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FIGURE 5. A bifurcating schematic separating species that show a in Description of Luciola aquatilis sp. nov., a new aquatic firefly (Coleoptera: Lampyridae: Luciolinae) from Thailand
FIGURE 5. A bifurcating schematic separating species that show a resemblance to L. aquatilis based on the related 11 species that possess linear elytral punctation.
FIGURE 6 in Separation of Pleuroxus pamirensis (Werestschagin, 1923) from P. annandalei (Daday, 1908) (Cladocera: Chydoridae)
FIGURE 6. Pleuroxus pamirensis, parthenogenetic females from Lake Zorkul (type series of Werestchagin, 1923) (F, H) and from a temporary freshwater body NE of Lake Zorkul (A-E, G, I-L), East Pamirs. (A) Ventral margin of valve. (B-D) Setae at antero-ventral, middle and postero-ventral portion of valve. (E-F) Postabdomen of adult. (G) Postabdominal claw. (H) Postabdomen of juvenile. (I-J) Antenna I and II of adult. (K) Distal portion of limb I. (L) Limb I, inner view. Scale bars: 0.1 mm.
FIGURE 5 in Separation of Pleuroxus pamirensis (Werestschagin, 1923) from P. annandalei (Daday, 1908) (Cladocera: Chydoridae)
FIGURE 5. Pleuroxus pamirensis, parthenogenetic females from Lake Zorkul (type series of Werestchagin, 1923) (A-C, J) and from a temporary freshwater body NE of Lake Zorkul (D-I), East Pamirs. (A-C) Lectotype, lateral, anterior and dorsal view. (D-E) Large adult, lateral and dorsal view. (F) Head, lateral view. (G) Head shield. (H) Tip of rostrum. (I) Dorsal head pores. Scale bars: 0.1 mm.
FIGURE 3 in Separation of Pleuroxus pamirensis (Werestschagin, 1923) from P. annandalei (Daday, 1908) (Cladocera: Chydoridae)
FIGURE 3. Pleuroxus annandalei, parthenogenetic female from Lake Khövsgöl (A-B) Limb I and its distal portion. (C- D) Limb II and distal armature of its gnathobase. (E-F) Limb III and its inner portion. (G-H) Limb IV and its inner portion. (I) Limb V. Scale bars: 0.1 mm.
FIGURE 1 in Separation of Pleuroxus pamirensis (Werestschagin, 1923) from P. annandalei (Daday, 1908) (Cladocera: Chydoridae)
FIGURE 1. Pleuroxus annandalei, parthenogenetic female from Lake Khövsgöl (A-B) Large adult, lateral and dorsal view. (C) Lateral projection of other individual. (D) Head, lateral view. (E-F) Tip of rostrum, anterior view. (G-H) Labrum, lateral view. (I) Head with labrum, ventral view. (J-K) Head shield and its posterior portion. (L) Dorsal head pores. (M) Valve. (N) Anterior portion of valve, external view. (O-P) Same, inner view. (Q) Medium portion of valve. (R-S) Postero-ventral portion of valve. Scale bars: 0.1 mm.
FIGURE 4 in Separation of Pleuroxus pamirensis (Werestschagin, 1923) from P. annandalei (Daday, 1908) (Cladocera: Chydoridae)
FIGURE 4. Pleuroxus annandalei, juvenile female from Lake Khövsgöl (A-E) and Achit Nuur (F-G), both in Mongolia. (A) General view. (B) Labrum. (C-D) Postabdomen and postabdominal claw. (E) antenna I. (F-G) Postabdomen and postabdominal claw. Scale bars: 0.1 mm.
FIGURE 2 in Separation of Pleuroxus pamirensis (Werestschagin, 1923) from P. annandalei (Daday, 1908) (Cladocera: Chydoridae)
FIGURE 2. Pleuroxus annandalei, parthenogenetic female from Lake Khövsgöl (A-B) Postabdomen. (C-D) Postabdominal claw, external view. (E-F) Antenna I. (G-I) Antenna II, its endopod and apical swimming seta. Scale bars: 0.1 mm.
FIGURE 7. Spiophanes uschakowi Zachs, 1933 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 7. Spiophanes uschakowi Zachs, 1933: A. Anterior end, dorsal view. B. Chaetiger 5–12, lateral view; arrow indicates simple vertical opening of glandular organ in chaetiger 11. C. Neuropodial hooks with reduced hood from chaetiger 19. — All Syntype, RAS 1/25826. Scale: A, B 0.5 mm; C 10 µm.
FIGURE 8 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 8. First presence of neuropodial hooks in relation to body width on chaetiger 4 in both Spiophanes bombyx and S. norrisi sp. nov.
FIGURE 5 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 5. Spiophanes norrisi sp. nov.: A. Anterior end, dorsal view; methyl green stained nuchal and dorsal ciliated organs. B. Anterior end, lateral view; methyl green stained openings of glandular organs on chaetigers 5, 7, and 8; arrow indicates simple vertical opening of glandular organ in chaetiger 14. C–F. Parapodium from chaetiger 2, 5, 11, and 19, all anterior view. G. Neuropodial hooks with reduced hood from chaetiger 19. H. Neuropodial chaeta from chaetiger 5. I. Sabre chaeta from chaetiger 11. K. Neuropodial chaeta from chaetiger 2. — B = LACM–AHF V. 1962–50 (Paratype); all others LACM–AHF V5102. Scale: A, B 0.5 mm, C–F 0.1 mm. G–K 5 µm.
FIGURE 2 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 2. Spiophanes bombyx (Claparède, 1870): A. Anterior end, dorsal view. B. Chaetigers 9–15 with dorsal ciliated organs and dorsal ciliated crests, dorsal view. — Specimens from the North Sea, German Bight, depth 24 m, leg. K. Meißner, Jul 2008. Scale: in µm.
FIGURE 10 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 10. Phylogenetic relationships among five Spiophanes species based on partial mitochondrial and nuclear sequences. A. Maximum–likelihood bootstrap consensus tree (1000 replicates) based on COI haplotypes. Numbers above branches are likelihood bootstrap values; numbers below branches are Bayesian posterior probabilities and parsimony consensus percentages. Trees are rooted using sequences of Prionospio as outgroup (P. steenstrupi EU835668; Prionospio sp.1 EU835667). B. Maximum–parsimony bootstrap consensus tree (1000 replicates) based on 18S haplotypes. Numbers above branches are parsimony bootstrap values; numbers below branches are Bayesian posterior probabilities and likelihood bootstrap percentages. Trees are rooted using sequences of Prionospio as outgroup (P. ehlersi EU340095; P. dubia EU418859).
FIGURE 3 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 3. Spiophanes bombyx (Claparède, 1870): Chaetiger 10–18, dorsal view, methyl green stained nuchal organs. — Specimen from Turkey, Iskenderum Bay, sublittoral, leg. E. Dagli, Sep 2005. Scale: 0.5 mm.
FIGURE 4 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 4. Spiophanes bombyx (Claparède, 1870): A. Chaetigers 4–9 with openings of glandular organs on chaetigers 5, 7, 8, 9, lateral view. B. Neuropodial hooks from chaetiger 16, dorsal apical view. C. Chaetigers 9–11, lateral view. D. Posterior end with stout curved notochaeta, dorsal view. — A, B, D specimens from the North Sea, German Bight, depth 24 m, leg. K. Meißner, Jul 2008; C specimen from the Gulf of Naples, depth 20 m, leg. P. Lanera, March 2005. Scale: in µm.
FIGURE 9 in Spiophanes norrisi sp. nov. (Polychaeta: Spionidae) — a new species from the NE Pacific coast, separated from the Spiophanes bombyx complex based on both morphological and genetic studies
FIGURE 9. Number of neuropodial hooks in relation to body width on chaetiger 4 in both Spiophanes bombyx and S. norrisi sp. nov.
FIGURE 3 in On the identity of Isoperla curtata (Plecoptera: Perlodidae): behavioural and molecular approaches show the existence of two separate species
FIGURE 3. Time intervals between beats in a male drumming call from a southern population (Arroyo de la Nava del Rey).
FIGURE 6 in On the identity of Isoperla curtata (Plecoptera: Perlodidae): behavioural and molecular approaches show the existence of two separate species
FIGURE 6. Isoperla morenica sp. n. Head and pronotum (a), ventral view of the male abdomen (b), penial armature (c), detail of the penial armature showing the scales (d), and ventral view of the tip of female abdomen (e).
FIGURE 9 in A new species of fiddler crab from the Ogasawara (Bonin) Islands, Japan, separated from the widely-distributed sister species Uca (Paraleptuca) crassipes (White, 1847) (Crustacea: Decapoda: Brachyura: Ocypodidae)
FIGURE 9. Genealogical network for the control region haplotypes observed within the clades of Uca crassipes (White, 1947) (collected from the Ryukyus, Taiwan, the Philippines, Guam, Indonesia, Cocos-Keeling, New Caledonia and Polynesia) and U. boninensis sp. nov. (from Ogasawara Is.). The ancestral haplotype, or root of the network, is indicated by a square. Unlabelled nodes indicate inferred haplotypes not found in the sampled population.
FIGURE 8. A in A new species of fiddler crab from the Ogasawara (Bonin) Islands, Japan, separated from the widely-distributed sister species Uca (Paraleptuca) crassipes (White, 1847) (Crustacea: Decapoda: Brachyura: Ocypodidae)
FIGURE 8. A minimum evolution (ME) tree for Uca crassipes (White, 1947), U. boninensis sp. nov., U. splendida (Stimpson, 1858) and U. chlorophthalmus (H. Milne Edwards, 1837), based on the combined cytochrome oxidase I and control region genes. Probability values at the nodes represent support values for ME, maximum parsimony (MP) and maximum likelihood (ML). For haplotype names, see Table 1. "*" means the haplotype is heteroplasmic obtained by cloning.
FIGURE 7 in A new species of fiddler crab from the Ogasawara (Bonin) Islands, Japan, separated from the widely-distributed sister species Uca (Paraleptuca) crassipes (White, 1847) (Crustacea: Decapoda: Brachyura: Ocypodidae)
FIGURE 7. Morphology of different sizes of male Uca chlorophthalmus (H. Milne Edwards, 1837) (CHL), U. crassipes (White, 1847) (CRA), U. boninensis sp. nov. (BON) and U. splendida (Stimpson, 1858) (SPL). A, CHL: CW 13.1 mm (Kenya; NCHUZOOL 13498), CRA: 13.1 mm (Cocos-Keeling; ZRC), BON: 13.0 mm (Ogasawara Is.; CBM 11245) and SPL: 13.0 mm (New Taipei, Taiwan; NCHUZOOL 13446). B, CHL: 19.2 mm (Mayotte; MNHN-IU-2011-5600), CRA: 19.1 mm (Philippines; NCHUZOOL 13473), BON: 18.8 mm (Ogasawara Is.; CBM-ZC 11245) and SPL: 19.2 mm (Penghu, Taiwan; NCHUZOOL 13456). C, CRA: 23.1 mm (Dongsha, Taiwan; NCHUZOOL 13464); BON: 21.6 mm (Ogasawara Is.; CBM-ZC 11245) and SPL: 23.5 mm (Penghu, Taiwan; NCHUZOOL 13488). Some males' chelae are separated from the body.
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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.