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176 results for “Scorpaenidae”
Fig. 7 in Newly Recognized Diagnostic Characters of the Poorly Known Lionfish Pterois brevipectoralis (Scorpaenidae: Pteroinae), with Notes on Fresh Coloration
Fig. 7. Relationship of position of longest pectoral-fin ray tip to standard length (mm) in Pterois brevipectoralis. A, D, and C represent the anal-fin base end, the dorsal-fin base end, and the caudalfin base, respectively; =,>,
Fig. 4 in Newly Recognized Diagnostic Characters of the Poorly Known Lionfish Pterois brevipectoralis (Scorpaenidae: Pteroinae), with Notes on Fresh Coloration
Fig. 4. Skin flaps on lacrimal (A and C) and preopercle (B and D) of Pterois brevipectoralis at different growth stages. A, B, USNM 392069, 49.2 mm SL; C, D, HUMZ 73848, 125.7 mm SL. Arrows indicate third preopercular spine.
Fig. 2 in Newly Recognized Diagnostic Characters of the Poorly Known Lionfish Pterois brevipectoralis (Scorpaenidae: Pteroinae), with Notes on Fresh Coloration
Fig. 2. Fresh specimen of Pterois brevipectoralis, HUMZ 73846, 115.8 mm SL, Saya de Malha Bank. Photo: HUMZ.
Fig. 1 in Newly Recognized Diagnostic Characters of the Poorly Known Lionfish Pterois brevipectoralis (Scorpaenidae: Pteroinae), with Notes on Fresh Coloration
Fig. 1. Lateral (top) and dorsal (bottom) views of head of Pterois brevipectoralis, HUMZ 73848, 125.7 mm SL. Shaded areas indicate skin flaps. 1, nasal spine; 2, preocular spine; 3, supraocular spine; 4, postocular spine; 5, coronal spine; 6, tympanic spine; 7, parietal spine; 8, nuchal spine; 9, pterotic spine; 10, lower posttemporal spine; 11, supracleithral spine; 12, sphenotic spine; 13, supplemental preopercular spine; 14, preopercular spine; 15, suborbital ridge/spine; 16, lateral lacrimal ridge/spine; 17, posterior lacrimal spine. Barbel on anteroventral lacrimal based on right side in lateral view; nasal spines and right supraocular skin flap not illustrated in dorsal view.
Fig. 1 in Scorpaena dabryi, a Junior Synonym of Scorpaena miostoma, with Notes on Morphological Ontogenetic Changes (Teleostei: Scorpaenidae)
Fig. 1. Photographs of Scorpaena miostoma. A, lectotype of S. dabryi (MNHN 6882, male, 75.5 mm SL); B, paralectotype of S. dabryi (MNHN 6882, 71.0 mm SL); C, holotype of S. miostoma (BMNH 1879.5.14.235, 106.4 mm SL).
Fig. 3 in Scorpaena dabryi, a Junior Synonym of Scorpaena miostoma, with Notes on Morphological Ontogenetic Changes (Teleostei: Scorpaenidae)
Fig. 3. Life stages of Scorpaena miostoma. A, KAUM–I. 71264, male, 43.8 mm SL; B, KAUM–I. 25862, 62.3 mm SL; C, KAUM–I. 71449, male, 81.5 mm SL; D, KAUM–I. 30796, 108.2 mm SL; E, KAUM–I. 10014, male, 124.4 mm SL.
Fig. 3 in Sex Differences And Sex Identification In The Small-Scaled Scorpionfish, Scorpaena Porcus (Scorpaenidae, Scorpaeniformes)
Fig. 3. Coefficient of variation (CV, %) for relative values of plastic features in adult males (M) and females (F).
Fig. 2 in Sex Differences And Sex Identification In The Small-Scaled Scorpionfish, Scorpaena Porcus (Scorpaenidae, Scorpaeniformes)
Fig. 2. Coefficient of variation (CV, %) for 21 plastic characters in adult males (M) and females (F).
Fig. 1 in Sex Differences And Sex Identification In The Small-Scaled Scorpionfish, Scorpaena Porcus (Scorpaenidae, Scorpaeniformes)
Fig. 1. Differentiation of males of the small-scaled scorpionfish on absolute values of 21 plastic characters.
Figure 2 in First report of the Ecuadorian deep-sea scorpionfish, Trachyscorpia verai Béarez & Motomura, 2009 (Actinopteri: Scorpaenidae) from Peruvian marine waters
Figure 2. – Lateral view of Trachyscorpia verai. A: IMARPE-18787, 223 mm SL. B: IMARPE-18789, 266 mm SL. Photographed approximately one hour after capture and prior to preservation (photo F. Zavalaga).
Figure 4 in First report of the Ecuadorian deep-sea scorpionfish, Trachyscorpia verai Béarez & Motomura, 2009 (Actinopteri: Scorpaenidae) from Peruvian marine waters
Figure 4. – Endoparasites of the genus Anisakis (larva L3) found in the mesentery of Trachyscorpia verai.
Figure 4 in Feeding habits of Scorpaena notata (Scorpaenidae) from eastern Adriatic Sea
Figure 4. – Diet composition of Scorpaena notata throughout the year, based on the %IRI values of the major prey groups.
Figure 1 in Feeding habits of Scorpaena notata (Scorpaenidae) from eastern Adriatic Sea
Figure 1. – Study area and sampling sites of Scorpaena notata in the eastern Adriatic Sea. A: Kvarner Archipelago; B: Near Dugi Island; C: Near Šolta Island; D: Near Hvar Island. All sampling sites supported biocoenosis on coastal terrigenous sediments.
Figure 5 in Feeding habits of Scorpaena notata (Scorpaenidae) from eastern Adriatic Sea
Figure 5. – Dendrogram for hierarchical clustering of the prey composition of Scorpaena notata according to sampling sites, using group-average linking of Bray-Curtis similarities calculated on standardized and double root-transformed data of prey abundance. A: Kvarner Archipelago (n = 177); B: Near Dugi Island (n = 220); C: Near Šolta Island (n = 190); D: Near Hvar Island (n = 211).
Fig. 4 in Expressed sequence tags in venomous tissue of Scorpaena plumieri (Scorpaeniformes: Scorpaenidae)
Fig. 4. Sequence alignment of putative lectin from Scorpaena plumieri. Alignment of a lectin-like EST in silico translated sequence from S. plumieri (ClustalW2 EBI) with fish-egg lectin from Oplegnathus fasciatus (BAL618145), Dicentrarchus labrax (CBK52298), Maylandia zebra (XP_004574029), and Oreochromis niloticus (XP003443389). The recombinant clone was isolated with antibody fraction derived from S. plumieri venom. * identifies and identical residue;: identifies a conserved residue. Underlined residues represent invariable sites, underlined IRLS = N-acetylation site.
Fig. 3 in Expressed sequence tags in venomous tissue of Scorpaena plumieri (Scorpaeniformes: Scorpaenidae)
Fig. 3. The classification of EST from Scorpaena plumieri based on their putative fractions. Three-hundred fifty-six EST edited sequences were initially analyzed with Blast and Swiss protein databanks. The consensus sequence was attributed a function based on the strongest match.
Fig. 2 in Expressed sequence tags in venomous tissue of Scorpaena plumieri (Scorpaeniformes: Scorpaenidae)
Fig. 2. Agarose gel electrophoresis of DNA isolated from clones. White colonies containing insert were grown and the plasmidial DNA isolated and digested with EcoRI enzyme. An aliquot from each clone (1-27) was electrophoresed on 1% Agarose gel and stained with ethidium bromide.
Fig. 1 in Expressed sequence tags in venomous tissue of Scorpaena plumieri (Scorpaeniformes: Scorpaenidae)
Fig. 1. Agarose- formaldehyde electrophoresis of RNA from Scorpaena plumieri. A) 1) 2 µg of E. coli tRNA; 2) 2 µg de rRNA de Rattus norvegicus; 3) and 4) 2 µg total RNA from S. plumieri spine gland. B) 1) 2 µg de total RNA from S. plumieri; 2) the same sample incubated 2 h a 37ºC before electrophoresis.
Fig. 10 in Fig. 2 in A New Species of Bleeker, 1876 (Teleostei: Scorpaenidae) from Taiwan.
Fig. 10. Range distribution of extant and fossil species of Akodon in Brazil and Paraguay. Localities: 1 – Fazenda Califórnia, Parque Nacional da Serra da Bodoquena (Brandão et al. 2021); 2 – Nossa Senhora Aparecida cave, Serra da Bodoquena (Boroni et al. 2020); 3 – Carneiro cave (Boroni 2019); 4 – Igrejinha cave (Salles et al. 1999); 5 – Gruta dos Moura cave (Tobelém et al. 2013); 6 – Gruta do Urso cave (Pires et al. 2018); 7 – Toca da Barra da Janela do Antonião cave (Guérin et al. 1996); 8 – Lagoa Santa (Winge 1887); 9 – Abismo Iguatemi site (Castro and Langer 2011); 10 – Garivaldino site (Stutz et al. 2017); 11 – Adelar Pilger site (Hadler et al. 2016); 12 – Deobaldino Marques site (Roth 2018); 13 – Sangão site (Stutz et al. 2018); 14 – Risso Cave, Paraguay (Torres et al. 2015). Also see table 1. Gray area was based on the geographic range of the extant species of genus Akodon according to Pardiñas et al. (2015).
Fig. 9 in Fig. 2 in A New Species of Bleeker, 1876 (Teleostei: Scorpaenidae) from Taiwan.
Fig. 9. Occlusal views of the upper and lower molar toothrows of Akodon sp. (A–D) and Akodon kadiweu (E–F). Legends: anteroloph (An); ectolophid (ect); mesoloph (Ms), mesolophid (msl). Vouchers: MN 57650 (A), MN 57631 (B), MN 57635 (C), MN 57642 (D), MZUSP 35767 (E, F).
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International Brain Laboratory public data
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OpenNeuro
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