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Figure 3 in Ornithodoros faccinii n. sp. (Acari: Ixodida: Argasidae) parasitizing the frog Thoropa miliaris (Amphibia: Anura: Cycloramphidae) in Brazil
Figure 3 Scanninc electron microscopy of cnatosoma and tarsus of larvae of Ornithodoros faccinii n. sp. A. Capitulum, ventral view. B. Details of capitulum showinc small spurs at the base of hypostome in the lateral position (black arrow). C. Detail of hypostome, palpi and chelicerae. D. Trochanter of palpi with 11 short spurs in the inner side, some of them are bifid (black arrow). E. Tibiotarsus of palpi. F. Hypostome with dental formula 3/3 in the anterior third, and then 2/2 posteriorly to the base. G. Tarsi I. Scale bars: A. 100 μm; B. 500 μm; C. 25 μm; D. 15 μm; E. 15 μm; F. 10 μm; G. 50 μm.
Figure 2 in Ornithodoros faccinii n. sp. (Acari: Ixodida: Argasidae) parasitizing the frog Thoropa miliaris (Amphibia: Anura: Cycloramphidae) in Brazil
Figure 2 Larvae of Ornithodoros faccinii n. sp. A. Chaetotaxy of dorsal idiosoma: DAL (dorsal anterolateral setae), DC (dorsal central setae), DPL (dorsal posterolateral setae). B. Chaetotaxy of ventral idiosoma: ST (sternal setae), CA (circumanal setae), VPL (ventral posterolateral setae). C. Chaetotaxy of tarsus I, A (anterior), DM (dorsomedian), PC (paracapsular), PM (posteromedian), B (basal), AV (anteroventral), MV (midventral), BV (basiventral), PL (posterolateral). D. Licht microcraph of tarsus I, capsule of Haller's orcan. Scale bars: A and B. 100 μm; C. 50 μm; D. 20 μm.
Figure 5 in Ornithodoros faccinii n. sp. (Acari: Ixodida: Argasidae) parasitizing the frog Thoropa miliaris (Amphibia: Anura: Cycloramphidae) in Brazil
Figure 5 Phylocenetic tree based on the 16S rDNA ticks. The alicnment was produced usinc Clustal X and the tree was inferred by means of the MP method with 500 replicates of random addition taxa. The species Ixodes holocyclus and Ixodes uriae were used as outcroup. The Bayesian support (posterior probability) values are derived from 1,000,000 replicates.
Figure 3 in Early to middle Pleistocene occurrences of Litoria, Neobatrachus and Pseudophryne (Anura) from the Nullarbor Plain, Australia: first frogs from the "frog-free zone"
Figure 3. Pleistocene frog ilia from Leaena's Breath Cave (prefix WAM) compared with modern specimens (prefix SAMA). a) WAM 09.3.264. Right ilium of holotype of Litoria lundeliusi sp. nov. from Leaena's Breath Cave (unit 3). b) WAM 09.3.264. Enlargement of acetabular region of holotype of Litoria lundeliusi sp. nov. c) SAMA R68398. Representative left ilium of Litoria adelaidensis. d) SAMA R68399. Representative right ilium of Litoria rubella sensu stricto. e–h) Representative ilia of Neobatrachus sudelli highlighting extreme divergence in the form of the dorsal prominence. e) WAM 09.3.265. f) WAM 09.3.261. g) WAM 09.3.269. h) WAM 09.3.273. i) Right ilium of Pseudophryne sp. indet.
Figure 1 in Early to middle Pleistocene occurrences of Litoria, Neobatrachus and Pseudophryne (Anura) from the Nullarbor Plain, Australia: first frogs from the "frog-free zone"
Figure 1. Map of Australia showing modern occurrence records extracted from the Atlas of Living Australia (www.ala.org.au) and location of Leaena's Breath Cave (black triangle). a) Anura. b) Neobatrachus sudelli. Note that the two most northwestern records may represent N. aquilonius (J. D. Roberts, pers. comm., 27 June 2015). c) Pseudophryne guentheri (light green) and P. occidentalis (dark green). d) Litoria adelaidensis (red), L. cyclorhyncha (purple) and L. moorei (light brown).
Figure 7. Indopolystoma parvum n. gen. n in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 7. Indopolystoma parvum n. gen. n. sp. from Zhangixalus omeimontis. Dorsal view of holotype. (A) A drawing; (B) A photograph. Scale bar: 1 mm.
Figure 5. Indopolystoma elongatum n. gen. n in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 5. Indopolystoma elongatum n. gen. n. sp. from Zhangixalus arboreus. Ventral view of holotype. (A) A drawing; (B) A photograph. Scale bar: 1 mm.
Figure 4. Indopolystoma viridi n. gen. n in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 4. Indopolystoma viridi n. gen. n. sp. from Zhangixalus viridis. Marginal hooklets from paratypes. (A) Marginal hooklet C1; (B) Marginal hooklet C8; (C) Marginal hooklets C2–C7. Scale bar: 20 µm.
Figure 3. Indopolystoma viridi n. gen. n in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 3. Indopolystoma viridi n. gen. n. sp. from Zhangixalus viridis. Hamuli from holotype and paratypes. (A–A') Holotype; (B–H) Paratypes. Scale bar: 100 µm.
Figure 6. Indopolystoma elongatum n. gen. n in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 6. Indopolystoma elongatum n. gen. n. sp. from Zhangixalus arboreus. Hamuli and marginal hooklets from holotype and paratypes. (A–A') Holotype; (A''–A''') Paratypes; (B) Marginal hooklet C1; (B') Marginal hooklet C3; (B'') Marginal hooklet C8. Scale bar: 100 µm (A–A'''), 20 µm (B–B'').
Figure 1 in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 1. Bayesian tree for neobatrachian polystomes inferred from the analysis of four concatenated genes, namely 18S, 28S, COI and 12S. Numbers on nodes indicate Bayesian Posterior Probabilities. Indopolystoma spp. were regarded earlier as Polystoma spp. in Badets et al. [2] and Héritier et al. [22]. B. w. refers to Blommersia wittei and Z. s. to Zhangixalus smaragdinus. See also Table 1 for other host species. Scale bar represents 0.1 substitution/site.
Figure 8. Indopolystoma parvum n. gen. n in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 8. Indopolystoma parvum n. gen. n. sp. from Zhangixalus omeimontis. Hamuli and marginal hooklets from holotype and paratype. (A–A') Holotype; (A''–A''') Paratype; (B) Marginal hooklet C1; (B') Marginal hooklet C2; (B'') Marginal hooklet C6 or C7. Scale bar: 100 µm (A–A'''), 20 µm (B–B'').
Figure 2. Indopolystoma viridi n. gen. n in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 2. Indopolystoma viridi n. gen. n. sp. from Zhangixalus viridis. Dorsal view of holotype. (A) A drawing; (B) A photograph. Scale bar: 1 mm.
Dataset: JFrog Ltd. (FROG) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
Fig. 1 in Choosy Outsiders? Satellite Males Associate With Sexy Hosts In The European Tree Frog Hyla Arborea
Fig. 1. Box plots for snout-urostyle length of sampled males of Hyla arborea, classified as satellites, callers or hosts. Boxes represent standard error of mean and whiskers represent standard deviation. Small squares represent mean
Figure 2 in A new species, Dactylosoma piperis n. sp. (Apicomplexa, Dactylosomatidae), from the pepper frog Leptodactylus labyrinthicus (Anura, Leptodactylidae) from Mato Grosso State, Brazil.
Figure 2. Consensus phylogram of haemogregarines based on 18S rDNA sequences. The topology trees with Bayesian inference (BI) and Maximum likelihood (ML) analyses were identical (represented by the ML tree). The scale bar represents 0.02 nucleotide substitutions per site. Adelina dimidiata (DQ096835), Adelina grylli (DQ096836), Klossia helicina (HQ224955) and Klossia equi (MH211602) were used as outgroups.
Figure 1. Dactylosoma piperis n in A new species, Dactylosoma piperis n. sp. (Apicomplexa, Dactylosomatidae), from the pepper frog Leptodactylus labyrinthicus (Anura, Leptodactylidae) from Mato Grosso State, Brazil.
Figure 1. Dactylosoma piperis n. sp. in blood smears of Leptodactylus labyrinthicus. Primary merogony (A–F): A) Trophozoite; B) Young primary meront; C–D) Primary large rounded meronts; E–F) Fan-like shaped primary meronts with merozoites. Secondary merogony (G–L): G–H) Young secondary meronts; I–J) Secondary meronts with dactylate appearance; K–L) Secondary meronts with merozoites. Scale bar: 10 µm.
Figure 3 in Colour variations in the European tree frog, Hyla arborea (Linnaeus, 1758), from two small adjacent ponds in the Vojvodina province, Serbia
Figure 3. Two green colour variations: the typical, bright green a) and paler, yellowish b). Photos: Aleksandar Simović.
Figure 1 in Colour variations in the European tree frog, Hyla arborea (Linnaeus, 1758), from two small adjacent ponds in the Vojvodina province, Serbia
Figure 1. Two ponds where the frogs were observed: a) the larger one, near a settlement, overgrown with reeds; b) small, shallow pond with open water. Photos: Sonja Đorđević.
FIGURE 2 in Extinction risk or lack of sampling in a threatened species: Genetic structure and environmental suitability of the neotropical frog Pristimantis penelopus (Anura: Craugastoridae)
FIGURE 2: (Left) Maximum clade credibility tree depicting the phylogenetic position of Pristimantis penelopus within the P. ridens series. Numbers on nodes indicate posterior probabilities. Numbers below nodes represent nodal support using the ultrafast bootstrap (see methods). Asterisks indicate nodal support above 95% in both Bayesian and ML methods. (Right) Haplotype network based on 460 bp of the COI region. Numbers of mutational steps are shown on the lines connecting haplotypes. Colors refer to geographic locations shown in Figure 1.
ScienceDex guides
Understand access before you commit
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.