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Fig. 2 in Wild carnivores and Thelazia callipaeda zoonotic eyeworms: A focus on wolves

Fig. 2. Thelazia callipaeda collected from the eyes of wolves. a) anterior end of a female; b) anterior end of a female highlighting the striated cuticle throughout the body; c) presence of L1 in the uterus; d) posterior end of a male highlighting the short and long spicules.

Fig. 2 in High Toxocara cati prevalence in wild, free-ranging Eurasian lynx (Lynx lynx) in Finland, 1999-2015

Fig. 2. The estimated Eurasian lynx (Lynx lynx) population size and Toxocara cati prevalence (%, 95% confidence interval) in Finland, by year.

Fig. 3 in High Toxocara cati prevalence in wild, free-ranging Eurasian lynx (Lynx lynx) in Finland, 1999-2015

Fig. 3. Number of Toxocara cati worms in Eurasian lynx (Lynx lynx) in Finland, by age and sex. Median, first and third quartiles, and minimum and maximum are shown.

Fig. 3 in Molecular screening for Sarcocystidae in muscles of wild birds from Brazil suggests a plethora of intermediate hosts for Sarcocystis falcatula

Fig. 3. Phylogenetic tree of Sarcocystis spp. based on ITS1 sequences. The tree was constructed through the maximum likelihood method, using the best-fit model HKY + I. The final alignment contained 78 sequences and 661 aligned nucleotide positions. All positions containing gaps and missing data were eliminated (complete deletion option). Numbers on branches represent bootstrap values after 1000 replicates. The black dots identify the sequences obtained in this study.

Fig. 1 in High Toxocara cati prevalence in wild, free-ranging Eurasian lynx (Lynx lynx) in Finland, 1999-2015

Fig. 1. The head, the cephalic alae and the body of the Toxocara cati found from female Eurasian lynx (Lynx lynx) from Finland. The measurement scale has red marks at 1 mm intervals. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 2. SAG1 in Molecular screening for Sarcocystidae in muscles of wild birds from Brazil suggests a plethora of intermediate hosts for Sarcocystis falcatula

Fig. 2. SAG1 (a), SAG2 (b) and SAG3 (c) haplotype networks for Sarcocystis falcatula and other closely related species obtained in this study. Perpendicular bars along the branches refer to mutation changes. The sizes of the circles are proportional to the numbers of haplotypes, and colors indicate the different orders of birds found. The numbers correspond to the sample IDs. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1 in Molecular screening for Sarcocystidae in muscles of wild birds from Brazil suggests a plethora of intermediate hosts for Sarcocystis falcatula

Fig. 1. Phylogenetic tree of Sarcocystis spp. based on ITS1 sequences. The tree was constructed through the maximum likelihood method, using the best-fit model K2P + G. The final alignment contained 24 sequences and 389 aligned nucleotide positions. All positions containing gaps and missing data were eliminated (complete deletion option). Numbers on branches represent bootstrap values after 1000 replicates. The black dots identify the sequences obtained in this study.

Fig. 1 in Wild carnivores and Thelazia callipaeda zoonotic eyeworms: A focus on wolves

Fig. 1. Presence of Thelazia callipaeda in the conjunctival sacs of wolves (Canis lupus) from the Italian Alps.

Fig. 1 in Sero-prevalence and risk factors of Toxoplasma gondii infection in wild cervids in Denmark

Fig. 1. The geographical distribution of wild cervids included in the study and the number of animals tested positive for antibodies against Toxoplasma gondii in the hunting season 2017–2018 in Denmark (n = 428). Shown by region and proportion of species sampled (roe deer, fallow deer or red deer) in each region. Pie charts indicate proportion of samples from each cervid species. Note Sika deer was only sampled in Mid-Jutland (n = 14), and hence not included in the map. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 2 in High species diversity of Echinococcus spp. in wild mammals of Namibia

Fig. 2. Species and numbers of examined animals in the seven study sites; in brackets numbers of infected animals and causative Echinococcus sp. (EC = E. canadensis, EE = E. equinus, EF = E. felidis, EG = E. granulosus sensu stricto, EO = E. ortleppi) (Source of modified map https://de.wikipedia.org/wiki/Datei:Namibia_relief_locatio n_map.jpg).

Fig. 1 in Baseline study of the morphological and genetic characteristics of Haemoproteus parasites in wild pigeons (Columba livia) from paddy fields in Thailand

Fig. 1. Haemoproteus columbae from the blood of wild pigeons (Columba livia); cytochrome b lineage HAECOL1 (a–d), COLIV03 (e–f) and COQUI05 (i–l); macrogametocytes (a–b; e–f; i–j) and microgametocytes (c–d; g–h; k–l); simple arrows: nuclei of erythrocytes; short triangle-head arrows: volutin granules; long trianglehead arrows: pigment granules; scale bar = 10 μm.

Fig. 1 in High species diversity of Echinococcus spp. in wild mammals of Namibia

Fig. 1. Location of the seven study sites in Namibia (Source of modified map https://de.wikipedia.org/wiki/Datei:Namibia_relief_location_map.jpg).

Fig. 2 in Baseline study of the morphological and genetic characteristics of Haemoproteus parasites in wild pigeons (Columba livia) from paddy fields in Thailand

Fig. 2. Haplotype network of partial cyt b sequence (479 bp) of Haemoproteus columbae from wild pigeons (Columba livia); (A) the three common haplotypes (HAECOL1, COLIV03 and COQUI05) found in this study and proportions between study sites; (B) proportions of each haplotype reported worldwide and in the two study sites; Nakhon Sawan (purple), Phitsanulok (pink), and previous reports (gray); number of sequences shown in a pie chart of the network, without number inside indicates one sequence. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 3 in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 3. Boxplot of tick abundance, female-to-male ratio and important climate factors change by months. A: Tick daily abundance; B: Daily female-to-male ratio of ticks; C: Daily temperature; D: Daily air pressure. Variables sharing the same letters among months were not significantly different. The five-day-rolling average values were calculated for all the variables that change by months.

Fig. 6 in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 6. Daily average tick abundance, daily average air pressure and daily average temperature with standard deviations by months. All the values are calculated with five-day-rolling average values.

Fig. 2. Ixodes. ovatus collected from the giant panda. A in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 2. Ixodes. ovatus collected from the giant panda. A: Dorsal of the adult female I. ovatus; B: Ventral of the adult female I. ovatus; C: Dorsal of the adult male I. ovatus; D: Ventral of the adult male I. ovatus.

Fig. 5 in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 5. The correlation plot of daily tick abundance and the daily air pressure with trending line. The five-day-rolling average values were calculated for tick abundance and the air pressure.

Fig. 1 in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 1. Experimental site was located in Daxiangling Natural Reserve, which is a part of the Giant Panda National Park in China. The orange area indicates the range of the Giant Panda National Park. The blue star is the location of this experimental site. Continents outline maps by Vemaps.com. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 4 in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 4. The correlation plot of daily tick abundance and the daily temperature with the trending line. The five-day-rolling average values were calculated for tick abundance and temperature.