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753 results for “Brazilian Atlantic forest”
FIGURE 14 in The herpetofauna of the Serra do Urubu mountain range: a key biodiversity area for conservation in the brazilian atlantic forest
FIGURE 14: Reptile species recorded at the Serra do Urubu mountain range. (A) Amerotyphlops arenensis, (B) Crotalus durissus, (C) Lachesis muta.
FIGURE 13 in The herpetofauna of the Serra do Urubu mountain range: a key biodiversity area for conservation in the brazilian atlantic forest
FIGURE 13: Reptile species recorded at the Serra do Urubu mountain range. (A) Philodryas olfersii (Photo by C.O. Gussoni), (B) Pseudoboa nigra, (C) Sibynomorphus sp. (D) Taeniophallus affinis, (E) Xenodon sp. (Photo by C.O. Gussoni), (F) Xenopholis scalaris, (G) Micrurus sp. (H) Micrurus lemniscatus carvalhoi.
FIGURE 9 in The herpetofauna of the Serra do Urubu mountain range: a key biodiversity area for conservation in the brazilian atlantic forest
FIGURE 9: Reptile species recorded at the Serra do Urubu mountain range. (A) Amphisbaena alba, (B) Amphisbaena pretrei, (C) Norops fuscoauratus, (D) Dactyloa punctata, (E) Diploglossus lessonae (juvenile), (F) Diploglossus lessonae (adult), (G) Ophiodes sp. (H) Hemidactylus mabouia (Photo by C.O. Gussoni).
FIGURE 7 in The herpetofauna of the Serra do Urubu mountain range: a key biodiversity area for conservation in the brazilian atlantic forest
FIGURE 7: Amphibians species recorded at the Serra do Urubu mountain range. (A) Proceratophrys renalis, (B) Lithobates palmipes, (C) Pristimantis ramagii, (D) Pristimantis sp.
FIGURE 5 in The herpetofauna of the Serra do Urubu mountain range: a key biodiversity area for conservation in the brazilian atlantic forest
FIGURE 5: Amphibians species recorded at the Serra do Urubu mountain range. (A) Scinax eurydice, (B) Scinax fuscomarginatus, (C) Scinax x-signatus pattern 1, (D) Scinax clade ruber, (E) Scinax nebulosus, (F) Scinax pachycrus, (G) Scinax x-signatus pattern 2, (H) Adenomera cf. hylaedactyla.
FIGURE 4 in The herpetofauna of the Serra do Urubu mountain range: a key biodiversity area for conservation in the brazilian atlantic forest
FIGURE 4: Amphibians species recorded at the Serra do Urubu mountain range. (A) Boana faber, (B) Boana freicanecae, (C) Boana raniceps (Photo by C.O. Gussoni), (D) Boana semilineata, (E) Phyllodytes edelmoi, (F) Phyllodytes gyrinaethes, (G) Pithecopus nordestinus, (H) Scinax auratus.
FIGURE 12 in The herpetofauna of the Serra do Urubu mountain range: a key biodiversity area for conservation in the brazilian atlantic forest
FIGURE 12: Reptile species recorded at the Serra do Urubu mountain range. (A) Tantilla melanocephala, (B) Atractus potschi, (C) Dipsas sazimai, (D) Erythrolamprus aesculapii (Photo by C.O. Gussoni), (E) Imantodes cenchoa, (F) Leptodeira annulata, (G) Oxyrhopus petolarius (Photo by C.O. Gussoni), (H) Oxyrhopus trigeminus.
Fig.3 in Biodiversity survey, ecology and new distribution records of Marchantiophyta in a remnant of Brazilian Atlantic Forest
Fig.3. Graphical representation of substrates colonized by liverwort species in the fragment of dense montane ombrophilous forest studied in the National Park of Boa Nova, Bahia, Brazil.
Fig. 3 in Avian Assemblages in Forest Fragments do not Sum to the Expected Regional Community in the Brazilian Atlantic Forest.
Fig. 3. The number of local Atlantic Forest species by forest fragment size (log10 scales), showing that the number increases with fragment size (F = 13.4, r2 = 0.625, p = 0.0065).
Fig. 2 in Avian Assemblages in Forest Fragments do not Sum to the Expected Regional Community in the Brazilian Atlantic Forest.
Fig. 2. Numbers of species and similarities (PCoA) among the 10 Atlantic Forest fragments in southern Bahia, Brazil. A) Species accumulation curves, illustrating that with over 5000 sightings, the predicted total number of species had not been reached in any fragment, or in all fragments combined. Also, the similarity of the curves and their lack of a relationship with fragment size suggests that all fragments are similar with respect to accumulation of species. Note that both axes are log10 scaled. B) Principal Coordinate Analysis, using Bray similarities, illustrating that similarity among fragments was always low. Larger symbols indicate fragment centroids, and each smaller point indicates a sample list of species (see text). No particular pattern is evident, and all fragments are variable and do not form groups based on fragment size.
Fig. 4 in Avian Assemblages in Forest Fragments do not Sum to the Expected Regional Community in the Brazilian Atlantic Forest.
Fig. 4. Functional diversity analysis comparing different-sized fragments and functional evenness, dispersion, and divergence. A–C: Black squares and lines indicate the Atlantic Forest expected regional assemblage, circles and lines indicate the observed assemblages, with blue indicated only the Atlantic Forest species, and the open circle indicates all observed species (all based on presence-absence). D–F: estimated from presence-absence data of the expected local assemblage that were absent from the fragment. Regression results are presented in table 3.
Figs 1–9 in Guaricicana, a new genus of Hyalojassini (Hemiptera: Cicadellidae: Iassinae) from the Brazilian Atlantic Forest
Figs 1–9. Guaricicana borgesi gen. et sp. nov., holotype, ♂ (DZUP 215374). External morphology. 1. Head and thorax, dorsal view. 2. Head and thorax, ventral view. 3. Head and thorax, lateral view. 4. Fore wing. 5. Hind wing. 6. Fore leg, anterior view. 7. Hind femur, anterior view. 8. Hind tibia, anterior view. 9. Hind tarsus, ventral view. Scale bars: 1–7 = 1.0 mm; 8–9 = 0.5 mm.
Figs 10–20 in Guaricicana, a new genus of Hyalojassini (Hemiptera: Cicadellidae: Iassinae) from the Brazilian Atlantic Forest
Figs 10–20. Guaricicana borgesi gen. et sp. nov., holotype, ♂ (DZUP 215374), terminalia. 10. Sternite VIII, ventral view. 11. Pygofer, dorsal view. 12. Pygofer and subgenital plate, lateral view. 13. Ventral process of pygofer, lateral view. 14. Ventral process of pygofer, ventral view. 15. Subgenital plate, ventral view. 16. Connective, dorsal view. 17. Style, dorsal view. 18. Style, lateral view. 19. Aedeagus, lateral view. 20. Aedeagus, ventral view. Scale bars: 10–12, 15, 17–18 = 0.5 mm; 13–14, 16, 19–20 = 0.25 mm.
Figs 28–29 in Guaricicana, a new genus of Hyalojassini (Hemiptera: Cicadellidae: Iassinae) from the Brazilian Atlantic Forest
Figs 28–29. Guaricicana borgesi gen. et sp. nov., holotype, ♂ (DZUP 215374). 28. Dorsal habitus. 29. Lateral habitus. Scale bars = 1 mm.
Figs 21–27 in Guaricicana, a new genus of Hyalojassini (Hemiptera: Cicadellidae: Iassinae) from the Brazilian Atlantic Forest
Figs 21–27. Guaricicana borgesi gen. et sp. nov., paratype, ♀ (DZUP 215378), terminalia. 21. Sternite VII, ventral view. 22. Pygofer, lateral view. 23. First valvifer and first valvula, lateral view. 24. Apex of first valvula, lateral view. 25. Second valvula, lateral view. 26. Apex of second valvula, lateral view. 27. Gonoplac, lateral view. Scale bars = 0.5 mm; 24, 26 = not to scale.
Fig. 2 in Spatial variation of dung beetle assemblages associated with forest structure in remnants of southern Brazilian Atlantic Forest
Fig. 2. Principal coordinates analysis (PCoA) of dung beetle species based on Bray–Curtis similarity and environmental variables based on Euclidean distance. The analysis was performed using presence–absence (a), abundance (b) and biomass (c) data of dung beetles, and 15 environmental variables (d). ANH: Anhatomirim Environmental Protection Area; ITA: Permanent Protection Areas of Itapema; PER: Peri Lagoon Municipal Park; RAT: Permanent Protection Areas of Ratones.
Fig. 2 in Dung beetle (Coleoptera, Scarabaeidae) assemblage of a highly fragmented landscape of Atlantic forest: from small to the largest fragments of northeastern Brazilian region
Fig. 2. Non-Metric Multidimensional Scaling (NMDS) ordination of fragments of Trapiche, CIMNC and Coimbra, based on dung beetle species composition.
Figure 1Sampling site and stations.1A in Living in the sunlight: micro-environments with higher exposure of sunlight have more abundance and diversity of Hymenoptera in a Brazilian Atlantic Forest fragment
Figure 1Sampling site and stations.1A) Study area including the RAPELD modules.Each black point represents a permanent plot.1B) Trap-nest stations and selected micro-environments: treefall gap (A), placed in wooden post at 1.5m height; understory (B), placed in a tree branch at approximately 1.5 meters height; canopy (C), suspended with thread in a tree (height between 19.0 and 9.1 meters).
Figure 2 in Living in the sunlight: micro-environments with higher exposure of sunlight have more abundance and diversity of Hymenoptera in a Brazilian Atlantic Forest fragment
Figure 2 Interpolation curves of the richness and diversity of trap-nesting Hymenoptera (Atlantic forest, Brazil) in relation to the lowest observed abundance brood cells sampled and assessed for three Hill numbers (0, 1 e 2). CAN= canopy; GAP= treefall gap; UND= Understory.
Figure 1 in Comparative evaluation of taxonomic and functional diversities of leaf-litter ants of the Brazilian Atlantic Forest
Figure 1. Map of the study area in the state of Bahia (A), Brazil (B), showing the locations of the 65 Atlantic Forest sites (C).
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Allen Brain Atlas
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International Brain Laboratory public data
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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.