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opencc-by-4.0Aug 2016View details →

Fig. 1 in Molecular characterization of trypanosomatid infections in wild howler monkeys (Alouatta caraya) in northeastern Argentina

Fig. 1. Location of study areas in Northeastern Argentina: San Cayetano (SC), Estacíon Bioĺogica Corrientes (EBCo), Isla Brasilera (IB) and Isla del Cerrito (IC).

opencc-by-4.0Aug 2016View details →

Fig. 3 in Molecular characterization of trypanosomatid infections in wild howler monkeys (Alouatta caraya) in northeastern Argentina

Fig. 3. Size variation of amplified kDNA fragments revealed by electrophoresis and ethidium bromide staining. Samples are indicated by their ID numbers. Reference strains used as positive controls: TR1 and TR2: T. rangeli, k98: T. cruzi I, ClBr: T. cruzi VI (Cl Brener). M: 1 kb DNA molecular ladder. Fragment size is indicated in base pairs.

Fig. 3 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 3. Single nucleotide polymorphisms in the ND2 gene of B. columnaris, compared to B. procyonis. Nucleotide position numbers are shown at the top of the figure. Speciesspecific SNPs are shown in bold.

Fig. 1 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 1. Single nucleotide polymorphisms in the Cox1 gene of B. columnaris, compared to B. procyonis. Nucleotide position numbers are shown at the top of the figure. Italicized numbers represent the position number from a previously published partial sequence of the B. columnaris Cox1 gene (Franssen et al., 2013). Species-specific SNPs are shown in bold.

Fig. 2 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 2. Single nucleotide polymorphisms in the Cox2 gene of B. columnaris, compared to B. procyonis. Nucleotide position numbers are shown at the top of the figure. Italicized numbers represent the position number from a previously published partial sequence of the B. columnaris Cox2 gene (Franssen et al., 2013).

Fig. 4 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 4. Single nucleotide polymorphisms in several tRNA genes of B. columnaris, compared to B. procyonis, B. transfuga and B. schroederi. Nucleotide position numbers are shown at the top of the figure. SNPs which distinguish B. columnaris from other Baylisascaris species are shown in bold.

Fig. 4 in Molecular characterization of Babesia peircei and Babesia ugwidiensis provides insight into the evolution and host specificity of avian piroplasmids

Fig. 4. Geographic distribution of the phylogenetic groups of avian piroplasmids (based on the 18S rRNA gene). Map prepared based on information provided in Criado et al. (2006), Yabsley et al. (2006, 2009), Jefferies et al. (2008), Paparini et al. (2014), Quillfeldt et al. (2014), Martínez et al. (2015), Montero et al. (2016) and Chavatte et al. (2017).

Fig. 4 in Molecular identification and characterization of partial COX1 gene from caecal worm (Aulonocephalus pennula) in Northern bobwhite (Colinus virginianus) from the Rolling Plains Ecoregion of Texas

Fig. 4. Molecular Phylogenetic analysis by Maximum Likelihood method. The evolutionary history was inferred using the ML method based on the General Time Reversible model. The phylogenetic tree illustrates COX1 gene sequences of nematodes related to A. pennula. Bootstrap values above 50 are shown in the tree. The tree is drawn to scale, with branch lengths measured in the number of substitutions-per-site. All positions containing gaps and missing data were eliminated. Evolutionary analyses were conducted in MEGA7.

Fig. 1. A in Molecular identification and characterization of partial COX1 gene from caecal worm (Aulonocephalus pennula) in Northern bobwhite (Colinus virginianus) from the Rolling Plains Ecoregion of Texas

Fig. 1. A. Caecum of the wild quail B. Morphology of male and female caecal worm. All the parts of male and female caecal worm Aulonocephalus pennula are marked in Fig. 1B.

Fig. 3 in Molecular identification and characterization of partial COX1 gene from caecal worm (Aulonocephalus pennula) in Northern bobwhite (Colinus virginianus) from the Rolling Plains Ecoregion of Texas

Fig. 3. Pairwise alignment of the sequences of A. pennula and H. gallinarum. Sequence variations between A. pennula and H. gallinarum are highlighted in red. (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 Molecular characterization of Babesia peircei and Babesia ugwidiensis provides insight into the evolution and host specificity of avian piroplasmids

Fig. 2. Maximum likelihood phylogenetic tree of the ITS-1 (445 bp) and ITS-2 regions sequences (290 bp) of select avian-infecting Babesia lineages. Sequences identified in this study are emphasized in red, and those of other avian-infecting lineages are shown in blue. For each sequence, the following information is provided: morphospecies (individual identification or Genbank code) host species. Branch lengths are drawn proportionally to evolutionary distance (scale bar shown corresponds to both trees). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Fig. 2. A in Molecular identification and characterization of partial COX1 gene from caecal worm (Aulonocephalus pennula) in Northern bobwhite (Colinus virginianus) from the Rolling Plains Ecoregion of Texas

Fig. 2. A. PCR amplification of COX1 gene using nematode primers. Lane M: 100 bp DNA ladder (Fermentas); lane 1‾4 COX1 gene amplicon (750 bp). B. PCR amplification of partial COX1 gene using gene specific primers. Lane M: 100 bp DNA Marker (Fermentas); lane 1‾4 partial COX1 amplified products (405bp).

Fig. 3 in Molecular characterization of Babesia peircei and Babesia ugwidiensis provides insight into the evolution and host specificity of avian piroplasmids

Fig. 3. Distribution of the phylogenetic groups of avian piroplasmids (based on the 18S rRNA gene) in relation to the phylogeny of avian orders (based on multiple nuclear genes). Avian orders investigated in this study are shown in red, and other avian orders known to host piroplasmids are shown in blue. Avian phylogeny was adapted from Yuri et al. (2013). (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 Molecular characterization of Babesia peircei and Babesia ugwidiensis provides insight into the evolution and host specificity of avian piroplasmids

Fig. 1. Maximum likelihood phylogenetic tree of the 18S rRNA gene sequences (1450 bp) of the studied Babesia lineages. Sequences obtained in this study are emphasized in red, and those of other avian-infecting lineages are shown in blue. For each sequence, the following information is provided: morphospecies (individual identification or GenBank code) host species. For avian-infecting lineages, the host order is indicated with colored circles (see legend). Branch lengths are drawn proportionally to evolutionary distance. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

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Рис. 6. МоΔеΛирование экоΛогических ниш коΛораΔского жука ΔΛя ΔаΛьневосточного, европейского и североамериканского ареаΛов метоΔом метрического Δвухмерного шкаΛирования с применением коэффициента Жаккара Fig. 6. Models of ecological niches of the Colorado potato beetle for the Far Eastern, European, and North-American habitats (metric multidimensional scaling, Jaccard index) in Comparative characterization of the ecology of native (Henosepilachna vigintioctomaculata) and invasive (Leptinoatrsa decemlineata) species under the conditions of the monsoon climate in the southern part of the Russian Far East

Рис. 6. МоΔеΛирование экоΛогических ниш коΛораΔского жука ΔΛя ΔаΛьневосточного, европейского и североамериканского ареаΛов метоΔом метрического Δвухмерного шкаΛирования с применением коэффициента Жаккара Fig. 6. Models of ecological niches of the Colorado potato beetle for the Far Eastern, European, and North-American habitats (metric multidimensional scaling, Jaccard index)

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Рис. 1. ЗасеΛенность посаΔок картофеΛя коΛораΔским жуком в Приморском крае (2008-2011 гг.) (по: Мацишина, Рогатных 2013) Примечание. БаΛΛ поврежΔения привеΔен по 6-баΛΛьной шкаΛе ВИЗР (Шапиро и Δр., 1980; 1993) in Comparative characterization of the ecology of native (Henosepilachna vigintioctomaculata) and invasive (Leptinoatrsa decemlineata) species under the conditions of the monsoon climate in the southern part of the Russian Far East

Рис. 1. ЗасеΛенность посаΔок картофеΛя коΛораΔским жуком в Приморском крае (2008-2011 гг.) (по: Мацишина, Рогатных 2013) Примечание. БаΛΛ поврежΔения привеΔен по 6-баΛΛьной шкаΛе ВИЗР (Шапиро и Δр., 1980; 1993)

opencc-by-4.0Dec 2012View details →

Fig. 1 in Prevalence survey and first molecular characterization of Echinococcus granulosus in France

Fig. 1 Origin of the hydatid cysts samples. In grey are the department surveyed. The numbers of cattle or sheep indicate the number and breeding species of infected animals by E. granulosus in each department

opencc-by-4.0Jun 2022View details →

Fig. 4 in Characterization of tongue worms, Linguatula spp. (Pentastomida) in Romania, with the first record of an unknown adult Linguatula from roe deer (Capreolus capreolus Linnaeus)

Fig. 4 Light and scanning electron microscopy images of male specimens of Linguatula sp. collected from Capreolus capreolus. A SEM of posterior hook (SPL1165-2), with sensory papillae #3. B Anterior hook with fulcrum (SPL1165-2). Scale bar = 100 µm. C Posterior hook with fulcrum (SPL1165-2). Scale bar = 100 µm. D Posterior hook opening "pit" (SPL1165-2), showing fine spines on cuticle (arrow). Scale bar = 10 µm. E Anterior hook base with fine spines (arrow) (SPL1165-2). Scale bar = 25 µm. F Buccal capsule (SPL1156-1). Scale bar = 100 µm. G SEM of male genital aperture with sensory papillae #4 on lateral edges (SPL1165-3). H SEM of tip of copulatory spicule emerging from male genital aperture (SPL1165- 2). I Dissected copulatory spicule (SPL1165-1). Scale bar = 100 µm

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Fig. 1 in Characterization of tongue worms, Linguatula spp. (Pentastomida) in Romania, with the first record of an unknown adult Linguatula from roe deer (Capreolus capreolus Linnaeus)

Fig. 1 Map of the collection locations for the pentastomes examined in this study. Locations are indicated by red (collected from Canis lupus), yellow (collected from Canis aureus), and blue (collected from Capreolus capreolus) markers. The number within the marker refers to the specimen listed in Table 1