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Fig. 2 in Can artificial retreat sites help frogs recover after severe habitat devastation? Insights on the use of "coqui houses" after Hurricane Maria in Puerto Rico
Fig. 2. Change in forest structure in the Palo Colorado forest transect (El Yunque) due to Hurricane Maria and corresponding damage/recovery stages according to Table 1. (A) Before the hurricane. (B) Same site after the hurricane, stage 1. (C) Moderate recuperation, stage 3. (D–E) Canopy dominated by Sierra Palm fronds showing signs of further recuperation of original understory vegetation, stage 4.
Fig. 9 in Can artificial retreat sites help frogs recover after severe habitat devastation? Insights on the use of "coqui houses" after Hurricane Maria in Puerto Rico
Fig. 9. Different uses ascribed to the two types of artificial habitats (=coqui houses) placed in the forest. (A) Coqui frog using bamboo house as retreat site during the day. (B) Bamboo house used as nesting site with a double clutch. Note that eggs are observed but the guarding male jumped away as the photo was taken. (C) PVC house used by a coqui as a nocturnal perching site. (D) PVC house used by a coqui as a calling site during the night.
Fig. 1 in Can artificial retreat sites help frogs recover after severe habitat devastation? Insights on the use of "coqui houses" after Hurricane Maria in Puerto Rico
Fig. 1. Map showing the location of El Yunque National Forest in Puerto Rico, and the location of the study transects.
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. 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 in Climate change and the fate of endemic Beyşehir Frog, Pelophylax caralitanus
Fig. 3. Current climatic habitat suitability map (A) and the eight RCP climatic change scenario maps for P. caralitanus based on RCP 2.6 (B–C), RCP 4.5 (D–E), RCP 6.0 (F–G), and RCP 8.5 (H–I) for either 2050 or 2070 as indicated.
Fig. 2 in Climate change and the fate of endemic Beyşehir Frog, Pelophylax caralitanus
Fig. 2. Variables with the highest contributions to the potential distribution of P. caralitanus according to MAXENT with the standard errors in blue. The Y-axis indicates the probability of presence (based on the Cloglog, or complementary log-log transform, values) and the X-axis shows the contribution of each variable.
Fig. 5 in Captive management, reproduction, and comparative larval development of Klappenbach's Red-bellied Frog, Melanophryniscus klappenbachi Prigioni and Langone, 2000
Fig. 5. Body size of different test groups. (A) Single tadpole, O‒1, and (B) five tadpoles per box, O‒5, in osmosis water. (C) Single tadpole, P‒1, and (D) five tadpoles per box, P‒5, in pond water.
Fig. 2. Keeping and rearing M in Captive management, reproduction, and comparative larval development of Klappenbach's Red-bellied Frog, Melanophryniscus klappenbachi Prigioni and Langone, 2000
Fig. 2. Keeping and rearing M. klappenbachi. (A) Terrarium of the adult group housing eight specimens. (B) Rearing of the tadpole test groups in a climate chamber.(C) Rearing containers for the young toadlets.
Fig. 1 in Captive management, reproduction, and comparative larval development of Klappenbach's Red-bellied Frog, Melanophryniscus klappenbachi Prigioni and Langone, 2000
Fig. 1. Melanophryniscus klappenbachi. (A) Dorsal and (B) ventral view of an adult female. (C) Amplexus.(D) Egg clump attached to moss. (E) Contrasting photo of a tadpole, used for evaluating the growth.
Fig. 4 in Captive management, reproduction, and comparative larval development of Klappenbach's Red-bellied Frog, Melanophryniscus klappenbachi Prigioni and Langone, 2000
Fig. 4. (A) Mortality rate of different test groups until metamorphosis. (B) Average growth rate of the different test groups. (C) Number of tadpoles metamorphosed per day after hatching (O = osmosis water, P = pond water, number indicates individuals per container).
Fig. 3 in Captive management, reproduction, and comparative larval development of Klappenbach's Red-bellied Frog, Melanophryniscus klappenbachi Prigioni and Langone, 2000
Fig. 3. Developing coloration in young toadlets of different ages. (A) Recently metamorphosed toadlet. (B) Ten days after metamorphosis. (C) Twenty-three days after metamorphosis. (D) Two months after metamorphosis.
FIGURE 7 in Morphology and Systematics of Kalophrynus interlineatus-pleurostigma Populations (Anura: Microhylidae: Kalophryninae) and a Taxonomy of the Genus Kalophrynus Tschudi, Asian Sticky Frogs
FIGURE 7. Images of lectotype of Kalophrynus interlineatus (NHMUK/BMNH 1947. 2.31.26, female) in (A) dorsal and (B) ventral views, and of paralectotype (NHMUK/BMNH 1947. 2.31.27, male) in (C) dorsal view [photographer G.R. Zug].
FIGURE 11 in Morphology and Systematics of Kalophrynus interlineatus-pleurostigma Populations (Anura: Microhylidae: Kalophryninae) and a Taxonomy of the Genus Kalophrynus Tschudi, Asian Sticky Frogs
FIGURE 11. Coloration of living representatives of pleurostigma-interlineatus group. (A) Dorsolateral view of a K. anya (USNM 520321) from the Chatthin Wildlife Sanctuary, Sagaing, Myanmar [photographer, C. Hansen]; (B) dorsolateral view of a K. anya (USNM 523966) from the Chatthin Wildlife Sanctuary, Sagaing, Myanmar [photographer, G.R. Zug]; (C) dorsolateral view of a K. interlineatus (CAS) from the Tanintharyi National Park, Tanintharyi, Myanmar [photographer, J.V. Vindum]; (D) dorsolateral view of a K. meizon (FMNH 242796) from Poring Station, Mt. Kinabulu Park, Ranua District, Sabah [photographer, R.F. Inger]; (E) dorsolateral view of a K. sinensis (UK 333148) from Agusan del Norte, Mindanao, Philippines [photographer, R.M. Brown]; (F) dorsolateral view of a K. pleurostigma (UK 333148) from Gunung Kunyit, Jambi, Sumatra [photographer, E.N. Smith].
FIGURE 6 in Morphology and Systematics of Kalophrynus interlineatus-pleurostigma Populations (Anura: Microhylidae: Kalophryninae) and a Taxonomy of the Genus Kalophrynus Tschudi, Asian Sticky Frogs
FIGURE 6. Burmese distribution of voucher specimens of Kalophrynus anya sp. nov. in northern Myanmar and K. interlineatus in southern and peninsular Myanmar. The three reported localities of K. orangensis are also shown; all lie within the Brahmaputra river valley. Solid circles denote specimens examined in this study; open circles are literature or unexamined museum records; and stars represent type localities of available names.
FIGURE 4 in Morphology and Systematics of Kalophrynus interlineatus-pleurostigma Populations (Anura: Microhylidae: Kalophryninae) and a Taxonomy of the Genus Kalophrynus Tschudi, Asian Sticky Frogs
FIGURE 4. General distribution of the Kalophrynus interlineatus-pleurostigma group. Solid circles denote specimens examined in this study; open circles are literature records and museum records of specimens not seen; stars represent type localities of available names. Source of the locality records are in Appendix Specimens examined section.
FIGURE 1 in Morphology and Systematics of Kalophrynus interlineatus-pleurostigma Populations (Anura: Microhylidae: Kalophryninae) and a Taxonomy of the Genus Kalophrynus Tschudi, Asian Sticky Frogs
FIGURE 1. Morphology of the glandular skin of a northern Myanmar Kalophrynus individual (USNM 537421). (A) compact, columnar macroglands comprising the skin in the dorsolateral pre-inguinal region; (B) sketch of the preceding image A to assist the identification of structures; incision is immediately below and parallel to white diagonal dorsolateral stripe; tile-like pattern on dorsal surface identifies individual macroglands, each with a single duct opening (lighter area in each tile); (C) lateral view of head and neck displaying the abrupt termination of thick glandular skin, equivalent to a supratympanic fold; (D) belly pebbly skin just anterior to pubic area; (E) white glandular epidermal patches on chest. Abbreviations: D, dorsolateral stripe; G, columns of glandular tissue; St, supratympanic fold. Scale bars equal 1 mm in figures B, D, E, and 10 mm in C.
Figure 4 in Ornithodoros faccinii n. sp. (Acari: Ixodida: Argasidae) parasitizing the frog Thoropa miliaris (Amphibia: Anura: Cycloramphidae) in Brazil
Figure 4 Scanninc electron microscopy of nymphs of Ornithodoros faccinii n. sp. A. Idiosoma, dorsal view. B. Idiosoma, ventral view, showinc the preanal croove reachinc the sides of the body (white arrow). C. Genital primordium (white arrow) on the ventral idiosoma. D. Capitulum. E. Tarsi I and U-shaped capsule (white arrow), partially covered by a V-shaped membrane. Scale bars: A. 500 μm; B. 500 μm; C. 250 μm; D. 100 μm; E. 100 μm.
Figure 1 in Ornithodoros faccinii n. sp. (Acari: Ixodida: Argasidae) parasitizing the frog Thoropa miliaris (Amphibia: Anura: Cycloramphidae) in Brazil
Figure 1 Scanninc electron microscopy of idiosoma and capitulum of larvae of Ornithodoros faccinii n. sp. A. Idiosoma, dorsal view. B. Part of basis capituli and hypostome. C. Idiosoma, ventral view. D. Dorsal plate. E. Detail of ventral idiosoma, showinc the pair of setae VPL (ventral posterolateral) (black arrow). Scale bars: A. 500 μm; B. 50 μm; C. 500 μm; D. 100 μm; E. 250 μm.
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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.