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.
15
datasets available to search
ShareScore release 0.9.0
Dataset results
15 results for “Onchobothriidae”
FIGURES 19–21 in Two new and one redescribed species of Acanthobothrium (Cestoda: Onchoproteocephalidea: Onchobothriidae) from Dasyatis akajei (Myliobatiformes: Dasyatidae) in the China Sea
FIGURES 19–21. Scanning electron micrographs of Acanthobothrium guanghaiense n. sp. 19. Scolex. 20. Distal bothridial surface. 21. Enlarged view of bothridial surface at lateral margin of bothridium. Scale–bars: 19, 50 µm; 20–21, 1 µm.
FIGURES 8–14 in Two new and one redescribed species of Acanthobothrium (Cestoda: Onchoproteocephalidea: Onchobothriidae) from Dasyatis akajei (Myliobatiformes: Dasyatidae) in the China Sea
FIGURES 8–14. Scanning electron micrographs of Acanthobothrium ningdense n. sp. 8. Scolex. 9. Apical view of scolex. 10. Enlarged view of apical pad and apical sucker. 11. Distal bothridial surface. 12. Enlarged view of proximal bothridial surface. 13. Enlarged view of bothridial surface at lateral margin of bothridium. 14. Surface of cephalic peduncle. Scale–bars: 8–9, 100 µm; 10, 20 µm; 11–14, 1 µm.
FIGURES 28–34 in Two new and one redescribed species of Acanthobothrium (Cestoda: Onchoproteocephalidea: Onchobothriidae) from Dasyatis akajei (Myliobatiformes: Dasyatidae) in the China Sea
FIGURES 28–34. Scanning electron micrographs of Acanthobothrium macrocephalum Wang & Yang, 2001. 28. Scolex. 29. Enlarged apical view of muscular pad and hooks in Fig. 28. 30. Apical view of muscular pad. 31. Enlarged view of hooks after removing the apical sucker. 32. Distal bothridial surface. 33. Enlarged view of bothridial surface at lateral margin of bothridium. 34. Enlarged view of proximal bothridial surface. Scale–bars: 28, 1 mm; 29, 100 µm; 30–31, 50 µm; 32, 1 µm; 33– 34, 2 µm.
FIGURES 22–27 in Two new and one redescribed species of Acanthobothrium (Cestoda: Onchoproteocephalidea: Onchobothriidae) from Dasyatis akajei (Myliobatiformes: Dasyatidae) in the China Sea
FIGURES 22–27. Acanthobothrium macrocephalum Wang & Yang, 2001. 22. Scolex. 23. Muscular pad with its sucker and two prominent lobes. 24. Hooks. 25. Terminal genitalia. 26. Mature proglottid. 27. Gravid proglottid. Scale–bars: 22, 600 µm; 23–25, 50 µm; 26–27, 200 µm.
FIGURES 16–18. Acanthobothrium guanghaiense n in Two new and one redescribed species of Acanthobothrium (Cestoda: Onchoproteocephalidea: Onchobothriidae) from Dasyatis akajei (Myliobatiformes: Dasyatidae) in the China Sea
FIGURES 16–18. Acanthobothrium guanghaiense n. sp. 16. Scolex. 17. Hooks. 18. Mature proglottid. Scale–bars: 16–18, 50 µm.
FIGURES 15a–15b. 15a in Two new and one redescribed species of Acanthobothrium (Cestoda: Onchoproteocephalidea: Onchobothriidae) from Dasyatis akajei (Myliobatiformes: Dasyatidae) in the China Sea
FIGURES 15a–15b. 15a. Hooks of Acanthobothrium micracantha Yamaguti, 1952 (Paratype, MPM: 22636). 15b. Hooks of Acanthobothrium latum Yamaguti, 1952 (Holotype, MPM: 22637), the dotted line of the tip of axial hook of medial hook are broken in its holotype and we interpreted it according to the form of lateral hook. Abbreviation: B, connecting bar. Scale–bars: 15a, 25 µm; 15b, 50 µm.
FIGURES 1–7. Acanthobothrium ningdense n in Two new and one redescribed species of Acanthobothrium (Cestoda: Onchoproteocephalidea: Onchobothriidae) from Dasyatis akajei (Myliobatiformes: Dasyatidae) in the China Sea
FIGURES 1–7. Acanthobothrium ningdense n. sp. 1. Scolex. 2. Hooks. 3. Immature proglottid. 4. One of the anteriormost mature proglottids. 5. Terminal genitalia. 6. One of the posteriormost mature proglottids. 7. Gravid proglottid. Abbreviation: S, irregular shaped sclerite. Scale–bars: 1, 3, 4, 5, 7, 100 µm; 2, 6, 50 µm.
Figure 4 from: Zaragoza-Tapia F, Pulido-Flores G, Gardner SL, Monks S (2020) Host relationships and geographic distribution of species of Acanthobothrium Blanchard, 1848 (Onchoproteocephalidea, Onchobothriidae) in elasmobranchs: a metadata analysis. ZooKeys 940: 1-49. https://doi.org/10.3897/zookeys.940.46352
Figure 4 Number of species of Acanthobothrium reported from elasmobranchs in each biogeographic region (Last et al. 2016b).
Figure 1 from: Zaragoza-Tapia F, Pulido-Flores G, Gardner SL, Monks S (2020) Host relationships and geographic distribution of species of Acanthobothrium Blanchard, 1848 (Onchoproteocephalidea, Onchobothriidae) in elasmobranchs: a metadata analysis. ZooKeys 940: 1-49. https://doi.org/10.3897/zookeys.940.46352
Figure 1 Type localities of species of Acanthobothrium reported worldwide and the biogeographic regions (Last et al. 2016b) of the geographic distribution of their hosts (see Table 1).
Figure 3 from: Zaragoza-Tapia F, Pulido-Flores G, Gardner SL, Monks S (2020) Host relationships and geographic distribution of species of Acanthobothrium Blanchard, 1848 (Onchoproteocephalidea, Onchobothriidae) in elasmobranchs: a metadata analysis. ZooKeys 940: 1-49. https://doi.org/10.3897/zookeys.940.46352
Figure 3 Families of rays: A number of species of rays per family B number of species of rays parasitized by species of Acanthobothrium. Note: The first number within parentheses corresponds to the number of species of ray that have been reported as hosts of Acanthobothrium and the second is the number of species that have been described from that Family C percentage of species of rays reported to be parasitized within the total number of families of rays- note: Red color = parasitized; Blue color = not parasitized.
Figure 2 from: Zaragoza-Tapia F, Pulido-Flores G, Gardner SL, Monks S (2020) Host relationships and geographic distribution of species of Acanthobothrium Blanchard, 1848 (Onchoproteocephalidea, Onchobothriidae) in elasmobranchs: a metadata analysis. ZooKeys 940: 1-49. https://doi.org/10.3897/zookeys.940.46352
Figure 2 Families of sharks: A number of species of sharks per family B number of species of sharks parasitized by species of Acanthobothrium. Note: The first number within parentheses corresponds to the number of species of shark that have been reported as hosts of Acanthobothrium and the second is the number of species that have been described from that Family C percentage of species of shark reported to be parasitized within the total number of families of sharks- note: Red color = parasitized; Blue color = not parasitized.
Figure 4 from: Zaragoza-Tapia F, Pulido-Flores G, Violante-González J, Monks S (2019) Two new species of Acanthobothrium Blanchard, 1848 (Onchobothriidae) in Narcine entemedor Jordan & Starks, 1895 (Narcinidae) from Acapulco, Guerrero, Mexico. ZooKeys 852: 1-21. https://doi.org/10.3897/zookeys.852.28964
Figure 4 Light microscope photographs of holotype of Acanthobothriumvidali sp. nov. (CNHE-11134). A Scolex B details of bothridium C peduncle cephalic D genitalia. Scale bars: 400 µm (A); 40 µm (B);100 µm (C, D). Abbreviations: vg vagina; cs cirrus sac; gp genital pore.
Figure 3 from: Zaragoza-Tapia F, Pulido-Flores G, Violante-González J, Monks S (2019) Two new species of Acanthobothrium Blanchard, 1848 (Onchobothriidae) in Narcine entemedor Jordan & Starks, 1895 (Narcinidae) from Acapulco, Guerrero, Mexico. ZooKeys 852: 1-21. https://doi.org/10.3897/zookeys.852.28964
Figure 3 Holotype of Acanthobothriumvidali sp. nov. (CNHE-11134). A Scolex B hooks C mature proglottid D genitalia. Scale bars: 400 µm (A); 200 µm (B–D).
Figure 1 from: Zaragoza-Tapia F, Pulido-Flores G, Violante-González J, Monks S (2019) Two new species of Acanthobothrium Blanchard, 1848 (Onchobothriidae) in Narcine entemedor Jordan & Starks, 1895 (Narcinidae) from Acapulco, Guerrero, Mexico. ZooKeys 852: 1-21. https://doi.org/10.3897/zookeys.852.28964
Figure 1 Holotype of Acanthobothriumsoniae sp. nov. (CNHE-11136). A Scolex B hooks C mature proglottid D terminal proglottid E genitalia. Scale bars: 200 µm (A, D); 100 µm (B, E); 150 µm (C).
Figure 2 from: Zaragoza-Tapia F, Pulido-Flores G, Violante-González J, Monks S (2019) Two new species of Acanthobothrium Blanchard, 1848 (Onchobothriidae) in Narcine entemedor Jordan & Starks, 1895 (Narcinidae) from Acapulco, Guerrero, Mexico. ZooKeys 852: 1-21. https://doi.org/10.3897/zookeys.852.28964
Figure 2 Light microscope photographs of holotype of Acanthobothriumsoniae sp. nov. (CNHE-11136). A Scolex B details of bothridium C peduncle cephalic D genitalia. Scale bars: 200 µm (A); 40 µm (B), 100 µm (C, D). Abbreviations: mt microtriches; vg vagina; cs cirrus sac; gp genital pore.
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.