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Fig. 15 in Notes on Oriental Asilidae with six new species from Vietnam (Diptera: Brachycera)
Fig. 15. Damalis tamdaoensis sp. nov., holotype ♂. A, habitus, dorsal view. B, head, lateral view. C, habitus, right lateral view. D, habitus, left laterodorsal view.
Fig. 15 in The lanternflies from Andaman and Nicobar: one new Pyrops species, new records and illustrated key to the species (Hemiptera: Fulgoromorpha: Fulgoridae)
Fig. 15. Penthicodes (Ereosoma) atomaria (Weber, 1801). A–B, South Andaman, New Wandoor, 10 Mar. 2017, 18h30 (© A.V. Mohan).
Fig. 15 in The new stick insect genus Medauromorpha gen. nov. with one new species from Vietnam and notes on Medauroidea Zompro, 2000 (Phasmida: Phasmatidae: Clitumninae)
Fig. 15. Medauromorpha regina (Brunner von Wattenwyl, 1907) comb. nov., in nature. A, mating pair, Ba Be N.P., 2.VII.2015. B, ♀, Cham Chu N.R., 8.VII.2015.
Fig. 15 in Review of the Oriental stick insect genus Trachythorax Redtenbacher, 1908 with two new species from Vietnam and comments on egg parasitism and morphological counteradaptations (Phasmida, Lonchodidae, Necrosciinae)
Fig. 15. Trachythorax yunnanensis Gao & Liang, 2021 stat. nov., ♂ (RBINS). A, habitus, dorsal view. B, habitus, ventral view. C, head and thorax, dorsal view. D, habitus, lateral view. E, head and thorax, dorsolateral view.
Fig. 15. Polydictya affinis Atkinson, 1885 in Polydictya lanternflies of the Indochinese region: Six new species and identification key (Hemiptera: Fulgoromorpha: Fulgoridae)
Fig. 15. Polydictya affinis Atkinson, 1885, holotype ♀ (BMNH). A, habitus, dorsal view; B, habitus, ventral view. C, head, pro- and mesonotum, dorsal view. D, frons, normal view. E, labels.
Figure 3A-F. Migration pathways from French Frigate Shoals breeding site for 15 females and 2 in Ocean pathways and residential foraging locations for satellite tracked green turtles breeding at French Frigate Shoals in the Hawaiian Islands
Figure 3A-F. Migration pathways from French Frigate Shoals breeding site for 15 females and 2 males. The release location is shown with an open star and final tracking position is indicated by a colored circle. Year of tracking is indicated on the map.
Fig. 15 in An early Cambrian fauna of skeletal fossils from the Emyaksin Formation, northern Siberia
Fig. 15. Mollusc Enigmaconus? pyramidalis sp. nov., holotype, internal moulds from lower Cambrian Emyaksin Formation, Bol'shaya Kuonamka River, Anabar Uplift, Siberia; SMNH Mo 167676, sample 7/70. A. Upper view. B. Close-up of A, scaly texture on internal mould. C. Lateral view. D. View on the pegma-like sub-apical structure. E. Close-up of C. F. View on the side opposite to D. Scale bar 300 μm, except B, E, 60 μm.
Fig. 15 in The Hirnantian (Late Ordovician) brachiopod fauna of the East Baltic: Taxonomy of the key species
Fig. 15. Meristellid brachiopods of the genus Hindella from Porkuni Regional Stage, East Baltic, Kuldiga Formation, western Latvia (A–C, E, F) and Ärina Formation, northern Estonia (D). A, E, F. Hindella cf. crassa incipiens (Williams, 1951). A. Ventral valve, GIT 542-273, Aispute-41, depth 991.0 m, exterior (A 1), lateral (A 2), posterior (A 3), and anterior (A 4) views. E. Incomplete dorsal valve, GIT 542-278, Aispute-41, 991.0 m, interior view. F. Incomplete ventral valve, GIT 542-35, Stirnas-18, 907.5 m, interior view. B, C. Hindella sp. B. Ventral valve, GIT 542-34, Stirnas-18, 908.2 m, lateral (B 1) and exterior B 2) views. C. The bedding plane with brachiopods, including Hindella sp., GIT 542-4 (figured in Kaljo et al. 2008), Aispute-41, 998.25 m. D. Hindella cf. cassidea (Dalman, 1828), shell, GIT 542-267, erratics from the Kõnnu village, dorsal (D ) and posterior (D ) views. Scale bars 5 mm.
Fig. 15 in Late Viséan pelagic chondrichthyans from northern Europe
Fig. 15. Ichthyoliths from the upper Viséan of Todowa Grząba, north of Ostrówka Quarry, Gałęzice Region, Holy Cross Mountains, Poland (A–E), Cawdor Quarry, Matlock, Derbyshire, England, UK, sample Cawdor 5 (F–H), and Westenfeld Quarry, Rhenish Mountains, Germany (I–Q). A, F, I. Ctenacanth-type scales. A. MWGUW/Ps/11/24, in coronal view. F. NHMUK PV P73291, in lateral view. I. MWGUW/Ps/11/29, in coronal view. B, O. Hybodont-type scales. B. MWGUW/Ps/11/25, in coronal (B 1) and anterior/lateral (B 1) views. O. MWGUW/Ps/11/30, in anterior (O 1) and coronal/anterior (O 2) views. D, E, L–N. Symmoriiform branchial denticles ("Stemmatias"). D. MWGUW/Ps/11/27, in lateral view. E. MWGUW/Ps/11/26, in coronal view. L. MWGUW/ Ps/11/32, in anterior view. M. MWGUW/Ps/11/31, in lateral view. N. MWGUW/Ps/11/33, in lateral (N 1) and coronal (N 2) views. G, H. Neoselachian (NHMUK PV P73292) and holocephalian (NHMUK PV P73293) placoid scales, in lateral views. C, J. Acanthodes-type acanthodian scales. C. MWGUW/ Ps/11/28, in anterior/coronal view. J. MWGUW/Ps/11/37, in lateral/coronal view. K. Actinopterygian tooth, MWGUW/Ps/11/34, in lateral view. P, Q. Actinopterygian scales in external (P, MWGUW/Ps/11/35) and internal (Q, MWGUW/Ps/11/36) views.
Fig. 15 in The appendicular skeleton of Neuquensaurus, a Late Cretaceous saltasaurine sauropod from Patagonia, Argentina
Fig. 15. Phylogenetic relationships of Archosauriformes, showing main hypotheses of sauropod evolution (adapted from Wilson 2002; Nesbitt et al. 2009; Taylor 2009). Symbols indicate appendicular character evolution according the interpretation given in the present paper. The numbers indicate cladogram nodes as follows: 1, Archosauriformes; 2, Archosauria; 3, Ornithodira; 4, Dinosauromorpha; 5, Dinosauria; 6, Saurischia; 7, Sauropodomorpha; 8, Sauropoda; 9, Eusauropoda; 10, Neosauropoda; 11, Macronaria; 12, Titanosauriformes; 13, Somphospondili; 14, Titanosauria; 15, Saltasauridae; 16, Saltasaurinae.
Fig. 15 in Silicified Mississippian brachiopods from Muhua, southern China: Rhynchonellides, athyridides, spiriferides, spiriferinides, and terebratulides
Fig. 15. Athyridoid brachiopod Cleiothyridina deroissyi (Léveillé, 1835) from the Tornaisian Muhua Formation, southern China. A. Complete juvenile shell, PKUM02−0443, in dorsal (A1), lateral (A2), and anterior (A3) views. B, C. Two almost complete shells, PKUM02−0444 (B) and PKUM02−0445 (C), in dorsal (B1, C1), ventral (B2, C2), and anterior (B3, C3) views, and enlargement of ventral valve showing micro−ornamentation (C4). D. Dorsal valve, PKUM02−0446, viewed externally (D1) and internally (D2). E. Ventral valve, PKUM02−0447, in exterior (E1), interior (E2), and the same inclined anteriorly (E3) views. F. Dorsal valve, PKUM02−0448, in exterior (F1) and interior (F2) views and enlarged view of cardinalia (F3) and corroded surface micro−ornamentation (F4). G. Dorsal valve, PKUM02−0449, interior (G1) and enlarged view of cardinalia (G2). H. Complete shell, PKUM02−0450, in dorsal (H1), ventral (H2), lateral (H3), anterior (H4), and posterior (H5) views, and enlargement showing shell micro−ornamentation (H6). All from sample MH1.
Fig. 15 in Revision of the flexible crinoid genus Ammonicrinus and a new hypothesis on its life mode
Fig. 15. Schematic sketches of different LCEE of the mesistele in uncoiled (above) and coiled positions (below), indicating evolution of perfecting the crown−encasing in coiled position by modifying the extensions form Emsian to Givetian. A. Lateral view of Ammonicrinus kerdreoletensis Le Menn and Jaouen, 2003, showing similar shaped columnals with very short LCEE; thus, the crown is laterally nearly unprotected in coiled position. B. Lateral view of Ammonicrinus wanneri Springer, 1926, with lengthened LCEE of the similar shaped columnals, which lattice−like guarded the crown in coiled position. C. Lateral view of Ammonicrinus sulcatus Kongiel, 1958, showing smaller columnals of the mesistele, which are interconnected with longer ones and afford lateral density of the coiled stem. D. Lateral view of Ammonicrinus doliiformis Wolburg, 1938a (for 1937), showing regularly or irregularly arranged columnals with longer and shorter LCEE, which were interconnected with several columnals showing broadened convex and concave extensions that could interlock in coiled position.
Fig. 15 in New saurichthyid actinopterygian fishes from the Anisian (Middle Triassic) of southwestern China
Fig. 15. Photographs of saurichthyid fish Sinosaurichthys longimedialis gen. et sp. nov. from Middle Triassic of Dawazi Section, Luoping, Yunnan, China. A. Holotype GMPKU−P1927. Left pectoral fin (A1). Skeleton of posterior abdominal and caudal regions (A2). Magnification of squared region (A3) to show fringing fulcra in anal fin. B. Skeleton of posterior abdominal and caudal regions of GMPKU−P1388. Anterior facing left inA1 and right in A2, A3, B.
Fig. 15. Trochotomid gastropod Trochotoma vetusta Terquem, 1855 in Earliest Jurassic patellogastropod, vetigastropod, and neritimorph gastropods from Luxembourg with considerations on the Triassic-Jurassic faunal turnover
Fig. 15. Trochotomid gastropod Trochotoma vetusta Terquem, 1855 from Brouch (Mersch, Grand−Duchy of Luxembourg), Late Hettangian (Schlotheimia angulata Zone, Schlotheimia complanata Subzone), Early Jurassic. A. MNHNL BR704, dorsal (A1), apical (A2), lateral (A3), and apertural (A4) views. B. MNHNL BR754, dorsal (B1), apical (B2), subapertural (B3) views, and detail of the exhalant hole and of the shell seam (B4). C. – MNHNL BR710, apical (C1), dorsal (C2), basal (C3), and apertural (C4) views. D. MNHNL BR361, apertural (D1), basal (D2), dorsal (D3), apical (D4), and lateral (D5) views. E. MNHNL BR705, dorsal (E1) and apical (E2) views, and detail of the exhalant hole and of the shell seam (E3). The arrow indicates the position of the selenizone.
Fig. 15 in Osteology and relationships of Olorotitan arharensis, a hollow-crested hadrosaurid dinosaur from the latest Cretaceous of Far Eastern Russia
Fig. 15. Hadrosaurid dinosaur Olorotitan arharensis Godefroit, Bolotsky, and Alifanov, 2003 (AEHM 2/845, holotype), from the Upper Cretaceous of Kundur (Russia). A. Cranial dorsal vertebra, in cranial (A1) and right lateral (A2) views. B. Caudal dorsal vertebra, in cranial (B1) and left lateral (B2) views. C. Reconstruction of the articulated dorsal series, sacrum, and right pelvic girdle in right lateral view.
Fig. 15 in Fish remains, mostly otoliths, from the non-marine early Miocene of Otago, New Zealand
Fig. 15. Otoliths of marine fishes from the early Miocene Bannockburn Formation and from selected recent fishes for comparison. A. Eeyorius hutchinsi Paulin, 1986, Recent, off Tasmania, 41°00'S–147°23'E, WAM 27564−003, paratype, inner face (A), dorsal view (A). B, C. Lotella rhacina (Bloch and 1 2 Schneider, 1801). B. Recent, of Western Australia, collection W. Schwarzhans, donated by WAM, inner face (B1), dorsal view (B2). C. NMNZ S.52748, Manuherikia River, HH1a, inner face (C1), dorsal view (C2), posterior view (C3), outer face (C4). D. Lactarius sigmoidalis (Frost, 1933), NMNZ S.52749, Manuherikia River, HH1a, inner face (D1), ventral view (D2). E. Bleekeria viridianguilla (Fowler, 1931), Recent, Jakarta, SMF 15768, inner face (E1), ventral view (E2). F, G. Genus aff. Bleekeria sagittiformis (Schwarzhans, 1980), Manuherikia River. F. NMNZ S.52750, HH1b, anterior view (F1), inner face (F2), ventral view (F3). G. NMNZ S.52751, HH1a, inner face.
Fig. 15 in Morphological description and multilocus genotyping of Onchocerca spp. in red deer (Cervus elaphus) in Switzerland
Fig. 15. Dendrogram of Onchocerca from this study, various other Onchocerca sequences and Litomosoides sigmodontis as an outgroup based on a dataset of 579 positions of the mitochondrial cox1 gene, estimated by using the Maximum Likelihood method and TN93 + G + I substitution model (Tamura and Nei, 1993). The tree with the highest log likelihood (– 2902.13) is shown. Bootstrap values over 50 are shown next to the branches. Sequences newly generated in this study are in bold.
Fig. 15 in Emergence and collapse of the Frasnian conodont and ammonoid communities in the Holy Cross Mountains, Poland
Fig. 15. Playfordia primitiva (Bischoff and Ziegler, 1957) from the early Frasnian of Wietrznia Iquarry, sample Wtr−9; elements ZPAL CXVI/1061 (A), 1062 (B), and 1060 (C).
Fig. 15 in Frasnian-Famennian extinction and recovery of rhynchonellid brachiopods from the East European Platform
Fig. 15. Transverse serial sections of Globulirhynchiaminima sp. nov. from the early Famennian, Evlanovo Horizon, Don River basin, Zadonsk region, central Russia.Numbers refer to distances in mm from the top of the ventral umbo. A. CNIGR 15/13076. B. CNIGR 16/13076. C. CNIGR 17/13076.
Figures 15-17. 15 Calonola ectrocta female Thailand LGN893 in Review of the genus Calonola László, Ronkay & Witt, 2010 with description of a new species (Lepidoptera, Nolidae, Nolinae)
Figures 15-17. 15 Calonola ectrocta female Thailand LGN893; 16 Calonola orbiculata holotype female Thailand LGN146; 17 Calonola orbiculata paratype female Indonesia, Sumatra LGN435.
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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)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.