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668 results for “Mussels”
Figure 4 from: Wu R-W, Liu X-J, Wang S, Roe KJ, Ouyang S, Wu X-P (2019) Analysis of mitochondrial genomes resolves the phylogenetic position of Chinese freshwater mussels (Bivalvia, Unionidae). ZooKeys 812: 23-46. https://doi.org/10.3897/zookeys.812.29908
Figure 4 Hypotheses of phylogenetic relationships among subfamilies of the Unionidae form this and other studies. ALopes-Lima et al. (2017a)BBolotov et al. (2017a)CHuang et al. 2013; Burzyński et al. 2017; Huang et al. 2018; Wu et al. 2016, 2017bD This study.
Figure 2 from: Wu R-W, Liu X-J, Wang S, Roe KJ, Ouyang S, Wu X-P (2019) Analysis of mitochondrial genomes resolves the phylogenetic position of Chinese freshwater mussels (Bivalvia, Unionidae). ZooKeys 812: 23-46. https://doi.org/10.3897/zookeys.812.29908
Figure 2 The gene arrangement of the F-type mitochondrial genome of Acuticostachinensis, Schistodesmuslampreyanus, Cuneopsisheudei, and Cuneopsiscapitatus.
Figure 3 from: Wu R-W, Liu X-J, Wang S, Roe KJ, Ouyang S, Wu X-P (2019) Analysis of mitochondrial genomes resolves the phylogenetic position of Chinese freshwater mussels (Bivalvia, Unionidae). ZooKeys 812: 23-46. https://doi.org/10.3897/zookeys.812.29908
Figure 3 Phylogenetic trees of freshwater mussels obtained by Bayesian Inference (BI) and Maximum Likelihood (ML) analyses of 12 mitochondrial protein-coding gene sequences (except atp8) and two rRNA combined dataset. Support values above the branches are posterior probabilities and bootstrap support. (*) indicates 100 percent bootstrap support and posterior probabilities. Red font indicates Chinese species.
Figure 1 from: Wu R-W, Liu X-J, Wang S, Roe KJ, Ouyang S, Wu X-P (2019) Analysis of mitochondrial genomes resolves the phylogenetic position of Chinese freshwater mussels (Bivalvia, Unionidae). ZooKeys 812: 23-46. https://doi.org/10.3897/zookeys.812.29908
Figure 1 Shells of the unionids species in this study. AAcuticostachinensis (Lea, 1868) BSchistodesmuslampreyanus (Baird & Adams, 1867) CCuneopsisheudei (Heude, 1874) DCuneopsiscapitatus (Heude, 1874). Scale bar: 4 cm. Photogaphs R-W Wu.
Figure 1 from: Bolotov IN, Vikhrev IV, Lopes-Lima M, Gofarov MY, Konopleva ES, Lunn Z, Chan N, Bogan AE (2019) Indonaia rectangularis (Tapparone-Canefri, 1889), comb. nov., a forgotten freshwater mussel species from Myanmar (Bivalvia, Unionidae). ZooKeys 852: 23-30. https://doi.org/10.3897/zookeys.852.33898
Figure 1 Holotype of Indonaiarectangularis (Tapparone-Canefri, 1889), comb. nov. [MSNG]. A, B Shell, lateral view: inner side of the left valve and outer side of the right valve (A); vice versa (B) C shell, dorsal view D original label [probably by C.M. Tapparone-Canefri] E, F secondary labels [probably by B. Prashad]. Scale bar: 5 mm. (Photos: Ilya V. Vikhrev).
Figure 3 from: Bolotov IN, Vikhrev IV, Lopes-Lima M, Gofarov MY, Konopleva ES, Lunn Z, Chan N, Bogan AE (2019) Indonaia rectangularis (Tapparone-Canefri, 1889), comb. nov., a forgotten freshwater mussel species from Myanmar (Bivalvia, Unionidae). ZooKeys 852: 23-30. https://doi.org/10.3897/zookeys.852.33898
Figure 3 Map of the type locality of Indonaiarectangularis (Tapparone-Canefri, 1889), comb. nov. (dark blue circle). The digital elevation model and other layers of the map were added from the Esri Data & Maps 10 dataset.
Figure 2 from: Bolotov IN, Vikhrev IV, Lopes-Lima M, Gofarov MY, Konopleva ES, Lunn Z, Chan N, Bogan AE (2019) Indonaia rectangularis (Tapparone-Canefri, 1889), comb. nov., a forgotten freshwater mussel species from Myanmar (Bivalvia, Unionidae). ZooKeys 852: 23-30. https://doi.org/10.3897/zookeys.852.33898
Figure 2 Specimens of Indonaiaandersoniana (Nevill, 1877) and I.subclathrata (Martens, 1899) from Myanmar [RMBH biv450_2 and RMBH biv347_2, respectively]. A, B Shell of I.andersoniana, lateral view: inner side of the left valve and outer side of the right valve (A); vice versa (B) C shell of I.andersoniana, dorsal view D, E shell of I.subclathrata, lateral view: inner side of the left valve and outer side of the right valve (D); vice versa (E) F shell of I.subclathrata, dorsal view. Scale bar: 5 mm. (Photos: Ekaterina S. Konopleva).
Figure 2 in The gill morphology of the date mussel Lithophaga lithophaga (Bivalvia: Mytilidae)
Figure 2. Axial region of the ctenidia. a. A narrow axis and thin filaments of the gill of L. lithophaga. b. A prominent canal, full of food material (arrows) at the dorsal end of the axial region and a dentation at the lower edge (arrowhead). c. Protozoa trapped in the axial canal. Scale bar: a = 200 µm, b = 100 µm, c = 50 µm.
Figure 5 in The gill morphology of the date mussel Lithophaga lithophaga (Bivalvia: Mytilidae)
Figure 5. Ciliation on the filaments from the frontal view in the gill of L. lithophaga. a. Three very thick layers of cilia are prominent. b. Latero-frontal cilia in pairs. c. Duality in latero-frontal cilia and aggregated (arrowheads) or singly distributed (circles) food particles on the ciliary surface. lf: latero-frontal cilia. Scale bar: a = 40 µm, b = 10 µm, c = 4 µm.
Figure 1. a in The gill morphology of the date mussel Lithophaga lithophaga (Bivalvia: Mytilidae)
Figure 1. a. General anatomy of L. lithophaga. b. Schematic view of the gills showing very prominent double sheets within the mantle cavity. c. A ridged demibranch (*). Ml: mantle layers, Mc: mantle cavity, f: foot, ea: excurrent aperture, ia: incurrent aperture, aam: anterior adductor muscle, arm: anterior retractor muscle, ih: inner hemipalp, od: outer demibranches, id: outer demibranches.
Figure 7 in The gill morphology of the date mussel Lithophaga lithophaga (Bivalvia: Mytilidae)
Figure 7. Ostia (arrows) distributed unevenly along the abfrontal surface of the lamellae. Scale bar = 10 µm.
Fig. 9 in Pathobiology and first report of larval nematodes (Ascaridomorpha sp.) infecting freshwater mussels (Villosa nebulosa, Unionidae), including an inventory of nematode infections in freshwater and marine bivalves
Fig. 9. Second-stage larva of Ascaridomorpha sp. (Nematoda) infecting Villosa nebulosa, in lateral view. Body showing tripartite esophagus ([es], 1st part representing pharynx [p], 2nd part representing muscular anterior portion [amp], 3rd part representing muscular posterior portion [pme]), nerve ring (nr), genital primordium (gp), and anus (a).
Fig. 8 in Pathobiology and first report of larval nematodes (Ascaridomorpha sp.) infecting freshwater mussels (Villosa nebulosa, Unionidae), including an inventory of nematode infections in freshwater and marine bivalves
Fig. 8. Infected intestine of Villosa nebulosa showing ciliated columnar epithelium (ce), connective tissue (ct), and a nematode (ne).
Fig. 3 in Pathobiology and first report of larval nematodes (Ascaridomorpha sp.) infecting freshwater mussels (Villosa nebulosa, Unionidae), including an inventory of nematode infections in freshwater and marine bivalves
Fig. 3. Ventro-lateral aspect of an uninfected foot of Villosa nebulosa showing overlapping bundles of myofibers (mf), basophilic granulocytes (bg), and ciliated pedal epithelium (pe).
Fig. 11 in Pathobiology and first report of larval nematodes (Ascaridomorpha sp.) infecting freshwater mussels (Villosa nebulosa, Unionidae), including an inventory of nematode infections in freshwater and marine bivalves
Fig. 11. Second-stage larva of Ascaridomorpha sp. (Nematoda) infecting Villosa nebulosa, in lateral view. Anterior end of body showing vestibule (v).
Figure 2 in Effects of in vivo exposures to nanoparticles (Al O , CuO, TiO ) on the activities of ATPases in the gill and muscle of freshwater mussel (Unio tigridis)
Figure 2. Effects of NPs on Na-ATPase activity in the gill of mussels after 14 days. * indicates significant (p <0.05) differences compared to control.
Figure 13 in Structural and biological characterization of two freshwater mussel shells (Bivalvia: Unionidae)
Figure 13. Cell viability (%) of the freshwater mussel shell powder. *Significant differences compared to the control at p <0.05.
Figure 4 in Structural and biological characterization of two freshwater mussel shells (Bivalvia: Unionidae)
Figure 4. The periostracum on the outer surface of each shell of (A) P. semirugata and (B) L. wheatleyi.
Figure 2. Sinanodonta woodiana from Algeria, Oubeira Lake. A in First record of the occurrence of the Chinese pond mussel Sinanodonta woodiana (Lea, 1834) (Bivalvia: Unionidae) in African freshwaters: Oubeira Lake, Algeria
Figure 2. Sinanodonta woodiana from Algeria, Oubeira Lake. A: live specimens of S. woodiana collected from Oubeira sediment; B: general view of soft body (a: gills; b: foot; c: mantle); C: external view of the shell; D: internal view of the shell; E: details of umbonal sculptures. Photos: BensaâdBendjedid L.
Figure 2 in Environmental niche modelling of the Chinese pond mussel invasion in Europe under climate change scenarios
Figure 2. Response curves of the environmental variables selected for prediction of S. woodiana distribution under the recent climate scenario. Each curve (green line) shows how the logistic prediction changes as each environmental variable is varied. The orange dashed line crosses the maximum value of the variable.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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.