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Fig. 4 in The bony fishes (Teleostei) caught by industrial trawlers off the Brazilian North coast, with insights into its conservation
Fig. 4. Species of the order Anguilliformes, family Heterenchelyidae, (A) Pythonichthys sanguineus, MPEG 35269, 493 mm TL, family Moringuidae, (B) Neoconger sp., AZUSC 4931, 254 mm TL, family Muraenidae, (C) Enchelycore nigricans, AZUSC 5432, 298 mm TL, (D) Gymnothorax conspersus AZUSC 5059, 326 mm TL, (E) Gymnothorax ocellatus AZUSC 5069, 464 mm TL, family Ophichthidae, (F) Aplatophis chauliodus not calaloged, 520 mm TL, (G) Echiophis punctifer MPEG 35510, 932 mm TL, (H) Ophichthus cylindroideus MPEG 35152, 645 mm TL, (I) Ophichthus ophis AZUSC 5179, 1052 mm TL.
Fig. 8 in The bony fishes (Teleostei) caught by industrial trawlers off the Brazilian North coast, with insights into its conservation
Fig. 8. Species of the ordem Perciformes, family Centropomidae, (A) Centropomus ensiferus MPEG 35060, 352 mm TL, family Serranidae, (B) Alphestes afer MPEG 35142, 174 mm TL, (C) Cephalopholis fulva not cataloged, 240 mm TL, (D) Diplectrum radiale MPEG 35149, 221 mm TL, (E) Epinephelus morio AZUSC 5428, 368 mm TL, (F) Hyporthodus nigritus not cataloged, 140 mm TL, (G) Hyporthodus niveatus MPEG 35841, 113 mm TL, (H) Mycteroperca bonaci not cataloged, 420 mm TL, (I) Paralabrax dewegeri AZUSC 5183, 70 mm TL, (J) Paranthias furcifer not cataloged, 270 mm TL, (K) Serranus flaviventris AZUSC 5103, 71 mm TL, (L) Serranus phoebe, AZUSC 5526, 116 mm TL, family Opistognathidae, (M) Lonchopisthus higmani, not cataloged, 80 mm TL, family Priacanthidae, (N) Priacanthus arenatus MPEG 35707 323 TL, family Malacanthidae, (O) Caulolatilus guppyi AZUSC 5668, 180 mm TL, (P) Malacanthus plumieri not cataloged, 420 mm TL, family Pomatomidae, (Q) Pomatomus saltatrix not cataloged, 380 mm TL, family Echeneidae, (R) Echeneis naucrates MPEG 35159, 296 mm TL.
Fig. 2 in Organization of fish assemblages in blackwater Atlantic Forest streams
Fig. 2. Rarefaction curves calculated for each mesohabitat category (sand, leaf-litter and trunks), considering a total of 31 mesohabitats sampled in 13 blackwater streams of the alluvial plain of the Serra do Mar in the State of São Paulo. EstimateS 9.1 was used to plot species rarefaction curve (100 runs).
Fig. 3 in Genetic diversity and population structure of Brycon nattereri (Characiformes: Bryconidae): a Neotropical fish under threat of extinction
Fig. 3. Haplotype network based on partial sequencing of the D-loop region (mtDNA) of 92 individuals of Brycon nattereri from the Laranjinha River. Circle sizes are pro- portional to haplotype frequency.
Figs 22–29 in Three new Cryptochetum Rondani, 1875 (Diptera: Cryptochetidae) from Yunnan Province, China and an identification key to Chinese species
Figs 22–29. Wings of eight species of Cryptochetum. 22. C. curvatum Yang & Yang, 1996. 23. C. deltatum Yang & Yang, 1996. 24. C. tianmuense Yang & Yang, 2001. 25. C. acutulum Yang & Yang, 1996. 26. C. zalatilabium Xi & Yang, 2015. 27. C. kunmingense Yang & Yang, 1996. 28. C. fanjingshanum Yang & Yang, 1988. 29. C. maolanum Yang & Yang, 1996. Scale bar = 0.1 mm
Figs 15–17 in Three new Cryptochetum Rondani, 1875 (Diptera: Cryptochetidae) from Yunnan Province, China and an identification key to Chinese species
Figs 15–17. Cryptochetum longilingum sp. nov., holotype (CR154), ♂. 15. Head, lateral view. 16. Head, dorsal view. 17. Wing, dorsal view. Scale bar = 0.1 mm.
Figs 8–10 in Three new Cryptochetum Rondani, 1875 (Diptera: Cryptochetidae) from Yunnan Province, China and an identification key to Chinese species
Figs 8–10. Cryptochetum glochidiatusum sp. nov., holotype, ♂ (CR122). 8. Head, lateral view. 9. Head, dorsal view. 10. Wing, dorsal view. Scale bar = 0.1 mm.
Figs 1–3 in Three new Cryptochetum Rondani, 1875 (Diptera: Cryptochetidae) from Yunnan Province, China and an identification key to Chinese species
Figs 1–3. Cryptochetum euthyiproboscise sp. nov., holotype, ♂ (CR101). 1. Head, lateral view. 2. Head, dorsal view. 3. Wing, dorsal view. Scale bar = 0.1 mm.
Figs 11–14 in Three new Cryptochetum Rondani, 1875 (Diptera: Cryptochetidae) from Yunnan Province, China and an identification key to Chinese species
Figs 11–14. Cryptochetum glochidiatusum sp. nov., holotype, ♂ (CR122). 11. Dorsal view. 12. Lateral view. 13. Dorsal view. 14. Lateral view. Scale bars: 11–12 = 0.1 mm; 13–14 = 0.05 mm.
Fig. 7 in Thoridae (Crustacea: Decapoda) can penetrate the Abyss: a new species of Lebbeus from the Sea of Okhotsk, representing the deepest record of the family
Fig. 7. Phylogenetic relationships within Thoridae (Hippolyte Leach, 1814 as outgroup) based on COI mtDNA gene markers. Bootstrap support (> 50%) is shown by the numbers along the branches (BA/ML analysis). Line thickness is also correlated with support values.
Fig. 4 in Thoridae (Crustacea: Decapoda) can penetrate the Abyss: a new species of Lebbeus from the Sea of Okhotsk, representing the deepest record of the family
Fig. 4. Lebbeus sokhobio sp. nov., ♀ from st. 4-3 (paratype, ZMMU Ma6097) (A–H, J–K, M) and ♂ from st. 4-9 (paratype, SMF 51579) (I, L). A. Basal segments of pereiopods I–III. B. Maxilliped III. C. Antepenultimate segment of maxilliped III. D. Pereiopod I. E. Chela of pereiopod I. F. Proximal segments of pereiopod I. G. Pereiopod II. H. Pereiopod III. I. Merus of pereiopod III. J. Dactylus of pereiopod III. K. Pereiopod IV. L. Merus of pereiopod IV. M. Pereiopod V.
Fig. 2 in Thoridae (Crustacea: Decapoda) can penetrate the Abyss: a new species of Lebbeus from the Sea of Okhotsk, representing the deepest record of the family
Fig. 2. Lebbeus sokhobio sp. nov., general view, ♀ from st. 4-3 (paratype, ZMMU Ma6097) and ♂ from st. 4-9 (paratype, SMF 51579).
Fig. 3 in Thoridae (Crustacea: Decapoda) can penetrate the Abyss: a new species of Lebbeus from the Sea of Okhotsk, representing the deepest record of the family
Fig. 3. Lebbeus sokhobio sp. nov., ♀ from st. 4-3 (paratype, ZMMU Ma6097) (A–I) and ♂ from st. 4-10 (paratype, MIMB 39426) (J–K). A–B. Anterior part of carapace. C. Abdominal pleonites IV–V, lateral view. D–E. Antennula. F. Antenna. G. Telson and uropods. H. Distal margin of telson. I. Distolateral margin of exopod. J. Endopod of pleopod I. K. Endopod of pleopod II.
Figs 26–32 in Review of the Anthelephila maindroni complex, and description of four new species from the Indian subcontinent (Coleoptera: Anthicidae)
Figs 26–32. Anthelephila strigosa (Heberdey, 1934), male, Hambantota (ZKDC): 26 – front leg; 27 – sternum VII; 28 – median process of sternum VII, laterally; 29 – tergum VII; 30 – prong of sternite VIII; 31 – tergite VIII; 32 – apical portion of tegmen. Scale (0.5 mm): A – Fig. 19; B – Figs 15, 16; C – Figs 14, 17. (0.2 mm): C – Figs 18, 20.
Fig. 2 in Comparative cytogenetics of Astyanax (Teleostei: Characidae) from the upper Paraguay basin
Fig. 2. Karyotypes of Astyanax abramis (A and B), A. lacustris (C and D) and A. pirapuan (E and F) after Giemsa-stained and showing the distribution of constitutive heterochromatin revealed by C-banding. Insets show Ag-NOR and 18S-bearing chromosomes pairs. Scale bar = 10 µm.
Figs 33–38. 33–36 in Review of the Anthelephila maindroni complex, and description of four new species from the Indian subcontinent (Coleoptera: Anthicidae)
Figs 33–38. 33–36 – habitus: 33 – Anthelephila feminea sp. nov. (holotype); 34 – A. maindroni (Pic, 1903), Pondicherry (NHMW); 35 – A. sahyadrica sp. nov. (holotype); 36 – A. semistrigosa sp. nov. (holotype). 37–38 – antenna of females: 37 – A. feminea sp. nov. (holotype); 38 – A. maindroni, Hambantota (ZKDC). Scale (0.5 mm): Figs 37, 38.
Fig. 3 in Use of a nursery area by cownose rays (Rhinopteridae) in southeastern Brazil
Fig. 3. Methods to collect data of individuals: (top) information provided by fishermen (reports, pictures, and videos) and (down) field sampling by researchers.
Fig. 2. Relationships concentration x in Anesthesia of tambaqui Colossoma macropomum (Characiformes: Serrasalmidae) with the essential oils of Aniba rosaeodora and Aniba parviflora and their major compound, linalool
Fig. 2. Relationships concentration x anesthesia induction or recovery time in tambaqui, Colossoma macropomum, exposed to the linalools. a. synthetic linalool; light sedation: y=4.4+(4281/x), r2=0.716, deep sedation: y=-22.5+(12252/x), r2=0.773, deep anesthesia:y=15.3+(17878/x), r2=0.669, recovery: y=43.9+0.66x+0.0015x2, r2=0.712. b. linalool extracted from Aniba rosaeodora; deep sedation: y=29.0+(6010/x), r2=0.784, deep anesthesia: y=-151.3+(60541/x), r2=0.873. Light sedation and recovery: no significant relationship. y = time to reach stage or recovery (s) and x = concentration (µL L-1).
Fig. 3 in Histopathological alterations in Astyanax bifasciatus (Teleostei: Characidae) correlated with land uses of surroundings of streams
Fig. 3. Photomicrograph of liver of Astyanax bifasciatus in streams of the basin of the lower Iguaçu River. a. Normal liver, central vein (CV), and sinusoids capillary (S) in forest stream (F1). b. Tubular arrangement of hepatocytes (H), nucleus (arrow), nucleolus (head of arrow), and centrilobular vein (*) in forest stream (F1); c. Pancreatic tissue (*), presence of eosinophils around the hepatopancreas tissue (arrow) in forest stream (F2). d. Presence of picnotic nucleus (head of arrow) and nuclear hypertrophy (arrow) in rural stream (R2). e. Cytoplasmic degeneration (*), the picnotic nucleus (arrow), the nucleus in a lateral position (head of arrow) in urban stream (U2). f. Picnotic nucleus (head of arrow) and cytoplasmic vacuolization (*) in rural stream (R2). g. Leukocyte infiltration (arrow) in urban stream (U1). h. Melanomacrophage aggregates (arrows) around the central vein (CV) in urban stream (U2). Stained Hematoxylin Harris and eosin.
Fig. 3 in Water temperature affects aggressive interactions in a Neotropical cichlid fish
Fig. 3. Mean ± SE of initial (third day) and final (eighth day) frequencies of a. restrained aggression and b. overt aggression of group-housed fish. Different letters show differences among treatments. Mixed Model ANOVA completed by Fisher-LSD post hoc test.
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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.