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963 results for “Gobies”
MCR LTER: Coral Reef: Habitat Utilization and Pairing Patterns of Mutualistic Shrimps and Gobies from 7 Indo-Pacific regions
We analyzed network level specialization for eight Indo-Pacific networks of obligate, mutualistic gobies and shrimps, and elucidated ecological and evolutionary factors driving specialization. To accomplish this we collected and analyzed data on species pairings in Moorea, French Polynesia (lat. -17.49, long. -149.84), Kenting, Taiwan (lat. 21.95, long. 120.76), and Kimbe Bay, New Britain, Papua New Guinea (PNG; lat. -5.50, long. 150.12), and combined these observations with previously published data from Seychelles Islands (Polunin and Lubbock 1977), Great Barrier Reef, Australia (Cummins 1979), Red Sea, Israel (Karplus et al. 1981), Japan (Yanagisawa 1984), and the Gulf of Thailand, Thailand (Nakasone and Manthachitra 1986). We also systematically collected and analyzed habitat data for shrimps and gobies in Moorea, Taiwan, and PNG. We found specialization was affected by variability in habitat use for both gobies and shrimps and by phylogenetic history for shrimps. Habitat use was phylogenetically conserved among shrimp, and thus effects of shrimp phylogeny on partner choice were mediated in part by habitat. By contrast, habitat use and pairing patterns in gobies were not related to phylogenetic history. This asymmetry appears to result from evolutionary constraints on partner use in shrimps and convergence among distantly-related gobies to utilize burrows provided by multiple shrimp species. Results indicate that the evolution of mutualism is affected by life history characteristics that transcend environments and that different factors constrain interactions in disparate ecosystems. These data are associated with this publication: Thompson AR, Adam TC, Hultgren KM, Thacker CE (in press). Ecology and evolution affect network structure in an intimate marine mutualism. The American Naturalist. This is a collection of short term studies spanning 1972 to 2011.
FIGURE 4 in A new cleaner goby of the genus Elacatinus (Teleostei: Gobiidae), from Trindade Island, off Brazil
FIGURE 4: Trindade Island (20 ° 30 ' S, 29 ° 20 ' W), type locality of Elacatinus pridisi n. sp., off the state of Espírito Santo, Brazil (Photograph by J. L. Gasparini).
FIGURE 3 in A new cleaner goby of the genus Elacatinus (Teleostei: Gobiidae), from Trindade Island, off Brazil
FIGURE 3: Brazilian species of Elacatinus: Top: Elacatinus pridisi n. sp., holotype (MNRJ 21980), 23.6 mm SL (Photograph by J. L. Gasparini); middle: Elacatinus figaro, (LBRP 0728), 27.8 mm SL, from the Brazilian coast (Photograph by R. Z. P. Guimarães); bottom: Elacatinus randalli, (MNRJ 12054), 28.7 mm SL, from Fernando de Noronha Archipelago, photograph kindly provided by Dr. Gustavo Nunan. All specimens live, photographed in aquaria shortly after collection.
FIGURE 2 in A new cleaner goby of the genus Elacatinus (Teleostei: Gobiidae), from Trindade Island, off Brazil
FIGURE 2: Detail of anterior portion of body of Elacatinus pridisi n. sp., paratype (UFES 1424), 28.4 mm SL, photographed in an aquarium immediately after collection (Photograph by J. L. Gasparini).
FIGURE 1 in A new cleaner goby of the genus Elacatinus (Teleostei: Gobiidae), from Trindade Island, off Brazil
FIGURE 1: Lateral view of Elacatinus pridisi n. sp., holotype (MNRJ 21980), 23.6 mm SL (Photograph by J. L. Gasparini).
Fig. 3. Rhinogobius vermiculatus, CMK 15306 in Three New Freshwater Gobies Of The Genus Rhinogobius (Teleostei: Gobiidae) From Northeastern Laos
Fig. 3. Rhinogobius vermiculatus, CMK 15306, paratypes, (a) male, 34.1 mm SL, and (b) female, 41.1 mm SL; Laos: Nam Hang.
Fig. 7 in Three New Freshwater Gobies Of The Genus Rhinogobius (Teleostei: Gobiidae) From Northeastern Laos
Fig. 7. Rhinogobius milleri, holotype, ZRC 46581, 39.8 mm SL; cephalic colour pattern of male. Scale bar = 1 mm.
Fig. 6. Rhinogobius vermiculatus, CMK 15306, 47.7 in Three New Freshwater Gobies Of The Genus Rhinogobius (Teleostei: Gobiidae) From Northeastern Laos
Fig. 6. Rhinogobius vermiculatus, CMK 15306, 47.7 mm SL; head lateral-line system. Scale bar = 1 mm.
Fig. 4 in Three New Freshwater Gobies Of The Genus Rhinogobius (Teleostei: Gobiidae) From Northeastern Laos
Fig. 4. Rhinogobius milleri, holotype, ZRC 46581, 39.8 mm SL; head lateral-line system. Scale bar = 1 mm.
Fig. 1. Rhinogobius milleri, CMK 15249 in Three New Freshwater Gobies Of The Genus Rhinogobius (Teleostei: Gobiidae) From Northeastern Laos
Fig. 1. Rhinogobius milleri, CMK 15249, paratypes, (a) male, 39.2 mm SL, and (b) female, 45.8 mm SL; Laos: Nam Kuang.
Fig. 1 in First Record of a Sicydiine Goby, Stiphodon multisquamus (Actinopterygii: Gobioidei: Gobiidae), from Okinawa Island, Japan
Fig. 1. Map showing the locations of Okinawa Island and Hain- an and Guangdong Provinces, China, where Stiphodon multisquamus has been reported previously.
Fig. 3 in First Record of a Sicydiine Goby, Stiphodon multisquamus (Actinopterygii: Gobioidei: Gobiidae), from Okinawa Island, Japan
Fig. 3. Diagrammatic illustration of head showing arrangement of cephalic sensory pores (black dots) and cutaneous sensory papillae (A′–O′) in Stiphodon multisquamus (40.6 mm SL, NSMT- P 114246) from Okinawa Island. A, dorsal view; B, lateral view; C, ventral view. AN, anterior nostril; PN, posterior nostril.
Fig. 4 in Shape Analysis Of Otoliths Of The Round Goby, Neogobius Melanostomus (Gobiiformes, Gobiidae), From The Black Sea Basin
Fig. 4. Dendrogram for Euclidian distances between otolith contours of round goby (n = 786) from nine sampling areas, sampled during three years of study. Stippled line represents five clusters representing pairs of similar sampling sites. It shows that similarity of the sampling sites does not follow the pattern of their allocation chain along the coast of the Black sea visible in fig. 1.
Fig. 1 in Shape Analysis Of Otoliths Of The Round Goby, Neogobius Melanostomus (Gobiiformes, Gobiidae), From The Black Sea Basin
Fig. 1. Map of the study area with sampling localities: 1 — Lake Yalpuh; 2 — Snake Island; 3 — Dniester Estuary; 4 — Gulf of Odesa; 5 — Khadzhibey Estuary; 6 — Tylihul Estuary; 7 — Dnipro-Bug Estuary; 8 — Dzharylhach Bay; 9 — Obytichna Bay of the Sea of Azov.
Fig. 2 in Shape Analysis Of Otoliths Of The Round Goby, Neogobius Melanostomus (Gobiiformes, Gobiidae), From The Black Sea Basin
Fig. 2. Basic morphometric characters used for the shape description of the round goby otoliths. At the internal surface: 1 — dorsal part; 2 — ventral part; 3 — anterior margin; 4 — posterior margin; 5 — rostrum; 6 — pararostrum; 7 — acoustic groove.
Fig. 3 in Shape Analysis Of Otoliths Of The Round Goby, Neogobius Melanostomus (Gobiiformes, Gobiidae), From The Black Sea Basin
Fig. 3. The visualized reconstruction of the round goby otolith contour features predicated upon the first six Principal components (see Material and method for details).
Fig. 1 in Climatic niche defines geographical distribution of Mesobuthus eupeus mongolicus (Scorpiones: Buthidae) in Gobi desert
Fig. 1. Geographic and climatic features for the occurrence sites of Mesobuthus eupeus mongolicus and its suitable distributional areas predicted by ecological niche modeling. A. Field surveying sites (camping sites and stopovers) in Mongolia (dots) and occurrence points (crosses) of M. eupeus mongolicus is projected on the physical map of studied region. B. Scorpion occurring sites is projected on the map of Köppen-Geiger climatic classification. BWk: arid, desert, cold; BSk: arid, steppe, cold; Df(a-c): cold, without dry season; Dw(a-c) cold, dry winter; EF: polar, frost; ET: polar, tundra. C. Suitable distributional areas (red) predicted with MaxEnt basing on 98 presence-only data for M. eupeus mongolicus.
Fig. 4 in First Records of an Estuarine Goby Acentrogobius ocyurus (Gobiiformes: Gobiidae) from Japan and the Sulu Sea in the Philippines
Fig. 4. Map showing the sites where Acentrogobius ocyurus has been recorded. Solid circles represent new records described in the present study; open square represents type locality; open circles are other records in literatures (Jordan and Seale 1907; Herre 1936; Herre and Myers 1937; Fowler 1938; Koumans 1953; Blaber et al. 1990; Lim and Larson 1994; Anonymous 2003; Larson and Lim 2005; Larson et al. 2008; Zhong 2008; Tan et al. 2010; Satapoomin 2011; Ng et al. 2015; Shibukawa 2018); triangles are records in the online databases (Millen 2019; Museum and Art Gallery of the Northern Territory 2019; Western Australian Museum 2019; Australian Museum 2021; European Bioinformatics Institute 2021; Nakae and Shinohara 2021; Orrell 2021; Queensland Museum 2021; Shao 2021; Catania and Fong 2022; UMMZ Fish Division Data Group 2022).
Fig. 1 in First Records of an Estuarine Goby Acentrogobius ocyurus (Gobiiformes: Gobiidae) from Japan and the Sulu Sea in the Philippines
Fig. 1. Fresh specimens of Acentrogobius ocyurus from Manko in Okinawa-jima Island, Japan (A: OCF-P 3494, male, 27.6 mm SL; B: OCF-P 3813, 28.2 mm SL, female) and from Puerto Princesa in Palawan Island, Philippines (C: URM-P 49640, 30.4 mm SL, male).
Fig. 6 in First Records of an Estuarine Goby Acentrogobius ocyurus (Gobiiformes: Gobiidae) from Japan and the Sulu Sea in the Philippines
Fig. 6. Preserved (A–D) and fresh (E) specimens of Acentrogobius ocyurus and related species. A, holotype of Rhinogobius ocyurus (CAS-SU 9249, 30.7 mm SL); B and C, holotype or paratype of Quisquilius malayanus (CAS-SU 30963, B=29.4 mm and C=27.2 mm SL); D, holotype of Ctenogobius kranjiensis (CAS-SU 32999, 29.4 mm SL); E, Acentrogobius sp. "Suzume-haze" (URM-P 49641, 38.6 mm SL).
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International Brain Laboratory public data
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OpenNeuro
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