Uronychia transfuga (O. F. Müller, 1786) Stein, 1859 (Ciliophora, Hypotrichia, Uronychiidae): Cortical Structure and Morphogenesis during Division

Morphogenesis of cell division was investigated in Uronychia transfuga utilizing both light microscopy of living and stained specimens and SEM of preserved specimens. The cortical morphogenetic pattern of Uronychia is similar in several respects to that of the members of the family Euplotidae. These features include: the de novo development of the opisthe oral primordium in a subcortical pouch; the development of frontoventral and transverse cirri for both the proter and opisthe from 5 cirral primordia that form de novo within a single latitudinal developmental zone; and the absence of right marginal cirri. The members of the genus Uronychia also show a number of unique characteristics: development of a proter oral primordium that causes partial replacement of the parental adoral zone of oral polykinetids during development of the proter; a large oral membrane that is divided into a right and left component; large caudal cirri that bend to the left; and dorsal kineties comprised of closely set paired-kinetosome kinetids. When compared to the other euplotid-like ciliates, these unique features support the placement of the genus Uronychia in a separate family, Uronychiidae.     

Morphological,Biometric, and Morphogenetic Comparison of Two Closely Related Species,Stylonychia vorax and S. pustulata (Ciliophora: Oxytrichidae)1

Differences in the morphology of Stylonychia vorax Stokes, 1885 and S. pustulata (Müller, 1786) Ehrenberg, 1838 recognizable in vivo are the shape, the ventral cirral pattern, the caudal cirri, and the mode of moving. The dorsal-bristle complexes are distinguishable by the length of dorsal kinety four and the spaces among the pairs of basal bodies. When the ranges of variation of different populations and clones are compared by biometric analyses, S. vorax shows a relatively stable cortical pattern whereas in S. pustulata the cortical elements are regulated depending on the size of the body and the number of adoral membranelles. In S. vorax morphogenesis begins with a proliferation of basal bodies close to the transverse cirri. In contrast, in S. pustulata, the oral primordium appears de novo between the left marginal row and the postoral cirri. All other morphogenetic events are the same for both species. In proters and opisthes the six anlagen of the frontal-ventral-transverse cirri are of different origin and evolve independently. Three anlagen of the opisthe separate from the oral primordium, two originate from the right, and one from the left postoral cirrus. Three anlagen of the proter evolve from the posteriormost cirrus in the frontal area, one from the parental undulating membranes, one from the buccal cirrus, and one from the cirrus below the buccal cirrus. The anlagen one to six generate one, three, three, three, four, and four cirri. The characteristic arrangement of the undulating membranes and the participation of only two postoral cirri in the formation of primordia provide features that distinguish between the often confused genera Oxytricha and Stylonychia.     

Morphogenesis of the marine spirotrichous ciliate, Trachelostyla pediculiformis (Cohn, 1866) (Ciliophora, Stichotrichia), with consideration of its phylogenetic position

The cortical development during binary fission of the relatively poorly known stichotrich ciliate, Trachelostyla pediculiformis (Cohn, 1866) Borror, 1972, found in coastal waters near Qingdao, China, was investigated using the protargol impregnation method. The morphogenetic process reveals some pretty unusual characteristics, which do not follow the Oxytricha-pattern: (1) the parental oral apparatus is entirely renewed from an oral primordium formed de novo in the proter; (2) in the proter, the parental undulating membranes are not involved in the formation of the newly formed oral primordium; both undulating membrane-anlagen (UM-anlage) and frontoventral-transverse cirral anlagen (FVT-anlagen) develop from the oral primordium in the proter; (3) the dorsal kineties (DK) are generated in a unique way, that is, in both dividers, two separate groups of DK-anlagen develop in the right- and left-most DK, generate all the DK and evolve to replace the old structures; (4) three caudal cirri are formed at the posterior ends of three right-most dorsal kinety anlagen; (5) eight frontal, five ventral and five transverse cirri are derived from six streaks, namely, the UM-anlage and 5 FVT-anlagen; the cirri are segregated from these anlagen in the pattern 1:3:3:3:4:4 (from left to right) in the Oxytricha mode. Based on both SSrRNA gene sequencing and morphogenetic data, the systematic positions of the genus Trachelostyla Borror, 1972 as well as the family Trachelostylidae Small and Lynn, 1985 are briefly analyzed. The results indicate that this genus/family could be a highly isolated lineage and might be ancestral to other well-known oxytrichids.     

Morphology and Morphogenesis of a Novel Saline Soil Hypotrichous Ciliate,Gonostomum sinicum nov. spec. (Ciliophora,Hypotrichia, Gonostomatidae), Including a Report on the Small Subunit rDNA Sequence

Morphology, cirral pattern, and morphogenesis of the new saline soil hypotrich, Gonostomum sinicum nov. spec. collected from Longfeng Wetland in Daqing, north China, were studied, using detailed live observations and protargol‐stained specimens. The new species is characterized as follows: (i) a size in vivo of 100–125 × 30–40 μm, (ii) colorless cortical granules, 0.5 μm across, arranged in short rows, (iii) an adoral zone composed of 28–33 membranelles, (iv) three or four frontoventral rows, one of which extends onto the postoral area, (v) left and right marginal rows composed of 18–27 and 21–35, cirri, respectively, and (vi) usually two transverse cirri. Morphogenesis is as usual for the genus Gonostomum, i.e. the cirral primordia II–VI are primary primordia which split into two sets for proter and opisthe in division middle stages, except for anlage I which develops independently. However, the number of frontoventral transverse anlagen is either five or six not only in different individuals but even in proter and opisthe of the same divider. The phylogenetic analyses based on SSU rDNA sequences showed that the genus Gonostomum is nonmonophyletic, indicating that the patterns of cirri and dorsal kineties are homoplasious characters. The new species G. sinicum nov. spec. is perhaps closely related to Cotterillia bromelicola and two congeners.     

四核舍太虫的细胞发生学与Helix E10-1二级结构分析

利用蛋白银染色技术,观察和研究海洋游仆虫-四核舍太虫Certesia quadrinucleata(纤毛门,游仆目)二分裂期间的形态发生学。其主要特征如下:(1)老口围带完全被前仔虫继承;(2)后仔虫口原基独立产生于皮膜深层;(3)老口侧膜参与前仔虫口侧膜原基形成,前后仔虫的口侧膜原基均发生于细胞表面, 向前贡献出第一根额腹棘毛;(4)额-腹-横棘毛以初级5原基模式产生, 且以"3:3:3:3:3"的方式分化出新的棘毛;(5)背触毛与左缘棘毛原基均来自老结构, 无尾棘毛产生。研究首次给出了背面纤毛器的发生图示,为进一步探讨舍太虫的系统地位提供了一份补足性的发生学基础资料。游仆目纤毛虫的核糖体小亚基基因HelixE10-1区域二级结构一共存在9种模式, 该区域序列长度的变异性揭示了游仆目纤毛虫在进化中可能处于比较特殊的地位。       

变藓棘毛虫的形态学重描述及细胞发生学研究

通过活体观察和蛋白银染色法对采自青岛沙滩半咸水的变藓棘毛虫Sterkiella histriomuscorum(纤毛门, 腹毛目)进行了形态学及细胞发生学研究。该种群形态学与前人报道的土壤及淡水种群基本一致: 虫体近长椭圆形, 活体大小约(100-160) m (40-75) m; 无皮层颗粒; 2938片口小膜; 额棘毛3根; 额腹棘毛4根; 口后腹棘毛3根; 横前腹棘毛2根; 横棘毛3-5根; 左右缘棘毛列分别由17-23、20-24根棘毛组成; 6列背触毛; 2枚大核。其主要发生学特征如下: (1)老口围带完全保留, 老波动膜解体重建; 后仔虫口原基独立发生; (2)额腹横棘毛为5原基次级发生式, 部分原基来自老棘毛解体, 以2:3:3:4:4方式分化为新棘毛; (3)缘棘毛原基产生于老结构中, 并向两极延伸逐渐形成前后仔虫的新结构; (4)背触毛发生为典型Oxytricha模式; (5)大核在发生过程中完全融合。研究对首次在半咸水生境中发现的变藓棘毛虫种群进行了活体形态学和纤毛图式描述, 补充了显微照片、性状统计数据及发生过程的细节信息。       

Morphogenesis of a unique pseudourostylid ciliate,Trichototaxis songi (Ciliophora,Urostylida)

Divisional morphogenesis in the freshwater spirotrichous ciliate, Trichototaxis songi Chen et al., 2007, was investigated. The main morphogenetic events are characterised as follows: (1) the parental oral apparatus is completely renewed by the independently formed oral primordium in the proter; (2) the oral primordium in the opisthe is formed on the cell surface; (3) several left cirri of the midventral pairs participate in the formation of the oral primordium in the opisthe; (4) FVT-anlage I forms the leftmost pair of the bicorona; (5) the macronuclear nodules fuse into many masses rather than a single or branched mass as described in most pseudokeronopsids; and (6) usually, two marginal anlagen develop within each left marginal row separately. However, the number of left marginal anlagen is highly variable, even differing between the proter and opisthe of the same divider. The increase in the number of left marginal anlagen is by de novo generation of small anlagen to the left of the intrakinetal left marginal anlage, whereas the decrease in number is by resorption of the old marginal row(s). We posit that Trichototaxis is an intermediate form between the Pseudourostylidae and Pseudokeronopsidae as it shares morphogenetic features with both. Additionally, as in Uroleptopsis (Uroleptopsis), FVT-anlage I forms the leftmost pair of the bicorona in Trichototaxis indicating these genera may be closely related.     

卡龙游仆虫无性生殖期间的形态发生学研究：原生动物,纤毛虫

卡龙游仆虫为海洋中自由生纤毛虫,利用银染法对该种二分裂期间的形态发生学进行了初步的研究,其主要过程为：１．伴随大核改组带的出现和ＤＮＡ复制开始,口原基发生于老口围 方皮膜下一龛腔内,后由前至后组装成围口小膜而演化为后ＡＺＭ。老口围带及口侧膜在原位被被前仔虫继承;２．体棘毛场首先出现两组棘毛原基,其随后各自独立演化成９根前、后仔虫的额－腹－横棘毛;３．缘棘毛原基也为独立发生,初为单一,后断裂为二并分     

Morphology and cell division of the oxytrichids Architricha indica nov. gen., nov. sp., and Histriculus histrio (Müller, 1773), Corliss, 1960 (Ciliophora, Hypotrichida)

The oxytrichid ciliate Architricha indica nov. gen., nov. sp., isolated from the river Yamuna, Delhi, shows a new combination of characters. It possesses a flexible body, 18 frontal-ventral-transverse (FVT) cirri, 3 right and 2 left marginal cirral rows, 6 dorsal bristle rows and 3 caudal cirri (CC). The FVT cirri arise from 6 primordia, which utilize 6 parental cirri in their origin as is typical of Oxytricha species. Multiple marginal rows (MMR) develop through 5 independent marginal primordia arising "within-row", 1 in each parental marginal row. All the 5 marginal rows are thus morphogenetically active. Such a mode of formation of MMR has not been recorded among oxytrichids and has necessitated separation of A. indica at the generic level. Histriculus, on the other hand, has well-known characteristics, viz. rigid body, confluent marginal rows and absence of CC. The morphogenesis of Histriculus histrio has been described by Berger and Foissner [1997. Cladistic relationships and generic characterization of oxytrichid hypotrichs (Protozoa, Ciliophora). Arch. Protistenkd. 148, 125-155]. Reinvestigation of very early stages of development revealed that (i) the FVT cirral primordia utilize kinetosomes from 5 parental FVT cirri, (ii) the primordium II of the proter is of a composite origin: kinetosomes from the oral primordium merge with the primordium II that originates from the buccal cirrus II/2 and (iii) the FVT primordia V and VI for the 2 daughter cells arise sequentially from the parental cirrus V/4. Thus, the genus Histriculus exhibits a new combination of characters with respect to the origin of FVT cirri, an additional pattern to be added to the known 6 patterns of FVT development in oxytrichids [Berger and Foissner, 1997; Berger, H., 1999. Monograph of the Oxytrichidae (Ciliophora, Hypotrichida), Kluwer Academic Publishers, Dordrecht/Boston/London].     

The Cortical Morphogenetic Cycle Associated with Cell Division in Diophrys Dujardin, 1841 (Ciliophora,Hypotrichida)1

Morphogenesis of cell division was investigated in Diophrys scutum, D. oligothrix, and D. appendiculata utilizing both light microscopy of living and stained specimens and SEM of preserved specimens. The cortical morphogenetic pattern of Diophrys is similar to that of other members of the family Euplotidae. The opisthe oral primordium, which develops in a subsurface pouch, forms posterior to the parental buccal cavity. The proter inherits the parental adoral zone of membranelles (AZM) apparently unchanged. The endoral membrane forms to the right of the posterior end of the AZM in the proter, in association with the developing AZM in the opisthe. The paroral cirrus and membrane develop from a single streak that first appears along the right edge of the buccal cavity in the proter to the right of the developing buccal structures of the opisthe. Frontal and transverse cirri develop in both proter and opisthe from five separate cirral primordia that form to the right of the buccal cavity. Left marginal cirri do not develop in association with the corresponding parental structures. Kinetosomes formed within the opisthe oral primordium, or kinetosomes that were part of any parental ciliary structure, do not appear to become part of any developing paroral structures, frontal, transverse, or left marginal cirri. Speciation within the genus Diophrys and evolution of the family Euplotidae as they relate to the morphogenesis of cortical structure are discussed.     

Morphology,ontogeny and molecular phylogeny of a new urostylid ciliate,Bakuella (Pseudobakuella) guangdongica n. sp. (Ciliophora,Hypotrichia) from southern China

The morphology, morphogenesis, and molecular phylogeny of Bakuella (Pseudobakuella) guangdongica n. sp., isolated from southern China, were investigated. The new species is characterized by a body length of 150–225 μm in vivo; 35–42 adoral membranelles; 3–5 buccal, two frontoterminal, 7–12 transverse and two pretransverse ventral cirri; midventral complex comprised of 10–20 pairs and two rows extending to transverse cirri; posterior part of marginal rows slightly overlapping; colorless cortical granules about 1 μm across, arranged in small groups; soil habitat. Its main ontogenetic features are: (1) in the proter, the parental adoral zone of membranelles is completely renewed by new structures; (2) in the opisthe, the oral primordium originates apokinetally, some old midventral cirri join the formation of frontoventral-transverse cirral anlagen; (3) the anlagen for marginal rows and dorsal kineties develop intrakinetally; and (4) the numerous macronuclear nodules fuse into a single mass before dividing. Phylogenetic analyses based on the SSU rDNA sequence suggest the non-monophyly of the genus Bakuella.     

Morphology and morphogenesis of a new marine hypotrichous ciliate (Protozoa,Ciliophora, Pseudoamphisiellidae), including a report on the small subunit rRNA gene sequence

The morphology and morphogenesis of a new marine hypotrichous ciliate Pseudoamphisiella elongata sp. nov. isolated from mussel‐farming waters near Qingdao, China, are described based on living and protargol‐impregnated specimens. Morphologically, the new species can be distinguished from its known congeners by its elongate body shape, narrow oral field, having fewer dorsal kineties and caudal cirri, more marginal cirri, and differentiated pretransverse cirri. The identification as a new species is firmly supported by the sequences of the small subunit ribosomal rRNA (SSU rRNA) gene, compared with other known Pseudoamphisiella species, and the phylogenetic analysis. The morphogenetic characteristics can be summarized as follows: (1) the parental adoral zone of membranelles and undulating membranes are entirely rebuilt by the oral primordium, which develops de novo in the outermost region of the cortex; (2) the oral primordium in the opisthe and the frontoventral–transverse (FVT) anlagen in both dividers are formed independently on the cell surface; (3) an ‘extra’ marginal anlage originates to the right of the right marginal anlage, and develops into two or three ‘extra’ marginal cirri; (4) the FVT anlagen develop in the primary mode, and the last FVT streak contributes two migratory cirri (frontoterminal cirri), which are probably resorbed; (5) the right marginal anlagen in both dividers occur close together, independent of the old structure. © 2010 The Linnean Society of London, Zoological Journal of the Linnean Society, 2010, 158 , 231–243.     

A redescription of the oxytrichid Tetmemena pustulata () and notes on morphogenesis in the marine urostylid Metaurostylopsis salina Lei et al., 2005 (Ciliophora,Hypotrichia)

Two hypotrichous ciliates from China were investigated. The common oxytrichid species Tetmemena pustulata (Müller, 1786) Eigner, 1999, isolated from the estuary of the Pearl River in southern China, was investigated with emphasis on its living morphology and infraciliature. Tetmemena pustulata is characterized as follows: body elliptical to obovoid in shape; 75–115 × 40–60 μm in vivo; two macronuclear nodules and two micronuclei; one contractile vacuole left of midline and somewhat ahead of midbody positioned; three frontal, four frontoventral, one buccal, three postoral ventral, two pretransverse ventral and five transverse cirri; cirrus III/2 ahead of level of cirrus IV/3; cirrus IV/2 arranged more anteriorly than cirrus V/4; transverse cirri not forming two distinct groups; three prolonged and widely separated caudal cirri; six dorsal kineties in Oxytricha-pattern with dorsal kineties 3 and 4 bipolar. The marine urostylid species Metaurostylopsis salina Li et al., 2005, isolated from an aquarium in Qingdao, northern China, was investigated with emphasis on its morphogenesis which is characterized by the de novo formation of the oral primordium in the proter and the development of the marginal rows from two anlagen that form within each parental structure separately in both dividers.     

一种游仆虫无性分裂生殖的研究Ⅱ.无性分裂过程中皮层结构的形态发生

应用光学显微镜和扫描电子显微镜,观察到在一种游仆虫无性生殖周期中,新口围带发育时老口围带的更新、新波动膜原基的发生、棘毛原基发生的最早形态和背触毛发生等在其他种游仆虫中未见报道的现象。     

Description of the Rare Marine Ciliate, Uronychia multicirrus Song, 1997 (Ciliophora; Euplotida) based on Morphology, Morphogenesis and SS rRNA Gene Sequence

ABSTRACT. A population of the marine euplotid ciliate, Uronychia multicirru s Song 1997 , found in the littoral zone of the Daya Bay, Guangdong, South China, was investigated using live observation and protargol impregnation method. This species is diagnosed by possessing a long row of ventral cirri, which has never been seen in all other known congeners. Divisional process, described based on protargol-impregnated specimens, is typical of the genus regarding its general pattern: (1) the oral primordia in both proter and opisthe develop de novo in two subcortical pouches, while the UM-anlage forms de novo (i.e. does not develop from the oral primordium); (2) five frontoventral-transverse (FVT)-cirral anlagen develop in a primary-mode on the cell surface, and almost all the cirri are derived from the FVT-anlagen, except the first frontal cirri, which are formed de novo in both dividers; (3) the species characteristic ventral row derives from the right-most FVT-anlage; (4) the parental structures do not take part in the construction of the marginal anlagen, and (5) the caudal cirri originate in the right-most two dorsal kineties in a multi-segmentation mode. The small subunit rRNA gene of U. multicirrus (GenBank accession number: EU267929) is 1,773 bp and differs by 0.9–1.41% from its closely related congeners.     

Morphogenesis in the marine spirotrichous ciliate Apokeronopsis crassa (Claparède & Lachmann, 1858) n. comb. (Ciliophora: Stichotrichia), with the establishment of a new genus, Apokeronopsis n. g., and redefinition of the genus Thigmokeronopsis

Morphogenetic events during the division of the marine spirotrichous ciliate, Apokeronopsis crassa (Claparède & Lachmann 1858) n. comb. were investigated. Compared with members of the well-known genera Thigmokeronopsis, Uroleptopsis, and Pseudokeronopsis, A. crassa has one row of buccal cirri, high number of transverse cirri, clearly separated midventral rows, lacks thigmotactic cirri and a gap in adoral zone, its undulating membranes (UMs) anlage forms one cirrus and marginal rows and dorsal kineties form apokinetally during division. All these characteristics indicate that this organism represents a new taxon at the generic level, and hence a new genus is suggested, Apokeronopsis n. g. It is defined as thus: Pseudokeronopsidae with Pseudokeronopsis-like bicorona of frontal cirri and one marginal row on each side; one row of two or more buccal cirri in ordinary position; two midventral rows distinctly separated, hence of cirri that are not in a typical zig-zag pattern; high number of transverse cirri, caudal cirri absent, and frontoterminal cirri present; thigmotactic cirri absent, many macronuclear nodules fuse into many masses as well as marginal and dorsal kineties form apokinetally during morphogenesis. At the same time, the genus ThigmokeronopsisWicklow, 1981 is redefined, and one new combination, Apokeronopsis antarctica (Petz, 1995) n. comb. is proposed. The morphogenetic events of A. crassa are characterized as follows: (1) In the proter, the adoral zone of membranelles and UMs are completely renewed by the oral primordium. The UM anlage is formed apokinetally on the dorsal wall of the buccal cavity and is hence clearly separated from the frontoventral-transverse (FVT) cirral anlagen in the proter. (2) Frontoventral-transverse cirral anlagen are generated de novo in the outermost region of the cortex to the right of the old UMs. (3) A row of buccal cirri arises from FVT cirral streak I. (4) The marginal rows and dorsal kineties originate de novo in both dividers; no caudal cirri are formed. (5) The last FVT-streak contributes two frontoterminal cirri. (6) The many macronuclear nodules fuse into many masses (about 50 segments) during division, unlike a singular or branched mass as described in other urostylids.     

Cortical structure in non-dividing and dividing Diophrys japonica spec. nov. (Ciliophora, Euplotida) with notes on morphological variation

The morphology and morphogenesis of Diophrys japonica spec. nov., isolated from the Mie Port, Nagasaki, Japan, were investigated from life and following impregnation with protargol. The new species is recognized by the following characters: Body elliptical in outline and slightly greyish to yellowish in color; size in vivo about 80-120 x 50-70 microm; pellicle flexible, with underlying granules densely arranged in lines; ciliature comprising about 30-46 adoral membranelles, 4-7 frontal, 1-4 ventral and 4-7 transverse cirri, always 1 left marginal and 3 caudal cirri, and 4 dorsal kineties; usually two macronuclear nodules; fragment kinety with 2-5 dikinetids; marine habitat. The main morphogenetic events are: (1) the opisthe's oral primordium develops de novo in a subsurface pouch near the left transverse cirri; (2) the proter retains the parental AZM except for reorganization of some proximal membranelles; (3) cirral anlagen for the frontal, ventral and transverse cirri in both dividers develop separately from the oral primordium or parental cirri, and are derived from the separation of primary primordia that originate de novo; (4) the anlagen for the left marginal cirrus and fragment kinety also form de novo and separately; (5) dorsal kinety anlagen occur within the parental structures at mid-body and posterior end of the cell, of which the right-most one contributes three caudal cirri from its posterior portion. Based on available ontogenetic data, the author proposes that the numbers of left marginal and caudal cirri can be regarded as reliable characters for species identification, while the numbers of frontal, ventral and transverse cirri are not consistent enough for species distinction. A key to the eleven adequately known species of Diophrys is presented.     

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.     

Morphogenesis of the marine ciliate, Pseudoamphisiella alveolata (Kahl, 1932) Song & Warren, 2000 (Ciliophora, Stichotrichia, Urostylida) during binary fission

Morphogenesis during the binary fission of the stichotrich ciliate Pseudoamphisiella alveolata, isolated from Jiaozhou Bay near Qingdao, China, was investigated using protargol silver impregnation. The process is characterized as follows: (1) in the proter, only the posterior part of the parental adoral zone of membranelles is renewed, where the membranelles dedifferentiate and then rebuild the UM-anlage and the missing membranelles, (2) the oral primordium in the opisthe and the FVT-anlagen in both dividers are formed de novo on the cell surface, (3) an "extra" anlage, which is generated on the right of the right marginal anlage, develops into three or four "extra" marginal cirri that connect the caudal cirri with the marginal rows, (4) the right marginal anlage is formed within the old structure, (5) the FVT-cirri develop in a primary mode, and (6) unlike most stichotrichs, the right marginal anlagen in both dividers generate closely together. As an additional contribution, the diversity of morphogenetic patterns within the genus Pseudoamphisiella is discussed. Based on both morphogenetic and SS rRNA gene sequencing data, the systematic position of the genus Pseudoamphisiella as well as the family Pseudoamphisiellidae Song et al. 1997 is briefly analyzed. The results indicate that they should very possibly represent a higher evolved group in the order Urostylida.