Stomatocysts of Mallomonas hamata and M. heterospina (Mallomonadaceae, Synurophyceae) from South Swedish lakes

The stomato cysts of Mallomonas hamata and M. heterospina are described from lakes in South Sweden. These Mallomonas species develop cysts of similar appearance, size and form. Cyst formation for Mallomonas hamata was recorded at temperature 10–11°C and pH 5.9 and for M. heterospina at temperatures 4.2–11°C and pH 7.4. The cysts of M. hamata and M. heterospina are ovoid and easy to recognize, even with light microscopy, but difficult to distinguish from another. Thus their value as paleoindicators is limited, even if the two species have preference for waters of different nutrient and pH status.     

Salinity tolerance in Hyalophysa chattoni (Ciliophora, Apostomatida), a symbiont of the estuarine grass shrimp Palaemonetes pugio

The apostome ciliate Hyalophysa chattoni, a symbiont of the estuarine grass shrimp Palaemonetes pugio, was tested for its growth and reproductive ability in a wide range of salinities from 0.1 to 55 ppt. Shrimp, with their attached ciliates, were slowly acclimated to different salinities in order to assess protozoan cell size and division. The trophont and tomont stages of the ciliate life cycle were analyzed. In both stages, cell size increased with salinity from 0.1 to 20 ppt. Cell size leveled in the 20-35 ppt range, and decreased at higher salinities. The number of daughter cells produced per tomont cyst correlated with increased cell size, and also correlated with increased salinity. Additionally, increased salinity correlated with an increase in the percentage of cells able to divide and excyst as tomite stages. These results indicate that H. chattoni is able to grow and divide more effectively at salinities closer to seawater than in the estuarine environment from which they were collected. Though able to survive salinities from 0.1 to 55 ppt, the species is better adapted for an existence in the higher salt concentrations.     

海洋浮游纤毛虫包囊的研究进展*

作为微型浮游动物的重要组成部分,海洋浮游纤毛虫是连接微食物环和经典食物链的重要中介。有些浮游纤毛虫在生活周期中会形成包囊,条件适宜时包囊会萌发,这对纤毛虫种群动态有重要的意义。目前国际上对于浮游纤毛虫生态学的研究主要集中在其营养期细胞,浮游纤毛虫包囊的研究尚少,中国还没有这方面的研究。本文对浮游纤毛虫包囊研究进展进行概述,包括包囊的形态、沉积物中包囊的丰度、包囊形成的环境因素、包囊萌发过程及环境因素对包囊萌发的影响等方面,希望对国内开展浮游纤毛虫包囊的研究有所裨益。     

大亚湾海域锥状斯氏藻孢囊形成与萌发的季节变化

锥状斯氏藻(Scrippsiella trochoidea)是南海大亚湾海域优势甲藻。为了解该藻孢囊形成和萌发动态及其对营养细胞种群动态的影响,2001年1月-2002年1月在大亚湾澳头海域用沉积物捕捉器及TFO重力采泥器对其孢囊进行每月一次的周年监测,同时对浮游植物、水温、盐度、溶解氧等也进行了监测。孢囊形成和萌发分别以沉积物捕捉器中的孢囊形成率以及上表层沉积物中空孢囊的百分比来表示。钙质孢囊和非钙质孢囊年平均形成率分别为1.11×104 cysts m-2d-1和2.13×105 cysts m-2d-1。前者在冬季大量形成,而后者在夏季形成较多。孢囊多在春秋季节萌发,夏季萌发较少,而冬季几乎不萌发。在5月份和10月份营养细胞数量峰形成前,孢囊的萌发出现了高峰,而表层沉积物中的孢囊数量及孢囊形成率则在营养细胞数量峰后大幅度上升。由此可见,大亚湾沉积物中该藻孢囊的萌发给水体提供了丰富的营养细胞,反之水体中高密度营养细胞又促使孢囊的大量形成,从而造成了锥状斯氏藻赤潮在大亚湾海域接连发生。     

Serologic Changes Associated with the Encystment of Axenically Grown Hartmannella culbertsoni*

SYNOPSIS. Serologic reactions elicited by sonically ruptured trophic and cystic forms of Hartmannella culbertsoni were studied. The antigens of trophic amoebae reacted with their homologous rabbit antiserum showing multiple precipitin lines which could not be seen when the reacting antigens were treated with trypsin prior to application on the Ouchterlony plates. Antigens of trophic amoeba did not react with antiserum against cysts. Cyst antigens reacted with their homologous antiserum only after trypsin treatment. Antigens prepared from trophozoites excysting from cysts reacted positively with the antiserum against antigens of trophic amoebae. Antigens of trophic as well as cystic forms fixed guinea pig complement in presence of their homologous antisera. With the trophic form, this property was abolished after trypsin treatment. Non-specific complement fixation mediated by cyst antigens was abolished by treatment with cellulase. Antiserum against trophic amoebae immobilized trophozoites and, in the presence of guinea pig complement, led to their lysis.     

Encystment ofAzotobacter vinelandii in liquid culture

Cyst formation in liquid cultures ofAzotobacter vinelandii could be raised to 90% by including 0.6% CaCO₃ in the Burk's basal salts solution. The cysts were resistant to desiccation and possessed exine and intine capsular components when observed by electron microscopy of ultrathin sections. Cells grown in liquid medium containing no CaCO₃, but in which the pH was controlled by addition of 0.1m KOH, were not resistant to desiccation. The capsular material was loosely aggregated and not organized into the typical coat structure. The culture supernatant fluid became viscous and could be precipitated with CaCl₂, yielding a thick, polysaccharide-like gel. Calcium carbonate in the liquid encystment medium served both as a means of acid neutralization and as a source of calcium ions. Calcium ions appear to be structural units necessary for coordination of the coat components into the rigid cyst structure. Other metal ions examined could not substitute effectively for calcium in the encysting system. This investigation was supported by Public Health Service research grants AI-02924 and AI-05551 and by Public Health Service predoctoral fellowship 5-F1-GM-29, 322-02.     

Chlorella-bearing ciliates dominate in an oligotrophic North Patagonian lake (Lake Pirehueico, Chile): abundance, biomass and symbiotic photosynthesis

1. Large mixotrophic ciliates ( Stentor araucanus , S. amethystinus and Ophrydium naumanni ) were a characteristic component of a temperate, oligotrophic lake in North Patagonia. During a 1-year study, the abundance, biomass and primary production of these large Chlorella -bearing ciliates were compared with those of the total plankton community.
2. Mixotrophic ciliates peaked in spring and from late summer to autumn, accounting for 1.6–43% (annual average: 16.3%) and 67–99% (annual average: 92%) of total ciliate abundance and biomass, respectively. Their contribution to total zooplankton biomass, including flagellates, rotifers, ciliates and crustaceans, was 14–76%, or 47% as an annual average. Endosymbiotic algae accounted for up to 25% of total autotrophic biomass (annual mean: 3.9%).
3. Maximum cell-specific photosynthetic rates of S. araucanus and S. amethystinus at light saturation varied between 80 and 4400 pg C ciliate^–1 h^–1 with high values during autumn and winter, and low values during summer. The depth-integrated rates of photosynthesis (0–40 m) of algal endosymbionts contributed 1–25% to total photosynthesis (annual mean: 6.5%).
4. A comparison of calculated ingestion rates with photosynthetic rates of Stentor indicates that photosynthate produced by endosymbionts generally exceeded heterotrophic food supply of Stentor during autumn and winter, but was much lower during summer, when food supply was high.
5. The mixotrophic ciliates represent an important 'link' between nanoplankton and higher trophic levels within the plankton community because of their high heterotrophic biomass and considerable contribution to total photosynthesis.     

Morphological and Molecular Characterization of a New Protist Family, Sandmanniellidae n. fam. (Ciliophora, Colpodea), with Description of Sandmanniella terricola n. g., n. sp. from the Chobe Floodplain in Botswana

ABSTRACT. Sandmanniella terricola n. g., n. sp. was discovered in soil from the Chobe floodplain, Botswana, southern Africa. Its morphology and 18S rDNA gene sequence were studied with standard methods. Sandmanniella terricola is very likely an adversity strategist because it reaches peak abundances 6–12 h after rewetting the soil and maintains trophic food vacuoles with undigested bacteria in the resting cyst, a highly specific feature suggested as an indicator for an adversity life strategy. Possibly, the energy of the stored food vacuoles is used for reproduction and support of the cyst wall. Morphologically, Sandmanniella terricola is inconspicuous, having a size of only 50 × 40 μm and a simple, ellipsoidal shape. The main characteristics of the genus are a colpodid silverline pattern; a perioral cilia condensation; a flat, dish-shaped oral cavity, in the centre of which originates a long, conical oral basket resembling that of certain nassulid ciliates; and a vertically oriented left oral polykinetid composed of brick-shaped adoral organelles. This unique mixture of features and the gene sequence trees, where Sandmanniella shows an isolated position, suggest establishing a new family, the Sandmanniellidae n. fam., possibly related to the families Colpodidae or Bryophryidae. The curious oral basket provides some support for the hypothesis of a common ancestor of colpodid and nassulid ciliates.     

Mychonastes desiccatus Brown sp. nova (Chlorococcales, Chlorophyta)--an intertidal alga forming achlorophyllous desiccation-resistant cysts

An intertidal Chlorella-like alga Mychonastes desiccatus Brown sp. nova, capable of forming achlorophyllous desiccation-resistant cysts, has been grown in unialgal culture. This small alga was first isolated from a dried sample of a well-studied microbial mat. The mat, located at North Pond, Laguna Figueroa, San Quintin, Baja California, Mexico, is a vertically-stratified microbial community which forms laminated sediments. Morphology, pigment composition and G+C content are within the range typical for the genus Chlorella s. 1. Unlike other chlorellae, however, upon desiccation M. desiccatus forms an achlorophyllous, lipid-filled cyst (thick-walled resting stage) in which no plastid is evident. Rewetting leads to chloroplast differentiation, excystment and recovery of the fully green alga. During desiccation, sporopollenin is deposited within a thickening cell wall. Encystment cannot be induced by growth in the dark. The formation of desiccation-induced cysts allows the alga to survive frequent and intermittent periods of dryness. These chlorellae tolerate wide ranges of acidity and temperature; they both grow and form cysts in media in which sodium ions are replaced with potassium. Although the cysts tolerate crystalline salts, the cell grow optimally in concentrations corresponding from three-quarters to full-strength seawater.     

Water relations during desiccation of cysts of the potato-cyst nematode Globodera rostochiensis

The loss during desiccation of osmotically active water (OAW), which freezes during cooling to -45 degrees C, and osmotically inactive water (OIW), which remains unfrozen, from the cysts of the potato cyst nematode, Globodera rostochiensis, was determined using differential scanning calorimetry. Exotherms and endotherms associated with non-egg compartments were not detected after 5 min desiccation at 50% relative humidity and 20 degrees C. The pattern of water loss from the cysts indicates that water is lost from compartments outside the eggs first, that nearly all the non-egg water is OAW and that the OIW content of the cyst is contained within the eggs. Water is lost from the eggs only after the OAW content outside the eggs falls below that within the eggs. Both OAW and OIW are lost from the eggs during desiccation but the eggs retain a small amount of OIW. Other animals which survive some desiccation but which are not anhydrobiotic will tolerate the loss of OAW but not the loss of their OIW. Anhydrobiotic animals can survive the loss of both their OAW and a substantial proportion of their OIW.     

中国沿海甲藻包囊研究进展

休眠包囊是甲藻生活史中的一个重要阶段,它们对于甲藻种群的生存、延续以及扩散具有重要的生物学意义.能够形成休眠包囊的甲藻大部分时间以包囊的形式存在于沉积物中,因此研究包囊有助于揭示甲藻的物种多样性.根据沉积物中甲藻包囊的种类和数量还可以追溯各海区的富营养化历史,以及重建古海洋环境.本文介绍了甲藻包囊的研究方法,指出形态分...     

Cyst formation in a freshwater strain of the choanoflagellate Desmarella moniliformis Kent

Cyst formation in a freshwater strain of the colonial freshwater choanoflagellate Desmarella moniliformis Kent (Protozoa: Choanoflagellida) has been studied with light and electron microscopy for the first time. Batch cultures inoculated with motile vegetative cells start to produce cysts within 3 days during the exponential phase of growth. Cyst production proceeds until in late stationary phase there is a preponderance of cysts. Transfer of cysts to fresh medium results in limited excystment. Encystment involves the production of electron-dense fibrillar wall material, firstly around the neck of the cell and then around the posterior end. As the wall material is deposited the neck of the cell elongates and the dictyosome rotates from the horizontal to vertical plane. The number of mitochondrial profiles seen in individual sections of cells increases. Finally the neck of the cell is retracted, the flagellum and collar tentacles are withdrawn, and the bottom of the neck of the cyst wall is sealed with a diaphragm of wall material. Excystment, which has not been observed directly, appears to involve the disruption of the wall at the base of the neck, the remainder of the cyst wall remains intact. Comparisons are made between encystment in Desmarella and cyst development in other protists.     

Effects of development, temperature and salinity on metabolism in eggs and yolk-sac larvae of milkfish, Chanos chanos (Forsskål)

Oxygen uptake rates and yolk-inclusive dry weiGhts were measured during the egg and yolk-sac larval stages of milkfish, Chanos chanos (Forsskal). Oxygen uptake by eggs and yolk-sac larvae was measured to assess the effects of four salinities (20,25,30,35 ppt) at 28°C. The effects of three temperatures (23,28,33°C) on oxygen uptake by yolk-sac larvae were determined at a salinity of 35 ppt. Dry weights were measured throughout embryonic development at 28°C and the yolk-sac stage at 23.28 and 33°C.
Oxygen uptake rates of eggs increased more than fivefold during embryogenesis (0.07±0.03 to 0.40 ± 03 μl O₂ egg ⁻¹ h ⁻¹;blastula to prehatch stage). Larval oxygen uptake did not change with age but was affected by rearing temperature (0.33 ± 0.08, 0.44 ± 0.07 and 0.63 ± 0.13 μl O₂ larva ⁻¹ h⁻¹ at 23, 28 and 33°C, respectively; Q₁₀= 1.93). Acute temperature changes from 28 to 33°C caused significant increases in oxygen uptake by embryos (Q ₁₀= 1.69–3.58) and yolk-sac larvae (Q ₁₀=2.55). Salinity did not affect metabolic rates.
Dry weight of eggs incubated at 28°C decreased 13% from fertilization to hatching. Incubation temperatures from 23–33°C did not affect dry weights at hatching. Rearing temperatures significantly affected the rate of larval yolk absorption (Q ₁₀= 2.25).     

Induction of synchronous encystment in a hypotrichous ciliate, Histriculus sp

A method for the induction of synchronous encystment in a hypotrichous ciliate,Histriculus sp. is described. When the ciliates were transferred into 10× Osterhout's solution at around 7 h after disappearance of the food organisms, Tetrahymena, and were maintained at 20 °C, the organisms underwent synchronous encystment. Phase 1 cells (precystic cells) appeared at around 2 h after transfer into the 10× Osterhout solution, and almost all organisms had transformed into phase 1 cells approx. 3 h after transfer. The first cyst appeared at around 3 h after transfer into the 10× solution and essentially 100% of the organisms had transformed into cysts within approx. 4.5 h after transfer.     

Mxi1 influences cyst formation in three-dimensional cell culture

Cyst formation is a major characteristic of ADPKD and is caused by the abnormal proliferation of epithelial cells. Renal cyst formation disrupts renal function and induces diverse complications. The mechanism of cyst formation is unclear. mIMCD-3 cells were established to develop simple epithelial cell cysts in 3-D culture. We confirmed previously that Mxi1 plays a role in cyst formation in Mxi1-deficient mice. Cysts in Mxi1 transfectanted cells were showed by collagen or mebiol gels in 3-D cell culture system. Causative genes of ADPKD were measured by q RT-PCR. Herein, Mxi1 transfectants rarely formed a simple epithelial cyst and induced cell death. Overexpression of Mxi1 resulted in a decrease in the PKD1, PKD2 and c-myc mRNA relating to the pathway of cyst formation. These data indicate that Mxi1 influences cyst formation of mIMCD-3 cells in 3-D culture and that Mxi1 may control the mechanism of renal cyst formation. [BMB reports 2012; 45(3): 189-193].     

Dinoflagellate cysts from surface sediments of Saldanha Bay, South Africa: an indication of the potential risk of harmful algal blooms

The distribution and abundance of dinoflagellate cysts from recent coastal sediments in Saldanha Bay, was investigated, and compared to the cyst assemblages of the adjacent coastal upwelling system as reflected in the sediments off Lambert's Bay on the southern Namaqua shelf. Twenty-two cyst types were identified from three sample sites off Lambert's Bay with recorded abundances between 1726 and 1863 cysts ml⁻¹ wet sediment. At least 21 distinctive cyst types were identified from 32 sample sites within Saldanha Bay. Cyst abundance in Saldanha Bay was relatively low, averaging 116 cysts ml⁻¹ wet sediment. The region off Lambert's Bay is especially susceptible to the formation of harmful algal blooms attributed to high biomass dinoflagellate blooms. Owing to these blooms and the retentive circulation characteristics of this area, cyst formation and deposition is high. Blooms can be advected into Saldanha Bay, but their development and duration in the Bay is restricted by the system of exchange that operates between the Bay and the coastal upwelling system, in that there is a net export of surface waters from the Bay. Consequently, fewer cysts are formed and deposited within the Bay thereby reducing the likelihood of in situ bloom development initiated from the excystment of cysts.     

CYST–THECA RELATIONSHIP,LIFE CYCLE,AND EFFECTS OF TEMPERATURE AND SALINITY ON THE CYST MORPHOLOGY OF GONYAULAX BALTICA SP. NOV. (DINOPHYCEAE) FROM THE BALTIC SEA AREA1

A new species of Gonyaulax, here named Gonyaulax baltica sp. nov., has been isolated from sediment samples from the southeastern Baltic. Culture strains were established from individually isolated cysts, and cyst formation was induced in a nitrogen‐depleted medium. Although G. baltica cysts are similar to some forms attributed to Spiniferites bulloideus and the motile stage of G. baltica has affinities with G. spinifera, the combination of features of cyst and motile stage of G. baltica is unique. The culture strains were able to grow at salinity levels from 5 to 55 psu and formed cysts from 10 to 50 psu. Cultures at each salinity level were grown at 12, 16, and 20° C. Temperature‐ and salinity‐controlled morphological variability was found in the resting cysts. Central body size varied with temperature and salinity, and process length varied with salinity. Cysts that formed at extreme salinity levels displayed lower average process length than cysts formed at intermediate salinity levels, and central body length and width were lowest at higher temperature and lower salinity. Models for the relationship between central body size and temperature/salinity and process length and salinity have been developed and may be used to determine relative paleosalinity and paleotemperature levels. Our results on salinity‐dependent process length confirm earlier reports on short‐spined cysts of this species found in low salinity environments, and the model makes it possible to attempt to quantify past salinity levels.     

Population Dynamics of Active and Total Ciliate Populations in Arable Soil Amended with Wheat

Soil protozoa are characterized by their ability to produce cysts, which allows them to survive unfavorable conditions (e.g., desiccation) for extended periods. Under favorable conditions, they may rapidly excyst and begin feeding, but even under optimal conditions, a large proportion of the population may be encysted. The factors governing the dynamics of active and encysted cells in the soil are not well understood. Our objective was to determine the dynamics of active and encysted populations of ciliates during the decomposition of freshly added organic material. We monitored, in soil microcosms, the active and total populations of ciliates, their potential prey (bacteria and small protozoa), their potential competitors (amoebae, flagellates, and nematodes), and their potential predators (nematodes). We sampled with short time intervals (2 to 6 days) and generated a data set, suitable for mathematical modeling. Following the addition of fresh organic material, bacterial numbers increased more than 1,400-fold. There was a temporary increase in the number of active ciliates, followed by a rapid decline, although the size of the bacterial prey populations remained high. During this initial burst of ciliate growth, the population of cystic ciliates increased 100-fold. We suggest that internal population regulation is the major factor governing ciliate encystment and that the rate of encystment depends on ciliate density. This model provides a quantitative explanation of ciliatostasis and can explain why protozoan growth in soil is less than that in aquatic systems. Internally governed encystment may be an essential adaptation to an unpredictable environment in which individual protozoa cannot predict when the soil will dry out and will survive desiccation only if they have encysted in time.     

The primary and secondary spore cyst of Aphanomyces (Oomycetes, Saprolegniales)

The ultrastructural organization of the primary (1°) and secondary (2°) cysts of Aphanomyces astaci and A. laevis is extremely similar, and similar to that of the 1° and 2° cysts of A. eutekhes as presented earlier by Hoch and Mitchell. Synchronous populations of 2° cysts can be induced by mechanical shock and encystment appears to be essentially instantaneous. The cyst coat–wall appears to be formed extremely rapidly from material from the peripheral vesicles with flocculent content. After encystment the microtubule cytoskeleton found in the zoospore is maintained in the 1° and 2° cyst (i.e. the single microtubules which extend along the pyriform nucleus from the ki–netosomes–centrioles and the bundles of closely appressed microtubules are retained). The peripheral vesicles with granular content found in the zoospore are not seen in the 1° or 2° cyst. Multivesicular bodies and lomasomes are observed in the 1° and 2° cyst which are not found in the zoospore. The peripheral cisternae of the zoospore are lost upon encystment and may be formed from dictyosome–derived vesicles during excystment of the 1° and 2° cyst. The U–body of A. astaci has a paracrystalline content while the U–body of A laevis and A eutekhes has a tubular content. A microbody–lipid body complex (sensu Powell) is found in the 1° and 2° cysts of A laevis but not in A astaci or A eutekhes. The significance of the presence of a microbody–lipid body complex in a biflagellate zoospore is discussed.