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133 results for “wild boar”
Fig. 4 in Cystic echinococcosis in wild boars (Sus scrofa) from southern Italy: Epidemiological survey and molecular characterization
Fig. 4. Distribution of the 93 positive wild boars in the study area and details of prevalence, provinces, regional and national parks.
Figure 7 in Mitochondrial DNA control region variability of wild boar Sus scrofa with various external phenotypes in Turkey
Figure 7. Median-joining network of 68 haplotypes from 485 wild boars from different regions of the world. Circle sizes are proportional to haplotype frequencies and numbers refer to haplotype codes in Table 2. Numbers on the branches indicate the number of nucleotide substitutions, if more than one. Major haplogroups are delimited by dashed lines. A, Asian; NE, Near Eastern; E1, European E1; E2, European E2. Haplotypes exclusive to Turkey are labeled in green.
Figure 3 in Mitochondrial DNA control region variability of wild boar Sus scrofa with various external phenotypes in Turkey
Figure 3. Maximum likelihood phylogenetic tree of haplotypes of the Turkish wild boars (Sus scrofa) obtained in the present study, based on the partial D-loop sequences of mtDNA. Numbers above or below branches indicate bootstrap values. TR numbers refer to current haplotype numbers in Table 1 and H numbers refer to the published haplotype labels downloaded from GenBank (Table 2). E1: European 1 haplogroup/clade in Figure 5, NE: Near East haplogroup/ clade in Figure 5.
Figure 2 in Mitochondrial DNA control region variability of wild boar Sus scrofa with various external phenotypes in Turkey
Figure 2. Various phenotypes of obtained Turkish wild boar individuals from different localities studied presently.
Figure 6 in Mitochondrial DNA control region variability of wild boar Sus scrofa with various external phenotypes in Turkey
Figure 6. Bayesian inference tree based on 68 partial D-loop haplotypes of 485 wild boars (both obtained in this study and downloaded from GenBank). Posterior probabilities are indicated at nodes. Haplogroups: A, Asian; NE, Near Eastern; E1, European E1; E2, European E2. Outgroup taxa are Sus barbatus and Phacochoerus aethiopicus.
Figure 1 in Mitochondrial DNA control region variability of wild boar Sus scrofa with various external phenotypes in Turkey
Figure 1. Location map of the 70 samples examined in this study: black dots indicate local samples of one or more individuals and numbers refer to locality names in Table 1. TT (Turkish Thrace, 1–4), SWA (Southwestern Anatolia, 5–11), CA (Central Anatolia, 12–26), NEA (Northeastern Anatolia, 27–30), and SEA (Southeastern Anatolia, 31–34).
Figure 5 in Mitochondrial DNA control region variability of wild boar Sus scrofa with various external phenotypes in Turkey
Figure 5. Maximum likelihood tree based on 68 haplotypes from 485 wild boar D-loop region sequences (both obtained in this study and downloaded from GenBank). Numbers above or below branches indicate bootstrap support values. Haplogroups: A, Asian; NE, Near Eastern; E1, European E1; E2, European E2. Outgroup taxa are Sus barbatus and Phacochoerus aethiopicus.
Figure 4 in Mitochondrial DNA control region variability of wild boar Sus scrofa with various external phenotypes in Turkey
Figure 4. Bayesian phylogenetic tree constructed from haplotypes of the wild boar (Sus scrofa) samples collected in this study, based on the partial D-loop sequences of mtDNA. Posterior probabilities are indicated at nodes. TR numbers refer to current haplotype numbers in Table 1 and H numbers refer to the published haplotype labels downloaded from GenBank (Table 2). E1: European 1 haplogroup/clade in Figure 5, NE: Near East haplogroup/clade in Figure 5.
Fig. 2 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. 2. Wild boar lung with massive trauma after bullet penetration and visible bone fractures (A), dense nodule of the lobus caudalis dexter (B), and accumulation of nematodes in a bronchus (C).
Fig. 3 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. 3. Caudal ends of the 5 Metastrongylus species identified in this study: M. apri female (A) and male (B), M. asymmetricus female (C) and male (D), M. confusus female (E) and male (F), M. pudendotectus female (G) and male (H), M. salmi female (I) and male (J).
Fig. 1 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. 1. Map of Switzerland with sampling areas for the northern (Cantons of Aargau (AG), Schaffhausen (SH), Thurgau (TG) and Zürich (ZH)) and the southern (Canton of Ticino (TI)) wild boar population. N: number of lungs sampled.
Fig. 3 in A comparison of detection methods of Alaria alata mesocercariae in wild boar (Sus scrofa) meat
Fig. 3. Probability of detection of DMS using various methods (Digestion, D + P, Compressor) in relation to numbers of DMS in meat sample (basing on AMT method) (n = 43 for D + P, Digest, n = 19 for Compressor, for details, see Methods).
Fig. 1 in A comparison of detection methods of Alaria alata mesocercariae in wild boar (Sus scrofa) meat
Fig. 1. The scheme of the experiment. Legend: P – prevalence of infection has been determined, I – intensity of infection has been determined, S – sensitivity of method has been determined, DMS – Distomum musculorum suis (mesocercariae of Alaria alata), AMT-reference – Alaria alata mesocercariae migration technique – reference method, Compressor – compressor analysis, Digestion – digestion with digestion stirrer, D + P – modified digestion with Pancreatin® bile pancreatic enzymes.
Fig. 2 in A comparison of detection methods of Alaria alata mesocercariae in wild boar (Sus scrofa) meat
Fig. 2. Mean numbers of DMS in meat sample (30 g) and comparison with the Kruskall Wallis test (X2 = 64.34.03; df = 2; P <0.001, N = 43 in all cases) and pairwise comparison with the Mann-Whitney U test (statistical difference was stated in comparison of pairs: AMT-Digestion and AMT-D + P, p <0.001 in both cases).
Fig. 1 in Epidemiology of Trichinella infection in wild boar from Spain and its impact on human health during the period 2006-2019
Fig. 1. Prevalence of Trichinella infection in wild boar from several Spanish autonomous communities.
Fig. 4 in Epidemiology of Trichinella infection in wild boar from Spain and its impact on human health during the period 2006-2019
Fig. 4. Box-plot and post hoc pairwise comparison via Dunn's test of the incidence. Box-plot with different letters indicate a statistically significant difference.
Fig. 3 in Epidemiology of Trichinella infection in wild boar from Spain and its impact on human health during the period 2006-2019
Fig. 3. Three-dimensional plots for the interaction effects of the total number of wild boars hunted and the prevalence of the Trichinella infection in wild boar on incidence of trichinellosis in humans.
Fig. 2 in Predicting the risk of Alaria alata infestation in wild boar on the basis of environmental factors
Fig. 2. The prevalence of A. alata in wild boar in provinces in Poland calculated from literature values and data from the present study (A) and predicted by percentage of areas covered by WETLANDS (B) (for detailed information, see: Methods). The figure shows prevalence values for a given province and confidence intervals (lower; upper).
Fig. 1 in Toxoplasma gondii and Neospora caninum in invasive wild boars (Sus scrofa) and hunting dogs from Brazil
Fig. 1. Map highlighting the cities where wild boar and hunting dog samples were obtained, Brazil, 2024.
Fig. 4 in Prevalence, molecular characterisation and phylogenetic analyses of hydatid cysts and cysticercus tenuicollis isolates and first report of E. canadensis (G6/G7) in wild boars in Bingol province, Türkiye
Fig. 4. Haplotype network of G1/G3 haplotypes identified on the basis of partial nad5 gene (628 bp). The G1 isolates obtained in this study (Hap01-Hap04), G3 isolates (Hap05, Hap06). Hatch marks represent the number of mutations between the haplotypes and the size of circle corresponds to the frequency of each haplotype in the population. Haplotypes formed by the isolates obtained in this study are marked with an asterisk.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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
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