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Fig. 6. 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. 6. Mothocya andoni n. sp. Ƌ (12.0 mm total length, 5.0 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. 8. A in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria
Fig. 8. A, Dorsal view of Mothocya andoni n. sp. holotype ♀ (ovigerous, 15.0 mm total length, 8.0 mm width) (SAMC–A092737) (top) and Mothocya powelli n. sp. holotype ♀ (ovigerous, 7.0 mm total length, 5.0 mm width) (SAMC–A092739) (bottom); B, Ventral view of Mothocya andoni n. sp. holotype ♀ (top) and Mothocya powelli n. sp. holotype ♀ (bottom); C, Dorsal view of Mothocya andoni n. sp. holotype ♀ (left) and Mothocya andoni n. sp. Ƌ (12.0 mm total length, 5.0 mm width) (SAMC–A092738) (right).
Fig. 4 in A new species of the neopterygian fish Enchodus from the Duwi Formation, Campanian, Late Cretaceous, Western Desert, central Egypt
Fig. 4. Majority rule consensus of 222 equally parsimonious trees (TL = 263, CI = 0.53, HI = 0.47, RI = 0.75, and RC = 0.4). Numbers next to branches indicate the percentage of trees in which each clade is present.
Fig. 3 in A new species of the neopterygian fish Enchodus from the Duwi Formation, Campanian, Late Cretaceous, Western Desert, central Egypt
Fig. 3. Digital reconstructions of the aulopiform teleost Enchodus tineidae sp. nov. holotype (MUVP 59) from the Campanian of central Egypt. Right dentary showing its caudal extent, otherwise obscured by matrix, in lateral (A) and medial (B) views. Caudal portion of the left anguloarticular in lateral view (C), showing its dorsal aspect, otherwise obscured by matrix. Right ectopterygoid showing its caudal extent and dorsal aspect, otherwise obscured by matrix, in lateral (D), caudodorsal (E), showing V-shaped trough for articulation with the dermopalatine, and medial (F) views. Abbreviations: d, dentary tooth; E, ectopterygoid tooth; numbers 1–13 indicate tooth position in the respective bone.
Fig. 2 in A new species of the neopterygian fish Enchodus from the Duwi Formation, Campanian, Late Cretaceous, Western Desert, central Egypt
Fig. 2. Aulopiform teleost Enchodus tineidae sp. nov. holotype (MUVP 59) from the Campanian of central Egypt. A, B. Photographs of specimen in lateral (A1) and medial (B1) views; photographs with identifiable elements outlined, in lateral (A2) and medial (B2) views. C. Close up of denticles of the lateral tooth row.
Fig. 5 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 5. Ichthyodectiform fish Cladocyclus geddesi sp. nov. (QM F44329) from near Isisford, central-western Queensland, Australia; Lower Cretaceous (upper Albian) strata of the Winton Formation, area of articulation for the lower jaw. Photograph (A) and interpretive drawing (B). Hatched area indicates broken bone.
Fig. 1 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 1. Map showing the discovery site of Cladocyclus geddesi sp. nov. (QM F44329) near the town of Isisford, central-western Queensland, Australia. Gray area indicates the extent of the upper Albian–lower Turonian Winton Formation.
Fig. 6 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 6. Projection of the hyomandibular facet and angle of the parasphenoid in three ichthyodectiform fishes. A. Cladocyclus gardneri Agassiz, 1841 based on AMNH 19129). B. Aidachar pankowskii (Forey and Cavin, 2007) (after Forey and Cavin 2007: fig. 4). C. Ichthyodectes ctenodon Cope, 1871 after Badack 1965: 14). Also, note differences in proportions of the skull in these ichthyodectiforms. QM F44329 (Cladocyclus geddesi sp. nov.) has the same angle of the parasphenoid as Cladocyclus gardneri.
Fig. 4 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 4. Ichthyodectiform fish Cladocyclus geddesi sp. nov. (QM F44329) from near Isisford, central-western Queensland, Australia; Lower Cretaceous upper Albian) strata of the Winton Formation, braincase in dorsolateral view. Photograph (A) and interpretive drawing (B).
Fig. 3 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 3. Ichthyodectiform fish Cladocyclus geddesi sp. nov. (QM F44329) from near Isisford, central-western Queensland, Australia; Lower Cretaceous (upper Albian) strata of the Winton Formation, in lateral view. Photograph (A) and interpretive drawing (B).
Fig. 7 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 7. Outlines of various ichthyodectiform pectoral girdle (cleithrum, coracoid, and scapular) arrangements in lateral external view. A. Allothrissops mesogaster (Agassiz, 1843) (redrawn from Patterson and Rosen 1977: fig. 10). B. Thrissops formosus Agassiz, 1833 (redrawn from Taverne 1977: fig. 5). C. Unamichthys espinosai Alvarado-Ortega, 2004 (IGM 8373). D. Cladocyclus geddesi sp. nov. (QM F44329). E. Cladocyclus gardneri Agassiz, 1841 (AMNH 11877). F. Vallecillichthys multivertebratum Blanco and Cavin, 2003 (redrawn from Blanco-Piñón 2003: fig. 9.2).
Fig. 8 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 8. Phylogenetic relationships of Cladocyclus geddesi sp. nov. (QM F44329). Stratigraphically calibrated strict consensus of 3 most-parsimonious trees (length 223, CI 0.45, RI, 0.67) analysed using T.N.T. 1.1 (Goloboff et al. 2003), with a heuristic search (1000 replicates in "Traditional search" with TBR branch swapping). See Appendix 1 for new character descriptions, taxon-character matrix, and a list of character state transformation for each taxon. Age ranges correspond to those provided in Cavin et al. (2013).
Fig. 19 in A new species of the ginglymodian fish Isanichthys from the Late Jurassic Phu Kradung Formation, northeastern Thailand
Fig. 19. Phylogenetic hypothesis of ginglymodians interrelationships. A. Strict consensus tree of the 24 most parsimonious tree (305 steps; consistency index = 0.38; retention index = 0.65). All characters are unordered and have equal weight. In brackets are the bootstrap values of the nodes if superior to 50 (3840 replicates) and the Bremer supports if superi- or to 1. B. Relationships between the species of Isanichthys if I. luchowensis is removed from the analysis (strict consensus of three trees, 303 steps, CI = 0.38, RI = 0.65). The rest of the cladogram is similar to A.
Fig. 17 in A new species of the ginglymodian fish Isanichthys from the Late Jurassic Phu Kradung Formation, northeastern Thailand
Fig. 17. Ginglymodian fish Isanichthys lertboosi sp. nov., KS36-2 (holotype); Phu Kradung Formation, Late Jurassic; Kalasin Province, Northeastern Thailand. Caudal fin in right view. All branchings and segmentations of the rays are not drawn, although present, because they are hardly visible on the specimen.
Fig. 18 in A new species of the ginglymodian fish Isanichthys from the Late Jurassic Phu Kradung Formation, northeastern Thailand
Fig. 18. Skull of ginglymodian fish Isanichthys luchowensis sp. nov., cv 002; Early or middle Jurassic of Sichuan, China. A. Photograph. B. Semi-interpretative line drawing.
Fig. 12 in A new species of the ginglymodian fish Isanichthys from the Late Jurassic Phu Kradung Formation, northeastern Thailand
Fig. 12. Ventral views of the snout of the ginglymodian fish Isanichthys lertboosi sp. nov., KS36-2; Phu Kradung Formation, Late Jurassic; Kalasin Province, Northeastern Thailand; showing vormerine and ectopterygoid teeth. Photographs in different angles (A, B) and semi-interpretative line drawing (C).
Fig. 10 in A new species of the ginglymodian fish Isanichthys from the Late Jurassic Phu Kradung Formation, northeastern Thailand
Fig. 10. Snout region and mandible of the ginglymodian fish Isanichthys lertboosi sp. nov., KS34-281; Phu Kradung Formation, Late Jurassic; Kalasin Province, Northeastern Thailand; in left lateral view. A. Photograph. B. Semi-interpretative line drawing.
Fig. 9 in A new species of the ginglymodian fish Isanichthys from the Late Jurassic Phu Kradung Formation, northeastern Thailand
Fig. 9. Part of suspensorium and mandible of the ginglymodian fish Isanichthys lertboosi sp. nov., KS34-281; Phu Kradung Formation, Late Jurassic; Kalasin Province, Northeastern Thailand; in right lateral view. A. Photograph. B. Semi-interpretative line drawing.
Fig. 8 in A new species of the ginglymodian fish Isanichthys from the Late Jurassic Phu Kradung Formation, northeastern Thailand
Fig. 8. Braincase of the ginglymodian fish Isanichthys lertboosi sp. nov., KS34-380; Phu Kradung Formation, Late Jurassic; Kalasin Province, Northeastern Thailand; in left ventrolateral view (the dorsal side faces down) (A), left posteroventral (B), and posterior (C) views. Photographs (A 1 –C 1) and semi-interpretative line drawings (A 2 –C 2). Shaded areas in B 2 and C 2 correspond to matrix.
Fig. 6 in A new species of the ginglymodian fish Isanichthys from the Late Jurassic Phu Kradung Formation, northeastern Thailand
Fig. 6. Skull roof of the ginglymodian fish Isanichthys lertboosi sp. nov., KS36-2; Phu Kradung Formation, Late Jurassic; Kalasin Province, Northeastern Thailand; in dorsal views. A. KS34-380. B. KS36-3. Photographs (A1, B1) and semi-interpretative line drawings (A2, B2).
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
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.