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Figure 2 in Range extension of Periophthalmodon septemradiatus (Gobiidae) in southern Sumatra, Indonesia
Figure 2. – The specimen of P. septemradiatus caught in the Musi River, Palembang City, South Sumatra Province, Indonesia. Photo M. Iqbal.
Figure 3.– P in Range extension of Periophthalmodon septemradiatus (Gobiidae) in southern Sumatra, Indonesia
Figure 3.– P. septemradiatus caught on the Musi River; (A) dorsal-lateral view (B) first pectoral fin (C) ventral view showing pelvic fins. Photo M. Iqbal.
Figure 1 in Range extension of Periophthalmodon septemradiatus (Gobiidae) in southern Sumatra, Indonesia
Figure 1. – The habitat where Periophthalmodon septemradiatus was caught on 16 September 2017, in the Musi River, Palembang City, South Sumatra Province, Indonesia. Photo A. Halim.
Fig. 1 in SHORT COMMUNICATION Noblella lynchi Duellman 1991 (Anura: Craugastoridae): Geographic range extension, Peru
Fig. 1. Noblella lynchi (A and B: male, MUSM 28216, SVL 24.8 mm; C and D: young, MUSM 24886, SVL 7.8 mm; E and F: female, MUSM 26448, SVL 19.5 mm). Photos by D. Rodríguez.
Fig. 1 in Conservation status, range extension, and call analysis of the Littoral Glassfrog, Cochranella litoralis (Ruiz-Carranza and Lynch 1996)
Fig. 1. Distribution map of Cochranella litoralis. White circles indicate verifiable localities reported in the literature; the white star denotes the type locality; the blue X marks the iNaturalist observation from the Río Palenque Research Center, Los Ríos; and yellow plus symbols indicate new records reported herein.
Fig. 2 in Conservation status, range extension, and call analysis of the Littoral Glassfrog, Cochranella litoralis (Ruiz-Carranza and Lynch 1996)
Fig. 2. Dorsal and ventral aspects of Cochranella litoralis in life. (A) Adult male, CJ12588, from Los Laureles, Cotopaxi, Ecuador. (B–E) Adult male, CJ12587a–d, from Cristobal Colón Quininde, Esmeraldas, Ecuador. Photos by: Jaime Culebras (A); Ross J. Maynard (B–E).
Fig. 3 in Conservation status, range extension, and call analysis of the Littoral Glassfrog, Cochranella litoralis (Ruiz-Carranza and Lynch 1996)
Fig. 3. Audio spectrogram (top), oscillogram (middle), and power spectrum (bottom) of an adult male Cochranella litoralis from Los Laureles, Cotopaxi, Ecuador (A), and an adult male C. granulosa from Jardín de los Sueños, Cotopaxi, Ecuador (B).
Fig. 2 in Consistency in fruit preferences across the geographical range of the frugivorous bats Artibeus, Carollia and Sturnira (Chiroptera)
Fig. 2. Distribution of three bat genera (Artibeus, Carollia and Sturnira – solid gray) and the four most frequent plant genera (Cecropia, Ficus, Piper and Solanum – dotted pattern) in their diet in the Neotropical region. Sources: bat distribution follows GARDNER (2008); plant distribution follows JARAMILLO & MANOS (2001) for Piper; KNAPP et al. (2004) for Solanum, LOBOVA et al. (2003) for Cecropia; SHANAHAN et al. (2001) for Ficus.
Fig. 1 in Consistency in fruit preferences across the geographical range of the frugivorous bats Artibeus, Carollia and Sturnira (Chiroptera)
Fig. 1. Number of records for the four fruit genera most frequently consumed by Artibeus, Carollia and Sturnira (total number of records for each bat species) based on literature review.
Fig. 6 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 6. Mandibles and vertebrae of pinniped mammal Enaliarctos sp. (UWBM 89114) from Moolack Beach, Lincoln County, Oregon, Astoria Formation, late early Miocene. Two sides of the block (A, B). Photographs (A1, B1), explanatory drawings (A2, B2). Abbreviations: CV, cervical vertebra; TV, thoracic vertebra.
Fig. 1 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 1. Locality map for fossils of enaliarctines. Map of Oregon and California (A), the coastline near Newport, Oregon (B), the coastline near Point Arena, California (C).
Fig. 3 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 3. Mandible of pinniped mammal Enaliarctos mealsi (UCMP 114474) from Schooner Gulch, Mendocino County, California, earliest Miocene; in lingual (A), occlusal (B), and labial (C) views.
Fig. 5 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 5. Elements of pinniped mammal Enaliarctos sp., cf. E. tedfordi Berta, 1991 (UCMP 253400) from Ona Beach, Lincoln County, Oregon, Yaquina Formation, early late Oligocene; overview of original block (A), lingual (B), occlusal (C), and labial (D) views; matrix preserving impression of lingual side of p4 and m1 (E).
Fig. 8 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 8. Time calibrated composite phylogenetic hypothesis of early pinnipedimorphs and putative allies, with an emphasis on Oligo-Miocene pinnipedimorphs from the eastern North Pacific. Topology based on Boessenecker and Churchill (2015), except as follows: Enaliarctos from Berta (1991); Phocoidea after Boessenecker and Churchill (in press). Placement of Pacificotaria from Deméré and Berta (2001), conjectural placement (dashed lines) of Puijila and Kolponomos after Tedford et al. (1994) and Rybczynski et al. (2009), Enaliarctos sp. (UWBM 89114) based on shared dental synapomorphies with E. emlongi and E. mitchelli. Geochronologic ranges from Table 3 (this study), Boessenecker and Churchill (2015: supplementary information, in press: supplementary information), and Rybczynski et al. (2009).
Fig. 4 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 4. Metacarpal of pinniped mammal Enaliarctos mealsi Mitchell and Tedford, 1973 (UCMP 276804) from Schooner Gulch, Mendocino County, California, earliest Miocene; in dorsal (A), lateral (B), and ventral/palmar C) views.
Fig. 2 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 2. Stratigraphic columns of Oregon (A) and California (B) localities. Columns based on Snavely et al. (1964) and Phillips et al. (1976); paleomagnetic and K/Ar dates from Prothero et al. (2001a, b) and Phillips et al. (1976). In the interest of clarity non-enaliarctine marine carnivores are omitted. Modified from Moore (1963) and Phillips et al. (1976). Abbreviations: FAD, first appearance datum; LAD, last appearance datum; t, type locality/horizon.
Fig. 6 in A large hyaenodont from the Lutetian of Switzerland expands the body mass range of the European mammalian predators during the Eocene
Fig. 6. Bivariate plots representing the Relative Premolar Size (RPS) versus the Relative Blade Length (RBL) for some selected hyaenodonts from the Eocene of Europe.
Fig. 5 in A large hyaenodont from the Lutetian of Switzerland expands the body mass range of the European mammalian predators during the Eocene
Fig. 5. Results of the phylogenetic analysis of Hyaenodonta character-taxon matrix. Results are visualized as an "all compat" (majority rule plus compatible groups) consensus tree. Major named clades recovered or discussed in this analysis and recovered in other analyses are illustrated.
Fig. 7 in A large hyaenodont from the Lutetian of Switzerland expands the body mass range of the European mammalian predators during the Eocene
Fig. 7. Values of the body mass (in ln) of oxyaenids, mesonychids, and hyaenodonts (Hyaenodontoidea, "Sinopinae", "Arfiinae", Hyainailourinae, and Hyaenodontinae) from MP7 to MP19 with particular attention on the new species from Egerkingen γ (Hyaenodontinae + "Arfiinae"). Values from Table 1 (Cartierodon egerkingensis gen. et sp. nov.) and Solé et al. (2015). Egerkingen γ is here represented to be close to the MP13 reference-level. Abbreviations: ELMA, European Land Mammal Ages; ETM-2, Eocene Thermal Maximum 2; MECO, Middle Eocene Climatic Optimum; MDE, Mammal Dispersal Event; MP, Mammal Palaeogene; PETM, Paleocene–Eocene Thermal Maximum.
Fig. 4 in A large hyaenodont from the Lutetian of Switzerland expands the body mass range of the European mammalian predators during the Eocene
Fig. 4. Comparison of the ratio width/length estimated for the lower premolars of Paenoxyaenoides liguritor from late Eocene of France, Quercy Phosphorites (based on Lange-Badré 1979: table 10), Prodissopsalis eocaenicus from Eocene of Switzerland, Geiseltal-Obere Mittelkohle (MP12) and Geiseltal-Untere Mittelkohle (MP13) (based on Lange-Badré and Haubold 1990: table 3); Cartierodon egerkingensis gen. et sp. nov. from Eocene of Switzerland, Egerkingen γ (MP13?); and Cartierodon cf. egerkingensis from Eocene of France, Lissieu (MP14) (based on Lange-Badré 1972: table 1).
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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.