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66 results for “gastrointestinal parasite”
Dataset of host, habitat and vegetation parameters in relation to gastrointestinal parasite infections of small mammalian hosts in Madagascar
<p>The dataset contains information on the endoparasite infection status of 903 individuals of four small mammal species (<em>Microcebus murinus</em>, <em>M. ravelobensis</em>, <em>Eliurus myoxinus</em>, <em>Rattus rattus</em>) in relation to host-specific (sex, body condition, population density) and habitat-specific factors (degree of habitat fragmentation, fragment size, distance to the edge of the fragment, percentage of edge habitat, vegetation structure).</p>
Seasonal Effects in Gastrointestinal Parasite Prevalence, Richness and Intensity in Vervet Monkeys Living in a Semi-Arid Environment
<p>Data and R Notebook for Seasonal Effects in Gastrointestinal Parasite Prevalence, Richness and Intensity in Vervet Monkeys Living in a Semi-Arid Environment</p>
Fig. 3 in Gastrointestinal Parasite Community In A New Population Of The Przewalski'S Horse (Equus Ferus Przewalskii) In The Orenburg State Reserve, Russia
Fig. 3. Distribution of strongylid species from the Przewalski's horses in Pre-Urals Steppe, Orenburg State Reserve, on ten prevalence classes.
Fig. 1 in Gastrointestinal parasites in captive and free-ranging Cebus albifrons in the Western Amazon, Ecuador
Fig. 1. From left to right in each row: Hymenolepis sp., Capillaria sp., Strongyloides sp., Prosthenorchis elegans, Strongyle (unidentified), Entamoeba histolytica/dispar/moskovskii/ nuttalli. (40x).
Fig. 3 in Gastrointestinal parasite infestation in the alpine mountain hare (Lepus timidus varronis): Are abiotic environmental factors such as elevation, temperature and precipitation affecting prevalence of parasite species?
Fig. 3. Parasite infestation in faeces and ambient temperature. Correlation between parasite infestation in Alpine mountain hare faeces (n = 52) and average, minimal, and maximal temperature found in Vorarlberg (Austria) during the years 2014 and 2015. Count visualises the number of faecal samples. See text for details on statistics.
Fig. 2 in Gastrointestinal parasite infestation in the alpine mountain hare (Lepus timidus varronis): Are abiotic environmental factors such as elevation, temperature and precipitation affecting prevalence of parasite species?
Fig. 2. Number of parasite types per faeces and severity of parasitic infestation. Correlation between number of parasite types per Alpine mountain hare faeces and severity of parasitic infestation (n = 28) found in Vorarlberg (Austria) during the years 2014 and 2015. Count visualises the number of faecal samples. The severity of infestation is indicated by scattered ((+)), low (+), intermediate (++), and high (+++) infestation. See text for details on statistics.
Fig. 2. A in Multiple infestations of gastrointestinal parasites - Probable cause for high mortality of Spot-billed Pelican (Pelecanus philippensis) at Kokrebellur Community Reserve, India
Fig. 2. A. Larvae of Contracaecum sp. in fish, B. Adult Contracaecum sp. worms in the pelican, C. Eggs of Echinostoma sp. in pelican fecal and water samples, D. Eggs of Contracaecum sp. in pelican fecal and water samples and E. Eggs of Opisthorchis viverrini in pelican fecal samples.
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. 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 Gray wolves as sentinels for the presence of Echinococcus spp. and other gastrointestinal parasites in France
Fig. 4. Histogram of the total number of fecal samples analyzed for each French wolf pack with a minimum of 12 fecal samples available, with indication of the detection of cestodes (red), nematodes (orange) or absence of parasites (green).
Fig. 2 in Gray wolves as sentinels for the presence of Echinococcus spp. and other gastrointestinal parasites in France
Fig. 2. Spatial distribution of the 911 fecal samples collected from wolves (gray circle) in southeastern France submitted to copro-DNA analyses for identification of gastrointestinal parasites. The size of the circles is proportional to the number of samples collected per municipality. The departments (corresponding to NUTS3 level) are indicated by black lines.
Fig. 3 in Gray wolves as sentinels for the presence of Echinococcus spp. and other gastrointestinal parasites in France
Fig. 3. Location of the French wolf fecal samples positive for Echinococcus granulosus sensu stricto (green circles) and Echinococcus multilocularis (red circles). The E. multilocularis-positive fecal samples of dogs (red triangles) and wolves (small red diamonds) from Imperia (Italy) taken from Massolo et al., (2018) are also shown.
Fig. 3 in Gastrointestinal parasite diversity of South American camelids (Artiodactyla: Camelidae): First review throughout the native range of distribution
Fig. 3. Parasitic richness of South American camelid throught the native distribution range based on data available to date.
Fig. 2 in Gastrointestinal parasite diversity of South American camelids (Artiodactyla: Camelidae): First review throughout the native range of distribution
Fig. 2. Geographical location of the documents compiled in the present review (red dots). (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 Veterinary monitoring of gastrointestinal parasites in European bison, Bison bonasus designated for translocation: Comparison of two coprological methods
Fig. 5. The relationship between the prevalence of Eimeria spp. oocysts in European bison feces measured by the Willis and modified McMaster techniques (each point represents an individual parasite species).
Fig. 3 in Effect of urbanization on zoonotic gastrointestinal parasite prevalence in endemic toque macaque (Macaca sinica) from different climatic zones in Sri Lanka
Fig. 3. GI parasite genera types identified from fecal samples of toque macaques. I. Protozoan types: (A) Balantidium cyst, (B) Balantidium trophozoite, (C) Endolimax cyst, (D) Entamoeba cyst, (E) Isospora cyst. (F) Unidentified protozoan cyst; II. Cestode types: (G) Bertiella ova, (H) Diphyllobothrium ova, (I) Hymenolepis ova; III. Trematode types: (J–K) Unidentified trematode ova; IV. Acanthocephalan type: (L) Moniliformis ova; V. Nematode types: (M) Oesophagostomum ova, (N) Strongyloides ova, (O) Ascaris ova, (P) Trichuris ova, (Q) Strongyle/ Hookworm ova, (R) Enterobius ova, (S)Trichostrongylus ova, (T) Unidentified nematode ova.
Fig. 2 in Effect of urbanization on zoonotic gastrointestinal parasite prevalence in endemic toque macaque (Macaca sinica) from different climatic zones in Sri Lanka
Fig. 2. Map of Sri Lanka with sampling localities in the dry and the wet zones and the montane region.
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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.