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963 results for “Gobies”
Fig. 3 in First Records of an Estuarine Goby Acentrogobius ocyurus (Gobiiformes: Gobiidae) from Japan and the Sulu Sea in the Philippines
Fig. 3. Living Acentrogobius ocyurus showing various color markings in aquaria. A, Different individual; B, C, same individual under different light conditions. All specimens were collected from Manko in Okinawa-jima Island, Japan (no voucher).
Fig. 5. A in First Records of an Estuarine Goby Acentrogobius ocyurus (Gobiiformes: Gobiidae) from Japan and the Sulu Sea in the Philippines
Fig. 5. A living Alpheus richardsoni (WMNH-2019-INV-401), collected together with Acentrogobius ocyurus (OCF-P 3810) from Manko in Okinawa-jima Island, Japan.
Fig. 2 in First Records of an Estuarine Goby Acentrogobius ocyurus (Gobiiformes: Gobiidae) from Japan and the Sulu Sea in the Philippines
Fig. 2. Cephalic sensory organs of Acentrogobius ocyurus (27.6 mm SL, OCF-P 3494). A, Lateral view; B, dorsal view; C, ventral view. Arrows indicate the anteroventral end of the gill opening.
Effects of ecology on the sociality of coral dwelling gobies, genus Gobiodon
<p>We developed a framework to assess how ecological factors affected the sociality of animals, and we used coral dwelling gobies (genus Gobiodon) to model this framework. We identifed four categories of sociality to compare: form of sociality, degree of sociality, social plasticity, and hierarchy maintenance. We tested global and local ecological factors from climatic disturbances to habitat size, and assessed how they affected the different categories of sociality. We combined the findings of each category to determine to outlook of social maintenance in the taxa when considering the ecological factors tested. For coral dwelling gobies, we found that there is a very poor outlook for their social maintenance with respect to climatic disturbances.</p>
Fig. 7 in Rhinogobius mizunoi, A New Species of Freshwater Goby (Teleostei: Gobiidae) from Japan
Fig. 7. Freshly-collected specimens of Rhinogobius fluviatilis. A: OMNH-P 18393, male, 53.8 mm SL, Komenotsu-gawa River, Kagoshima Prefecture, Japan; B: OMNH-P 18429, female, 69.8 mm SL, Nabeno-gawa River, Kagoshima Prefecture, Japan. Photographed by T. Suzuki.
Fig. 5 in Rhinogobius mizunoi, A New Species of Freshwater Goby (Teleostei: Gobiidae) from Japan
Fig. 5. Freshly-collected (A and B) and alcohol-preserved (C) paratype of Rhinogobius mizunoi (OMNH-P 40618, female, 61.9 mm SL). Photographed by T. Suzuki.
Fig. 4 in Rhinogobius mizunoi, A New Species of Freshwater Goby (Teleostei: Gobiidae) from Japan
Fig. 4. Freshly-collected (A and B) and alcohol-preserved (C) holotype of Rhinogobius mizunoi (SPMN-PI 3196, male, 67.2 mm SL). Photographed by T. Suzuki..
Fig. 3 in Rhinogobius mizunoi, A New Species of Freshwater Goby (Teleostei: Gobiidae) from Japan
Fig. 3. Dorsal (top), lateral (middle), and ventral (bottom) views of head of holotype of Rhinogobius mizunoi (SPMN-PI 3196, male, 67.2 mm SL), showing freshlycollected coloration. Photographed by T. Suzuki.
Fig. 6 in Rhinogobius mizunoi, A New Species of Freshwater Goby (Teleostei: Gobiidae) from Japan
Fig. 6. Underwater photographs of male (A, KPM- NR 91331B) and female (B, KPM-NR 78800A) of Rhinogobius mizunoi, taking at lower reach of Okitsugawa River, Shizuoka Prefecture, Japan. Photographed by K. Uchino.
Fig. 1 in Rhinogobius mizunoi, A New Species of Freshwater Goby (Teleostei: Gobiidae) from Japan
Fig. 1. Dorsal view of head (A) and ventral view of pelvic fin (B) of paratype of Rhinogobius mizunoi (OMNH-P 40617, a male, 73.6 mm SL), stained with alizarin red. Black circle with black letters F, H, K, and L indicate sensory-canal pores; letter with prime mark indicates the terminal opening if sensory canal. Yellow dots indicate scales along edge of scaled area on nape and occipital region; letters P1, P2, and P3 indicate boundary of anterior extension of scaled area along predorsal midline, boundary of anterior extension of scaled area on side of occipital region, and boundary of most concave point of scaled area between P1 and P2, respectively. Black letters 1–5 indicate number of segmented rays of pelvic fin. Photographed and annotated by T. Suzuki.
Fig. 2 in Rhinogobius mizunoi, A New Species of Freshwater Goby (Teleostei: Gobiidae) from Japan
Fig. 2. Dorsal (top), lateral (middle), and ventral (bottom) views of head of holotype of Rhinogobius mizunoi (SPMN-PI 3196, male, 67.2 mm SL), showing cephalic sensory pores and papillae. Red circle with red letters indicate sensory canal pores (letters with prime marks indicate terminal opening of sensory canal); yellow dots indicated by yellow letters represent sensory papillae; black arrows show positions of dorsal and ventral most of gill opening. Abbreviations: AN, anterior narial pore; PN, posterior narial pore. Photographed and annotated by T. Suzuki.
Fig. 9 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint
Fig. 9: Histogram of the Mantel test assessing the relationship between genetic and morphologic distance for Gobius niger. Sim: simulations; Frequency: frequency values of the correlation between the genetic and morphologic distances. The dot represents the original value of the correlation between the distance matrices.
Fig. 6 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint
Fig. 6: PCA of the morphological variables of Gobius niger (standard length, SL; body height, BH; head length, HL; snout length, SnL; eye diameter, ED; first dorsal fin, DF1; second dorsal fin, DF2; anal fin, AF; pectoral fin, PF; ventral fin, VF) with projection of phenotypic groups. PC1 vs. PC2 and PC2 vs. PC3. The percentage of variation explained by each PC axis is given within parentheses.
Fig. 3 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint
Fig. 3: Cluster analysis associated with the similarity profile test (SIMPROF), based on abundances of Gobius niger, reveals reciprocal relations among the 20 sampled stations in the Marchica Lagoon using the Bray–Curtis distance.
Fig. 2 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint
Fig. 2: Picture of Gobius niger from the Marchica Lagoon showing the main measurements taken: total length (TL), standard length (SL), head length (LT), snout length (SnL), body height (BH), and eye diameter (ED).
Fig. 7 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint
Fig. 7: Linear regression of the principal component score axis (PC1) from morphometric measurements on the log standard length of Gobius niger with projection of phenotypic groups.
Fig. 8 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint
Fig. 8: Haplotype network constructed from 16S rDNA sequences of Gobius niger. The size of a particular circle reflects the haplotype frequency. The numbers indicate the nodes.
Fig. 1 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint
Fig. 1: Map showing the geographical localization of the Marchica Lagoon and the sampling stations of Gobius niger.
Fig. 4 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint
Fig. 4: Two-dimensional redundancy analysis (RDA) ordination representing the spatial distribution of Gobius niger related to the predictor variables selected through the best linear models based on distance (DISTLM). SM: suspended matter.
Fig. 7 in Skull of a dromaeosaurid dinosaur Shri devi from the Upper Cretaceous of the Gobi Desert suggests convergence to the North American forms
Fig. 7. Comparison of silhouettes of the velociraptorine skulls from different sites of the Upper Cretaceous of the Gobi Desert. A. Shri devi Turner, Montanari, and Norell, 2021, ZPAL MgD-I/97. B, D, E. Velociraptor mongoliensis Osborn, 1924. B. AMNH FARB 6515. D. MPC-D 100/25. E. MPC-D 100/54. C. Velociraptor sp. MPC-D 100/982. F. "Velociraptor" osmolskae Godefroit, Currie, Li, Shang, and Dong, 2008, IMM 99NM-BYM-3/3. G. Linheraptor exquisitus Xu, Choinere, Pittman, Tan, Xiao, Li, Tan, Clark, Norell, Hone, and Sullivan, 2010, IVPP V16923. H. Tsaagan mangas Norell, Clark, Turner, Makovicky, Barsbold, and Rowe, 2006, MPC-D 100/1015. Known elements from any side of the specimen are in grey. Lines present some of the features distinguishing S. devi from other velociraptorines: the maximum height of the antorbital fenestra and its perpendicular projection showing elongation of the fenestra (red lines), the position of the last maxillary alveoli (blue), the anteriormost projection of the quadratojugal (green), and the position of the ventral margin of the external mandibular fenestra (purple).
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.