Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
65
datasets available to search
ShareScore release 0.9.0
Dataset results
65 results for “Odorrana”
Frequency jumps and subharmonic components in calls of female Odorrana tormota differentially affect the vocal behaviors of male frogs
<p><span>Many studies have demonstrated that sounds containing nonlinear phenomena (NLP) can influence the behavior of receivers. However, the specific functions of different NLP components have received less attention. In most frog species, females produce few or no vocalizations; in contrast, female <em>O</em></span><span><em>dorrana</em> <em>tormota</em></span><span> exhibit a diverse range of calls that are rich in NLP components. Previous field playbacks have shown that female calls can elicit responses from male frogs. Therefore, we conducted a phonotaxis experiment to investigate the differential effects of different NLP calls by female <em>O. tormota</em> on the vocal behavior of male frogs. The results of our study revealed that calls with subharmonics elicited a greater number of short calls and answering calls from male frogs than calls with frequency jumps. Conversely, calls with frequency jumps triggered more staccato calls from males than calls with subharmonics. Additionally, during the phonotaxis experiments, we recorded the initial vocalizations of males in response to playbacks of female calls. The majority of males first produced short calls. Under calls with frequency jumps, most of the male frogs approaching within 10 cm of the loudspeaker produced staccato calls instead of "meow" calls or short calls. While under calls with subharmonics, most male frogs preferred to produce short calls. Our findings demonstrate that frequency jumps and subharmonic components in the calls of female <em>O. tormota</em> have different effects on male vocal behaviors.</span></p>
Frequency jumps and subharmonic components in calls of female Odorrana tormota differentially affect the vocal behaviors of male frogs
Open the record for dataset details and reuse information.
FIGURE 5 in A new frog species of the genus Odorrana (Anura: Ranidae) from Yunnan, China
FIGURE 5. (A) Habitat of Odorrana dulongensis sp. nov. near Dulong river in Gaoligongshan National Nature Reserve, Yunnan Province, China.
FIGURE 4 in A new frog species of the genus Odorrana (Anura: Ranidae) from Yunnan, China
FIGURE 4. (A) Dorsal and (B) ventral views of the front feet, and (C) dorsal and (D) ventral views of the back feet of Odorrana dulongensis sp. nov. (KIZ 035029) in life.
FIGURE 3 in A new frog species of the genus Odorrana (Anura: Ranidae) from Yunnan, China
FIGURE 3. (A) Dorsolateral, dorsal (B), ventral (C) and head (D) views of Odorrana dulongensis sp. nov. (KIZ 035029) in life.
FIGURE 2 in A new frog species of the genus Odorrana (Anura: Ranidae) from Yunnan, China
FIGURE 2. Bayesian phylogenetic tree of the genus Odorrana inferred from a fragment of 16S gene. "-" denotes low support by Bayesian posterior probabilities (BPP <95%), and bootstrap support (BS <70%). The scale bar represents 0.05 nucleotide substitutions per site. The seven clades (A-G) were revealed by Chen et al. (2013).
FIGURE 1 in A new frog species of the genus Odorrana (Anura: Ranidae) from Yunnan, China
FIGURE 1. Type locality (red cycle) of Odorrana dulongensis sp. nov. in Dulongjiang, Gaoligongshan National Nature Reserve, Yunnan Province, China.
FIGURE 6 in Inter- and intra-island divergence in Odorrana ishikawae (Anura, Ranidae) of the Ryukyu Archipelago of Japan, with description of a new species
FIGURE 6. Chromosomes observed in spermatogenetic meioses of Amami common type control (A, B) and hybrids between Amami common type female and Okinawa male (C–F).
FIGURE 3. The Maximum Likelihood tree reconstructed from 16S in Inter- and intra-island divergence in Odorrana ishikawae (Anura, Ranidae) of the Ryukyu Archipelago of Japan, with description of a new species
FIGURE 3. The Maximum Likelihood tree reconstructed from 16S and sequence divergence data. The most parsimonious tree has the same topology.
FIGURE 4 in Inter- and intra-island divergence in Odorrana ishikawae (Anura, Ranidae) of the Ryukyu Archipelago of Japan, with description of a new species
FIGURE 4. Tailbud embryos of Okinawa control (A) and hybrid between Okinawa female and Amami common type male (B). In hybrid embryos, development was inhibited and showed exogastrulation and microcephaly. Scale bar = 2 mm.
FIGURE 7 in Inter- and intra-island divergence in Odorrana ishikawae (Anura, Ranidae) of the Ryukyu Archipelago of Japan, with description of a new species
FIGURE 7. Holotype (IABHU F2179) of Odorrana splendida sp. nov. Dorsal (A) and ventral (B) aspects. The chest was cut for collecting blood sample. Scale bar = 20 mm.
FIGURE 5 in Inter- and intra-island divergence in Odorrana ishikawae (Anura, Ranidae) of the Ryukyu Archipelago of Japan, with description of a new species
FIGURE 5. Structure of the testes of Amami common type control (A) and hybrid between Amami common type female and Okinawa male (B). Arrows indicate pycnotic nuclei showing failure of normal spermatogenesis. Scale bar = 50μm.
FIGURE 2 in Inter- and intra-island divergence in Odorrana ishikawae (Anura, Ranidae) of the Ryukyu Archipelago of Japan, with description of a new species
FIGURE 2. Dorsal and ventral aspects of the Amami large type (A, D), Amami common type (B, E), and Okinawa type (C, F). Scale bar = 20 mm.
FIGURE 1 in Inter- and intra-island divergence in Odorrana ishikawae (Anura, Ranidae) of the Ryukyu Archipelago of Japan, with description of a new species
FIGURE 1. (A) Frequencies of discriminant scores of the Amami and Okinawa types of O. ishikawae. Each numeral on abscissa includes the range ± 0.5. (B) Plots of scores of discriminant function 1 (CA1) and those of discriminant function 2 (CA2). Amami-C and Amami-L indicate Amami common type and Amami large type, respectively.
FIGURE 2 in A new species of the genus Odorrana (Amphibia: Ranidae) and the first record of Odorrana bacboensis from China
FIGURE 2. Bayesian inference tree derived from partial DNA sequences of the mitochondrial 12S rRNA and 16S rRNA gene with Bayesian posterior probabilities (BPP>80% retained) and maximum-likelihood bootstrap values (500 replicates; BS>60 retained), respectively.
FIGURE 6 in A new species of the genus Odorrana (Amphibia: Ranidae) and the first record of Odorrana bacboensis from China
FIGURE 6. Habitat of O. fengkaiensis sp. nov. in the type locality of Heishiding Nature Reserve, Fengkai County, Guangdong Province.
FIGURE 5 in A new species of the genus Odorrana (Amphibia: Ranidae) and the first record of Odorrana bacboensis from China
FIGURE 5. Morphology and colour pattern of Odorrana hainanensis and O. bacboensis in life. A: SYS a001046, adult female O. bacboensis, from Bainan village, Napo County, Guangxi, China. B: adult female O. hainanensis, from Diaoluoshan Mountain, Hainan Island. C: SYS a000377, adult male O. hainanensis, from Diaoluoshan Mountain, Hainan Island. D: velvety nuptial pad on thumb in SYS a000377. Photos by Qing Du and JHY.
FIGURE 3. The holotype SYS a002265 in A new species of the genus Odorrana (Amphibia: Ranidae) and the first record of Odorrana bacboensis from China
FIGURE 3. The holotype SYS a002265 of Odorrana fengkaiensis sp. nov.. A: dorsal view in life; B: ventral view in life; C: ventral spinules; D: dorsal view of hand; E: ventral view of hand; F: ventral view of foot. Photos by YLL and YYW.
FIGURE 4 in A new species of the genus Odorrana (Amphibia: Ranidae) and the first record of Odorrana bacboensis from China
FIGURE 4. Variation in morphology and colour pattern of Odorrana fengkaiensis sp. nov. in life. A: dorsolateral view of an adult male; B: dorsolateral view of an adult male (SYS a000176) and a gravid young female (SYS a000183); C: dorsal view of male froglet; D: dorsolateral view of a gravid young female (SYS a002262); E: an old adult female found on 3rd November, 2012; F: SYS a001045, an gravid old female from Tongling Canyon, Guangxi. Photos by YYW and JHY.
FIGURE 7 in A new species of the genus Odorrana (Amphibia: Ranidae) and the first record of Odorrana bacboensis from China
FIGURE 7. Comparisons of sister species O. hainanensis and O. fengkaiensis sp. nov. A: The specimen SYS a000377 of adult male O. hainanensis; B: CIB40548 of adult male O. hainanensis; C: SYS a002265 of adult male O. fengkaiensis sp. nov.; D: SYS a000176 of adult male O. fengkaiensis sp. nov.; 1: showing eye, tympanum and tympanum–eye distance; 2: showing disk width of finger III and width of distal phalanx of finger III.
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.