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.

806

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

806 results for “cavities”

Learn how ShareScore rates datasets ↗
zenodo40/100

Text-fig. 1. CT slices on Block 1. Details of the internal bone structure (a, b), teeth (b, c). Invertebrate imprints (a, c). Holes, cracks and empty cavities in both the limestone matrix and within the vertebrate fossil (b). in Hidden Treasures Uncovered: Successful Detection Of Fossils Below The Surface In Large Limestone Blocks Using A Standard Medical X-Ray Ct Scanner

Text-fig. 1. CT slices on Block 1. Details of the internal bone structure (a, b), teeth (b, c). Invertebrate imprints (a, c). Holes, cracks and empty cavities in both the limestone matrix and within the vertebrate fossil (b).

opencc-by-4.0Dec 2021View details →
zenodo40/100

Text-fig. 5. Mastixiopsis nyssoides KIRCHH. a, b, g–n: Organic preservation. a, b: Lignitic, unpermineralized, early Eocene Dorset Pipe clays at Arne, V. 40762. a: Ventral view (original illustration from pl. 18, fig. 1 of Chandler 1962). b: Transverse fracture, somewhat distorted by compression. c–f: Pyrite permineralization. c: Ventral view, V. 22963(1) from Sheppey, originally listed as Mastixia cantiensis. d: Lateral view, V. 22969 from Sheppey (identified as Mastixia grandis by Reid and Chandler 1933: pl. 25, fig. 8). e: Equatorial transverse physical section from (c). f: Equatorial transverse physical section from (d). g: Detail of pericarp from (e), showing endocarp formed of dense fibrous tissue, surrounded by mesocarp of anticlinally oriented larger cells. h: Detail of pericarp from (f). i–n: Type material from Eocene of Riestadt, Germany, MNB. i: Ventral view. j, k: Ventral and apical views of holotype. l: View of the transversely fractured surface from (j) showing horseshoe shaped locule. m: Equatorial transverse physical cut of the specimen in (i); note yellow resin cavity (arrow). n: Scanning electron microscopy of pericarp from (l) with locule lining at lower edge of image. Note dense endocarp tissue composed of small cells (fibres and sclereids), extending about 3/5 of distance to periphery, surrounded by mesocarp of larger, anticlinally oriented cells. Scale bars 1 cm in (a–f), (i–k), 1 mm in (g), 2 mm in (h), 3 mm in (l), m, 250 Μm in (n). Bar in (d) applies also to (c). Bar in (l) also applies to (m). Bar in (i) also applies to (j) and (k). in Mastixioid Fruits (Cornales) From The Early Eocene London Clay Flora: Morphology, Anatomy And Nomenclatural Revision

Text-fig. 5. Mastixiopsis nyssoides KIRCHH. a, b, g–n: Organic preservation. a, b: Lignitic, unpermineralized, early Eocene Dorset Pipe clays at Arne, V. 40762. a: Ventral view (original illustration from pl. 18, fig. 1 of Chandler 1962). b: Transverse fracture, somewhat distorted by compression. c–f: Pyrite permineralization. c: Ventral view, V. 22963(1) from Sheppey, originally listed as Mastixia cantiensis. d: Lateral view, V. 22969 from Sheppey (identified as Mastixia grandis by Reid and Chandler 1933: pl. 25, fig. 8). e: Equatorial transverse physical section from (c). f: Equatorial transverse physical section from (d). g: Detail of pericarp from (e), showing endocarp formed of dense fibrous tissue, surrounded by mesocarp of anticlinally oriented larger cells. h: Detail of pericarp from (f). i–n: Type material from Eocene of Riestadt, Germany, MNB. i: Ventral view. j, k: Ventral and apical views of holotype. l: View of the transversely fractured surface from (j) showing horseshoe shaped locule. m: Equatorial transverse physical cut of the specimen in (i); note yellow resin cavity (arrow). n: Scanning electron microscopy of pericarp from (l) with locule lining at lower edge of image. Note dense endocarp tissue composed of small cells (fibres and sclereids), extending about 3/5 of distance to periphery, surrounded by mesocarp of larger, anticlinally oriented cells. Scale bars 1 cm in (a–f), (i–k), 1 mm in (g), 2 mm in (h), 3 mm in (l), m, 250 Μm in (n). Bar in (d) applies also to (c). Bar in (l) also applies to (m). Bar in (i) also applies to (j) and (k).

opencc-by-4.0Aug 2022View details →
zenodo40/100

Lid-Driven Cavity Re=400 flow solution computed using LUMA and Code_Saturne coupled to each other

<p>This dataset is the result of running the Code_Saturne and LUMA codes coupled to each other to simulate a standard Re=400 Lid-Driven Cavity problemon ARCHER2. &nbsp;This is a test case for the coupling of the two codes.</p> <p>The domain is a unit cube. &nbsp;LUMA evolved&nbsp;the portion $x \le 0.6$, and Code\_Saturne evolved&nbsp;the portion $x \ge 0.4$. &nbsp;The boundary $x=0$ was&nbsp;driven with a velocity $u_y = 1$. &nbsp;Boundary data at the coupling boundaries is obtained from the other code using the PLE library.</p> <p>See&nbsp;https://github.com/cfdemons/cs-luma-archer/blob/main/tutorial.md for details to reproduce this dataset.</p> <p>&nbsp;</p>

opencc-by-4.0Oct 2022View details →
zenodo40/100

Plate III. Tyrannosaurus rex. Section of skull showing brain cavity. Amer. Mus. No. 5029: Scale 1/2. in Crania of Tyrannosaurus and Allosaurus

Plate III. Tyrannosaurus rex. Section of skull showing brain cavity. Amer. Mus. No. 5029: Scale 1/2.

opencc-by-4.0Jul 1906View details →
zenodo40/100

parallel-fibered bone; A5, osteocyte lacunae with well-preserved canaliculi; B3, osteocyte lacunae lacking canaliculi; B4, B5, growth pattern with preserved residuals of the thick annuli and zones (zo I–III) and thin annuli and zones (zo IV–VII); A6, growth pattern with preserved thin annuli and thick zones (zo I–IV), the dotted line marks the border between the perimedullary region and the cortex. Arrows in A5 and B3 indicate osteocyte lacunae; in B4, B5, and A6 indicate the annuli. Growth pattern in B4 figured on the lateral section side, in B5 and A5 on the ventral side; note the cortex thickness variation between B4 and B5. A1, A3, A4, A6, B1, B4, B5 in polarized light and A2, A5, B2, B3 in normal transmitted light. Abbreviations: an, annulus; ec, erosion cavity; pmr, perimedullary region; pos, primary osteon; sos, secondary osteon; zo, zone. in Palaeohistology helps reveal taxonomic variability in exceptionally large temnospondyl humeri from the Upper Triassic of Krasiejów, SW Poland

parallel-fibered bone; A5, osteocyte lacunae with well-preserved canaliculi; B3, osteocyte lacunae lacking canaliculi; B4, B5, growth pattern with preserved residuals of the thick annuli and zones (zo I–III) and thin annuli and zones (zo IV–VII); A6, growth pattern with preserved thin annuli and thick zones (zo I–IV), the dotted line marks the border between the perimedullary region and the cortex. Arrows in A5 and B3 indicate osteocyte lacunae; in B4, B5, and A6 indicate the annuli. Growth pattern in B4 figured on the lateral section side, in B5 and A5 on the ventral side; note the cortex thickness variation between B4 and B5. A1, A3, A4, A6, B1, B4, B5 in polarized light and A2, A5, B2, B3 in normal transmitted light. Abbreviations: an, annulus; ec, erosion cavity; pmr, perimedullary region; pos, primary osteon; sos, secondary osteon; zo, zone.

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

◂Fig. 5 Gametogenesis in male and female Veneriserva pygoclava. A–D Semi-thin histological sections of female Veneriserva pygoclava, stained with toluidine blue. A Cross-section of a female Veneriserva. B Close-up of large mature oocytes without discernible nurse cells. C Developing oocytes attached to mesenteries (mes), and oogonia proliferating from the ventral side of the dorsal blood vessel (bv). D Details of vitellogenic oocytes and nurse cells. Arrowheads indicate brownstained yolk platelets and yolk bodies. E Live sperm cells captured in a light micrograph. F–G Cross-sections of male Veneriserva. Note the absence of a gut in the cross-sections. Abbreviations—ac acicula, acr acrosome, bv blood vessel, coe coelomic cavity, mes mesentery, nc nurse cell, nn nurse cell nucleus, nu sperm cell nucleus, Oo oocyte, on oocyte nucleus, sp spermatogonia, vnc ventral nerve cord in Hardly Venus's servant-morphological adaptations of Veneriserva to an endoparasitic lifestyle and its phylogenetic position within Dorvilleidae (Annelida)

◂Fig. 5 Gametogenesis in male and female Veneriserva pygoclava. A–D Semi-thin histological sections of female Veneriserva pygoclava, stained with toluidine blue. A Cross-section of a female Veneriserva. B Close-up of large mature oocytes without discernible nurse cells. C Developing oocytes attached to mesenteries (mes), and oogonia proliferating from the ventral side of the dorsal blood vessel (bv). D Details of vitellogenic oocytes and nurse cells. Arrowheads indicate brownstained yolk platelets and yolk bodies. E Live sperm cells captured in a light micrograph. F–G Cross-sections of male Veneriserva. Note the absence of a gut in the cross-sections. Abbreviations—ac acicula, acr acrosome, bv blood vessel, coe coelomic cavity, mes mesentery, nc nurse cell, nn nurse cell nucleus, nu sperm cell nucleus, Oo oocyte, on oocyte nucleus, sp spermatogonia, vnc ventral nerve cord

opencc-by-4.0Jan 2024View details →
zenodo40/100

Fig. 5 in Towards incorporating insect isotope analysis using cavity ring-down spectroscopy into area-wide insect pest management programs

Fig. 5. Cumulative standard deviation of the mean carbon isotope signature of individual moths, field-caught LBAM (circles), mass-reared pink bollworm (squares) and mass-reared LBAM (triangles), analysed using the CM-CRDS module.

opencc-by-4.0Jun 2016View details →
zenodo40/100

Fig. 3 in Towards incorporating insect isotope analysis using cavity ring-down spectroscopy into area-wide insect pest management programs

Fig. 3. Carbon isotope signature of common cutworm leg samples from different moths reared on the artificial laboratory diet or caught in the wild (circles, n = 5, Bars +/- 3 SD). The spermatophore data point (triangle) is the carbon isotope signature of spermatophores dissected from laboratory-reared females mated with field-caught males (n = 5, Bars +/- 3 SD). All samples measured using CM-CRDS.

opencc-by-4.0Jun 2016View details →
zenodo40/100

Fig. 1 in Towards incorporating insect isotope analysis using cavity ring-down spectroscopy into area-wide insect pest management programs

Fig. 1. Carbon isotope ratios of 16 different common dietary components measured using either elemental analysis isotope ratio mass spectrometry (EAIRMS) or combustion module cavity ring down spectrometry (CM-CDRS).

opencc-by-4.0Jun 2016View details →
zenodo40/100

Fig. 2 in Towards incorporating insect isotope analysis using cavity ring-down spectroscopy into area-wide insect pest management programs

Fig. 2. Carbon isotope ratios of 3 populations of the common cutworm measured using either elemental analysis isotope ratio mass spectrometry (EA-IRMS) or combustion module cavity ring down spectrometry (CM-CDRS): Field-caught moths: squares; synthetic diet-reared moths: circles and laboratory-reared on castor diet moths: triangles.

opencc-by-4.0Jun 2016View details →
zenodo40/100

Figure 1 in Euryglossina (Euryglossina) perpusilla (Hymenoptera: Colletidae: Euryglossinae) nesting in pre-formed cavities in Bankisa atenuata (Proteaceae)

Figure 1. Nesting holes (preformed) in a branch of a live, yet partially burnt tree of Banksia attenuata Brown located at Star Swamp Reserve, Western Australia. A number of individuals of Euryglossina (Euryglossina) perpusilla Cockerell (Colletidae: Euryglossinae) were observed entering and exiting the holes, and two specimens, both females, were collected on 9 January 2017.

opencc-by-4.0Dec 2018View details →
zenodo40/100

Fig. 2. Morphological characters used for the analysis and key. A–D. Pronotum. E–F. Prosternal process. G–H. Mesoventral cavity. I. Elytral striae. J. Aedeagus. K in The world fauna of Synchroidae Lacordaire, 1859 (Coleoptera, Tenebrionoidea, Synchroidae)

Fig. 2. Morphological characters used for the analysis and key. A–D. Pronotum. E–F. Prosternal process. G–H. Mesoventral cavity. I. Elytral striae. J. Aedeagus. K. Ovipositor.

opencc-by-4.0Feb 2018View details →
zenodo40/100

Data from Figures in "Selection rules for cavity-enhanced Brillouin light scattering from magnetostatic modes"

<p>Data from figures in&nbsp;our paper &quot;Selection rules for cavity-enhanced Brillouin light scattering from magnetostatic modes&quot; in Physical Review B. The figures are in an Origin file (OriginPro 2016). Matlab code (R2016b) that can be used to generate plots of the magneto-static modes is also included.</p>

opencc-by-4.0Jun 2018View details →
zenodo40/100

Text-fig. 2—The articular surface of the frontal for the prefrontal in anterior view. A, Right frontal of Albertosaurus cf. A. lancensis, LACM 23845. B, Left frontal of Tyrannosaurus sp., MMS 51-2004. The diagonal lines indicate broken surfaces. Abbreviations: ec, endocranial cavity; po, articular surface of frontal for postorbital; prf, articular surface of frontal for prefrontal. MMS 51-2004 includes portions of the laterosphenoid and prootic in addition to the frontal. Bars represent 1 cm. in An albertosaur from the Hell Creek formation of Montana

Text-fig. 2—The articular surface of the frontal for the prefrontal in anterior view. A, Right frontal of Albertosaurus cf. A. lancensis, LACM 23845. B, Left frontal of Tyrannosaurus sp., MMS 51-2004. The diagonal lines indicate broken surfaces. Abbreviations: ec, endocranial cavity; po, articular surface of frontal for postorbital; prf, articular surface of frontal for prefrontal. MMS 51-2004 includes portions of the laterosphenoid and prootic in addition to the frontal. Bars represent 1 cm.

opencc-by-4.0Jan 1980View details →
zenodo40/100

Subgenus Lestes (15-28). L. sponsa: 15. Left side of head of ♂ showing ridge behind antennal cavity; 16. pterostigma of right forewing; 17-18. anal appendages dorsally and from left; 19. prophallus; 20. terminal segments and ovipositor sheath and vulvar scale at its base (all Germany except prophallus from Japan). L. barbarus (Morocco): 21. right anal appendages from above; 22. prophallus. L. dryas (California): 23. anal appendages dorsally, 24. prophallus. L. macrostigma (Turkey): 25, 26. the same. L. virens (Germany): 27, 28. the same. f = flange, hd = hood, li = ligula, sc = scoop, sh = shelf. in A revision of African Lestidae (Odonata) (excerpt)

Subgenus Lestes (15-28). L. sponsa: 15. Left side of head of ♂ showing ridge behind antennal cavity; 16. pterostigma of right forewing; 17-18. anal appendages dorsally and from left; 19. prophallus; 20. terminal segments and ovipositor sheath and vulvar scale at its base (all Germany except prophallus from Japan). L. barbarus (Morocco): 21. right anal appendages from above; 22. prophallus. L. dryas (California): 23. anal appendages dorsally, 24. prophallus. L. macrostigma (Turkey): 25, 26. the same. L. virens (Germany): 27, 28. the same. f = flange, hd = hood, li = ligula, sc = scoop, sh = shelf.

opencc-by-4.0Dec 1980View details →
zenodo40/100

Text-fig. 3. Rhinoppioides quadrituberculatus MIKO gen. et sp. nov. Above: assumed fragments of legs as seen in body cavity of holotype (Aa – in dorsal view, Ab – in ventral view) and paratype (B, only dorsal view available). Below: speculative reconstruction of legs, assumed segments leg IV in above rows (numbers 1, 3, 5, 7, 12, 13, 14), assumed segments of leg I below (numbers 6, 9, 10). Rest of the segments assumed to belong to legs II and III. Only trochanters III (nr. 8) and IV (nr. 7, 12) undoubtedly belonging to the new species. Bars indicating 50 µm, numbers indicate identity of segments. in Oribatid Mite Fossils From Quaternary And Pre-Quaternary Sediments In Slovenian Caves I.Two New Genera And Two New Species Of The Family Oppiidae From The Early Pleistocene

Text-fig. 3. Rhinoppioides quadrituberculatus MIKO gen. et sp. nov. Above: assumed fragments of legs as seen in body cavity of holotype (Aa – in dorsal view, Ab – in ventral view) and paratype (B, only dorsal view available). Below: speculative reconstruction of legs, assumed segments leg IV in above rows (numbers 1, 3, 5, 7, 12, 13, 14), assumed segments of leg I below (numbers 6, 9, 10). Rest of the segments assumed to belong to legs II and III. Only trochanters III (nr. 8) and IV (nr. 7, 12) undoubtedly belonging to the new species. Bars indicating 50 µm, numbers indicate identity of segments.

opencc-by-4.0Jul 2012View details →
zenodo40/100

Fig. 4 in Experimental manipulation of cavity temperature produces differential effects on parasite abundances in blue tit nests at two different latitudes

Fig. 4. Differences in the body mass of adult blue tit males by heat treatment of nest boxes and locality. Means ± intervals of confidence at 95% are shown.

opencc-by-4.0Apr 2021View details →
zenodo40/100

Fig. 2 in Experimental manipulation of cavity temperature produces differential effects on parasite abundances in blue tit nests at two different latitudes

Fig. 2. Blowfly pupae abundance observed in control and heated nests of blue tits (Cyanistes caeruleus) in both localities (Spain and Germany). The data presented was controlled for the locality and the interaction between locality and treatment. Means ± intervals of confidence at 95% are shown.

opencc-by-4.0Apr 2021View details →
zenodo40/100

Fig. 3 in Experimental manipulation of cavity temperature produces differential effects on parasite abundances in blue tit nests at two different latitudes

Fig. 3. Differences in the abundance of Haemoproteus/Plasmodium in blue tit males by treatment and locality. Means ± intervals of confidence at 95% are shown.

opencc-by-4.0Apr 2021View details →
zenodo40/100

Fig. 1 in Experimental manipulation of cavity temperature produces differential effects on parasite abundances in blue tit nests at two different latitudes

Fig. 1. Daily variation of temperature in nests of blue tits. Temperature is decreasing at 00:00 and lower values for the day are attained close to 8:00 h. Data from two different nests with nestling of 7 days old are represented from A) Spain and B) Germany.

opencc-by-4.0Apr 2021View 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