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Fig. 1 in Predicting seasonal infection of eyeworm (Oxyspirura petrowi) and caecal worm (Aulonocephalus pennula) in northern bobwhite quail (Colinus virginianus) of the Rolling Plains Ecoregion of Texas, USA

Fig. 1. Contour and scatterplot of relationships between temperature and precipitation on parasite worm burdens and egg shedding. a) Predicted caecal worm intensity against temperature and precipitation contour plot. b) Scatterplot of predicted caecal worm reproduction against precipitation. d) Predicted eyeworm reproduction against temperature and precipitation contour plot.

opencc-by-4.0Apr 2019View details →
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Fig. 2 in The wild world of Guinea Worms: A review of the genus Dracunculus in wildlife

Fig. 2. Dracunculus insignis infection in definitive host raccoon (Procyon lotor) and intermediate host (Cyclopoid copepod): (A) lesion from emergence of gravid female D. insignis (marked by arrow); (B) in situ photograph of patent D. insignis infection in forelimb of raccoon; (C) first-stage larvae (L1) of D. insignis (0.596–0.857 mm); (D) thirdstage larvae (L3) of D. insignis (0.434–0.605 mm) with trilobed tail, a distinguishing morphologic characteristic; (E) a copepod infected with D. insignis (L3s marked with arrow).

opencc-by-4.0Dec 2018View details →
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Fig. 1 in The wild world of Guinea Worms: A review of the genus Dracunculus in wildlife

Fig. 1. Life-cycle of Dracunculus insignis in wildlife and domestic dogs. Arrows in red represent transmission from (A) definitive hosts to intermediate hosts (Cyclopoid copepods) and (B) transmission to definitive hosts via consumption of intermediate hosts. Arrows in blue represent (C) transmission from intermediate hosts to paratenic and transport hosts (amphibains and fish) via consumption of infected copepods and (D) transmission to definitive hosts via consumption of paratenic/transport hosts. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Dec 2018View details →
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Fig. 3 in A comparison of helminth infections as assessed through coprological analysis and adult worm burdens in a wild host

Fig. 3. The relationship between adult lungworm (A. falciformis) burden and number of larvae per g of faeces in Irish badgers (n = 289).

opencc-by-4.0Dec 2018View details →
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Fig. 2 in A comparison of helminth infections as assessed through coprological analysis and adult worm burdens in a wild host

Fig. 2. The relationship between adult hookworm (U. criniformis) burden and faecal egg counts (e.p.g) in Irish badgers (n = 289).

opencc-by-4.0Dec 2018View details →
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Fig. 8. Myzomolgus cucullatus n in Three new species of Myzomolgus (Copepoda, Cyclopoida, Catiniidae) associated with sipunculan worms from a tidal flat in Phuket, Thailand

Fig. 8. Myzomolgus cucullatus n. sp., female. A, anal somite and caudal rami, dorsal; B, paragnath; C, maxillule; D, maxilla; E, distal segment of maxilla; F, leg 1; G, leg 2; H, leg 4; I, leg 5. Scale bars: A, D, E, 0.02 mm; B, C, 0.01 mm; F-I, 0.05 mm.

opencc-by-4.0Dec 2021View details →
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Fig. 7. Myzomolgus cucullatus n in Three new species of Myzomolgus (Copepoda, Cyclopoida, Catiniidae) associated with sipunculan worms from a tidal flat in Phuket, Thailand

Fig. 7. Myzomolgus cucullatus n. sp., female. A, habitus, dorsal; B, urosome, dorsal; C, urosome, ventral; D, rostral area, ventral; E, antennule; F, antenna; G, mandible; H, right genital area, ventral. Scale bars: A, 0.1 mm; B-E, 0.05 mm; F-H, 0.02 mm.

opencc-by-4.0Dec 2021View details →
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Fig. 6. Myzomolgus spatulatus n in Three new species of Myzomolgus (Copepoda, Cyclopoida, Catiniidae) associated with sipunculan worms from a tidal flat in Phuket, Thailand

Fig. 6. Myzomolgus spatulatus n. sp., male. A, habitus, dorsal; B, urosome, ventral; C, antennule; D, labrum; E, maxilla; F, maxilliped. Scale bars: A, 0.1 mm; B, 0.02 mm; C-F, 0.01 mm.

opencc-by-4.0Dec 2021View details →
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Fig. 4. Myzomolgus spatulatus n in Three new species of Myzomolgus (Copepoda, Cyclopoida, Catiniidae) associated with sipunculan worms from a tidal flat in Phuket, Thailand

Fig. 4. Myzomolgus spatulatus n. sp., female. A, habitus, dorsal; B, urosome, dorsal; C, urosome, ventral; D, cephalic region, ventral; E, antennule; F, mandible; G, maxillule. Scale bars: A, 0.1 mm; B, C, 0.05 mm; D, E, 0.02 mm; F, G, 0.01 mm.

opencc-by-4.0Dec 2021View details →
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Fig. 3. Myzomolgus leptocercosus n in Three new species of Myzomolgus (Copepoda, Cyclopoida, Catiniidae) associated with sipunculan worms from a tidal flat in Phuket, Thailand

Fig. 3. Myzomolgus leptocercosus n. sp., male. A, habitus, dorsal; B, urosome, ventral; C, distal part of urosome, dorsal; D, antenna; E, labrum; F, maxilliped. Scale bars: A, 0.1 mm; B, C, 0.05 mm; D-F, 0.02 mm.

opencc-by-4.0Dec 2021View details →
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Fig. 5. Myzomolgus spatulatus n in Three new species of Myzomolgus (Copepoda, Cyclopoida, Catiniidae) associated with sipunculan worms from a tidal flat in Phuket, Thailand

Fig. 5. Myzomolgus spatulatus n. sp., female. A, antenna; B, maxilla; C, leg 1; D, leg 2; E, leg 4. Scale bars: A, C-E, 0.02 mm; B, 0.01 mm.

opencc-by-4.0Dec 2021View details →
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Fig. 2. Myzomolgus leptocercosus n in Three new species of Myzomolgus (Copepoda, Cyclopoida, Catiniidae) associated with sipunculan worms from a tidal flat in Phuket, Thailand

Fig. 2. Myzomolgus leptocercosus n. sp., female. A, maxillule; B, maxilla; C, leg 1; D, leg 2; E, leg 4; F, leg 5; G, left genital area, dorsal. Scale bars: A, 0.01 mm; B-G, 0.02 mm.

opencc-by-4.0Dec 2021View details →
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Fig. 1. Myzomolgus leptocercosus n in Three new species of Myzomolgus (Copepoda, Cyclopoida, Catiniidae) associated with sipunculan worms from a tidal flat in Phuket, Thailand

Fig. 1. Myzomolgus leptocercosus n. sp., female. A, habitus, dorsal; B, urosome, dorsal; C, urosome, ventral; D, egg sac; E, rostral area, ventral; F, antennule; G, antenna; H, labrum; I, mandible. Scale bars: A, D, 0.1 mm; B, C, E, 0.05 mm; F-H, 0.02 mm; I, 0.01 mm.

opencc-by-4.0Dec 2021View details →
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Fig. 3 in New record of commensal scale worms, Arctonoe vittata (Grube, 1855) and Hyperhalosydna striata (Kinberg, 1856) (Polychaeta: Polynoidae) from Korean waters

Fig. 3. Various host invertebrates of Arctonoe vittata (Grube, 1855) found in this study. A, Solaster dawsoni Verrill, 1880; B and C, Aphelasterias japonica (Bell, 1851); D, Haliotis discus hannai Ino, 1953; E, Scelidotoma gigas (Martens, 1881); F, Triopha catalinae (Cooper, 1863); G and H, Cadlina japonica Baba, 1937; I, Niveotectura pallida (Gould, 1859); J, Apostichopus japonicus (Selenka, 1867).

opencc-by-4.0Oct 2016View details →
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Fig. 2 in New record of commensal scale worms, Arctonoe vittata (Grube, 1855) and Hyperhalosydna striata (Kinberg, 1856) (Polychaeta: Polynoidae) from Korean waters

Fig. 2. Hyperhalosydna striata (Kinberg, 1856), NIBRIV0000326200. A, Anterior end with elytra, dorsal view; B, Proboscis, frontal view; C, Right elytron from segment 11; D, Posterior end, dorsal view; E, Anterior end without elytra, dorsal view (arrow indicate dorsal cirrophore); F, Notopodium with notochaeta (arrow) from segment 14; G, Cirrigerous parapodium from segment 14, anterior view; H, Posterior end, ventral view; I, Posterior segments with nephridial papillae, ventral view; J, Neurochaeta from segment 14. Scale bar: A-E, H = 1 mm; F, J = 0.05 mm; G = 0.3 mm; I = 0.2 mm.

opencc-by-4.0Oct 2016View details →
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Fig. 5 in New record of commensal scale worms, Arctonoe vittata (Grube, 1855) and Hyperhalosydna striata (Kinberg, 1856) (Polychaeta: Polynoidae) from Korean waters

Fig. 5. Distribution of Arctonoe vittata (Grube, 1855) and Hyperhalosydna striata (Kinberg, 1856) in eastern Asia based on the present study (P) and literatures (1-19). 1: Uschakov (1982), 2: Uchida (1992), 3: Imajima (2001), 4: Uchida (1988), 5: Moore (1903), 6: Okuda (1936), 7: Imajima (2001), 8: Imajima and Hartman (1964); Imajima (2001), 9: Imajima (2001), 10: Okuda (1936), 11 and 12: Imajima (2001), 13: Okuda (1936), 14: Imajima (1988), 15-19: Uschakov (1955).

opencc-by-4.0Oct 2016View details →
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Fig. 6 A in Extensive cryptic diversity in the cosmopolitan sludge worm Limnodrilus hoffmeisteri (Clitellata, Naididae)

Fig. 6 A scatter plot of the length of the penis sheath against the ratio between length and basal width (right corner) of species. Species (SHSs) labeled I–IV and VI–X are identified as members of the L. hoffmeisteri complex, CC as BL. claparedianus-cervix,^ LM as L. maumeensis, and LC as L. claparedianus

opencc-by-4.0Jan 2017View details →
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Fig. 3 in Extensive cryptic diversity in the cosmopolitan sludge worm Limnodrilus hoffmeisteri (Clitellata, Naididae)

Fig. 3 The morphology of penis sheaths. Species labeled I–IV and VI–X are identified as members of the L. hoffmeisteri complex, CC as BL. claparedianus-cervix,^ LM as L. maumeensis

opencc-by-4.0Jan 2017View details →
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Orthonectids are highly degenerate annelid worms

<p>These datasets hold the individual alignments and phylogenetic trees (including full PhyloBayes output) presented in our study showing that Mesozoa are polyphyletic and Orthonectida are annelids. A detailed description can be found in the manuscript.</p> <p>Briefly, there is a mitochondrial dataset, the full alignment and PhyloBayes data for the nuclear genes, and lastly several jackknife datasets subsampled from the full alignment and run under different evolutionary models and with different subset of genes.</p>

opencc-by-4.0Apr 2018View details →
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Figure 3 in Note on rare knot worm, Polygordius madrasensis Aiyar and Alikunhi, 1944 (Polychaeta, Polygordiidae) from India

Figure 3. Light microscopy image of neotype (MB/SBN/VD8) (pp: paired palps, hf: head fold, pr: prostomium, mo: mouth opening, pc: pygidial cirri, py: pygidium, s: segments, gc: gut content).

opencc-by-4.0Dec 2022View details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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

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