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.     

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.     

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.     

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.     

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.     

RNA:DNA ratios and growth of herring (Clupea harengus) larvae reared in mesocosms

Autumn-spawned North Sea herring larvae (Clupea harengus L.) were released in two outdoor mesocosms of 2500 m³ (A) and 4000 m³ (B). The mesocosms were monitored for temperature, salinity, oxygen, chlorophyll a, zooplankton and herring larvae abundance. The density of suitable prey for first feeding larvae (mainly copepod nauplii) was initially low in Mesocosm A (<0.11^-1) compared to in Mesocosm B (>11^-1). Half-way through the experiment the situation was reversed, with higher densities of prey in Mesocosm A (>31^-1) as compared to Mesocosm B (11^-1). The average temperature declined steadily in both mesocosms from 18°C at release to 11–12°C by the end of the experiment 60 d later. The RNA:DNA values of individual herring larvae were related to protein growth rates and temperature adjusted according to Buckley (1984). A corresponding DNA growth index (Gdi) was given as: Gdi=0.68 TEMP+3.05 RNA:DNA-9.92. The RNA:DNA based growth indices were significantly correlated with other somatic growth estimates. The average estimated protein growth rate in the two mesocosms followed the same temporal pattern as the somatic growth rate, but with a lag of 2 d or more. Residual analysis of the regression of ln RNA versus ln DNA also showed the same temporal pattern as the RNA:DNA ratios, but the shift in condition as estimated by this method occurred more in synchrony with the other somatic growth measures. Larvae in Mesocosm A had RNA:DNA values similar to the starvation control kept in the laboratory the first days after release, confirming that larvae in Mesocosm A initially were in poor nutritional condition. On the other hand, the majority of the herring from Mesocosm B were characterised as starving or in poor nutritional condition towards the end of the experiment. The assessment of growth and nutritional condition were in accordance with independent survival estimates which suggested that the majority of the total mortality occurred during the first 15 d in Mesocosm A and there-after in Mesocosm B.     

Ammonium excretion by gelationous zooplankton and their contribution to the ammonium requirements of microplankton in Chesapeake Bay

Ammonium excretion rates of recently collected specimens of gelatinous zooplankton, the scyphomedusan Chrysaora quinquecirrha DeSor and the etenophore Mnemiopsis leidyi A. Agassiz, were correlated with body mass and water temperature in measurements made from April to October 1989 and 1990. Rates ranged between 3.5 and 5.0 g atoms NH ₄ ⁺ -N (g dry wt)^-1h^-1 for C. quinquecirrha and 3.0 to 4.9 g atoms NH ₄ ⁺ -N (g dry wt)^-1h^-1 for M. leidyi. Excretion rate equations and in situ data on the size distributions and biomasses of gelatinous zooplankters and water temperature were used to estimate the contribution of ammonium by medusae and ctenophores to mesohaline Chesapeake Bay waters on several dates during April to October 1989 and 1990. We then compared the estimated contributions to direct measurements of ¹⁵NH ₄ ⁺ uptake by microplankton. The maximum estimated regeneration by gelatinous zooplankton was 5.8 g atoms NH ₄ ⁺ -N m^-3h^-1 at night in August 1990, when medusae biomass was greatest. This represents about 4% of the ammonium required by the microplankton. During the daytime on all dates, less than 1% of the ammonium required by microplanktion was supplied by gelatinous zooplankton. Therefore, gelatinous zooplankton appear to play a minor role in the ammonium cycle of Chesapeake Bay.     

RNA:DNA ratio during the critical period and early larval growth of the red drum Sciaenops ocellatus

Eggs from two separate spawning stocks of the red drum Sciaenops ocellatus (Linnaeus) were hatched, and the larvae were reared in the laboratory for 2 wk under closely controlled conditions. Total RNA, DNA, and soluble protein were measured in each population daily in triplicate pooled samples of larvae from each of three tanks. Growth rate in mm d^-1 was determined for each population at 2 d intervals. Growth rate explained 72 and 95% of the variation in the RNA:DNA ratios of the two populations individually, and 86% of the variation in the RNA:DNA ratio when data from the two populations were combined. The RNA:DNA ratio appeared to be most effective as an indicator of growth in rapidly growing larvae, and to lose some resolution when growth was intermittent. The rates of deposition of RNA, DNA, and protein into tissue were all highly correlated with growth rate and with each other. Mean population RNA:DNA ratios of red drum yolk-sac larvae decreased from Day 1 post-hatch until larvae initiated successful feeding behavior, and then increased steadily throghout the remainder of the experimental period. This pattern of change in the RNA:DNA ratios during the yolk-sac stage appears to be an intrinsic developmental pattern of red drum ontogeny. The lowest values for the RNA:DNA ratio were observed just prior to the initiation of feeding or during the critical period, indicating that red drum larvae experience a decrease in capacity for protein synthesis as they initiate feeding. Intrinsic variation in the RNA:DNA ratio during development suggests that caution be used when comparing the RNA:DNA ratios of yolk-sac larvae to a critical ratio calculated from Buckley's general model.     

Grazing of Acartia hudsonica (A. clausi) on Skeletonema costatum in Narragansett Bay (USA): Influence of food concentration and temperature

Grazing experiments were performed with temperatureacclimated Acartia hudsonica fed the diatom Skeletonema costatum in concentrations ranging from 50 to 3×10⁴ cell ml^-1 at 5°, 10° and 15°C. The ingestion data were best fit by an Ivlev equation. Feeding threshold values of 39 and 59 cells ml^-1 were not significantly different from zero; however, filtration rates were depressed at low food concentrations. Maximum filtration rates increased exponentially with temperature, reaching a maximum with copepods collected at 14°–15°C, and then declining. Both the increase in ingestion rate with increasing food concentration and the maximum ingestion rate were significantly greater as experimental temperature was increased. Maximum ingestion rates were reached at concentrations greater than 6×10³ cells ml^-1. Percent of body carbon ingested per day at 5 g C L^-1 increased from 1.5% at 5°C to 6.7% at 15°C. At 500 g C L^-1, the ingestion increased from 84% (5°C) to 660% (15°C). Percent of body nitrogen at 0.5 g N L^-1 increased from 0.6% per day at 5°C to 2.5% per day at 15°C. At 50 g N L^-1, the ingestion was 42% body nitrogen at 5°C and 250% at 15°C. The influence of grazing by A. hudsonica on phytoplankton in Narragansett Bay, USA was estimated for 1972–1977. The percent of standing stock removed by grazing rarely exceeded 5% per day except during the late spring when S. costatum growth becomes nutrient limited and higher temperatures favor the rapid population growth of A. hudsonica.     

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.     

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.     

Effects of temperature,salinity, and predators on mortality of and colonization by the invasive hydrozoan<Emphasis Type="Italic"> Moerisia lyonsi</Emphasis>

The successful invasion of non-indigeneous species depends on initial colonization as well as establishing a self-maintaining population. The invasive hydrozoan Moerisia lyonsi (Boulenger, 1908), possibly originating from low-salinity waters in the Black Sea and Middle East regions, has become established in low-salinity waters in several estuaries of North America, including Chesapeake Bay. The effects of temperature and salinity on mortality of M. lyonsi polyps were examined in the laboratory in February 2001 in the presence of abundant food. The polyps of M. lyonsi were directly transferred from 20°C and 10 salinity to one of 45 combinations of temperature (10–29°C) and salinity (1–40). Polyp mortality within 7 days occurred only in low-temperature treatments with salinities of 35–40. Surviving polyps reproduced asexually in salinities of 1–40 at 20–29°C, and in salinities of 1–25 at 15°C, but not in any salinities at 10°C. The greatest asexual reproduction rates, an index for population survival potential, occurred at salinities of 5–20. Survival and reproduction of M. lyonsi over such broad temperature and salinity ranges indicate that M. lyonsi may colonize and establish populations throughout the Chesapeake Bay; however, M. lyonsi medusae were reported only at salinities <9.3 there. This discrepancy may be due to the effects of predators. The scyphomedusan Chrysaora quinquecirrha (Desor, 1848), but not the ctenophore Mnemiopsis leidyi (A. Agassiz, 1865) consumed M. lyonsi medusae in laboratory experiments in August–September 2001. Populations of M. lyonsi do not appear to be limited by temperature and salinity conditions; however, their distribution in Chesapeake Bay may be restricted to low salinities not inhabited by predators.Communicated by J.P. Grassle, New Brunswick     

The common jellyfish Aurelia aurita: standing stock,excretion and nutrient regeneration in the Kiel Bight,Western Baltic

The population dynamics, ammonia and inorganic phosphate excretion, and nutrient regeneration of the common jellyfish Aurelia aurita was investigated from 1982 to 1984 in the Kiel Bight, western Baltic Sea. During summer 1982, medusae abundance ranged between 14 and 23 individuals 100 m^-3, biomass was estimated at about 5 g C 100 m^-3 and the mean final diameter of individuals was 22 cm. Abundance, based on numbers, in 1983 and 1984 was an order of magnitude lower; biomass was less than 2 g C 100 m^-3 and jellyfish grew to 30 cm. During the summers of 1983 and 1984, A. aurita biomass constituted roughly 40% of that of the total zooplankton>200 m. In 1982, for which zooplankton data were lacking, it was assumed that medusae biomass was greater than that of all other zooplankton groups. Total ammonia excretion ranged between 6.5 and 36 mol h^-1 individual^-1, whereas inorganic phosphate release was 1.4 to 5.7 mol h^-1 individual^-1. Allometric equations were calculated and exponents of 0.93 for NH₄–N release and 0.87 for PO₄–P excretion were determined. Nitrogen and phosphorus turnover rates were 5.4 and 14.6% d^-1, respectively. In 1982, the medusae population released 1 100 mol NH₄–N m^-2 d^-1, about 11% of the nitrogen requirements of the phytoplankton. The inorganic phosphate excretion (150 mol m^-2 d^-1) sustained 23% of the nutrient demands of the primary producers. In the other two years the nutrient cycling of the medusae was much less important, and satisfied only 3 to 6% of the nutrient demands. It is suggested that in some years A. aurita is the second most important source of regenerated nutrients in Kiel Bight, next to sediment.     

Feeding rates of the jellyfish Aurelia aurita on fish larvae

We quantified feeding rates of field caught Aurelia aurita feeding on yolk sac cod (Gadus morhua) larvae in a series of incubation experiments. A short-time (~1 h) functional response experiment with a wide range of prey concentrations (0.5–16 prey l⁻¹, initial concentration) revealed that ingestion rates increased linearly over this range, such that clearance rates were similar between the different prey concentrations. This suggests that A. aurita is capable of efficiently utilizing dense prey patches. This indication was further supported by a linear increase of prey captured by A. aurita during 2.5 h of feeding at extremely high prey concentration (>200 prey l⁻¹). Clearance rate in darkness scaled with jellyfish diameter to a power of ~1.7 for jellyfish 3.9–9.5 cm in diameter. The jellyfish did not alter their umbrella pulse frequency in response to presence of fish larvae. There were no significant differences between A. aurita feeding rates in light and darkness for yolk sac prey ages 0–7 days (at 7.5°C). Although prey vision and escape abilities of fish may develop rapidly during early larval ontogeny, these factors apparently have little impact on interactions with predators such as A. aurita during the yolk sac stage.     

Study by evolution of nucleic acid content of prepuberal growth in the shrimp Crangon vulgaris

Growth of the shrimp Crangon vulgaris was studied by following the evolution of its nucleic acid concentration and total content. Deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) analysis were effected on homogenates of whole shrimps. Cell multiplication was estimated from evolution of total DNA content, and cell size increment from evolution of fresh weight: DNA ratio. DNA puric bases ratio and RNA monoribonucleotides percentages were constant throughout the investigation period. A decrease in DNA concentration was observed from 50 to 20 M/g dry defatted weight (DDP), when fresh weight increases from 40 to 570 mg. This decrease was more marked in the first half of the period studied (prepuberal phase). The DNA content in the whole shrimp increases with fresh weight without slowing down at sexual maturity. However, at the beginning of the prepuberal phase the cell-multiplication rate seems to be graduated rather than continuous; this is still to be explained. Cell size, calculated from fresh weight: DNA ratio, increases until the shrimp weighs 300 mg; beyond this weight, cell increment proceeds much more slowly. The weight gain of shrimps throughout the growth period studied is mainly attributable to hyperplasia — which occurs constantly — while hypertrophy insures only 21% weight increment in the largest shrimps. As protein content, RNA content is a linear function of shrimp weight. RNA:DNA ratio evolution is similar to that of cell size and protein content. We suggest that cells have attained a physiological balance when shrimps reach a weight of 300 mg.     

Mantle protein excretion and calcification in the hardshell clam Mercenaria mercenaria. II. Protein synthesis and excretion by the isolated mantle

Sheets of mantle tissue from above the mantle line of Mercenaria mercenaria were incubated for 2, 6 and 20 h at 20°C in 50 Ci ³H-glycine in 50 ml artificial seawater. Incorporation of tritium into soluble proteins excreted by the mantle and into tissue proteins was followed. The excretion of soluble protein continued throughout the experiment; the proportion of incorporated label excreted reached 17% by 20 h. The initiation of excretion of labelled protein seemed to lag 60 to 70 min behind the initiation of protein synthesis. Protein synthesis by the mantle contributed to proteins of the extrapallium and mantle chambers and, thus, may be involved in synthesis and regulation of proteins involved in the shell-formation process.     

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.     

Combined effects of temperature and salinity on fed and starved larvae of the mediterranean mussel Mytilus galloprovincialis and the Japanese oyster Crassostrea gigas

The combined effects of temperature, salinity and nutrition on survival and growth of larvae of the Mediterranean mussel Mytilus galloprovincialis and the Japanese oyster Crassostrea gigas were studied over a period of 7 d in the laboratory. Ripe adults, collected in spring and summer 1987 from natural populations in the Bay of Arcachon, France, were induced to spawn. Larvae of both species were cultured at four temperatures (15°, 20°, 25° and 30°C), four salinities (20, 25, 30 and 35S) per temperature, and two levels of nutrition (fed and unfed) per temperature/salinity combination. The fed larvae received a mixed algal diet of 50 cells each of Isochrysis galbana and Chaetoceros calcitrans forma pumilum per microlitre. In both bivalve species, larvae survived over a wide range of temperature and salinity, with the exception of mussel larvae, which died at 30°C. Statistical analysis indicated that nutrition had the greatest effect on larval development, explaining 64 to 75% of the variance in growth of M. galloprovincialis and 54 to 70% in growth of Crassostrea gigas. Unfed mussel larvae displayed little growth. Compared with temperature, the effect of salinity was very slight. M. galloprovincialis larvae exhibited best growth at 20°C and 35S and C. gigas at 30°C and 30S.     

Routine oxygen consumption of Mugil cephalus,Liza dumerili and L. richardsoni at Different temperatures and salinities

Oxygen consumption studies were undertaken with 3 mullet species to determine b, the exponent of w, as well as a, as indices of metabolic rate in the equation M=aw ^bwhere M=metabolic rate, a=the intensity of metabolism, W=body weight, and b=the exponent of w. This was done under 5 experimental temperatures (13°, 18°, 23°, 28°, 33°C) for Mugil cephalus and Liza dumerili at 1 and at 35 S, and for L. richardsoni at 35S only. Mean b values were approximately 0.85. The a values depended on temperature, and increased according to Van't Hoff's law except for L. dumerili (1 S) and L. richardsoni (35 S) for a temperature increase from 23° to 28°C. It was found that handling had a profound influence on metabolic rate and led to considerably increased consumption rates during the first 8 h after introduction into the respiration chambers. Fasting in L. dumerili resulted in a total drop of 27% in oxygen consumption over a period of 6 days, of which 10% occurred over the first 24 h. Oxygen consumption displayed diurnal rhythms during the 6 day period, with lowest consumption rates at midday and midnight and highest just after sunrise and sunset.     

Invading <Emphasis Type="Italic">Aurelia aurita</Emphasis> has established scyphistoma populations in the Caspian Sea

The Caspian Sea has no endemic Scyphozoa. In 1999, a mass accumulation of Aurelia medusae was recorded, indicating that sometime earlier, jellyfish had invaded the basin, but since then no scyphozoans have been reported in the Caspian. In the fall of 2008, we found scyphistomae (scyphoid polyps) during a cruise to the eastern Middle Caspian. The scyphistomae were numerous (100–10,000 ind. m⁻²) and occupied a depth range of 30–73 m. Genetic data (18S rDNA, ITS-1 and COI) showed that the scyphistomae belonged to the species A. aurita. The current genetic data set is insufficient to determine the source region(s) of the invasive A. aurita. It remains unclear why no moon jellies have been recorded in the Caspian in the last 10 years. Because swarming scyphomedusae are often pests, the presence of scyphistomae should be considered as a warning of a possible outbreak of A. aurita medusae in the Caspian.