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956 results for “Cichlidae”
Fig. 27 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 27. Haplochromis falcatus sp. nov. a. Photograph of preserved holotype (RMCA 2018.008.P.0401; 101.3 mm SL). b. X-ray image of holotype. c–d. Photographs of freshly caught specimens. c. Dominant male (RMCA 2017.006.P.0416; 119.1 mm SL). d. Female (RMCA 2016.035.P.0257; 112.8 mm SL) to illustrate the live colour patterns. The contrast was slightly enhanced.
Fig. 2. a in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 2. a. Differences in total number of outer teeth and premaxillary dentition between the macro- and microdontic groups of piscivores from the Lake Edward system. b. Schematic presentation of the dominant male colour patterns in life, in the various groups studied. For H. sp. 'latifrons' the female and for H. sp. 'curvidens' the non-dominant colour patterns are shown, as those of dominant males are unknown.
Fig. 28 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 28. Haplochromis falcatus sp. nov. (RMCA 2018.008.P.0397; 103.3 mm SL). a. Dorsal view of the lower pharyngeal jaw. b. Lateral view of the lower pharyngeal jaw.
Fig. 6 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 6. Haplochromis latifrons sp. nov. a. Photograph of preserved holotype (RMCA 2018.008.P.0330; 158.2 mm SL). b. X-ray image of holotype. c–d. Photographs of freshly caught specimens. c. Holotype. d. Another female (RMCA 2017.006.P.0340; 105.4 mm SL) to illustrate the live colour patterns. The contrast was slightly enhanced.
Fig. 8. Haplochromis mentatus Regan, 1925 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 8. Haplochromis mentatus Regan, 1925, holotype, ♀, 93.1 mm SL (MCZ 31523) reconstructed with a straightened vertebral column. Drawn by N. Vranken.
Fig. 18 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 18. Haplochromis glaucus sp. nov. a. Photograph of preserved holotype (RMCA 2019.002.P.0016; 106.2 mm SL). b. X-ray image of holotype c–d. Photographs of freshly caught specimens. c. Dominant male, the holotype. d. Female (RMCA 2019.002.P.0017; 102.1 mm SL) to illustrate the live colour patterns. The contrast was slightly enhanced.
Fig. 30 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 30. Haplochromis curvidens sp. nov. a. Photograph of preserved holotype (RMCA 2016.035.P.0219; 112.0 mm SL). b. X-ray image of holotype. c–d. Photographs of freshly caught specimens. c. Holotype, an adult male. d. Female (RMCA 2018.008.P.0340); 90.2 mm SL) to illustrate the live colour patterns. The contrast was slightly enhanced.
Fig. 19 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 19. Haplochromis glaucus sp. nov. (RMCA 2019.002.P.0020; 110.9 mm SL). a. Dorsal view of the lower pharyngeal jaw. b. Lateral view of the lower pharyngeal jaw.
Fig. 31 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 31. Haplochromis curvidens sp. nov. (RMCA 2016.035.P.0217; 102.5 mm SL). a. Dorsal view of the lower pharyngeal jaw. b. Lateral view of the lower pharyngeal jaw.
Figure 10 in Parasites of Moroccan desert Coptodon guineensis (Pisces, Cichlidae): transition and resilience in a simplified hypersaline ecosystem
Figure 10. Abundance of infection of Coptodon guineensis at Sebkha Imlili by acanthocephalan Acanthogyrus (Acanthosentis) cf. tilapiae according to fish total length. Infection occurred in fish as small as 20 mm. Larger fish were more often infected than smaller fish.
Figure 5 in Parasites of Moroccan desert Coptodon guineensis (Pisces, Cichlidae): transition and resilience in a simplified hypersaline ecosystem
Figure 5. Unidentified metacercariae from Coptodon guineensis at Sebkha Imlili. A. Metacercaria (arrow) showing ocelli and associated with intense granulocytic reaction in intestinal mucosa. B. Fresh squash of spleen showing numerous metacercariae.
Figure 4 in Parasites of Moroccan desert Coptodon guineensis (Pisces, Cichlidae): transition and resilience in a simplified hypersaline ecosystem
Figure 4. Metacercariae of heterophyid Pygidiopsis genata from Coptodon guineensis at Sebkha Imlili. A. Numerous metacercariae encysted on the outer wall of stomach. B & C. Fresh squashes of infected tissues with clusters of live metacercariae. D. SEM of excysted metacercariae showing a pyriform scaled body with terminal oral sucker (arrow) and subequatorial acetabulum (arrowhead). E. Oral sucker unarmed. F. small ventral sucker. Insert: pectinate body scales.
Figure 6 in Parasites of Moroccan desert Coptodon guineensis (Pisces, Cichlidae): transition and resilience in a simplified hypersaline ecosystem
Figure 6. Prevalence of infection (%) of Coptodon guineensis at Sebkha Imlili. Blue bars = acanthocephalan Acanthogyrus (Acanthosentis) cf. tilapiae (December 2018: n = 93; April 2019: n = 80; July 2019: n = 92; October 2019: n = 57); Orange bars = metacercariae of Pygidiopsis genata (Dec 2018: n = 92; April 2019: n = 80; July 2019: n = 39; October 2019: n = 53); Grey bars = unidentified metacercariae (December 2018: n = 92; April 2019: n = 80; July 2019: n = 25; October 2019: n = 35).
Figure 2 in Parasites of Moroccan desert Coptodon guineensis (Pisces, Cichlidae): transition and resilience in a simplified hypersaline ecosystem
Figure 2. Acanthocephalan Acanthogyrus (Acanthosentis) cf. tilapiae from Coptodon guineensis at Sebkha Imlili. Fresh preparations. A. Female worm (gravid). B. Male worm. C. Ellipsoid eggs in gravid female. D. Proboscis and anterior trunk (montage) of male worm. Note strong anterior hooks and abruptly smaller middle and posterior hooks as well as regular rows of spines that were lost and leave rosette marks on tegument. E. Posterior end of male worm showing terminal genital opening and everted copulatory bursa. F. Posterior end of female showing terminal genital opening.
Figure 9 in Parasites of Moroccan desert Coptodon guineensis (Pisces, Cichlidae): transition and resilience in a simplified hypersaline ecosystem
Figure 9. Mean trunk length of females of acanthocephalan Acanthogyrus (Acanthosentis) cf. tilapiae in Coptodon guineensis at Sebkha Imlili (December 2018: n = 41; April 2019: n = 42; July 2019: n = 47; October 2019: n = 50). Worms were significantly smaller in April and October compared to December and July.
Figure 8 in Parasites of Moroccan desert Coptodon guineensis (Pisces, Cichlidae): transition and resilience in a simplified hypersaline ecosystem
Figure 8. Proportions of females of acanthocephalan Acanthogyrus (Acanthosentis) cf. tilapiae in Coptodon guineensis at Sebkha Imlili according to stage of maturity. Solid bars = immature females (no genitalia visible); dotted bars = ovigerous females (ovarian balls visible); striped bars = gravid females (December 2018: n = 41; April 2019: n = 42; July 2019: n = 47; October 2019: n = 50). Gravid females were present throughout the year but significantly more abundant proportionally in December and July, which may indicate a short life span of the worms and quick turnover in the fish.
Figure 3 in Parasites of Moroccan desert Coptodon guineensis (Pisces, Cichlidae): transition and resilience in a simplified hypersaline ecosystem
Figure 3. Acanthocephalan Acanthogyrus (Acanthosentis) cf. tilapiae from Coptodon guineensis at Sebkha Imlili. SEM. A. Male proboscis showing large anterior hooks markedly separated from small posterior hooks. B. Anterior trunk of female showing rows of spines. C. Female body spine.
Figure 2 in Gyrodactylus magadiensis n. sp. (Monogenea, Gyrodactylidae) parasitising the gills of Alcolapia grahami (Perciformes, Cichlidae), a fish inhabiting the extreme environment of Lake Magadi, Kenya
Figure 2. Line drawings of the haptoral sclerites and MCO of Gyrodactylus magadiensis n. sp. from Alcolapia grahami in Lake Magadi, Kenya. (A) Haptoral sclerites with hamulus (ha), dorsal bar (db), and ventral bar (vb); (B) marginal hook; (C) male copulatory organ (MCO). Scale bars – (A) 20 µm; (B and C) 5 µm.
Figure 4 in Gyrodactylus magadiensis n. sp. (Monogenea, Gyrodactylidae) parasitising the gills of Alcolapia grahami (Perciformes, Cichlidae), a fish inhabiting the extreme environment of Lake Magadi, Kenya
Figure 4. Evolutionary history of Gyrodactylus magadiensis n. sp. based on Bayesian Inference approaches using ITS sequences for selected gyrodactylids. Statistical support for Bayesian inference (BI) and maximum likelihood (ML) methods indicated at branch nodes with posterior probabilities and bootstrap support indicated, respectively (ML/BI).
Figure 1 in Gyrodactylus magadiensis n. sp. (Monogenea, Gyrodactylidae) parasitising the gills of Alcolapia grahami (Perciformes, Cichlidae), a fish inhabiting the extreme environment of Lake Magadi, Kenya
Figure 1. Collection sites from which Alcolapia grahami were collected. (A) Silhouette of Africa showing area of study; (B) map of study area indicating countries, water bodies, and relation of Lake Magadi to Nairobi; (C) fish spring lagoon of Lake Magadi from which the fish specimens were collected.
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OpenNeuro
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