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.
123
datasets available to search
ShareScore release 0.9.0
Dataset results
123 results for “Mormyridae”
FIGURE 9 in A new Stomatorhinus (Osteoglossomorpha: Mormyridae) from the Ivindo River, Gabon, West Central Africa
FIGURE 9. Waveforms and power spectra of EODs from Stomatorhinus walkeri (A – D), S. ater (E, F) and S. patrizii (G, H) on the same time scale as those shown in Fig. 5. EOD waveforms are centered about the largest headnegative peak, normalized to the same peaktopeak height and plotted with head positivity upward for each trace. Power spectra are normalized so that the peak energy is adjusted to 0 dB. Individual specimen numbers are indicated beneath waveforms; F = female, M = male.
FIGURE 8 in A new Stomatorhinus (Osteoglossomorpha: Mormyridae) from the Ivindo River, Gabon, West Central Africa
FIGURE 8. Scores from types of S. ivindoensis n. sp. and five other Stomatorhinus species on the second and third factors of a principal components analysis of the covariance matrix calculated from 24 logtransformed morphometric measures. Twelve nontype specimens of S. walkeri and one nontype of S. polli included. Variables loading most heavily on the second principal component are caudal peduncle depth, interorbital distance and internostril distance. Variables loading most heavily on the third principal component are eye diameter, postorbital head length and caudal
FIGURE 5 in A new Stomatorhinus (Osteoglossomorpha: Mormyridae) from the Ivindo River, Gabon, West Central Africa
FIGURE 5. EOD waveforms (left) and power spectra (right) for Stomatorhinus ivindoensis n. sp. The holotype of S. ivindoensis, a male, is shown in A and B. Peaks are numbered in order from P 0 to P 3. EOD waveforms are centered about the largest headnegative peak and plotted with head positivity upward. Power spectra are normalized so that the peak energy is adjusted to 0 dB. EODs of reproductive males (E, F) are longer in duration and have a lower peak power frequency than those of females (C, D). Individual specimen numbers are indicated beneath waveforms; F = female, M = male, H = holotype. Time base = 0.1 millisecond.
FIGURE 7 in A new Stomatorhinus (Osteoglossomorpha: Mormyridae) from the Ivindo River, Gabon, West Central Africa
FIGURE 7. Selected morphometric ratios of S. ivindoensis n. sp. compared to those in S. fuliginosus (A) and S. polli (B). IO = interorbital distance, HW = head width, CPD = caudal peduncle depth measured at terminus of anal fin, CPL = caudal peduncle length, E = eye diameter, HL = head length.
FIGURE 4 in A new Stomatorhinus (Osteoglossomorpha: Mormyridae) from the Ivindo River, Gabon, West Central Africa
FIGURE 4. Typical forest creek habitat of Stomatorhinus ivindoensis n. sp.: upper “ Balé Creek ” within the Ipassa Plateau Reserve near Makokou, Gabon.
FIGURE 3 in A new Stomatorhinus (Osteoglossomorpha: Mormyridae) from the Ivindo River, Gabon, West Central Africa
FIGURE 3. Collection sites of Stomatorhinus ivindoensis n. sp. (circles) and S. walkeri (triangles) in the Ivindo and Ogooué River basins of Gabon and the KouilouNiari basin of the Republic of Congo. Shaded areas delimit the boundary of the Lower Guinea ichthyofaunal province of West Central Africa.
FIGURE 2 in A new Stomatorhinus (Osteoglossomorpha: Mormyridae) from the Ivindo River, Gabon, West Central Africa
FIGURE 2. Photograph (A) and radiograph (B) of preserved holotype of Stomatorhinus ivindoensis n. sp., CU 85157, 43.8 mm SL, male; (C) live paratype specimen no. 1004, CU 75437, 40.8 mm SL, male; (D) preserved paratype, CU 85465, 52.2 mm SL, female.
FIGURE 1 in A new Stomatorhinus (Osteoglossomorpha: Mormyridae) from the Ivindo River, Gabon, West Central Africa
FIGURE 1. Drawing of Stomatorhinus ivindoensis n. sp. holotype, 43.8 mm SL. Drawn by Vera Ming Wong.
FIGURE 6 in A new Stomatorhinus (Osteoglossomorpha: Mormyridae) from the Ivindo River, Gabon, West Central Africa
FIGURE 6. Species of Stomatorhinus to which Stomatorhinus ivindoensis n. sp. is closely compared in study: (A) S. walkeri syntype BMNH 1867.5. 3.16, 85.6 mm SL; (B) S. walkeri live specimen no. 2880, CU 80237, 95 mm SL; (C) S. fuliginosus syntype MRAC 6652, 37.7 mm SL; (D) S. fuliginosus syntype MRAC 6648, 33.5 mm SL; (E) S. polli paratype MRAC 138993, 61.3 mm SL; (F) S. polli paratype MRAC 138977, 58.7 mm SL.
FIG. 1. — A in From fin rays to DNA: supplementary morphological and molecular data to identify Mormyrus subundulatus Roberts, 1989 (Pisces: Mormyridae) from the Bandama River in Côte d'Ivoire
FIG. 1. — A, radiography of the paratype SU 63507 Mormyrus subundulatus Roberts, 1989 from the Tano River (© California Academy of Sciences, Dept. of Ichthyology); B, specimen number MNHN-IC-2018-0558 caught in the Bandama River near the type locality; C, specimen number MNHN-IC-2018-0559. Scale bar: A, 10 cm.
FIG. 4. — A in From fin rays to DNA: supplementary morphological and molecular data to identify Mormyrus subundulatus Roberts, 1989 (Pisces: Mormyridae) from the Bandama River in Côte d'Ivoire
FIG. 4. — A, Distribution of Mormyrus subundulatus Roberts, 1989 according to available data; B, the Bandama River in the type locality is impacted by the Taabo dam just upstream; C, preserved stream habitat downstream the type locality where M. subundulatus still lives. This part of the River will be lost after the impoundment of another big dam, planned for the next few years; D, aerial view (GoogleEarth) of the Tano River in the type locality (red dot); E, upstream, showing the important buildup of soil and mud due to mining activities. The Tano River does not seem to host suitable habitat for M. subundulatus anymore, at least around the historical locality.
FIG. 3 in From fin rays to DNA: supplementary morphological and molecular data to identify Mormyrus subundulatus Roberts, 1989 (Pisces: Mormyridae) from the Bandama River in Côte d'Ivoire
FIG. 3. — Distribution of the dorsal fin rays counts for the specimens of M. subundulatus Roberts, 1989 examined by us (blue bars) and for the specimens of M. rume Valenciennes, 1847 (data from Lévêque and Bigorne, 1985; orange bars). Yellow bars: specimens presumably from the Sassandra River population. (1) position of paratype CAS-SU63507 from the Tano River in Ghana (red bar); (2) position of specimen MNHN-IC-2018-0558, for which genetic data confirms the identification as M. subundulatus.
FIG. 2 in From fin rays to DNA: supplementary morphological and molecular data to identify Mormyrus subundulatus Roberts, 1989 (Pisces: Mormyridae) from the Bandama River in Côte d'Ivoire
FIG. 2. — Bayesian phylogenetic analyses base on Cyt b gene fragment (A) and COI gene fragment (B). Numbers on branch node indicate posterior probability values, only node with posterior probability above 85 are represented. Nodes with probability> 98 are identified with *. Numbers on specimens indicate the GenBank accession number of the sequence or, when many specimens shared the same haplotype, the haplotype names in Table 1.
Figure 5 in Notes on the electric organ discharges (EODs) of four Mormyrus-species (Osteoglossomorpha: Mormyridae) from the Nilo-Sahelo-Sudan ichthyofaunal province of Africa
Figure 5. - Scatterplot of logarithmic total signal duration in µs versus logarithmic peak of fast Fourier transformation in Hz. Each symbol represents a single EOD from M. caschive (open triangle, n = 8), M. hasselquistii (open inverse triangle, n = 31), M. kannume (filled triangle, n = 3) and M. rume (filled inverse triangle, n = 7).
Figure 4 in Notes on the electric organ discharges (EODs) of four Mormyrus-species (Osteoglossomorpha: Mormyridae) from the Nilo-Sahelo-Sudan ichthyofaunal province of Africa
Figure 4. - Boxplots of selected signal characteristics. A: Total EOD duration in µs; B: Relative amplitude of main positive phase; C: Peak frequency of fast Fourier transformation in Hz.
Figure 3 in Notes on the electric organ discharges (EODs) of four Mormyrus-species (Osteoglossomorpha: Mormyridae) from the Nilo-Sahelo-Sudan ichthyofaunal province of Africa
Figure 3. - Exemplary AC coupled measurements of electric organ discharges (EODs) of Mormyrus species. A: M. caschive, 97 mm SL, White Nile at Kosti, Sudan. B: M. kannume, 169 mm SL, White Nile at Khartoum, Sudan. C: M. hasselquistii, 188 mm SL, Mare Diwouni, Pendjari National Park, Benin. D: M. rume, 230 mm SL, Ouémé at Kpoto, Benin.
Figure 2 in Notes on the electric organ discharges (EODs) of four Mormyrus-species (Osteoglossomorpha: Mormyridae) from the Nilo-Sahelo-Sudan ichthyofaunal province of Africa
Figure 2. - AC coupled measurement of electric organ discharge (EOD) of Mormyrus caschive (97 mm SL; White Nile at Kosti, Sudan) showing nomenclature of waveform characteristics as used in this study. m-POS = main positive phase; m-NEG = main negative phase; p-POS = posterior positive phase. Beginning and end of the signal is given by exceeding 1.5% of the total amplitude; beginning and end of phases within the signal by zero-crossings.
Figure 1 in Notes on the electric organ discharges (EODs) of four Mormyrus-species (Osteoglossomorpha: Mormyridae) from the Nilo-Sahelo-Sudan ichthyofaunal province of Africa
Figure 1. - Outline of the African continent showing sampling sites of the study. Only sampled river systems are displayed.
A new genome of an African weakly electric fish (Campylomormyrus compressirostris, Mormyridae) indicates rapid gene family evolution in Osteoglossomorpha
Background <p>Teleost fishes comprise more than half of the vertebrate species. Within teleosts, most phylogenies consider the split between Osteoglossomorpha and Euteleosteomorpha/Otomorpha as basal, preceded only by the derivation of the most primitive group of teleosts, the Elopomorpha. While Osteoglossomorpha are generally species-poor, the taxon contains the African weakly electric fish (Mormyroidei), which have radiated into numerous species. Within the mormyrids, the genus <em>Campylomormyrus</em> is mostly endemic to the Congo Basin. <em>Campylomormyrus</em> serves as a model to understand mechanisms of adaptive radiation and ecological speciation, especially with regard to its highly diverse species-specific electric organ discharges (EOD). Currently, there are few well-annotated genomes available for electric fish in general and mormyrids in particular. Our study aims at producing a high-quality genome and to use this to examine genome evolution in relation to other teleosts. This will facilitate further understanding of the evolution of the osteoglossomorph fish in general and of electric fish in particular.</p> Results <p>A high-quality weakly electric fish (<em>C. compressirostris</em>) genome was produced from a single individual with a genome size of 862Mb, consisting of 1,497 contigs with an N50 of 1,399 kb and a GC-content of 43.69%. Gene predictions identified 34,492 protein-coding genes, which is a higher number than in the two other available Osteoglossomorpha genomes of <em>Paramormyrops</em> <em>kingsleyae</em> and <em>Scleropages</em> <em>formosus</em>. A CAFE5 analysis of gene family evolution comparing 33 teleost fish genomes suggests an overall faster gene family turnover rate in Osteoglossomorpha than in Otomorpha and Euteleosteomorpha. Moreover, the ratios of expanded/contracted gene family numbers in Osteoglossomorpha are significantly higher than in the other two taxa, except for species that had undergone an additional genome duplication (<em>Cyprinus</em> <em>carpio</em> and <em>Oncorhynchus</em> <em>mykiss</em>). As potassium channel proteins are hypothesized to play a key role in EOD diversity among species, we put a special focus on them, and manually curated 16 Kv1 genes. We identified a tandem duplication in the KCNA7a gene in the genome of <em>C</em>. <em>compressirostris</em>.</p> Conclusions <p>We present the fourth genome of an electric fish and the third well-annotated genome for Osteoglossomorpha, enabling us to compare gene family evolution among major teleost lineages. Osteoglossomorpha appears to exhibit rapid gene family evolution, with more gene family expansions than contractions. The curated Kv1 gene family showed seven gene clusters, which is more than in other analyzed fish genomes outside Osteoglossomorpha. The KCNA7a, encoding for a potassium channel central for EOD production and modulation, is tandemly duplicated which may related to the diverse EOD observed among <em>Campylomormyrus</em> species.</p>
A new genome of an African weakly electric fish (Campylomormyrus compressirostris, Mormyridae) indicates rapid gene family evolution in Osteoglossomorpha
Open the record for dataset details and reuse information.
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.