Skip to main content
Powered by ShareScore

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.

3,015

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

3,015 results for “occurrences”

Learn how ShareScore rates datasets ↗
zenodo40/100

Fig. 7 in Youngest occurrences of rhomaleosaurid plesiosaurs indicate survival of an archaic marine reptile clade at high palaeolatitudes

Fig. 7. Left ilium of the plesiosaur Rhomaleosauridae indet., SGM 1445-99, from the Lower Callovian Hlebnovka Formation of "Konnyi barak" ravine, Russia, in lateral (A), posterior (B), medial (C), anterior (D), and ventral (E) views.

opencc-by-4.0Jun 2015View details →
zenodo40/100

Fig. 3 in Youngest occurrences of rhomaleosaurid plesiosaurs indicate survival of an archaic marine reptile clade at high palaeolatitudes

Fig. 3. Left ischium of the plesiosaur Rhomaleosauridae indet., CAMSM X.50215, from the Callovian Peterborough Member of Fletton, United Kingdom, in dorsal view (articulated with left ilium) (A), and ventral (B), lateral (C), dorsomedial (D), and anterior (E) views.

opencc-by-4.0Jun 2015View details →
zenodo40/100

Fig. 1. A in Shallow-Water Occurrence ofWiwaxiain the Middle Cambrian of the Barrandian Area, Czech Republic

Fig. 1. A. Location of the Skryje−Týřovice Basin and the studied area within the Bohemian Massif and Czech Republic. B. Geology of the area of "Orthis small quarry" (modified after Mašek et al. 1997). C. Stratigraphy of the Skryje−Týřovice Basin (according to Fatka et al. 2011).

opencc-by-4.0Dec 2011View details →
zenodo40/100

Fig. 3 in Shallow-Water Occurrence ofWiwaxiain the Middle Cambrian of the Barrandian Area, Czech Republic

Fig. 3. Palaeogeographical distribution of the genus Wiwaxia in the lower and middle Cambrian. 1, Wiwaxia corrugata (Matthew, 1899), Burgess Shale of the Stephen Formation, British Columbia, USA (Conway Morris 1985a); 2, Wiwaxia corrugata (Matthew, 1899), Mount Cap Formation, northwestern Canada (Butterfield 1994); 3, Wiwaxia cf. corrugata (Matthew, 1899), Spence Shale, west−central Utah, USA (Conway Morris and Robison 1988; Robison 1991); 4, Wiwaxia taijiangensis Zhao, Qian, and Li, 1994, Kaili Formation, Guizhou, China (Zhao et al. 1994); 5, Wiwaxia sp., Emu Bay Shale, South Australia (Nedin unpublished material, Porter 2004); 6, Wiwaxia sp., Monastery Creek Formation, North Australia (Southgate and Shergold 1991; Porter 2004); 7, Wiwaxia sp., Sinsk Formation, Siberia (Ivantsov et al. 2005a, b); 8, Wiwaxia sp. cf. Wiwaxia corrugata (Matthew, 1899), Slapnice Member, Buchava Formation, Czech Republic (this paper). Early Cambrian palaeogeography modified after McKerrow et al. (1992).

opencc-by-4.0Dec 2011View details →
zenodo40/100

Fig. 2 in Shallow-Water Occurrence ofWiwaxiain the Middle Cambrian of the Barrandian Area, Czech Republic

Fig. 2. Isolated sclerites of Wiwaxia sp. cf. Wiwaxia corrugata (Matthew, 1899), Slapnice Member of the Buchava Formation, Skryje−Týřovice Basin, Barrandian area, Czech Republic. A, B. Part and counterpart of CGS XB 800a. C. CGS XB 800b. D. CGS XB 800c. E. CGS XB 800d. F. CGS XB 800e. A1–C1, D, E1–F1. Photos of scales. A2–C2, E2–F2. Drawings of the respective specimens. A3. Example of a typical assemblage of the sclerite of Wiwaxia (arrow) with fragments of graptolites; slab CGS XB 800.

opencc-by-4.0Dec 2011View details →
zenodo40/100

Fig. 4 in Mapping a brain parasite: occurrence and spatial distribution in fish encephalon

Fig. 4. Transmission electron micrographs showing the tegument and capsule walls of metacercariae of Cardiocephaloides longicollis. A and F illustrate the capsule wall of monocyst and multicyst metacercariae; B and I represent diagrams of monocyst and multicyst metacercariae showing the location of the following TEM micrographs. C – E Longitudinal section through the capsule wall and tegument of a monocyst. G, H, J-M Longitudinal section through the inner capsule wall and tegument of a multicyst metacercaria. D, E, J-M Detail of necrotic material accumulated on the capsule wall surrounding the metacercaria. K, Detail of inner capsule walls merging together within a multicyst. CW, capsule wall; F, fibrocyte; Gx, glycocalyx; GxF, glycocalyx filaments; ICW, inner capsule wall; M, metacercaria; M1- M3 number of metacercaria in a multicyst; MA, macrophage; Mt, metacercarial tegument; N, nucleus; NC, necrotic cells. Head arrows indicate glycocalyx filaments, asterisks (*) outside of the cyst, (**) inside of the cyst, (***) inside of the cyst when encysted with more than one capsule wall. Scale bars: D, E = 1 μm; C, G, H, J, L, M = 5 μm; K = 10 μm.

opencc-by-4.0Aug 2023View details →
zenodo40/100

Fig. 3 in Mapping a brain parasite: occurrence and spatial distribution in fish encephalon

Fig. 3. Occupation of the fish brain by Cardiocephaloides longicollis in fresh (A, B) and histological samples (C–F). Cardiocephaloides longicollis metacercariae within (A) the PGZ and (B) the medulla oblongata in experimentally-infected fish one month after infection. Asterisks indicate the position of metacercariae. Cardiocephaloides longicollis metacercariae are found at 6 dpi in the tectal ventricle (C), and as they grow (D, 21 dpi; E, 8 mpi; F, 15 mpi) they occupy larger part of the tectal ventricle, and also the PGZ. The representations of brains indicate the sections and positions (yellow square) where metacercariae have been found. Legend: TeO striped, cerebellum in dots and Mo squared. ICL, inferior cerebellar lobe; Mo, medulla oblongata; PGZ, periventricular gray zone of optic tectum; TeO, tectum opticum; TV, tectal ventricle. Scale bars: A = 300 μm; B = 450 μm; C–F = 200 μm. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Aug 2023View details →
zenodo40/100

Fig. 1 in Mapping a brain parasite: occurrence and spatial distribution in fish encephalon

Fig. 1. Distribution of metacercariae of Cardiocephaoides longicollis in the different fish brain regions, i.e., olfactory bulbs (Olf-B), olfactory lobes (Olf-L), optic lobe region (Op-L), inferior and superior cerebellar lobes (ICL, SCL), medulla oblongata (Mo), and spinal cord (SC). Metacercarial distribution in different fish species sampling locations are provided. N, number of infected brains used for metacercarial distribution; P, prevalence (based on total number of fish, see Table 1); MI, mean intensity. Note that the number of metacercariae in the brain of fish from the marine pond is based only of half brain (see Materials and methods).

opencc-by-4.0Aug 2023View details →
zenodo40/100

Fig. 2 in Mapping a brain parasite: occurrence and spatial distribution in fish encephalon

Fig. 2. Variation in the number of metacercariae of Cardiocephaloides longicollis encysted in different fish groups. Box plots represent the median number of metacercariae per brain region, upper and lower quartile (box) with maximum and minimum ranges (whiskers). Olfactory bulbs (Olf-B), olfactory lobes (Olf-L), optic lobe region (Op-L), inferior and superior cerebellar lobes (ICL, SCL), medulla oblongata (Mo), and spinal cord (SC). Y-axis is represented in logarithmic scale, and dots represent jittered raw data.

opencc-by-4.0Aug 2023View details →
zenodo40/100

Text-fig. 1. Simplified map of the Bohemian Cretaceous Basin (grey) showing the occurrence of Stramentum (Stramentum) pulchellum (G. B. SOWERBY JR., 1843). in A Systematic Revision Of Stramentum (Stramentum) Pulchellum (G.B. Sowerby Jr., 1843) (Cirripedia, Thoracica, Stramentidae) From The Bohemian Cretaceous Basin, The Czech Republic

Text-fig. 1. Simplified map of the Bohemian Cretaceous Basin (grey) showing the occurrence of Stramentum (Stramentum) pulchellum (G. B. SOWERBY JR., 1843).

opencc-by-4.0Dec 2013View details →
zenodo40/100

FIGURE 2 in RNames, a stratigraphical database designed for the statistical analysis of fossil occurrences - the Ordovician diversification as a case study

FIGURE 2. Structure of algorithm for time binning of stratigraphical units of the RNames Database (available under https://github.com/bjoekroe/RNames). Time bins are selected via three correlation routes (colour codes) and six rules resulting in six tables with referenced bins from which only those are selected which are most precise (i.e., range through lowest number of bins). Abbreviations: bio.unit, biostratigraphic unit; non-bio. unit, non-biostratigraphic unit. Colour code: red, correlation exclusively based on biostratigraphy; orange; correlation indirectly based on biostratigraphy; yellow, correlation based on direct or indirect assignments to time bins. -> arrow refers to referenced relations in RNames.

opencc-by-4.0Apr 2017View details →
zenodo40/100

FIGURE 1 in RNames, a stratigraphical database designed for the statistical analysis of fossil occurrences - the Ordovician diversification as a case study

FIGURE 1. Simplified structure of the RNames Database (rnames.luomus.fi/). The database contains eight related tables (blue and red objects) of which the object "Relations" is central. In "Relations" correlated stratigraphic units are listed by reference. Three output tables (yellow objects) list time binned stratigraphic units based on a search algorithm that uses "Relations" via R-Package RMySQL (the scripts are available under https://github.com/bjoekroe/ RNames). Global Stages after Cooper et al. (2012). Abbreviations: ID, identifier; StS, Stage Slice (Bergström et al., 2009); TS, Time Slice (Webby et al., 2004)

opencc-by-4.0Apr 2017View details →
zenodo40/100

FIGURE 5 in RNames, a stratigraphical database designed for the statistical analysis of fossil occurrences - the Ordovician diversification as a case study

FIGURE 5. Quality of PaleobioDB data used for diversity calculations. 1. Number of collections available per time bin. 2. Mean stratigraphic range of collections through time bins. Diamonds, two-time-bin resolution; triangles, one-time bin resolution; squares, all collections. Red, Global Stages after Cooper et al. (2012), green; Stage Slices, Bergström et al. (2009); blue, Time Slices, Webby et al. (2004).

opencc-by-4.0Apr 2017View details →
zenodo40/100

FIGURE 4 in RNames, a stratigraphical database designed for the statistical analysis of fossil occurrences - the Ordovician diversification as a case study

FIGURE 4. Ordovician genus-level diversity trends of PaleobioDB occurrence data, based on three different time binning approaches. 1. Total mean standing diversity (after Cooper, 2004). 2. Rarefied diversity with time bins of <100 collections culled, with quota 600. Diamonds, two-time-bin resolution; triangles, one-time bin resolution; stars, all collections. Red, Global Stages after Cooper et al. (2012), green; Stage Slices, Bergström et al. (2009); blue, Time Slices, Webby et al. (2004). Error bars reflect 95% confidence interval.

opencc-by-4.0Apr 2017View details →
zenodo40/100

FIGURE 6 in New occurrences of the endangered Notholebias minimus (Cyprinodontiformes: Rivulidae) in coastal plains of the State of Rio de Janeiro, Brazil: populations features and conservation

FIGURE 6 | Land use and cover (%) in 11 different localities (Protected/Conservation Units vs. Unprotected) and periods (1985–2021) at areas (buffer 250 m) of occurrence of Notholebias minimus.

opencc-by-4.0Aug 2023View details →
zenodo40/100

FIGURE 5 in New occurrences of the endangered Notholebias minimus (Cyprinodontiformes: Rivulidae) in coastal plains of the State of Rio de Janeiro, Brazil: populations features and conservation

FIGURE 5 | Unfertilized eggs ofNotholebias minimus, evidencing mushroom-like projections and polygonal grooves in the zona pellucida. Scale bar = 100 µm.

opencc-by-4.0Aug 2023View details →
zenodo40/100

FIGURE 3 in New occurrences of the endangered Notholebias minimus (Cyprinodontiformes: Rivulidae) in coastal plains of the State of Rio de Janeiro, Brazil: populations features and conservation

FIGURE 3 | Temporary wetlands in the Guandu River Hydrographic Region (coastal drainages of the Sepetiba Bay, State of Rio de Janeiro, Brazil) with new occurrences of Notholebias minimus. A–B. Swamps of open vegetation in Chaperó locality, C–D. Swamps in forest fragments in the campus of the Universidade Federal Rural do Rio de Janeiro – UFRRJ, and in the Área de Proteção Ambiental das Brisas, respectively.

opencc-by-4.0Aug 2023View details →
zenodo40/100

FIGURE 2 in New occurrences of the endangered Notholebias minimus (Cyprinodontiformes: Rivulidae) in coastal plains of the State of Rio de Janeiro, Brazil: populations features and conservation

FIGURE 2 | Males of Notholebias minimus captured in (A) Área de Proteção Ambiental das Brisas, Rio de Janeiro Municipality, and (B) in the campus of the Universidade Federal Rural do Rio de Janeiro – UFRRJ (Seropédica Municipality). Scale bar = 4 mm.

opencc-by-4.0Aug 2023View details →
zenodo40/100

FIGURE 1 in New occurrences of the endangered Notholebias minimus (Cyprinodontiformes: Rivulidae) in coastal plains of the State of Rio de Janeiro, Brazil: populations features and conservation

FIGURE 1 | Map of occurrences of Notholebias minimus in coastal plains of the State of Rio de Janeiro, Brazil. Black triangles indicate the new records in this study. Black dots, records from previous studies (e.g., Costa, Amorim, 2013; Costa, 2016). Occurrence references (codes) are available in Tab. 2.

opencc-by-4.0Aug 2023View details →
zenodo40/100

Figure 2. Alien spionid polychaetes from Sukhum Bay, Black Sea. A in First occurrence of the invasive alien species Streblospio gynobranchiata (Rice & Levin, 1998) and Polydora cornuta Bosc, 1802 (Polychaeta: Spionidae) on the coast of Abkhazia (Sukhum Bay, Black Sea)

Figure 2. Alien spionid polychaetes from Sukhum Bay, Black Sea. A – general view of Streblospio gynobranchiata (female, length 6.35 mm), B,C – Polydora cornuta morphology (fifth chaetiger): major spines with tooth (at) and companion chaetae (bc). Scale bars: 10 μm.

opencc-by-4.0Aug 2018View details →

ScienceDex guides

Understand access before you commit

These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

Compare curated 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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record