nanos expression at the embryonic posterior pole and the medusa phase in the hydrozoan Podocoryne carnea

Summary The distinction between soma and germline is an important process in the development of animals with sexual reproduction. It is regulated by a number of germline-specific genes, most of which appear conserved in evolution and therefore can be used to study the formation of the germline in diverged animal groups. Here we report the isolation of two orthologs of one such gene, nanos (nos), in the cnidarian Podocoryne carnea, a species with representative zoological features among the hydrozoans. By studying nos gene expression throughout the Podocoryne biphasic life cycle, we find that the germline differentiates exclusively during medusa development, whereas the polyp does not contribute to the process. An early widespread nos expression in developing medusae progressively refines into a mainly germline-specific pattern at terminal stages of medusa formation. Thus, the distinction between germline and soma is a late event in hydrozoan development. Also, we show that the formation of the medusa is a de novo process that relies on active local cell proliferation and differentiation of novel cell and tissue types not present in the polyp, including nos-expressing cells. Finally, we find nos expression at the posterior pole of Podocoryne developing embryos, not related to germline formation. This second aspect of nos expression is also found in Drosophila, where nos functions as a posterior determinant essential for the formation of the fly abdomen. This raises the possibility that nos embryonic expression could play a role in establishing axial polarity in cnidarians.     

Cell adhesion to extracellular matrix is different in marine hydrozoans compared with vertebrates

Extracellular matrices (ECMs) of phylogenetically very distant organisms were tested for their ability to support cell adhesion, spreading and DNA replication in reciprocal xenograft adhesion tests. Mechanically dissociated cells of the medusa Podocoryne carnea (Cnidaria, Hydrozoa) were seeded on ECMs of polyps and medusa, and on several ECM glycoproteins or entire ECMs from vertebrates. In reciprocal experiments, cells from different vertebrate cell-lines were seeded on ECMs of polyps, medusae and also on electrophoresed and blotted extracts of both types of ECMs. The results demonstrate that medusa cells adhere and spread on polyp and medusa ECMs but do not recognize vertebrate ECMs or purified ECM glycoproteins. Vertebrate cells in contrast adhere, spread and proliferate on ECMs of polyps and medusae. The number of attached cells depends on the cell type, the type of ECM and, in certain cases, on the stage of the cell cycle. Cell adhesion experiments with pretreated ECMs of polyps and medusae, e.g. oxidation of carbohydrate residues with sodium-metaperiodate, or blocking of certain carbohydrate moieties with the lectin wheat germ agglutinin or a carbohydrate-specific monoclonal antibody, demonstrate that ECM carbohydrates are more important for cell-ECM interactions of medusa cells than for vertebrate cells. Furthermore, the experiments indicate that polyp and medusa ECMs contain different components which strongly modulate adhesion, spreading and DNA replication of vertebrate cells.     

Polypengeneration und Entwicklungsgeschichte vonEucheilota maculata (Thecata-Leptomedusae)

Polyps and medusae differ in regard to habitats, evolution, and morphological structures. In order to replace the former taxonomic systems which deal with polyp and medusa generations separately, by a single valid classification including both generations, knowledge of all essential life history phases is necessary. Modern methods of culturing marine hydroids are outlined briefly. Successful culturing provides the means to link formerly unidentified polyps or medusae with one another. The present paper is concerned with the hydroidEucheilota maculata Hartlaub, the medusa of which is common in the southern North Sea. The polyps formerly unknown have been reared from fertilized eggs of the medusae. They were raised to full size, formed colonies, and produced gonangia and medusae. Thus the morphology of the single polyp, the polyp colony, and of the young medusa could be investigated in detail. The nematocyst equipment of the two generations and of all developmental stages is described as well as the number of chromosomes. The systematic position of the genusEucheilota is discussed and the diagnosis of the speciesE. maculata, including the two generations, given.     

Molecular characterization of aspartylglucosaminidase,a lysosomal hydrolase upregulated during strobilation in the moon jellyfish,Aurelia aurita

The life cycle of the moon jellyfish, Aurelia aurita, alternates between a benthic asexual polyp stage and a planktonic sexual medusa (jellyfish) stage. Transition from polyp to medusa is called strobilation. To investigate the molecular mechanisms of strobilation, we screened for genes that are upregulated during strobilation using the differential display method and we identified aspartylglucosaminidase (AGA), which encodes a lysosomal hydrolase. Similar to AGAs from other species, Aurelia AGA possessed an N-terminal signal peptide and potential N-glycosylation sites. The genomic region of Aurelia AGA was approximately 9.8 kb in length and contained 12 exons and 11 introns. Quantitative RT-PCR analysis revealed that AGA expression increased during strobilation, and was then decreased in medusae. To inhibit AGA function, we administered the lysosomal acidification inhibitors, chloroquine or bafilomycin A1, to animals during strobilation. Both inhibitors disturbed medusa morphogenesis at the oral end, suggesting involvement of lysosomal hydrolases in strobilation.     

Telomerase activity is not related to life history stage in the jellyfish Cassiopea sp.

The polyp (scyphistoma) of the jellyfish Cassiopea sp. can be maintained in culture for a long time, as polyps repeatedly reproduce asexually via formation of vegetative buds or propagules. The medusa, which is the sexually reproducing stage, typically has a relatively short life span. As a first step to understand the difference in life spans of the polyp and medusa stages of Cassiopea sp., we measured telomerase activity in different life cycle stages. We found telomerase activity in tissues of aposymbiotic polyps and propagules and symbiotic ephyrae (newly budded medusae) and adult medusae. No significant difference in telomerase activity was found between polyps and the bell region of the medusae. The cloned elongation products of the stretch PCR contained the TTAGGG repeats suggesting that the jellyfish has the ‘vertebrate’ telomere motif (TTAGGG)_n. This is the first study to show that somatic tissues of both polyp and medusa stages of a cnidarian had telomerase activity. Telomerase activity in somatic tissues may be related to the presence of multipotent interstitial cells and high regenerative capacity of cnidarians.     

Polypengeneration und Entwicklung vonEutonina indicans (Thecata-Leptomedusae)

The medusaEutonina indicans (Romanes 1876) represents a circumpolar northern boreal species. In the European seas it has its southern limits of distribution in the southern North Sea, where it is common during late spring and early summer. The present paper is concerned with the formerly unknown polyp generation. It was possible to rear polyps from fertilized medusa eggs to full size; they formed colonies and produced gonangia and young medusae. Thus, morphology and development of the single polyp, colony, and young medusa could be described in detail. The systematic position ofEutonina indicans is discussed briefly, and a diagnosis of the species, including the two generations, given.     

Life Cycle Reversal in Aurelia sp.1 (Cnidaria,Scyphozoa)

The genus Aurelia is one of the major contributors to jellyfish blooms in coastal waters, possibly due in part to hydroclimatic and anthropogenic causes, as well as their highly adaptive reproductive traits. Despite the wide plasticity of cnidarian life cycles, especially those recognized in certain Hydroza species, the known modifications of Aurelia life history were mostly restricted to its polyp stage. In this study, we document the formation of polyps directly from the ectoderm of degenerating juvenile medusae, cell masses from medusa tissue fragments, and subumbrella of living medusae. This is the first evidence for back-transformation of sexually mature medusae into polyps in Aurelia sp.1. The resulting reconstruction of the schematic life cycle of Aurelia reveals the underestimated potential of life cycle reversal in scyphozoan medusae, with possible implications for biological and ecological studies.     

EVOLUTION OF LIFE CYCLE,COLONY MORPHOLOGY,AND HOST SPECIFICITY IN THE FAMILY HYDRACTINIIDAE (HYDROZOA,CNIDARIA)

Biased transitions are common throughout the tree of life. The class hydrozoa is no exception, having lost the feeding medusa stage at least 70 times. The family hydractiniidae includes one lineage with pelagic medusae (Podocoryna) and several without (e.g., Hydractinia). The benthic colony stage also varies widely in host specificity and in colony form. The five‐gene phylogeny presented here requires multiple transitions between character states for medusae, host specificity, and colony phenotype. Significant phylogenetic correlations exist between medusoid form, colony morphology, and host specificity. Species with nonfeeding medusae are usually specialized on a single host type, and reticulate colonies are correlated with nonmotile hosts. The history of feeding medusae is less certain. Podocoryna is nested within five lineages lacking medusae. This requires either repeated losses of medusae, or the remarkable re‐evolution of a feeding medusa after at least 150 million years. Traditional ancestral reconstruction favors medusa regain, but a likelihood framework testing biased transitions cannot distinguish between multiple losses versus regain. A hypothesis of multiple losses of feeding medusae requires transient selection pressure favoring such a loss. Populations of species with feeding medusae are always locally rare and lack of feeding medusae does not result in restricted species distribution around the world.     

Fish assemblage structure in urban streams of Puerto Rico: the importance of reach- and catchment-scale abiotic factors

Cotylorhiza tuberculata is a common symbiotic scyphozoan in the Mediterranean Sea. The medusae occur in extremely high abundances in enclosed coastal areas in the Mediterranean Sea. Previous laboratory experiments identified thermal control on its early life stages as the driver of medusa blooms. In the present study, new ecological aspects were tested in laboratory experiments that support the pelagic population success of this zooxanthellate jellyfish. We hypothesized that planulae larvae would have no settlement preference among substrates and that temperature would affect ephyra development, ingestion rates and daily ration. The polyp budding rate and the onset of symbiosis with zooxanthellae also were investigated. Transmission electron microscopy revealed that zooxanthella infection occurred by the polyp stage. Our results showing no substrate selectivity by planulae and high polyp budding rates in high temperatures suggest increased benthic polyp populations, which would lead to higher medusa abundances. Rates of transition from ephyrae to medusae and the feeding of early medusa stages also increased with temperature. Continuing changes in coastal ecosystems such as future climate warming and marine construction may lead to increased populations of jellyfish to the detriment of fish globally.     

Phylogeny of Medusozoa and the evolution of cnidarian life cycles

To investigate the evolution of cnidarian life cycles, data from the small subunit of the ribosome are used to derive a phylogenetic hypothesis for Medusozoa. These data indicate that Cnidaria is monophyletic and composed of Anthozoa and Medusozoa. While Cubozoa and Hydrozoa are well supported clades, Scyphozoa appears to be paraphyletic. Stauromedusae is possibly the sister group of either Cubozoa or all other medusozoans. The phylogenetic results suggest that: the polyp probably preceded the medusa in the evolution of Cnidaria; within Hydrozoa, medusa development involving the entocodon is ancestral; within Trachylina, the polyp was lost and subsequently regained in the parasitic narcomedusans; within Siphonophorae, the float originated prior to swimming bells; stauromedusans are not likely to be descended from ancestors that produced medusae by strobilation; and cubozoan polyps are simplified from those of their ancestors, which possessed polyps with gastric septa and four mesogleal muscle bands and peristomial pits.     

Morphological and ultrastructural analysis of Turritopsis nutricula during life cycle reversal

The hydrozoa life cycle is characterized, in normal conditions, by the alternation of a post-larval benthic polyp and an adult pelagic medusa; however, some species of Hydrozoa react to environmental stress by reverting their life cycle: i.e. an adult medusa goes back to the juvenile stage of polyp. This very uncommon life cycle could be considered as some sort of inverted metamorphosis. A morphological study of different stages during the reverted life cycle of Turritopsis nutricula led to the characterization of four different stages: healthy medusa, unhealthy medusa, four-leaf clover and cyst. The ultrastructural study of the cellular modifications (during the life cycle reversion of T. nutricula) showed the presence of both degenerative and apoptotic processes. Degeneration was prevalent during the unhealthy medusa and four-leaf clover stages, while the apoptotic rate was higher during the healthy medusa and cyst stages. The significant presence of degenerative and apoptotic processes could be related to the occurrence of a sort of metamorphosis when an adult medusa transforms itself into a polyp.     

A newly discovered oxidant defence system and its involvement in the development of Aurelia aurita (Scyphozoa, Cnidaria): reactive oxygen species and elemental iodine control medusa formation

In Aurelia aurita, applied iodine induces medusa formation (strobilation). This process also occurs when the temperature is lowered. This was found to increase oxidative stress resulting in an increased production of iodine from iodide. One polyp produces several medusae (initially termed ephyrae) starting at the polyp's oral end. The spreading of strobilation down the body column is controlled by a feedback loop: ephyra anlagen decrease the tyrosine content in adjacent polyp tissue by producing melanin from tyrosine. Endogenous tyrosine is able to remove iodine by forming iodiferous tyrosine compounds. The reduced level of tyrosine causes the ephyra-polyp-border to move towards the basal end of the former polyp. We argue that an oxidant defence system may exist which makes use of iodide and tyrosine. Like other marine invertebrates, polyps of Aurelia contain iodide ions. Inevitably produced peroxides oxidise iodide into iodine. The danger to be harmed by iodine is strongly decreased by endogenous tyrosine which reacts with iodine to form iodiferous tyrosine compounds including thyroxin. Both substances together, iodide and tyrosine, form an efficient oxidant defence system which shields the tissue against damage by reactive oxygen species. In the course of evolution (from a species at the basis of the animal kingdom like Aurelia to a highly evolved species like man) the waste product thyroxin (indicating a high metabolic rate) has developed into a hormone which controls the metabolic rate.     

Synchronized release of medusae from three species of hydrozoan fire corals

 The release of medusae from three hydrozoan fire corals, Millepora dichotoma, M. murrayi and M. platyphylla, was investigated at three sites in southern Taiwan from February 1994 to July 1995. All three species were gonochoristic, and developed and released several batches of medusae between April and May. The duration of open ampulla appearing on the surface of coralla was short, about three months, and could be used to infer the reproductive season of the fire corals between April and May. No obvious lunar cycles of medusa release were found in these species. Medusa release started before dark at approximately 17:00 h and continued for several hours. Males began releasing medusae earlier than females. Synchronization of medusa release between colonies, i.e., the probability of occurring on the same nights, was significantly higher within a species than between different species. Hybridization in nature among the three species is, therefore, unlikely due to segregation in the spawning dates. Moreover, the synchronization within each species was often significantly higher within versus between sites. The free-swimming medusae released gametes within approximately one hour, and the spent medusae lived for a few more hours. Medusae may facilitate fertilization rates as a result of an apparently negatively geotactic swimming response that results in medusa aggregation at the surface. No differences in the sizes of medusae, eggs and sperm were detected among the three species; however, some characteristic differences of medusa nematocysts were found. Accepted: 25 September 1997     

Cnidarians as a model system for understanding evolution and regeneration

Hydra and Podocolyne are two cnidarian animals which provide complementary advantages for analysing developmental mechanisms possibly reflecting the basic developmental processes shared by most bilaterians. Interestingly, these mechanisms remain accessible all along the life of these animals, which bud and regenerate, whatever their age. The Hydra polyp permits a direct study of the molecular cascades linking amputation to regeneration. Podocoryne displays a complete life cycle, polyp and medusa stages with a fast and inducible sexual cycle and an unparalleled In vitro transdifferentiation potential. In both cases, a large number of evolutionarily conserved molecular markers are available, and analysis of their regulation highlights the molecular mechanisms which underly pattern formation in these two species.     

Bau und Lebensgeschichte des Polypen vonTripedalia cystophora (Cubozoa,class. nov., Carybdeidae) und seine Bedeutung für die Evolution der Cnidaria

FollowingHaeckel (1880), most zoologists have grouped the Cubomedusae with the class Scyphozoa. However, the actual systematic position and evolution of the Cubomedusae remained unclear because essential phenomena of the life cycle, i. e. life history and structure of the polyp generation and the process of medusa formation were unknown. Successful cultivation of the Carribean larviparousTripedalia cystophora Conant, 1898 elucidated for the first time the complete life cycle of a cubomedusa. Primary polyps could be raised from planulae which were transferred by air mail from La Parguera, Puerto Rico. The sessile polyp is solitary. Its morphology, anatomy, and behaviour are described. The body (length 0.6–1.0 mm) is radially constructed without any trace of tetramerous structures. 6 to 11 solid capitate tentacles insert in one circle, above which the body ends in a long contractile snout-like mouth cone (proboscis). The body is sac-like without gastric septa or gastric pockets; its base is enveloped by a small cup of thin, structureless periderm. Asexual reproduction by which the stock is enlarged quickly envolves lateral budding of small secondary polyps. After detachment these small polyps go through a creeping phase. The fully grown polyp shows a remarkable behavioural plasticity as it can migrate and change into an inactive encysted stage. The whole polyp metamorphoses into a single medusa. All externally visible metamorphosis phases are described. First, the polyp's body becomes tetramerous due to 4 longitudinal folds. The tentacles congregate into 4 groups, each in one quadrant. While the distal parts of the tentacles are resorbed, their bases develop into 4 perradial sensory organs (rhopalia). Interradially, 4 new tentacles are formed and become the primary tentacles of the medusa. Simultaneously, the complete body of the polyp transforms into the bell of the medusa. At the end of the metamorphosis which takes 5 to 6 days at 25 to 27° C, the young medusa begins to pulsate quickly and swims away leaving behind the empty peridermal cup. The morphology of the young medusa is described.T. cystophora has a tricnidom of basitrich haplonemes, holotrich haplonemes, and heterotrich microbasic euryteles. The ecology of both, polyp and medusa generation, is briefly outlined. A critical comparison between the polyp and medusa ofT. cystophora and the Scyphozoa and Hydrozoa reveals important differences. Consequently, a new class, Cubozoa, must be established and given the evolutionary position between Scyphozoa and Hydrozoa. Diagnoses are presented for the polyp ofT. cystophora and the class Cubozoa.     

Induction of segmentation in polyps of Aurelia aurita (Scyphozoa, Cnidaria) into medusae and formation of mirror-image medusa anlagen

Polyps of Aurelia aurita can transform into several medusae (jellyfish) in a process of sequential subdivision. During this transformation, two processes take place which are well known to play a key role in the formation of various higher metazoa: segmentation and metamorphosis. In order to compare these processes in bilaterians and cnidarians we studied the control and the kinetics of these processes in Aurelia aurita. Segmentation and metamorphosis visibly start at the polyp's head and proceed down the body column but do not reach the basal disc. The small piece of polyp which remains will develop into a new polyp. The commitment to the medusa stage moves down the body column and precedes the visible onset of segmentation by about one day. Segmentation and metamorphosis can start at the cut surface of transversely cut body columns, leading to a mirror-image pattern of sequentially developing medusae.     

Larval necrophilia: the odd life cycle of a pandeid hydrozoan in the Weddell Sea shelf

Colonies of an athecate hydroid were found at six stations in the high Antarctic (Weddell Sea) growing on dead specimens of Flabelligera mundata (Annelida, Polychaeta). All living specimens of F. mundata at the same stations were free of epibionts. Transplantation experiments showed that hydropolyps did not produce stolons on substrates other than the epidermal jelly coat and chetae of dead F. mundata specimens. The largest colonies (>1,000 polyps) producing medusa buds were cultured until medusa liberation: growth of medusae was then surveyed for the next 5 weeks, but development of adult features was extremely slow. Young medusae were ascribed to the suborder Pandeida by the presence of two main characters, namely (1) hollow marginal tentacles, and (2) a mouth with four simple lips. Considering polyp and young medusa features, this species is acknowledged as newly recorded for the Southern Ocean, and assigned to the genus Neoturris (Hydroidomedusae, Pandeidae).     

Heat dissociation and maceration of marine Cnidaria

Summary The effect of increased temperature on the tissue integrity of polyps and medusae ofPodocoryne carnea is described. Animals exposed for 10 to 20 min to a temperature of 35°C are easily dissociated into single cells. These dissociated cells round up, form reaggregates and, depending on their origin, regenerate polyp or medusa structures. However, as the exposure time is increased, the dissociated cells gradually lose the ability to reaggregate or to regenerate defined structures. At incubation times exceeding 50 min, the tissue separates into single cells which retain their normalin vivo shapes but which do not form reaggregates. These are termed macerated cells. The ultrastructure and protein profile of macerated cells demonstrate no major changes from those of untreated cells. Both the dissociation and maceration methods are applicable to other cnidarian species for developmental, histological and biochemical studies.