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34 results for “dendrobatid”
FIG, 1. John William Daly (1933–2008) on the upper Río San Juan. This paper is dedicated to John Daly, our late friend and colleague, who helped collect three of the new species here described. In addition to his globally acclaimed discoveries in chemistry and pharmacology, John was an accomplished field herpetologist who contributed importantly to the systematics and natural history of dendrobatoid frogs (see Grant et al., 2006; Myers, 2009). This photograph shows John at age 37, with the upper Río San Juan behind him and branches overhead of a madroño tree (probably Garcinia magnifolia, syn. Rheedia chocoensis, Clusiaceae). When in South America, John was never far from a dendrobatid frog—this time, in the tree above his head, a tiny, undescribed semiarboreal species (also collected and later named "Dendrobates fuguritus" by our colleague Philip Silverstone). Other dendrobatids found nearby included Phyllobates aurotaenia (Boulenger, 1913), which was then being used for poisoning blowgun darts, and also the nontoxic species that we name Silverstoneia dalyi herein. (Photograph by C. W. Myers, 2 km above Playa de Oro, Chocó, February 16, 1971.) in Review of the Frog Genus Silverstoneia, with Descriptions of Five New Species from the Colombian Chocó (Dendrobatidae: Colostethinae)
FIG, 1. John William Daly (1933–2008) on the upper Río San Juan. This paper is dedicated to John Daly, our late friend and colleague, who helped collect three of the new species here described. In addition to his globally acclaimed discoveries in chemistry and pharmacology, John was an accomplished field herpetologist who contributed importantly to the systematics and natural history of dendrobatoid frogs (see Grant et al., 2006; Myers, 2009). This photograph shows John at age 37, with the upper Río San Juan behind him and branches overhead of a madroño tree (probably Garcinia magnifolia, syn. Rheedia chocoensis, Clusiaceae). When in South America, John was never far from a dendrobatid frog—this time, in the tree above his head, a tiny, undescribed semiarboreal species (also collected and later named "Dendrobates fuguritus" by our colleague Philip Silverstone). Other dendrobatids found nearby included Phyllobates aurotaenia (Boulenger, 1913), which was then being used for poisoning blowgun darts, and also the nontoxic species that we name Silverstoneia dalyi herein. (Photograph by C. W. Myers, 2 km above Playa de Oro, Chocó, February 16, 1971.)
Physiological thermal niches, elevational ranges and thermal stress in dendrobatid frogs: an integrated approach
<p><strong>Aim: </strong>We investigated the relationship between thermal physiology, elevational distribution, and thermal stress among nine closely related dendrobatid frogs during their aquatic stage by employing an integrated approach, combining thermal physiology, environmental temperature modelling, and predictive assessments of current and future exposure to thermal variation.</p> <p><strong>Location:</strong> Ecuador</p> <p><strong>Taxon:</strong> Amphibians; Anura, Dendrobatidae, Epipedobates, Hyloxalus</p> <p><strong>Methods:</strong> We determined the Thermal Performance Curves of larval growth (TPCs) for each species and modelled the thermal variation in contrasting aquatic larval environments for both present and future times. This allowed us to estimate the expected elevational distributions and forecast periods of exposure to stressful temperatures that inhibit larval growth due to elevation and global warming.</p> <p><strong>Results:</strong> We found significant correlations between optimum temperature (Topt), 50 % maximum performance temperature (maxB50), 50% minimum performance temperature (minB50), and cold resistance (survival at 9 ºC) with the current elevational distributions. However, thermal physiology predicted lower than observed distributions for high-elevation dendrobatids and higher than observed maximum elevations for lowland species. Nonetheless, our models predicted that low thermal variability habitats (i.e. streams and deep permanent ponds) can buffer the future increase in temperatures for all taxa, even when considering the most extreme scenario. In contrast, all species within high thermal variation habitats (open forest temporary ponds) are expected to experience stressful temperatures under present conditions.</p> <p><strong>Main Conclusions:</strong> The findings indicate that thermal physiology may not be a limiting factor for dendrobatid frog species' ranges in this equatorial mountain gradient. Highland species may need to adapt to suboptimal performance, while some lowland species could occupy higher elevations. This study emphasizes the importance of habitat buffering to mitigate thermal stress in the face of climate change for amphibians in tropical mountains.</p>
Data from: Sexy fingers: Pheromones in the glands of male dendrobatid frogs
<p>Our study investigates the role of the swollen fingers of two dendrobatid species, <em>Leucostethus brachistriatus, </em>and <em>Epipedobates anthonyi,</em> in pheromone production using whole-transcriptome sequencing (RNAseq). We examined differential gene expression in the swollen versus non-swollen fingers and toes. The overwhelming pattern of gene expression in both species was strong upregulation of sodefrin precursor-like factors (SPFs) in swollen fingers, a well-known pheromone system in salamanders. As part of the results, we include a fasta-file with the RNA-seq assemblies from each species, as well as their annotation and Differential expression (DE) analyses. Likewise, we include the alignment of some of the most highly expressed sodefrin precursor-like-factor (SPF) sequences</p>
Wild dendrobatid frog microbiomes - bacteria
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Wild dendrobatid microbiomes - fungi
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Ecuadorian Dendrobatid frog alkaloid profiles
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Data from: Physiological thermal niches, elevational ranges and thermal stress in dendrobatid frogs: An integrated approach
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Data from: Sexy fingers: Pheromones in the glands of male dendrobatid frogs
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FIGURE 2 in A new dendrobatid frog (Anura: Dendrobatidae: Colostethus) from Aprada tepui, southern Venezuela
FIGURE 2. View of the type locality (Cueva de El Fantasma, Aprada tepui) from inside. Note the size of the two helicopters at the entrance. This is the first geographic report and photograph of such immense "cave". Photo by Charles BrewerCarías.
FIGURE 6 in A new dendrobatid frog (Anura: Dendrobatidae: Anomaloglossus) from the Orinoquian rainforest, southern Venezuela
FIGURE 6. Natural habitat of the type locality of Anomaloglossus verbeeksnyderorum sp. nov., Tobogán de la Selva, Estado Amazonas, Venezuela.
FIGURE 3 in A new dendrobatid frog (Anura: Dendrobatidae: Anomaloglossus) from the Orinoquian rainforest, southern Venezuela
FIGURE 3. Anomaloglossus verbeeksnyderorum sp. nov. in life. A. Male. B. Female. Specimens not collected. Photo by Zelimir Cernelic.
FIGURE 2 in A new dendrobatid frog (Anura: Dendrobatidae: Anomaloglossus) from the Orinoquian rainforest, southern Venezuela
FIGURE 2. Hands and feet of Anomaloglossus verbeeksnyderorum sp. nov. A. Palmar view of the left hand of the holotype (MHNLS 19649). B. Palmar view of the left hand of the female paratopotype MHNLS 16944. C. Sole view of the right foot of the holotype (MHNLS 19649). D. Sole view of the left foot of the paratotype (MHNLS 19644), showing a median metatarsal tubercle. Note that there are only four toes instead five. See explanation on the text. Scale equals 2 mm.
FIGURE 5 in A new dendrobatid frog (Anura: Dendrobatidae: Anomaloglossus) from the Orinoquian rainforest, southern Venezuela
FIGURE 5. Distribution of the genus Anomaloglossus in Venezuela. 1. A. verbeeksnyderorum sp. nov. type locality. 2. A. wothuja. 3. A. guanayensis. 4. A. shrevei. 5. A. parimae. 6. A. tamacuarensis. 7. A. ayarzagüenai. 8. A. moffetti. 9. A. tepuyensis. 10. A. triunfo. 11. A. murisipanensis. 12. A. parkerae. 13. A. praderioi and A. roraima. 14. A. breweri.
FIGURE 4 in A new dendrobatid frog (Anura: Dendrobatidae: Anomaloglossus) from the Orinoquian rainforest, southern Venezuela
FIGURE 4. Anomaloglossus verbeeksnyderorum sp. nov. A. Audiospectrogram and B. oscillogram of a complete trill call with 152 notes. 24.5 ºCelsius. C. audiospectrogram and D. oscillogram of an amplified random section of the complete call sequence.
FIGURE 1 in A new dendrobatid frog (Anura: Dendrobatidae: Anomaloglossus) from the Orinoquian rainforest, southern Venezuela
FIGURE 1. Anomaloglossus verbeeksnyderorum sp. nov. A. Left profile of the head of the holotype (MHNLS 19649). B. Dorsal view of the head of the holotype (MHNLS 19649). C. Ventral view of the head of the holotype (MHNLS 19649). D. Ventral view of female paratopotype MHNLS 16944 showing the sexual dichromatism explained in the text. Scale equals 2 mm. E. Dorsal view of the holotype (MHNLS 19649). F. Ventral view of the holotype (MHNLS 19649).
FIGURE 2 in A new striking dendrobatid frog (Dendrobatidae: Aromobatinae, Aromobates) from the Venezuelan Andes
FIGURE 2. Dorsal (A) and ventral (B) views of the holotype (EBRG 5292) of Aromobates ornatissimus sp. nov.
FIGURE 3 in A new striking dendrobatid frog (Dendrobatidae: Aromobatinae, Aromobates) from the Venezuelan Andes
FIGURE 3. Lateral view of the head (A), dorsal view of the head (B), palmar view of the right hand (C) and plantar view of the right foot (D) of the holotype (EBRG 5292) of Aromobates ornatissimus sp. nov. Scale equals 2 mm.
FIGURE 6 in A new striking dendrobatid frog (Dendrobatidae: Aromobatinae, Aromobates) from the Venezuelan Andes
FIGURE 6. One note of the call of Aromobates ornatissimus sp. nov. taken at 19ºC. (A) waveform and (B) spectrogram.
FIGURE 5 in A new striking dendrobatid frog (Dendrobatidae: Aromobatinae, Aromobates) from the Venezuelan Andes
FIGURE 5. Series of 5 notes in the call of Aromobates ornatissimus sp. nov., taken at 19ºC. (A) waveform and (B) spectrogram. Note distinct harmonics.
FIGURE 1 in A new striking dendrobatid frog (Dendrobatidae: Aromobatinae, Aromobates) from the Venezuelan Andes
FIGURE 1. Maximum likelihood tree of Aromobates ornatissimus sp. nov., other dendrobatids, and closely related hyloids. The phylogeny was inferred using a 12S-16S rRNA segment. Support values are based on 200 non-parametric bootstrap replicates. Museum catalog numbers and GenBank accession numbers are provided.
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