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1.
SYNOPSIS. The protargol technic was used in a study of the development of oral, cirral, and dorsal primordia of Urostyla weissei fixed during division, reorganization, and regeneration following transection at different levels. While the course of development is similar in all situations, differences were observed in the way in which some primordia are initiaily formed. The primordium of the new AZM always appears posterior to the old AZM. It develops into an entire new membranellar band in dividing cells and in opimers (posterior fragments from equatorial transections), while it eventually joins with a portion of the old AZM in reorganizers, promers (anterior fragments from equatorial transections) and “large opimers” (cells whose anterior tip has been cut off). The UM-primordium of proters is derived from disaggregation of the kinetosomes of the 2 old UM's, that of opisthes and opimers is formed “de novo” to the right of the AZM-primordium, while the UM-primordium of reorganizers, promers, and “large opimers” is of composite origin, partly “de novo” and partly from the old UM's. The UM primordium differentiates into the new UM's and the 1st frontal cirrus. The primordia of the remaining frontal, ventral, transversal (F-V-T) and marginal cirri originate as “streaks” of cilia, most of which are derived from re-alignment of the constituent cilia of certain pre-existing cirri. New cirri differendiate from the streaks, and replace the remaining old cirri. The streaks are formed similarly in all developmental situations, except for the 1st 3 F-V-T streaks. In proters, reorganizers, and promers, these originate from the posterior 3 frontal cirri, while in opisthes and opimers they are formed “de novo” to the right of the UM-primordium. In the “large opimers” these streaks are formed “de novo” behind the 1st 3 frontal cirri, in spite of the continued presence of these cirri at the anterior tip of the fragments. The site of formation of these streaks thus appears to be determined by an anteriorposterior gradient, rather than by any preformed cortical structure. The new dorsal bristle rows I to III develop from the proliferation of portions of the old rows, while rows IV and V originate from short kineties formed “de novo” on the right margin. New caudal cirri differentiate at the posterior ends of the new rows I to III. The numbers of ventral cirral rows and transversal cirri are variable; these variations are correlated, and related to variations in numbers of developing streaks. A survey of hypotrich developmental patterns revealed extensive parallels, especially in the sites of appearance of primordia. The primordium site appears to be a more constant feature of cortical development than is the “source” of ciliary units. It is concluded that sites of primordia are determined by cellular gradients, with competent preformed structures being utilized if they are appropriately positioned within these gradients.  相似文献   

2.
A new hypotrichous ciliate, Apoterritricha lutea n. g., n. sp., was discovered in a sample of a terrestrial liverwort from Korea. Its morphology was studied using detailed in vivo observation and protargol impregnation. Its phylogenetic relationships were revealed by analyses of the 18S rRNA gene. This new taxon is characterized by a combination of the following traits: (i) ellipsoidal to narrowly ellipsoidal body with an average size of 230 × 85 μm; (ii) two macronuclear nodules and two to five micronuclei; (iii) golden yellow cortical granules, forming small groups along the microtubular appendages of cirri, adoral membranelles, and dorsal kineties; (iv) typically three frontal cirri, one buccal cirrus, four frontoventral cirri, seven midventral cirri, two pretransverse cirri, seven transverse cirri, ca. 38 left, and ca. 36 right marginal cirri; and (v) on average six dorsal kineties, three dorsomarginal kineties, and three caudal cirri. In molecular phylogenies, A. lutea clusters with strong support within a clade containing Afrokeronopsis aurea and several “typical” oxytrichids having golden yellow to brown cortical granules. In this light we propose a hypothesis that is not unambiguously rejected by the present phylogenetic analyses, which shows how the Afrokeronopsis‐like pattern could have evolved from a Rubrioxytricha‐like ancestor via an Apoterritricha‐like stage by cirri‐multiplication.  相似文献   

3.
A new species, Pleurotricha indica n. sp., is described, characterized by an average size of 220 × 119 μm, a firm and inflexible body, six rows of dorsal kineties, one left and two right rows of marginal cirri, and an “Oxytricha-like” pattern of ventral cirri. The parts of the macronucleus are variable in shape and number. The comparison with other members of the genus shows that P. indica differs from other congeneric species in the combination of these characters.  相似文献   

4.
Hypotrichs are among the most complex ciliates in terms of morphology and development. To study the fine structure of cortical morphogenesis associated with cell division in Euplotes eurystomus, three different methods of observation were employed: light microscopy of protargol-stained specimens, scanning electron microscopy of cells prepared by critical point drying, and transmission electron microscopy of sectioned material. Observations on the stages of morphogenesis give much new information about cortical development, particularly about proliferation and aggregation of kinetosomes (basal bodies), ciliary outgrowth, the topography of morphogenesis, cirrus resorption, and growth of the pellicle. During the formation of new cirrus the process of kinetosome proliferation is atypical, i.e., groups of prokinetosomes are seen oriented at random and, in some cases, prokinetosomes apparently are formed at a distance from nearby young kinetosomes. That the new cirri develop in surface grooves, the grooves elongate into “tracks,” and (in some cases) grooves are partitioned into separate tracks suggests that the grooves play a role in the orderly migration of the new cirri on the cell surface. Conspicuous morphogcnctic changes in the cell surface involve local growth of the pellicle. The process of pellicle growth apparently involves two basic steps: (a) growth of the outer cell membrane to form “bare regions,” and (b) formation of alveoli in the bare regions. Alveolar sheets are formed by fusion of alveolus precursor particles. Cirrus resorption is sequential over several stages of development, and old cirri are resorbed as the new cirri impinge on them. As the old cirri regress, both in situ resorption and retraction of axonemes into the cytoplasm occur.  相似文献   

5.
ABSTRACT. Based on both morphological and molecular information, two new euplotid genera Apodiophrys n. g. and Heterodiophrys n. g. are described in the present paper. Apodiophrys n. g. is defined as sculptured Diophryinae with bipartite adoral zone; frontoventral cirri arranged in Diophrys‐pattern; marginal cirri located in two clearly separated groups. Heterodiophrys n. g. is recognizable by the combination of Diophrys‐like frontoventral cirri and the unique structure of several marginal cirri that are arranged in a long row. The type species for both new genera, Apodiophrys ovalis n. sp. and Heterodiophrys zhui n. sp., collected from southern China sea, are described. The small subunit rRNA (SSU rRNA) gene sequences for both new taxa are determined. Phylogenetic analyses based on these data indicate that Apodiophrys is most closely related to Paradiophrys, which then clusters with Uronychia species. Thus, Apodiophrys–Paradiophrys is separated from other typical Diophrys‐like genera in the SSU rRNA gene trees. The new genus Heterodiophrys is basal to the sister group of Diophrys–Diophryopsis, hence belongs to the “core”Diophrys‐complex.  相似文献   

6.
In the hypotrich ciliate Euplotes, many individual basal bodies are grouped together in tightly packed clusters, forming ventral polykinetids. These groups of basal bodies (which produce compound ciliary organelles such as cirri and oral membranelles) are cross-linked into ordered arrays by scaffold structures known as “basal-body cages.” The major protein comprising Euplotes cages has been previously identified and termed “cagein.” Screening a Eaediculatus cDNA expression library with anti-cagein antisera identified a DNA insert containing most of a putative cagein gene; standard PCR techniques were used to complete the sequence. Probes designed from this gene identified a macronuclear “nanochromosome” of ca. 1.5 kb in Southern blots against whole-cell DNA. The protein derived from this sequence (463 residues) is predicted to be hydrophilic and highly charged; however, the native cage structures are highly resistant to salt/detergent extraction. This insolubility could be explained by the coiled-coil regions predicted to extend over much of the length of the derived cagein polypeptide. One frameshift sequence is found within the gene, as well as a short intron. BLAST searches find many ciliates with evident homologues to cagein within their derived genomic sequences.  相似文献   

7.
L'infraciliature ventrale est presque entièrement détruite lors de la conjugaison: la totalité des structures buccales, tous les cirres fronto-ventraux et transversaux, certains cirres caudaux. Le retour à l'état végétatif s'effectue en 2 étapes. Première Etape.–Différenciation d'un nouvel ensemble de cirres, dépourvu du cirre 1/I (selon la nomenclature de Wallengren); néoformation, à partir d'une ébauche située sur le territoire présomptif du cirre manquant, d'une partie des structures buccales (la moitié antérieure de la frange adorale de membranelles). Deuxième Etape.–Remplacement de tous les cirres par un nouvel ensemble comportant le cirre 1/I; différenciation des structures buccales manquantes (moitié postérieure de la frange adorale, ciliature parorale) Les rapports morphogénétiques entre le cirre 1/I et la ciliature parorale suggèrent que le territoire de ce “cirre paroral” est homologue des territoires stomatogènes d'autres Hypotriches tels que Kahliella et Stylonychia. SYNOPSIS. During conjugation of Euplotes, the ventral ciliature, including the entire oral apparatus, all the fronto-ventral and transverse cirri, and some of the caudal cirri, is nearly completely lost. As followed in silver-stained preparations, the redifferentiation of the ciliature proceeds in 2 steps. The first step entails differentiation of a new complement of cirri, except for cirrus 1/I (according to the nomenclature of Wallengren), and neoformation of the anterior part of the adoral zone of membranelles (AZM) from a primordium located in an area that would be expected to give rise to the missing 1/I cirrus. The 2nd step involves replacement of all the cirri, including 1/I, and completion of the oral apparatus by redifferentiation of the posterior half of the AZM and of the paroral ciliature. The spatial morphogenetic relationships between cirrus 1/I and the paroral ciliature suggest that the area of this “paroral cirrus” is homologous with the stomatogenic areas of other Hypotrichida, such as Kahliella and Stylonychia.  相似文献   

8.
Small-sized vegetative cells were found to co-occur with normal-sized cells in populations of the European bloom-forming dinoflagellate Gymnodinium cf. nagasakiense Takayama et Adachi, currently known as Gyrodinium aureolum Hulburt, but not in populations of the closely related Japanese species Gymnodiniumn agasakiense. We examined how cell size differentiation may influence growth and cell cycle progression under a 12:12-h light: dark cycle in the European taxon, as compared to the Japanese one. Cell number and volume and chlorophyll red fluorescence in both species varied widely during the photocycle. These variations generally appeared to be related lo the division period, which occurred at night, as indicated by the variations of the fraction of binucleated cells (mitotic index) as well as the distribution of cellular DNA content. “Small” cells of G. cf. nagasakiense divided mainly during the first part of the dark period, although a second minor peak of dividing cells could occur shortly before light onset. In contrast, “large” cells displayed a sharp division peak that occurred 9 h after the beginning of the dark period. The lower degree of synchrony of “small” cells could be a consequence of their faster growth. Alternatively, these data may suggest that cell division is lightly controlled by an endogenous clock in “large” cells and much more loosely controlled in “small” cells. Cells of the Japanese species, which were morphologically similar to “large” cells of the European taxon, displayed an intermediate growth pattern between the two cell types of G. cf. nagasakiense, with a division period that extended to most of the dark period.  相似文献   

9.
SYNOPSIS. A quantitative method for the analysis of cirral patterns in the genus Euplotes is developed and contrasted with alternative approaches. Inherent variations in cirral pattern, as they are reflected in frequency distributions of intercirral distances, are ascertained through subclonal analyses of Euplotes harpa samples grown under different conditions. This assessment of the extent of variation within a form having 10 frontoventral cirri provides a basis for a comparative study of other Euplotes of cirrotype 10. These results suggest that all marine cirrotype 10 forms with a single dargyrome have the same configuration of frontoventral and transverse cirri. Similarly, most marine double dargyrome forms of cirrotype 10 have this same cirral pattern, and thus constitute variations upon the same morphometric theme.  相似文献   

10.
ABSTRACT. Species belonging to the genus Diophrys Dujardin, 1841, are easily recognized due to possession of the usual complement of approximately seven frontoventral cirri, five transverse cirri, two left marginal cirri, and three large caudal cirri. Separation of these species has been based upon differences in cell length and width, the number and arrangement of cilia in dorsal kinetics, the configuration of the adoral zone of oral polykinetids, the number and distribution of cirri within cirral groups, and the number and arrangement of macronuclei. Jankowski used some of these characteristics to divide the genus into two genera, Diophrys and Paradiophrys, with several subgenera [Jankowski, A. W. 1978. Systematic revision of the class Polyhymenophora (Spirotricha), morphology, systematics and evolution. Tezisy Dokl. Zool. Inst. Akad. Nauk SSSR, 197839-40. (in Russian); Jankowski, A. W. 1979. Systematics and phylogeny of the order Hypotrichida Stein, 1859 (Protozoa, Ciliophora). Trudy. Zool. Inst. Akad. Nauk SSSR, 86 :48–85. (in Russian with English summary)]. Data obtained from light microscopic examination of stained (nigrosin-butanol, Chatton-Lwoff, and Protargol) cells in interphase or division supports and modifies the use of particular structural features of these ciliates for the purpose of taxonomic classification. The structural variability within and among populations of different species within the genera Diophrys (D. appendiculata, D. oligothrix, and D. scutum) and Paradiophrys (P. irmgard and P. multinucleata) is described. D. hystrix is redescribed as the type of the new genus Diophryopsis n. g. Comparative information on the cortical morphogenesis of division of selected species within each genus is reviewed. Two taxonomic classifications of these hypotrichs are discussed: 1) a listing of diagnoses and synonymies and 2) a binary key for identification of all species at the light microscope level. An alternative evolutionary explanation of variations among isolates is presented.  相似文献   

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