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Fig. 6 in Two new species of the genus Cylindrophis Wagler, 1828 (Squamata: Cylindrophiidae) from Southeast Asia
Fig. 6. Coloration of Cylindrophis mirzae sp. nov. holotype, MNHN-RA 3279 (A) head in dorsal view, (B) head in ventral view, (C) head in lateral view, (D) midbody in dorsal view, (E) midbody in ventral view, and (F) tail in ventral view.
Fig. 1 in Two new species of the genus Cylindrophis Wagler, 1828 (Squamata: Cylindrophiidae) from Southeast Asia
Fig. 1. Coloration of Cylindrophis ruffus MZB 1418 (A) head in dorsal view, (B) head in ventral view, (C) head in lateral view, (D) midbody in dorsal view, (E) midbody in ventral view, and (F) tail in ventral view.
Fig. 4 in Two new species of the genus Cylindrophis Wagler, 1828 (Squamata: Cylindrophiidae) from Southeast Asia
Fig. 4. Coloration of Cylindrophis jodiae sp. nov. holotype, MNHN-RA 1911.0196 (A) head in dorsal view, (B) head in ventral view, (C) head in lateral view, (D) midbody in dorsal view, (E) midbody in ventral view, and (F) tail in ventral view.
Figs. 4-6 in Two new species of Dermestidae (Coleoptera) from Bolivia and Venezuela.
Figs. 4-6.- Cryptorhopalum bastidasi sp. nov: 4.- Habitus dorsal aspect. 5.- Head and antenna. 6.- Male genitalia
Figs. 1-3 in Two new species of Dermestidae (Coleoptera) from Bolivia and Venezuela.
Figs. 1-3.- Cryptorhopalum ayolasi sp. nov: 1.- Habitus dorsal aspect. 2.- Head, pronotum and antenna. 3.- Male genitalia.
Fig. 2 in Two new species of the genus Cylindrophis Wagler, 1828 (Squamata: Cylindrophiidae) from Southeast Asia
Fig. 2. Coloration of Cylindrophis burmanus lectotype, BMNH 1940.3.3.1 (A) head in dorsal view, (B) head in ventral view, (C) head in lateral view, (D) midbody in dorsal view, (E) mid-body in ventral view, and (F) tail in ventral view.
Fig. 3 in Two new species of the genus Cylindrophis Wagler, 1828 (Squamata: Cylindrophiidae) from Southeast Asia
Fig. 3. Scalation of Cylindrophis burmanus lectotype, BMNH 1940.3.3.1 (A) head in dorsal view, (B) head in ventral view, (C) head in lateral view, (D) tail in ventral view, (E) midbody in dorsal view, (F) midbody in ventral view.
Fig. 1 in Pathological findings associated with Dipetalonema spp. (Spirurida, Onchocercidae) infection in two species of Neotropical monkeys from Brazil
Fig. 1 Gross lesions in Alouatta guariba clamitans and Sapajus nigritus monkeys infected by Dipetalonema spp. (a; case 2) Thoracic cavity with multifocal areas of fibrous adhesions in the visceral and parietal pleura associated with filarial nematodes (arrowhead) in an individual with polyserositis. (b; case 12) Thoracic cavity with proliferation of fibrous connective tissue in the visceral pleura causing adhesions in the lung. (c; case 7) Liver, marked proliferation of fibrous connective tissue in the form of fringes over the organ capsule. (d; case 13) Abdominal cavity, filarial nematodes in the mesentery. (e; case 13) Heart with epicardium presenting pale multifocal areas, and moderate adherence by fibrous and fibrinous serositis associated with filarial nematodes. (f; case 20) Small intestine with entrapment of intestinal segment by focal area of fibrosis with fibrous polyserositis caused by filarial nematodes
Fig. 2. A in First population assessment of two cryptic Tiger Geckos (Goniurosaurus) from northern Vietnam: Implications for conservation
Fig. 2. A: Macrohabitat and B: Microhabit of Goniurosaurus luii in Ha Lang District, Cao Bang Province, North Vietnam; specimens of G. luii from C: Cao Bang Province and D: Lang Son Province (new record). Photos Mona van Schingen, Marta Bernardes, and Tao Thien Nguyen.
Fig. 3 in On the distribution and conservation of two "Lost World" tepui summit endemic frogs, Stefania ginesi Rivero, 1968 and S. satelles Señaris, Ayarzagüena, and Gorzula, 1997
Fig. 3. Phylogenetic relationships as recovered in the MrBayes analysis (concatenated dataset, 2359 bp), outgroup not shown. Values at each node represent Bayesian posterior probabilities; asterisks indicate values> 95%. Stefania ginesi sensu stricto, and S. satelles sensu stricto are highlighted in red. Relation between eye color and tepui summit surface is indicated on the right side of the figure. Photos PJRK.
Fig. 2 in On the distribution and conservation of two "Lost World" tepui summit endemic frogs, Stefania ginesi Rivero, 1968 and S. satelles Señaris, Ayarzagüena, and Gorzula, 1997
Fig. 2. Typical Pantepui landscape. Photograph taken on 8th June 2012 from the summit of Upuigma-tepui, showing Angasima-tepui on the left and Akopán-tepui and Amurí-tepui on the right. Note stretches of savannah mainly caused by anthropogenic fires. Photo PJRK.
Fig. 4. A in First population assessment of two cryptic Tiger Geckos (Goniurosaurus) from northern Vietnam: Implications for conservation
Fig. 4. A: Average population structure of Goniurosaurus catbaensis and a continental G. luii population from Cao Bang Province (May–August vs. June, respectively); B: Frequency histogram of Snout-vent length of G. catbaensis for the months May, July, and August.
Fig. 1 in On the distribution and conservation of two "Lost World" tepui summit endemic frogs, Stefania ginesi Rivero, 1968 and S. satelles Señaris, Ayarzagüena, and Gorzula, 1997
Fig. 1. Left: Map of Pantepui and its location within South America (inset); the thick blue line indicates the Río Caroní. Right: Map of the area under study showing localities mentioned in the text (yellow dots represent known localities of occurrence of Stefania satelles, white dots represent known localities of occurrence of Stefania ginesi). Numbers indicate sampled localities and Roman numerals indicate unsampled localities, as follows: (1) Aprada-tepui, Venezuela; (2) Murisipán-tepui, Venezuela; (3) Upuigmatepui, Venezuela; (4) Angasima-tepui, Venezuela; (5) Abakapá-tepui, Venezuela; (6) Chimantá-tepui, Venezuela; (7) Amurí-tepui, Venezuela; (i) Kamarkawarai-tepui, Venezuela; (ii) Murei-tepui, Venezuela; (iii) Churí-tepui, Venezuela; (iv) Akopán-tepui, Venezuela.
Fig. 3. A in First population assessment of two cryptic Tiger Geckos (Goniurosaurus) from northern Vietnam: Implications for conservation
Fig. 3. A: Macrohabitat of Goniurosaurus catbaensis at the coast of Cat Ba Island; B: Limestone cliffs, the typical microhabitat of G. catbaensis; C: Adult male of G. catbaensis marked for population assessment; D: First evidence for the occurrence of G. catbaensis within limestone cave of small offshore Island in Ha Long Bay archipelago. Photos Hai Ngo, Tao Thien Nguyen, and Minh Le Pham.
Fig. 1 in First population assessment of two cryptic Tiger Geckos (Goniurosaurus) from northern Vietnam: Implications for conservation
Fig. 1. Distribution of the cryptic species Goniurosaurus catbaensis (gray circles) and G. luii (black circles): Filled circles represent study areas; dashed circle represents new record of G. luii; questions marks indicate former localities or sites where the current presence is unclear. Occurrence records were represented as big circles to prevent showing exact locality data.
FIG. 1 in Two new species of the genus Empis Linnaeus, 1758 (Diptera, Empididae, Empidinae) from French nature reserves
FIG. 1. — Empis (Empis) cartusiana n. sp.: A, male habitus; B, male hypopygium; C, female habitus. Abbreviations: see Material and methods. Scale bars: A, C, 1 mm; B, 0.2 mm.
Fig. 10 in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships
Fig. 10. Type locality of Petracola shurugojalcapi, Área de Conservación Privada Llamapampa-La Jalca, District of la Jalca Grande, Province of Chachapoyas, Department ofAmazonas.
Fig. S1 in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships
Fig. S1. Phylogenetic relationships of Cercosaurini (log likelihood = -54268.289, ultrafast bootstrap = 10,000) constructed from the data set of 2,384 nucleotides for mitochondrial genes (12S, 16S, cyt-b, and ND4) and a nuclear gene (c-mos).
Fig. 9 in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships
Fig. 9. Holotype in life of Petracola shurugojalcapi from La Jalca Grande (PFAUNA 431, SVL = 51.0 mm, TL = 39.0 mm, adult female).
Fig. 7 in Two new species of gymnophthalmid lizards of the genus Petracola (Squamata: Cercosaurinae) from the Andes of northeastern Peru, and their phylogenetic relationships
Fig. 7. Holotype of Petracola shurugojalcapi, adult female PFAUNA 431 (SVL = 51.0 mm, TL = 39.0 mm).
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.