Morphology and morphogenesis of a freshwater ciliate, Epistylis chlorelligerum Shen, 1980 (Ciliophora, Peritrichia)

An oligohalobic peritrichous ciliate, Epistylis chlorelligerum Shen, 1980, was collected from a ditch in Hangzhou, China. The morphology, oral infraciliature, and morphogenesis of the species were studied using living and protargol-impregnated specimens. Zooids of E. chlorelligerum are 160-230 × 50-60 μm in vivo, and characterized by green-colored endoplasm containing symbiotic algae. The oral infraciliature presents a well-developed filamentous reticulum linked to the circular fiber of the cytostome; the outer two rows of P3 extend adstomally over P1 and usually enfold it. During binary fission, one daughter cell inherits most part of the old buccal apparatus and the reorganized haplokinety and germinal kinety (Hk' and G'), and new buccal apparatus of the other daughter cell is mostly developed from the original germinal kinety (G) and haplokinety (Hk): new peniculi 2, 3 (2P2, 2P3), new haplokinety (2Hk), and new germinal kinety (2G) are formed from G, while the new peniculus 1 (2P1) and its peristomial extention (2Pk) originate from Hk. The epistomial membrane can be observed until the two sets of buccal apparatus begin to separate from each other.     

Infraciliature and myoneme system of Campanella umbellaria (Protozoa, Ciliophora, Peritrichida)

The infraciliature and myoneme system of Campanella umbellaria were revealed using the protargol impregnation technique. The main characteristics of the infraciliature are the peristomial ciliary rows (haplokinety and polykineties), which make four and a half turns around the peristomial disc before plunging into the infundibulum, and the aboral infraciliature, which is made up of the aboral ciliary wreath (trochal band) and the scopula. The myoneme system is composed of: 1) longitudinal fibers, which include 60-84 (mean 72.3) short longitudinal fibers, 40-56 (mean 45.8) medium-length longitudinal fibers, and numerous long longitudinal fibers; and 2) circular fibers, which include 8-12 (mean 9.3) peristomial ring fibers, linking fibers, support fibers, and peristomial disc fibers. The various fibers in C. umbellaria are interconnected to form a single myoneme system that may act as a cell skeleton as well as providing the mechanism by which the zooid contracts and relaxes.     

Morphology and Morphogenesis of Two Species of the Genus Lembadion (Ciliophora, Oligohymenophora): Lembadion lucens and Lembadion bullinum

ABSTRACT. The morphology and morphogenesis of two species of the genus Lembadion, L. lucens and L. bullinum , are described. In both species, left and right ventral kineties converge behind the mouth forming a postoral suture. Buccal infraciliature is formed by one polykinety and two very close paroral kineties (inner and outer). During stomatogenesis, the new oral structures originate from the paroral kineties. The inner paroral kinety forms the new adoral polykinety and regenerates the outer paroral kinety of the proter, while the paroral kineties of the opisthe originate from the outer paroral kinety of the parental cell. Somatic proliferation starts before the stomatogenesis at the equatorial level of the cell, and extends towards the poles forming an equatorial band. Two large invariant zones, anterior and posterior, remain in the dividing cell. Moreover, the kinetodesmal fibers disappear in the proliferation band during the bipartition (fission) process.     

Pseudovorticella zhengae n. sp., P. difficilis (Kahl, 1933) Jankowski, 1976, and P. punctata (Dons, 1918) Warren, 1987, three marine peritrichous ciliates from north China

The morphology, infraciliature and silverline system of three marine peritrichous ciliates, Pseudovorticella zhengae n. sp., P. difficilis (Kahl, 1933) Jankowski, 1976 and P. punctata (Dons, 1918) Warren, 1987, were investigated by observation in vivo and silver-staining methods. The new species is characterized by its body shape, the appearance of the peristomial lip, the number of transverse silverlines, and the configuration of infundibular polykinety 3; P. difficilis by its body shape, the configuration of infundibular polykinety 3, and unusual annular swellings on the stalk; and P. punctata by the appearance of the pellicle, the configuration of infundibular polykinety 3, and the number of transverse silverlines.     

Taxonomic characterization of two marine peritrichous ciliates, Epicarchesium corlissi n. sp. and Pseudovorticella jiangi n. sp. (Ciliophora: Peritrichia), from northern China

Two new marine peritrich ciliates, Epicarchesium corlissi n. sp. and Pseudovorticella jiangi n. sp., were discovered in mariculture waters on the coast of northern China near Qingdao. Their morphology, infraciliature and silverline system were investigated based on both living and silver-impregnated specimens. E. corlissi is characterized as follows: marine Epicarchesium with dichotomously branched stalk; zooids elongate, approximately 60–70×25–35 μm in vivo; peristomial collar double-folded; macronucleus J-shaped; single, small contractile vacuole ventrally positioned; more than 60 striations between peristome and aboral trochal band, 13–18 from aboral trochal band to scopula; abstomal end of row 1 of infundibular polykinety 3 terminating at same level as rows 2 and 3 of infundibular polykinety 3; rows 2 and 3 of infundibular polykinety 3 much longer than row 1 and converging adstomally with infundibular polykinety 1. The new species P. jiangi is diagnosed as follows: marine Pseudovorticella; zooid inverted bell-shaped, approximately 80×60 μm in vivo and with a broad, flat, thin peristomial collar that measures approximately 90 μm across; pellicle with transparent cortical vesicles; macronucleus J-shaped; number of silverlines between peristome and aboral trochal band 20–24, from aboral trochal band to scopula 9–11; abstomal end of row 1 of infundibular polykinety 3 diverges from the other two rows of this polykinety and ends alongside row 3 of infundibular polykinety 2.     

Observations on Opisthonecta henneguyi Fauré-Fremiet: Infraciliature, Argyrome, and Myonemic System

The infraciliature, argyrome, and myonemic system of Opisthonecta henneguyi have been examined after impregnation with the Fernández-Galiano silver impregnation method. The oral infraciliature is formed by one haplokinety and three polykineties while the aboral infraciliature is formed by the trochal band—six kinetosomes wide—and the scopula. The trochal band has three fibrillar systems: orally directed fibers, aboral fibers, and oblique fibers. The argyrome is formed by 90 to 135 fine circular striations, which cover the whole organism with the exception of the peristome. The myonemic system is located in two regions: the oral and the aboral ones. The oral myonemic system is formed by a fibrous ring which surrounds the peristome underneath the spiral of the peristomial infraciliature and by a group of fibers which depart from the peristomial disc. The aboral myonemic system is much simpler, and it is formed by fibers which extend radially from the scopula. Biometrical characterizations of the vegetative cells and living cysts were also made, and our data are compared with the results obtained previously by other authors.     

The Stomatogenic Process in Opercularia coarctata (Ciliophora, Peritrichida)

ABSTRACT. Stomatogenesis in Opercularia coarctata has been studied in specimens treated with Fernández-Galiano's silver impregnation method. The new buccal structures originate from the germinal row and from the parental haplokinety.     

Description of Opisthonecta Matiensis N. Sp. (Protozoa, Ciliophora), A New Peritrich Ciliate From Wastewater

Opisthonecta matiensis n. sp. was isolated from the inlet water of a wastewater treatment plant near Madrid, Spain, and studied in vivo, with silver methods, and using electronic and indirect immunofluorescence microscopy. This new species shows an amphora-like cell shape and has a size of 45-73 microns (x 58.2) x 25-40 microns (x 31.3). The oral infraciliature is formed by one haplokinety, three polykineties, and a short row of kinetosomes (epistomial membrane). The aboral infraciliature is made up of the trochal band and the scopula. From the trochal band arise three fibrillar systems: oral fibers, aboral fibers, and oblique fibers. The myoneme system is composed of a delicate peristomial ring, longitudinal branched fibers that reach the trochal band and of radial fibers extending from the scopula to the trochal band. The silverline system consists of an average of 147 lines. This new species is separated from other known forms by its smaller size, the presence of one single vacuole, and its higher number of silverlines.     

Two New Species of Zoothamnium (Ciliophora,Peritrichia) from Korea,with New Observations of Z. parahentscheli Sun et al., 2009

Three peritrichous ciliates, Zoothamnium arcuatum n. sp., Z. grossi n. sp., and Z. parahentscheli Sun et al., 2009, were collected from an estuary of the Taehwagang River, Korea. All these species were investigated based on live observations and silver staining, and their small subunit (SSU) rRNA gene was also sequenced. Zoothamnium arcuatum can be identified by a goblet‐shaped colony, double‐layered peristomial lip, and abstomally shortened row 3 of infundibular polykinety 3 (P3). Zoothamnium grossi is morphologically characterized by an alternately branched stalk with the lowest secondary stalk diverging from the main part of colony, asymmetrically bell‐shaped zooids, and three short, parallel ciliary rows in P3. Phylogenetic analysis revealed that the three Zoothamnium species described in this paper clustered with other members of the family Zoothamniidae, as expected.     

Morphological and Molecular Identification of a New Ciliate,Zoothamnium palmphlatum nov. spec. (Ciliophora,Peritrichia) from North China

A new peritrichous ciliate, Zoothamnium palmphlatum nov. spec., was collected from an estuary in Yantai, China. It was investigated, using both live observation and silver staining. The new species can be identified by a palm‐shaped colony consisting of highly developed and alternately arranged secondary branches, a double‐layered peristomial lip, and an infundibular polykinety 3 composed of two parallel kinetosomal rows. Phylogenetic analyses of the small subunit (SSU) rRNA gene sequence show that Z. palmphlatum clusters with other members of the family Zoothamniidae. Furthermore, the comparison of primary and secondary SSU rDNA structures indicates that Z. palmphlatum is distinctly different from its morphologically similar species (93.2–97.0% in sequence similarity) in combination of H10 and H31 regions. Although Z. palmphlatum shares highest sequence similarity with Zoothamnium mucedo (98.9%), the new species has distinctly different structures in the H11, H12, H18, and H31 regions compared to Z. mucedo, which indicates that sequence similarity may not determine the similarity of the secondary structure.     

Morphology and Phylogeny of Four New Vorticella Species (Ciliophora: Peritrichia) from Coastal Waters of Southern China

Four new species of Vorticella, V. parachiangi sp. n., V. scapiformis sp. n., V. sphaeroidalis sp. n., and V. paralima sp. n., were isolated from coastal brackish waters of southern China. Their morphology, infraciliature, and silverline system were investigated based on observations of specimens both in vivo and following silver staining. Vorticella parachiangi sp. n. is distinguished by: a J‐shaped macronucleus; a single dorsally located contractile vacuole; a two‐rowed infundibular polykinetid 3, in which row 1 is shorter than row 2; 21–31 silverlines between peristome and aboral trochal band, 6–11 between aboral trochal band and scopula. Vorticella scapiformis sp. n. is characterized by its conspicuously thin and irregularly edged peristomial lip; a J‐shaped macronucleus; a single, ventrally located contractile vacuole; row 1 of the infundibular polykinetid 3 proximally shortened; 18–25 silverlines between peristome and aboral trochal band, 8–12 between aboral trochal band and scopula. Vorticella sphaeroidalis sp. n. can be identified by its small, sub‐spherical zooid; a C‐shaped macronucleus; a ventrally located contractile vacuole; an aboral trochal band adjacent to the scopula; 16–18 silverlines between persitome and aboral trochal band, two between aboral trochal band and scopula. Vorticella paralima sp. n. can be identified by its ovoidal zooid; a J‐shaped macronucleus; a dorsally positioned contractile vacuole; rows 1 and 2 of the infundibular polykinetid 3 proximally shortened; 26–35 silverlines from peristome to aboral trochal band, and 7–13 from aboral trochal band to scopula. The SSU rDNA genes of these four species were sequenced and their phylogeny was analyzed.     

Morphology,Morphogenesis and Molecular Phylogeny of a New Obligate Halophile Ciliate,Schmidtiella ultrahalophila gen. nov., spec. nov. (Ciliophora,Hypotrichia) Isolated from a Volcanic Crater on Sal (Cape Verde Islands)

A new hypotrichous ciliate, Schmidtiella ultrahalophila gen. nov., spec. nov., was isolated from a solar saltern on the island of Sal, Cape Verde. The possession of only one short dorsal kinety clearly distinguishes S. ultrahalophila from other known hypotrichous genera and species. Further diagnostic characters include: a flexible and slender body, an average size of 85 × 15 μm in vivo; a bipartite adoral zone with two hypertrophied frontal adoral membranelles and nine to twelve ventral adoral membranelles; three frontal, one parabuccal, two frontoventral, two or three postoral ventral, and two or three frontoterminal cirri; and marginal cirral rows variable in number, usually one on each side. Ontogenetic data indicate the following: the frontal‐ventral cirri originate from six or five anlagen; the proter inherits the parental adoral zone; the frontal and ventral cirri originate from five or six anlagen; and the marginal cirral rows and the dorsal kinety tend to originate intrakinetally. Additional marginal rows are rarely derived from de novo anlagen. Based on its morphology, morphogenesis and its SSU rRNA phylogenetic placement, the new species should be assigned to the order Sporadotrichida Fauré‐Fremiet, 1961. Due to low taxon sampling, however, its exact position in this order remains enigmatic.     

Morphology and molecular analyses of four epibiotic peritrichs on crustacean and polychaete hosts,including descriptions of two new species (Ciliophora,Peritrichia)

Four epibiotic sessilid peritrichs, i.e., Zoothamnium wilberti n. sp., Baikalonis microdiscus n. sp., Epistylis anastatica (Linnaeus, 1767) Ehrenberg, 1830, and Rhabdostyla commensalis Möbius, 1888, were isolated from one syllid polychaete and three crustacean hosts in Qingdao, China. For each species, specimens were observed both in vivo and following silver staining. Their SSU rDNA was also sequenced for phylogenetic analyses. Zoothamnium wilberti n. sp. is characterized by the appearance of its colony, which is up to 350 μm high, and usually has fewer than 16 zooids, and the dichotomously branched stalk with transverse wrinkles, the conspicuously conical peristomial disc, and infundibular polykinety 3 comprising three isometric ciliary rows. Baikalonis microdiscus n. sp. can be recognized by its barrel-shaped zooid, small peristomial disc, smooth and short stalk, and its unusual infundibular polykinety 3 comprising a long inner row and a short outer row. Two poorly known species, i.e., Epistylis anastatica and Rhabdostyla commensalis, are redescribed and redefined. Phylogenetic analyses reveal that: (i) R. commensalis is closely related to the family Astylozoidae rather than to the morphologically similar Epistylididae; (ii) B. microdiscus n. sp. is sister to the family Scyphidiidae; (iii) E. anastatica groups with vorticellids and ophrydiids, which further supports the polyphyly of the genus Epistylis; and (iv) Z. wilberti n. sp. is nested within the Zoothamniidae, as expected.     

Cortical Ultrastructure of the Scuticociliates Dexiotricha media and Dexiotricha colpidiopsis (Hymenostomata)*†

SYNOPSIS. Cortical ultrastructure of the scuticociliates Dexiotricha media and Dexiotricha colpidiopsis was investigated. The following elements of the somatic cortex were studied: the cell membrane, alveolar membranes and the epiplasm, kinetodesmal fibers, postciliary and transverse microtubular ribbons, and transverse fibers associated with single and paired kinetosomes; mitochondria and single microtubules located in interkinetal ridges; mature and early extrusion stages of mucocysts: the expulsion vacuole pore and tube, the nephridioplasm and the cytoproct. In the buccal cortex, the paroral kinety-ribbed wall complex, the 3 polykineties, and the cytostome-cytopharynx were investigated. Comparative survey of ciliate ultrastructure indicates 2 principal orientation patterns for kinetodesmal and postciliary fibers, recognition of which leads to reevaluation of the theory of paroral kinety formation and the ideas of homology based on this theory. Ultrastructurally, the scuticociliates are not distinct from tetrahymenines and peniculines; the 3 groups appear to be 1 assemblage.     

Variability in the number of tooth rows in the pharyngeal dentition of Barbus intermedius (Teleostei; Cyprinidae): genetic,hormonal and environmental factors

The variability of pharyngeal dentition in a natural population of B. intermedius and effects of genetic, hormonal and environmental factors on the number of tooth rows in the pharyngeal dentition in offspring from wild‐caught parents have been investigated. It was revealed that: (i) about 10% of fish from natural population have four‐rowed dentition instead of three‐rowed dentition characteristic for this species; (ii) the presence of the additional tooth row is not an abnormality of tooth replacement since it occurs symmetrically on both sides; (iii) occurrence of the fourth row of teeth is heritable since laboratory‐reared offspring from parents with four‐rowed dentition have the same dentition. Even if one of the parents had four‐rowed dentition the percentage of four‐rowed individuals in the progeny was significantly higher than in progeny from parents with normal (three rowed) dentition; (iv) the number of tooth rows appears to be hormonally controlled: high levels of thyroid hormone result in a decrease in the number of tooth rows to two. In contrast, deficiency of this hormone results in an increase to four rows; (v) no differences in the number of tooth rows were found in fish reared under 17°C, 24°C, 30°C and room temperature (20–26°C).     

Morphology of two new marine peritrich ciliates from Yellow Sea,Pseudovorticella dingi nov. spec. and P. wangi nov. spec., with supplementary descriptions of P. plicata,P. banatica and P. anomala (Ciliophora,Peritrichia)

Two new marine peritrich ciliates, Pseudovorticella dingi nov. spec. and Pseudovorticella wangi nov. spec. were collected from coastal waters of Qingdao, China. Their living morphology, infraciliature and silverline system were studied using light microscopy and silver staining methods. Pseudovorticella dingi is characterized mainly by the apically located contractile vacuole and the presence of pellicular granules. There are 28–36 and 13–18 transverse silverlines above and below the trochal band, respectively. Infundibular polykinety 3 is composed of three rows, with row 1 conspicuously shorter than the other two. P. wangi is distinguished mainly by having two ventrally located contractile vacuoles. There are 17–20 and 9–11 transverse silverlines above and below the trochal band, respectively. Abstomal end of row 1 of infundibular polykinety 3 diverges from the other two and ends alongside row 3 of infundibular polykinety 2. Pseudovorticella plicata, P. banatica, and P. anomala have been described in Sun et al. (2009); we supplement morphometric data and photographs from life and after silver staining of these three species in the present study.     

Scanning Electron Microscope Observations on Some Life History Stages of Carchesium polypinum (Ciliata,Peritrichia)1

SYNOPSIS. Sessile zooids, and mobile telotrochs and microgamonts of Carchesium polypinum (Protozoa, Ciliata, Peritrichia), were examined by scanning electron microscopy. The results were compared to earlier light and electron microscope studies in order to investigate structural changes concerned with adaptation and differentiation. Telotrochs and microgamonts always had a contracted peristome and usually had a long phalange of cilia. Striae around the contracted buccal apparatus in all 3 stages were convoluted and often had thickened margins; those in telotrochs and microgamonts had oral-aboral ectoplasmic cross-connections. Nonbuccal striae of telotrochs and microgamonts varied in structure and height differences between epiplasmic peaks and alveoli surface membranes. The number of striae were constant in all 3 stages. Pellicular pore structure did not vary in any of the stages examined and resembled parasomal sacs located near buccal structures. Fully relaxed sessile zooids had ectoplasmic ridges coursing from polykinety kinetosomes and cilia to an area in front of the ciliated portion of the haplokinety; these ridges were interpreted to be the interkinetal fibers. Telotroch bands of sessile zooids consisted of 2 or 3 parallel ectoplasmic ridges which circled the aboral region and contained structures resembling pores. Telotroch bands in telotrochs and microgamonts had 2 enlarged, parallel ectoplasmic ridges circling the aboral region; telotroch band cilia were found between these ridges. In addition, a fold-like, ectoplasmic structure extended beyond the 2 ridges and was located between the telotroch band cilia and the aboral ridge. The epiplasmic shelf surrounding the stalk in sessile zooids was enlarged in telotrochs, and cilia were seen in the scopula depression. No scopula organelle was seen in any microgamont.