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Fig. 1 in Prevalence of avian haemosporidia among injured wild birds in Tokyo and environs, Japan
Fig. 1. Locations of the four facilities in the Kanto region that samples were collected. A. Kanagawa Prefecture Natural Conservation Center, B. Inokashira Animal Hospital, C. Gyotoku Wild Bird Hospital, D. Bird Clinic Kanesaka Animal Hospital.
Fig. 2 in Prevalence of avian haemosporidia among injured wild birds in Tokyo and environs, Japan
Fig. 2. Hemacolor ® stained blood smears from rescued birds: (a) Plasmodium sp. from Cyanopica cyanus, (b) P. reluctum from Hypisipetes amaurotis, (c) P. circumflexum from Fulica atra, (d) Haemoproteus sp. from Hypisipetes amaurotis, (e) Haemoproteus sp. from Larus canus, (f) H. minutus from Turdus cardis, (g) Leucocytozoon sp. from Anas acuta, (h) Leucocytozoon sp. from Aythya marila.
Fig. 1 in Seasonal prevalence of queens and males in colonies of tawny crazy ants (Hymenoptera: Formicidae) in Florida
Fig. 1. Mean ± SE (n = 3–11) number of queens (including female dealates), volume of brood (mL), and number of male alates per colony, collected monthly in Gainesville (Alachua County), Florida, USA, to show monthly fluctuations within seasons designated as winter (Dec–Feb), spring (Mar–May), summer (Jun–Aug), and fall (Sep–Nov).
Fig. 1 in Prevalence of avian haemosporidians among understorey birds of Mt. Banahaw de Lucban, Philippines.
Fig. 1 Avian haemosporidian prevalence according to altitude. P=Plasmodium, L=Leucocytozoon, H=Haemoproteus.
Fig. 1 in The prevalence of Leucocytozoon spp. in nestlings of three wild raptor species including implications on haematological and blood chemistry values
Fig. 1. Prevalence of Leucozytozoon spp. infection in nestlings of common buzzards (Buteo buteo), red kites (Milvus milvus) and northern goshawks (Accipiter gentilis). Asterisks refer to P-values ≤0.05, determined by GLMM. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in The prevalence of Leucocytozoon spp. in nestlings of three wild raptor species including implications on haematological and blood chemistry values
Fig. 3. Results of linear discriminant analysis (LDA) comparing 15 selected blood parameters between uninfected and infected raptor nestlings. a) Distribution of the LDA according to uninfected and infected nestlings. b) Correlation plot of the first axis of the 15 selected variables.
Fig. 6 in Prevalence and gross pathology of liver fluke in macropods cohabiting livestock farms in north eastern NSW, Australia, and diagnosis using cELISA
Fig. 6. Livestock farms in the Northern Tablelands region of NSW, Australia, with Macropods harbouring liver fluke infections (December 2018–June 2021).
Fig. 5 in Prevalence and gross pathology of liver fluke in macropods cohabiting livestock farms in north eastern NSW, Australia, and diagnosis using cELISA
Fig. 5. Scatter plot of Fasciola hepatica coproantigen concentration (optical density, 450 nm) and total fluke count in Macropods.
Fig. 4. A in Prevalence and gross pathology of liver fluke in macropods cohabiting livestock farms in north eastern NSW, Australia, and diagnosis using cELISA
Fig. 4. A. Common wallaroo liver (visceral surface) with prominent fibrotic capsules. B. Liver cross-section of fibrous capsules. C. Eastern grey kangaroo liver (visceral surface) with irregular form, hepatomegaly, fibrotic lesions and bile duct hyperplasia. D. Necrotic tracks generated by immature fluke. E. Immature fluke (mm).
Fig. 3. Rainfall and temperature data throughout 2019–2020 in Prevalence and gross pathology of liver fluke in macropods cohabiting livestock farms in north eastern NSW, Australia, and diagnosis using cELISA
Fig. 3. Rainfall and temperature data throughout 2019–2020 recorded at the Armidale airport NSW, Australia (Australian Government of Bureau of Meteorology, 2019, 2020).
Fig. 1 in Prevalence and gross pathology of liver fluke in macropods cohabiting livestock farms in north eastern NSW, Australia, and diagnosis using cELISA
Fig. 1. Geographical location of livestock farms (A–G) surveyed in the Northern Tablelands region of NSW, Australia, to assess liver fluke prevalence in Macropods (ArcGIS 10.4.1 software, 2018).
Fig. 2 in Prevalence and gross pathology of liver fluke in macropods cohabiting livestock farms in north eastern NSW, Australia, and diagnosis using cELISA
Fig. 2. Liver fluke prevalence in Macropods (infected/total sampled) cohabiting farms in the Northern Tablelands region of NSW, Australia. Number of farms by risk site: low – 2 farms, medium – 3 farms, high – 2 farms.
Fig. 2 in The prevalence of Leucocytozoon spp. in nestlings of three wild raptor species including implications on haematological and blood chemistry values
Fig. 2. Proportion of infected individuals of common buzzard (Buteo buteo), red kite (Milvus milvus) and northern goshawk (Accipiter gentilis) nestlings (n = 528) in relation to the proportion of the nestling period, determined by age and the species-specific average nestling duration. Calculated nestling periods were grouped into steps of ten percent (0.2–0.9). Each step represents the proportion of all individuals examined within this period. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 5 in Host and geographic differences in prevalence and diversity of gastrointestinal helminths of foxes (Vulpes vulpes), coyotes (Canis latrans) and wolves (Canis lupus) in Quebec´, Canada
Fig. 5. On the left, whole mounted Cryptocotyle lingua adult trematode stained with borax carmine (credit: Brent Wagner). On the right, distribution of foxes (Vulpes vulpes) infected with C. lingua in the Subarctic (samples (n) collected along James Bay and the St Lawrence estuary) and Humid Continental climate collected during winter 2016–2017 by trappers from Qu´ebec, Canada. Arrows indicate major waterways.
Fig. 2. A in Host and geographic differences in prevalence and diversity of gastrointestinal helminths of foxes (Vulpes vulpes), coyotes (Canis latrans) and wolves (Canis lupus) in Quebec´, Canada
Fig. 2. A) Parasite genus richness in foxes (Vulpes vulpes, blue), coyotes (Canis latrans, orange), and wolves (Canis lupus, gray) from Qu´ebec, Canada, determined by gross examination and fecal flotation combined (N = 250). Fewer foxes were uninfected than coyotes (p = 0.006). More foxes were infected by two parasite genera than coyotes (p = 0.004). B) Parasite genus richness between Subarctic (yellow) and Humid Continental climate (green) in foxes from Qu´ebec, Canada, determined by gross examination and fecal flotation combined (N = 155). No significant difference in parasite genera was seen in foxes between Subarctic and Humid Continental climate regions. Parasites counted in both histograms were: diphyllobothriids (likely Dibothriocephalus spp.), Echinococcus spp., Taenia spp., Capillaria spp., Toxascaris sp., Toxocara sp., Trichuris sp., Uncinaria sp., Alaria sp., Cryptocotyle sp., and Metorchis sp. Parasites observed in both fecal and gross examination were only counted once. Bars represent 95% confidence intervals. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 5 in Prevalence and genetic diversity of Haemoproteus and Plasmodium in raptors from Thailand: Data from rehabilitation center
Fig. 5. Heatmap of pairwise genetic distances estimated from nucleotide sequences of the cytochrome b gene (479 nucleotides) of Plasmodium spp. using the JukesCanter model.
Fig. 6 in Host and geographic differences in prevalence and diversity of gastrointestinal helminths of foxes (Vulpes vulpes), coyotes (Canis latrans) and wolves (Canis lupus) in Quebec´, Canada
Fig. 6. Distribution of foxes (Vulpes vulpes), coyotes (Canis latrans), and wolves (Canis lupus) infected with Toxascaris leonina (left, N = 55) and Toxocara canis (right, N = 19) in the Subarctic and Humid Continental climate collected during winter 2016–2017 by hunters and trappers from Qu´ebec, Canada.
Fig. 1. K in Host and geographic differences in prevalence and diversity of gastrointestinal helminths of foxes (Vulpes vulpes), coyotes (Canis latrans) and wolves (Canis lupus) in Quebec´, Canada
Fig. 1. K¨oppen climate regions and sampling distribution of foxes (Vulpes vulpes, N = 176), coyotes (Canis latrans, N = 77), and wolves (Canis lupus, N = 23) collected during winter 2016–2017 by hunters and trappers from Qu´ebec, Canada. Arrows indicate major waterways.
Fig. 4 in Prevalence and genetic diversity of Haemoproteus and Plasmodium in raptors from Thailand: Data from rehabilitation center
Fig. 4. Bayesian phylogeny based on the partial cytochrome b gene (479 base pairs) of Plasmodium lineages. The lineages isolated in this study are given in red bold. MalAvi lineage codes and GenBank accession numbers are given after species names. Node values indicate percentages of posterior probabilities. Plasmodium isolated from this study are clustered into three clades (clade I, II and II). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4 in Host and geographic differences in prevalence and diversity of gastrointestinal helminths of foxes (Vulpes vulpes), coyotes (Canis latrans) and wolves (Canis lupus) in Quebec´, Canada
Fig. 4. Mixed taeniid infections in the Humid Continental climate in coyotes (Canis latrans) and wolves (Canis lupus) from Qu´ebec, Canada, following molecular analyses. Abbreviations on x-axis: E. can, Echinococcus canadensis; T. hyd, Taenia hydatigena; T. twi, T. twitchelli; T. kra, T. krabbei; T. pis, T. pisiformis-"like"; T. cra, T. crassiceps.
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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.