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Fig. 1 in Effects of introduced sika deer (Cervus nippon) and population control activity on the distribution of Haemaphysalis ticks in an island environment

Fig. 1. Map of Niijima Island, with locations of foot snare traps (black circle), and tick collection routes for the tick survey conducted June, August, and November of 2018 and February of 2019 (orange area). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Aug 2020View details →

Fig. 2 in Small-mammal characteristics affect tick communities in southwestern Tennessee (USA)

Fig. 2. Mean number of ticks per host by sex and age of rodent hosts (Peromyscus leucopus, Sigmodon hispidus, Peromyscus maniculatus, Microtus pinetorum, and Ochrotomys nuttalli) captured at Hobart Ames Plantation, Fayette and Hardeman counties, Tennessee.

opencc-by-4.0Aug 2020View details →

Fig. 1 in Small-mammal characteristics affect tick communities in southwestern Tennessee (USA)

Fig. 1. Number of ticks present on rodent hosts (Peromyscus leucopus, Sigmodon hispidus, Peromyscus maniculatus, Microtus pinetorum, and Ochrotomys nuttalli) captured at the Hobart Ames Plantation, Fayette and Hardeman counties, Tennessee. (a) Number of ticks by host sex x weight interaction (males y = 0.009x + 2.135; females y = 0.022x - 0.09). (b) Number of ticks by host age x weight interaction (adult y = 0.051x + 0.203; subadult = 0.310x - 3.499).

opencc-by-4.0Dec 2020View details →

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).

opencc-by-4.0Dec 2020View details →

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. 2b in Tick abundance and life-stage segregation on the American black bear (Ursus americanus)

Fig. 2b. Diagram of tick segregation on American black bears, based on 17 body regions surveyed on black bears from June 2018–December 2019 in Pennsylvania, USA. Darker colors indicate higher percentages of adult ticks and lower percentages of immature ticks observed and lighter colors indicate lower percentages of adult ticks and higher percentages of immature ticks observed; based on percentages of adult ticks out of all ticks recorded in that body region (table). Percentages based on bears that had at least one tick recorded in the surveyed body locations. Body region descriptors- A: ear; B: cheek; C: neck; D: upper spine; E: lower spine; F: chest; G: front outer leg; H: front inner leg; I: front axillary region; J: front inner toes; K: stomach; L: hip; M: hind outer leg; N: hind inner leg; O: hind axillary region; P: hind inner toes; Q: muzzle. (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 Tick abundance and life-stage segregation on the American black bear (Ursus americanus)

Fig. 3. Photograph of a bear with severe sarcoptic mange. Note the high loss of fur and thickened skin on the ears, face, and along the sides of the body and higher amounts of fur remaining along the spine and lower limbs. This pattern of hair loss and thickened crusting skin is typical for bears with moderate to severe cases of sarcoptic mange in Pennsylvania, with mild cases also frequently exhibiting higher hair loss and clinical signs of sarcoptic mange on the face and front regions of the body.

Fig. 2a in Tick abundance and life-stage segregation on the American black bear (Ursus americanus)

Fig. 2a. Diagram of tick abundance on American black bears, based on 17 body regions surveyed on black bears from June 2018–December 2019 in Pennsylvania, USA. Figure colors based on percentage of observed tick presence out of all observations of that body region (table), to represent where ticks were most frequently observed within the body regions surveyed. Darker colors indicate higher percentages of observations when ticks were present and lighter colors indicate lower percentages of observations that had ticks present in that body region. Body location descriptors- A: ear; B: cheek; C: neck; D: upper spine; E: lower spine; F: chest; G: front outer leg; H: front inner leg; I: front axillary region; J: front inner toes; K: stomach; L: hip; M: hind outer leg; N: hind inner leg; O: hind axillary region; P: hind inner toes; Q: muzzle. (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 Tick abundance and life-stage segregation on the American black bear (Ursus americanus)

Fig. 1. Map of capture locations for bears surveyed for tick burden in Pennsylvania from June 2018–December 2019.

Fig. 1 in Molecular screening of ticks of the genus Amblyomma (Acari: Ixodidae) infesting South African reptiles with comments on their potential to act as vectors for Hepatozoon fitzsimonsi (Dias, 1953) (Adeleorina: Hepatozoidae)

Fig. 1. Maximum likelihood analysis of Amblyomma tick species based on the 16S rRNA sequences. Bootstrap values at the major nodes are of percentage agreement among 1000 replicates. The branch scale represents substitutions per site.

Fig. 2 in Molecular screening of ticks of the genus Amblyomma (Acari: Ixodidae) infesting South African reptiles with comments on their potential to act as vectors for Hepatozoon fitzsimonsi (Dias, 1953) (Adeleorina: Hepatozoidae)

Fig. 2. Maximum likelihood analysis of species of Hepatozoon based on the 18S rRNA sequences. Bootstrap values at the major nodes are of percentage agreement among 1000 replicates. The branch scale represents substitutions per site.

Fig. 10 in Micropathogen community identification in ticks (Acari: Ixodidae) using third-generation sequencing

Fig. 10. Phylogenetic analysis of the isolated bacteria/viruses. Reference oligonucleotide sequences were selected by BLAST searches of the NCBI nt database. (A) Subtrees of the experimental sequences from the Borrelia burgdorferi 16S rRNA gene. (B) Subtrees of the experimental sequences from the Coxiella burnetii 16S rRNA gene. (C) Subtrees of the experimental sequences from the Anaplasma phagocytophilum MSP4 gene. (D) Subtrees of the experimental sequences from the Simian foamy virus pathogen. (E) Subtrees of the experimental sequences from the Crimean-Congo haemorrhagic fever orthonairovirus segment-S gene.

Fig. 7 in Micropathogen community identification in ticks (Acari: Ixodidae) using third-generation sequencing

Fig. 7. Population distribution of micropathogens in different samples. Note: "%" represents the proportion of micropathogen in the total community from each sample.

Fig. 3 in Micropathogen community identification in ticks (Acari: Ixodidae) using third-generation sequencing

Fig. 3. Venn diagram based on the eggNOG database. Note: The corresponding functional categories and non-supervised orthologous group (NOG) numbers were obtained from the eggNOG database.

Fig. 5 in Micropathogen community identification in ticks (Acari: Ixodidae) using third-generation sequencing

Fig. 5. Heat maps of community composition based on genera. Note: X-axis, template name; Y-axis, genus. The darker the blue colour is, the higher the enrichment of the genus in the sample.

Fig. 2 in Micropathogen community identification in ticks (Acari: Ixodidae) using third-generation sequencing

Fig. 2. Summary of the tag length distribution following the sequencing of genes from the four samples.

Fig. 9 in Micropathogen community identification in ticks (Acari: Ixodidae) using third-generation sequencing

Fig. 9. Pie chart of the distribution of viral abundances in different samples. Note: "%" represents the proportion of the virus in the total community from each sample, and the different colours represent different viruses. A: The primary micropathogens analysed in G1. B: The primary micropathogens analysed in G2. C: The main micropathogens analysed in G3. D: The main micropathogens analysed in G4.

Fig. 4 in Micropathogen community identification in ticks (Acari: Ixodidae) using third-generation sequencing

Fig. 4. Venn diagram based on the KEGG Orthology database. Note: DIAMOND was used to compare gene sequences with the KEGG database, and the corresponding metabolic pathway information and KEGG orthology results of the genes were obtained from the KEGG database.

Fig. 1 in Micropathogen community identification in ticks (Acari: Ixodidae) using third-generation sequencing

Fig. 1. The genomic DNA library was generated according to the PacBio Sequel sample preparation instructions.