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6,859 results for “parasitism”
Figure 8 in Parasites of Moroccan desert Coptodon guineensis (Pisces, Cichlidae): transition and resilience in a simplified hypersaline ecosystem
Figure 8. Proportions of females of acanthocephalan Acanthogyrus (Acanthosentis) cf. tilapiae in Coptodon guineensis at Sebkha Imlili according to stage of maturity. Solid bars = immature females (no genitalia visible); dotted bars = ovigerous females (ovarian balls visible); striped bars = gravid females (December 2018: n = 41; April 2019: n = 42; July 2019: n = 47; October 2019: n = 50). Gravid females were present throughout the year but significantly more abundant proportionally in December and July, which may indicate a short life span of the worms and quick turnover in the fish.
Figure 3 in Parasites of Moroccan desert Coptodon guineensis (Pisces, Cichlidae): transition and resilience in a simplified hypersaline ecosystem
Figure 3. Acanthocephalan Acanthogyrus (Acanthosentis) cf. tilapiae from Coptodon guineensis at Sebkha Imlili. SEM. A. Male proboscis showing large anterior hooks markedly separated from small posterior hooks. B. Anterior trunk of female showing rows of spines. C. Female body spine.
Figure 4. Genus Pogonomystrongylus Smales, 2014. Body sections. A–D in Revision of the genera of Heligmonellidae (Nematoda, Heligmosomoidea), parasitic in Muridae from New Guinea
Figure 4. Genus Pogonomystrongylus Smales, 2014. Body sections. A–D' Pogonomystrongylus domaensis Smales, 2014. A–B' within proximal body. A, A' male, B, B' female. C–D' at midbody. C, C' male, D, D' female. Source: A–D redrawn from [36]. A'–D', modified figures: A'–C' reversed on their frontal axes with respect to the originals, then slightly rotated clockwise. D' rotated 45° clockwise.
Figure 9. Genus Flannerystrongylus Smales, 2019. Body sections. A–C Flannerystrongylus abulus Smales, 2019. A, A in Revision of the genera of Heligmonellidae (Nematoda, Heligmosomoidea), parasitic in Muridae from New Guinea
Figure 9. Genus Flannerystrongylus Smales, 2019. Body sections. A–C Flannerystrongylus abulus Smales, 2019. A, A' within proximal body, female. B, C at midbody. B male, C female. D–E' Flannerystrongylus chisholmae Smales, 2020. D–E' at midbody. D, D' male. E, E' female. Abbreviation: cu, cuticle. Sources: A–C redrawn from [42]; D, E redrawn from [43]. A', B', D', E': modified figures: A' rotation clockwise, re-numbering of ridges with respect to the original. B' rotation clockwise. D', E' addition of external cuticular lining. D' re-numbering of ridges.
Figure 8. Genus Missimstrongylus Smales, 2018. A-A in Revision of the genera of Heligmonellidae (Nematoda, Heligmosomoidea), parasitic in Muridae from New Guinea
Figure 8. Genus Missimstrongylus Smales, 2018. A-A" Missimstrongylus oweni Smales, 2018, section at midbody, male. Source: A redrawn from [41]. A', A" modified figures: A' rotated 90° clockwise with respect to the original, A" further reversion of A' on its frontal axis.
Figure 3b. I–K Montistrongylus karungi Smales, 2012. I, I in Revision of the genera of Heligmonellidae (Nematoda, Heligmosomoidea), parasitic in Muridae from New Guinea
Figure 3b. I–K Montistrongylus karungi Smales, 2012. I, I' within proximal body, male. J, K at midbody. J male, K female. L–O Montistrongylus kaindiensis Smales, 2015. L, M within proximal body. L male, M female. N–O at midbody. N, N' male, O female. Sources: I–K redrawn from [35]; L–O redrawn from [37]. I', N', modified figures. I' body displaced inside the cuticle to obtain a section congruent with Figure 3K. N' reversed on its sagittal axis then rotated 30° clockwise with respect to the original.
Figure 2 in Revision of the genera of Heligmonellidae (Nematoda, Heligmosomoidea), parasitic in Muridae from New Guinea
Figure 2. Genus Mawsonema Smales & Heinrich, 2010. Body sections. A–F' Mawsonema mokwanense Smales & Heinrich, 2010. A, A' within proximal body, male. B, C at midbody. B male, C female. D, E within distal body. D male, E female. F, F' within proximal body, female. A–E synlophe of type I. F, F' synlophe of type II. Source: A–F redrawn from [45]. A', F' modified figures: reversed on their frontal axes with respect to the originals. F' axis of orientation reinterpreted as subfrontal.
Figure 2 in Prevalence of Blastocystis sp. in Morocco: Comparative assessment of three diagnostic methods and characterization of parasite forms in Jones' culture medium
Figure 2. Occurrence of Blastocystis sp. infection on its own or in conjunction with other protozoan species.
Figure 7. Genus Parvinema Smales, 2017. Midbody sections. A, B Parvinema bafunminense Smales, 2017. A male, B, B in Revision of the genera of Heligmonellidae (Nematoda, Heligmosomoidea), parasitic in Muridae from New Guinea
Figure 7. Genus Parvinema Smales, 2017. Midbody sections. A, B Parvinema bafunminense Smales, 2017. A male, B, B' female. C, C' Parvinema helgeni Smales, 2017, male. Source: A–C redrawn from [40]. B', C' modified figures with respect to the original: B' numbering of ridges added. C' reversed on its frontal axis, then rotated 30° clockwise.
Figure 1. Genus Melomystrongylus Smales, 2009. Body sections. A–D Melomystrongylus sepikensis Smales, 2009. A, B within proximal body. A male, B in Revision of the genera of Heligmonellidae (Nematoda, Heligmosomoidea), parasitic in Muridae from New Guinea
Figure 1. Genus Melomystrongylus Smales, 2009. Body sections. A–D Melomystrongylus sepikensis Smales, 2009. A, B within proximal body. A male, B female; C, D at midbody. C male, D, female. E–H Melomystrongylus somoroensis Smales & Heinrich, 2010. E, F within proximal body. E male, F female. G, G' at midbody, male. H female "at posterior end of midbody" (sic). Sources: A–D redrawn from [30]. E–H redrawn from [45]. G' modified figure, reversed on its frontal axis with respect to the original.
Figure 3 in Host conservation through their parasites: molecular surveillance of vector-borne microorganisms in bats using ectoparasitic bat flies
Figure 3. Comparison of detected microorganism prevalence (prevalence of infection) between bats and bat flies. Different bars represent hosts (black), all bat flies (dark grey), and consensus fly results, meaning that at least one infected fly individual was present on the host (light grey).
Figure 5 in Toxoplasma gondii in beef consumed in France: regional variation in seroprevalence and parasite isolation
Figure 5. Comparison of observed values versus predicted values by the final model according to age. The observed values are in green bars, while for the predicted values the red point represents the mean prediction and the blue segment the 95% confidence interval of the prediction. The number above the blue segment is the number of observations for this particular class of age.
Figure 2 in Toxoplasma gondii in beef consumed in France: regional variation in seroprevalence and parasite isolation
Figure 2. Geographical variation of Toxoplasma gondii seroprevalence of French bovine samples according to the area of slaughtering and to age categories: (A) calves; (B) adults; (C) bovines overall (calves and adults). The numbers represent the number of samples collected for each region.
Figure 1 in Toxoplasma gondii in beef consumed in France: regional variation in seroprevalence and parasite isolation
Figure 1. (A) Map of French beef production according to the Ministry of Agriculture database. The colour gradient represents the number of cattle slaughtered in 2007. (B) The numbers represent the number of slaughterhouses per region that were included in the cross-sectional survey of Toxoplasma gondii presence in beef produced in France.
Figure 2 in Host conservation through their parasites: molecular surveillance of vector-borne microorganisms in bats using ectoparasitic bat flies
Figure 2. Prevalence of Bartonella spp., Polychromophilus spp., and Trypanosoma spp. infection in nycteribiid flies collected from 28 bats, which carried between 2 and 7 flies. Black: all flies are infected, dark grey: all flies are non-infected, light grey: both infected and non-infected flies occurred on the same host.
Figure 4 in Toxoplasma gondii in beef consumed in France: regional variation in seroprevalence and parasite isolation
Figure 4. Seroprevalence of Toxoplasma gondii infection in bovines of French origin (adults + calves) accordingly to the age and the titer (6; 10; 25; 50; 100; 200).
Figure 3 in Toxoplasma gondii in beef consumed in France: regional variation in seroprevalence and parasite isolation
Figure 3. Terminal titer of the modified agglutination test (MAT) for French origin samples in relation to age (A) for all samples (n = 2348) (age in years); (B) only for bovines less than 1 year (n = 601) (age in months). The number of observations at each month of age is given at the top of the corresponding bar.
Figure 1 in Host conservation through their parasites: molecular surveillance of vector-borne microorganisms in bats using ectoparasitic bat flies
Figure 1. Number of detected vector-borne microorganisms in bats (A) and bat flies (B). Black colour corresponds to Miniopterus natalensis (A), and Nycteribia schmidlii scotti (B), whereas grey shows Miniopterus schreibersii (A) and Nycteribia schmidlii (B).
Figure 2. Dendrogram resulting from a in Host specificity and the structure of helminth parasite communities of fishes in a Neotropical river in Mexico
Figure 2. Dendrogram resulting from a similarity matrix based on the Sørensen measure for component communities of adult autogenic helminth parasites of 10 fish species from Apazapan, Río La Antigua, Veracruz, Mexico. Host species are: Amex, A. mexicanus; Rgua, R. guatemalensis; Smar, S. marmoratus; Hbim, P. bimaculata; Pmex, Poecilia mexicana; Pgra, Poeciliosis gracilis; Psph, Poecilia sphenops; Xell, X. helleri; Tell, T. ellioti; Vfen, V. fenestrata.
Figure 1 in Host specificity and the structure of helminth parasite communities of fishes in a Neotropical river in Mexico
Figure 1. Patterns of relative abundance of 24 species of helminths in 11 component communities of freshwater fishes from Río Apazapan, Río La Antigua basin, Mexico (fish species: Am, A. mexicanus; Rg, Rhamdia guatemalensis; Hb, Pseudoxiphophorus bimaculata; Pm, Poecilia mexicana; Ps, P. sphenops; Pg, Poeciliopsis gracilis; Xh, Xiphophorus helleri; Te, Thorichthys helleri; Vf, Vieja fenestrata; Sm, Sicydium gymnogaster).
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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.