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43 results for “parasitic worm”
Figure 7 from: Chiu M-C, Huang C-G, Wu W-J, Lin Z-H, Chen H-W, Shiao S-F (2020) A new millipede-parasitizing horsehair worm, Gordius chiashanus sp. nov., at medium altitudes in Taiwan (Nematomorpha, Gordiida). ZooKeys 941: 25-48. https://doi.org/10.3897/zookeys.941.49100
Figure 7 Phylogenetic relationship of Gordius/Acutogordius spp. restructured using COI partial sequences compared with C. formosanus, E. nigromaculatus, and P. diblastus as out groups. Numbers at the nodes represent the percentage of 1000 bootstrap replicates.
Supplementary material 1 from: Chiu M-C, Huang C-G, Wu W-J, Lin Z-H, Chen H-W, Shiao S-F (2020) A new millipede-parasitizing horsehair worm, Gordius chiashanus sp. nov., at medium altitudes in Taiwan (Nematomorpha, Gordiida). ZooKeys 941: 25-48. https://doi.org/10.3897/zookeys.941.49100
Video S1
Figure 5 from: Chiu M-C, Huang C-G, Wu W-J, Lin Z-H, Chen H-W, Shiao S-F (2020) A new millipede-parasitizing horsehair worm, Gordius chiashanus sp. nov., at medium altitudes in Taiwan (Nematomorpha, Gordiida). ZooKeys 941: 25-48. https://doi.org/10.3897/zookeys.941.49100
Figure 5 Field observation of Gordius chiashanus sp. nov. A hazy appearance (arrows) surrounding the body surface in hot water B spermatophore (arrow) on a female collected on the surface of the soil C rainbow-like reflection on the body surface D free-living adult collected in wet soil E, F infected host, Spirobolus sp. nov. (Hsu and Chang, unpublished), harboring (E) three immature worms (arrow) and (F) an adult worm. Photographs courtesy of (D) Fang, Hua-Te and (F) Hung, Ming-Chin. Scale bars: 1 cm (E).
Figure 8 from: Chiu M-C, Huang C-G, Wu W-J, Lin Z-H, Chen H-W, Shiao S-F (2020) A new millipede-parasitizing horsehair worm, Gordius chiashanus sp. nov., at medium altitudes in Taiwan (Nematomorpha, Gordiida). ZooKeys 941: 25-48. https://doi.org/10.3897/zookeys.941.49100
Figure 8 Seasonal occurrence of free-living adults of Gordius chiashanus sp. nov. Numbers at the bottom indicate the actual number of each bar.
Figure 4 from: Chiu M-C, Huang C-G, Wu W-J, Lin Z-H, Chen H-W, Shiao S-F (2020) A new millipede-parasitizing horsehair worm, Gordius chiashanus sp. nov., at medium altitudes in Taiwan (Nematomorpha, Gordiida). ZooKeys 941: 25-48. https://doi.org/10.3897/zookeys.941.49100
Figure 4 Female Gordius chiashanus sp. nov. A, B anterior end examined using a (A) stereomicroscope and (B) SEMC–E posterior end with the terminal view examined using a (C) stereomicroscope and (D) SEM, and the (E) lateral view examined using a stereomicroscope F, G mid-body examined using a (F) stereomicroscope and (G) compound microscope. Co, cloacal opening. Scale bars: 1 mm (A, F, G), 200 μm (B–D).
Figure 2 from: Chiu M-C, Huang C-G, Wu W-J, Lin Z-H, Chen H-W, Shiao S-F (2020) A new millipede-parasitizing horsehair worm, Gordius chiashanus sp. nov., at medium altitudes in Taiwan (Nematomorpha, Gordiida). ZooKeys 941: 25-48. https://doi.org/10.3897/zookeys.941.49100
Figure 2 Posterior end of male Gordius chiashanus sp. nov. A stereomicroscopic image of the posterior end B–DSEM images of (B) overview of the posterior end with bristles concentrated on the (C) lobe tips (arrow), and (D) inner side of the lobe tips and the formation of a bristle field on each tail lobe posterior to the tips of the postcloacal crescent (arrows) E cloacal opening with areoles on the inside wall. Scale bars: 1 mm (A), 500 μm (B), 200 μm (C–D), 50 μm (E).
Figure 3 from: Chiu M-C, Huang C-G, Wu W-J, Lin Z-H, Chen H-W, Shiao S-F (2020) A new millipede-parasitizing horsehair worm, Gordius chiashanus sp. nov., at medium altitudes in Taiwan (Nematomorpha, Gordiida). ZooKeys 941: 25-48. https://doi.org/10.3897/zookeys.941.49100
Figure 3 Mid-body of male Gordius chiashanus sp. nov. A, BSEM images of (A) cuticle in the mid-body with scattered short bristles (arrows) and (B) close-up view of a short bristle C, D white spots and dorsal and ventral dark pigmented line examined using (C) a compound microscope and (D) a stereomicroscope. Scale bars: 1 mm (A, C, D), 5 μm (B).
Figure 1 from: Chiu M-C, Huang C-G, Wu W-J, Lin Z-H, Chen H-W, Shiao S-F (2020) A new millipede-parasitizing horsehair worm, Gordius chiashanus sp. nov., at medium altitudes in Taiwan (Nematomorpha, Gordiida). ZooKeys 941: 25-48. https://doi.org/10.3897/zookeys.941.49100
Figure 1 Anterior end of male Gordius chiashanus sp. nov. A stereomicroscopic image of the ventral side of the anterior end showing a white cap, dark-brown collar, and vertical white stripe on the ventral side B, CSEM images of the anterior end surface that is (B) smooth with scattered short bristles and (C) wrinkled D close-up view of the dotted square in C showing the short bristles (arrows) covered by a wrinkled structure. Scale bars: 2 mm (A), 200 μm (B–D).
Figure 2 from: Martins MF, de Moraes SC, Cohen SC, Cárdenas MQ, Galvão C (2020) First record of a mermithid worm (Nematoda, Mermithidae) parasitizing a third instar nymph of Triatoma sordida (Stål, 1859) (Hemiptera, Reduviidae, Triatominae) from Mato Grosso, Brazil. ZooKeys 980: 79-91. https://doi.org/10.3897/zookeys.980.55865
Figure 2 Mermithid: A specimen emerging from the posterior end of the third stage nymph of Triatoma sordida (Stål, 1859) collected in a chicken coop in Araguaiana, Mato Grosso, Brazil in December 2018 B specimen on microscope slide.
Figure 1 from: Martins MF, de Moraes SC, Cohen SC, Cárdenas MQ, Galvão C (2020) First record of a mermithid worm (Nematoda, Mermithidae) parasitizing a third instar nymph of Triatoma sordida (Stål, 1859) (Hemiptera, Reduviidae, Triatominae) from Mato Grosso, Brazil. ZooKeys 980: 79-91. https://doi.org/10.3897/zookeys.980.55865
Figure 1 Map of the distribution of Triatoma sordida, showing the studied locality "Fazenda Lago Azul" in Araguaiana, Mato Grosso, Brazil (15°43'47"S, 51°49'26"W).
Figure 3 from: Martins MF, de Moraes SC, Cohen SC, Cárdenas MQ, Galvão C (2020) First record of a mermithid worm (Nematoda, Mermithidae) parasitizing a third instar nymph of Triatoma sordida (Stål, 1859) (Hemiptera, Reduviidae, Triatominae) from Mato Grosso, Brazil. ZooKeys 980: 79-91. https://doi.org/10.3897/zookeys.980.55865
Figure 3 Chicken coop on "Fazenda Lago Azul", Araguaiana, Mato Grosso, Brazil where the nymph of Triatoma sordida was found.
Figure 4 from: Martins MF, de Moraes SC, Cohen SC, Cárdenas MQ, Galvão C (2020) First record of a mermithid worm (Nematoda, Mermithidae) parasitizing a third instar nymph of Triatoma sordida (Stål, 1859) (Hemiptera, Reduviidae, Triatominae) from Mato Grosso, Brazil. ZooKeys 980: 79-91. https://doi.org/10.3897/zookeys.980.55865
Figure 4 Mermithid nematode of Triatoma sordida observed by differential interference contrast (DIC). A Anterior portion B posterior portion showing the tail end ring. Scale bars: 60 mm (A); 150 mm (B).
Figure 8 from: Chiu M-C, Huang C-G, Wu W-J, Shiao S-F (2017) A new orthopteran-parasitizing horsehair worm, Acutogordius taiwanensis sp. n., with a redescription of Chordodes formosanus and novel host records from Taiwan (Nematomorpha, Gordiida). ZooKeys 683: 1-23. https://doi.org/10.3897/zookeys.683.12673
Figure 8 - Male adult Chordodes formosanus from novel hosts. A Posterior end B Anterior end C–D Variable crowned areole morphologies from different individuals E Close view of (C) with typical C. formosanus crowned areoles; F Close view of (D) with smaller crowned areoles. Ca, crowned areole. Scale bars 100 µm (A), 10 µm (B), 100 µm (C–D), and 10 µm (E–F).
Figure 5 from: Chiu M-C, Huang C-G, Wu W-J, Shiao S-F (2017) A new orthopteran-parasitizing horsehair worm, Acutogordius taiwanensis sp. n., with a redescription of Chordodes formosanus and novel host records from Taiwan (Nematomorpha, Gordiida). ZooKeys 683: 1-23. https://doi.org/10.3897/zookeys.683.12673
Figure 5 - Morphological variation of the cuticle that may result from mucus. A Smooth cuticle B–C Wrinkled cuticle D–E Cracked surface of cuticle F Areole-like structures on the anterior end of the cuticle G–J Indentations on the G–I mid-body and J anterior end of the cuticle surface. Scale bars 100 µm (A), 10 µm (B), 50 µm (C–E), 100 µm (F), 20 µm (G), 100 µm (H), 10 µm (I), and 100 µm (J).
Figure 2 from: Chiu M-C, Huang C-G, Wu W-J, Shiao S-F (2017) A new orthopteran-parasitizing horsehair worm, Acutogordius taiwanensis sp. n., with a redescription of Chordodes formosanus and novel host records from Taiwan (Nematomorpha, Gordiida). ZooKeys 683: 1-23. https://doi.org/10.3897/zookeys.683.12673
Figure 2 - Posterior end of male Acutogordius taiwanensis sp. n. A–C Images of the posterior end with the postcloacal crescent extending A, C over or B anterior to the starting point of the tail lobe bifurcation D–F SEM images of the posterior end with a D angled E slightly curved, and F semicircular postcloacal crescent A–F are images from the same individual, respectively. Scale bars 500 µm (A–C), and 200 μm (D–F).
Figure 4 from: Chiu M-C, Huang C-G, Wu W-J, Shiao S-F (2017) A new orthopteran-parasitizing horsehair worm, Acutogordius taiwanensis sp. n., with a redescription of Chordodes formosanus and novel host records from Taiwan (Nematomorpha, Gordiida). ZooKeys 683: 1-23. https://doi.org/10.3897/zookeys.683.12673
Figure 4 - Female Acutogordius taiwanensis sp. n. A Anterior end B Posterior end. Clo, cloacal opening. Scale bars 100 µm (A–B).
Figure 7 from: Chiu M-C, Huang C-G, Wu W-J, Shiao S-F (2017) A new orthopteran-parasitizing horsehair worm, Acutogordius taiwanensis sp. n., with a redescription of Chordodes formosanus and novel host records from Taiwan (Nematomorpha, Gordiida). ZooKeys 683: 1-23. https://doi.org/10.3897/zookeys.683.12673
Figure 7 - Neighbor-joining tree of Acutogordius taiwanensis sp. n. and Chordodes formosanus compared to C. japonensis, Gordius attoni, G. cf robustus, G. balticus, and Paragordius sp. Numbers at the nodes represent the percentage of 5,000 bootstrap replicates.
Figure 1 from: Chiu M-C, Huang C-G, Wu W-J, Shiao S-F (2017) A new orthopteran-parasitizing horsehair worm, Acutogordius taiwanensis sp. n., with a redescription of Chordodes formosanus and novel host records from Taiwan (Nematomorpha, Gordiida). ZooKeys 683: 1-23. https://doi.org/10.3897/zookeys.683.12673
Figure 1 - Anterior end of Acutogordius taiwanensis sp. n. A–C Images of the anterior end showing the (A) white cap and dark-brown collar and B–C white spots scattered on the brown collar D–F SEM images of the anterior end surface that is D smooth E smooth but wrinkled on the tip with holes scattered on the dark-brown collar, and F wrinkled A–F are images from the same individual, respectively. Scale bars 500 µm (A–C), and 200 μm (D–F).
Figure 3 from: Chiu M-C, Huang C-G, Wu W-J, Shiao S-F (2017) A new orthopteran-parasitizing horsehair worm, Acutogordius taiwanensis sp. n., with a redescription of Chordodes formosanus and novel host records from Taiwan (Nematomorpha, Gordiida). ZooKeys 683: 1-23. https://doi.org/10.3897/zookeys.683.12673
Figure 3 - Detailed diagnostic characteristics of male Acutogordius taiwanensis sp. n. A Tiny bristles scattered anterior to postcloacal crescent B Tiny bristles scattered in concentrated groups on tail lobes C Lobe tips covered by moderately flat areoles with short spines amongst areoles D–E Short bristles scattered on the mid-body cuticle. Scale bars 200 µm (A–B), 100 µm (C–D), and 10 μm (E).
Figure 6 from: Chiu M-C, Huang C-G, Wu W-J, Shiao S-F (2017) A new orthopteran-parasitizing horsehair worm, Acutogordius taiwanensis sp. n., with a redescription of Chordodes formosanus and novel host records from Taiwan (Nematomorpha, Gordiida). ZooKeys 683: 1-23. https://doi.org/10.3897/zookeys.683.12673
Figure 6 - Immature stages of Acutogordius taiwanensis sp. n. A–B Live A cyst-form and B worm-form larvae in water C Posterior view of a worm-form larva D Cysts in an infected snail; E Worm-form larva under SEM F Anterior view of a larva showing the hook arrangement G Egg strings H Close-up of the proboscis. DS, dorsal spines; Ho, hooklet; LS, lateral spines; Peo, pseudointestine exterior opening; PostS, postseptum; PreS, preseptum; Pro, proboscis; PS, proboscis sheath; PsI, pseudointestine gland. Scale bars 50 µm (A–B), 2 µm (C), 50 µm (D), 10 µm (E), 5 µm (F), 1 cm (G), and 2 µm (H).
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