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Figs 39–53 in Comparative analysis of male calling signals in closely related species of Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Eurymelinae: Macropsini) reveals possible ways of evolution of the signal temporal pattern
Figs 39–53. Oscillograms of male calling signals: 39–47 — Macropsis milkoi; 48–53 — M. aselae. Faster oscillograms of the parts of signals indicated as "40", "46–47", and "52–53" are given under the same numbers. Рис. 39–53. Осциллограммы приЗывных сигналов: 39–47 — Macropsis milkoi; 48–53 — M. aselae. Фрагменты сигналов, обоЗначенные цифрами "40", "46–47" и "52–53", представлены на осциллограммах под такими же номерами.
Figs 15–29 in Calling signal pattern vs. genitalia morphology in Planaphrodes Hamilton, 1975 (Homoptera: Auchenorrhyncha: Cicadellidae: Aphrodinae) - which trait evolves faster?
Figs 15–29. Planaphrodes spp.: 15–21 — P. bifasciatus; 22–29 — P. monticola; 15–20 and 22–28 — oscillograms of male calling signals; 21 and 29 — penis, side view; 15, 17, and 19 — male from Mytishchi District; 16, 18, and 20–21 — male from Serpukhov District (both in Moscow Oblast); 22–23, 25, 27, and 29 — male from Western Tien-Shan Mts.; 24, 26, and 28 — male from Central Tien-Shan Mts. Faster oscillograms of the parts of signals indicated as "17–20" and "25–28" are given under the same numbers. Рис. 15–29. Planaphrodes spp.: 15–21 — P. bifasciatus; 22–29 — P. monticola; 15–20, 22–28 — осциллограммы приЗывных сигналов самца; 21, 29 — пенис сбоку; 15, 17, 19 — самец иЗ МытиЩинского р-на; 16, 18, 20–21 — самец иЗ Серпуховского р-на (оба — МосковскаЯ обл.); 22–23, 25, 27, 29 — самец с Западного ТЯнь-ШанЯ; 24, 26, 28 — самец с Центрального ТЯнь-ШанЯ. Фрагменты сигналов, обоЗначенные цифрами "17–20" и "25–28", представлены на осциллограммах под такими же номерами.
Fig. 10 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships
Fig. 10. Phylogenetic relationships within the Pristimantis "unistrigatus group" in the Guiana Shield as recovered in the MrBayes analysis (438 bp of the 16S rRNA gene sequence). Values at each node represent statistical support (* = 0.99 or 1). Pristimantis marmoratus (Boulenger, 1900) is highlighted in red.
Fig. 9 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships
Fig. 9. Habitat of Pristimantis marmoratus (Boulenger, 1900). Left. Submontane rainforest inKaieteur NationalParkatca630melevation.Right.MontanerainforestontheslopesofMaringma-tepui,Guyana at ca 1376 m elevation. Photographs by PJRK.
Fig. 6.A in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships
Fig. 6.A. Guzmania cf. sphaeroidea (André)André ex Mez, an arboreal bromeliad species used as egg deposition site by Pristimantis marmoratus (Boulenger, 1900) in the Wokomung Massif. B. Egg clutch of Pristimantis marmoratus deposited on a leaf of the arboreal bromeliad Guzmania cf. sphaeroidea in theWokomung Massif.C. Egg clutchof Anomaloglossus beebei(Noble, 1923) (white arrow) deposited in the phytotelmata of the same plant as in B. D. Dorsolateral view of IRSNB 17916, 11.3 mm SVL, a juvenile of P. marmoratus collected on the slopes of Maringma-tepui, Guyana. PhotographsA–C by DBM, D by PJRK.
Fig. 8 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships
Fig. 8. Vocalization of Pristimantis marmoratus (Boulenger, 1900); oscillogram and spectrogram obtained using Seewave v. 1.6.4 in R. Spectrogram (top) and oscillogram (below) of one call of IRSNB 14472 from Kaieteur National Park, Guyana. Call recorded at a temperature of 24°C.
Fig. 7 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships
Fig. 7. Vocalization of Pristimantis marmoratus (Boulenger, 1900); oscillograms and spectrograms obtained using Raven v. 1.4. A. Oscillogram (top) and spectrogram (below) of three calls of IRSNB 14472 from Kaieteur National Park, Guyana (ca 16 s recording). B. Expanded oscillogram (top) and spectrogram (below) of one call of IRSNB 14471 from Kaieteur National Park, Guyana. C. Expanded oscillogram (top) and spectrogram (below) of one call of IRSNB 14472 from Kaieteur National Park, Guyana. Calls recordedat a temperature of 24°C.
Fig. 5 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships
Fig. 5. Pristimantis marmoratus (Boulenger, 1900). Intraspecific variation in dorsal (top) and ventral (below) colour patterns in preserved specimens.Photographs by PJRK.
Fig. 3 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships
Fig. 3. Pristimantis marmoratus (Boulenger, 1900). Ventral view of left hand and left foot of a male (top), and ventral view of right hand and right foot of a female (below), both from Kaieteur National Park, Guyana.Photographs by PJRK.
Fig.4 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships
Fig.4.Pristimantismarmoratus(Boulenger,1900)(fourindividualsatthetop)andP.pulvinatus(Rivero, 1968) (twoindividuals below).Intraspecificvariation in dorsalcolour pattern and sexualdimorphism in living specimens. Note: the subtle hint of green visible on the lower body and legs of some specimens of P. marmoratus is due to a reflection of the substrate (green leaf). Photographs by PJRK, except the uncollected P.pulvinatus, which is by CBA.
Fig.2 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships
Fig.2.Pristimantismarmoratus(Boulenger,1900).Preservedadult♂,holotype(BMNH1947.2.16.92). A. Dorsal view. B. Ventral view. C. Dorsolateral view. Grid squares = 5 mm. Photographs by PJRK.
Fig. 1 in Amended diagnosis and redescription of Pristimantis marmoratus (Boulenger, 1900) (Amphibia: Craugastoridae), with a description of its advertisement call and notes on its breeding ecology and phylogenetic relationships
Fig. 1.MapoftheEasternPantepuiDistrictshowingtheknowndistributionof Pristimantismarmoratus (Boulenger,1900).Reddotsdenotelocalitiesofconfirmedoccurrencebasedeitheronmuseumspecimens or colour photographs.
FIGURE 1 in The advertisement call of Centrolene notostictum (Anura, Centrolenidae) with a new record of geographic distribution in Tolima, Colombia
FIGURE 1. Oscillogram (A) and audiospectrogram (B) of the advertisement call of C. notostictum (C). Voucher specimen CZUT-A 2080, snout-to-vent length: 23.96 mm. Call sample deposited at Fonoteca Zoológica, FZ_ Sound Code: 9982.
FIGURE 1 in The aggressive call of Dendropsophus cruzi (Pombal & Bastos, 1998) (Anura; Hylidae) in Central Brazil
FIGURE 1. Spectrogram (top) and oscilogram (bottom) of the advertisement and aggressive calls) of Dendropsophus cruzi from Itajá municipality, state of Goiás, Brazil (air temperature = 22.6 °C; SVL = 17.5; mass = 0.2 g).
FIGURE 1 in The advertisement call of Proceratophrys branti Brandão, Caramaschi, Vaz-Silva & Campos, 2013 (Amphibia, Anura, Odontophrynidae)
FIGURE 1. (A) Male of Proceratophrys branti (CEPB9501) from the recorded population in municipality of Novo Acordo, state of Tocantins, Brazil; (B) Power spectrum of a single advertisement call of P. branti (bandwidth = 256 Hz); (C) Oscillogram and (D) spectrogram of a single advertisement call of P. branti, air temperature at time of recording = 28.4°C.
FIGURE 2 in The advertisement calls of two species of Brachycephalus (Anura: Brachycephalidae) from southern Atlantic Forest, Brazil
FIGURE 2. Advertisement call of Brachycephalus quiririensis: (A) oscillogram of three consecutive calls; and (B) spectrogram and (C) oscillogram of a single call. Voucher CFBHT 21178, recorded at Campos do Quiriri, Municipality of Garuva, Santa Catarina State, Brazil, on 27 November 2013, 0715 p.m., air temperature 16°C and air relative humidity 100%.
FIGURE 1 in The advertisement calls of two species of Brachycephalus (Anura: Brachycephalidae) from southern Atlantic Forest, Brazil
FIGURE 1. Advertisement call of Brachycephalus olivaceus: (A) oscillogram of three consecutive calls; and (B) spectrogram and (C) oscillogram of a single call. Non-vouchered recording made at Castelo dos Bugres, Municipality of Joinville, Santa Catarina State, Brazil, on 29 November 2013, 0530 p.m., air temperature 21°C and air relative humidity 100%.
Training material for Calling variants in non-diploid systems
<p>The majority of life on Earth is non-diploid and represented by prokaryotes, viruses and their derivatives such as our own mitochondria or plant’s chloroplasts. In non-diploid systems allele frequencies can range anywhere between 0 and 100% and there could be multiple (not just two) alleles per locus. The main challenge associated with non-diploid variant calling is the difficulty in distinguishing between sequencing noise (abundant in all NGS platforms) and true low frequency variants. </p>
FIGURE 8 in A new species of Pseudopaludicola Miranda-Ribeiro (Anura: Leptodactylidae: Leiuperinae) from eastern Brazil, with novel data on the advertisement call of Pseudopaludicola falcipes (Hensel)
FIGURE 8. Live specimens of Pseudopaludicola pocoto from Pico das Almas, Rio de Contas, state of Bahia, Brazil. (A) ZUEC 23510 (adult male, call voucher, SVL = 12.3 mm); (B) ZUEC 23511 (adult female, SVL = 14.8 mm).
FIGURE 3 in A new species of Pseudopaludicola Miranda-Ribeiro (Anura: Leptodactylidae: Leiuperinae) from eastern Brazil, with novel data on the advertisement call of Pseudopaludicola falcipes (Hensel)
FIGURE 3. Holotype and three paratypes of Pseudopaludicola florencei sp. nov. in life. (A) ZUEC 23521 (holotype, adult male, call voucher, SVL = 12.9 mm), (B) ZUEC 23523 (adult female, SVL = 15.5 mm), (C) ZUEC 23520 (adult male, call voucher, SVL = 13.2 mm), and (D) ZUEC 23522 (adult male, SVL = 12.8 mm).
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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.