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56 results for “Intestinal Parasites”
Fig. 3 in Gastro-intestinal parasites of urban rhesus macaques (Macaca mulatta) in the Kathmandu Valley, Nepal
Fig. 3. Photomicrographs of various GI parasites of the rhesus macaques at 400×: Trophozoite of E. histolytica (A), Cyst of E. histolytica (B), Cyst of E. coli (C), Cyst of Iodomoeba butschlii (D), Cyst of Giardia spp. (E), Trophozoite of Balantioides coli (F), Cyst of Balantioides coli (G), Egg of Trichuris spp. (H), Egg of Strongyloides spp. (I), Larva of Strongyloides spp. (J), Egg of Hookworm (K), Egg of Trichostrongylus spp. (L), Egg of Ascarid spp. (M), Egg of Physaloptera spp. (N), Egg of Toxocara spp.(O), Egg of Toxocara spp. (P), Egg of Strongyle spp. (Q), Egg of Strongyle spp.(R), Oocyst of Cryptosporidium spp. (S), Unknown spp. 1 (T).
Fig. 1 in Gastro-intestinal parasites of urban rhesus macaques (Macaca mulatta) in the Kathmandu Valley, Nepal
Fig. 1. Map showing the four fecal collection sites of the urban rhesus macaques in the Kathmandu Valley.
Figure 1 in Prevalence of intestinal parasitic diseases in school children of rural areas of district Lower Dir, Pakistan
Figure 1. Parts of the region studied.
Fig. 4. Metastrongylus spp. eggs from a in Lungworms (Metastrongylus spp.) and intestinal parasitic stages of two separated Swiss wild boar populations north and south of the Alps: Similar parasite spectrum with regional idiosyncrasies
Fig. 4. Metastrongylus spp. eggs from a wild boar faecal sample.
Fig. 2 in Gastro-intestinal parasites of urban rhesus macaques (Macaca mulatta) in the Kathmandu Valley, Nepal
Fig. 2. Prevalence of gastro-intestinal parasites in the rhesus macaques of Kathmandu Valley.
Fig. 4 in Gastro-intestinal parasites of urban rhesus macaques (Macaca mulatta) in the Kathmandu Valley, Nepal
Fig. 4. Location-wise richness of parasitic infection in rhesus macaques of the Kathmandu Valley.
Fig. 5 in Gastro-intestinal parasites of urban rhesus macaques (Macaca mulatta) in the Kathmandu Valley, Nepal
Fig. 5. Species Richness of GI parasite infection in rhesus macaques of the Kathmandu Valley.
Age specific impacts of vegetation functional traits on gastro-intestinal nematode parasite burdens in a large herbivore
<ol> <li>Gastro-intestinal nematode (GIN) parasites play an important role in the ecological dynamics of many animal populations. Recent studies suggest fine-scale spatial variation in GIN infection dynamics is important in wildlife systems, but the environmental drivers underlying this variation remain poorly understood.</li> <li>We used data from over two decades of GIN parasite egg counts, host space use, and spatial vegetation data from a long-term study of Soay sheep on St Kilda to test how spatial autocorrelation and vegetation in an individual's home range predict parasite burden across three age groups. We developed a novel approach to quantify the plant functional traits present in a home range to describe the quality of vegetation present. </li> <li>Effects of space and vegetation varied between age classes. In immature lambs, strongyle parasite faecal egg counts (FEC) were spatially structured, being highest in the north and south of our study area. Independent of host body weight and spatial autocorrelation, plant functional traits predicted parasite egg counts. Higher egg counts were associated with more digestible and preferred plant functional traits, suggesting the association could be driven by host density and habitat preference.</li> <li>In contrast, we found no evidence that parasite FEC were related to plant functional traits in the host home range in yearlings or adult sheep. Adult FEC were spatially structured, with highest burdens in the north-east of our study area, while yearling FEC showed no evidence of spatial structuring.</li> <li>Our findings support the importance of fine-scale environmental variation for wildlife disease ecology and provide new evidence that such effects may vary across demographic groups within a population. Parasite burdens in immature individuals appear more readily influenced by fine-scale spatial variation in the environment, highlighting the importance of such heterogeneity for our understanding of wildlife epidemiology and health.</li> </ol>
Data from: Intestinal nematode infection confers a benefit to a non-declining frog species, while a fungal parasitic infection has sublethal impacts on reproductive investment
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Age specific impacts of vegetation functional traits on gastro-intestinal nematode parasite burdens in a large herbivore
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FIGURE 3 in Leidynema bestium sp. n. (Oxyuridomorpha: Thelastomatidae) an intestinal parasite of blaberid cockroaches from Yaroslavl Zoo, Russia
FIGURE 3. Leidynema bestium sp. n., males, scanning electron microscopy. A—anterior end, ventral view; B—posterior end, ventral view; C—posterior end, sublateral view; D—posterior end, lateral view; E—posterior end, ventral view; F—posterior end, sublateral view; G—tail tip and structure of genital papillae.
FIGURE 2 in Leidynema bestium sp. n. (Oxyuridomorpha: Thelastomatidae) an intestinal parasite of blaberid cockroaches from Yaroslavl Zoo, Russia
FIGURE 2. Leidynema bestium sp. n., females, scanning electron microscopy. A–C—anterior end, sub-apical view; D— posterior end, subventral view; E—female juvenile 4th stage, subdorsal view.
FIGURE 1 in Leidynema bestium sp. n. (Oxyuridomorpha: Thelastomatidae) an intestinal parasite of blaberid cockroaches from Yaroslavl Zoo, Russia
FIGURE 1. Leidynema bestium sp. n. A–F: female; A—total view; B—cephalic end; C—pharynx basal bulb; D—excretory pore and adjoining channels; E—vulvar opening and vagina; F—posterior end, ventral view; G–K: male; G—total view; H— cephalic end; I—oesophageal region; K—posterior end. All in lateral aspect if not otherwise specified. Scales in micrometers.
FIGURE 4 in Leidynema bestium sp. n. (Oxyuridomorpha: Thelastomatidae) an intestinal parasite of blaberid cockroaches from Yaroslavl Zoo, Russia
FIGURE 4. Phylogenetic tree inferred from analysis of D2–D3 LSU rDNA sequences of Leidynema nematodes. Bootstrap support values in the format MP/NJ/ML. Two groups of taxa: A and B are two subclades of Leidynema appendiculatum with a nucleotide difference in 10 bp between.
Impact of Hand Hygiene Activities on the Prevention of Intestinal Parasitic Infections and Anaemia Among School Children
ClinicalTrials.gov study NCT01619254. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Pattern of Intestinal Parasitic Infection Among Cirrhotic Patients in Sohag University Hospital
ClinicalTrials.gov study NCT05856721. IPD Sharing: UNDECIDED. Countries: 1. Publications: 4.
Effects of Vitamin A Supplementation on Intestinal Parasitic Reinfections
ClinicalTrials.gov study NCT00936091. IPD Sharing: Not stated. Countries: 1. Publications: 5.
Impact of Health Education Learning Package Against Intestinal Parasitic Infections Among Orang Asli Children
ClinicalTrials.gov study NCT03930901. IPD Sharing: NO. Countries: 1. Publications: 1.
Data from: High gut microbiota diversity provides lower resistance against infection by an intestinal parasite in bumblebees
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Data from: Fine-scale population epigenetic structure in relation to gastro-intestinal parasite load in red grouse (Lagopus lagopus scotica)
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International Brain Laboratory public data
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OpenNeuro
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