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PL
Two oxytrichids Architricha indica Gupta et al., 2006 and Pleurotricha curdsi (Shi et al. 2002) Gupta et al., 2003 collected in East China, were studied using live observation and the silver staining method. The description and morphometric characterization of the new populations were supplied. The Shanghai population of A. indica differs from the Indian population in the number of cirri in the third right marginal row (average of 16.8 vs. 21.1). The Shanghai population of P. curdsicorresponds well with the Indian population, but it differs from the other Chinese population in the number of right marginal rows (two vs. three). The early process of reorganization of A. indica was studied, and a difference on the formation of anlage V was found compared to the original report. The small subunit rRNA genes of both species were sequenced for the first time. The phylogenetic analyses based on SSU rRNA gene sequence data revealed that Architricha is sister to the assemblage of Pseudouroleptus caudatus and two Strongylidium, while P. curdsi clusters with its congener P. lanceolata and is located in Stylonychinae.
PL
The morphology and infraciliature of two marine scuticociliates, Pleuronema puytoraci Grolière and Detcheva, 1974, and Parauronema longum Song, 1995, collected from China, were investigated using live observation and protargol impregnation methods. Based on the data obtained for the China population, new information of the living morphology of Pleuronema puytoraci is documented and details of the complete infraciliature is available for the first time. The stomatogenesis of Parauronema longum is basically similar to that of its congeners and can be summarized as follows: membranelle 1, membranelle 2 and the scutica of the opisthe originate from the parental paroral membrane, whereas membranelle 3 of the opisthe develops from the parental scutica; the paroral membrane originates from the parental paroral membrane.
PL
Living observation and silver impregnation methods were used to investigate the morphology and infraciliature of three Frontonia ciliates (F. guangdongensis spec. nov., F. ocularis Bullington, 1939 and F. schaefferi Bullington, 1939) that were isolated from coastal waters of the South China Sea. Frontonia guangdongensis spec. nov. may be recognized by the combination of the following characteristics: cells about 160 × 35 μm in vivo; elongated body with right margin depressed in anterior third; length to width ratio 4:1 to 5:1; three or four vestibular and four or five postoral kineties; peniculi 1 and 2 each with four rows of kineties, peniculus 3 with two rows; one contractile vacuole in mid-body region right of cell median; brackish water habitat. A key based on morphological data for fourteen marine or brackish water Frontonia species found in China is also provided. In addition, the small subunit (SSU) rDNA gene was sequenced for F. ocularis Bullington, 1939. Our phylogenetic analyses support the contention that the genus Frontonia is not monophyletic.
PL
The morphology and infraciliature of four marine scuticociliates, Pleuronema elegans spec. nov., P. setigerum Calkins, 1902, P. grolierei Wang et al., 2008 and Uronema orientalis spec. nov., collected from China seas, were investigated through live observation and protargol staining methods. Pleuronema elegans spec. nov. can be recognized by the combination of the following characters: size in vivo 90–115 × 45–60 µm, slender oval in outline with a distinctly pointed posterior end; about 10 prolonged caudal cilia; consistently two preoral kineties and 18 or 19 somatic kineties; membranelle 2a double-rowed with its posterior end straight; membranelle 3 three-rowed; one macronucleus; marine habitat. Uronema orientalis spec. nov. is distinguished by the following features: in vivo about 40–55 × 20–30 μm with a truncated apical plate; consistently twenty somatic kineties; membranelle 1 single-rowed and divided into two parts which comprise four and three basal bodies respectively; contractile vacuole pore positioned at the end of the second somatic kinety; marine habitat. We also provide improved diagnoses for P. grolierei Wang et al., 2008 and P. setigerum Calkins, 1902 based on current and previous reports. The small subunit rRNA gene of U. orientalis, P. elegans, P. grolierei and P. puytoraci were sequenced. Phylogenetic analyses indicate that Uronema and Pleuronema are not monophyletic.
PL
Eight marine scuticociliates, Pseudoplatynematum denticulatum (Kahl, 1933) nov. comb., Protocyclidium sinica nov. spec., Histiobalantium marinum Kahl, 1933, Porpostoma notata Möbius, 1888, Philaster hiatti Thompson, 1969, Parauronema longum Song, 1995, Uronemella parafilificum Gong et al., 2007, and Paranophrys magna Borror, 1972, collected from Chinese coastal waters, were investigated using live observations and silver impregnation methods. Investigations of a Chinese population of Platynematum denticulatum (Kahl, 1933) reveal that it has a highly strengthened pellicle and distinct spines and thus corresponds well with the definition of Pseudoplatynematum Bock, 1952. A new combination, Pseudoplatynematum denticulatum (Kahl, 1933) nov. comb., is therefore proposed and an improved species diagnosis is supplied. Protocyclidium sinica nov. spec. is characterized by: small body size with buccal field approximately 60% of body length; extrusomes present; 13 or 14 somatic kineties; somatic kinety 1 comprising approximately 24 densely arranged kinetids; somatic kinety n shortened posteriorly; single macronucleus. Additional information is documented on the morphology of six other species of scuticociliates based on the China populations.
PL
During faunistic studies of ciliates in coastal waters of Daya Bay and Bohai Bay, China, two previously unknown ciliates were discovered and investigated using standard taxonomic methods. Morphological comparative analyses revealed that they represent two novel species in the genus Chaenea. Chaenea paucistriata spec. nov. can be distinguished from its congeners by the following traits: body length in vivo about 180–250 µm; eight somatic kineties; dorsal brush rows 1–4 consisting of three, five, seven, and two dikinetids, respectively; rod-like extrusomes, 8 µm long; 63–94 macronuclei; cortical granules minute and colourless. Chaenea sinica spec. nov. differs from its congeners in having: body length in vivo about 140–240 µm; 17–21 somatic kineties; dorsal brush rows 1–4 consisting of 3–7, 10 or 11, 11–13, and 3–6 dikinetids, respectively; rod-like extrusomes about 6–8 µm long; 71–164 macronuclei. A key is presented to assist the identification of all Chaenea species.
PL
The morphology, infraciliature, and silverline system of three marine scuticociliates, Uronema marinum Dujardin, 1841, U. heteromarinum nov. spec. and Pleuronema setigerum Calkins, 1902, isolated from coastal waters off Qingdao, China, were investigated using living observation and silver impregnation methods. Due to the great confusion in the species definition of the well-known species U. marinum, we have documented a detailed discussion/comparison and believe that most of the confusion is due to the fact that at least 2 closely-related sibling morphotypes exist which are often not recognized. Based on the data available, U. marinum is strictly defined as follows: marine Uronema ca. 30 × 10 μm in size, with truncated apical frontal plate and smooth pellicle, extrusomes inconspicuous, cytostome located equatorially, 12–14 somatic kineties and one contractile vacuole pore near posterior end of kinety 2. Uronema heteromarinum nov. spec. resembles U. marinum but can be distinguished morphologically by its notched pellicle with conspicuous extrusomes and reticulate ridges, the 15–16 somatic kineties, widely separated membranelle 1 and membranelle 2, as well as the subequatorially positioned cytostome. Based on the Qingdao population, an improved diagnosis for the poorly known Pleuronema setigerum is: marine slender oval-shaped form, in vivo about 40–50 × 15–20 μm; 3–5 preoral kineties and 14–22 somatic kineties; membranelle 1 and 3 three-rowed, and posterior end of M2a ring-like. The small subunit (SSU) rRNA gene for all three organisms were sequenced and analyzed with standard methods.
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