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.
6,025
datasets available to search
ShareScore release 0.9.0
Dataset results
6,025 results for “Science of science”
Figure 6 from: Van Roie M, De Wint F, Güngor A, Huyghe C, Dekoninck W, Sekerka L (2019) An annotated checklist of the leaf beetles (Coleoptera, Chrysomelidae) from El Salvador, with additions from the Bechyné collection in the Royal Belgian Institute of Natural Sciences. In: Schmitt M, Chaboo CS, Biondi M (Eds) Research on Chrysomelidae 8. ZooKeys 856: 137-196. https://doi.org/10.3897/zookeys.856.32017
Figure 6 Dorsal pictures of the species of Galerucinae excluding Alticini from El Salvador currently present in the collections of the RBINS. AAcalymmasemicaeruleaBAmphelasmanigrolineatumCCoraiaclarkiDC.maculicollisEDiabroticabalteataFD.circulataGD.curvilineataHD.pulchraID.viridulaJNeobroticaornataKPyesiadetritalaevicollis. High resolution images can be found at http://collections.naturalsciences.be/ssh-entomology.
Figure 6 from: Cunha CM, Rosenberg G (2019) Type specimens of Aplysiida (Gastropoda, Heterobranchia) in the Academy of Natural Sciences of Philadelphia, with taxonomic remarks. Zoosystematics and Evolution 95(2): 361-372. https://doi.org/10.3897/zse.95.33707
Figure 6 Aplysiida types. A–D. Syntype of Aplysiawillcoxi (=A.fasciata). A. Whole specimen, L = ca 114 mm, ANSP A2262, in dorsal view. B. Same in right lateral view. C. Shell in ventral view, L = 50 mm. D. Same, in dorsal view.
Figure 4 from: Cunha CM, Rosenberg G (2019) Type specimens of Aplysiida (Gastropoda, Heterobranchia) in the Academy of Natural Sciences of Philadelphia, with taxonomic remarks. Zoosystematics and Evolution 95(2): 361-372. https://doi.org/10.3897/zse.95.33707
Figure 4 Aplysiida types. A–E. Holotype of Tethyswillcoxivar.perviridis (=A.perviridis), A. Whole specimen, L. ca 105 mm, ANSP A2250 in right lateral view. B. Same, detail of opaline gland in dorsal view showing the uniporous and multiparous apertures. C. Same, opaline deflected showing the opaline gland spread on the roof of haemocoel. D. Shell of the same, L 60 mm, in ventral view. E. Same in dorsal view. F–H. Syntype of Tethyspilsbryi (= A.pilsbryi). F. Whole specimen, L 97 mm, ANSP A7036 in right lateral view. G. Same in dorsal view. H. Same, detail of pallial cavity showing the upturned edge to the rim of the mantle border (ed); legend: pa - parapodium, sr - seminal groove, ha - hermaphrodite aperture, ed - upturned edge, ma - mantle; gi - gill, as - anal siphon. Scale bar: 5 mm.
Figure 2 from: Cunha CM, Rosenberg G (2019) Type specimens of Aplysiida (Gastropoda, Heterobranchia) in the Academy of Natural Sciences of Philadelphia, with taxonomic remarks. Zoosystematics and Evolution 95(2): 361-372. https://doi.org/10.3897/zse.95.33707
Figure 2 Aplysiida types. A–B. Syntype of Syphonotaelongata (=Aplysiaparvula), A. Shell, L 11.3 mm, ANSP 20686 in dorsal view. B. Same, in ventral view. C–E. Syntypes of Tethysfloridensis (=A.fasciata), C. Shell, L ca 45 mm, ANSP 63529 in dorsal view. D. Same species, whole specimen, L ca 90 mm, ANSP A7034 in right lateral view. E. Same, in dorsal view. F. Syntype of Dolabriferafusca (= D.dolabrifera), shell, L 7.7, ANSP 20710 in dorsal view. G. Same, in ventral view. H–K. Syntypes of D.jacksoniensis (= D.brazieri), H. Shell, L 6.7 mm, ANSP 64931 in dorsal view. I. Same, in ventral view. J. Same species, whole specimen, L ca 16.7 mm, ANSP A7040 in dorsal view. K. Same in ventral view.
Figure 5 from: Cunha CM, Rosenberg G (2019) Type specimens of Aplysiida (Gastropoda, Heterobranchia) in the Academy of Natural Sciences of Philadelphia, with taxonomic remarks. Zoosystematics and Evolution 95(2): 361-372. https://doi.org/10.3897/zse.95.33707
Figure 5 Aplysiida types. A–D. Holotype of Tethysrobertsi (= A.robertsi), A. Whole specimen, L ca 92 mm, ANSP A7029 in dorsal view. B. Same in right lateral view. C. Same in ventral view. D. Same, detail showing the sole covered by small black dots. E–G. Syntype of Dolabriferaswiftii (=D.dolabrifera), D. Shell, L 10.5 mm, ANSP 67519 in dorsal view. F. Same in ventral view. G. Same in lateral view. H–L. Syntype of Tethyspulmonicavar.tryoniana (=A.pulmonica), H. Whole specimen, L ca 122 mm, ANSP A7037 in right lateral view. I. Same in dorsal view. J. Same in ventral view. K. Shell, L ca 58 mm, ANSP 66306, in dorsal view. L. Same in ventral view. Scale bar: 5 mm
Figure 3 from: Cunha CM, Rosenberg G (2019) Type specimens of Aplysiida (Gastropoda, Heterobranchia) in the Academy of Natural Sciences of Philadelphia, with taxonomic remarks. Zoosystematics and Evolution 95(2): 361-372. https://doi.org/10.3897/zse.95.33707
Figure 3 Aplysiida types. A–E. Syntypes of Dolabriferanicaraguana, A. Shell, L 8.2 mm, ANSP 67518 in dorsal view. B. Same, in ventral view. C. Same species, shell, L 9.2 mm, ANSP 67517 in dorsal view. D. Same in lateral view. E. Same in ventral view. F–I. Syntypes of Tethyspanamensis (= A.dactylomela), F. whole specimen, L ca 52 mm, ANSP A7042 in right lateral view. G. Same in dorsal view. H. Shell, L 16 mm, ANSP 20693 in ventral view. I. Same in dorsal view.
Figure 1 from: Cunha CM, Rosenberg G (2019) Type specimens of Aplysiida (Gastropoda, Heterobranchia) in the Academy of Natural Sciences of Philadelphia, with taxonomic remarks. Zoosystematics and Evolution 95(2): 361-372. https://doi.org/10.3897/zse.95.33707
Figure 1 Aplysiida types. A. Holotype of Aplysiaaequorea (=A.dactylomela), shell, L 35 mm, ANSP 66519 in dorsal view. B. Same, in ventral view. C–G. Types of A.badistes, C. Shell, L 18.7 mm, ANSP 187712 in dorsal view. D. Same, in ventral view. E. Same species, whole specimen, L 45.8mm, ANSP A7028 in dorsal view. F. Same, in ventral view. G. Same, in right lateral view. H–J. Syntypes of A.benedicti (=Aplysiaargus), whole specimens ANSP A7027. H. Specimen L 79 mm in dorsal view. I. Same, in right lateral view. J. Specimen L 76 mm in right lateral view.
Citizen Science SOPARC sheet
<p>Citizen Science SOPARC sheet</p>
Figure 4 from: Croce A, Nazzaro R (2017) An atlas of orchids distribution in the Campania region (Italy), a citizen science project for the most charming plant family. Italian Botanist 4: 15-32. https://doi.org/10.3897/italianbotanist.4.14916
Figure 4 - Richness of taxa based on field data (observations). The number includes hybrids. Coordinates are expressed in metres, UTM WGS84 33N. Province abbreviations: AV = Avellino, BN = Benevento, CE = Caserta, NA = Naples, SA = Salerno.
Figure 3 from: Croce A, Nazzaro R (2017) An atlas of orchids distribution in the Campania region (Italy), a citizen science project for the most charming plant family. Italian Botanist 4: 15-32. https://doi.org/10.3897/italianbotanist.4.14916
Figure 3 - number of field data (observations) in the 10 km × 10 km cells of the grid on 31 December 2016. Coordinates are expressed in metres, UTM WGS84 33N. Province abbreviations: AV = Avellino, BN = Benevento, CE = Caserta, NA = Naples, SA = Salerno.
Figure 2 from: Croce A, Nazzaro R (2017) An atlas of orchids distribution in the Campania region (Italy), a citizen science project for the most charming plant family. Italian Botanist 4: 15-32. https://doi.org/10.3897/italianbotanist.4.14916
Figure 2 - Richness of taxa based on literature data. The number includes hybrids but also species sensu lato. Coordinates are expressed in metres, UTM WGS84 33N. Province abbreviations: AV = Avellino, BN = Benevento, CE = Caserta, NA = Naples, SA = Salerno.
Figure 1 from: Croce A, Nazzaro R (2017) An atlas of orchids distribution in the Campania region (Italy), a citizen science project for the most charming plant family. Italian Botanist 4: 15-32. https://doi.org/10.3897/italianbotanist.4.14916
Figure 1 - Number of bibliographic records (citations) in the 10 km × 10 km cells of the grid on 31 December 2016. Coordinates are expressed in metres, UTM WGS84 33N. Province abbreviations: AV = Avellino, BN = Benevento, CE = Caserta, NA = Naples, SA = Salerno.
Figure 5 from: Croce A, Nazzaro R (2017) An atlas of orchids distribution in the Campania region (Italy), a citizen science project for the most charming plant family. Italian Botanist 4: 15-32. https://doi.org/10.3897/italianbotanist.4.14916
Figure 5 - Distribution of the observations over time, collected in research projects or by volunteer contributors.
Supplementary material 2 from: Croce A, Nazzaro R (2017) An atlas of orchids distribution in the Campania region (Italy), a citizen science project for the most charming plant family. Italian Botanist 4: 15-32. https://doi.org/10.3897/italianbotanist.4.14916
Checklist of the taxa recorded in the database : Data type: Table
Figure 6 from: Croce A, Nazzaro R (2017) An atlas of orchids distribution in the Campania region (Italy), a citizen science project for the most charming plant family. Italian Botanist 4: 15-32. https://doi.org/10.3897/italianbotanist.4.14916
Figure 6 - Distribution of the localities of the observations (punctual type) inside (black circles) and outside (open circles) protected areas (grey areas).
Figure 7 from: Croce A, Nazzaro R (2017) An atlas of orchids distribution in the Campania region (Italy), a citizen science project for the most charming plant family. Italian Botanist 4: 15-32. https://doi.org/10.3897/italianbotanist.4.14916
Figure 7 - Distribution of the localities of the observations (punctual type) inside (black circles) and outside (open circles) a 2 km buffer around the main roads (bands).
Figure 3 from: Heard J, Chen J-P, Wen CKC (2019) Citizen science yields first records of Hippocampus japapigu and Hippocampus denise (Syngnathidae) from Taiwan: A hotspot for pygmy seahorse diversity. ZooKeys 883: 83-90. https://doi.org/10.3897/zookeys.883.39662
Figure 3 Comparison of AHippocampus denise in situ, Orchid Island, Taiwan at 28 m depth, with its most similar congener BHippocampus bargibanti in situ, Green Island, Taiwan. Note the differences in body colouration (orange in H. denise vs. purple in H. bargibanti), the number and size of tubercles (fewer and less pronounced in H. denise), snout length (bulbous tip in H. bargibanti vs. non-bulbous in H. denise) and overall shape (slender and elongate in H. denise vs. rotund in H. bargibanti) (Photographs A Yung-Kuang Ting B Ryan Ku).
Figure 2 from: Heard J, Chen J-P, Wen CKC (2019) Citizen science yields first records of Hippocampus japapigu and Hippocampus denise (Syngnathidae) from Taiwan: A hotspot for pygmy seahorse diversity. ZooKeys 883: 83-90. https://doi.org/10.3897/zookeys.883.39662
Figure 2 Hippocampus japapigu in situ A Green Island, Taiwan B Hejie, Kenting, Taiwan at 5 m depth C Hejie, Kenting, Taiwan D 82.5 k near Longdong, northern Taiwan (Photographs A Jolly Huang B Jay Chiu C Chao-Tsung Chen D Jung-Chao Yeh).
Figure 4 from: Heard J, Chen J-P, Wen CKC (2019) Citizen science yields first records of Hippocampus japapigu and Hippocampus denise (Syngnathidae) from Taiwan: A hotspot for pygmy seahorse diversity. ZooKeys 883: 83-90. https://doi.org/10.3897/zookeys.883.39662
Figure 4 Comparison of A–CHippocampus colemani in situ, Green Island, Taiwan with D–FHippocampus pontohi in situ, Green Island, Taiwan. Note the differences in the shape and angle of the coronet (low and rounded in H. colemani vs. distinct and angular in H. pontohi), as well as differences in body colouration (H. colemani is known only to occur in shades of off-white, whereas H. pontohi is highly variable) (Photographs A Joe Chiu B Ryan Ku C, E, F Ming-Hung Yu D Ryan Ku).
Figure 1 from: Heard J, Chen J-P, Wen CKC (2019) Citizen science yields first records of Hippocampus japapigu and Hippocampus denise (Syngnathidae) from Taiwan: A hotspot for pygmy seahorse diversity. ZooKeys 883: 83-90. https://doi.org/10.3897/zookeys.883.39662
Figure 1 Map showing A the original collection locations of specimens for the five pygmy seahorse species recorded in Taiwan during this study, as well as B their distributions in Taiwan and surrounding islands (Penghu islands, Green Island, and Orchid Island). Symbols are scaled relatively according to the number of observations per species at each location obtained through social media.
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.