribution surrounding central part of Amazon Basin. Records from Paraguay are suspicious. in Phyllostomidae
Distribution. Colombia, Venezuela, the Guianas, N, W, S & SE Brazil, Ecuador, Peru, Bolivia, and NW Argentina resulting in arc-type distribution surrounding central part of Amazon Basin. Records from Paraguay are suspicious.
Distribution. Known only from vicinity of type locality along Rio Orinoco in Bolivar and Amazonas states, Venezuela. in Phyllostomidae
Distribution. Known only from vicinity of type locality along Rio Orinoco in Bolivar and Amazonas states, Venezuela.
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.