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Portrait of the haptorid ciliate, Chaenea teres (Dujardin,1841). Probably synonymous with C. stricta (Dujardin 1841, Foissner, 1995) which is also found in freshwater habitats. The cell is elongate,ovoid in cross section,flexible but only slightly contractile. There is a short anterior snout with an inconspicuous apical cytostome. Small trichites support the cytopharynx. Longitudinal somatic kineties are widely spaced. The short snout has densely packed slightly spiral kineties with longer cilia. There is a single posterior terminal contractile vacuole (not seen in this image). The macronucleus is in many small rounded parts throughout the cytoplasm. The cytoplasm of this individual contains multiple highly refractile crystalline inclusions.This specimen was collected from a commercial saltwater aquarium in Boise, Idaho May 2004. DIC optics.
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Detail of the anterior end of the haptorid ciliate, Chaenea teres (Dujardin,1841). Probably synonymous with C. stricta (Dujardin 1841, Foissner, 1995) which is also found in freshwater habitats. The cell is elongate,ovoid in cross section,flexible but only slightly contractile. There is a short anterior snout with an inconspicuous apical cytostome. Small trichites support the cytopharynx. Longitudinal somatic kineties are widely spaced. The short snout has densely packed slightly spiral kineties with longer cilia (seen well here). The cytoplasm of this individual contains highly refractile crystalline inclusions.This specimen was collected from a commercial saltwater aquarium in Boise, Idaho May 2004. DIC optics.
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Portrait of the haptorid ciliate, Chaenea teres (Dujardin,1841). Probably synonymous with C. stricta (Dujardin 1841, Foissner, 1995) which is also found in freshwater habitats. The cell is elongate,ovoid in cross section,flexible but only slightly contractile. There is a short anterior snout with an inconspicuous apical cytostome. Small trichites support the cytopharynx. Longitudinal somatic kineties are widely spaced. The short snout has densely packed slightly spiral kineties with longer cilia. The cytoplasm of this individual contains highly refractile crystalline inclusions.This specimen was collected from a commercial saltwater aquarium in Boise, Idaho May 2004. DIC optics.
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Portrait of the haptorid ciliate, Chaenea teres (Dujardin,1841). Probably synonymous with C. stricta (Dujardin 1841, Foissner, 1995) which is also found in freshwater habitats. The cell is elongate,ovoid in cross section,flexible but only slightly contractile. There is a short anterior snout with an inconspicuous apical cytostome. Small trichites support the cytopharynx. Longitudinal somatic kineties are widely spaced. The short snout has densely packed slightly spiral kineties with longer cilia (seen well here). The cytoplasm of this individual contains highly refractile crystalline inclusions.This specimen was collected from a commercial saltwater aquarium in Boise, Idaho May 2004. DIC optics.
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Detail of the anterior end of the haptorid ciliate, Chaenea teres (Dujardin,1841). Probably synonymous with C. stricta (Dujardin 1841, Foissner, 1995) which is also found in freshwater habitats. The cell is elongate,ovoid in cross section,flexible but only slightly contractile. There is a short anterior snout with an inconspicuous apical cytostome. Small trichites support the cytopharynx. Longitudinal somatic kineties are widely spaced. The short snout has densely packed slightly spiral kineties with longer cilia (seen well here). The cytoplasm of this individual contains highly refractile crystalline inclusions.This specimen was collected from a commercial saltwater aquarium in Boise, Idaho May 2004. DIC optics.
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Enchelyodon (ench-elly-owe-don), a cylindrical predatory ciliate, body fairly flexible, mouth is a slit zone at anterior end, underlain by a number of extrusomes. Differential interference contrast.
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Trachelophyllum, small predatory ciliate, with a wreath of flagella projecting from the front of the cell. This cell has two large macronuclei, one on each side of the small micronucleus. From Lake Donghu, China. Phase contrast micrograph.
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Trachelophyllum, a predatory haptorid ciliate. The mouth is located at the anterior pole. Extrusomes lie internal to the mouth. Contractile vacuole located at posterior end. Differential interference contrast optics.
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Trachelophyllum, a predatory haptorid ciliate. The mouth is located at the anterior pole. Extrusomes lie internal to the mouth. Contractile vacuole located at posterior end.
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Two of the three types of lepidosomes of Luporinophrys micelae (FOISSNER,2005). The type II are not seen in this image.Stained by the silver carbonate technique (see Foissner, W. Europ. J. Protistol., 27:313-330;1991).Brightfield.
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Luporinophrys micelae (FOISSNER,2005). Collected from an ephemeral puddle on a flood-irrigated grass lawn in Boise, Idaho, 2007.Phase contrast.
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Luporinophrys micelae (FOISSNER,2005). Collected from an ephemeral puddle on a flood-irrigated grass lawn in Boise, Idaho, 2007.Phase contrast.
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Enchelyodon armatus (KAHL,1926) KAHL,1930 from a freshwater pond near Boise, Idaho. Oblique illumination.
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Enchelyodon armatus (KAHL, 1926) KAHL, 1930.DIC.
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In vivo portrait of Enchelyodon armatus (KAHL,1926),KAHL,1930 demonstrating the band-form macronucleus.
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Trachelophyllum apiculatum (Perty, 1852) Claparède & Lachmann, 1859.Predatory ciliate with surface coated with a single type (probably Type I) of fine organic scales (i.e. lepidosomes). Identification is tentative since scanning electron microscopy is required for diagnostic lepidosome characterization. Collected from a freshwater pond near Boise, Idaho.DIC.
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Trachelophyllum apiculatum (Perty, 1852) Claparède & Lachmann, 1859. Predatory ciliate with surface coated with a single type (probably Type I) of fine organic scales (i.e. lepidosomes). Identification is tentative since scanning electron microscopy is required for diagnostic lepidosome characterization.Yellow arrows mark the surface layer of fine organic scales (i.e. lepidosomes). Collected from a freshwater pond near Boise, Idaho.DIC.