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258 results for “freshwater mussel”
Fig. 12 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. 12. Second-stage larva of Ascaridomorpha sp. (Nematoda) infecting Villosa nebulosa, in lateral view. Posterior end of body showing anus (a), rectal glands (rg).
Fig. 7 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. 7. Uninfected intestine of Villosa nebulosa showing ciliated columnar epithelium (ce), and connective tissue (ct).
Fig. 2 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. 2. Ventral portion of infected foot of Villosa nebulosa showing a nematode infection (ne), myofibers (mf), basophilic granulocytes (bg), and pedal epithelium (pe).
Fig. 10 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. 10. Second-stage larva of Ascaridomorpha sp. (Nematoda) infecting Villosa nebulosa, in lateral view. Anterior end of body showing lips (l), pharynx (p), and esophagus (es).
Fig. 1 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. 1. Ventral portion of an uninfected foot of Villosa nebulosa showing myofibers (mf), basophilic granulocytes (bg), and pedal epithelium (pe).
Fig. 13 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. 13. Phylogenetic interrelationships of nematodes (Cosmocercoidea, Seuratoidea) based on sequences of the 18S rDNA, generated from Bayesian inference. Nodal supports were estimated by Bayesian posterior probability (BPP) after running the Markov chain Monte Carlo (2 runs 4 chains, 4 × 106 generations, sampling frequency = 4 × 103, burn-in = 1 × 106). Sequence obtained in the present study is in bold.
Figure 6 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 6. Effects of NPs on Ca-ATPase activity in the muscle of mussels after 14 days. * indicates significant (p <0.05) differences compared to control.
Figure 4 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 4. Effects of NPs on Ca-ATPase activity in the gill of mussels after 14 days. * indicates significant (p <0.05) differences compared to control.
Figure 3 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 3. Effects of NPs on Mg-ATPase activity in the gill of mussels after 14 days. * indicates significant (p <0.05) differences compared to control.
Figure 5 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 5. Effects of NPs on Mg-ATPase activity in the muscle of mussels after 14 days. * indicates significant (p <0.05) differences compared to control.
Figure 1 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 1. TEM images of Al O (a), CuO (b), and TiO (c) nanoparticles in stock solutions (Canli and Canli, 2020).
Figure 1 in A new genus of ultra-elongate freshwater mussels from Vietnam and eastern China (Bivalvia: Unionidae)
Figure 1. Examples of Sinosolenaia gen. nov. shells (external view of the left valves). (A) S. recognita (Heude, 1877) gen. & comb. nov., Hanoi, Red (Hồng Hà) River basin, northern Vietnam. (B) S. oleivora (Heude, 1877) comb. nov., Yangtze River basin, eastern China. (C) S. carinata (Heude, 1877) comb. nov., Yangtze River basin, eastern China. Scale bars = 25 mm. (Photo: Yulia S. Kolosova [A], Huang et al. (2019) [B-C]).
Figure 12 in Structural and biological characterization of two freshwater mussel shells (Bivalvia: Unionidae)
Figure 12. (A) Hemolytic activity (%) of the freshwater mussel shell powder. (B) BCI (%) of the freshwater mussel shell powder. *Significant differences for all pairwise analyses at p <0.05.
Figure 9 in Structural and biological characterization of two freshwater mussel shells (Bivalvia: Unionidae)
Figure 9. SEM-EDS of the different surfaces of the L. wheatleyi shells: (A) periostracum layer and (B) nacreous layer.
Figure 8 in Structural and biological characterization of two freshwater mussel shells (Bivalvia: Unionidae)
Figure 8. View of the nacre layer of (A) P. semirugata and (B) L. wheatleyi, where the individual aragonite layers are horizontally overlapping.
Figure 7 in Structural and biological characterization of two freshwater mussel shells (Bivalvia: Unionidae)
Figure 7. Lateral view of the prismatic layer showing the columnar convergent prisms of (A) P. semirugata and (B) L. wheatleyi.
Figure 10 in Structural and biological characterization of two freshwater mussel shells (Bivalvia: Unionidae)
Figure 10 SEM-EDS of the different surfaces of the P. semirugata shells: (A) periostracum layer and (B) nacreous layer.
Figure 3 in Structural and biological characterization of two freshwater mussel shells (Bivalvia: Unionidae)
Figure 3. The growth front of the outer surface of each shell of (A) P. semirugata and (B) L. wheatleyi.
Figure 1 in First record of the occurrence of the Chinese pond mussel Sinanodonta woodiana (Lea, 1834) (Bivalvia: Unionidae) in African freshwaters: Oubeira Lake, Algeria
Figure 1. Location of Oubeira Lake in the boundaries of El-Kala National Park (modified from Sarri, 2017).
Figure 3 in First record of the occurrence of the Chinese pond mussel Sinanodonta woodiana (Lea, 1834) (Bivalvia: Unionidae) in African freshwaters: Oubeira Lake, Algeria
Figure 3. Scheme of measurements for S. woodiana from Oubeira Lake (photos by Bensaâd-Bendjedid L.): shell's length (SL), height (SH), and width (SW).
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
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)
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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.