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19 results for “Haemoparasites”
Fig. 2 in Biodiversity of frog haemoparasites from sub-tropical northern KwaZulu-Natal, South Africa
Fig. 2. Micrographs of various frog haemoparasites encountered in the current study. Haemoparasites from the peripheral blood of 15 frog species collected from three localities in northern KwaZulu-Natal, stained with Giemsa stain (A–E) gamonts of Hepatozoon species; (F–G) primary and secondary stage gamonts of Dactylosoma species; (H–J) viral or bacterial inclusions; (K) microfilarid nematode species; (L–T) Trypanosoma species. Scale bar: 10 μm.
Fig. 1 in Biodiversity of frog haemoparasites from sub-tropical northern KwaZulu-Natal, South Africa
Fig. 1. Map displaying the three sampling localities in northern KwaZulu-Natal, South Africa. Map displaying the three sampling localities at which frogs were surveyed for haemoparasite biodiversity, top to bottom: Ndumo Game Reserve (NGR), outside NGR and Kwa Nyamazane Conservancy, in northern KwaZulu-Natal, South Africa. All sampling sites were directly or indirectly linked to the Phongolo River.
Fig. 3. Minimum spanning network for Haemoproteus and Plasmodium mitochondrial DNA cytochrome b in Spatial, temporal, molecular, and intraspecific differences of haemoparasite infection and relevant selected physiological parameters of wild birds in Georgia, USA
Fig. 3. Minimum spanning network for Haemoproteus and Plasmodium mitochondrial DNA cytochrome b haplotypes detected in four species of passerines from Georgia (USA). Circles are drawn proportional to the frequency at which haplotypes were observed. Color represents the host species from which haplotypes originated: red for Northern Cardinal (Cardinalis cardinalis), blue for Indigo Bunting (Passerina cyanea), yellow for White-throated Sparrow (Zonotrichia albicollis), and grey for Tufted Titmouse (Baeolophus bicolor). A single mutation separates nodes unless explicitly indicated by number. Letters within each node refer to Table 8 which indicates the haplotype name, sampling location, and other factors associated with hosts.
Fig. 1 in Spatial, temporal, molecular, and intraspecific differences of haemoparasite infection and relevant selected physiological parameters of wild birds in Georgia, USA
Fig. 1. Map of Georgia (USA) indicating the location of the six sampling sites for identifying haemoparasite infections of birds in the northern and southern regions of the state.
Fig. 2 in Spatial, temporal, molecular, and intraspecific differences of haemoparasite infection and relevant selected physiological parameters of wild birds in Georgia, USA
Fig. 2. Average percent cell volume (PCV) values for five target bird species from Georgia (USA). Different letters indicate significant differences between bird species (p <0.05).
Fig. 4 in The distribution and host-association of a haemoparasite of damselfishes (Pomacentridae) from the eastern Caribbean based on a combination of morphology and 18S rDNA sequences
Fig. 4. Phylogenetic analysis of the Haemohormidium-like parasite based on 18S rDNA sequences. Bayesian inference (BI) analysis showing the phylogenetic relationships for 8 Haemohormidium-like parasite isolates, 6 from the present study (GenBank: MH401637-42) (in bold) and 2 from Renoux et al. (2017), isolated from three species of Stegastes including Stegastes adustus, Stegastes diencaeus and Stegastes planifrons, from 5 sites in the eastern Caribbean. Comparative sequences representing known coccidia, with Adelina dimidiata (DQ096835) as outgroup, were downloaded from the GenBank database. Nodal support values> 50% are represented on the tree.
Fig. 2 in The distribution and host-association of a haemoparasite of damselfishes (Pomacentridae) from the eastern Caribbean based on a combination of morphology and 18S rDNA sequences
Fig. 2. Peripheral blood stages of the Haemohormidium-like parasite infecting species of Stegastes. Giemsa stained light micrographs of the Haemohormidium-like parasite as observed in the peripheral blood of Stegastes diencaeus from St Thomas, eastern Caribbean (Genbank accession number MH401641). A. rare possible trophozoite stage. B. possible meront stages undergoing transverse binary fission. C. possible meront stages undergoing longitudinal binary fission. Scale bar = 10 μm.
Fig. 3 in The distribution and host-association of a haemoparasite of damselfishes (Pomacentridae) from the eastern Caribbean based on a combination of morphology and 18S rDNA sequences
Fig. 3. Prevalence of infection differences among six Stegastes spp., averaged across six study sites. 95% confidence intervals calculated using the Wilson procedure with continuity corrections. Different lower-case letters above each bar indicates a significant (p ≤ 0.05) difference between species, as indicated by a binomial logistic regression (GLMM results shown in Table 1).
Fig. 1 in The distribution and host-association of a haemoparasite of damselfishes (Pomacentridae) from the eastern Caribbean based on a combination of morphology and 18S rDNA sequences
Fig. 1. Map of the Eastern Caribbean region showing collection sites for the current study and Cook et al., 2015.
Fig. 1 in Haemoparasites in endemic and non-endemic passerine birds from central Mexico highlands
Fig. 1. Location of study sites. (A) Location of the State of Mexico, (B) Location of Nevado de Toluca Natural Protected Area (NTNPA), and Valle de Bravo Natural Protected Area (VBNPA), (C) Parque Ecológico Ejidal de Cacalomacán (PEEC) and (D) Parque Ecoturístico Corral de Piedra (PECP). Datum WGS_1984_UTM Zone 14.
Fig. 1 in Evaluation of haemoparasite and Sarcocystis infections in Australian wild deer
Fig. 1. Location of eight deer sampling sites in eastern Australia. Queensland: north-east Queensland (1). New South Wales: Liverpool Plains (2), Wollongong (3), and Kiah (4). Victoria: Alpine National Park (5), Upper Yarra Flats and Yellingbo (6). ACT: Canberra (7).
Fig. 2 in Evaluation of haemoparasite and Sarcocystis infections in Australian wild deer
Fig. 2. Total number of deer samples collected in eastern Australia between March 2018 and November 2019.
Haemoparasite Infection Risk in Multi-Host Avian System: An Integrated Analysis
<p><strong>Data used in the study: Haemoparasite Infection Risk in Multi-Host Avian System: An Integrated Analysis</strong></p> <ul> <li><strong>Podmokła et al. 2024_data.csv</strong> - This file contains the processed data used in the analysis.</li> <li><strong>Podmokła et al. 2024_raw data_landscape and population variables.csv</strong> - This file includes raw data on landscape and population variables. <ul> <li><strong>Population Metrics</strong>: Density of the same species and all species combined in the study area.</li> <li><strong>Landscape Variables</strong>: High-resolution satellite remote-sensing data reflecting vegetation cover (NDVI), moisture levels (NDMI), and distances to key landscape features such as forest edges, coastlines, pastures, and fields.<br><br></li> </ul> </li> <li><strong>Podmokła et al. 2024_raw data_parasites.csv</strong> - This file contains raw data on <em>Haemoproteus</em>, <em>Plasmodium</em>, and <em>Trypanosoma</em> infection status</li> </ul>
Pleiotropic effects of melanin pigmentation: Haemoparasite infection intensity but not telomere length is associated with morph in black sparrowhawks
Open the record for dataset details and reuse information.
Fig. 2 in Haemoparasites in endemic and non-endemic passerine birds from central Mexico highlands
Fig. 2. Triple infection of Haemoproteus spp./Leucocytozoon spp./microfilaria in a Catharus occidentalis. (A). Leucocytozoon spp. () and Haemoproteus spp. () parasites. (B). Microfilaria (➤), Leucocytozoon spp. () and Haemoproteus spp. () parasites. (C). Catharus occidentalis infected. Photomicrographs. Scale-bar: 10 μm.
Figure 4 in Haemoparasites of falcons in France: a 2 - year survey in the Cevennesı with description of two new Haemoproteid species from poly-parasitised birds
Figure 4. Microphotographs of Haemoproteus deharoi n. sp. in the blood of Falco tinnunculus. A. Mature microgametocyte with kidney-shaped aspect; B. mature macrogametocyte with kidneyshaped aspect and colloidal area; C. mature macrogametocyte with ellipsoidal aspect; D. old microgametocyte; E. old roundish macrogametocyte with two colloidal areas; F. old roundish macrogametocyte with a colloidal area and numerous white vacuoles throughout the cytoplasm. Giemsa staining. Scale bar = 5 μm.
Figure 3 in Haemoparasites of falcons in France: a 2 - year survey in the Cevennesı with description of two new Haemoproteid species from poly-parasitised birds
Figure 3. Microphotographs of Haemoproteus obainae n. sp. in the blood of Falco sp. A. Mature microgametocyte slightly curved; B. mature macrogametocyte; C. mature microgametocyte with diffuse nucleus; D. mature macrogametocyte displacing upwards the RBC nucleus; E. mature microgametocyte harbouring a red granule in its nucleus and displacing upwards the RBC nucleus; F and G. mature microgametocytes with fine cytoplasmic projections; H. mature macrogametocyte fine pigment granules; I. unstained smear: pigment of gametocyte; arrows indicate pigments. A–F, I, from the blood of Falco subbuteo; G, H, from the blood of Falco tinnunculus. Giemsa staining. Scale bar = 5 µm.
Figure 2 in Haemoparasites of falcons in France: a 2 - year survey in the Cevennesı with description of two new Haemoproteid species from poly-parasitised birds
Figure 2. Microphotographs of Haemoproteus brachiatus in the blood of Falco tinnunculus. A. Microgametocyte; B. macrogametocyte. Giemsa staining. Scale bar = 5 µm.
Figure 1 in Haemoparasites of falcons in France: a 2 - year survey in the Cevennesı with description of two new Haemoproteid species from poly-parasitised birds
Figure 1. Microphotographs of Haemoproteus tinnunculi in the blood of Falco tinnunculus. A. Macrogametocyte; B. microgametocyte. Giemsa staining. Scale bar = 5 µm.
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International Brain Laboratory public data
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OpenNeuro
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