SPORE FORMATION IN THE LIFE CYCLES OF THE DIATOMS CHAETOCEROS DIADEMA AND LEPTOCYLINDRUS DANICUS1

A nitrogen limitation technique elicited the entire life cycle of the marine centric diatoms Chaetoceros diadema (Ehr.) Gran and Leptocylindrus danicus Cleve. In C. diadema the sexual cycle followed the same pattern as in the previously investigated C. didymus. Sexuality took place in narrow diameter cells, only at 2 and 5° C, and was seldom seen. Resting spore formation took place in cells of all sizes and at all temperatures at which the species grew vegetatively (2–15° C). The L. danicus life cycle is probably unique among diatoms. Nitrogen depletion induced sexuality in the entire culture at 10 and 15° C if the cell diameter was narrow (3–8 μm). Auxospore formation was followed by resting spore formation directly within the auxospore. In C. diadema, as in most centric diatoms, resting spores are not an obligate part of the life cycle, but they are in L. danicus. Resting spore formation is a versatile adaptive response in C. diadema, depending only on nitrogen depletion, although promoted by low temperatures. In L. danicus the linkage to the sexual process sharply limits conditions under which resting spores can form.     

Monterey Bay Phytoplankton. II. Resting Spore Cycles in Coastal Diatom Populations

The purpose of this study is to examine the role of "restingspores" in natural population cycles of temperature, neriticdiatoms. Resting spores are a conspicuous element of centricdiatom populations in most neritic and some deep-water environmentsof the world oceans. Until recently the spores have been accepted,almost axiomatically, as surviving as a seasonal benthic stagewhich reinoculate the water column at the onset of favorablegrowth conditions. Data to support this hypothesis, however,is limited and contradictory. In my study, I am examining theoccurrence of resting spores in relation to vegetative cellcycles and oceanographic conditions in Monterey Bay, California,a nearshore upwelling-dominated system. I have utilized samplesfrom the water column, from settling-tubes, and from sedimentcores to document the cycles. Resting spore cycles were observed for many neritic species,and spore cycles for abundant species were considered in detail.Resting spore formation was associated with low nitrate concentrationsin surface waters. After spore formation in the water columnspores were found in settling-tubes and in sediment samples.Spore formation was a frequent event and spores were often presentin the water column and in the sediments. Observations of spore cycles in the present study were consistentwith the prevailing idea that resting spores function as benthicresting stages in coastal populations. The pelagic retentionand/or dispersal in coastal circulation cells, however, alsoappeared to be highly likely. The study has demonstrated thepotential for resting spores to function as survival stagesin Monterey Bay and in other regions with similar hydrographicconditions. The present evidence regarding the role of restingspores suggests that resting spores may have a wide range offunctions, and a more inclusive (or alternate) resting sporehypothesis is suggested.     

Evidence for Regular Sporulation by Haplosporidium nelsoni (MSX) (Ascetospora; Haplosporidiidae) in Spat of the American Oyster, Crassostrea virginica

The spore stage of Haplosporidium nelsoni , the ascetosporan parasite causing multinucleated sphere unknown (MSX) disease in oysters, Crassostrea virginica , has been reported so rarely (≥0.01% of infected oysters) that a second host has been postulated. However, recent intensive sampling of young (≥1 year) oysters in Delaware Bay, U.S. suggests that spore formation occurs regularly in this group and that spores are produced in at least 75–85% of all infections reaching the advanced stage. Sporulation was seasonal, occurring over two to three weeks in late June/early July and again in late summer/early fall. Our data indicate that sporulation by H. nelsoni in oysters is more common than previously suspected, occurring in a segment of the host population that may not have been sufficiently sampled in the past, and that a direct life cycle should be reconsidered.     

Evidence for regular sporulation by Haplosporidium nelsoni (MSX) (Ascetospora; Haplosporidiidae) in spat of the American oyster, Crassostrea virginica.

The spore stage of Haplosporidium nelsoni, the ascetosporan parasite causing multinucleated sphere unknown (MSX) disease in oysters, Crassostrea virginica, has been reported so rarely (less than 0.01% of infected oysters) that a second host has been postulated. However, recent intensive sampling of young (less than 1 year) oysters in Delaware Bay, U.S. suggests that spore formation occurs regularly in this group and that spores are produced in at least 75-85% of all infections reaching the advanced stage. Sporulation was seasonal, occurring over two to three weeks in late June/early July and again in late summer/early fall. Our data indicate that sporulation by H. nelsoni in oysters is more common than previously suspected, occurring in a segment of the host population that may not have been sufficiently sampled in the past, and that a direct life cycle should be reconsidered.     

The explosive diversification of the diatom genus Chaetoceros across the Eocene/Oligocene and Oligocene/Miocene boundaries in the Norwegian Sea

Eocene to middle Miocene stratigraphic changes in species richness, abundance and valve size of Chaetoceros resting spores in the Norwegian Sea (DSDP Site 338) were investigated in order to understand past productivity and paleoenvironmental changes in upwelling regions. As a result, drastic resting spore events were recognized in a 6 myr interval across the Eocene/Oligocene boundary (EO Event), the Oligocene/Miocene boundary (OM Event) and in the early middle Miocene (emM Event). The EO Event was characterized by explosive diversification at both the morpho-generic and specific levels, an increase in abundance, and a decrease in valve size from the upper Eocene through the lowest Oligocene. The OM Event was defined by a two-fold increase in species richness. During the emM Event spore abundance decreased rapidly, and species richness and valve size decreased gradually. These changes may indicate changes in the nutrient supply, especially in upwelling regions. The increased species richness suggests a change from a stable water column with a constant nutrient supply in the Eocene to an unstable one with a sporadic nutrient supply by increased vertical mixing in the Oligocene, based on evaluation of the ecologic differences between dinoflagellate cysts and Chaetoceros resting spores. The role of main primary producer might have switched from dinoflagellates and/or nannoplankton in the Eocene to diatoms, especially Chaetoceros, in the Oligocene in the Norwegian Sea. Increased resting spore species richness during the OM Event may show that environmental changes such as global cooling and nutrient mixing led to a diversification of the spore producing genus Chaetoceros. The emM Event might have been affected by changes in paleoceanographic conditions, perhaps a decrease in nutrient supply. This study presents the first paleoceanographic analysis using not only the total resting spore abundance but also the abundances of individual species, and establishes the value of spore taxonomy and diatom analysis including spores.     

Resting spore formation ofLeptocylindrus danicus (Bacillariophyceae) during short time-scale upwelling and its significance as predicted by a simple model

Resting spore formation during short time-scale upwelling and its significance were investigated in the field and by a simple theoretical model. Field observations of spore formation ofLeptocylindrus danicus were made off Izu Peninsula, Japan. A rapid increase in ratio of resting spore to vegetative cell numbers indicated thatL. danicus formed resting spores quickly as a response to nutrient depletion in the upwelled water, although only a very low number of resting spores was found in the upwelling. A simple model was constructed to investigate the possible advantages of spore formation during short time-scale upwelling. This showed that there is a critical time-scale for resting spore formation to be advantageous. The nutrient depletion period of the upwelling off Izu was shorter than the critical time-scale determined by the model. Rapid-sinking of resting spores may increase further the critical time-scale, unless spores return with upwelling water. For short time-scale upwelling, the vegetative cell may be better suited than the resting spore for enduring a short period of nutrient depletion. Contribution from Shimoda Marine Research Center, University of Tsukuba, No. 475.     

Macroalgal spore dysfunction: ocean acidification delays and weakens adhesion

Early life stages of marine organisms are predicted to be vulnerable to ocean acidification. For macroalgae, reproduction and population persistence rely on spores to settle, adhere and continue the algal life cycle, yet the effect of ocean acidification on this critical life stage has been largely overlooked. We explicitly tested the biomechanical impact of reduced pH on early spore adhesion. We developed a shear flume to examine the effect of reduced pH on spore attachment time and strength in two intertidal rhodophyte macroalgae, one calcified (Corallina vancouveriensis) and one noncalcified (Polyostea robusta). Reduced pH delayed spore attachment of both species by 40%–52% and weakened attachment strength in C. vancouveriensis, causing spores to dislodge at lower flow‐induced shear forces, but had no effect on the attachment strength of P. robusta. Results are consistent with our prediction that reduced pH disrupts proper curing and gel formation of spore adhesives (anionic polysaccharides and glycoproteins) via protonation and cation displacement, although experimental verification is needed. Our results demonstrate that ocean acidification negatively, and differentially, impacts spore adhesion in two macroalgae. If results hold in field conditions, reduced ocean pH has the potential to impact macroalgal communities via spore dysfunction, regardless of the physiological tolerance of mature thalli.     

广东沿海洛氏角毛藻复合群物种多样性的探究

为了澄清洛氏角毛藻复合群的物种多样性, 并明确洛氏角毛藻和并基角毛藻的种间界限, 文章以广东沿海为例, 建立了洛氏角毛藻复合群的22个单克隆培养株系, 利用光学显微镜和电子显微镜技术, 开展了基于生活史的连续形态学观察; 结合基于核糖体大亚基编码基因D1-D3区序列的分子系统学分析。结果表明: 文章支持近年研究的观点, 认为“角毛基部并行融合”不是稳定特征, 不宜继续作为并基角毛藻的标志特征; 发现洛氏角毛藻形态相似藻株聚类在2个分支上, 确认了洛氏角毛藻确实存在隐藏的物种多样性。其中一类与目前认知的洛氏角毛藻最为接近, 而另一类在角毛孔纹、休眠孢子上存在明显区别。经过对洛氏角毛藻历史文献的对比研究, 发现洛氏角毛藻的物种界定存在混乱和模糊的情况, 如休眠孢子形态, 及其初生壳面是否具有二叉状分布结构等, 均存在相互矛盾或不一致的历史报道。     

氮、硅限制对赤潮藻扁面角毛藻休眠孢子形成的影响

休眠孢子的形成对于赤潮藻种群的保存、延续以及分布扩散等均具有重要的意义。通过单因子营养限制研究氮、硅对赤潮藻扁面角毛藻（Chaetoceros compressus）休眠孢子形成的影响,结果表明：培养基中氮的初始浓度对休眠孢子的出现时间有一定影响。氮的初始浓度越低,休眠孢子出现的时间越早：反之,氮的初始浓度越高,休眠孢子出现的时间越晚。氮缺乏是硅藻形成休眠孢子的必需条件之一,当培养基中氮含量低于10μmol·L^-1时,扁面角毛藻可以形成休眠孢子。氮缺乏诱发的休眠孢子的形成需要大量的硅,当培养基中硅含量低于23μmol·L^-1时,即使氮缺乏,扁面角毛藻也几乎不再继续形成休眠孢子。这说明硅藻休眠孢子的形成不仅受氮浓度的影响,还与硅浓度有关。     

AUTECOLOGICAL STUDIES ON THE MARINE DIATOM RHIZOSOLENIA FRAGILISSIMA BERGON. II. ENRICHMENT AND DARK VIABILITY EXPERIMENTS1

Nutrient enrichment experiments were conducted with a Narragansett Bay clone of Rhizosolenia fragilissima to examine the potential influence of nutrients in regulating its seasonal cycle in this embayment, and their contribution to its coastal tendencies. Growth rates were measured at 18 C and 1000 ft-c continuous illumination in surface waters enriched in 15 different ways. Narragansett Bay was sampled in March, May, September, and December. Six stations on a transect from this Bay to the Sargasso Sea were sampled during late summer. The data and our previous autecological observations are consistent with the idea that the annual cycle of this species in Narragansett Bay is associated with temperature, chemical “water quality,” and unknown factors. Its absence during late fall and winter may reflect low temperatures and a trace metal (Co, Mo) inadequacy. In early spring, low temperature appears to be the limiting factor, whereas in late spring and early summer trace metals again appear to prevent active growth. A late summer-early autumn bloom occurs periodically during optimal temperature conditions; this can terminate independently of grazing pressure, and in spite of seemingly adequate light-temperature-salinity and phosphate conditions.     

The life stages of Entomophthora virulenta (Entomophthorales: Entomophthoraceae)

An illustrated scheme of the life cycle of Entomophthora virulenta shows that an alternation of the conidal and resting spore stages is involved. The resting spores are azygospores; chlamydospores are also present.     

氮、硅限制对赤潮藻扁面角毛藻休眠孢子形成的影响

休眠孢子的形成对于赤潮藻种群的保存、延续以及分布扩散等均具有重要的意义。通过单因子营养限制研究氮、硅对赤潮藻扁面角毛藻 (Chaetoceros compressus )休眠孢子形成的影响, 结果表明: 培养基中氮的初始浓度对休眠孢子的出现时间有一定影响。氮的初始浓度越低, 休眠孢子出现的时间越早; 反之, 氮的初始浓度越高, 休眠孢子出现的时间越晚。氮缺乏是硅藻形成休眠孢子的必需条件之一, 当培养基中氮含量低于10 mmol.L^-1时, 扁面角毛藻可以形成休眠孢子。氮缺乏诱发的休眠孢子的形成需要大量的硅, 当培养基中硅含量低于23 mmol.L^-1时, 即使氮缺乏, 扁面角毛藻也几乎不再继续形成休眠孢子。这说明硅藻休眠孢子的形成不仅受氮浓度的影响, 还与硅浓度有关。     

Application of nested-PCR technique to resting spores from the Entomophthora muscae species complex: implications for analyses of host-pathogen population interactions

We developed new Entomophthora-specific primers for nested-PCR of the ITS II region to be used on in vivo material and combined it with RFLP. Resting spores from Scathophaga stercoraria (3 specimens), Delia radicum (9 specimens), Botanophila fugax (1 specimen), and two syrphid host species, Platycheirus peltatus and Melanostoma mellinum (one specimen of each) were characterized genetically after analysis of RFLP-profiles of the PCR-products. The genetic characterization of the resting spore isolates was compared with twenty isolates of known primary conidial morphology (in vitro and in vivo) from the E. muscae species complex. The analysis allowed for the first time a separation of resting spore isolates into the species level, which is not possible only using morphological characters (diameter). Isolates originating from different specimens of the same host taxa appeared to be strongly clonal even they were sampled at different localities in different years. Isolates morphologically belonging to E. muscae s. str. (e.g., including E. scatophagae) could be separated genetically further into sub-groups entirely depending on the host taxa; each fungal genotype, either present at the conidial stage or at the resting spore stage, is correlated with one host species. Furthermore, E. muscae s. str. originating from D. radicum proved to be much more closely related to E. scatophagae than to E. muscae s. str. originating from M. domestica. None of the resting spore isolates could be assigned to E. schizophorae. The nested-PCR approach accompanied by RFLP proved its usefulness for identification of resting spores and for more detailed studies clarifying host-pathogen specificity and interactions. It seems that different members of the E. muscae species complex are able to complete their life cycle in only one host species and, further, that each pathogen-host system is independent.     

Entomophthora muscae resting spore formation in vivo in the host Delia radicum

The formation in vivo of Entomophthora muscae resting spores was investigated in the host, Delia radicum (cabbage root fly), by analysis of field data on the seasonal occurrence of E. muscae resting spores over 4 years. E. muscae resting spores in D. radicum were spherical with an average diameter of 39.4 microm, and the average numbers produced were estimated at 5.7 x 10(4) resting spores/female cadaver. Resting spores were found only after midsummer in D. radicum and almost exclusively in females. The proportion of infected females with resting spores was negatively correlated with average weekly day length after midsummer. We did not detect any significant year effect; thus, the results support the hypothesis that the photoperiod is the most important abiotic factor controlling E. muscae resting spore formation in D. radicum.     

Synchytrium solstitiale: reclassification based on the function and role of resting spores

Studies were made about resting spores of Synchytrium solstitiale, a chytrid that causes false rust disease of yellow starthistle (YST). During evaluation of this fungus for biological control of YST, a protocol for resting spore germination was developed. Details of resting spore germination and study of long-term survival of the fungus were documented. Resting spores from dried leaves germinated after incubating them on water agar at least 7 d at 10-15 C. Resting spores were viable after storage in air-dried leaves more than 2 y at room temperature, suggesting they have a role in off-season and long-term survival of the fungus. Each resting spore produced a single sorus that contained a single sporangium, which on germination released zoospores through a pore. YST inoculated with germinated resting spores developed symptoms typical of false rust disease. All spore forms of S. solstitiale have been found to be functional, and the life cycle of S. solstitiale has been completed under controlled laboratory and greenhouse conditions. Resting spore galls differ from sporangial galls both morphologically and biologically, and in comparison, each sporangial gall cleaves into several sori and each sorus produces 5-25 sporangia that rupture during release of zoospores. For this reason S. solstitiale should be reclassified as diheterogallic sensu Karling (Am J Bot 42:540-545). Because resting spores function as prosori and produce an external sorus, S. solstitiale is best placed in into the subgenus Exosynchytrium.     

In vitro formation of resting spores by the insect pathogenic fungus Entomophaga maimaiga

Field-collected resting spores (azygospores) of the fungal pathogen of Lymantria dispar (gypsy moth), Entomophaga maimaiga, have been used to release this biological control agent in areas where this pathogen is not established. We have found that E. maimaiga can produce resting spores in vitro using Grace's insect tissue culture medium (95%) plus fetal bovine serum (5%). The majority of spores become mature between 7 and 21 days after cultures are initiated. Spore production varies by fungal isolate; of 38 isolates tested, 10 produced no resting spores while 7 produced >1000 resting spores/ml. Resting spore production was not affected when isolates were mixed. Glycerol (used for fungal storage), trehalose, and selected amino acids each inhibited resting spore formation. Fetal bovine serum was required for spore production but the presence of >5% yielded lower resting spore densities. A large surface area:volume ratio (12.5 cm(2):ml versus 4.2 cm(2):ml) was required for abundant formation of resting spores. At present, resting spores have only been produced in small volumes with a maximum of 3 x 10(4) resting spores/ml.     

Fine structure of resting spore formation and germination in Entomophthora virulenta

The fine structure during the formation and germination of resting spores of Entomophthora virulenta is described. There were many microbodies in contact with oil droplets, and the microbodies appeared to participate in spore germination. The mature resting spore had an epispore layer with two regions and an endospore layer with five regions. Dictyosomes, numerous vesicles, and lomasomes were produced during the formation of the endospore layer. Prior to spore germination, the single large oil droplet separated into numerous small oil droplets, and the new cell wall was formed beneath the endospore layer which gradually disintegrated possibly by enzymatic actions. The germ tube perforated the epispore layer mainly by mechanical pressure.     

Cytological and genetic studies of the life cycle of Saccharomycopsis lipolytica

Summary In the alkane yeast Saccharomycopsis lipolytica (formerly: Candida lipolytica) the variability in the ascospore number is caused by the absence of a correlation between the meiotic divisions and spore wall formation. In four spored yeasts, after meiosis II, a spore wall is formed around each of the four nuclei produced by meiosis II. However, in the most frequently occurring two spored asci of S. lipolytica, the two nuclei are already enveloped by the spore wall after meiosis I due to a delay of meiosis II. This division takes place within the spore during the maturation of the ascus. In this case germination of the binucleate ascospore is not preceded by a mitosis. It follows that the cells of the new haploid clones are mononucleate. In the three spored asci, which occur rarely, only one nucleus is surrounded by a spore wall after meiosis I; the other nucleus undergoes meosis II before the onset of spore wall formation. The result is one binucleate and two mononucleate spores. In the one spored asci the two meiotic divisions occur within the young ascospore, i.e. spore wall formation starts immediately after development of the ascus. These cytological observations were substantiated by genetic data, which in addition confirmed the prediction that binucleate spores may be heterokaryotic. This occurs when there is a postreduction of at least one of the genes by which the parents of the cross differ. This also explains the high frequency of prototrophs in the progeny on non-allelic auxotrophs since random spore isolates are made without distinguishing between mono-and binucleate spores. The possibility of analysing offspring of binucleate spores by tetrad analysis is discussed. These findings enable us to understand the life cycle of S. lipolytica in detail and we are now in a position to start concerted breeding for strain improvement especially with respect to single cell protein production.     

小绒泡菌生活史及其形态建成期显微结构的观察

在完成小绒泡菌Physaum pusillum生活史的同时,观察了小绒泡菌P. pusillum生活史不同阶段显微结构的形成。生活史研究结果表明：小绒泡菌P. pusillum的孢子萌发方式为裂式,黏变形体具两根鞭毛,较短一根不易观察到,原质团类型为显型原质团,子实体形态建成过程约需12-13h。显微结构观察结果表明：石灰结和孢丝结构在原质团隆起约6h后开始形成,孢子在原质团隆起约9h后开始形成,石灰结和孢丝先于孢子形成。     

Development of Acaulospora rehmii spore and hyphal swellings under root-organ culture

A strain of Acaulospora rehmii was, for the first time, successfully grown in vitro on Ri T-DNA transformed carrot roots allowing the in situ observation of Acaulospora spore development and of extraradical thin-walled hyphal swellings. The sporogenous hypha developed intercalarly along thin-walled coenocytic hyphae. The distal part of the sporogenous hypha swelled slightly as a sporiferous saccule primordium followed by the differentiation of a lateral spore primordium along the neck of the sporogenous hypha. Both structures matured simultaneously, and the sporiferous saccule began to collapse after spore maturation and complete differentiation of the spore wall. Several of the in situ observations on in vitro differentiated A. rehmii spores are concordant with previous ontogenic studies done on other Acaulospora species obtained from in vivo cultures. New and original observations on the early developmental stages of sporiferous saccules and spores and on the occurrence of small diameter intercalary hyphal swellings provide additional elements in the study of Acaulospora sporulation process and life cycle.