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.
150
datasets available to search
ShareScore release 0.9.0
Dataset results
150 results for “parasitic Copepoda”
Figure 14 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 14. Chondracanthus kabatai sp. n., paratype male from Zenopsis conchifer Lowe. A. Habitus, lateral view. B. Antennule. C. Antenna. D. Mandible. E. Maxillule. F. Maxilla. G. Maxilliped. H. Leg 1. I. Leg 2. J. Lateral view of genito-abdomen. K. Rami.
Figure 8 in New species of Acanthochondria Oakley, 1930 and Chondracanthus Delaroche, 1811 (Copepoda: Cyclopoida: Chondracanthidae) parasitizing marine fishes from Indian waters
Figure 8. Chondracanthus kabatai sp. n. from Zenopsis conchifer Lowe. A–C. Holotype, female, dorsal, ventral and lateral views. D–F. Paratype, female, dorsal, ventral and dorso-lateral views.
Fig. 3. Tracheliastes sachalinensis Markevich, 1936 in First Records of Tracheliastes sachalinensis (Copepoda: Lernaeopodidae), a Fin Parasite of Cyprinids, from Japan
Fig. 3. Tracheliastes sachalinensis Markevich, 1936, adult female from Tribolodon sachalinensis in the Jirô-sawa River, Hokkaido. A, first antenna, medial; B, second antenna, lateral; C, same, tip of endopod, lateral; D, mandible, lateral; E, first maxilla, lateral; F, bulla and tips of second maxillae, dorsal; G, maxilliped, dorsal. 1, endopod of second antenna; 2, exopod of second antenna; 3, anchor; 4, manubrium. Scale bars: A–D, G, 20 µm; E, 10 µm; F, 0.2 mm.
Fig. 1 in First Records of Tracheliastes sachalinensis (Copepoda: Lernaeopodidae), a Fin Parasite of Cyprinids, from Japan
Fig. 1. Distribution records of Tracheliastes sachalinensis Markevich, 1936 in Far East Asia. Collection localities (solid circles) in this study (Hokkaido: 1, Lake Abashiri; 2, Lake Shirarutoro; 3, Lake Tôro; 4, Mena River; 5, Jirô-sawa River); type locality of Tra. sachalinensis (solid triangle) (Sakhalin: 6, Tym River [Markevich 1936]); collection localities (open circles) in the previous studies (Sakhalin: 7, Aslanbekova Passage; 8, Poronai River (including the Leonidovka River); 9. Uglegorka River; 10. Tatar Strait at Lomonon Cape; 11, Ainskoye Lake; 12, Naiva River; 13. Mal Takoy River; 14. Lake Tunaycha; 15, Vavaiskoe Lake; 16, Lebyazh'ye Lake [Shedko et al. 2005; Sokolov et al. 2012]; the Shantar Islands: 17, Bol'shoye Lake [Shedko et al. 2005]; the Primorsky Krai: 18, Koppi River; 19, Samarga River; 20, Amgu River [Shedko et al. 2005]). The species was also reported from the Amur River basin (Dogiel and Akhmerov 1952) including Lake Khivanda (Smirnova 1971), but this lake is not shown herein because its location was not determined.
Fig. 1 in Salmincola markewitschi (Copepoda: Lernaeopodidae) Parasitic on Whitespotted Char, Salvelinus leucomaenis, in a Mountain Stream of Honshu Island, Central Japan
Fig. 1. Salmincola markewitschi, female, NSMT-Cr 28337, from whitespotted char, Salvelinus leucomaenis, from the Zako River, a tributary of the upper Nakatsu River, Nagano Prefecture, central Honshu Island, Japan. A, habitus, lateral view; B, habitus, dorsal view; C, cephalothorax, second maxillae and bulla, anterior view; D, first antenna, dorsal view; E, second antenna, anterolateral view; F, exopod of second antenna, lateral view; G, H, mandibles, lateral view; I, first maxilla, lateral view; J, maxilliped, dorsolateral view; K, maxilliped, palp, dorsolateral view. Abbreviations: h1, hook 1; p, palp; p4, process 4; p5, process 5; s2, spine 2; t3, tubercle 3. Scale bars: A–C, 1 mm; D, 20 µm; E, 50 µm; F–H, 20 µm; I, 30 µm; J, 100 µm; K, 20 µm.
Fig. 3 in Salmincola edwardsii (Copepoda: Lernaeopodidae) Parasitic on Southern Asian Dolly Varden, Salvelinus malma krascheninnikova, from Hokkaido Island, Japan, with the Southernmost Distribution Record of the Copepod in Asia
Fig. 3. Map of Hokkaido Island and the southern Kuril Islands, showing the collection localities of Salmincola edwardsii in the previous (closed triangles, Shedko and Shedko, 2002) and present (closed circles) studies. Open circles show no copepod infection on southern Asian Dolly Varden. 1, Olya Inlet (Prostor Bay), Iturup Island; 2, Kuibyshev Bay, Iturup Island; 3, Petrova River, Kunashir Island; 4, a nameless creek, Kunashir Island; 5, Rusha River; 6, Rausu River; 7, Shari River; 8, Shibetsu River; 9, Saru River; 10, Yoichi River; 11, Shiribetsu River; 12, Notto River; 13, Chihase River.
Fig. 2 in Salmincola edwardsii (Copepoda: Lernaeopodidae) Parasitic on Southern Asian Dolly Varden, Salvelinus malma krascheninnikova, from Hokkaido Island, Japan, with the Southernmost Distribution Record of the Copepod in Asia
Fig. 2. Female of Salmincola edwardsii attached to the base of gill filament of southern Asian Dolly Varden, Salvelinus malma krascheninnikova, from the Shari River, Hokkaido Island. Formalinfixed and later ethanol-preserved specimen, lateral view. Abbreviations: c, cephalothorax; es, egg sac; ga, gill arch; gf, gill filament; mx2, second maxilla; mxp, maxilliped; t, trunk. Scale bar: 1 mm. Note most portions of the infected gill filament lost, and a bulbous swelling (*) enveloping the bulla.
Fig. 1 in Salmincola edwardsii (Copepoda: Lernaeopodidae) Parasitic on Southern Asian Dolly Varden, Salvelinus malma krascheninnikova, from Hokkaido Island, Japan, with the Southernmost Distribution Record of the Copepod in Asia
Fig. 1. Salmincola edwardsii, female, from southern Asian Dolly Varden, Salvelinus malma krascheninnikova, from the Shari River, Hokkaido Island. A, habitus, anterolateral view; B, second antenna, lateral view; C, mandible, lateral view; D, first maxilla, lateral view; E, maxilliped, lateral view. Abbreviations: ant2, second antenna; b, bulla; c, cephalothorax; es, egg sac; ex, exopod; h1, hook 1; mx2, second maxilla; mxp, maxilliped; p, palp; p4, process 4; p5, process 5; s2, spine 2; sy, sympod; t, trunk. Scale bars: A, 1 mm; B, 50 µm; C, 20 µm; D, 100 µm; E, 200 µm.
Figs 15–17 in Microsporidia in a Woodland Pool I. Lanatospora costata sp. n. (Opisthosporidia, Microsporidia), Parasite of Megacyclops viridis (Crustacea, Copepoda): Fine Structure and Molecular Phylogeny
Figs 15–17. Lanatospora costata, parasite of Megacyclops viridis, structure of spores as seen in SEM and TEM. 15 – Spore surface ornamentation as seen by SEM. Note that the exospore ribs form a complex armour on the spore surface. Scale bar: 1 µm. 16 – Detail of the polaroplast lamellae (pl) in the apical part of the spore, pf – polar filament. Scale bar: 200 nm. 17 – Details of the polar filament coils (pf) in cross section. Scale bar: 500 nm.
Fig. 19 in Microsporidia in a Woodland Pool I. Lanatospora costata sp. n. (Opisthosporidia, Microsporidia), Parasite of Megacyclops viridis (Crustacea, Copepoda): Fine Structure and Molecular Phylogeny
Fig. 19. The woodland pool near Přerov nad Labem, Central Bohemia Region, Czech Republic (50°167′N, 14°810′E), the type habitat of Lanatospora costata sp. n.
Fig. 3 in New records of Colobomatus mylionus Fukui, 1965 and Clavellisa chinensis (Yü, 1933) (Crustacea: Copepoda) parasitic on marine fish of Korea
Fig. 3. Clavellisa chinensis (Yü, 1933), adult female. A. habitus, dorsal view. B. habitus, lateral view. C. antennule. D. antenna. E. mandible. F. maxillule. G. maxilliped. Scale bars: A, B = 500 μm; C, D, G = 200 μm; E, F = 100 μm.
Fig. 2 in An alien parasite affects local fauna-Confirmation of Sinergasilus major (Copepoda: Ergasilidae) switching hosts and infecting native Silurus glanis (Actinopterygii: Siluridae) in Hungary
Fig. 2. Evolutionary history of Sinergasilus based on Bayesian Inference (BI) analysis of 18S rDNA with Ergasilus anchoratus Markewitsch, 1940 designated as outgroup. Support for both maximum likelihood (ML, 1000 bootstrap replicates) and BI (10 million MCMC) indicated at nodes (ML/BI), only nodes with more than 50% support annotated.
Fig. 1 in An alien parasite affects local fauna-Confirmation of Sinergasilus major (Copepoda: Ergasilidae) switching hosts and infecting native Silurus glanis (Actinopterygii: Siluridae) in Hungary
Fig. 1. Micrographs using light microscopy (LM) and scanning electron microscopy (SEM) of Sinergasilus major; (A) Total body (SEM), (B) rostral plate with integumental pores and tactile setules (SEM), (C) thoracic plate with pectinate denticles (SEM), (D) ventral aspect of cephalon (SEM), (E) everted mouth (SEM), (F) inverted mouth (SEM), (G) ventral view of mouth parts (SEM), (H) mouth parts (LM). A1 – antennule 1, A2 – antenna, Ip – integumental pore, Gs – genital somite, Lb – labium, Lr – labrum, M – mouth, Md – mandible, Ml – maxillule, Mx – maxilla, Ps4 – pedigerous somite 4, Pd – pectinate denticles, Tp – thoracic plate, Ts – tactile setules.
Fig. 1 in First step towards understanding the specific identity of fish muscle parasites of the genus Sarcotaces (Copepoda: Philichthyidae)-New species and first molecular ID in the genus
Fig. 1. Photographs documenting copepod (Sarcotaces izawai sp. nov.) infection of fish (Mora moro); (A) Parasite-induced black-stained void in the body of host fish, (B) parasite gall in the muscles of host fish, (C) The same with myomeres removed, (D) Composite microphotograph of the male parasite, lateral view. Scale bars: A–C = 30 mm, D = 0.5 mm. Photos A–C: by Karolina Po´łtorak.
Fig. 4 in First step towards understanding the specific identity of fish muscle parasites of the genus Sarcotaces (Copepoda: Philichthyidae)-New species and first molecular ID in the genus
Fig. 4. SEM micrographs of Sarcotaces izawai sp. nov.; male; (A) Cephalon, dorsal, (B) Cephalothorax, ventral, (C) Cephalon, anterior view, (D) Antennule, dorsal, (E) Antennule, ventral, (F) Antenna, ventral.
Fig. 3 in First step towards understanding the specific identity of fish muscle parasites of the genus Sarcotaces (Copepoda: Philichthyidae)-New species and first molecular ID in the genus
Fig. 3. Line drawings of Sarcotaces izawai sp. nov.; male; (A–E) Caudal rami of other male specimens, ventral; (F) Antennule, ventral; (G) Antenna, ventral; (H) Mandible (Mdb), and maxillae (Mx), ventral; above—protuberances of supramandibular ridge; left mandible omitted), (I) First leg (right side), ventral, (J) Second leg (left side), ventral; Scale bars: A–E = 0.1 mm, F–J = 0.01 mm.
Fig. 5 in First step towards understanding the specific identity of fish muscle parasites of the genus Sarcotaces (Copepoda: Philichthyidae)-New species and first molecular ID in the genus
Fig. 5. SEM micrographs of Sarcotaces izawai sp. nov.; male; (A) Antenna, mandible and maxillule, ventral, (B) Mandibular claw and maxillule, ventral, (C) Maxillae, ventral, (D) Exopod of first thoracopod (left side), (E) Caudal rami of other male specimens, ventral, (F) Caudal ramus of another male specimens, ventral.
Fig. 2 in First step towards understanding the specific identity of fish muscle parasites of the genus Sarcotaces (Copepoda: Philichthyidae)-New species and first molecular ID in the genus
Fig. 2. Line drawings of Sarcotaces izawai sp. nov.; (A) Female (allotype), habitus, semi-ventral view; small black silhouettes on the right represent the males at the same scale (the highest number found in a single gall), (B) Male (holotype), habitus, ventral, (C, D, E) Other males, habitus, ventral, (F, G) Caudal rami of other male specimens; Abbreviations: M = mouth area, T IV–T VII = thoracic somites, A I–A IV = abdominal somites; Scale bars: A = 10 mm, B–E = 0.5 mm, F–G = 0.1 mm.
Linked collectors and determiners for: Parasitic copepods of the family Lernanthropidae Kabata, 1979 (Copepoda: Siphonostomatoida) from Australian fishes, with descriptions of seven new species.
Natural history specimen data linked to collectors and determiners held within, "Parasitic copepods of the family Lernanthropidae Kabata, 1979 (Copepoda: Siphonostomatoida) from Australian fishes, with descriptions of seven new species". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/c76ec731-0dc9-4fc4-8ea4-d90d90da9438">https://bionomia.net/dataset/c76ec731-0dc9-4fc4-8ea4-d90d90da9438</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/c76ec731-0dc9-4fc4-8ea4-d90d90da9438">https://gbif.org/dataset/c76ec731-0dc9-4fc4-8ea4-d90d90da9438</a>. Formatted as a Frictionless Data package.
FIGURE 44 in Parasitic copepods of the family Lernanthropidae Kabata, 1979 (Copepoda: Siphonostomatoida) from Australian fishes, with descriptions of seven new species
FIGURE 44. Sagum lativentris (Heller, 1865) n. comb., adult ♀. A, habitus, dorsal; B, habitus, lateral; C, habitus, ventral. Scale bar 1 mm.
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.