The jellyfish and its polyp: a comparative study of gene expression monitored by the protein patterns, using two-dimensional gels with double-label autoradiography

The life cycle of Podocoryne carnea (Coelenterata, Anthomedusae) shows several distinct stages which differ considerably in terms of their ecology, morphology, cellular composition, and ultrastructure. Previously these stages had even been described as separate species. Using two-dimensional gel electrophoresis and a new method of double-label autoradiography, we show here for the first time for metagenic hydrozoans that only minor differences in gene expression exist between the various life cycle stages. Our results demonstrate the high resolution power of these techniques and show that the different life stages of P. carnea remain rather similar on the protein level. Most of the prominent spots of the two-dimensional gel protein patterns are common to all stages studied. These data show that the hydrozoan life cycle and development are regulated by only minor distinctions in gene expression which possibly explains the great morphogenetic repertoire of these animals described in many studies.     

Effects of variation in resource acquisition during different stages of the life cycle on life‐history traits and trade‐offs in a burying beetle

Individual variation in resource acquisition should have consequences for life‐history traits and trade‐offs between them because such variation determines how many resources can be allocated to different life‐history functions, such as growth, survival and reproduction. Since resource acquisition can vary across an individual's life cycle, the consequences for life‐history traits and trade‐offs may depend on when during the life cycle resources are limited. We tested for differential and/or interactive effects of variation in resource acquisition in the burying beetle Nicrophorus vespilloides. We designed an experiment in which individuals acquired high or low amounts of resources across three stages of the life cycle: larval development, prior to breeding and the onset of breeding in a fully crossed design. Resource acquisition during larval development and prior to breeding affected egg size and offspring survival, respectively. Meanwhile, resource acquisition at the onset of breeding affected size and number of both eggs and offspring. In addition, there were interactive effects between resource acquisition at different stages on egg size and offspring survival. However, only when females acquired few resources at the onset of breeding was there evidence for a trade‐off between offspring size and number. Our results demonstrate that individual variation in resource acquisition during different stages of the life cycle has important consequences for life‐history traits but limited effects on trade‐offs. This suggests that in species that acquire a fixed‐sized resource at the onset of breeding, the size of this resource has larger effects on life‐history trade‐offs than resources acquired at earlier stages.     

LIFE CYCLE OF THE HETEROTROPHIC DINOFLAGELLATE PFIESTERIA PISCICIDA (DINOPHYCEAE)1

The putatively toxic dinoflagellate Pfiesteria piscicida (Steidinger et Burkholder) has been reported to have an unusual life cycle for a free‐living marine dinoflagellate. As many as 24 life cycle stages were originally described for this species. During a recent phylogenetic study in which we used clonal cultures of P. piscicida, we were unable to confirm many reported life cycle stages. To resolve this discrepancy, we undertook a rigorous examination of the life cycle of P. piscicida using nuclear staining techniques combined with traditional light microscopy, high‐resolution video microscopy, EM, and in situ hybridization with a suite of fluorescently labeled peptide nucleic acid (PNA) probes. The results showed that P. piscicida had a typical haplontic dinoflagellate life cycle. Asexual division occurred within a division cyst and not by binary fission of motile cells. Sexual reproduction of this homothallic species occurred via the fusion of isogamous gametes. Examination of tanks where P. piscicida was actively feeding on fish showed that amoebae were present; however, they were contaminants introduced with the fish. Whole cell probing using in situ hybridization techniques confirmed that these amoebae were hybridization negative for a P. piscicida‐specific PNA probe. Direct observations of clonal P. piscicida cultures revealed no unusual life cycle stages. Furthermore, the results of this study provided no evidence for transformations to amoebae. We therefore conclude that P. piscicida has a life cycle typical of free‐living marine dinoflagellates and lacks any amoeboid or other specious stages.     

Observations on the life histories of Paramacroderoides pseudoechinus sp. n. (Digenea: Plagiorchioidea) and P. echinus Venard 1941, trematodes from the Florida gar.

Paramacroderoides pseudoechinus sp. n. is described from the intestine of Lepisosteus platyrhincus. Life history studies reveal that developmental stages previously reported for P. echinus from gars belong instead to the new species. The account of the life history of P. echinus is emended accordingly and differences in structure and behavior between that species and P. pseudoechinus are described.     

Organization of vertebrate annual cycles: implications for control mechanisms

The majority of vertebrates have a life span of greater than one year. Therefore individuals must be able to adapt to the annual cycle of changing conditions by adjusting morphology, physiology and behaviour. Phenotypic flexibility, in which an individual switches from one life history stage to another, is one way to maximize fitness in a changing environment. When environmental variation is low, few life history stages are needed. If environmental variation is large, there are more life history stages. Each life history stage has a characteristic set of sub-stages that can be expressed in various combinations and patterns to determine state at any point in the life of the individual. Thus individuals have a finite number of states that can be expressed over the spectrum of environmental conditions in their life spans. Life history stages have three phases-development, mature capability (when characteristic sub-stages can be expressed) and termination. Expression of a stage is time dependent (probably a minimum of one month), and termination of one stage overlaps development of the next stage. It follows that the more life history stages an individual expresses, the less flexibility it will have in timing those stages. Having fewer life history stages increases flexibility in timing, but less tolerance of variation in environmental conditions. To varying degrees it is possible to overlap mature capability of some life history stages to effectively reduce 'finite stage diversity' and maximize flexibility in timing. Theoretical ways by which this can be done, and the implications for neuroendocrine and endocrine control mechanisms are discussed. Twelve testable hypotheses are posed that relate directly to control mechanisms.     

REPLY TO COMMENT ON THE LIFE CYCLE AND TOXICITY OF PFIESTERIA PISCICIDA REVISITED1

Free‐living, marine dinoflagellates are typified by a well‐defined, haplontic life cycle with relatively few stages. The most unusual departure from this life cycle is one reported for the heterotrophic dinoflagellate Pfiesteria piscicida Steidinger et Burkholder. This species is alleged to have at least 24 life cycle stages including amoebae and a chrysophyte‐like cyst form ( Burkholder et al. 1992 , Burkholder and Glasgow 1997a ) not previously known in free‐living marine dinoflagellates. Litaker et al. (2002) redescribed the life cycle of P. piscicida from single‐cell isolates and found only life cycle stages typical of free‐living marine dinoflagellates. The discrepancy between these observations and the life cycle reported in the literature prompted a rigorous study to resolve the life cycle of P. piscicida. Burkholder and Glasgow (2002) took exception to this study, arguing that Litaker et al. (2002) misunderstood the life cycle of P. piscicida and ignored recent publications. We present a rebuttal of their criticisms and suggest a simple way to resolve the discrepancies in the P. piscicida life cycle.     

Flexibility in annual cycles of birds: implications for endocrine control mechanisms

Life cycles of birds and other vertebrates are composed of series of life history stages each with unique combinations of morphological, physiological and behavioral characteristics. For example, in the white-crowned sparrow, Zonotrichia leucophrys, the nonbreeding stage (winter), vernal migration, breeding, moult and autumn migration stages occur in a fixed and repeated sequence where each cycle is 1 year. The sequence of stages cannot be reversed. Transition from one life history stage to the next and the duration of each stage are dependent upon a combination of genetic factors and environmental cues. The latter include the annual change in photoperiod and the former may involve endogenous circannual rhythms. All vertebrates also express the emergency life history stage in response to perturbations of the environment that allow individuals to cope with the unpredictable. Each stage has a unique repertoire of sub-stages (physiological and behavioral, and to a lesser extent morphological), which can be expressed in any sequence or combination to give the state of the individual at any point in its life cycle. This state is presumably maximally adapted to the environmental conditions at that time. Although the sequence of life history stages appears to be innate, the rate of transition from stage to stage, and the expression of sub-stages can be modified by the local environmental factors and, particularly, by social cues. These environmental cues acting on the phenotype result in neuroendocrine and endocrine secretions that regulate development of the life history stage, its onset once mature capability has been attained, and then terminate it at the appropriate times. The environmental cues (from the physical and social environment) impart a strong experiential component. Because, there is a set number of life history stages and their sub-stages, there is a finite number of states that can be expressed in response to the environmental variation experienced by the individual. The more life history stages a phenotype expresses, the less flexibility is there in the overall timing of these stages owing to the time taken to develop one stage and terminate the last (about 1 month). However, many phenotypes have increased flexibility in their life cycles by overlapping some life history stages (i.e., with overlapping mature capability of two or perhaps even more stages). Another potential strategy is to dissociate some components of a life history stage so they are expressed at other times of year thus spreading out potential costs associated with that life history stage. Examples of both overlap and dissociation of life history stages are given including implications for hormonal control mechanisms.     

Redefinition of Peridinium lomnickii Wołoszynska (Dinophyta) by scanning electronmicroscopical survey

Peridinium lomnickii Wo?oszynska was investigated by scanning electron microscopy with special attention to the importance of development of thecal plate during the life cycle. Different life cycle stages (gymnodinoid-, glenodinoid-, peridinioid) are described on the basis of development of cell wall, presence and development of sutures, appearance of pore and the change of the cell shape. Differences and possible relationships between the three existing varieties of the species are discussed. We suggest that the three varieties of P. lomnickii, P. lomnickii var. lomnickii, P. lomnickii var. wierzejskii and P. lomnickii var. splendida,represent the different life cycle stages of the species. These results and the known ontogenic cycle of dinophyta taxa should be taken into consideration, when a phylogenic tree of the dinophytes is constructed.     

The life cycle and transmission dynamics of the larval stages of Hypoderaeum conoideum

The morphology of the different larval stages and life cycle of Hypoderaeum conoideum (Trematoda: Echinostomatidae) are described. The freshwater snail species Lymnaea peregra (Gastropoda: Lymnaeidae) serves as the natural first intermediate host and this and L. corvus serve as experimental first intermediate hosts. These and other freshwater snails, such as Physella acuta and Gyraulus chinensis, in turn serve as second intermediate hosts. Adult worms were obtained from chicks and ducks, but not from rats, mice and golden hamsters. The morphology of the larval stages is compared with previous work on H. conoideum. Several aspects of the biology of the life history stages are described with emphasis on the transmission dynamics of the free-living stages. Differential suitability of the snail species that may act as first and/or second intermediate hosts is studied and discussed.     

Nomadic behaviour and colony fission in a cooperative spider: life history evolution at the level of the colony?

The concept of colony-level life history evolution is introduced for the cooperative spiders by describing the life cycle and demography of Atbuhna binotata (Araneae: Dictynidae), a species living in groups containing up to several dozen adult females plus their offspring. In a life cycle remarkably similar to that of army ants, the colonies of A binotata were found to reproduce by fission and to alternate nomadic and sedentary phases in tight association with their internal demography. Colonies of other cooperative spiders, on the other hand, remain stationary as they grow for a number of generations before producing propagules that are relatively small subsets of the maternal colony. It is suggested that A. binotata!% peculiar life cycle may have unfolded as a consequence of the two-dimensional architecture of its nests. Expanding two-dimensional nests may fragment more easily than the three-dimensional nests characteristic of other species. A long distance group migration or nomadic phase, described here for the first time for a spider, may have followed as a mechanism to cope with potential disadvantages of fission while selecting for strict synchronization of individual life cycle stages within the nests. It is shown, however, that, as in other cooperative spiders, A. binotatd% sex ratio is also highly female biased. The theoretical implications of biased sex ratios in a species with fissioning colonies are briefly discussed.     

Evaluation of malacosporean life cycles through transmission studies

Myxozoans, belonging to the recently described Class Malacosporea, parasitise freshwater bryozoans during at least part of their life cycle, but no complete malacosporean life cycle is known to date. One of the 2 described malacosporeans is Tetracapsuloides bryosalmonae, the causative agent of salmonid proliferative kidney disease. The other is Buddenbrockia plumatellae, so far only found in freshwater bryozoans. Our investigations evaluated malacosporean life cycles, focusing on transmission from fish to bryozoan and from bryozoan to bryozoan. We exposed bryozoans to possible infection from: stages of T. bryosalmonae in fish kidney and released in fish urine; spores of T. bryosalmonae that had developed in bryozoan hosts; and spores and sac stages of B. plumatellae that had developed in bryozoans. Infections were never observed by microscopic examination of post-exposure, cultured bryozoans and none were detected by PCR after culture. Our consistent negative results are compelling: trials incorporated a broad range of parasite stages and potential hosts, and failure of transmission across trials cannot be ascribed to low spore concentrations or immature infective stages. The absence of evidence for bryozoan to bryozoan transmissions for both malacosporeans strongly indicates that such transmission is precluded in malacosporean life cycles. Overall, our results imply that there may be another malacosporean host which remains unidentified, although transmission from fish to bryozoans requires further investigation. However, the highly clonal life history of freshwater bryozoans is likely to allow both long-term persistence and spread of infection within bryozoan populations, precluding the requirement for regular transmission from an alternate host.     

N‐P utilization of Acer mono leaves at different life history stages across altitudinal gradients

The relationship between plants and the environment is a core area of research in ecology. Owing to differences in plant sensitivity to the environment at different life history stages, the adaptive strategies of plants are a cumulative result of both their life history and environment. Previous research on plant adaptation strategies has focused on adult plants, neglecting saplings or seedlings, which are more sensitive to the environment and largely affect the growth strategy of subsequent life stages. We compared leaf N and P stoichiometric traits of the seedlings, saplings, and adult trees of Acer mono Maxim and different altitudes and found significant linear trends for both life history stages and altitude. Leaf N and P content by unit mass were greatly affected by environmental change, and the leaf N and P content by unit area varied greatly by life history stage. Acer mono leaf N‐P utilization showed a significant allometric growth trend in all life history stages and at low altitudes. The adult stage had higher N‐use efficiency than the seedling stage and exhibited an isometric growth trend at high altitudes. The N‐P utilization strategies of A. mono leaves are affected by changing environmental conditions, but their response is further dependent upon the life history stage of the plant. Thus, this study provides novel insights into the nutrient use strategies of A. mono and how they respond to the environmental temperature, soil moisture content along altitude and how these changes differ among different life history stages, which further provide the scientific basis for the study of plant nutrient utilization strategy on regional scale.     

Studies on the Life History of a Neogregarine Parasite Found in Leptothorax Ants from North America

Pupal stages of Leptothorax ants collected near West Yellowstone, MT, USA, displayed striking signs and symptoms of disease, i.e., grey to black coloration, irregular pigmentation of compound eyes and toothless mandibles. Light microscope studies revealed heavy infections by a neogregarine, the life history of which is described. The life cycle of the pathogen includes micronuclear and macronuclear schizogonies, gametogony and sporogony. Schizonts of both types vary in size depending on the number of nuclei which is usually defined by doubling, thus giving rise to 8, 16, 32, 64 or even 128 uninucleate merozoites. In smears and sections, micronuclear merozoites are typically arranged in rosettes. In the early transformation of zygotes, sickle-shaped developmental stages have been encountered, so far undescribed from neogregarines. Two spores (oocysts), each developing eight sporozoites, evolve from each gametocyst, as is typical of the genus Mattesia. Mature lemon-shaped spores measure 13.8 9.3 μm in fresh preparations. Infections can be readily transmitted to healthy colonies and to other Leptothorax species by feeding crushed infected pupae. Vegetative life cycle stages grow and multiply in the haemocoel, only to some extent they infect fat body cells. Macronuclear merozoites invade the hypodermis and the fat body but also settle extracellularly in the haemocoel. The disease process terminates with the death of the pupae that harbour abundant spores. Infections of adults have not been observed. Despite some minor differences that may result from development of the pathogen in this host, from the type, sequence and morphology of life cycle stages and from the signs and symptoms of disease, this Mattesia species is identified with M. geminata, first discovered in the tropical fire ant, Solenopsis geminata (Fabricius).     

A NEW CELL STAGE IN THE HAPLOID‐DIPLOID LIFE CYCLE OF THE COLONY‐FORMING HAPTOPHYTE PHAEOCYSTIS ANTARCTICA AND ITS ECOLOGICAL IMPLICATIONS1

Few members of the well‐studied marine phytoplankton taxa have such a complex and polymorphic life cycle as the genus Phaeocystis. However, despite the ecological and biogeochemical importance of Phaeocystis blooms, the life cycle of the major bloom‐forming species of this genus remains illusive and poorly resolved. At least six different life stages and up to 15 different functional components of the life cycle have been proposed. Our culture and field observations indicate that there is a previously unrecognized stage in the life cycle of P. antarctica G. Karst. This stage comprises nonmotile cells that range in size from ～4.2 to 9.8 μm in diameter and form aggregates in which interstitial spaces between cells are small or absent. The aggregates (hereafter called attached aggregates, AAs) adhere to available surfaces. In field samples, small AAs, surrounded by a colony skin, adopt an epiphytic lifestyle and adhere in most cases to setae or spines of diatoms. These AAs, either directly or via other life stages, produce the colonial life stage. Culture studies indicate that bloom‐forming, colonial stages release flagellates (microzoospores) that fuse and form AAs, which can proliferate on the bottom of culture vessels and can eventually reform free‐floating colonies. We propose that these AAs are a new stage in the life cycle of P. antarctica, which we believe to be the zygote, thus documenting sexual reproduction in this species for the first time.     

放射孢子虫在中国的首次发现

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拟衣藻属一新种——中华拟衣藻及其生活史的研究

报道了团藻目衣藻科拟衣藻属一新种。此种从中国科学院武汉植物研究所一浇园粪缸中采得,在分离室内单种培养过程中,对其形态学和生活史进行了研究。营养细胞具有多个盘状色素体,与拟衣藻属已知的种类有明显的差别。经培养观察,作者发现除细胞分裂、无性生殖外,还有同宗异配式有性生殖,在生活史各阶段该藻中绿体中均未见蛋白核,因此,拟衣藻作为分类单元是一个有效的属。     

Identification of amoebae implicated in the life cycle of Pfiesteria and Pfiesteria-like dinoflagellates

This study was undertaken to assess whether amoebae commonly found in mesohaline environments are in fact stages in the life cycles of Pfiesteria and Pfiesteria-like dinoflagellates. Primary isolations of amoebae and dinoflagellates were made from water and sediment samples from five tributaries of the Chesapeake Bay. Additional amoebae were also cloned from bioassay aquaria where fish mortality was attributed to Pfiesteria. Electron microscopy and small subunit (SSU) rRNA gene sequence analysis of these isolates clearly demonstrated that the commonly depicted amoeboid form of Pfiisteria is very likely a species of Korotnevella and is unrelated to Pfiesteria or Pfiesteria-like dinoflagellates. We have determined that the Pfiesteria and Pfiesteria-like dinoflagellates examined in this study undergo a typical homothallic life cycle without amoeboid stages. Furthermore, we have demonstrated that cloned amoebae sharing morphological characteristics described for stages in the life cycle of Pfiesteria do not transform into dinozoites. The strict clonal isolation and cultivation techniques used in this study substantially support the conclusion that the amoebae and some of the flagellates depicted in the life cycle of Pfiesteria are environmental contaminants of the Pfiesteria culture system and that the Ambush Predator Hypothesis needs to be rigorously reevaluated.