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1,085 results for “Ciliophora”
Fig. 2 in Morphological and molecular identification of epibiontic sessilid Epistylis semiciculus n. sp. (ciliophora, Peritrichia) from Procambarus clarkia (Crustacea, Decapoda) in China
Fig. 2. Telotrochs of morphotype II of Epistylis semiciculus n. sp. in vivo. A. Apical view of telotroch. B. Oral of telotroch (arrow). C. Oral infraciliature (arrow). D. Transverse striations on oral pellicle (arrow). E. Macronucleus and infraciliature. F. Macronucleus (arrow). ATB, aboral trochal band; CV, Contractile vacuole; Ma, macronucleus; P, polykinety. Scale bars = 10 μm.
Fig. 6 in Morphological and molecular identification of epibiontic sessilid Epistylis semiciculus n. sp. (ciliophora, Peritrichia) from Procambarus clarkia (Crustacea, Decapoda) in China
Fig. 6. Consensus tree constructed from both trees generated by phylogenetic analyses of nuclear ITS1-5.8S-ITS2 sequence. The sequences investigated in the present study are in bold. Numbers on branches indicate the posterior probability (BI) and bootstrap (ML) values, respectively. 1, morphotype I; 2 and 3, morphotype II; 4, Telotrochs of morphotype II.
Fig. 5 in Morphological and molecular identification of epibiontic sessilid Epistylis semiciculus n. sp. (ciliophora, Peritrichia) from Procambarus clarkia (Crustacea, Decapoda) in China
Fig. 5. Consensus tree constructed from both trees generated by phylogenetic analyses of nuclear SSU rDNA sequences. The sequences investigated in the present study are formatted in bold. Numbers at nodes of branches indicate the posterior probability (BI) and bootstrap (ML) values, respectively. 1 and 2, morphotype I; 3, morphotype II; 4, Telotrochs of morphotype II.
Figure 3 in Ten new records of Protozoan Ciliates (Protozoa: Ciliophora) from India
Figure 3. Photomicrographs of protargol impregnated specimens. A, B. Leptopharynx costatus, ventral (A) and dorsal (B) views, arrowheads point to the food vacuoles. C, D. Rimaleptus mucronatus. E1, type 1 extrusomes; E2, type 2 extrusomes; MA, macronuclear nodules; MI, micronuclei. Scale bars 15 μm (A, B), 100 μm (D).
Figure 4 in Ten new records of Protozoan Ciliates (Protozoa: Ciliophora) from India
Figure 4. Photomicrographs of protargol impregnated specimens. A, B. Dileptus beersi. Arrowheads point to the oral opening. C, D. Pseudomonilicaryon falciforme. Arrowhead points to the oral opening. E1, type 1 extrusomes; E2, type 2 extrusomes; MA, macronuclear nodules; MI, micronuclei. Scale bars 80 μm (A, D), 15 μm (B, C).
Figure 2 in Ten new records of Protozoan Ciliates (Protozoa: Ciliophora) from India
Figure 2. Photomicrographs of protargol impregnated specimens of Cyrtolophosis muscicola Indian population. A, B. Vegetative specimens, arrowheads mark the oral concavity. C. A specimen in divisional stage. MA, macronuclear nodules; MI, micronuclei. Scale bars 10 μm.
Figure 1 in Ten new records of Protozoan Ciliates (Protozoa: Ciliophora) from India
Figure 1. Photomicrographs of protargol impregnated specimens. A. Anteholosticha intermedia. B. Rigidosticha italiensis, arrowhead marks the paroral membrane. C. Monomicrocaryon balladyna. D. Urosoma karinae. E. Diophrys oligothrix. AZM, adoral zone of membranelles; BC, buccal cirrus; CC, caudal cirri; LM, left marginal row; MA, macronuclear nodules; MI, micronuclei; MVP, midventral cirral pairs; RM, right marginal row; TC, transverse cirri. Scale bars 40 μm (A, B, D), 20 μm (C, E).
Figure 1 in Morphology of Indian populations of Coleps elongatus (Ehrenberg, 1830) Kahl, 1930 and C. amphacanthus Ehrenberg, 1833 (Ciliophora: Prostomatea: Prorodontida)
Figure 1. Photomicrography of Coleps elongatus Mahananda Wildlife Sanctuary population from live (A-E) and after protargol impregnation (F-H), Senhati Jheel population from live (I-L) and after protargol impregnation (M-O). A. Specimen showing typical barrel shaped body. B. Arrows showing anteriormost plates. C. Arrow indicating globular macronucleus. D. Arrowhead indicating contractile vacuole at the posterior body end. E. Arrow showing two distinct caudal cilia. F, G. Specimen showing ciliature on the dorsal and ventral surface. H. Oral ciliature. I. Specimen showing body shape, arrow indicates anterior spine and arrowheads point caudal spines. J. Specimen showing armour plate and 3rd caudal spine in different focus. K. hirtus-type of armour. L. pretzel-shaped window. M. Specimen showing dorsal ciliature. N. Macronucleus. O. Oral ciliature with perioral kineties. Scale bars: A, F, G, M- 15 µm; I, J- 20 µm; N- 10 µm.
Figure 2 in Morphology of Indian populations of Coleps elongatus (Ehrenberg, 1830) Kahl, 1930 and C. amphacanthus Ehrenberg, 1833 (Ciliophora: Prostomatea: Prorodontida)
Figure 2. Photomicrography ofColeps amphacanthus small natural pond, Kolkata population from live (A-E) and after protargol impregnation (F-I), Senhati Jheel population from live (J-P). A. Specimen showing broad barrel shaped body. B. hirtus-type windows. C. Arrowhead showing posterior spine. D. Arrow indicating contractile vacuole. E. Specimen showing caudal cilia. F. Specimen showing body ciliature. G. Macronucleus. H. Oral ciliature. I. caudal cilia. J. Specimen showing typical barrel shaped body. K. Arrowheads showing two anterior spines. L. Specimens showing typical hirtus-type armour plates. M. Enlarged view of the ruptured specimen showing 8-shaped windows. N. Specimen showing body shape with armoured plates. O. Caudal cilia. P. Arrow indicating contractile vacuole. Scale bars: A, F, J, N- 25 µm; G- 15 µm.
Figure 2 in Trichodinid fauna of freshwater fishes with infestation indices in the Lower Kızılırmak Delta in Turkey and a checklist of trichodinids (Ciliophora: Trichodinidae) in Turkish waters
Figure 2. Trichodinid parasites identified on Lower Kızılırmak Delta fishes: A) T. lepsii, B) T. puytoraci, C) T. domerguei, D) T. heterodentata, E) Paratrichodina corlissi, F) T. domerguei, G) T. modesta, H) Tripartiella macrosoma, I) T. acuta, J) T. lucioperca, K) T. tenuidens, L) Trichodina sp1, M) T. cobitis, N) Trichodina sp2, O) Trichodina sp3.
Figure 3 in Tintinnina (Ciliophora) and Foraminifera in plankton of hypersaline Lagoon Bardawil (Egypt): spatial and temporal variability
Figure 3. Dependence of number of found tintinnid species on number of analyzed samples in Lagoon Bardawil (a) and the Mediterranean Sea (b).
Figure 2 in Tintinnina (Ciliophora) and Foraminifera in plankton of hypersaline Lagoon Bardawil (Egypt): spatial and temporal variability
Figure 2. Dependence of total tintinnid abundance on number of tintinnid species in Lagoon Bardawil during 2009 and 2010 (a- winter, b- all seasons).
Figure 3 in The first finding of sessile ciliates Vorticella pyriforme Stiller, 1939 and Zoothamnium sinense Song, 1991 (Ciliophora, Peritrichia) in the Black Sea
Figure 3. General view of the colony Zoothamnium sinense Song, 1991 (original, in vivo), scale bar: 250 µm.
Figure 4. Zoothamnium sinense Song, 1991. A, C in The first finding of sessile ciliates Vorticella pyriforme Stiller, 1939 and Zoothamnium sinense Song, 1991 (Ciliophora, Peritrichia) in the Black Sea
Figure 4. Zoothamnium sinense Song, 1991. A, C – original, in vivo, scale bar: 35 µm; В – modified from Ji et al., 2006, scale bar: 20 µm.
Figure 20 in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 20. Results of cluster analysis (Simpson index) of species compositions of tintinnid ciliates in the world's oceans; in nodes of dendrogram, the results of bootstrap-analysis are marked.
Figure 10 in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 10. Results of cluster analysis (Simpson index) of species compositions of tintinnid ciliates in the Atlantic Ocean; in nodes of dendrogram, the results of bootstrap-analysis are marked.
Figure 23. A in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 23. A log-log plots of semivariance versus distance for tintinnid alpha-diversity (A – for distances ranged 100 to 2,500 km; B – for distances ranged 1,500 to 16,000 km). DF – fractal dimension; r - correlation coefficient.
Figure 5 in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 5. Species accumulation curve for tintinnid ciliates diversity in the Black Sea and the Sea of Azov.
Figure 8 in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 8. Results of cluster analysis (Simpson index) of species compositions of tintinnid ciliates in the Mediterranean Sea; in nodes of dendrogram, the results of bootstrap-analysis are marked.
Figure 14 in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 14. Results of cluster analysis (Simpson index) of species compositions of tintinnid ciliates in the Indian Ocean; in nodes of dendrogram, the results of bootstrap-analysis are marked.
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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.