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169 results for “Epibiont”
Figure 9 in Protozoan ciliate epibionts on the freshwater shrimp Caridina (Crustacea, Decapoda, Atyidae) from the Malili lake system on Sulawesi (Indonesia)
Figure 9. Cothurnia, view of the attachment of the ciliate to the surface of the basibiont.
Figure 6 in Protozoan ciliate epibionts on the freshwater shrimp Caridina (Crustacea, Decapoda, Atyidae) from the Malili lake system on Sulawesi (Indonesia)
Figure 6. Thuricola, the zooid inside the lorica and the operculum.
Figure 3 in Protozoan ciliate epibionts on the freshwater shrimp Caridina (Crustacea, Decapoda, Atyidae) from the Malili lake system on Sulawesi (Indonesia)
Figure 3. Acineta, view of the apical area with the tentacles (SEM).
Figure 5. Acineta, a specimen with a in Protozoan ciliate epibionts on the freshwater shrimp Caridina (Crustacea, Decapoda, Atyidae) from the Malili lake system on Sulawesi (Indonesia)
Figure 5. Acineta, a specimen with a larval stage in the apical surface.
Figure 4 in Protozoan ciliate epibionts on the freshwater shrimp Caridina (Crustacea, Decapoda, Atyidae) from the Malili lake system on Sulawesi (Indonesia)
Figure 4. Acineta, lateral view showing the actinophores and the stalk.
Figure 8 in Protozoan ciliate epibionts on the freshwater shrimp Caridina (Crustacea, Decapoda, Atyidae) from the Malili lake system on Sulawesi (Indonesia)
Figure 8. Cothurnia, arrangement of the individuals on the surface of the shrimp.
Figure 7 in Protozoan ciliate epibionts on the freshwater shrimp Caridina (Crustacea, Decapoda, Atyidae) from the Malili lake system on Sulawesi (Indonesia)
Figure 7. Cothurnia, an individual showing the lorica and the zooid.
Figure 12 in Protozoan ciliate epibionts on the freshwater shrimp Caridina (Crustacea, Decapoda, Atyidae) from the Malili lake system on Sulawesi (Indonesia)
Figure 12. Zoothamnium, several individuals of a colony.
Figure 11 in Protozoan ciliate epibionts on the freshwater shrimp Caridina (Crustacea, Decapoda, Atyidae) from the Malili lake system on Sulawesi (Indonesia)
Figure 11. Opercularia, two individuals in their loricae.
Figure 1 in Epibiontic communities on the freshwater shrimp Caridina ensifera (Crustacea, Decapoda, Atyidae) from Lake Poso (Sulawesi, Indonesia)
Figure 1. Geographical area of the study.
FIG. 4 in Middle Devonian Calceola sandalina (Linnaeus, 1771) (Anthozoa, Rugosa) from Moravia (Czech Republic): aspects of functional morphology, gerontic growth patterns, and epibionts
FIG. 4. — Calceola with calice facing downstream (A) and upstream (B).
A review of epibiont hydrozoans on Sargassum
<p>This database collects the information of hydroid epibionts of <em>Sargassum</em> records worldwide since 1802 to 2020. This database is part of the article titled "A review of epibiont hydrozoans on Sargassum", authored by Cecilia Odette Carral-Murrieta, Antonio C. Marques, Elisa Serviere-Zaragoza, Mariae C. Estrada-González, Amanda F. Cunha, Marina Oliveira Fernandez, Alejandra Mazariegos-Villarreal, Karla León-Cisneros, Juan Manuel López-Vivas, José Agüero, María A. Mendoza-Becerril.</p> <pre> </pre>
Data from: Oyster aquaculture impacts Zostera marina epibiont community composition in Akkeshi-ko estuary, Japan
Open the record for dataset details and reuse information.
Data from: Bacterial epibiont communities of panmictic Antarctic krill are spatially structured
<p>Antarctic krill (<i>Euphausia superba</i>) are amongst the most abundant animals on Earth, with a circumpolar distribution in the Southern Ocean. Genetic and genomic studies have failed to detect any population structure for the species, suggesting a single panmictic population. However, the hyper-abundance of krill slows the rate of genetic differentiation, masking potential underlying structure. Here we use high-throughput sequencing of bacterial 16S rRNA genes to show that krill bacterial epibiont communities exhibit spatial structuring, driven mainly by distance rather than environmental factors, especially for strongly krill-associated bacteria. Estimating the ecological processes driving bacterial community turnover indicated this was driven by bacterial dispersal limitation increasing with geographic distance. Furthermore, divergent epibiont communities generated from a single krill swarm split between aquarium tanks under near identical conditions suggests physical isolation in itself can cause krill-associated bacterial communities to diverge. Our findings show that Antarctic krill-associated bacterial communities are geographically structured, in direct contrast with the lack of structure observed for krill genetic and genomic data.</p>
FIGURE 7. Acineta sulcata Dons, 1927 in An overview of Suctorian ciliates (Ciliophora, Suctorea) as epibionts of halacarid mites (Acari, Halacaridae)
FIGURE 7. Acineta sulcata Dons, 1927 from Barents Sea halacarid mites (after Jankowski 1981). FIGURE 8. Acineta sulcata Dons, 1927 from freshwater halacarid mite found in Unava river (orig.). Scale bar 10 µm.
FIGURE 10 in An overview of Suctorian ciliates (Ciliophora, Suctorea) as epibionts of halacarid mites (Acari, Halacaridae)
FIGURE 10. Budding of Praethecacineta halacari (Schulz 1933) (orig.). Scale bar 10 µm. FIGURE 11. The settlement of Praethecacineta halacari on the halacarid mite from India (orig.). FIGURE 12. Thecacineta calix (Schroder 1907) found in the Black Sea (orig.). Scale bar 20 µm.
FIGURE 5 in A new Clathria (Demospongiae, Microcionidae) from Peru occurring on rocky substrates as well as epibiontic on Eucidaris thouarsii sea urchins
FIGURE 5. Spicule composition of a red Clathria (Microciona) aculeofila sp. nov. (MNRJ 11449) in SEM. A–C, principal subtylostyles; D–F, details of respectively A–C; G–I, accessory acanthostyles; J, detail of I; K–M auxillary styles and subtylostyles; N–P, details of the base of K–M; Q–R, details of the extremities of L–M; S, toxas; T, isochelae. Scale bars: A–C = 100 ìm; G–I = 20 ìm; J = 5 ìm; K–M = 50 µm; N–R = 10 µm; S = 20 µm; T = 5 µm.
FIGURE 4 in A new Clathria (Demospongiae, Microcionidae) from Peru occurring on rocky substrates as well as epibiontic on Eucidaris thouarsii sea urchins
FIGURE 4. Ground section of a spine of the sea urchin Eucidaris thouarsii covered by Clathria (Microciona) aculeofila sp. nov. MNRJ 13317. Scale bar = 200 µm.
FIGURE 6 in A new Clathria (Demospongiae, Microcionidae) from Peru occurring on rocky substrates as well as epibiontic on Eucidaris thouarsii sea urchins
FIGURE 6. Spicule composition of a yellow Clathria (Microciona) aculeofila sp. nov. (MNRJ 12982) in SEM. A–C, principal subtylostyles; D–E, details of respectively A–B; F–G, accessory acanthostyles; H, detail of G; I–J auxillary styles and subtylostyles; K–N, details of various auxillary styles and subtylostyles; O, toxas; P, isochelae. Scale bars: A–C = 100 ìm; D– E = 10 ìm; F–G = 20 ìm; H = 5 µm; I–J = 50 µm; K–N = 10 µm; O = 20 µm; P = 5 µm.
FIGURE 3 in A new Clathria (Demospongiae, Microcionidae) from Peru occurring on rocky substrates as well as epibiontic on Eucidaris thouarsii sea urchins
FIGURE 3. Transversal fracture of a spine of the sea urchin Eucidaris thouarsii (SEM) showing the structure of the skeleton of Clathria (Microciona) aculeofila sp. nov. MNRJ 13317. 1 = basal layer of spongin, 2 = echinated paucispicular fibres.
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