Find research datasets worth reusing

Figure 5 in First record of five fish species from Réunion Island observed during the inventory of the Marine Natural Zones of Interest for Ecology, Flora and Fauna (ZNIEFF)

Figure 5. – Specimen of Trichonotus marleyi photographed on 6 April 2017 at 20°55'30.54"S and 55°17'55.32"E.

Figure 3 in First record of five fish species from Réunion Island observed during the inventory of the Marine Natural Zones of Interest for Ecology, Flora and Fauna (ZNIEFF)

Figure 3. – Specimen of Fusigobius neophytus photographed on 22 November 2017 at 21°1'16.32"S and 55°13'31.84"E.

Figure 1 in First record of five fish species from Réunion Island observed during the inventory of the Marine Natural Zones of Interest for Ecology, Flora and Fauna (ZNIEFF)

Figure 1. – Location of the observation stations of the 5 fish species present- ed in this study on a geomorphological map of the Reunionese coastline.

Figure 4 in First record of five fish species from Réunion Island observed during the inventory of the Marine Natural Zones of Interest for Ecology, Flora and Fauna (ZNIEFF)

Figure 4. – Specimen of Samariscus triocellatus photographed on 4 May 2016 at 21°6'20.92"S and 55°46'16.72"E.

Figure 2 in First record of five fish species from Réunion Island observed during the inventory of the Marine Natural Zones of Interest for Ecology, Flora and Fauna (ZNIEFF)

Figure 2. – Specimen of Fusigobius inframaculatus photographed on 8 April 2016 at 21°21'18.54"S and 55°47'31.31"E.

Fig. 3 in Copepod consumption by amphibians and fish with implications for transmission of Dracunculus species

Fig. 3. Average copepods ingested by tadpole species during the feeding trial. Bars represent average copepods ingested, error bars represent standard error, and dotted line shows average copepod loss in control trials. The lack of significant differences (p <0.05) determined by Tukey post-hoc contrasts are indicated by 'a'.

Fig. 2 in Copepod consumption by amphibians and fish with implications for transmission of Dracunculus species

Fig. 2. Average copepods ingested by fish species during the feeding trial. Bars represent average copepods ingested, error bars represent standard error, and dotted line shows average copepod loss in control trials. Significant differences (p <0.05) determined by Tukey post-hoc contrasts are indicated by 'a' and 'b'.

Fig. 1 in Copepod consumption by amphibians and fish with implications for transmission of Dracunculus species

Fig. 1. Average copepods ingested by animal type during the feeding trial. Bars represent average copepods ingested, error bars represent standard error, and dotted line shows average copepod loss in control trials. Significant differences (p <0.05) determined by Tukey post-hoc contrasts are indicated by 'a', 'b', and 'c'.

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.)

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).

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. 1 in Caryophyllidean tapeworms (Cestoda), Nearctic parasites of fish in Mexico, including description of a new species of Isoglaridacris and the first report of Khawia japonensis, an invasive parasite of common carp (Cyprinus carpio)

Fig. 1. Archigetes sp. 1 from Notropis caliensis, Michoac´an (CNHE 6800) (A, C, F); Archigetes (?) sp. 2 from Notropis nazas, Durango (CNHE 6797) (B, E); Archigetes sp. 3 from Chirostoma sp., Michoac´an (CNHE 6801) (D). A, B – total view, dorsally; C, E – anterior part with scolex; note different position of anterior-most testes and vitelline follicles between C and E; D – total view, ventrally; F – ovarian and uterine region, dorsally. Abbreviations: cs – cirrus-sac; eb – excretory bladder; eg – eggs; esv – external seminal vesicle; lo – loculi; ov – ovary; sr – seminal receptacle; te – testes; vf – vitelline follicles.

Fig. 3 in Caryophyllidean tapeworms (Cestoda), Nearctic parasites of fish in Mexico, including description of a new species of Isoglaridacris and the first report of Khawia japonensis, an invasive parasite of common carp (Cyprinus carpio)

Fig. 3. Khawia japonensis (Yamaguti, 1934) from Cyprinus carpio, Durango (CNHE 6516). A – total view, ventrally (median preovarian vitelline follicles omitted except for anterior-most follicles); B – anterior end; C – posterior end, ventrally. Abbreviations: cgp – common genital pore; cs – cirrus-sac; Mg – Mehlis' gland; ov – ovary; povf – postovarian vitelline follicles; sd – sperm duct (vas deferens); sr – seminal receptacle; te – testes; ug – uterine glands; ut – uterus; va – vagina; vf – vitelline follicles.

Fig. 2 in Caryophyllidean tapeworms (Cestoda), Nearctic parasites of fish in Mexico, including description of a new species of Isoglaridacris and the first report of Khawia japonensis, an invasive parasite of common carp (Cyprinus carpio)

Fig. 2. Isoglaridacris brevicollis sp. n. from Catostomus nebuliferus, Durango (CNHE 6802; IPCAS C-885; 2x CNHE 6761) (A–D), Catostomus bernardini, Sonora (CNHE 6796) (E), and Moxostoma astrinum, Jalisco (CNHE 6799) (F); Pseudoglaridacris confusa (Hunter, 1929) from Ictiobus meridionalis, Oaxaca (CNHE 6798) (G). A – total view, ventrally; B – anterior end; C – posterior end, ventrally; D – slightly contracted scolex; E – cirrus-sac with external seminal vesicle, ventrally; F – ovary with overlapping posterior wings, dorsally (uterine loops are omitted at level of ovarian isthmus and more posteriorly); G – total view, dorsally. Abbreviations: cgp – common genital pore; cs – cirrus-sac; eb – excretory bladder; esv – external seminal vesicle; lo – loculi; ov – ovary; povf – postovarian vitelline follicles; sd – sperm duct (vas deferens); te – testes; ut – uterus; va – vagina; vd – vitelline duct; vf – vitelline follicles.

Fig. 5. Mothocya andoni n in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria

Fig. 5. Mothocya andoni n. sp. Ƌ (12.0 mm total length, 5.0 mm width) (SAMC–A092738). A, Antennula; B, Antenna; C, Maxilliped; D, Tip of maxillula; E, Mandible palp; F, Maxilla.

Fig. 2. Mothocya andoni n in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria

Fig. 2. Mothocya andoni n. sp. paratype ♀ (non-ovigerous, 18.0 mm total length, 9.0 mm width) (SAMC–A092738). A, Antennula; B, Antenna; C, Mandible; D, Maxillula; E, Maxilla; F, Maxilliped.

Fig. 3. Mothocya andoni n in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria

Fig. 3. Mothocya andoni n. sp. paratype ♀ (non-ovigerous, 18.0 mm total length, 9.0 mm width) (SAMC–A092738). A, Pleopod 1 ventral view; B, Pleopod 2 ventral view; C, Pleopod 3 ventral view; D, Pleopod 4 ventral view; E, Pleopod 5 ventral view; F, Pleopod 1 dorsal view; G, Pleopod 2 dorsal view; H, Pleopod 3 dorsal view; I, Pleopod 4 dorsal view; J, Pleopod 5 dorsal view.

Fig. 1. Mothocya andoni n in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria

Fig. 1. Mothocya andoni n. sp. holotype ♀ (ovigerous, 15.0 mm total length, 8.0 mm width) (SAMC–AA092737). A, Dorsal body; B, Lateral body; C, Oostegites; D, Dorsal view of cephalon and pereonite 1; E, Uropod; F, Ventral cephalon; G, Dorsal view of pleon; H, Pereopod 1; I, Pereopod 7.

Fig. 4. Mothocya andoni n in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria

Fig. 4. Mothocya andoni n. sp. Ƌ (12.0 mm total length, 5.0 mm width) (SAMC–A092738)A, Dorsal body; B, Lateral body; C, Pereopod 1; D, Pereopod 7; E, Penes; F, Uropod; G, Dorsal view of cephalon with pereonite 1; H, Dorsal view of pleon.

Fig. 7. Mothocya powelli n in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria

Fig. 7. Mothocya powelli n. sp. holotype ♀ (ovigerous, 7.0 mm total length, 5.0 mm width) (SAMC–A092739). A, Dorsal body; B, Lateral body; C, Oostegites; D, Dorsal view of cephalon with pereonite 1; E, Uropod; F, Ventral cephalon; G, Dorsal view of pleon; H, Pereopod 1; I, Pereopod 7.