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4,648 results for “frog”
Fig. 1 in New records, range extension and call description for the stream-breeding frog Hyloscirtus lascinius (Rivero, 1970) in Venezuela
Fig. 1. Hyloscirtus lascinius from Venezuela. (A) Campamento Guacharaca, Sierra de Perijá, Zulia state; (B) Near La Macana, Mérida state; (C) Quebrada La Rana, Mérida state. Photos: F.J.M. Rojas-Runjaic (A) and C.L. Barrio-Amorós (B and C).
Fig. 1 in SHORT COMMUNICATION New records of the Critically Endangered frog Pristimantis pardalinus (Craugastoridae) in the eastern Andean slopes of central Peru
Fig. 1. Map showing the currently known distribution of Pristimantis pardalinus. The yellow triangle indicates the location of the type locality and the red stars indicate the location of new records reported in this study. The inset shows the location of the study area in Peru (red box).
Fig. 5 in Historical biogeography highlights the role of Miocene landscape changes on the diversification of a clade of Amazonian tree frogs
Fig. 5 Dorsolateral views of Osteocephalus. a O. leprieurii sensu stricto, Kaw mountain, French Guiana. b O. leprieurii, AF1824, Mana, French Guiana. c O. yasuni sensu stricto, QCAZ69010, Estación Cientí- fica Yasuní, Orellana, Ecuador. d O. yasuni, QCAZ55994, Lorocachi, Pastaza, Ecuador. e O. deridens, QCAZ56031, Lorocachi, Pastaza, Ecuador. f O. fuscifacies, QCAZ59887, Parque Nacional Llanganates, Pastaza, Ecuador. g O. aff. leoniae 2, AF4513 (sequenced), San Martín, Peru. h O. planiceps, QCAZ55881, Lorocachi, Pastaza, Ecuador. Photographs: a–b, g by Antoine Fouquet; c–f, h by Santiago Ron (BIOWEB, Licence: CC BY-NC-ND 4.0)
Fig. 4 in Historical biogeography highlights the role of Miocene landscape changes on the diversification of a clade of Amazonian tree frogs
Fig. 4 Dorsolateral and ventral views of Osteocephalus. a O. cabrerai, CORBIDI120, Tara- poa, Sucumbíos, Ecuador. b O. helenae, AF2427 (sequenced), Nassau, Suriname. c O. helenae, Amapá, Brazil. d O. helenae, Voltaire, French Guiana. e–f O. aff. helenae 2 'morph cabrerai', AF2357 (sequenced), Mapaou, French Guiana. g O. aff. helenae 2 'morph cabrerai', AF3358 (sequenced), Bakhuis, Surinam. h O. aff. helenae 2 'morph cabrerai', St. Georges, French Guiana. Photographs: a by Pablo Venegas (BIOWEB, Licence: CC BY-NC-ND 4.0); b–h by Antoine Fouquet
Fig. 3 in Historical biogeography highlights the role of Miocene landscape changes on the diversification of a clade of Amazonian tree frogs
Fig. 3 Dorsolateral views of Osteocephalus. a O. alboguttatus sensu stricto, QCAZ15972, Puyo-Canelos Road, Pastaza, Ecuador. b O. mimeticus sensu stricto, AF4442 (sequenced), San José, San Martín, Peru. c O. buckleyi sensu stricto, Canelos, Pastaza, Ecuador. d O. vilmae, QCAZ51205, Pompeya-Iro Road km 80, Orellana, Ecuador. e O. mutabor, QCAZ56066, Lorocachi, Pastaza, Ecuador. f O. mutabor, QCAZ39588, Río Pucayacu, Pastaza, Ecuador. g O. taurinus sensu stricto, Reserva Ducke, Amazonas, Brazil. h O. oophagus sensu stricto, Reserva Ducke, Amazonas, Brazil. Photographs: a, d–f by Santiago Ron (BIOWEB, Licence: CC BY-NC-ND 4.0); b by Antoine Fouquet; c, g–h by Diego Ortiz
ly a misidentification as today the recognized distribution of this species is restricted to western Africa. It is possible that the Cabinda frog may be referable to Phrynobatrachus auritus Boulenger, 1900. MAP 96. Distribution of Phrynobatrachus plicatus in Angola. in Diversity and Distribution of the Amphibians and Terrestrial Reptiles of Angola Atlas of Historical and Bibliographic Records (1840-2017)
ly a misidentification as today the recognized distribution of this species is restricted to western Africa. It is possible that the Cabinda frog may be referable to Phrynobatrachus auritus Boulenger, 1900. MAP 96. Distribution of Phrynobatrachus plicatus in Angola.
Spatial capture-recapture data of Darwin's frogs captured between 2014-2017
<p>Search-encounter spatial capture-recapture data from <em>R. darwinii</em> individuals captured between 2014-2017 at two plots located near Neltume, Southern Chile.</p> <p>x and y coordinates in meters are provided for each capture as text files. These are matrices with 64 columns (secondary capture occasions) and 311 rows (frogs). The 16 primary capture occasions are separated by a 3-month period, and each of these occasion is composed of four secondary capture occasions. With these data you can reconstruct the capture-history matrix used in non-spatial capture-recapture models.</p> <p>Snout-to-vent length (SVL) during each capture occasion are provided in mm for each frog. With these data you can reconstruct the age of the individuals (juveniles or adults).</p> <p>Id data is provided for each individual. The first column represents the frog’s code, and the second one represents the plot where the frog was captured (1= HUI1, 2= HUI2).</p> <p>Any question can be addressed to andresvalenzuela.zoo@gmail.com</p>
Training datasets for 16S Metagenomics analysis with FROGS
<p>This training dataset is from 2 imaginary microbiome samples. Each one is from a paired end 16S amplicon sequencing run and contains 2 fastq files (forwards and reverse.)</p> <p>It is a useful dataset for demonstrating:</p> <ul> <li>16S metagenomics analysis techniques</li> <li>Differences between microbiome samples</li> </ul>
Survey data and individual characterists for northeastern leopard frogs
<p>Data supporting Schlesinger, M.D. et al. In press. Follow-up ecological studies for cryptic species discoveries: decrypting the leopard frogs of the eastern U.S. PLOS ONE.</p>
Figure 6 in Genetic divergences of South and Southeast Asian frogs: a case study of several taxa based on 16S ribosomal RNA gene data with notes on the generic name Fejervarya
Figure 6. Maximum likelihood (ML) tree of bufonid frogs based on nucleotide sequences of the mitochondrial 16S rRNA gene with Leptophryne borbonica as an outgroup. The bootstrap support (>50%) is indicated at nodes in the order of ML (500) replicates. Asterisks represent Bayesian posterior probability (BPP; * ≥95%). Specimens examined in this study are indicated by boldface type.
Figure 2 in Genetic divergences of South and Southeast Asian frogs: a case study of several taxa based on 16S ribosomal RNA gene data with notes on the generic name Fejervarya
Figure 2. Maximum likelihood (ML) tree based on nucleotide sequences of the mitochondrial 16S rRNA gene from 88 haplotypes of frogs (Table 1), with Xenopus laevis as an outgroup. Bootstrap support (>50%) is indicated at nodes in the order of ML (1000) replicates. Asterisks represent Bayesian posterior probability (BPP; * ≥95%).
Figure 2 in Additional information on the Giant Himalayan Horned Frog, Megophrys periosa Mahony, Kamei, Teeling & Biju, 2018 (Anura: Megophryidae)
Figure 2. Field photographs of the specimens of M. periosa from Sessa, West Kameng, Arunachal Pradesh; a – V/A/NERC/1526 (♂) from EWS, and b – V/A/NERC/1527 (♀) from SOWS.
Figure 1 in 'Endangered' or 'Near Threatened', distribution status of Karaavali Skittering frog from the west coast of peninsular India
Figure 1. Map showing the distribution range of E. karaavali in the west coast of India (red star, type locality; red circle, other collection localities by Priti et al. (2016); blue circle, genetically identified by Anoop et al. (2017); orange circle, genetically confirmed sample in the present study; yellow circle, museum collection localities in the present study).
Figure 4 in Microhabitat partitioning of closely related Sarawak (Malaysian Borneo) frog species previously assigned to the genus Hylarana (Amphibia: Anura)
Figure 4. NMDS configuration showing ecological groupings from microhabitat characteristics of Sarawak frogs. Each point represents a species: Hba = Pulchrana baramica (N = 62 individuals), Hg = Pulcharana glandulosa (N = 10 individuals), Hsig = Pulcharana signata (N = 26 individuals), Hp = Pulcharana picturata (N = 27 individuals, Hra = Chalcorana raniceps (N = 112 individuals), He = Hylarana erythraea (N = 46 individuals), and Oh = Odorrana hosii (N = 21 individuals).
Figure 2 in Microhabitat partitioning of closely related Sarawak (Malaysian Borneo) frog species previously assigned to the genus Hylarana (Amphibia: Anura)
Figure 2. Dendrogram of Morisita's similarity resulting from average linkage clustering using the unweighted pair-group (UPGMA) method on data based on counts of individuals of frogs' species associated with habitats and microhabitats.
Figure 3 in Microhabitat partitioning of closely related Sarawak (Malaysian Borneo) frog species previously assigned to the genus Hylarana (Amphibia: Anura)
Figure 3. Final coordinate dimension (FDC) 1(A) and 2(B) of NMDS (PROXSCAL) of microhabitat characteristics of Sarawak frogs.
Fig. 3 in Development of in-country live food production for amphibian conservation: The Mountain Chicken Frog (Leptodactylus fallax) on Dominica, West Indies
Fig. 3. (A) Two rows of cricket breeding containers and cockroach breeding bins below. (B) Inside of a cricket breeding container, including refugia, food items, and several egg laying containers, transplanted into an empty container to allow eggs to hatch. (C) Inside view of a cockroach breeding bin, including substrate, refugia, and several food items. Photos: D. Nicholson.
Fig. 2 in Development of in-country live food production for amphibian conservation: The Mountain Chicken Frog (Leptodactylus fallax) on Dominica, West Indies
Fig. 2. Cultured species at the CBP in Dominica. (A) Gryllodes sigillatus. (B) Gryllus assimilis. (C) Caribacusta dominica. (D) Blaberus discoidalis. (E) Zophobas atratus. (F) Veronicella sloanii. (G) Pleurodonte dentiens. (H) Leptogoniulus sp. Photos: D. Nicholson.
Figure 3 in Rediscovery of pearly tree frog, Nyctixalus margaritifer Boulenger, 1882 (Amphibia: Rhacophoridae) from Mt. Wilis after 135 years
Figure 3. Discovery site of Nictyxalus margaritifer (a). The only one individual is attached on the ventral side of the coffee leaf. (b). A collapsed coffee tree as its microhabitat (Photographer: Richo Firmansyah).
Figure 2 in Rediscovery of pearly tree frog, Nyctixalus margaritifer Boulenger, 1882 (Amphibia: Rhacophoridae) from Mt. Wilis after 135 years
Figure 2. Habitat topography of Gunung Sigogor Nature Reserve. (a). High lands consist of hills and slopes. (b). A streamline flowing at the edge and inside the conservation area (Photographer: Richo Firmansyah).
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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.