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2,390 results for “rainforests”
FIGURE 2 in A new species of Phyllodytes (Anura: Hylidae) from the Atlantic Rainforest of southern Bahia, Brazil
FIGURE 2. Phyllodytes amadoi SP. nov. in preservative (holotype, MZUESC 14954, SVL = 20 mm).
FIGURE 2 in Unrealized diversity in an urban rainforest: A new species of Lygosoma (Squamata: Scincidae) from western Sarawak, Malaysia (Borneo)
FIGURE 2. Map of Borneo indicating sampling localities for holotype (red) and paratype (orange).
FIGURE 3 in Unrealized diversity in an urban rainforest: A new species of Lygosoma (Squamata: Scincidae) from western Sarawak, Malaysia (Borneo)
FIGURE 3. Photo in life of the holotype of Lygosoma samajaya sp. nov.
FIGURE 4 in Unrealized diversity in an urban rainforest: A new species of Lygosoma (Squamata: Scincidae) from western Sarawak, Malaysia (Borneo)
FIGURE 4. Preserved holotype (upper) and paratype (lower) of Lygosoma samajaya sp. nov.
Fig. 2 in Nothrolohmannia Baloghi Sp. N. (Acari: Oribatida), From Rainforest In Papua New Guinea, And Reevaluation Of Nothrolohmanniidae
Fig. 2. Nothrolohmannia baloghi sp. n., adult female: ventral aspect. Setae of legs, lateral lips of subcapitulum, and some epimere I setae represented only by dots marking their insertions; detail at
FIGURE 2 in Physical habitat as predictor of fish trophic structure in Brazilian Atlantic rainforest streams
FIGURE 2 | Proportion of fish species richness, biomass, and number of individuals in each trophic group for each sampling point in the Paranapanema river basin, São Paulo state, Brazil.
FIGURE 4 in Physical habitat as predictor of fish trophic structure in Brazilian Atlantic rainforest streams
FIGURE 4 | Biplot of the first two canonical functions showing how substrate composition (SC), mesohabitat variability (MH), and bank stability (BS) correlate with number of individuals of carnivores (NCar), invertivores (NInv), omnivores (NOmn), and herbivorous-detritivores (NHD).
Fig. 6 in Crepuscular and nocturnal hawkmoths (Lepidoptera: Sphingidae) from a fragment of Atlantic rainforest in the state of São Paulo, southeastern Brazil
Fig. 6. Individual-based rarefaction curves, with 95% confidence intervals, of the samplings at the Serra do Japi Biological Reserve (this study; solid line) and at the Boraceia Biological Station (Duarte et al. 2008; dashed line).
Fig. 3 in Crepuscular and nocturnal hawkmoths (Lepidoptera: Sphingidae) from a fragment of Atlantic rainforest in the state of São Paulo, southeastern Brazil
Fig. 3. Fluctuation of richness (A) and relative abundance (B) of the subfamilies during the sampling period.
Fig. 1 in Crepuscular and nocturnal hawkmoths (Lepidoptera: Sphingidae) from a fragment of Atlantic rainforest in the state of São Paulo, southeastern Brazil
Fig. 1. Location of the Serra do Japi Biological Reserve. (A) Brazil with detail showing the state of São Paulo. (B) State of São Paulo with detail of the municipality of Jundiaí. (C) Municipality of Jundiaí and the Serra do Japi Biological Reserve.
Figure 5 from: Studer A, Cardoso de Sousa M, Barcena Goyena B (2018) Breeding biology and nest success of Short-tailed Antthrush Chamaeza campanisona (Aves: Formicariidae) in the Atlantic rainforest of northeastern Brazil. Zoologia 35: 1-8. https://doi.org/10.3897/zoologia.35.e12906
Figure 5 Cumulative number of active nests between 1986–2016 and the average precipitation in Quebrangulo (Agência Nacional de Águas 2009).
Figures 2-4 from: Studer A, Cardoso de Sousa M, Barcena Goyena B (2018) Breeding biology and nest success of Short-tailed Antthrush Chamaeza campanisona (Aves: Formicariidae) in the Atlantic rainforest of northeastern Brazil. Zoologia 35: 1-8. https://doi.org/10.3897/zoologia.35.e12906
Figures 2-4 (2) Detail of C. campanisona nest location; (3) nest and eggs of C. campanisona at cavity bottom; (4) adult of C. campanisona at nest entrance carrying a large quantity of arthropods. All photos by A. Studer on March 2009.
Figure 4 from: Scherz MD, Hawlitschek O, Razafindraibe JH, Megson S, Ratsoavina FM, Rakotoarison A, Bletz MC, Glaw1 F, Vences M (2018) A distinctive new frog species (Anura, Mantellidae) supports the biogeographic linkage of two montane rainforest massifs in northern Madagascar. Zoosystematics and Evolution 94(2): 247-261. https://doi.org/10.3897/zse.94.21037
Figure 4 Photographs of Gephyromantis (Vatomantis) lomorina sp. n. and its habitat in Sorata. (a,d) ZSM 1545/2012; (b,e) ZSM 1547/2012; and (c,f) ZSM 1549/2012, not to scale; (g) habitat where several specimens were found in Sorata, showing (h,i) the appearance of the species in situ whilst calling at night.
Figure 3 from: Scherz MD, Hawlitschek O, Razafindraibe JH, Megson S, Ratsoavina FM, Rakotoarison A, Bletz MC, Glaw1 F, Vences M (2018) A distinctive new frog species (Anura, Mantellidae) supports the biogeographic linkage of two montane rainforest massifs in northern Madagascar. Zoosystematics and Evolution 94(2): 247-261. https://doi.org/10.3897/zse.94.21037
Figure 3 Morphological and chromatic variation among paratypes of Gephyromantis (Vatomantis) lomorina sp. n. from Marojejy in life. (a–b) ZSM 420/2016; (c–d) UADBA 60296; (e–f) UADBA 60295; and (g–h) ZSM 418/2016. Scale bars indicate 2 mm.
Figure 2 from: Scherz MD, Hawlitschek O, Razafindraibe JH, Megson S, Ratsoavina FM, Rakotoarison A, Bletz MC, Glaw1 F, Vences M (2018) A distinctive new frog species (Anura, Mantellidae) supports the biogeographic linkage of two montane rainforest massifs in northern Madagascar. Zoosystematics and Evolution 94(2): 247-261. https://doi.org/10.3897/zse.94.21037
Figure 2 The holotype of Gephyromantis lomorina sp. n., ZSM 419/2016 (ZCMV 15221) in life. (a) Dorsal; (b) ventral; and (c) dorsolateral view. Scale bars indicate 5 mm.
Figure 1 from: Scherz MD, Hawlitschek O, Razafindraibe JH, Megson S, Ratsoavina FM, Rakotoarison A, Bletz MC, Glaw1 F, Vences M (2018) A distinctive new frog species (Anura, Mantellidae) supports the biogeographic linkage of two montane rainforest massifs in northern Madagascar. Zoosystematics and Evolution 94(2): 247-261. https://doi.org/10.3897/zse.94.21037
Figure 1 Preliminary phylogenetic tree of Gephyromantis (Vatomantis) lomorina sp. n., based on Maximum Likelihood analysis of a 532 bp fragment of the mitochondrial 16S rRNA gene. Numbers at nodes indicate bootstrap values in percent (500 replicates, above) and posterior probabilities from a Bayesian Inference analysis (20 million generations, below), shown only if >50 % (bootstrap) or >90 % (posterior probabilities). Each specimen/species is followed by the corresponding GenBank accession number used in the alignment. Schematic drawings of femoral glands of all species in the subgenera Laurentomantis and Vatomantis as well as of G. klemmeri are shown to the right of the phylogeny, and coloured according to the subgenus to which they are assigned.
Figure 5 from: Scherz MD, Hawlitschek O, Razafindraibe JH, Megson S, Ratsoavina FM, Rakotoarison A, Bletz MC, Glaw1 F, Vences M (2018) A distinctive new frog species (Anura, Mantellidae) supports the biogeographic linkage of two montane rainforest massifs in northern Madagascar. Zoosystematics and Evolution 94(2): 247-261. https://doi.org/10.3897/zse.94.21037
Figure 5 Spectrogram (above) and waveform (below) of a call of the holotype of Gephyromantis (Vatomantis) lomorina sp. n., ZSM 419/2016, from Marojejy. (a) A full call (spectrogram shown using FFT of 512 points to visualise call structure); and (b) a 250 ms section from the middle of a call, showing the degree of pulsation of each note (spectrogram shown using FFT of 128 points to visualise note structure).
Figure 6 from: Scherz MD, Hawlitschek O, Razafindraibe JH, Megson S, Ratsoavina FM, Rakotoarison A, Bletz MC, Glaw1 F, Vences M (2018) A distinctive new frog species (Anura, Mantellidae) supports the biogeographic linkage of two montane rainforest massifs in northern Madagascar. Zoosystematics and Evolution 94(2): 247-261. https://doi.org/10.3897/zse.94.21037
Figure 6 Distribution of Gephyromantis (Vatomantis) lomorina sp. n. in northern Madagascar. Areas with diagonal lines are official protected areas. The dotted outline indicates the proposed area with the scope of the WWF protection plan for this part of Madagascar (Biodev Madagascar Consulting 2014, WWF Madagascar 2015). Three arc second SRTM data from Jarvis et al. (2008).
FIGURE 19 in Two new genera of predatory katydids (Orthoptera: Tettigoniidae: Meconematinae) from the Amazon rainforest
FIGURE 19. Geographical records of Arboraptor gen. nov. and Tyrannoraptor gen. nov.
FIGURE 17. Tyrannoraptor arboreus comb. nov., live immatures. A in Two new genera of predatory katydids (Orthoptera: Tettigoniidae: Meconematinae) from the Amazon rainforest
FIGURE 17. Tyrannoraptor arboreus comb. nov., live immatures. A: male; B: female.
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.