Life cycle of the rhizostome jellyfish <Emphasis Type="Italic">Rhizostoma octopus</Emphasis> (L.) (Scyphozoa,Rhizostomeae), with studies on cnidocysts and statoliths

Stages in the life cycle of the rhizostome jellyfish Rhizostoma octopus (L.) were reared in the laboratory from planula to young medusa and are described here. Fertilization of eggs was external, and planulae, 110–150 μm in length, appeared after 2 days. These settled and developed into the scyphistoma stage. Scyphistomae reached a maximum size of 2.3 mm, bore up to 24 tentacles, and had a large manubrium. Polyps reproduced asexually mainly by podocysts. Strobilation was induced by temperature change. Each strobila released up to five ephyrae that measured 2.7–5.8 mm in diameter at liberation. During transformation from newly released ephyra to young medusa, velar lappets appeared and increased in number, the manubrium developed eight branched oral arms with epaulettes, and a marginal gastric network arose. Only one cnidocyst type, the “a”-atrichous haploneme, was present in the planula. In addition to these haplonemes, heterotrichous microbasic euryteles were observed in polyps, ephyrae, and medusae. Statoliths, located in the rhopalia, had a characteristic compact shape. These sensory structures increased in number and size with the growth of ephyrae and medusae.     

Life cycle ofRhopilema nomadica: a new immigrant scyphomedusan in the Mediterranean

Rhopilema nomadica is an Indopacific scyphomedusan, which has migrated into the eastern Mediterranean in recent years. Large aggregations of the medusae were recorded in Haifa Bay, Israel, reaching 5.5×10⁵ medusae per square nautical mile during summer 1989. The life cycle ofR. nomadica from planula to young medusa is described. Fertilization is external and planulae are formed within a few hours at 20°C. After settlement, polyps were fed withArtemia sp. nauplii and developed into polydisc strobilae within 45 d. The strobilation process was completed within 7 d, and the liberated ephyrae developed into young medusae within 2 mo. Asexual reproduction occurred mainly via podocyst formation. The population explosion ofR. nomadica could be attributed to its high reproductive potential.     

A comparative ecological study on the scyphozoans Aurelia aurita,Cyanea capillata and C. lamarckii in the Gullmar Fjord,western Sweden, 1982 to 1986

During the years 1982 to 1986, the life cycles and population dynamics of three scyphozoans, Aurelia aurita (L.), Cyanea capillata (L.) and C. lamarckii (Person and Lesueur), were studied in the Gullmar Fjord on the Swedish west coast. The settling of planulae, strobilation of scyphistomae and release of ephyrae were followed on ceramic settling plates in the laboratory and in the field. Weekly to bi-weekly hauls with Bongo nets were used to study the abundance of ephyrae and medusae. The results show great differences in the life cycles and ecology of the three species. A. aurita utilizes the best season for scyphistoma growth (August to September) and strobilates during the highest zooplankton abundance in October. C. capillata strobilates during the spring (March to May), and the abundance of C. capillata medusae is more dependent on immigration from the North Sea than A. aurita. C. lamarckii does not reproduce at all in the Gullmar Fjord and is totally dependent on immigration from the North Sea. The possibility of interspecific competition between A. aurita and C. capillata is discussed. A preliminary experiment showed that scyphistomae of A. aurita eat planula larvae of C. capillata during the autumn.     

Carbon metabolism and strobilation in Cassiopea andromedea (Cnidaria: Scyphozoa): Significance of endosymbiotic dinoflagellates

Scyphopolyps and scyphomedusae of Cassiopea andromeda Forskål (Cnidaria, Scyphozoa) containing dinoflagellate endosymbionts (zooxanthellae) were investigated for rates and pathways of carbon fixation. Photosynthesis by the algae, accounting for 80 and 15 mol C h^-1 on a dry weight basis in medusae and polyps, respectively, by far exceeds dark incorporation of inorganic carbon by the intact association. Photosynthetic carbon fixation is operated via C₃ pathway of carbon reduction. DCMU-treatment (1×10^-6 M and 1×10^-5 M) completely inhibits light-dependent carbon assimilation. Major photosynthates presumably involved in a metabolite flow from algal symbionts to animal tissue are glycerol and glucose. A total of 5–10% net algal photosynthate appears to be seleased in vivo to the host. This is probably less than the energy supply ultimately required for the nutrition of the polyps and medusae. The presence of zooxanthellae proved to be indispensable for strobilation in the scyphopolyps. However, photosynthesis by algal symbionts as well as photosynthate release is obviously not essential for the initiation of ephyrae as is shown by DCMU-treatment, culture in continous darkness, and aposymbiotic controls. It is therefore concluded that strobilation is supported, but not triggered by algal photosynthetic activity. The induction of strobilation thus seems to depend on a more complex system of regulation.     

Life cycle of the jellyfish <Emphasis Type="Italic">Lychnorhiza lucerna</Emphasis> (Scyphozoa: Rhizostomeae)

The life cycle of Lychnorhiza lucerna (Scyphozoa: Rhizostomeae) and the settlement preferences of its larvae were studied using laboratory-based rearing experiments. Mature medusae of L. lucerna were collected from the beach of the Río de la Plata estuary, Argentina. This species displayed the typical metagenetic, (i.e. medusoid and polypoid), life cycle reported for other rhizostomes. The fertilized eggs developed into motile and short lived planulae. The majority of planulae settled on the air-water interface (p < 0.001). Of those that settled on the settlement plates provided, no significant differences were observed between styrene slides, glass slides and shells of the bivalve Mactra isabelleana (p > 0.05). No planulae settled on stones. Several hours after planulae settled, they metamorphosed into sessile four-tentacled scyphistomae. Most scyphistomae attached onto the air-water interface. At 19–22°C, the scyphistomae grew up to 22 tentacles and reached 1,500 μm height. The scyphistomae increased their numbers by means of formation of podocysts from which new polyps emerged and strobilated. Strobilation occurred 46 days after settlement. Only polydisk strobilation was observed and each strobila always produced three ephyrae. After releasing ephyrae, strobilae returned to normal scyphistomae and were capable of repeating strobilation. A single founder polyp was estimated to produce up to 60 ephyrae over 4 months. Ephyrae developed into metephyrae 15 days after release at 19–22°C. In this paper we describe the morphological and some behavioural features of L. lucerna in the polypoid and early medusoid stages.     

Laboratory observations on the life history of Rhopilema verrilli (Scyphozoa: Rhizostomeae)

The life history of the scyphozoan Rhopilema verrilli is described from the planula to the young medusa stages. Planulae are retained within the gonadal tissue of the medusa until fully developed. On liberation, most planulae set and developed into small scyphistomae within 7 to 10 days. The scyphistoma differs from those of other described species in having an unusually large, clavate manubrium. The only means of asexual reproduction observed in the scyphistoma cultures involved the formation of podocysts. Strobilation was usually of the monodisc variety, although polydics strobilation was not infrequent. The process of strobilation was completed within 7 days at 20°C. Newly liberated ephyrae typically had 8 pairs of lappets, and 8 rhopalia. Ephyral development resembled that of the closely related rhizostome Rhizostoma pulmo. The cnidome of the planula and scyphistoma consisted of atrichous isorhizas (a atrichs) and microbasic heterotrichous euryteles, while that of the strobila and ephyra consisted of a atrichs, euryteles, and holotrichous haplonemesContribution No. 546 from the Virginia Institute of Marine Science, Gloucester Point, Virginia 23062, USA.     

Derivation of the reduced life cycle of <Emphasis Type="Italic">Thecoscyphus zibrowii</Emphasis> Werner, 1984 (Cnidaria,Scyphozoa)

The species Thecoscyphus zibrowii Werner, 1984 has an exceptional life cycle, which lacks a medusa stage but develops an extraordinary structure (egg sac) for reproduction. Investigation of the life cycle, as well as anatomical and histological studies of the different developmental stages of T. zibrowii were performed to provide evidence for a possible homology of the egg sac with the medusa stage and to determine whether the reduced metagenesis of T. zibrowii is derived from strobilation. The egg sac showed several characteristics, which were compared to those of coronate medusae. The ectodermis of the egg sac had a plate-like appearance and was completely ciliated as is typical for coronate medusae. The number and the location of the gonads were similar to those of coronate medusae. The cnidocysts were significantly larger in the egg sac than in the polyp. A size difference of cnidocysts in the medusa and the polyp stage is known for several Coronatae. Characteristics of egg sac formation were compared to characteristics of strobilation. The formation of the early operculum was similar in T. zibrowii and N. eumedusoides. The constriction of egg sac and strobila occurred in the same mode and the gastric cavities of two egg sacs stayed in contact in a similar fashion to the gastric cavities of the strobila discs. The developmental zones of cnidoblasts of the egg sac and polyp were separated during the formation of the egg sac which showed a similar developmental gradient to a strobila. The existence of all of these consistent characteristics makes it very likely that the egg sac structure was homologous to a medusa. The species T. zibrowii would therefore be derived from a metagenetic ancestor. This species has reduced the medusa generation to the greatest extent within the Nausithoidae and has demonstrated thus far the endpoint of a regressive evolution of the medusa generation.     

Significance of food type for growth of ephyrae Aurelia aurita (Scyphozoa)

We studied growth of newly released Aurelia aurita ephyra larvae fed five different food types, including a large-sized copepod, a phytoflagellate, and suspended POM (particulate organic matter) made from bivalve meat. Experiments were run at saturated food concentration in two different temperatures over 10 days. The effect of small differences in temperature was inconsistent and interacted with the effect of food type, which, in turn, was highly significant. A low average growth rate (4-9% day^-1) was shown when feeding on the large-sized copepod Calanus finmarchicus (80 µg AFDW individual^-1), in spite of an extremely high daily ration of up to 1500% of body AFDW. When feeding on the cryptophyte Rhodomonas baltica (ca. 8 µm cell diameter), the ephyrae showed an average growth rate over the 10 day experiment of 7-11%, but with a considerably higher growth rate during the first days. Suspended POM generated an average growth rate of 7-9% day^-1, whereas fresh bivalve meat, manually placed into the stomach of the ephyra, gave an average growth rate of 12-14% day^-1. Artemia nauplii (ca. 3 µg AFDW individual^-1), used as a general reference, resulted in higher growth rates than any of the other food types (17-31% day^-1). We conclude that A. aurita ephyrae can capture and feed on phytoplankton, large copepods, and POM; that phytoplankton might be of nutritive significance early in development; and that the high quantity of large-sized copepods ingested is inefficiently converted to growth during early development. POM is a potential food source because of the ability of the ephyrae to encounter and ingest it, although concentration, size distribution, and nutritional composition of natural POM probably constrain its effect on growth.     

Morphology and development of benthic and pelagic life stages of North Sea jellyfish (Scyphozoa, Cnidaria) with special emphasis on the identification of ephyra stages

Jellyfish blooms or invasions could be detected in an early phase of development if the youngest medusa stages (ephyrae) and their early growth stages (post-ephyrae) were identifiable in plankton samples but a useful identification key for ephyrae in early growth stages is lacking for most species. In the present study, the identification characteristics of adult North Sea scyphomedusae (Aurelia aurita, Cyanea capillata, Cyanea lamarckii, Chrysaora hysoscella, Rhizostoma octopus) collected around the island of Helgoland (German Bight) in July?CAugust 2003 and 2004 are described. Planula larvae were measured and reared to polyps in the laboratory. The process of ephyrae development asexually produced by the polyps (strobilation) was photo-documented. Photographs of the ephyrae growth stages were combined with drawings of features useful for the species identification. The provided identification key allows discrimination among post-ephyrae from plankton samples, probably leading to conclusions on the development of jellyfish blooms and their causes.     

Comparison of the statolith structures of <Emphasis Type="Italic">Chironex fleckeri</Emphasis> (Cnidaria,Cubozoa) and <Emphasis Type="Italic">Periphylla periphylla</Emphasis> (Cnidaria,Scyphozoa): a phylogenetic approach

The rhopalia and statocysts of Periphylla periphylla (Péron and Lesueur in Ann Mus Hist Nat Marseille 14:316–366,1809) and Chironex fleckeri Southcott (Aust J Mar Freshw Res 7(2):254–280 1956) were examined histologically and showed several homologous characteristics. Differences in sensory area distribution could be connected to a slightly different functionality of equilibrium sensing. In P. periphylla, the statoliths (crystals) grow independently of each other; whereas in C. fleckeri, one large crystal covers the smaller ones. The structures of both statoliths were examined in detail with single-crystal diffraction, microtomography and diffraction contrast tomography. The single compact statolith of C. fleckeri consisted of bassanite as was previously known only for other rhopaliophoran medusae. An origin area with several small oligocrystals was located in the centre of the cubozoan statolith. The origin areas and the accretion of statoliths are similar in both species. Our results lead to the assumption that the single bassanite statolith of C. fleckeri (Cnidaria, Cubozoa) is a progression of the scyphozoan multiplex statolith. It is therefore suggested that the Cubozoa are derived from a scyphozoan ancestor and are a highly developed taxa within the Rhopaliophora.     

Rate-temperature responses in scyphozoan medusae and polyps

The effects of temperature on oxygen consumption and spontaneous rhythmic activity have been investigated in various stages of the life histories of 3 species of jellyfish from the Chesapeake Bay, USA. All 3 species clearly show the ability to acclimate positively to temperature change. Thermal sensitivity of metabolism in the winter medusa Cyanea capillata fulva is fairly low at temperature intervals which are experienced in nature. Polyps of the two summer medusae, Chrysaora quinquecirrha and Aurelia aurita, show reduced metabolic sensitivity at temperatures normally accompanying high developmental activity and the onset of strobilation.     

Nucleic acid and protein levels in strobilating polyps of Chrysaora quinquecirrha and Aurelia aurita

Levels of DNA, RNA, and protein were measured in scyphistomae of the scyphozoans Aurelia aurita and Chrysaora quinquecirrha during strobilation. In synchronously developing populations of A. aurita, the amount of DNA per polyp increases 41 to 260% during strobilation, whereas RNA and protein remain relatively constant. The RNA/DNA ratio drops by about 50% during strobilation in both C. quinquecirrha and A. aurita, and protein/DNA decreases by 50% in A. aurita. Specific RNA reserves are probably not accumulated in advance of strobilation, since strobilation is blocked immediately in both species by 1 to 3 g/ml actinomycin D. The size and DNA content of polyps are usually increased by prolonged incubation at temperatures of 12° to 15°C, which facilitates strobilation; however, the RNA/DNA and protein/DNA ratios of such polyps are not significantly increased by the cold conditioning.Contribution No. 472 from the Virginia Institute of Marine Science.     

Strobilation,budding and initiation of scyphistoma morphogenesis in the rhizostome Cassiopea andromeda (Cnidaria: Scyphozoa)

Scyphistomae of Cassiopea andromeda Forskål, 1775 containing symbiontic zooxanthellae did not develop medusae at a constant temperature of 20°C, but monodisc strobilation was initiated after transfer of the polyps to 24°C. After release of the ephyrae and regeneration of the hypostome and tentacular region, the recovered polyps either produced vegetative buds or entered a new strobilation phase. Formation of motile, planula-like buds was not found to be indicative of unfavourable environmental conditions. Intensity of budding was positively correlated with available food and with increase of temperature. Budding was negatively correlated with the number of polyps maintained per dish and with the conditioning of the sea water. Under optimal feeding and temperature conditions, polyps could simultaneously produce chains of buds at 2 to 4 budding regions. Settlement and development of buds into scyphistomae was suppressed in pasteurized sea water and in pasteurized sea water containing antibiotics, but polyps developed from buds in the presence of algal material taken from the aquarium, debris or egg shells of Artemia salina, or on glass slides which had been incubated in used A. salina culture medium. Several species of marine bacteria were detected after staining these slides. One, a Gramnegative coccoid rod, which was identified as a nonpathogenic Vibrio species, was isolated, cultivated as a pure strain, and was proved to induce the development of C. andromeda buds into polyps. Millipore filter-plates coated with Vibrio sp. cells grown in suspension culture were ineffectual, but diluted filtrate initiated polyp morphogenesis. The inducing factor is obviously not a constituent of the bacterial cell surface, but is a product of growing Vibrio sp. cells released into the medium. This product was found to be relatively heat-stable and dialyzable. As to the basic mechanism involved in the induction of polyp formation, it is suggested that the inducing factor (s) acts bimodally by inducing pedal disc development and by eliminating a head inhibitor originating from the basal end of the bud. The life history, and various aspects of medusa-formation and of vegetative reproduction in scyphozoans are reviewed and discussed with particular reference to rhizostome species. Special attention has been paid to some reports of larval metamorphosis controlled by marine bacteria.     

Prey selection by the scyphomedusan predator Aurelia aurita

We describe feeding behavior of Aurelia aurita (Linnaeus) using gut content analyses of field-collected specimens and a mesocosm experiment. The field studies were conducted in Narragansett Bay, Rhode Island, USA from March to April 1988, and the mesocosm studies were done at the Marine Ecosystems Research Laboratory at the University of Rhode Island. Patterns of prey selection changed with medusa diameter. Smaller medusae (12 mm diameter) consumed mostly hydromedusan prey whereas larger medusae (up to 30 mm diameter) ingested greater numbers of copepod prey. While larger medusae did feed on copepods, their diet also contained more barnacle nauplii and hydromedusae than expected from the relative abundances of these prey types in plankton samples. A marginal flow mechanism of feeding by A. aurita provided an explanation for the patterns of prey selection we observed in medusae of different sizes and among widely divergent prey types. Our data indicated that large prey, with escape speeds slower than the marginal flow velocities around the bell margins of A. aurita, made up a substantial fraction of the daily ration when they were available. Such prey species may be more important to nutrition than the more abundant copepods and microzooplankton. Successful development of young medusae may depend upon an adequate supply of slowly escaping prey.     

Seasonal variations in the densities of fecal pellets produced by Oikopleura vanhoeffeni (C. Larvacea) and Calanus finmarchicus (C. Copepoda)

Two abundant macrozooplankters, Oikopleura vanhoeffeni (Lohmann) and Calanus finmarchicus (Gunnerus) were collected from the coastal waters off Newfoundland in different seasons during 1990–1991 and incubated in natural seawater to collect freshly egested, field produced, fecal pellets. The densities of fecal pellets from O. vanhoeffeni and C. finmarchicus were measured in an isosmotic density gradient. These are the first reported seasonal measurements of fecal pellet densities from two different types of macrozooplankters, O. vanhoeffeni, a larvacean, filter feeder and C. finmarchicus, a crustacean, suspension feeder. Pellet density ranges and medians were significantly different among seasons for both species, depending primarily on the type of phytoplankton ingested and its ability to be compacted. Winter O. vanhoeffeni and fall C. finmarchicus feces filled with nanoplankters and soft bodied organisms had less open space [packing index (% open area) = 3.5 and 4% for O. vanhoeffeni and C. finmarchicus, respectively] and were more dense (1.23 and 1.19 g cm^-3) than spring feces filled with diatoms (packing index = 15 and 23%, density = 1.13 and 1.11 gcm^-3). For copepods, these results contrast with previously published density values and with the predicted copepod fecal pellet density calculated, in the present study, using the conventional mass/volume relationship. Copepod spring and summer diatom-filled feces had a calculated density of 1.12 and 1.24 gcm^-3 vs a measured median density of 1.11 gcm^-3 for both spring and summer feces; the fall feces containing nanoplankters had a calculated density of 1.08 gcm^-3 vs a measured median density of 1.19 gcm^-3. Knowledge of the seasonal variations in fecal pellet densities is important for the development of flux models.     

The effect of light on strobilation in the Chesapeake Bay Sea Nettle Chrysaora quinquecirrha

Previous work (Loeb, 1972) showed that strobílation could be induced in Chrysaora quinquecirrha (Desor) by subjecting polyps to a period of chilling followed by warming. It is shown here, that the onset of strobilation and the rate at which this process occurs in a population of C. quinquecirrha polyps is positively related to the amount of light received during chilling and in the period following warming. The absence of light during either period delays the onset of strobilation. The intensity of coloration of C. quinquecirrha polyps before strobilation appears to be correlated with the amount of light to which they have been exposed during chilling.     

Seasonal development of scyphozoan medusae and the predatory impact of Aurelia aurita on the zooplankton community in the Bornholm Basin (central Baltic Sea)

The annual cycle of abundance and distribution of the scyphozoan medusae Aurelia aurita and Cyanea capillata was studied in the Bornholm Basin (central Baltic Sea) in 2002. Seasonal changes in prey composition and predatory impact were investigated by analyzing stomach contents. A. aurita occurred from July to November, with a maximum mean abundance of 2.3 ind. per 100 m³ in August, whereas C. capillata was caught in much smaller numbers from July to September. No ephyrae of either species were found; therefore, advection of medusae from the western Baltic Sea is assumed. From July to October, ~80% of A. aurita medusae was distributed in the upper 20 m above the thermocline, whereas C. capillata occurred only in the halocline below 45 m. A. aurita did not migrate vertically and fed mainly on the most abundant cladoceran species Bosmina coregoni maritima. Further prey organisms were the cladocerans Evadne nordmanni and Podon spp., mollusk larvae and copepods. Copepod nauplii and copepodite stages I–III were not eaten by the medusae, neither were fish eggs and larvae used as prey. Based on mean medusa and zooplankton abundance from the upper 20 m, the predatory impact was very low. In August, when mean abundance of A. aurita was highest, only 0.1% of the copepod and 0.5% of the cladoceran standing stock were eaten per day. However, in regions with higher medusa or lower zooplankton abundance, up to 7.9% of the cladoceran standing stock was consumed per day. Hence, A. aurita did not regulate the zooplankton community in the Bornholm Basin, and fish larvae did not suffer from competition with and predation by the medusae.Communicated by O. Kinne, Oldendorf/Luhe     

An individual-based numerical model of medusa swimming behavior

Scyphomedusae are ubiquitous in marine and estuarine systems, where they frequently play an important role in trophodynamics. Many scyphomedusae are cruising predators, and feeding rates depend, in part, on swimming behavior. Yet, no model of medusa swimming exists. An individual-based correlated random walk (CRW) model of medusa swimming behavior in three dimensions was developed. The model was validated using a previously published dataset of the swimming of 19 Chrysaora quinquecirrha (Desor, 1848) medusae that were observed in the presence or absence of zooplankton prey in laboratory mesocosms in August–October 1998 (Matanoski et al. in Mar Biol 139:191–200, 2001). In the presence of prey, medusae swam at a constant moderate rate in looping trajectories. In the absence of prey, medusae alternated periods of slow and fast swimming in more linear trajectories. In the model, looping trajectories were reproduced only when changes in movement by a medusa were oriented to its current position and orientation; more linear trajectories were reproduced by movement oriented to a fixed framework. This suggests that medusae change from swimming behavior oriented to local stimuli (e.g., contact with prey) to long-range stimuli (e.g., gravity) depending on the availability of prey. The model reproduced cyclical changes in swimming speeds by medusae in the absence of prey by simulating switching in the behavior controlling the strength of swimming bell pulsations using a probabilistic function. Model results also demonstrated that medusae tend to swim toward the surface, avoid contact with the bottom, increase time spent in prey patches if they alter swimming patterns in the presence of prey, and exhibit significant periodicities in swimming patterns that are the result of deterministic behavior. The model will permit the simulation of the complex behavior of medusae.     

Quantitative feeding ecology of the hydromedusan Nemopsis bachei in Chesapeake Bay

We determined feeding rates of the hydromedusan Nemopsis bachei L. Agassiz in the mesohaline region of Chesapeake Bay, USA during the spring of 1989 and 1990 from gut contents, digestion rates and abundances of medusae and zooplankton. The medusae consumed primarily copepodites of Acartia tonsa, selecting against naupliar stages. The peak abundance of N. bachei medusae was in April to May, when densities averaged more than 10 m^-3. Medusa densities were similar in both years, but were greatest (maximum of 132 medusae m^-3) along a southern transect sampled only in 1990. At peak densities, N. bachei medusae consumed 30% d^-1 of the copepodite standing stocks, but they consumed <1% d^-1 at the lower densities typical of late May or early June. The predation effects were generally greater than those reported for other hydromedusan species. But even at peak predation, N. bachei medusae could not have controlled or reduced A. tonsa copepod populations, which had a production rate of 85% d^-1 at that time. Medusa feeding rates were highest at nighttime, and were correlated with prey density in the field, but not in the laboratory.Communicated by J. Grassle, New Brunswick     

Bioenergetics of ephyra larvae of the scyphozoan jellyfish Aurelia aurita in relation to temperature and salinity

The body mass of Aurelia aurita ephyrae was better correlated with the diameter of the central disc than with the distance between opposite rhopaliae or distance between opposite lappet tips. Body dry weight (y, in μg) related to the disc diameter (x, in mm) through the equation y = 22.33 x ^1.99. The exponent 1.99 was significantly lower than that for the medusa stage, indicating a tendency to grow in diameter rather than in weight through the ephyra stage. The average ash-free dry weight (AFDW) of ephyrae was 38.0% of the dry weight. The AFDW/diameter relationship was used to convert measured diameters to body AFDW and calculate succession in body mass, daily ration, daily growth rate and gross growth efficiency. Effects of temperature (6, 9.5, 12, 15 and 18 °C) and salinity (17.5, 22, 26, 30.5 and 35 PSU) on these parameters and feeding were studied at saturated prey concentration (222 Artemia nauplii l⁻¹ initial concentration) by daily measurements over 10 d. There was a strong effect of temperature for total ingestion, growth rate, growth efficiency and final body mass of individual ephyrae, whereas the daily ration was not significantly different between the different temperatures. The experimental group kept at the highest temperature (18 °C) diverged the most, and ephyrae at this temperature ingested 2.7 times more and increased in weight 5.4 times more than at 6 °C. The average daily growth rate and gross growth efficiency of these ephyrae were 34.5% and 25.1%, respectively, significantly higher than at 6, 9.5 and 15 °C. Significant effects of salinity were shown for total ingestion, daily ration, daily growth rate and final weight, although only total ingestion and daily ration diverged sufficiently to show effects in a post-hoc test. This test showed that total ingestion was significantly different for all salinities except between 22 and 35 PSU and between 17.5 and 26 PSU. The daily ration for 35 PSU diverged from all other salinities, whereas none of the other salinities showed any significant differences. Thus, provided food in excess A. aurita can double its weight every 2 to 4 d, dependent on temperature and can therefore develop to the medusa stage in short time. Differences in environmental salinity in the range 17.5 to 35 PSU have little or no effect on growth rate and growth efficiency, whereas our results indicate that the full seawater salinity (35 PSU) causes significantly higher ingestion rate compared to lower salinities. Received: 11 January 1999 / Accepted: 11 May 1999