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Figure 1 in Two southeastern Atlantic records of the rare largetooth cookiecutter shark, Isistius plutodus (Selachii, Squaliformes, Dalatiidae)
Figure 1. - Isistius plutodus female, 420 mm TL, AtlantNIRO 23074. A: Dorsal view; B: Ventral view; C: Lateral view; D: Head in dorsal view; E: head in ventral view.
Figure 2 in Two southeastern Atlantic records of the rare largetooth cookiecutter shark, Isistius plutodus (Selachii, Squaliformes, Dalatiidae)
Figure 2. - Isistius plutodus female, 330 mm TL, AtlantNIRO 24000, in dorsal (A), ventral (B) and lateral (C) views.
Figure 1 in Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part two
Figure 1. – Acropoma lecorneti, MNHN-IC-2008-1612, 141.9 mm SL, from Vanuatu. A: Lateral view of left side; B: Inside of the abdominal region of right side (dissected and outlined luminous gland).
Figure 5 in Distribution patterns of ocellated eagle rays, Aetobatus ocellatus, along two sites in Moorea Island, French Polynesia
Figure 5. – Percentage of observations for the ten different behaviours according to the study site: swimming, foraging, chafing, cruising, escape, pre-mating, jumping, conspecific interaction, heterospecific interaction, come-close. See Table II for details on each behaviour.
Figure 2 in Distribution patterns of ocellated eagle rays, Aetobatus ocellatus, along two sites in Moorea Island, French Polynesia
Figure 2. – Multiple Correspondence Analysis factor map (2 first components, 34.5% and 19.4%, respectively) representing the relationship between the study sites (ClubMed/Mareto), ontogenetic stage of the eagle rays (male/female/juvenile), seasons (wet/dry), and the time of the day (am/pm).
Figure 1 in Distribution patterns of ocellated eagle rays, Aetobatus ocellatus, along two sites in Moorea Island, French Polynesia
Figure 1. – Map highlighting the two study sites on Moorea Island, French Polynesia: Mareto and ClubMed.
Figure 3 in Temporal dynamics of the recruitment of glass eels in two valleys of French Polynesia (Tahiti and Moorea Islands)
Figure 3. – Annual monitoring of glass eels recruitment for each of the three species in: A: Moorea; B: Tahiti; C: Moorea and Tahiti, given in number of specimens per month.
Figure 4 in Temporal dynamics of the recruitment of glass eels in two valleys of French Polynesia (Tahiti and Moorea Islands)
Figure 4. – Composition of the recruitment of Anguilla species from Moorea and Tahiti Islands given in percent; * test chiº, p-value <0.001.
Figure 5 in Temporal dynamics of the recruitment of glass eels in two valleys of French Polynesia (Tahiti and Moorea Islands)
Figure 5. – Mean length (in mm) of the glass eel specimens at recruitment, for the three species in Moorea and Tahiti islands; * test chiº, p-value <0.001.
Figure 4 in Distribution patterns of ocellated eagle rays, Aetobatus ocellatus, along two sites in Moorea Island, French Polynesia
Figure 4. – Abundance (number of macroinvertebrate individuals) and biomass (grams) for the two study sites. The boxes represent the first and third quartiles, black lines are the medians (second quartiles), and whiskers cor- respond to the range (min-max) of the distributions. An asterisk indicates sta- tistically significant differences.
Figure 3 in Distribution patterns of ocellated eagle rays, Aetobatus ocellatus, along two sites in Moorea Island, French Polynesia
Figure 3. – Multiple Factor Analysis scatter plots (2 first components, 18% and 13%, respectively) representing the relationship between sex (male/ female/ juvenile), the site (ClubMed/Mareto) and the environmental factors: wave and wind direction (east/north/south/ west), wind speed (high/medium/low) and current strength (no/light/medium/ strong).
Figure 2 in Temporal dynamics of the recruitment of glass eels in two valleys of French Polynesia (Tahiti and Moorea Islands)
Figure 2. – Annual monitoring of glass eels recruitment in the Opunohu River on the Moorea Island and in the Vaituoru River on the Tahiti Island per year, given in number of specimens caught per day.
Fig. 5. A in Two new species of frogs of the genus Phrynopus (Anura: Terrarana: Craugastoridae) from the Peruvian Andes
Fig. 5. A) Habitat of the type locality of Phrynopus valquii sp. nov.; B) Microhabitat of Phrynopus valquii sp. nov.; C) Habitat of the type locality of Phrynopus daemon sp. nov.; D) Microhabitat of Phrynopus daemon sp. nov. Photographs: A–B by Germán Chávez and C–D by Roy Santa-Cruz.
Fig. 3 in Two new species of frogs of the genus Phrynopus (Anura: Terrarana: Craugastoridae) from the Peruvian Andes
Fig. 3. Distribution of Phrynopus valquii sp. nov. (green circles) and Phrynopus daemon sp. nov. (red circles). Map by Ca- terina H. Cosmopolis.
Fig. 4 in Two new species of frogs of the genus Phrynopus (Anura: Terrarana: Craugastoridae) from the Peruvian Andes
Fig. 4. Dorsal (left) and ventral (right) views of the type series of Phrynopus daemon sp. nov.: A–B) Holotype (CORBIDI 15364, adult female, SVL = 24.3 mm); C–D) Female paratype (MUSA 4916, adult female, SVL = 21.4 mm); E–F) Male paratype (MUSM 32747, SVL = 21.7). Photographs: A–D by Roy Santa-Cruz and E–F by Daniel Rodriguez.
Fig. 2 in Two new species of frogs of the genus Phrynopus (Anura: Terrarana: Craugastoridae) from the Peruvian Andes
Fig. 2. Ventral view of: A) right hand of the holotype of Phrynopus valquii; B) right foot of the holotype of Phrynopus valquii; C) right hand of the holotype of Phrynopus daemon; D) right foot of the holotype of Phrynopus daemon. Photographs by Germán Chávez.
Fig. 1 in Two new species of frogs of the genus Phrynopus (Anura: Terrarana: Craugastoridae) from the Peruvian Andes
Fig. 1. Dorsal (left) and ventral (right) views of specimens of the type series of Phrynopus valquii sp. nov.: A–B) Holotype (COR- BIDI 14005, adult female, SVL = 31.2 mm); C–D) Paratype (CORBIDI 14007, adult female, SVL = 28.07 mm); E–F (CORBIDI 13993, adult male, SVL = 25.2 mm). Photographs by Germán Chávez.
Fig. 8 in New biological data for two rare reedfrog species, Hyperolius nimbae Laurent, 1958, and H. chlorosteus (Boulenger, 1915) (Anura: Hyperoliidae)
Fig. 8. Number of Hyperolius chlorosteus captured from 2 August 2019 to 8 July 2020 along lowland forest streams at Mount Nimba.
Fig. 6 in New biological data for two rare reedfrog species, Hyperolius nimbae Laurent, 1958, and H. chlorosteus (Boulenger, 1915) (Anura: Hyperoliidae)
Fig. 6. (A) Hyperolius nimbae usually calls perched between branches and leaves of trees. (B) Waveform (above), spectogram (center), and powerspectrogram (below) of the advertisement calls of a H. nimbae male from Yéalé, western Ivory Coast.
Fig. 2 in New biological data for two rare reedfrog species, Hyperolius nimbae Laurent, 1958, and H. chlorosteus (Boulenger, 1915) (Anura: Hyperoliidae)
Fig. 2. Habitats of Hyperolius nimbae at the foothills of the Ivorian part of the Nimba Mountains. In Yéalé, the species was found in heavily degraded habitats at the edge of large swamps.
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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.