莫氏肾形虫武汉种群的形态学及表膜下纤毛系研究

肾形纲的代表属肾形虫属是土壤间隙生境中最为重要的纤毛虫类群之一,其中的某些种类也常见于湖泊、池塘等淡水水体中[1—7]。Foissner 1993年修订后的肾形虫属(包括30个种),其将迅捷(快速)肾形虫Colpoda fastigataKahl,1931,固囊肾形虫C·matritensisOcariz,et al·,1965和莫氏拟肾形虫Paracolpoda maupasi(Enriques,1908)Lynn,1975等纤毛虫作为莫氏肾形虫C·maupasiEnriques,1908的同物异名[2]。之后,Foissner又报道了2新种和1新亚种[3,8]。因为原生动物现代研究技术是始于近几十年,所以不少纤毛虫种类的形态分类特征还未被详细地研究…     

Identification of Precystic Stages and Encystment Kinetics Analysis of Colpoda inflata by Using an Immunofluorescent Method

ABSTRACT. The application of an immunocytochemical method to identify precystic stages and to analyse the encystment kinetics, by using a polyclonal antiserum against isolated cyst walls from the ciliate Colpoda inflata , is reported for the first time. Three different precystic phases were chosen on the basis of morphological changes and degree of cyst wall formation. By using this procedure a better identification of mature resting cysts with regard to precystic cells or young cysts is provided. An average consensus encystment kinetics of C. inflata , by using an accumulated class frequency analysis, is reported.     

Experimental evolution of protozoan traits in response to interspecific competition

Decades of experiments have demonstrated the ecological effect of competition, but experimental evidence for competitive effects on trait evolution is rare. I measured the evolution of six protozoan traits in response to competitors from the inquiline community of pitcher plants. Replicate populations of Colpoda, a ciliated protozoan, were allowed to evolve in response to intra- and interspecific competition for 20 days (approximately 100 generations), before traits were measured in two common garden environments. Populations that evolved with interspecific competition had smaller cell sizes, produced fewer cysts and had higher population growth rates relative to populations grown in monoculture. The presence of interspecific competitors led to differential lineage sorting, most likely by increasing the strength of selection. These results are the first to demonstrate protozoan evolution in response to competition and may have implications for species coexistence in this system.     

Cortical and Nuclear Events During Cell Division and Resting Cyst Formation in Colpoda inflata

Nuclear and cortical phenomena during dividing and resting cyst formation of Colpoda inflata are described. Cell division forms a cyst and produces two or four tomites. In each tomite, the right oral field results from the proliferation of the anterior extreme of a single kinety, and the left oral field results from the proliferation of four, five, or six somatic kineties. After macronuclear division, each macronuclear mass undergoes a chromatinic extrusion process. During resting cyst formation, the oral infraciliature of the vegetative cell is resorbed. The somatic kineties dispose in a radial way and some pairs of kinetosomes disappear. As in cell division, there is an extrusion process. From these results we conclude that the resting cysts of Colpoda inflata cannot be included in any group of the previous classifications for hypotrich resting cysts. Thus, we propose a new additional group to Walker and Maugel's classification called PKR (partial-kinetosome-resorbing) cysts.     

Ontogenetic Shifts in the Ability of the Cladoceran,Moina macrocopa Straus and Ceriodaphnia cornuta Sars to Utilize Ciliated Protists as Food Source

The ontogenetic diet shifts and age specific ability of the two cladoceran species Moina macrocopa and Ceriodaphnia cornuta to derive energy from ciliated protists have been investigated in laboratory. The postembryonic developmental rates and life table demography (longevity, age and size at first reproduction, fecundity and intrinsic rate of natural increase) of the cladocerans have been elucidated on algae (Chlorella vulgaris) and the ciliated protists (Tetrahymena pyriformis, Colpoda (c.f.) steini) as food. For either of the cladoceran, the somatic growth rate and average body size at first reproduction were higher with algal diet. During initial stages of development (0–5 days), either cladoceran realized higher rate of somatic growth on algal diet, subsequently ciliated protists supported significantly higher growth rate than the alga. Algal and ciliate diets did not differ in maximum body size (C. cornuta: 539–554 μm; M. macrocopa: 1274.8–1309 μm) reached by either of the cladocerans. The maximum body sizes were larger than size at first reproduction with either of the ciliated protists, however, with algal diet the maximum body sizes did not differ from the size at first reproduction in each case. In case of C. cornuta the generation time (20.5 ± 0.3 days on ciliate; 15.6 ± 0.17 days on algal diet), reproductive rates (net reproductive rate: 20.05 ± 3.2 on ciliate; 15.5 ± 1.2 on algal diet), and average life expectancy at hatching (27 ± 0.8 days on ciliate; 22.7 ± 0.71 days on alga) were higher, whereas the size at first reproduction (482 μm on ciliate; 521 μm on alga) was smaller with the ciliate than with an algal diet. The algal and the ciliate diets did not differ in survival (life expectancy at hatching: 9.2 ± 0.7 days) and fecundity (NRR: 23.6 ± 2.4) for M. macrocopa. The two ciliates used in the experiment did not differ in their performance as food source for either cladoceran species. Our results suggest that both the cladoceran species are able to utilize smaller ciliate (e.g., T. pyriformis, C. (c.f.) steini) as food; however with differential ability to derive energy from the ciliate diet and this ability is size and age structured in both cases. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Protozoan predation of bacterial cells in soil aggregates

Abstract The development and survival of Aerobacter aerogenes IAM11022 in the inner and outer zones of soil aggregates (1–2 mm) was investigated in relation to a protozoan ( Colpoda sp.). With different dilutions of the bacterial cell suspension, a constant partition ratio of these cells was observed between outer and inner zones of the aggregates. Protozoa inoculated in the same manner were generally recovered only from the outer zone of the aggregates.
In the presence of protozoa, prey cell numbers of the outer zone were reduced from more than 10⁸ to approx. 10⁴ cells · g soil⁻¹ in 12 days. In contrast, 10⁸ cells · g soil⁻¹ remained in the inner zone of the aggregates, even after 12 days.
The increase in predator cell number was proportional to initial prey densities in the outer zone of the aggregates. At a constant initial prey density (1.8 × 10⁷ cells · g soil⁻¹), Colpoda sp. multiplied in proportion to the initial number of predators. When the initial density of the predator was low more prey cells survived in the outer zone.
Prey persistence was associated with 3 different types of protection: (1) small pore necks of the inner zone space of the aggregates; (2) the division of the outer zone space into compartments; and (3) the distribution of protozoan cells among soil aggregates. The latter two were closely related to the moisture condition of the soil.     

Colpoda spiralis sp. n., a Colpodid Ciliate Found Inhabiting Treeholes (Colpodida,Ciliophora)*

SYNOPSIS A new species of the family Colpodidae, genus Colpoda O. F. Müller, Colpoda spiralis sp. n. is described. This organism has been found only in treehole fluid. Its species status is based on the possession of a unique and prominent preoral protuberance, multimicronuclearity, and the preference for a treehole habitat. Its range is known to include the tri-state area of Arizona, New Mexico and Utah, and the mixed-deciduous forests of Maryland. This species prefers treehole fluids with a pH > 7 and is naturally limited to tree species which possess these alkaline treeholes. It encysts as a treehole dries and excysts when the treehole is again filled by fluids from the tree, or rainwater.     

Culture Age, Intracellular Ca2+ Concentration, and Protein Phosphorylation in Encystment-Induced Colpoda cucullus

In Colpoda cucullus, intracellular Ca²⁺ mediates the encystment induction and protein phosphorylation that occur just prior to morphogenetic transformation into the resting form. When rapidly growing cells were stimulated to encyst, encystment was not readily induced, and the protein phosphorylation level was lower. On the other hand, in post-growing cells stimulated to encyst, the encystment rate and protein phosphorylation level were elevated. These results suggest that protein phosphorylation is closely linked to encystment induction. Why, then, are the protein phosphorylation level and encystment rate difficult to elevate in the rapidly growing cells? Fura 2 ratiometry showed that the intracellular Ca²⁺ concentration (F₃₄₀/F₃₈₀ ratio) was raised in rapidly growing cells as well as in post-growing cells when the cells were stimulated to encyst. It is presumed that the Ca²⁺-mediated signal transduction pathways for protein phosphorylation and encystment may be triggered in rapidly growing cells, but downstream certain steps may be suppressed by certain intracellular components.