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Fig. 4 in Experimental manipulation of cavity temperature produces differential effects on parasite abundances in blue tit nests at two different latitudes
Fig. 4. Differences in the body mass of adult blue tit males by heat treatment of nest boxes and locality. Means ± intervals of confidence at 95% are shown.
Fig. 2 in Experimental manipulation of cavity temperature produces differential effects on parasite abundances in blue tit nests at two different latitudes
Fig. 2. Blowfly pupae abundance observed in control and heated nests of blue tits (Cyanistes caeruleus) in both localities (Spain and Germany). The data presented was controlled for the locality and the interaction between locality and treatment. Means ± intervals of confidence at 95% are shown.
Fig. 3 in Experimental manipulation of cavity temperature produces differential effects on parasite abundances in blue tit nests at two different latitudes
Fig. 3. Differences in the abundance of Haemoproteus/Plasmodium in blue tit males by treatment and locality. Means ± intervals of confidence at 95% are shown.
Fig. 1 in Experimental manipulation of cavity temperature produces differential effects on parasite abundances in blue tit nests at two different latitudes
Fig. 1. Daily variation of temperature in nests of blue tits. Temperature is decreasing at 00:00 and lower values for the day are attained close to 8:00 h. Data from two different nests with nestling of 7 days old are represented from A) Spain and B) Germany.
Fig. 4. Mothocya andoni n in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria
Fig. 4. Mothocya andoni n. sp. Ƌ (12.0 mm total length, 5.0 mm width) (SAMC–A092738)A, Dorsal body; B, Lateral body; C, Pereopod 1; D, Pereopod 7; E, Penes; F, Uropod; G, Dorsal view of cephalon with pereonite 1; H, Dorsal view of pleon.
Fig. 4 in Predictors of helminth parasite infection in female chacma baboons (Papio ursinus)
Fig. 4. An interaction between host reproductive state and progestagen concentrations in the infection intensity of Protospirura. Pregnant females (blue) exhibit increased infection intensity of Protospirura with rising progestagen concentrations. Non-pregnant females (red) exhibit decreased infection intensity of Protospirura with rising progestagen concentrations. Confidence intervals are in gray. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in Predictors of helminth parasite infection in female chacma baboons (Papio ursinus)
Fig. 2. Plots showing associations between log Protospirura intensity (eggs per gram; epg) in female baboons and marginal effects of each predictor variable. Plots are (A) pregnant (no or yes); (B) log progestagen concentrations (low = below median; high = above median; ng/g); (C) season (dry or wet); (D) presence/absence of Oesophagostomum; and (E) log Trichuris intensity (epg). Points and whiskers on the plot represent the mean and confidence intervals. For Fig. 2E, the values of each fixed effect are divided into tertiles. Numbers above each bar indicate sample size.
Fig. 3 in Predictors of helminth parasite infection in female chacma baboons (Papio ursinus)
Fig. 3. Plots showing associations between log Trichuris intensity (eggs per gram; epg) in female baboons and marginal effects of each predictor variable. Plots are (A) cycling (no or yes); (B) log fecal glucocorticoid concentrations (ng/g); (C) season (dry or wet); (D) presence/absence of Oesophagostomum; and (E) log Protospirua intensity (epg). Points and whiskers on the plot represent the mean and confidence intervals. For Fig. 3B and E, the values of each fixed effect are divided into tertiles. Numbers above each bar indicate sample size. Photograph by Bobby Habig.
Fig. 1 in Predictors of helminth parasite infection in female chacma baboons (Papio ursinus)
Fig. 1. Population and host level processes proposed to drive within group variation in helminth infection risk among female chacma baboon hosts (partially adapted from Akinyi et al., 2019; Habig et al., 2019). Four key drivers of parasite risk are examined: environmental conditions; reproductive stage; steroid hormones; and patterns of coinfection.
Fig. 5 in Gastrointestinal parasites of a reintroduced semi-wild plains bison (Bison bison bison) herd: Examining effects of demographic variation, deworming treatments, and management strategy
Fig. 5. The average sum of FECs counts by year, demonstrating and increasing trend in FECs between 2015 and 2019. Black horizontal lines denote median values, while the top and bottom of boxes denote the upper and lower interquartile ranges (75th and 25th percentiles). Extending "whiskers" denote values of 1.5 times the interquartile range; points outside of this range constitute outliers.
Fig. 4 in Gastrointestinal parasites of a reintroduced semi-wild plains bison (Bison bison bison) herd: Examining effects of demographic variation, deworming treatments, and management strategy
Fig. 4. The sum of FECs counted per gram of individual bison, demonstrating variation FECs between and among individuals. Black horizontal lines denote median values, while the top and bottom of boxes denote the upper and lower interquartile ranges (75th and 25th percentiles). Extending "whiskers" denote values of 1.5 times the interquartile range; points outside of this range constitute outliers.
Fig. 3 in Gastrointestinal parasites of a reintroduced semi-wild plains bison (Bison bison bison) herd: Examining effects of demographic variation, deworming treatments, and management strategy
Fig. 3. The sum of FECs types, including "STRONGs" (Strongyle-type), "COCCs" (Coccidia), "NEMAs" (Nematodirus), "TRICHs" (Trichuris), "MONs" (Moniezia) counted per gram of sample from bison of various age classes. Ages classes included "NC" (New Calf; 0–1), "YR" (Yearling; 1–2), "JA" (Juvenile to Adult Transition; 2–4), "YA" (Young Adult; 4–6), "PA" (Peak Adult; 6–9), "MA" (Mature Adult; 9+). Black horizontal lines denote median values, while the top and bottom of boxes denote the upper and lower interquartile ranges (75th and 25th percentiles). Extending "whiskers" denote values of 1.5 times the interquartile range; points outside of this range constitute outliers.
Fig. 7. Mothocya powelli n in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria
Fig. 7. Mothocya powelli n. sp. holotype ♀ (ovigerous, 7.0 mm total length, 5.0 mm width) (SAMC–A092739). A, Dorsal body; B, Lateral body; C, Oostegites; D, Dorsal view of cephalon with pereonite 1; E, Uropod; F, Ventral cephalon; G, Dorsal view of pleon; H, Pereopod 1; I, Pereopod 7.
Fig. 6. Mothocya andoni n in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria
Fig. 6. Mothocya andoni n. sp. Ƌ (12.0 mm total length, 5.0 mm width) (SAMC–A092738). A, Pleopod 1 ventral view; B, Pleopod 2 ventral view; C, Pleopod 3 ventral view; D, Pleopod 4 ventral view; E, Pleopod 5 ventral view; F, Pleopod 1 dorsal view; G, Pleopod 2 dorsal view; H, Pleopod 3 dorsal view; I, Pleopod 4 dorsal view; J, Pleopod 5 dorsal view.
Fig. 8. A in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria
Fig. 8. A, Dorsal view of Mothocya andoni n. sp. holotype ♀ (ovigerous, 15.0 mm total length, 8.0 mm width) (SAMC–A092737) (top) and Mothocya powelli n. sp. holotype ♀ (ovigerous, 7.0 mm total length, 5.0 mm width) (SAMC–A092739) (bottom); B, Ventral view of Mothocya andoni n. sp. holotype ♀ (top) and Mothocya powelli n. sp. holotype ♀ (bottom); C, Dorsal view of Mothocya andoni n. sp. holotype ♀ (left) and Mothocya andoni n. sp. Ƌ (12.0 mm total length, 5.0 mm width) (SAMC–A092738) (right).
Fig. 2 in Gastrointestinal parasites of a reintroduced semi-wild plains bison (Bison bison bison) herd: Examining effects of demographic variation, deworming treatments, and management strategy
Fig. 2. The sum of FECs counted per gram of sample from bison of various age classes, including "NC" (New Calf; 0–1), "YR" (Yearling; 1–2), "JA" (Juvenile to Adult Transition; 2–4), "YA" (Young Adult; 4–6), "PA" (Peak Adult; 6–9), "MA" (Mature Adult; 9+). Black horizontal lines denote median values, while the top and bottom of boxes denote the upper and lower interquartile ranges (75th and 25th percentiles). Extending "whiskers" denote values of 1.5 times the interquartile range; points outside of this range constitute outliers.
Fig. 1 in Gastrointestinal parasites of a reintroduced semi-wild plains bison (Bison bison bison) herd: Examining effects of demographic variation, deworming treatments, and management strategy
Fig. 1. Aerial image of the Crane Trust bison pastures. The smaller North metapopulation was continuously grazed in the Visitor Center ("VC" – 50 acres) pasture (outlined in pink). The larger South metapopulation was rotated through Ruge-South Brown ("RS" – 387 acres) pasture (outlined in orange), Calving-Office ("CO" – 267 acres) pasture (outlined in yellow), and North Meadow ("NM" – 177 acres) pasture (outlined in green). The North (orange) and South (pink) metapopulation pastures were separated by a minimum distance of 200 m, including an 80 m channel of the Platte River. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4 in Louse flies in Azorean and mainland populations of four Passeriformes species: A new perspective to parasite Island syndromes
Fig. 4. Map showing the prevalence (represented by different color; yellow color represent the prevalence of uninfested birds) of hippoboscid fly species in blackbirds, blackcaps, chaffinches and robins in the each of the sampled Azorean Islands (S˜ao Miguel, Terceira and Flores) and the mainland Portugal. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Louse flies in Azorean and mainland populations of four Passeriformes species: A new perspective to parasite Island syndromes
Fig. 1. Map of the mainland Portugal and Azores Islands with the geographic distribution of the study areas (Silves, Olh˜ao, S˜ao Miguel Island, Terceira Island and Flores Island).
Fig. 3 in Louse flies in Azorean and mainland populations of four Passeriformes species: A new perspective to parasite Island syndromes
Fig. 3. Prevalence (%) of hippoboscid fly species found on blackbirds, blackcaps, chaffinches and robins from the Azores Islands and mainland Portugal.
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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.
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.