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15,460 results for “Neotropical”
Figure 13 in New tribes, overview and checklist of Neotropical Cladonotinae (Orthoptera: Caelifera: Tetrigidae)
Figure 13. Mucrotettix gibbosus Perez-Gelabert, Hierro and Otte, 1998, holotype male. A) Left lateral view. B) Right lateral view. C) Dorsal view, highlighting the shape of the posterior margin of the pronotum (outlined in white). D) Frontal view. E) Labels. Scale bar = 0.5 cm.
Figure 9 in A new Colombian pest species of the genus Poecilocloeus Bruner (Orthoptera: Acrididae: Proctolabinae) on coffee, with a key to the Neotropical species
Figure 9. Accumulated mortality of Poecilocloeus coffeaphilus nymphs with a strain of Metarhizium acridum by the immersion method (T1) and spraying (T2), spraying with a commercial formulation of Metarhizium anisopliae (T3) and control treatment with water (T4).
Figure 7 in A new Colombian pest species of the genus Poecilocloeus Bruner (Orthoptera: Acrididae: Proctolabinae) on coffee, with a key to the Neotropical species
Figure 7. Damage caused by adults of Poecilocloeus coffeaphilus n. sp. on coffee plants. A) Close-up of leaf damage. B) Scrapings on the bark of stems and branches. C) Damage of ripe fruit. D-E) Damage of unripe and near ripe fruits. F) Fruits with the pulp consumed. G) Coffee fruits with the exocarp and pulp completely eaten off and the grains exposed.
Figure 5 in A new Colombian pest species of the genus Poecilocloeus Bruner (Orthoptera: Acrididae: Proctolabinae) on coffee, with a key to the Neotropical species
Figure 5. Different stages of development of Poecilocloeus coffeaphilus n. sp. A) First instar. B) Second instar. C) Third instar. D) Fourth instar. E) Fifth instar. F) Sixth instar. G) Adult male. H) Adult female.
Fig. 6 in Plasticity in the shape and growth pattern of asteriscus otolith of black prochilodus Prochilodus nigricans (Teleostei: Characiformes: Prochilodontidae) freshwater Neotropical migratory fish
Fig. 6. Regressions between radius of each increments and increments growth estimated in Prochilodus nigricans from Solimões (red), Japurá (blue) and Negro (black) Amazon Basin, Brazil.
Fig. 5 in Plasticity in the shape and growth pattern of asteriscus otolith of black prochilodus Prochilodus nigricans (Teleostei: Characiformes: Prochilodontidae) freshwater Neotropical migratory fish
Fig. 5. Canonical variate analysis of the organized data of the analysis cluster. Representation the four different morphotypes of asteriscus otoliths of Prochilodus nigricans. (red cross) Morphotype 3; (blue square) Morphotype 2; (purple asterisk) Morphotype 4; (green ex) Morphotype 1.
Fig. 4 in Plasticity in the shape and growth pattern of asteriscus otolith of black prochilodus Prochilodus nigricans (Teleostei: Characiformes: Prochilodontidae) freshwater Neotropical migratory fish
Fig. 4. Four morphotype asteriscus otolith Prochilodus nigricans established by cluster analysis from the amplitudes of wavelets. a. morphotype 1; b. morphotype 2; c. morphotype 3 and d. morphotype 4 respectively, sampled of rivers Solimões, Japurá and Negro. Scale bars: 1 mm.
Fig. 1 in Plasticity in the shape and growth pattern of asteriscus otolith of black prochilodus Prochilodus nigricans (Teleostei: Characiformes: Prochilodontidae) freshwater Neotropical migratory fish
Fig. 1. Partial map of the Amazon basin showing the study area where Prochilodus nigricans were collected. Rivers: Solimões, Japurá and Negro, Brazil.
Fig. 1 in Divergence in energy sources for Prochilodus lineatus (Characiformes: Prochilodontidae) in Neotropical floodplains
Fig. 1. Map of the floodplain of the Upper Paraná River, highlighting the areas sampled in this study. The subsystems sampled were A = Paraná River, B = Baía River and C = Ivinheima River. The numbers indicate sampled sites in each subsystem.
Fig. 4 in Divergence in energy sources for Prochilodus lineatus (Characiformes: Prochilodontidae) in Neotropical floodplains
Fig. 4. The average percentage contribution of each carbon source in different subsystems. The width of arrows represents the strength of resource utilization in each environment studied (MB = microbial biomass).
Fig. 1 in Preface: How far has Neotropical Ichthyology progressed in twenty years?
Fig. 1. Accumulative curve of valid freshwater species described by year from 1977 to 2017 (last 40 years) in the Neotropical region (based on Reis et al., 2003, and Fricke et al., 2018), showing an increased rate of species description in the beginning of the twenty-first century, and the estimate number of total valid species for the region based on Jackknife 1.
Fig. 7 in The changing course of the Amazon River in the Neogene: center stage for Neotropical diversification
Fig. 7. Growth of mega-wetlands in northern South America. Geological time scale at top. Eustatic sea-level estimates from Zachos et al. (2001). Area estimates of for Atlantic and Caribbean draining mega-wetlands from paleogeographic reconstructions in Wesselingh, Hoorn (2010) and Hoorn et al. (2017), and for the Orinoco basin by Jaramillo et al. (2017). Caribbeandraining Andean foreland basins in orange; Atlantic-draining basins contributing to transcontinental Amazon in yellow. Areas estimated using ImageJ (Abràmoff et al., 2004). Curves smoothed using a third-order Bezier Spline.
Figure 3 in New records and combinations in Neotropical Premnobius Eichhoff (Coleoptera: Curculionidae: Scolytinae: Ipini) with an illustrated key to New World species
Figure 3. Premnobius flechtmanni (Wood), female. A) Dorsal view. B) Lateral view. C) Frontal view. D) Declivity. Photos by T.H. Atkinson.
Fig. 2 in Molecular phylogeny and biogeographic history of the Neotropical tribe Glandulocaudini (Characiformes: Characidae: Stevardiinae)
Fig. 2. Calibrated Bayesian tree based on concatenated dataset (16S+COI+RAG2, 1,829 bp) showing the relationships within the Glandulocaudini. Numbers at branches are posterior probabilities and bootstrap values. Species/populations from Brazilian crystalline shield are highlighted in brown (upland areas) and species/populations from Brazilian coastal drainages in green (lowland areas).
Figure 1-4 in Two new species of Xanthopimpla (Hymenoptera, Ichneumonidae) from Western Amazonia, with a revised key to the Neotropical species of the genus
Figure 1-4. Xanthopimpla amazonica sp. n. 1 Holotype female, lateral view. 2 propodeum, dorsal view. 3 propodeum, lateral view. 4 head, postero-lateral view.
Figure 8. E in Phylogenetic analysis of species of the neotropical social wasp Epipona Latreille, 1802 (Hymenoptera, Vespidae, Polistinae, Epiponini)
Figure 8. E. niger, propodeum, dorsal view. Scale bar = 1.0 mm. Figure 9. E. guerini, propodeum, dorsal view. Scale bar = 1.0 mm. Figure 10. E. niger, head, dorsal view. Scale bar = 1.0 mm. Figure 11. E. guerini, head, dorsal view. Scale bar = 1.0 mm. Figure 12. E. tatua, Tergum II, dorsal view. Scale bar = 1.0 mm. Figure 13. E. media, Tergum II, dorsal view. Scale bar = 1.0 mm.
Figure 1. E in Phylogenetic analysis of species of the neotropical social wasp Epipona Latreille, 1802 (Hymenoptera, Vespidae, Polistinae, Epiponini)
Figure 1. E. quadrituberculata, humeri, dorsal view. Scale bar = 1.0 mm. Figure 2. E. tatua, humeri, dorsal view. Scale bar = 1.0 mm. Figure 3. E. guerini, propodeal concavity, frontal view. Scale bar = 1.0 mm. Figure 4. E. tatua, propodeal cancavity, frontal view. Scale bar = 1.0 mm. Figure 5. E. quadrituberculata, Tergum I, dorsal view. Scale bar = 1.0 mm. Figure 6. E. tatua, Tergum I, dorsal view. Scale bar = 1.0 mm.
Figure 13 in Phylogenetic analysis of species of the neotropical social wasp Epipona Latreille, 1802 (Hymenoptera, Vespidae, Polistinae, Epiponini)
Figure 13. Cladogram of species of Epipona. Character numbers (see table 1) are placed above hash marks, with the state numbers below, separated by ">" to indi- cate the transitions between states. Filled hash marks indicate an uncontroverted step, while open hash marks indicate homoplastic change.
Figs 48–51 in Studies on neotropical Phasmatodea XVIII: Four new species of Lobolibethra Hennemann & Conle, 2007 from Peru and Ecuador (Phasmatodea: "Anareolatae": Diapheromeridae)
Figs 48–51. Lobolibethra tricarinata sp. nov. 48. ♂, PT: dorsal view (MNHN). 49. ♂, PT: lateral view (MNHN). 50. ♂, PT: head and pronotum in lateral view (MNHN). 51. ♂, PT: apex of abdomen in dorsal view (MNHN).
Figs 20–23 in Studies on neotropical Phasmatodea XVIII: Four new species of Lobolibethra Hennemann & Conle, 2007 from Peru and Ecuador (Phasmatodea: "Anareolatae": Diapheromeridae)
Figs 20–23. Lobolibethra mutica (Hennemann & Conle, 2007). 20. ♂ (FH, 0401-1). 21. ♂, apex of abdomen in dorsal view (FH, 0401-1). 22. ♂, apex of abdomen in lateral view (FH, 0401-1). 23. ♂, apex of abdomen in ventral view (FH, 0401-1).
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.