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Fig. 4 in New biological data for two rare reedfrog species, Hyperolius nimbae Laurent, 1958, and H. chlorosteus (Boulenger, 1915) (Anura: Hyperoliidae)

Fig. 4. Dorsolateral views of the Hyperolius nimbae female (A) and males (B–H) from Yéalé, western Ivory Coast. Note the variation in coloration.

Fig. 7 in New biological data for two rare reedfrog species, Hyperolius nimbae Laurent, 1958, and H. chlorosteus (Boulenger, 1915) (Anura: Hyperoliidae)

Fig. 7. (A–B) Typical forest streams in the Mount Nimba Integrated Nature Reserve where Hyperolius chlorosteus breeds. A calling male (C), a female (D), a couple in amplexus (E), and their clutch (F) which was deposited on a leaf above a forest stream.

Fig. 1 in New biological data for two rare reedfrog species, Hyperolius nimbae Laurent, 1958, and H. chlorosteus (Boulenger, 1915) (Anura: Hyperoliidae)

Fig. 1. Geographical location of the Mount Nimba Integrated Nature Reserve within the westernmost extension of Ivory Coast at the border crossing point with Guinea and Liberia. The altered forest area where Hyperolius nimbae and H. chlorosteus were found at Yéalé is represented by a purple star; the habitats of H. chlorosteus ranged from dense, broadleaf and evergreen forests from lower to mid-elevations (yellow star). The inset figure indicates the location of Ivory Coast (green patch) on the African continent.

Fig. 5 in New biological data for two rare reedfrog species, Hyperolius nimbae Laurent, 1958, and H. chlorosteus (Boulenger, 1915) (Anura: Hyperoliidae)

Fig. 5. Ventral views of Hyperolius nimbae males (A and B) and female (C) adults, and the eggs (D) from Yéalé, western Ivory Coast.

Fig. 10 in New biological data for two rare reedfrog species, Hyperolius nimbae Laurent, 1958, and H. chlorosteus (Boulenger, 1915) (Anura: Hyperoliidae)

Fig. 10. Calling male of Hyperolius chlorosteus (A) with (B) waveform (above), spectogram (centre) and powerspectrogram (below), of the species' advertisement call, from Mount Nimba Integrated Nature Reserve. Note that the data for five calls are shown.

Fig. 3 in New biological data for two rare reedfrog species, Hyperolius nimbae Laurent, 1958, and H. chlorosteus (Boulenger, 1915) (Anura: Hyperoliidae)

Fig. 3. Number of Hyperolius nimbae individuals recorded from 2 August 2019 to 8 July 2020 at Yéalé.

Fig. 9 in New biological data for two rare reedfrog species, Hyperolius nimbae Laurent, 1958, and H. chlorosteus (Boulenger, 1915) (Anura: Hyperoliidae)

Fig. 9. Variation of color pattern of Hyperolius chlorosteus from Mount Nimba Integrated Nature Reserve, western Ivory Coast.

Fig. 4 in Distribution and habitat suitability of two neighboring Lycian salamanders

Fig. 4. Variables with the highest contributions to the potential distributions of L. flavimembris (a) and L. fazilae (b) according to MaxEnt, with the standard errors in shown blue. In each graph, the y-axis indicates the probability of presence and the x-axis shows the contribution of each variable. See Table 1 for definitions of the environmental variables.

Fig. 6 in Distribution and habitat suitability of two neighboring Lycian salamanders

Fig. 6. Frequencies of Bedrock types on the different presence points of L. flavimembris and L. fazilae. Bedrock type abbreviations: Alluvion [All], Breccias [Brec], Pebble Stone-Sandstone-Mudstone [PS-SS-MS], Chert [Cher], Cherty Limestone [Cher LS], Dolomite [Dol], Limestone [LS], Melange [Mel], Peridotite [Per], Spilite-Basalt-Tuff [SBT], Sandstone-Mudstone [SS-MS], Sandstone-Mudstone-Limestone [SS-MS-LS], Volcanite-Sedimentary Rock [V-SR], and all unknown rock types [Unknown].

Fig. 3 in Distribution and habitat suitability of two neighboring Lycian salamanders

Fig. 3. Results of the Jackknife test for evaluating the relative importance of environmental variables for L. flavimembris (a) and L. fazilae (b). See Table 1 for definitions of the environmental variables.

Fig. 2 in Distribution and habitat suitability of two neighboring Lycian salamanders

Fig. 2. The receiver operating characteristic (ROC) curves for L. flavimembris (a) and L. fazilae (b).

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Fig. 5 in Fish blood flukes (Digenea: Aporocotylidae) from Indonesia: Two new genera and species infecting the banded eagle ray, Aetomylaeus nichofii (Bloch and Schneider, 1801) Capape´and Desoutter, 1979 (Myliobatiformes: Myliobatidae) from Borneo

Fig. 5. Phylogenetic relationships of chondrichthyan blood flukes based on morphological characters (tegumental spines, shape of intestines). Host affiliations are included. Dashed lines indicate species with no nucleotide sequences. Boxes indicate spine rows: blue = 2 + spine rows, green = 1 spine row, and red ⋂ = no spines. Shape of the intestine () inverse U-shaped and (X) X-shaped. (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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Fig. 1-2. Aetohemecus kirstenjensenae Warren and Bullard n. gen., n in Fish blood flukes (Digenea: Aporocotylidae) from Indonesia: Two new genera and species infecting the banded eagle ray, Aetomylaeus nichofii (Bloch and Schneider, 1801) Capape´and Desoutter, 1979 (Myliobatiformes: Myliobatidae) from Borneo

Fig. 1-2. Aetohemecus kirstenjensenae Warren and Bullard n. gen., n. sp. (Digenea: Aporocotylidae) from the heart of the banded eagle ray, Aetomylaeus nichofii (Bloch and Schneider, 1801) Capape´and Desoutter, 1979 (Myliobatiformes: Myliobatidae). (1) Body of holotype (USNM No. 1642775), dorsal view. Bar = 250 μm. (2) Genitalia, paratype (USNM No. 1642776), ventral view. Bar = 100 μm. Mouth (mo), nerve commissure (nc), oesophagus (os), vitellarium (vit), intestine (i), testis (t), uterus (u), metraterm (met), ovary (o), vas deferens (v), seminal vesicle (sv), cirrus sac (cs), cirrus (c), vitelline duct (vd), common genital pore (cgp), oviducal ampullae (oa), and o¨otype (oo).

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Fig. 3-4. Homestios janinecairae Warren and Bullard n. gen., n in Fish blood flukes (Digenea: Aporocotylidae) from Indonesia: Two new genera and species infecting the banded eagle ray, Aetomylaeus nichofii (Bloch and Schneider, 1801) Capape´and Desoutter, 1979 (Myliobatiformes: Myliobatidae) from Borneo

Fig. 3-4. Homestios janinecairae Warren and Bullard n. gen., n. sp. (Digenea: Aporocotylidae) from the heart of the banded eagle ray, Aetomylaeus nichofii (Bloch and Schneider, 1801) Capape´and Desoutter, 1979 (Myliobatiformes: Myliobatidae). (3) Body of holotype (USNM No. 1642774), dorsal view. Bar = 250 μm. (4) Genitalia of holotype (USNM No. 1642774), dorsal view. Bar = 100 μm. Mouth (mo), oesophagus (os), vitellarium (vit), intestine (in), testis (t), ovary (ov), vas deferens (vd), uterus, (u), ascending uterus (au), descending uterus (du), seminal vesicle (sv), cirrus (c), and common genital pore (cgp).

Fig. 7. Stained microfilariae from amphibian blood. A – Neofoleyellides steyni n in Two new species of Neofoleyellides (Nematoda: Onchocercidae) parasitising anuran amphibians in South Africa

Fig. 7. Stained microfilariae from amphibian blood. A – Neofoleyellides steyni n. sp. from Amietia delalandii (Dum´eril et Bibron, 1841); B – Neofoleyellides martini n. sp. from Leptopelis natalensis (Smith, 1849).

Fig. 4. Neofoleyellides martini n in Two new species of Neofoleyellides (Nematoda: Onchocercidae) parasitising anuran amphibians in South Africa

Fig. 4. Neofoleyellides martini n. sp. from Leptopelis natalensis (Smith, 1849), line drawings. A – fragment of body at anterior end, female, lateral view; B – fragment of body at anterior end, male, lateral view; C – anterior extremity, female, lateral view; D–F – anterior extremity, female, apical view, optical sections at different depth of focus; G – posterior end of body, male, ventral view; H – microfilaria; I – posterior end of body, female, lateral view; J – spicules, lateral view.

Fig. 8 in Two new species of Neofoleyellides (Nematoda: Onchocercidae) parasitising anuran amphibians in South Africa

Fig. 8. Phylogeny of selected amphibian and reptilian filarial nematodes from the family Onchocercidae. Phylogram based on partitioned and concatenated datasets of 18S rDNA, and COI mtDNA sequences using Maximum Likelihood. Filaria latala (GenBank Accession numbers – 18S: KP760135 and COI: KP760186] was chosen as the outgroup. The total length of datasets is 1293 nucleotides, containing 11 taxa. The scale bar represents 0.09 nucleotide substitutions per site.

Fig. 6. Neofoleyellides martini n in Two new species of Neofoleyellides (Nematoda: Onchocercidae) parasitising anuran amphibians in South Africa

Fig. 6. Neofoleyellides martini n. sp. from Leptopelis natalensis (Smith, 1849), photomicrographs. A – transverse section at posterior end of body, male, a – ala; B – area rugosa.

Fig. 1. Neofoleyellides steyni n in Two new species of Neofoleyellides (Nematoda: Onchocercidae) parasitising anuran amphibians in South Africa

Fig. 1. Neofoleyellides steyni n. sp. from Amietia delalandii (Dum´eril et Bibron, 1841), line drawings. A – fragment of body at anterior end, female, lateral view; B – fragment of body at anterior end, male, lateral view; C – anterior extremity, female, lateral view; D–G – anterior extremity, female, apical view, optical sections at different depth of focus; H – microfilaria; I – posterior end of body, female, lateral view.

Fig. 5. Neofoleyellides martini n in Two new species of Neofoleyellides (Nematoda: Onchocercidae) parasitising anuran amphibians in South Africa

Fig. 5. Neofoleyellides martini n. sp. from Leptopelis natalensis (Smith, 1849), line drawings. A–D – posterior end of body, male, ventral view, variations of the arrangements of caudal papillae.