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Fig. 1 in Morphological and molecular identification of Cryptocotyle lingua metacercariae isolated from Atlantic cod (Gadus morhua) from Danish seas and whiting (Merlangius merlangus) from the English Channel

Fig. 1 Infected Atlantic cod (Gadus morhua) (a) and microscope observation of encysted metacercariae in caudal fin (b)

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Figure 2 in Molecular identification of Trichinella species by multiplex PCR: new insight for Trichinella murrelli

Figure 2. Electrophoretic profiles of Trichinella murrelli uniplex PCR amplifications.DNA from T. murrelli (isolate code ISS35) reference larvae was used. Lane L = 50 bp ladder. The genes targeted were the Expansion Segment V (ESV, lane 1), Internal Transcribed Spacer 1 II (ITS1 II, Lane 2), ITS1 III (lane 3), ITS2 IV (lane 4), and ITS2 V (lane 5).

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Figure 3 in Molecular identification of Trichinella species by multiplex PCR: new insight for Trichinella murrelli

Figure 3. Alignment of the 256 bp fragment of ITS1 II of Trichinella murrelli obtained by uniplex PCR.BLAST analysis revealed 99.6% identity with different clones of T. murrelli, including clone 5 (Accession number KC006421).

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Figure 1 in Molecular identification of Trichinella species by multiplex PCR: new insight for Trichinella murrelli

Figure 1. Electrophoretic profiles of Trichinella murrelli and T. britovi larva amplicons after multiplex PCR amplification.DNA extracts from 1 and 10 larvae of T. murrelli (isolate code ISS35) in lane 1 and lanes 2–4, respectively; and of T. britovi (isolate code ISS235) larva in lane 5. Lane L1 = 100 bp ladder.

Figure 10 in Morphological and molecular identification of Cladosporium sphaerospermum isolates collected from tomato plant residues

Figure 10. Nucleotide sequence alignment of the ITS (ITS1, 5.8S rDNA and ITS4) region of the C. sphaerospermum isolate 10 and the other isolates already recorded in NCBI.

Figure 8 in Morphological and molecular identification of Cladosporium sphaerospermum isolates collected from tomato plant residues

Figure 8. Nucleotide sequence alignment of the ITS (ITS1, 5.8S rDNA and ITS4) region of the C. sphaerospermum isolate 9 and the other isolates already recorded in NCBI.

Figure 5. A phylogenetic tree was generated using the neighbor-joining method which shows the genetic relationship between C. sphaerospermum 2 in Morphological and molecular identification of Cladosporium sphaerospermum isolates collected from tomato plant residues

Figure 5. A phylogenetic tree was generated using the neighbor-joining method which shows the genetic relationship between C. sphaerospermum 2 (as indicated in red circle) and the other C. sphaerospermum isolates deposited in GenBank (NCBI)

Figure 3. A in Morphological and molecular identification of Cladosporium sphaerospermum isolates collected from tomato plant residues

Figure 3. A phylogenetic tree constructed by the neighbor-joining method depending on a comparison of the nucleotide sequences obtained from the C. sphaerospermum isolates (1-13).

Figure 2 in Morphological and molecular identification of Cladosporium sphaerospermum isolates collected from tomato plant residues

Figure 2. The similarity and difference in the nucleotide sequences of the C. sphaerospermum isolates (1-13) identified in the present study. Similar nucleotides are stated in dots. Numbers given on the right side of the figure represent the nucleotide sequences obtained from the C. sphaerospermum isolates.

Figure 1. 1 in Morphological and molecular identification of Cladosporium sphaerospermum isolates collected from tomato plant residues

Figure 1. 1% Agarose gel electrophoresis of PCR products amplified using the primer pair ITS1 and ITS4 from the C. sphaerospermum isolates (1-13) obtained from tomato plant residues collected from different regions of Najaf and Karbala provinces. M: 1Kbp DNA Ladder (Promega, USA).

Fig. 6 in Morphological and molecular identification of cyathostomine gastrointestinal nematodes of Murshidia and Quilonia species from Asian elephants in Myanmar

Fig. 6. Molecular phylogenetic analysis of COI gene sequences of cyathostomine species using the maximum likelihood method in MEGA7. The percentage of trees in which associated taxa clustered together is shown next to the branches. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. GenBank accession numbers are indicated alongside taxa name.

Fig. 5 in Morphological and molecular identification of cyathostomine gastrointestinal nematodes of Murshidia and Quilonia species from Asian elephants in Myanmar

Fig. 5. Photomicrographs of Quilonia travancra. A, anterior end of a male, showing head papillae (arrows) and mouth collars (*); B, head of a male, showing crown leaflets (arrow); C, bursa of a male, lateral view, showing two branches (arrows) and three sub-branches of the posterior branch at approximately the same length (*); D, posterior branch of dorsal ray of bursa of a male, showing an appearance of trifurcation although the median and internal sub-branches are fused (*).

Fig. 2 in Morphological and molecular identification of cyathostomine gastrointestinal nematodes of Murshidia and Quilonia species from Asian elephants in Myanmar

Fig. 2. Photomicrographs of Murshidia indica. A, anterior end of a male, showing the appearance of plumose sculpturing on anterior portion of oesophagus (arrows); B, head of a male, showing coronal leaflets (*); C, copulatory bursa and spicules (arrow) of a male; D, dorsal ray of bursa of a male, showing two branches (arrows), in which the posterior branch has a pointed extremity (*).

Fig. 4 in Morphological and molecular identification of cyathostomine gastrointestinal nematodes of Murshidia and Quilonia species from Asian elephants in Myanmar

Fig. 4. Photomicrographs of Quilonia renniei. A, anterior end of a female, showing cylindrical shape of oesophagus (arrow); B, head of a female, showing a small buccal capsule (arrow) and curved coronal leaflets project above head (*); C, posterior end of a female; D, dorsal ray of bursa of a male, showing two branches (arrows), in which the posterior branch divided two sub-branches and the inner sub-branch is slightly bifid at the extremity (*).

Fig. 3 in Morphological and molecular identification of cyathostomine gastrointestinal nematodes of Murshidia and Quilonia species from Asian elephants in Myanmar

Fig. 3. Photomicrographs of Murshidia neveulemairei. A, anterior end of a female, showing the appearance of plumose sculpturing on anterior portion of oesophagus (arrows); B, posterior extremity of a female, showing anus (arrow) and vulva (*); C, dorsal ray of bursa of a male, showing two branches (arrows), in which the anterior branch is bifurcated in the distal half (*).

Fig. 1 in Morphological and molecular identification of cyathostomine gastrointestinal nematodes of Murshidia and Quilonia species from Asian elephants in Myanmar

Fig. 1. Photomicrographs of Murshidia falcifera. A, anterior end of a female, showing the appearance of two lateral lips of mouth collar with prominent head papillae (arrows) and coronal leaflets (*); B, head of a male, showing cuticular lining of buccal capsule (arrows) and funnel-shaped throat (*); C, dorsal ray of bursa of a male, showing three branches, in which anterior branch is composed of two sub-branches (arrows) and the posterior one is longer (*); D, posterior end of a female, showing anus (arrow).

Fig. 4 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 4. Vizcainocypria viator gen. nov. sp. nov., male (MUVHNZY0011). A: A2. B: Right prehensile palp. C: Left prehensile palp. D: Hemipenis. E: Zenker organ. Scale bars: A–E = 50 µm.

Fig. 2 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 2. Vizcainocypria viator gen. nov. sp. nov., female (MUVHNZY0012). A: A1 (arrow pointing to apical claw on penultimate segment). B: A2. C: Md coxa. D: Md palp. E: Detail of α and β setae. F: Mxl. Scale bars: A–F = 50 µm.

Fig. 3 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 3. Vizcainocypria viator gen. nov. sp. nov., female (MUVHNZY0012). A: T1. B: T2. C: T3. D: CR. E: Caudal attachment. Scale bars: A–E = 50 µm.

Fig. 6 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 6. Male copulatory organs (hemipenes) of different species of Cyclocyprididae. A: Cyclocypris, B: Cypria, C: Physocypria, D: Dentocypria, E: Keysercypria, F: Brasilocypria, G: Claudecypria, H: Vizcainocypria. Redrawn from Almeida et al. (2023): F, G; Karanovic (2011): C (P. bullata), E; Hartmann (1959): H (V. granadae); Meisch (2000): A, B (C. exsculpta, C. ophtalmica), C (P. kraepelini); Savatenalinton (2017): D; Smith and Janz (2008): B (C. matzkeae), C (P. nipponica, P. biwaensis); Wouters (1984): B (C. subsalsa). Scale bars are shown when available: D. smithi = 46 µm; C. ovum, C. ophtalmica, C. subsalsa, P. nipponica, P. biwaensis, D. mesquitai, B. pea, B. alisonae, C. mesquitai, C. rochei, V. viator = 50 µm; C. matzkeae, P. bullata, K. affinis, K. deformis = 100 µm.