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
Dataset results
806 results for “cavities”
FIGURE 1 in Redescription of the monotypic genus Cinusa Schioedte and Meinert, 1884 (Isopoda, Cymothoidae), a buccal-cavity isopod from South Africa
FIGURE 1. Cinusa tetrodontis, female lectotype (25.5 mm) (ZMUC CRU-20224). A. Full length dorsal view, B. Antennule, C. Antenna, D. Uropod, E. Lateral view of body. Scale bar: 1 mm.
FIGURE 4 in Redescription of the monotypic genus Cinusa Schioedte and Meinert, 1884 (Isopoda, Cymothoidae), a buccal-cavity isopod from South Africa
FIGURE 4. Cinusa tetrodontis, female, fresh material (19 mm) (SAMC A46771). A. Full length dorsal view, B. Ventral view of oostegites, C. Dorsal view of pleotelson, D. Lateral view of body. Scale bar: 2 mm.
FIGURE 8 in Redescription of the monotypic genus Cinusa Schioedte and Meinert, 1884 (Isopoda, Cymothoidae), a buccal-cavity isopod from South Africa
FIGURE 8. Cinusa tetrodontis, male paralectotype (17.5 mm) (ZMUC CRU-9140). A. Full length dorsal view, B. Lateral view of body. Scale bar: 2 mm.
FIGURE 7 in Redescription of the monotypic genus Cinusa Schioedte and Meinert, 1884 (Isopoda, Cymothoidae), a buccal-cavity isopod from South Africa
FIGURE 7. Cinusa tetrodontis, female, fresh material (19 mm) (SAMC A46771). A. Pleopod 1, dorsal, B. Pleopod 2, dorsal, C. Pleopod 3, dorsal, D. Pleopod 4, dorsal, E. Pleopod 5, dorsal. F. Pleopod 1, ventral, G. Pleopod 2, ventral, H. Pleopod 3, ventral, I. Pleopod 4, ventral, J. Pleopod 5, ventral, Scale bar: 1 mm.
FIGURE 3 in Redescription of the monotypic genus Cinusa Schioedte and Meinert, 1884 (Isopoda, Cymothoidae), a buccal-cavity isopod from South Africa
FIGURE 3. Cinusa tetrodontis, female lectotype (25.5 mm) (ZMUC CRU-20224). A. Pereopod 1, B. Pereopod 2, C. Pereopod 3, D. Pereopod 4, E. Pereopod 5, F. Pereopod 6, G. Pereopod 7. Scale bar: 2 mm.
FIGURE 10 in Redescription of the monotypic genus Cinusa Schioedte and Meinert, 1884 (Isopoda, Cymothoidae), a buccal-cavity isopod from South Africa
FIGURE 10. Cinusa tetrodontis, male, fresh material (12 mm) (SAMC A46772). A. Left maxillule, B. Left maxilliped, C. Antennule, D. Antenna, E. Left mandible, F. Left maxilla. Scale bar: 1 mm.
FIGURE 11 in Redescription of the monotypic genus Cinusa Schioedte and Meinert, 1884 (Isopoda, Cymothoidae), a buccal-cavity isopod from South Africa
FIGURE 11. Cinusa tetrodontis, male, fresh material (12 mm) (SAMC A46772). A. Pereopod 1, B. Pereopod 2, C. Pereopod 3, D. Pereopod 4, E. Pereopod 5, F. Pereopod 6, G. Pereopod 7. Scale bar: 1 mm.
FIGURE 2 in Redescription of the monotypic genus Cinusa Schioedte and Meinert, 1884 (Isopoda, Cymothoidae), a buccal-cavity isopod from South Africa
FIGURE 2. Cinusa tetrodontis, female lectotype (25.5 mm) (ZMUC CRU-20224). A. Ventral view of cephalon, B. Ventral view of oostegites, C. Dorsal view of cephalosome, D. Ventral view of pleotelson, E. Dorsal view of pleon and pleotelson. Scale bar: 1 mm.
FIGURE 3 in A new species of Domene Fauvel, 1873 (Coleoptera: Staphylinidae: Paederinae) from a granitic cavity in Serra da Estrela (Portugal)
FIGURE 3. SEM photographs of structural features of Domene viriatoi n.sp.: (a), head (dorsal view); (b), detail of the eye and chaetotaxy (lateral view); (c), labrum (dorsal view); (d), antennae (dorsal view); (e), part of the cleaning organ in foretibia (latero‒ventral view); (f), part of the cleaning organ in forefemur (latero‒ventral view); (g), pronotum (dorsal view); (h), elytra (dorsal view).
FIGURE 7 in A new species of Domene Fauvel, 1873 (Coleoptera: Staphylinidae: Paederinae) from a granitic cavity in Serra da Estrela (Portugal)
FIGURE 7. Aedeagus of Domene viriatoi n. sp.: (a), lateral view; (b), dorsal view; (c), ventral view.
FIGURE 5 in A new species of Domene Fauvel, 1873 (Coleoptera: Staphylinidae: Paederinae) from a granitic cavity in Serra da Estrela (Portugal)
FIGURE 5. SEM photographs of structural features of Domene viriatoi n. sp.: (a), III abdominal sternite (latero‒ventral view); (b), detail of intersegmental area between III and IV abdominal sternites (latero‒ventral view); (c), VII, VIII and IX abdominal sternites (ventral view); (d), detail of middle posteriad region of VII abdominal sternite (male, ventral view); (e), detail of VIII abdominal sternite (male, ventral view); (f), detail of the cluster of stout striate setae in VIII abdominal sternite (ventral view).
FIGURE 3 in Labrorostratus caribensis, a new oenonid polychaete from the Grand Caribbean living in the body cavity of a nereidid, with emendation of the genus
FIGURE 3. World distribution of parasitic Oenonid species with reduced maxillary apparatus (numbers matching those on the list of species from Table 2).
FIGURE 2. Labrorostratus caribensis n in Labrorostratus caribensis, a new oenonid polychaete from the Grand Caribbean living in the body cavity of a nereidid, with emendation of the genus
FIGURE 2. Labrorostratus caribensis n. sp. (A) Parapodium 100. (B) Modified ventral chaetae from medium parapodium. (C) Simple limbate chaetae from medium parapodium. (D) Simple bilimbate chaetae from posterior parapodium. Nereis sp. (E) Notopodial homogomph falciger from posterior parapodium. (F) Posterior parapodium, chaetae removed. Scale bars: A = 150 µm; B = 50 µm; C = 40 µm; D = 70 µm; E = 20 µm; F = 50 µm.
FIGURE 1. Labrorostratus caribensis n in Labrorostratus caribensis, a new oenonid polychaete from the Grand Caribbean living in the body cavity of a nereidid, with emendation of the genus
FIGURE 1. Labrorostratus caribensis n. sp. (A) Anterior region, lateral view. (B) Mandibles, ventral view. (C) maxillary carriers fused, ventral view. (D) Parapodium 6. (E) Parapodium 15. (F) Parapodium 30. (G) Parapodium 80. Scale bars: A = 250 µm; B = 100 µm; C = 150 µm; D-F = 100 µm; G = 150 µm.
FIGURE 5. Buccal cavity and third maxillipeds. A in Ankerius aenigmaticus, a new genus and new species of aphanodactylid crab symbiotic with polychaetes from the Red Sea coast of Saudi Arabia (Crustacea: Decapoda: Brachyura: Aphanodactylidae)
FIGURE 5. Buccal cavity and third maxillipeds. A, Selwynia laevis Borradaile, 1903, holotype male (7.1 × 5.6 mm) (CUMZ I.63872), Hulule Atoll, Maldives, coll. J.S. Gardiner, 1900; B, Gandoa brevipes (H. Milne Edwards, 1853), female (7.2 × 5.0 mm) (ZSM 1277/1) [holotype of Voeltzkowia zanzibarensis Lenz, 1905], Kokotoni, Zanzibar, coll. July 1889; C, Gustavus mecognathus Ahyong & Ng, 2009, paratype female (13.9 × 8.0 mm) (ZRC 2010.0252), SW Cocos Barrier, Guam, near small pass on large terebellid worm, coll. G. Paulay, 20 March 2000; D, Ankerius aenigmaticus gen. et sp. nov., female holotype (7.2 × 7.0 mm) (UF), Red Sea coast of Saudi Arabia.
Figs. 3–9. Strigister species. 3 in A New Genus and Species of North American Exosternini Associated with Cavity-Nesting Owls and a Reassignment ofPhelister simoniLewis (Coleoptera: Histeridae: Histerinae)
Figs. 3–9. Strigister species. 3) Dorsal habitus of S. tecolotito; 4) Dorsal habitus of S. simoni; 5) Frons of S. tecolotito; 6) Frons of S. simoni; 7) Ventral habitus of S. tecolotito; 8) Pro- and mesosterna of S. simoni; 9) Lateral habitus of S. tecolotito.
Fig. 10 in A New Genus and Species of North American Exosternini Associated with Cavity-Nesting Owls and a Reassignment ofPhelister simoniLewis (Coleoptera: Histeridae: Histerinae)
Fig. 10. Male genitalia of Strigister tecolotito. T8 = 8th tergite, S8 = 8th sternite, T9 = 9th tergite, S9 = 9th sternite, T10 = 10th tergite, tg = tegmen, bp = basal piece, ml = median lobe.
Figure 4 in Body cavity cells of Parachela during their active life
Figure 4. Histochemical staining of Hypsibius dujardini, Macrobiotus polonicus, Xerobiotus pseudohufelandi, and Isohypsibius granulifer granulifer; arrows indicate a positive reaction. A–C, histochemical staining of the storage cells of I. g. granulifer. LM. A, Periodic Acid-Schiff (PAS) method, scale bar = 7 µm. B, Sudan black B staining, scale bar = 5 µm. C, bromophenol blue staining (BPB), scale bar = 6 µm. D–F, histochemical staining of the storage cells of H. dujardini. LM. D, PAS method, scale bar = 6 µm; E, Sudan black B staining, scale bar = 6 µm; F, BPB, scale bar = 6 µm. G–I, histochemical staining of the storage cells of M. polonicus. LM. G, PAS method, scale bar = 9 µm; H, Sudan black B staining, scale bar = 7 µm; I, BPB, scale bar = 8 µm. J–L, histochemical staining of the storage cells of X. pseudohufelandi. LM. J, PAS method, scale bar = 11 µm; K, Sudan black B staining, scale bar = 11 µm; L, BPB, scale bar = 11 µm. LM, light microscope.
Coupled cluster cavity Born-Oppenheimer approximation for electronic strong coupling
<p>File to recreate the findings in: Coupled cluster cavity Born-Oppenheimer approximation for electronic strong coupling</p>
The effect of urbanization and temperature on thermal tolerance, foraging performance, and competition in cavity dwelling ants
<p>Human disturbance including rapid urbanization and increased temperatures can have profound effects on the ecology of local populations. Eusocial insects, such as ants, have adapted to stressors of increasing temperature and urbanization, however these evolutionary responses are not consistent among populations across geographic space. Here we asked how urbanization and incubation temperature influence critical thermal maximum (CT<sub>max</sub>) and various ecologically relevant behaviors in three ant species in urban and rural locations in Worcester, MA, USA. We did this by incubating colonies of three species of cavity dwelling ant (<em>Aphaenogaster picea, Tapinoma sessile, </em>and <em>Temnothorax longispinosus</em>) from 2 habitat types (Rural and Urban), for 60-days at multiple temperatures. We found that incubation temperature, urbanization and species of ant all significantly affected overall colony critical thermal maximum. We also found that recruitment time, colonization time and defense response were significantly affected by incubation temperature and varied between species of ant, while recruitment and colonization time were additionally affected by urbanization. These variable changes in performance and competitive traits across species suggest that responses to urbanization and shifting temperatures are not universal across species. Changes in behavioral responses caused by urbanization may disrupt biodiversity, creating unusual competitive environments as a consequence of natural adaptations and cause both direct and indirect mechanisms for which human disturbance can lead to local species extinction.</p> <p> </p>
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.