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Figure 3 in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran

Figure 3. Immatures of Hyalomma asiaticum collected from Meriones persicus in western Iran (nymphal stage): left: dorsal and right: ventral views.

Figure 5 in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran

Figure 5. Phylogenetic tree of Hyalomma asiaticum ticks inferred from ITS2 sequence data constructed using Bayesian Inference (BI) method. Nodes indicated with posterior probability values. Branch lengths are proportional to evolutionary changes (substitutions/site). Tree was rooted by Rhipicephalus sanguineus.

opencc-by-4.0Jul 2017View details →

Figure 2 in Infestation of Zebu cattle (Bos indicus Linnaeus) by hard ticks (Acari: Ixodidae) in Maiduguri, Northeastern Nigeria

Figure 2. Numbers of individual ticks of different species collected from different body parts of cattle.

Figure 1 in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran

Figure 1. Three rodent collection sites located in Lorestan province western Iran inlcuding: 1. Khorramabad-Kuhdasht road, Zamzam village; 2. Khorramabad-Tehran road, LUMS Campus; 3. Dorud-Azna road, Zarnan village.

Figure 2. A in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran

Figure 2. A rodent specimen infested by a number of immature ticks (red arrow) (animal is restrained through the ear by forceps and treated by insecticied for killing of ectoparasites).

opencc-by-4.0Oct 2021View details →

Figure 1. A in The Caspian red deer, Cervus elaphus maral (Mammalia: Cervidae): a new host record for Rhipicephalus (Boophilus) annulatus (Acari: Ixodidae) in northern Iran

Figure 1. A combined phylogenetic tree constructed using Bayesian Inference method based on ITS2/16S rRNA sequence data of Rhipicephalus (Boophilus) species in this study with sequences originated from various part of world retrieved from GenBank database. The main R. (B.) annulatus clade separated by a vertical double headed line. The taxa were defined with a name of species, country, GenBank accession number (taxon of the present study is bold). Posterior probability values inserted in the place of nodes. Branch lengths are proportional to the evolutionary changes. Rhipicephalus sanguineus assigned as outgroup taxon.

Figure 4 in Ornithodoros faccinii n. sp. (Acari: Ixodida: Argasidae) parasitizing the frog Thoropa miliaris (Amphibia: Anura: Cycloramphidae) in Brazil

Figure 4 Scanninc electron microscopy of nymphs of Ornithodoros faccinii n. sp. A. Idiosoma, dorsal view. B. Idiosoma, ventral view, showinc the preanal croove reachinc the sides of the body (white arrow). C. Genital primordium (white arrow) on the ventral idiosoma. D. Capitulum. E. Tarsi I and U-shaped capsule (white arrow), partially covered by a V-shaped membrane. Scale bars: A. 500 μm; B. 500 μm; C. 250 μm; D. 100 μm; E. 100 μm.

Figure 1 in Ornithodoros faccinii n. sp. (Acari: Ixodida: Argasidae) parasitizing the frog Thoropa miliaris (Amphibia: Anura: Cycloramphidae) in Brazil

Figure 1 Scanninc electron microscopy of idiosoma and capitulum of larvae of Ornithodoros faccinii n. sp. A. Idiosoma, dorsal view. B. Part of basis capituli and hypostome. C. Idiosoma, ventral view. D. Dorsal plate. E. Detail of ventral idiosoma, showinc the pair of setae VPL (ventral posterolateral) (black arrow). Scale bars: A. 500 μm; B. 50 μm; C. 500 μm; D. 100 μm; E. 250 μm.

Fig. 2 in Description of a new tick species, Ixodes collaris n. sp. (Acari: Ixodidae), from bats (Chiroptera: Hipposideridae, Rhinolophidae) in Vietnam

Fig. 2 Ventral idiosomal setae of a Ixodes collaris n. sp. (holotype) and b Ixodes vespertilionis in a similar state of encorcement. Note that I. collaris n. sp. has shorter setae anteriorly to the cenital aperture than posteriorly, whereas setae of I. vespertilionis are similar in lencth both anteriorly and posteriorly to the cenital aperture. I. collaris n. sp.: c perianal setae; d spiracular plate

Fig. 1 in Description of a new tick species, Ixodes collaris n. sp. (Acari: Ixodidae), from bats (Chiroptera: Hipposideridae, Rhinolophidae) in Vietnam

Fig. 1 Dorsal view of female of Ixodes collaris n. sp. a Holotype: posteriorly broad scutum (arrow), as contrasted to that of Ixodes vespertilionis female (b); c Basis capituli and palps of paratype No. 1. showinc convex loncitudinal flanks (arrow) enclosinc the porose areas, which are loncer than broad, as contrasted to those of I. vespertilionis female (d)

Fig. 5 in Description of a new tick species, Ixodes collaris n. sp. (Acari: Ixodidae), from bats (Chiroptera: Hipposideridae, Rhinolophidae) in Vietnam

Fig. 5 Drawincs of structures with diacnostic importance in the female (1) and nymph (2) of Ixodes collaris n. sp. Labels: 1.a and 2.a, capitulum dorsal view; 1.b and 2b, capitulum ventral view; 1.c and 2.c, coxae (downward: I-IV) with the collar overlayinc coxa I; 1.d and 2.d, scutum; 1.e, Haller's orcan

Figure 3 in Ornithodoros faccinii n. sp. (Acari: Ixodida: Argasidae) parasitizing the frog Thoropa miliaris (Amphibia: Anura: Cycloramphidae) in Brazil

Figure 3 Scanninc electron microscopy of cnatosoma and tarsus of larvae of Ornithodoros faccinii n. sp. A. Capitulum, ventral view. B. Details of capitulum showinc small spurs at the base of hypostome in the lateral position (black arrow). C. Detail of hypostome, palpi and chelicerae. D. Trochanter of palpi with 11 short spurs in the inner side, some of them are bifid (black arrow). E. Tibiotarsus of palpi. F. Hypostome with dental formula 3/3 in the anterior third, and then 2/2 posteriorly to the base. G. Tarsi I. Scale bars: A. 100 μm; B. 500 μm; C. 25 μm; D. 15 μm; E. 15 μm; F. 10 μm; G. 50 μm.

Fig. 4 in Description of a new tick species, Ixodes collaris n. sp. (Acari: Ixodidae), from bats (Chiroptera: Hipposideridae, Rhinolophidae) in Vietnam

Fig. 4 Nymphs of Ixodes collaris n. sp. (paratype No. 2) (a, b) and I. vespertilionis (c). a I. collaris n. sp., dorsal view. b I. collaris n. sp., cnathosoma, ventral view. Note semitransparent collars extendinc above the first coxae (arrows). c Gnathosoma of I. vespertilionis, ventral view

Fig. 3 in Description of a new tick species, Ixodes collaris n. sp. (Acari: Ixodidae), from bats (Chiroptera: Hipposideridae, Rhinolophidae) in Vietnam

Fig. 3 Ventral view of female a Ixodes vespertilionis and b Ixodes collaris n. sp. (holotype). a I. vespertilionis shows lateral flance on basis capituli (blue arrow) and a few, lonc coxal setae (especially on coxa III: white arrows). Note: V-shaped arrancement of some of these setae is due to reflection. b I. collaris n. sp. with ventral collar on basis capituli (yellow arrow) and multiple, short coxal setae (black arrows)

Figure 2 in Ornithodoros faccinii n. sp. (Acari: Ixodida: Argasidae) parasitizing the frog Thoropa miliaris (Amphibia: Anura: Cycloramphidae) in Brazil

Figure 2 Larvae of Ornithodoros faccinii n. sp. A. Chaetotaxy of dorsal idiosoma: DAL (dorsal anterolateral setae), DC (dorsal central setae), DPL (dorsal posterolateral setae). B. Chaetotaxy of ventral idiosoma: ST (sternal setae), CA (circumanal setae), VPL (ventral posterolateral setae). C. Chaetotaxy of tarsus I, A (anterior), DM (dorsomedian), PC (paracapsular), PM (posteromedian), B (basal), AV (anteroventral), MV (midventral), BV (basiventral), PL (posterolateral). D. Licht microcraph of tarsus I, capsule of Haller's orcan. Scale bars: A and B. 100 μm; C. 50 μm; D. 20 μm.

Figure 5 in Ornithodoros faccinii n. sp. (Acari: Ixodida: Argasidae) parasitizing the frog Thoropa miliaris (Amphibia: Anura: Cycloramphidae) in Brazil

Figure 5 Phylocenetic tree based on the 16S rDNA ticks. The alicnment was produced usinc Clustal X and the tree was inferred by means of the MP method with 500 replicates of random addition taxa. The species Ixodes holocyclus and Ixodes uriae were used as outcroup. The Bayesian support (posterior probability) values are derived from 1,000,000 replicates.

Fig. 9 in Description of the female, nymph and larva and mitochondrial genome, and redescription of the male of Ixodes barkeri Barker, 2019 (Acari: Ixodidae), from the short-beaked echidna, Tachyglossus aculeatus, with a consideration of the most suitable subgenus for this tick

Fig. 9 Mitochondrial genomes of Ixodes (Endopalpiger) australiensis, I. (Endo.) barkeri, I. (Endo.) woyliei and I. (Exopalpiger) fecialis. Protein-coding genes are shown in green, tRNAs are in yellow, rRNAs are in red, and the two control regions are in blue. Protein-coding genes are labelled by their four-character abbreviations, tRNAs are labelled by their one-letter amino acid abbreviations, and the two control regions are labelled as CR1 and CR2. Mitochondrial genome size variation is indicated in parentheses. The arrangement of genes in these four species is identical except that the main cluster of tRNA genes has the arrangement ARNSEF in the three species of Endopalpiger [I. (Endo.) australiensis, I. (End.) barkeri and I. (End.) woyliei], whereas in the one species of Exopalpiger [I. (Exo.) fecialis] the arrangement is ARNESF. The arrangement in I. (Exo.) fecialis is the first known arrangement in an Ixodidae tick that is different from ARNSEF.Thus, ARNESF might be a synapomorphy for the subgenus Exopalpiger

Fig. 7 Ixodes barkeri Barker, 2019 in Description of the female, nymph and larva and mitochondrial genome, and redescription of the male of Ixodes barkeri Barker, 2019 (Acari: Ixodidae), from the short-beaked echidna, Tachyglossus aculeatus, with a consideration of the most suitable subgenus for this tick

Fig. 7 Ixodes barkeri Barker, 2019, scanning electron micrographs of larva. A Scutum. B Gnathosoma, dorsal view. C Gnathosoma, ventral view. D Gnathosoma, anteroventral view. E Coxae. Scale bars: A, E 0.1 mm; B–D, 0.05 mm

Fig. 1 in Description of the female, nymph and larva and mitochondrial genome, and redescription of the male of Ixodes barkeri Barker, 2019 (Acari: Ixodidae), from the short-beaked echidna, Tachyglossus aculeatus, with a consideration of the most suitable subgenus for this tick

Fig. 1 The four known localities in Australia, Queensland (Qld), of Ixodes barkeri Barker, 2019, are indicated by white-with-red dots

Fig. 10 in Description of the female, nymph and larva and mitochondrial genome, and redescription of the male of Ixodes barkeri Barker, 2019 (Acari: Ixodidae), from the short-beaked echidna, Tachyglossus aculeatus, with a consideration of the most suitable subgenus for this tick

Fig. 10 Maximum likelihood (ML) phylogenetic tree from entire mt genomes (14,935 bps). The sequence alignment was put though Gblocks to remove regions with alignment gaps.Tip labels indicate NCBI accession numbers and (Barker & Barker Collection reference nos.). Numbers above branches show maximum likelihood bootstrap support, whereas numbers below branches show the Bayesian posterior probability support. Ixodes pavlovskyi Pomerantzev, 1946, one of the species "Other Ixodes" (sensu Barker & Murrell, 2004), for which an entire mitochondrial (mt) genome was available in GenBank, was set as the outgroup. The scale bar indicates 0.06 nucleotide substitutions per nucleotide site for the 14,935 nucleotide sites in our alignment of theses entire mt genomes. So, for example, there were about 896 nucleotide substitutions along the branch that leads to I. (Ceratixodes) uriae plus I. (Sternalixodes) holocyclus plus I. (Exopalpiger) fecialis, which is marked with an asterisk [i.e. 0.06 nucleotide substitutions per nucleotide site × 14,935 nucleotide sites (bps) = 1896 nucleotide substitutions]. Ticks in bold were sequenced in the present study