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Fig. 2 in Disseminated protozoal infection in a wild feathertail glider (Acrobates pygmaeus) in Australia

Fig. 2. Relationship of the novel apicomplexan taxon (in bold) from the liver of the feathertail glider with representative sequences from members of the Eimeriidae, Lankesterellidae and the Sarcocystidae, established based on a phylogenetic analysis of small subunit of nuclear ribosomal RNA gene (SSU) sequence data employing distance and Bayesian methods. Branch supports include neighbor-joining bootstrap percentages followed by Bayesian posterior probabilities. Members of the genus Goussia were used as outgroups.

Fig. 1 in Disseminated protozoal infection in a wild feathertail glider (Acrobates pygmaeus) in Australia

Fig. 1. Histological image of clusters of zoites (arrow) in the liver (A) and lung (B) of a feathertail glider. Haematoxylin and eosin stain; 1000-times magnification.

Fig. 1 in Rickettsia parkeri strain Atlantic rainforest in ticks (Acari: Ixodidae) of wild birds in Arauca, Orinoquia region of Colombia

Fig. 1. Localities sampled in the municipalities of Arauca, Cravo Norte, and Tame and reports of Rickettsia spp. in the study area (▴Rickettsia parkeri strain Atlantic rainforest).

Fig. 2 in Rickettsia parkeri strain Atlantic rainforest in ticks (Acari: Ixodidae) of wild birds in Arauca, Orinoquia region of Colombia

Fig. 2. Phylogenetic tree based on partial sequences of the outer membrane protein gene ompB present only in SFG Rickettsia species. The tree was inferred through Maximum Likelihood with the Tamura 3-parameter evolution model. The sequences obtained in this study appear in bold and the GenBank accessions numbers are provided within square brackets.

Fig. 1 in Review on parasites of wild and captive giant pandas (Ailuropoda melanoleuca): Diversity, disease and conservation impact

Fig. 1. Distribution of wild giant pandas in six mountain regions (Qinling, Minshan, Qionglai, Liangshan, Daxiangling and Xiaoxiangling) in three Provinces (Gansu, Shaanxi, and Sichuan) of China. Adapted from Wang et al. (2018).

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Figure 1 in First release of a captured Sumatran striped rabbit Nesolagus netscheri (Schlegel, 1880) into the wild

Figure 1. Two young individuals of N.netscheri received by Nature Conservation Agency of Bengkulu Province from local people, late September 2021, Rejang Lebong District, Bengkulu Province (Photo: Said Jauhari).

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Fig. 2. The 2019 in Wild bee pollinators foraging in peanut and cotton adjacent to native wildflower strips

Fig. 2. The 2019 mean (± SE) of bees per bee bowl captured in cotton and those with cotton pollen and unidentified pollen (= other) (a), and the mean (± SE) of bees per bee bowl captured in cotton with G. pulchella (IB), Monarda citriodora (mint), and Rudbeckia hirta (susan) (b).

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Fig. 1. The 2018 in Wild bee pollinators foraging in peanut and cotton adjacent to native wildflower strips

Fig. 1. The 2018 mean (± SE) of bees per bee bowl captured in peanut and those with peanut pollen (a), and the mean (± SE) of bees per bee bowl captured in peanut with Gaillardia pulchella (IB), and both G. pulchella and peanut pollen (b).

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Fig. 1 in Prevalence of avian haemosporidia among injured wild birds in Tokyo and environs, Japan

Fig. 1. Locations of the four facilities in the Kanto region that samples were collected. A. Kanagawa Prefecture Natural Conservation Center, B. Inokashira Animal Hospital, C. Gyotoku Wild Bird Hospital, D. Bird Clinic Kanesaka Animal Hospital.

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Fig. 2 in Prevalence of avian haemosporidia among injured wild birds in Tokyo and environs, Japan

Fig. 2. Hemacolor ® stained blood smears from rescued birds: (a) Plasmodium sp. from Cyanopica cyanus, (b) P. reluctum from Hypisipetes amaurotis, (c) P. circumflexum from Fulica atra, (d) Haemoproteus sp. from Hypisipetes amaurotis, (e) Haemoproteus sp. from Larus canus, (f) H. minutus from Turdus cardis, (g) Leucocytozoon sp. from Anas acuta, (h) Leucocytozoon sp. from Aythya marila.

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Fig. 3 in Diversity and density-dependence relationship between hymenopteran egg parasitoids and the corn leafopper (Hemiptera: Cicadellidae) in maize agroecosystem vs. teosinte wild habitat

Fig. 3. Relationship between the number of exposed Dalbulus maidis eggs and number of Anagrus virlai within the crop maize habitat on (A) maize sentinel plants, and (B) teosinte sentinel plants.

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Fig. 1 in Diversity and density-dependence relationship between hymenopteran egg parasitoids and the corn leafopper (Hemiptera: Cicadellidae) in maize agroecosystem vs. teosinte wild habitat

Fig. 1. Relationship between the number of exposed Dalbulus maidis eggs and number of adult parasitoids (of any species) found in the crop maize habitat on (A) maize sentinel plants, and (B) teosinte sentinel plants.

Fig. 1 in The prevalence of Leucocytozoon spp. in nestlings of three wild raptor species including implications on haematological and blood chemistry values

Fig. 1. Prevalence of Leucozytozoon spp. infection in nestlings of common buzzards (Buteo buteo), red kites (Milvus milvus) and northern goshawks (Accipiter gentilis). Asterisks refer to P-values ≤0.05, determined by GLMM. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 3 in The prevalence of Leucocytozoon spp. in nestlings of three wild raptor species including implications on haematological and blood chemistry values

Fig. 3. Results of linear discriminant analysis (LDA) comparing 15 selected blood parameters between uninfected and infected raptor nestlings. a) Distribution of the LDA according to uninfected and infected nestlings. b) Correlation plot of the first axis of the 15 selected variables.

Fig. 2 in The prevalence of Leucocytozoon spp. in nestlings of three wild raptor species including implications on haematological and blood chemistry values

Fig. 2. Proportion of infected individuals of common buzzard (Buteo buteo), red kite (Milvus milvus) and northern goshawk (Accipiter gentilis) nestlings (n = 528) in relation to the proportion of the nestling period, determined by age and the species-specific average nestling duration. Calculated nestling periods were grouped into steps of ten percent (0.2–0.9). Each step represents the proportion of all individuals examined within this period. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1 in Blastocystis occurrence and subtype diversity in wild European terrestrial mammals - The case of Białowieza˙Primeval Forest (NE Poland)

Fig. 1. Study area with localization and number of Blastocystis-positive and Blastocystis-negative animals of particular mammalian species.

Fig. 2 in Blastocystis occurrence and subtype diversity in wild European terrestrial mammals - The case of Białowieza˙Primeval Forest (NE Poland)

Fig. 2. Bayesian inference tree based on fragment of sequences obtained from the small subunit rRNA gene (SSU rDNA) of Blastocystis isolates of the present study, performed using MrBayes 3.2.7a. The Bayesian posterior probabilities are shown adjacent to branch nodes.

Fig. 1. A–C in The first case of Spiroxys contortus in European pond turtle (Emys orbicularis) in the wild in Poland

Fig. 1. A–C Female of Spiroxys contortus (Gnathostomatidae) parasite of wild Emys orbicularis (European pond turtle) in Poland. A. Anterior region (a) median lobe with a tooth; (b) the lip with submedian papilla; (c) cuticular spine on the margin of the collar; B. Posterior region with a conical tip (arrow) C. Vulvar opening (arrow).

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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. 4 in First record of an infection by tissue cyst-forming coccidia in wild vizcachas (Lagostomus maximus, Rodentia) of Argentina

Fig. 4. Morphological structure of the cyst wall. Cortical brain photomicrograph shows a thin cyst wall (A). A detailed view shows that the cyst wall is made up of host-nucleated cells indicated by black arrowheads (B). In contrast, tissue cysts seen in organs other than the nervous system show a thicker cystic wall. Such is the case for those tissue cysts observed in the mammary (C–D), adrenal (E) and spleen (F) glands. The most notorious differential feature is the thick collagen outer layer in cysts outside the nervous system (white arrowheads). Bz: bradyzoites. A–B: Giemsa staining; C–D: Masson's trichrome staining. E–F: hematoxilin-eosin staining.