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”
Figure 7 in It's a Trap! An evaluation of different passive trap types to effectively catch and control the invasive red swamp crayfish (Procambarus clarkii) in streams of the Santa Monica Mountains
Figure 7. Mean catches by stream habitat type. Differences in mean catches between stream Pools vs. Runs was evaluated using Wilcoxon rank-sum tests. * P-value <0.05.
Figure 3 in It's a Trap! An evaluation of different passive trap types to effectively catch and control the invasive red swamp crayfish (Procambarus clarkii) in streams of the Santa Monica Mountains
Figure 3. Mean catch per trap type with standard errors. Letters indicate significantly different mean counts within groups.
Figure 6 in It's a Trap! An evaluation of different passive trap types to effectively catch and control the invasive red swamp crayfish (Procambarus clarkii) in streams of the Santa Monica Mountains
Figure 6. Mean chub counts by size class across twelve trap types with standard error bars. Size classes include small as ≤ 60mm, medium as 61–89 mm, and large as 89–150mm as described by O'Brien et al. (2011).
SI Figure 3: Compositional difference among eukaryotic microinvertebrate external and internal microbiomes, using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars centroid location of each microbiome type. Communities do not cluster by animal, microbiome type, mat type, or stream. in External and internal microbiomes of Antarctic nematodes are distinct, but more similar to each other than the surrounding environment
SI Figure 3: Compositional difference among eukaryotic microinvertebrate external and internal microbiomes, using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars centroid location of each microbiome type. Communities do not cluster by animal, microbiome type, mat type, or stream.
SI Figure 2: Compositional differences among bacterial microinvertebrate external and internal microbiomes as well as mats they were isolated from using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars show centroids of microbiome types for each animal host. All host microbiomes (internal and external) are distinct from mat communities (P<0.05), but external microbiomes are more similar to mats than internal microbiomes are to mats. in External and internal microbiomes of Antarctic nematodes are distinct, but more similar to each other than the surrounding environment
SI Figure 2: Compositional differences among bacterial microinvertebrate external and internal microbiomes as well as mats they were isolated from using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars show centroids of microbiome types for each animal host. All host microbiomes (internal and external) are distinct from mat communities (P<0.05), but external microbiomes are more similar to mats than internal microbiomes are to mats.
SI Figure 1: Dispersion values (a boxplot using distance to centroids based on Bray Curtis distance matrix) of external and internal bacterial microbiome composition for different hosts. In a mixed linear model, microinvertebrates did not significantly impact dispersion (P=0.44), but microbiome type did (P=0.03). Pairwise contrasts show that while external microbiomes of P. murrayi and Tardigrada are more variable than their internal microbiomes, E. antarcticus external and internal microbiomes are equally variable. in External and internal microbiomes of Antarctic nematodes are distinct, but more similar to each other than the surrounding environment
SI Figure 1: Dispersion values (a boxplot using distance to centroids based on Bray Curtis distance matrix) of external and internal bacterial microbiome composition for different hosts. In a mixed linear model, microinvertebrates did not significantly impact dispersion (P=0.44), but microbiome type did (P=0.03). Pairwise contrasts show that while external microbiomes of P. murrayi and Tardigrada are more variable than their internal microbiomes, E. antarcticus external and internal microbiomes are equally variable.
Fig. 7 in A photographic type catalogue of Platygastroidea (Insecta, Hymenoptera) in the Natural History Museum Vienna
Fig. 7. Some unsorted material from the Förster collection. A. Cigar boxes donated to the NHMW by G. Mayr. B. Assorted pill boxes, mostly from a pharmacy in Aachen. C. Platygaster specimens found in one of the pill boxes.
Fig. 6 in A photographic type catalogue of Platygastroidea (Insecta, Hymenoptera) in the Natural History Museum Vienna
Fig. 6. Sparasionid types in the NHMW. A. Sparasion aenescens Förster, holotype male, NHMWHYM#0005326. B. Sparasion aeneus Kieffer, syntype male, NHMW-HYM#0006880. C. Sparasion lepidum Förster, holotype male, NHMW-HYM#0005372. D. Sparasion sublevis Kieffer, syntype female, NHMW-HYM#0006876.
Fig. 4 in A photographic type catalogue of Platygastroidea (Insecta, Hymenoptera) in the Natural History Museum Vienna
Fig. 4. Microphanurus schimitscheki Szelényi, paratype female, NHMW-HYM#0005416. A. Dorsal habitus. B. Lateral head and mesosoma, metapleural setation indicated. C. Head in dorsal view.
Fig. 2 in A photographic type catalogue of Platygastroidea (Insecta, Hymenoptera) in the Natural History Museum Vienna
Fig. 2. Baeus maculatus (Förster) comb. nov., holotype male, NHMW-HYM#0006908. A. Lateral habitus. B. Labels. C. Head in anterior view. D. Dorsal habitus.
Fig. 1 in A photographic type catalogue of Platygastroidea (Insecta, Hymenoptera) in the Natural History Museum Vienna
Fig. 1. Leptacis foersteri Kieffer, lectotype female, NHMW-HYM#0006906. A. Anterior habitus. B. Lateral habitus. C. Dorsal habitus.
Fig. 2 in Redescription of the type specimens for the Late Jurassic rhynchocephalian Opisthias rarus and a new specimen of Theretairus antiquus from Quarry 9, Morrison Formation, Wyoming, USA
Fig. 2. Teeth of rhynchocephalians Opisthias sp. (A–D) and Theretairus antiquus Simpson, 1926 (E) from Quarry 9, Como Bluff, Wyoming, USA, Upper Jurassic. A. USNM 6126, right dentary fragment with a relatively complete coronoid process in labial view. B. USNM 26080, fragment of palatine in?lingual view with four teeth attached. C. USNM 508532, rock matrix with fragments of right maxilla in lingual view (C1), close-up detail (C2), maxillary teeth (C3). D. USNM 7767 and USNM 26086, fragments of a right dentary, in lingual (D1), labial (D2), and occlusal (D3) views, close-up detail of the four distalmost additional teeth (D3), close-up detail of the four distalmost additional teeth in labial (D4) and lingual (D5) views. E. USNM 26088, anterior fragment of a left dentary, in labial (E1), lingual (E2), and occlusal (E3) views.
Fig. 1 in Redescription of the type specimens for the Late Jurassic rhynchocephalian Opisthias rarus and a new specimen of Theretairus antiquus from Quarry 9, Morrison Formation, Wyoming, USA
Fig. 1. Teeth in the type specimens of the rhynchocephalian Opisthias rarus Gilmore, 1909, Quarry 9, Como Bluff, Wyoming, USA, Upper Jurassic. A. USNM 2860 (holotype), nearly complete left dentary, in labial (A1, A4), lingual (A2, A5), and occlusal (A3, A6) views. B. USNM 2858 (paratype), partial left dentary, in labial (B1, B4), lingual (B2, B5), and occlusal (B3, B6) views. C. Fragment of rock matrix belonging to the holotype. D. Holotype when it is superimposed to the rock matrix.
Fig. 11. The tommotiid Shetlandia multiplicata Wrona, 2004, unknown type sclerite fragments from the Cambrian Series 2, Stages 3, 4 in Camenellan tommotiids from the Cambrian Series 2 of East Antarctica: Biostratigraphy, palaeobiogeography, and systematics
Fig. 11. The tommotiid Shetlandia multiplicata Wrona, 2004, unknown type sclerite fragments from the Cambrian Series 2, Stages 3, 4, Shackleton Limestone, Holyoake Range, Transantarctic Mountains, East Antarctica. A. NRM X10020, general view (A1), detail showing arched growth series (A2). B. NRM X10021, general view (B1), detail of broken margin (B2). C. NRM X10022, general view (C1), detail of comarginal ribs and broken edge (C2). D. NRM X10023. E. NRM X10024. Scale bars 200 µm, except B2, 100 µm. A–C taken with backscattered electron detector.
Fig 2 in Ordovician enigmatic sclerite-type elements from western Argentina: possible oldest axial components of alcyonacean octocorals
Fig 2. Alcyonacean octocoral Catenatus argentinus gen. et sp. nov. sclerite-type elements from the Middle Ordovician (Darriwilian), Lenodus variabilis– Yangtzeplacognathus crassus zones, San Juan Formation, San Juan Province, Argentina and its chemical composition by surface EDX analysis. A. Siliceous sclerite-type element, CEGH-UNC 27474, sample LG42 (unpolished sample). B. Phosphatic sclerite-type, CEGH-UNC 27475, sample RIN34. C. Partially broken element showing a solid inner structure, CEGH-UNC 27471, sample LG42. D, E. Thin sections of isolated elements of Catenatus argentinus gen. et sp. nov., showing the internal homogeneous structure, CEGH-UNC 27472, sample LG42 (D), and CEGH-UNC 27473, sample FSJ 3º hardground (E). Scale bars 100 μm.
Fig. 1 in Ordovician enigmatic sclerite-type elements from western Argentina: possible oldest axial components of alcyonacean octocorals
Fig. 1. The geographical and geological context of the Ordovician alcyonacean octocoral Catenatus argentinus gen. et sp. nov. from the San Juan Formation, Argentina. A. Location map of the studied localities with Ordovician alcyonacean sclerite-type elements from the Argentine Precordillera, San Juan Province, Argentina (1, Oculta Creek, Sierra de Los Cauquenes; 2, Los Gatos Creek, Cerro Viejo; 3, Amarilla Creek, Cerro Viejo; 4, Punta Negra Anticline; 5, Sierra de Rinconada). B. Simplified stratigraphic column of the San Juan Formation in the Argentine Precordillera, with location of the productive samples.
Fig. 17 in Sieve-type normal pore canals in Jurassic ostracods: A review with description of a new genus
Fig. 17. Cytherid ostracod Minyocythere tuberculata (Luppold, 2012) from Borehole Rodewald WA12, 404.5 m, NW Germany, Lower Bajocian. A. SMF Xe 23754, female left valve in external (A1) and internal (A4) views, micro sieve-type pore canals (StPC-m) (A2), macro sieve-type normal pore canals (StPC-M) A3), hinge, posterior (A5) and anterior (A6) parts. B. SMF Xe 23755, female right valve in external view.
Fig. 10 in Sieve-type normal pore canals in Jurassic ostracods: A review with description of a new genus
Fig. 10. Cytherid ostracod Minyocythere sp. cf. M. macroporosa sp. nov. from Borehole Rodewald WA12, 404.5 m (A), 386 m (B–E), 404.5 m (F, G), NW Germany, Witchellia laeviuscula Zone (Braun Jura γ upper), Lower Bajocian. A. SMF Xe 23725, male left valve in external view (A1), antero-dorsal area (A2), macro sieve-type normal pore canals (StPC-M) (A3), and micro sieve-type normal pore canals (StPC-m) (A4). B. SMF Xe 23726, female left valve in external view. C. SMF Xe 23727, female carapace in right (C1) and dorsal (C2) views. D. SMF Xe 23728, female right valve in external view. E. SMF Xe 23729, male carapace in dorsal view. F. SMF Xe 23730, fragment of female right valve in internal view. G. SMF Xe 23731, male left valve, internal view (G1), hinge (G2).
Fig. 16 in Sieve-type normal pore canals in Jurassic ostracods: A review with description of a new genus
Fig. 16. Normal pore canals (NPC) on juvenile left valves (A, stage A-2; B, stage A-3; C, stage A-4) in cytherid ostracod Minyocythere maculosa (Bate, 1963) from Borehole Rodewald WA6, 390 m, NW Germany, Lower Bajocian (Braun Jura γ). A. SMF Xe 23751, general view (A1), micro sieve-type pore canals (StPC-m) on the outer side of the valve (A2), macro sieve-type normal pore canals (StPC-M) on the outer side of the valve (A3, A4), StPC-M on the inner side of the valve (A5), and simple NPC on the outer side of the valve (A6). B. SMF Xe 23752, general view (B1), StPC-m on the outer side of the valve (B2), StPC-M on the inner side of the valve (B3). C. SMF Xe 23753, general view (C1), StPC-m on the outer side of the valve (C2), StPC-M on the outer side of the valve (C3).
Fig. 3 in Sieve-type normal pore canals in Jurassic ostracods: A review with description of a new genus
Fig. 3. Sieve-type normal pore canals (StPC) in Aphelocythere and Camptocythere spp. A. Aphelocythere perforata Plumhoff, 1963, from Borehole Wesendorf 51a, 1031–1035 m, NW Germany, Upper Aalenian. SMF Xe 5608 (Plumhoff Collection), carapace in external right view (A1), macro StPC (StPC-M) (A2–A4). B, C. Camptocythere praecox Triebel, 1950 from Borehole Hambühren WA 2, 341 m, NW Germany, Leioceras opalinum Zone, Lower Aalenian (Braun Jura α). B. Paratype, SMF Xe 1448, male right valve in external view (B1), mid-anterior area behind marginal rim, ornamentation and pores (large and small) (B2), StPC-M with a peripheral large pore (B3), micro StPC (StPC-m) (B4). C. Paratype, SMF Xe 1448, male right valve in internal view (C1), hinge (C2), StPC-m (C3). D. Camptocythere media Triebel, 1950 from Borehole Altencelle 1014, 212/16 m, NW Germany, Upper Aalenian (Braun Jura β). Paratype, SMF Xe 1513, female left valve in external view (D1), detail, antero-dorsal area, ornamentation and pores (large and small) (D2), round StPC-M (D3), elongate StPC-M (D4), StPC-m (D5).
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.