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Fig. 1 in Daily and seasonal activity patterns of a felid assemblage in a forest-grassland mosaic in southern Brazil
Fig. 1. Study area: Papagaios-de-Altitude Private Protected Area in Urupema, Santa Catarina, Brazil. On the top-right panel, colors indicate the type of soil-use in the area and its limits. The black dots in the map indicate the location of the camera traps.
Fig. 3 in Daily activity patterns and occurrence of Leopardus guttulus (Carnivora, Felidae) in Lami Biological Reserve, southern Brazil
Fig. 3. Temporal overlap of Leopardus guttulus (Hensel, 1872) activity during the different seasons: autumn/winter and spring/summer; the gray area represents the overlap between the activity observed in the two periods of the year and the vertical lines represent sunrise and sunset in each period (autumn/winter: 06h 45min sunrise and 18h 05min sunset; spring/summer: 06h 08min sunrise and 19h 33min sunset).
Fig. 4 in Daily activity patterns and occurrence of Leopardus guttulus (Carnivora, Felidae) in Lami Biological Reserve, southern Brazil
Fig. 4. Circular graph showing the distribution of Leopardus guttulus (Hensel, 1872) records in BRLJL, Rio Grande do Sul, Brazil, throughout the 12 months sampled. The black lines represent the concentration of records.
Fig. 2 in Daily activity patterns and occurrence of Leopardus guttulus (Carnivora, Felidae) in Lami Biological Reserve, southern Brazil
Fig. 2. Circular graphs showing the daily activity of Leopardus guttulus (Hensel, 1872) at the BRLJL, Rio Grande do Sul, Brazil, based on all records obtained for the species (n=25, all seasons), on records obtained during spring/summer (n=15), and on records from autumn/winter (n=10). The arrow on each circular graphs indicates the direction of the angular mean.
Fig. 1 in Daily activity patterns and occurrence of Leopardus guttulus (Carnivora, Felidae) in Lami Biological Reserve, southern Brazil
Fig. 1. Location of the study area in South America and the State of Rio Grande do Sul (left panel), with the indication of the geographic range of Leopardus guttulus (Hensel, 1872) (grey area) in Brazil, Paraguay and Argentina (above), and the Biological Reserve Lami JosÉ Lutzenberger – BRLJL in the municipality of Porto Alegre, Rio Grande do Sul, Brazil (below). On the right panel, a detailed map of the study area showing the limits of the BRLJL (black line), the vegetation types occurring in the area, the grid sQuares of 1 x 1 km (grey lines) designed to delimitate the zones where sampling stations (camera stations) were installed (black triangles).
FIG. 13 in Field inventory reveals high diversity of new species of mountain catfishes, genus Cambeva Katz, Barbosa, Mattos & Costa, 2018 (Siluriformes: Trichomycteridae), in south-eastern Serra Geral, southern Brazil
FIG. 13. — Urohyal, ventral view. A, Cambeva diffusa n. sp.; B, Cambeva pericoh n. sp.; C, Cambeva imaruhy n. sp.; D, Cambeva orbitofrontalis n. sp.; E, Cambeva panthera n. sp.; F, Cambeva grisea n. sp.; G, Cambeva duplimaculata n. sp.; H, Cambeva longipalata n. sp.; I, Cambeva notabilis n. sp.; J, Cambeva urubici n. sp.
FIG. 12 in Field inventory reveals high diversity of new species of mountain catfishes, genus Cambeva Katz, Barbosa, Mattos & Costa, 2018 (Siluriformes: Trichomycteridae), in south-eastern Serra Geral, southern Brazil
FIG. 12. — Left suspensorium and opercular series, lateral view: A, Cambeva diffusa n. sp.; B, Cambeva pericoh n. sp.; C, Cambeva imaruhy n. sp.; D, Cambeva orbitofrontalis n. sp.; E, Cambeva panthera n. sp.; F, Cambeva grisea n. sp.; G, Cambeva duplimaculata n. sp.; H, Cambeva longipalata n. sp.; I, Cambeva notabilis n. sp.; J, Cambeva urubici n. sp. Abbreviations of structures indicated by arrows are: iac, interopercular anterior concavity; ppe, preopercular postero-dorsal expansion; odc, opercular dorsal constriction; odp, opercular dorsal process; ppp, parurohyal posterior process. Larger stippling represents cartilaginous areas.
FIG. 10. — Cambeva urubici n in Field inventory reveals high diversity of new species of mountain catfishes, genus Cambeva Katz, Barbosa, Mattos & Costa, 2018 (Siluriformes: Trichomycteridae), in south-eastern Serra Geral, southern Brazil
FIG. 10. — Cambeva urubici n. sp., UFRJ 6967, holotype, 65.6 mm SL: A, left lateral view; B, dorsal view; C, ventral view.
FIG. 9. — Cambeva notabilis n in Field inventory reveals high diversity of new species of mountain catfishes, genus Cambeva Katz, Barbosa, Mattos & Costa, 2018 (Siluriformes: Trichomycteridae), in south-eastern Serra Geral, southern Brazil
FIG. 9. — Cambeva notabilis n. sp., UFRJ 6965, holotype, 71.7 mm SL: A, left lateral view; B, dorsal view; C, ventral view.
FIG. 8. — Cambeva longipalata n in Field inventory reveals high diversity of new species of mountain catfishes, genus Cambeva Katz, Barbosa, Mattos & Costa, 2018 (Siluriformes: Trichomycteridae), in south-eastern Serra Geral, southern Brazil
FIG. 8. — Cambeva longipalata n. sp., UFRJ 6944, holotype, 86.0 mm SL: A, left lateral view; B, dorsal view; C, ventral view.
FIG. 7. — Cambeva duplimaculata n in Field inventory reveals high diversity of new species of mountain catfishes, genus Cambeva Katz, Barbosa, Mattos & Costa, 2018 (Siluriformes: Trichomycteridae), in south-eastern Serra Geral, southern Brazil
FIG. 7. — Cambeva duplimaculata n. sp., UFRJ 6949, holotype, 83.4 mm SL: A, left lateral view; B, dorsal view; C, ventral view.
FIG. 6. — Cambeva grisea n in Field inventory reveals high diversity of new species of mountain catfishes, genus Cambeva Katz, Barbosa, Mattos & Costa, 2018 (Siluriformes: Trichomycteridae), in south-eastern Serra Geral, southern Brazil
FIG. 6. — Cambeva grisea n. sp., UFRJ 6936, holotype, 43.1 mm SL: A, left lateral view; B, dorsal view; C, ventral view.
FIG. 5. — Cambeva panthera n in Field inventory reveals high diversity of new species of mountain catfishes, genus Cambeva Katz, Barbosa, Mattos & Costa, 2018 (Siluriformes: Trichomycteridae), in south-eastern Serra Geral, southern Brazil
FIG. 5. — Cambeva panthera n. sp., UFRJ 6984, holotype, 66.5 mm SL: A, left lateral view; B, dorsal view; C, ventral view.
FIG. 2. — Cambeva pericoh n in Field inventory reveals high diversity of new species of mountain catfishes, genus Cambeva Katz, Barbosa, Mattos & Costa, 2018 (Siluriformes: Trichomycteridae), in south-eastern Serra Geral, southern Brazil
FIG. 2. — Cambeva pericoh n. sp., UFRJ 6969, holotype, 97.3 mm SL: A, left lateral view; B, dorsal view; C, ventral view.
FIG. 1. — Cambeva diffusa n in Field inventory reveals high diversity of new species of mountain catfishes, genus Cambeva Katz, Barbosa, Mattos & Costa, 2018 (Siluriformes: Trichomycteridae), in south-eastern Serra Geral, southern Brazil
FIG. 1. — Cambeva diffusa n. sp., UFRJ 6968, holotype, 112.3 mm SL.: A, left lateral view; B, dorsal view; C, ventral view.
FIG. 14 in Field inventory reveals high diversity of new species of mountain catfishes, genus Cambeva Katz, Barbosa, Mattos & Costa, 2018 (Siluriformes: Trichomycteridae), in south-eastern Serra Geral, southern Brazil
FIG. 14. — Map of geographical distribution of Cambeva Katz, Barbosa, Mattos & Costa, 2018 in the southeastern nucleus of the Serra Geral (SESG), southern Brazil.
FIGURE 3 in New species and new records of Benthana Budde-Lund, 1908 (Isopoda: Oniscidea: Philosciidae) from southern Brazil
FIGURE 3: Map distribution of the species of Benthana from southern Brazil. *: Benthana carijos sp. nov.; : Benthana cairensis; : Benthana longicornis; : Benthana moreirai; ·: Benthana picta; ·: Benthana serrara; : Benthana taeniata.
FIGURE 2 in New species and new records of Benthana Budde-Lund, 1908 (Isopoda: Oniscidea: Philosciidae) from southern Brazil
FIGURE 2: Benthana carijos sp. nov. (male paratype). A: pereopod 1; B: pereopod 7; C: uropod; D: genital papilla; E: pleopod 1; F: pleopod 2; G: pleopod 5 exopod.
Fig. 1 in Plasma ion levels of freshwater and marine/estuarine teleosts from Southern Brazil
Fig. 1. Ion regulation curves for Na+ (a), Cl- (b), Ca2+ (c), Mg2+ (d), and K+ (e) in the plasma of M. furnieri () and G. barbus (O) collected from water at different salinities from the São Gonçalo channel. Data are expressed as the means ± SEM (n = 12) (P <0.05); the traced line represents the isoionic line. The following equations were fitted to the data: Micropogonias furnieri (Na+: y=214.52+0.051x, r2=0.87; Cl-: y=130.45+0.110, r2=0.94; K+: y=14.44-0.396x, r2=0.71; Ca2+: y=1.73+0.067x, r2=0.70; Mg2+: y=0.62+0.020x, r2=0.70); Genidens barbus (Na+: y=223.74+0.048x, r2=0.70; Cl-: y=150.56+0.133x, r2=0.98; K+: y=14.23-0.419x, r2=0.97; Ca2+: y=2.29+0.087x, r2=0.82; Mg2+: y=0.66+0.037x, r2=0.85), where x = salinity and y = plasma ion concentration (mmol L-1).
Fig. 7 in Age, growth, and reproductive aspects of the dusky grouper Mycteroperca marginata (Actinopterygii: Epinephelidae) in a man-made rocky habitat in southern Brazil
Fig. 7. Percentages of immature (white) and mature-resting females (black) per size classes (total length, mm) for Mycteroperca marginata individuals collected in the study area. n = 111.
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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)
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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.