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Figure 5 in Relative tolerance of some tropical freshwater microcrustaceans to acidification

Figure 5. (a) Relative survival of 3 test species exposed to H O+ additions after 3 24 h; (b) dose–response curve of species against pH at 24 h.

Figure 1 in Relative tolerance of some tropical freshwater microcrustaceans to acidification

Figure 1. Annual occurrence of 3 species (numbers per milliliter) in freshwater wetlands of Midnapore during 2010 (M = Moina sp., H = Heliodiaptomus sp., and D = Daphnia sp.).

Figure 4 in Relative tolerance of some tropical freshwater microcrustaceans to acidification

Figure 4. (a) Relative survival in 3 test species exposed to H O+ additions after 1 h; 3 (b) dose–response curve of species against pH at 1 h (D = D. lumholtzi, M = adult M. brachiata, H = H. viduus).

Figure 7 in Gammarus baysali sp. nov., a new freshwater amphipod species from Turkey (Amphipoda: Gammaridae)

Figure 7. Gammarus baysali sp. nov. Allotype female: A) pereopod 5; B) pereopod 7; C) pereopod 6; D) antenna 1; E) telson; F) uropod 3; G) uropod 2; H) uropod 1; I) pereopod 5; J) uropod 3; K) telson; L) pereopod 7; M) pereopod 6.

Figure 5 in Gammarus baysali sp. nov., a new freshwater amphipod species from Turkey (Amphipoda: Gammaridae)

Figure 5. Gammarus baysali sp. nov. Holotype male: A) pereopod 5; B) pereopod 6; C) pereopod 7; D) pereopod 3; E) pereopod 4; F) epimeral plates.

Figure 4 in Gammarus baysali sp. nov., a new freshwater amphipod species from Turkey (Amphipoda: Gammaridae)

Figure 4. Gammarus baysali sp. nov. Holotype male: A) uropod 2; B) uropod 1; C) antenna 2; D) gnathopod 1 (inner view); D') detail of gnathopod 1 (outer view); E) gnathopod 2 (inner view); E') detail of gnathopod 2 (outer view); F) antenna 1; F') accessory flagellum; G) uropod 3; G') tip of uropod 3.

Fig. 6. Batrachocamallanus xenopodis, photomicrographs. A in Novel information on the morphology, phylogeny and distribution of camallanid nematodes from marine and freshwater hosts in South Africa, including the description of Camallanus sodwanaensis n. sp.

Fig. 6. Batrachocamallanus xenopodis, photomicrographs. A – male, general view; B – anterior part of body, male, apical view; C – optical section at base of buccal capsule level, male, apical view; D – buccal capsule, female, lateral view; E – female, general view; F – posterior part of body, male, lateral view; G – part of body at vulva region, lateral view; H – posterior part of body, female, lateral view. Scale bars: A, E, F–H – 100, B–D – 50.

Fig. 8 in Novel information on the morphology, phylogeny and distribution of camallanid nematodes from marine and freshwater hosts in South Africa, including the description of Camallanus sodwanaensis n. sp.

Fig. 8. Phylogenetic tree of Camallanidae nematodes based on 491 nucleotides long alignments of 28 rDNA gene. Nodal support presented for Bayesian Inference and Maximum Likelihood analyses (BI/ML).

Fig. 3. Paracamallanus cyathopgharynx, photomicrographs. A in Novel information on the morphology, phylogeny and distribution of camallanid nematodes from marine and freshwater hosts in South Africa, including the description of Camallanus sodwanaensis n. sp.

Fig. 3. Paracamallanus cyathopgharynx, photomicrographs. A – anterior part of body, male, lateral view; B – buccal capsule, male, lateral view; C – anterior part of body, male, apical view; D – female, general view; E - optical section at level of buccal capsule valves mid-length, male, dorsal view; F - part of body at vulva region, lateral view; G – posterior end of body, female, lateral view; H – posterior end of body, male, lateral view. Scale bars: A–C, E–H – 100; D – 1 mm.

Fig. 1. Camallanus sodwanaensis n in Novel information on the morphology, phylogeny and distribution of camallanid nematodes from marine and freshwater hosts in South Africa, including the description of Camallanus sodwanaensis n. sp.

Fig. 1. Camallanus sodwanaensis n. sp., line-drawings. A – anterior part of body, female, lateral view; B – buccal capsule, female, lateral view; C – anterior part of body, female, apical view; D – posterior part of body, male, ventral view; E – dorsal trident, male, lateral view; F – posterior part of body, female, lateral view; G – spicules, lateral view. Scale bars: A – 500; B–D, F–G – 100; E – 50.

Fig. 2. Camallanus sodwanaensis n in Novel information on the morphology, phylogeny and distribution of camallanid nematodes from marine and freshwater hosts in South Africa, including the description of Camallanus sodwanaensis n. sp.

Fig. 2. Camallanus sodwanaensis n. sp., photomicrographs. A – male, general view; B – anterior part of body, female, lateral view; C – buccal capsule, female, lateral view; D – optical section at level of buccal capsule valves mid-width, male, dorsal view; E – dorsal trident, male, dorsal view; F – anterior part of body, female, apical view; G - optical section at level of buccal capsule valves mid-length, male, apical view; H – right spicule, lateral view; I – posterior end of body, male, ventral view; J – part of body at vulva region, lateral view; K – posterior end of body, female, lateral view. Scale bars: A – 1 mm, B – 500, C–K – 100.

Fig. 12 in Pathobiology and first report of larval nematodes (Ascaridomorpha sp.) infecting freshwater mussels (Villosa nebulosa, Unionidae), including an inventory of nematode infections in freshwater and marine bivalves

Fig. 12. Second-stage larva of Ascaridomorpha sp. (Nematoda) infecting Villosa nebulosa, in lateral view. Posterior end of body showing anus (a), rectal glands (rg).

Fig. 7 in Pathobiology and first report of larval nematodes (Ascaridomorpha sp.) infecting freshwater mussels (Villosa nebulosa, Unionidae), including an inventory of nematode infections in freshwater and marine bivalves

Fig. 7. Uninfected intestine of Villosa nebulosa showing ciliated columnar epithelium (ce), and connective tissue (ct).

Fig. 2 in Pathobiology and first report of larval nematodes (Ascaridomorpha sp.) infecting freshwater mussels (Villosa nebulosa, Unionidae), including an inventory of nematode infections in freshwater and marine bivalves

Fig. 2. Ventral portion of infected foot of Villosa nebulosa showing a nematode infection (ne), myofibers (mf), basophilic granulocytes (bg), and pedal epithelium (pe).

Fig. 10 in Pathobiology and first report of larval nematodes (Ascaridomorpha sp.) infecting freshwater mussels (Villosa nebulosa, Unionidae), including an inventory of nematode infections in freshwater and marine bivalves

Fig. 10. Second-stage larva of Ascaridomorpha sp. (Nematoda) infecting Villosa nebulosa, in lateral view. Anterior end of body showing lips (l), pharynx (p), and esophagus (es).

Fig. 1 in Pathobiology and first report of larval nematodes (Ascaridomorpha sp.) infecting freshwater mussels (Villosa nebulosa, Unionidae), including an inventory of nematode infections in freshwater and marine bivalves

Fig. 1. Ventral portion of an uninfected foot of Villosa nebulosa showing myofibers (mf), basophilic granulocytes (bg), and pedal epithelium (pe).

Fig. 13 in Pathobiology and first report of larval nematodes (Ascaridomorpha sp.) infecting freshwater mussels (Villosa nebulosa, Unionidae), including an inventory of nematode infections in freshwater and marine bivalves

Fig. 13. Phylogenetic interrelationships of nematodes (Cosmocercoidea, Seuratoidea) based on sequences of the 18S rDNA, generated from Bayesian inference. Nodal supports were estimated by Bayesian posterior probability (BPP) after running the Markov chain Monte Carlo (2 runs 4 chains, 4 × 106 generations, sampling frequency = 4 × 103, burn-in = 1 × 106). Sequence obtained in the present study is in bold.

Figure 2 in Two freshwater flagellates from the Mahananda Wildlife Sanctuary, West Bengal

Figure 2. Photomicrographs of Entosiphon sulcatum from live (A-C) and silver stained preparations (D-F). A-C. Slightly pressed specimen due to cover slip pressure, showing the body shape, cytoplasmic crystals, lipid droplets, granules on the surface, food vacuoles and vacuole. Arrows point to the flagella. Note the protruding feeding organelles D-F. Specimens showing the body size variation, differences in the flagella length, and nucleus position. The irregular nucleolus and base of the flagellum is visible in the stained preparations. C, crystals; F1,2, flagellum 1, 2; FB, flagella base; FO, feeding organelle; FV, food vacuoles; G, granules; L, lipid droplet; N, nucleus; Nu, nucleolus; V, vacuole. Scale bars, 10 μm.

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Figure 2 in DNA barcoding of freshwater fish from different drainage systems of Telangana in Southern India

Figure 2. Neighbour-joining phylogeny of the studied fish species depicting distinctive species clades corresponding to the morphospecies. Scale bar corresponds to the length of clade from each node.