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403 results for “captivity”
Fig. 4 in Fatal infection caused by Cytauxzoon felis in a captive-reared jaguar (Panthera onca)
Fig. 4. Micrograph of the pancreas on infected jaguar. The macrophages are enlarged up to twice normal size and contained cytoplasmic schizonts. Note eccentric and pyknotic nuclei of macrophages. HE.
Fig. 3 in Fatal infection caused by Cytauxzoon felis in a captive-reared jaguar (Panthera onca)
Fig. 3. Micrograph of the pancreas on infected jaguar. The central blood vessel is partially obstructed by macrophages containing high numbers of C. felis schizonts. HE.
Fig. 2 in Fatal infection caused by Cytauxzoon felis in a captive-reared jaguar (Panthera onca)
Fig. 2. Gross findings of Cytauxzoon felis fatal infection in a jaguar. The spleen is severely enlarged.
Fig. 1 in Fatal infection caused by Cytauxzoon felis in a captive-reared jaguar (Panthera onca)
Fig. 1. Gross findings of Cytauxzoon felis fatal infection in a jaguar. Moderate icterus in the ocular mucosa. The enophthalmos indicates severe dehydration.
Fig. 3 in Fatal avian malaria in captive Atlantic puffins (Fratercula arctica) in Switzerland
Fig. 3. Modified Wright-stained peripheral blood smear of a captive Atlantic puffin (case 5). Intra-erythrocytic stages of Plasmodium relictum: trophozoites (short arrows); mature meront (long arrow) with marked displacement of the erythrocyte's nucleus; pigment granules (arrowheads). Picture: Veterinary Laboratory, Vetsuisse Faculty, University of Zurich.
Fig. 1. H&E in Fatal avian malaria in captive Atlantic puffins (Fratercula arctica) in Switzerland
Fig. 1. H&E-stained histological sections of the liver (A, B, C) and the spleen (D) of captive Atlantic puffins at 400x magnification. A: Case 1, multiple protozoan Plasmodium schizonts of up to 20 μm in diameter (arrows). B: Case 2, periportal infiltration with lymphocytes and presence of multiple intracytoplasmic Plasmodium schizonts, which contain numerous merozoites (arrows). C: Case 3, Plasmodium merozoites within the liver parenchyma (arrow). D: Case 5, multiple histiocytes with intracytoplasmic brown, finely granular pigment (accumulation of iron-based pigment). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2. H&E in Fatal avian malaria in captive Atlantic puffins (Fratercula arctica) in Switzerland
Fig. 2. H&E-stained histological sections of the liver (A, B, D) and the spleen (C) of captive Atlantic puffins at 1000x magnification, showing Plasmodium schizonts of up to 15 μm in diameter, containing multiple merozoites of 1–2 μm (arrows): A: Case 2, B: Case 4, C: Case 6, D: Case 7.
Fig. 1 in Unveiling a novel parasitosis: Trichostrongylus colubriformis infection in captive ring-tailed lemurs (Lemur catta)
Fig. 1. Morphology of Trichostrongylus colubriformis adult stages: A) anterior end, scale bar 50 μm; B) detail of anterior end of female showing three small lips and a circle of cephalic papillae; C) detail of ovijector, scale bar 50 μm; D) detail of the cuticle; E) posterior end of male showing the structure of bursa, the gubernaculum (g) and short subequal spicules (sp); F) egg, scale bar 50 μm.
Fig. 4. Phylogenetic relationship among the S in Fatal hepatic sarcocystosis in three captive and one free-ranging pinniped
Fig. 4. Phylogenetic relationship among the S. canis-like variants from two Hawaiian monk seals (Monachus schauinslandi) and two California sea lions (Zalophus californianus), a Pacific harbor seal (MT460246) compared against S. canis sequences from two black bears (OR336049, MW136927), a polar bear (DQ176645) and various other Sarcocystis spp. at the complete ITS1 locus. Evolutionary distances were computed using the Tamura-Nei genetic distance model. A Neighbor-Joining midpoint rooted bootstrap consensus tree was inferred from 1000 MUSCLE alignment iterations. Bootstrap percentage values are indicated at the branch points.
Fig. 2 in Fatal hepatic sarcocystosis in three captive and one free-ranging pinniped
Fig. 2. TEM of a schizont with protozoa similar to S. canis in the hepatocyte of a California sea lion (Zalophus californianus) "CSL 1". Merozoites contained micronemes (Mn), a conoid (Co), and a prominent nucleus (Nu), but no rhoptries. Bar = 500 nm.
Fig. 1 in Fatal hepatic sarcocystosis in three captive and one free-ranging pinniped
Fig. 1. Histologic liver sections of a California sea lion (Zalophus californianus) "CSL 2" with numerous coalescing foci of acute necrosis. A. Lower magnification of acute necrosis with Sarcocystis schizonts (black arrow). B. Higher magnification of mature protozoal schizonts with a rosette of merozoites (red arrow) and a schizont with greater than 30 free merozoites (black arrow) within a foci of hepatic necrosis.
Fig. 3 in Fatal hepatic sarcocystosis in three captive and one free-ranging pinniped
Fig. 3. Phylogenetic relationship of the S. canis-like variant isolate CSL-2 that infects pinnipeds from a California sea lion (Zalophus californianus) compared against S. canis from a black bear isolate 11–3173 (OR654898) and various other Sarcocystis spp. Within a 994 nucleotide fragment of the 18S rRNA locus. Evolutionary distances were computed using the Tamura-Nei genetic distance model. A Neighbor-Joining bootstrap consensus tree was inferred from 1000 MUSCLE alignment iterations. Bootstrap percentage values are indicated at the branch points. Toxoplasma gondii was used as an outgroup.
Fig. 2 in Unveiling a novel parasitosis: Trichostrongylus colubriformis infection in captive ring-tailed lemurs (Lemur catta)
Fig. 2. The evolutionary history was inferred by using the Maximum Likelihood method based on the Tamura 3-parameter model. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. The analysis involved 27 nucleotide sequences. There were a total of 684 positions in the final dataset.
Fig. 2 in Endoparasite loads and the efficacy of conventional anthelmintics against gastrointestinal nematodes in captive European bison
Fig. 2. Mean (±SE) number of Eimeria species in European bison without ungulate neighbors (N0) and kept near other ungulates (YES) for seasons, calculated in a generalized linear model. Differences were statistically significant in the pairwise comparison for autumn and winter (p values shown above the bars).
Fig. 1 in Endoparasite loads and the efficacy of conventional anthelmintics against gastrointestinal nematodes in captive European bison
Fig. 1. Location of coproscopically examined European bison enclosures and other ungulate species in the vicinity of these enclosures in Poland.
Fig. 1 in Molecular detection and characterization of Giardia spp., Cryptosporidium spp., and Blastocystis in captive wild animals rescued from central Colombia
Fig. 1. Cryptosporidium species in wild animals kept in captivity. The chord diagram shows the relation between Cryptosporidium species and the order and species of infected animals.
Fig. 5 in Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation
Fig. 5. Morphological comparison of Malayemys subtrijuga no. 5 between week 0 (A and B) and week 17 (C and D).
Fig. 4 in Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation
Fig. 4. Symptoms of Placobdelloides siamensis infection on Malayemys subtrijuga: (A) Leech penetration beneath the keratin layer (scute) on plastron from no. 8; (B) Shell holes resulting from leech penetration on plastron from no. 7; (C) Epidermal lesion on the hind foot from no. 6; (D) Keratin mandible jaw with leech consumption from no. 4.
Fig. 3 in Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation
Fig. 3. Trend analysis of red blood cell count (RCC) (left) and white blood cell count (WCC) (right) of Malayemys subtrijuga during captivity recovery from 2 November 2018 (week 0) to 1 March 2019 (week 17). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation
Fig. 1. Analysis of the mean red blood cell count (RCC) (blue line) and white blood cell count (WCC) (green line) of Malayemys subtrijuga during captivity recovery from 2 November 2018 (week 0) to 1 March 2019 (week 17). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
ScienceDex guides
Understand access before you commit
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)
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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.