Single and combined effects of two trace elements (Cd and Cu) on the asexual reproduction of Aurelia sp. polyps

Aquatic Ecology - Jellyfish blooms are an increasingly common event in our seas. Occurring via polyps’ asexual reproduction induced by human stresses, they represent a hazard for ecosystems...     

The effects of X irradiation on the metamorphosis and budding of Aurelia aurita

With the aid of the Aurelia metamorphosis test system, the acute and subtle developmental and behavioral effects of X irradiation in the presence and absence of thyroxine on the Norfolk Aurelia aurita were described. Radiation doses were 0 (control), 50, 100, 150, 200, and 400 Gy. Morphology of the ephyrae, and statolith and rhopalia numbers were recorded using the light microscope. Developmental abnormalities of the polyps and ephyrae were recorded with the scanning electron microscope and light microscope. Major findings from this investigation were the absence of rhopalia and statoliths in ephyrae at 150 and 200 Gy, a reduction in pulses per minute in the ephyrae at 100, 150, and 200 Gy, a reduction in ephyrae released at 150, 200, and 400 Gy, and the development of polyp monsters. There was a significantly higher frequency of polyp monsters in the group exposed to thyroxine prior to radiation than in the thyroxine-free group prior to radiation.     

Indomethacin induction of metamorphosis from the asexual stage to sexual stage in the moon jellyfish, Aurelia aurita

We found while screening a chemical library that indomethacin, an inhibitor of prostaglandin biosynthesis, induced strobilation (metamorphosis from the asexual to sexual stage) in the moon jellyfish, Aurelia aurita. Indomethacin initiated strobilation in a dose-dependent manner, but was not involved in the progression of strobilation. Pharmacological experiments suggested that indomethacin could induce strobilation independently of prostaglandin biosynthesis.     

Food regulation of growth and maturation in a natural population of Aurelia aurita (L.)

Growth and maturity development of the moon jellyfish. Aureliaaurita, were recorded in Vgsbpollen, a small and semi-enclosedbay on the Norwegian west coast, and compared to those of medusaetransferred to excess food and starving conditions, respectively.Mesozooplankton were extremely scarce in Vgsbpollen. The abundanceand biomass of the medusae in the poll were higher than thosetypicallyfound in open waters, reaching a maximum of 22 ind.m^–3 and 710 mg C m^–3 in June. The average diameterof medusae in the p increased to 8 cm until the last part ofJune, with an instantaneous growth rate between 1.5 and 20%day^–1, thereafter retarding somewhat, giving a negativegrowth rate of up to 2.6% day^–1. Starving medusae showeda negative growth rate ofup to 13.4% day^–1, and all thernedusae were dead after 49 days. Well-fed medusae showed avery stable growth over a 56 day period, diverging from thepollpopulation from early June, and with a growth rate between3.8 and 9.8% day^–1. Medusae from the pollpopulation begancarrying planulae on their oral arms when at least 5 cm in diameter,whereas not even the largest medusa of 15.6 cm diameter amongthose in the well-fed group produced any planulae. For the firsttime, it is thus explicitly shown that thesize and maturityof A.aurita are externally controlled through food availability.Scarcity of food reduces the growth rate, but also changes theenergy allocation towards reproduction, which thus occurs ata smaller size than for well-fed rnedusae. Its plasticity makesit possible for this species to exploit environments with lowadvection of food and develop high abundance in such environments,without losing fecundity.     

Grazing by the jellyfish, Aurelia aurita, on microzooplankton

The medusa of the scyphozoan, Aurelia aurita, is a seasonallyimportant predator of copepods and fish larvae in coastal watersbut little is known about its grazing on microzooplanltton.Medusae preferentially remove large (     

Population dynamics of the scyphomedusa Aurelia aurita in Southampton Water

The population dynamics of the scyphomedusa Aurelia aurita inSouthampton Water is characterized. Strobilation, indicatedby the presence of 1 mm ephyrae, occurred from the end of Januaryto the middle of March. Maximum abundances of up to 8.71 m^–3occurred soon after ephyrae release, after which numbers declinedsteadily until the end of June, when the population was absentfrom Southampton Water. The residence time of 3–4 monthsis somewhat less than that reported in many other areas, includingKiel Bight and Gullmarfjord. The carbon biomass of A.auritaaccounted for 92–97% of the predominant gelatinous biomass(A.aurita, Pleurobrachia pileus and Phialidium hemisphericum)in the upper estuary, and this reached a maximum of 30.2 mgC m^–3 in May 1990 and 27.6 mg C m^–3 in June 1991.Coincident with increased water temperature and mesozooplanktonabundance during May, growth rates increased from 0.02–0.30mm day^–1 to a peak of 4.8 mm day^–1, with a maximumbell diameter of 120–140 mm reached in late May/earlyJune. Size to maturity was variable, although the smallest medusaobserved to be ‘ripe’, i.e. containing dividingeggs and planula larvae in the brood sacs on the oral arms,were 64–71 mm. Aurelia aurita is believed to be endemicto Southampton Water, but because of the double high water inthe area, short flushing rates of between 4.5 and 20 days maybe responsible for such short residence times of Aurelia medusae.The effects of strong NE winds were considered as factors governingthe distribution of medusae in years of atypical temporal abundance.     

Protein composition of mesoglea and mesogloeal cells of medusa Aurelia aurita

Protein composition of mesoglea of the scyphomedusa Aurelia aurita was revealed in SDS-PAGE. Some major bands are visible in mesoglea of a mature medusa: 30, 45-47, 85 kDa, three bands between 100-200 kDa, and several bands with molecular weights > 300 kDa. Polyclonal antisera RA45/47 against protein 45 kDa were raised. RA45/47 react with 45-47 kDa protein in mesogleal sample and protein 120 kDa in mesogleal cells on immunoblot. Immunohistochemical analysis of A. aurita histological sections of young and mature medusae showed antigen localization in mesogleal cell granules and in the apical part of ectodermal cells. In mature medusae, the antigen was localized also in elastic fibers. We can conclude that in A. aurita mesogleal cells, along with ectodermal cells, take part in the formation of extracellular matrix of mesoglea.     

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.     

Development time of planula larvae on the oral arms of the scyphomedusa Aurelia aurita

The development time from zygote to late stage of planula larvaeon the oral arms of Aurelia aurita was found to be 270 and 170h at 12 and 22°C, respectively. The mean ratio of the diameterof the long axis to the short axis in newly released planulaewas 2.27.     

In situ estimation of ephyrae liberated from polyps of Aurelia aurita using settling plates in Tokyo Bay, Japan

The continuous changes in the number of newly established polyps of Aurelia aurita (L.) on settling plates under natural conditions were observed from August 1998 to September 1999 in Tokyo Bay, Japan. A sharp decline in survivorship of newly settled polyps was observed within the first few days, however, survivorship of polyps settled in October increased by budding up to 399% after two months. The number of discs in each strobila varied from 1 to 6, however, most of the strobilae formed single discs. The percentage ratios of the total number of ephyrae to the initial number of polyps on settling plates were generally lower than 10%, but the highest ratio of 594.4% was estimated for the polyps settled in October. It is considered that most of the liberated ephyrae originate from the polyps settled in October in Tokyo Bay. This study suggests that the occurrence of ripe medusae with planula larvae throughout the year contributes to the success of settlement and growth of the polyp stage in Tokyo Bay.     

Constraints on the evolution of asexual reproduction

Sexual reproduction is almost ubiquitous among multicellular organisms even though it entails severe fitness costs. To resolve this apparent paradox, an extensive body of research has been devoted to identifying the selective advantages of recombination that counteract these costs. Yet, how easy is it to make the transition to asexual reproduction once sexual reproduction has been established for a long time? The present review approaches this question by considering factors that impede the evolution of parthenogenesis in animals. Most importantly, eggs need a diploid chromosome set in most species in order to develop normally. Next, eggs may need to be activated by sperm, and sperm may also contribute centrioles and other paternal factors to the zygote. Depending on how diploidy is achieved mechanistically, further problems may arise in offspring that stem from 'inbreeding depression' or inappropriate sex determination systems. Finally, genomic imprinting is another well-known barrier to the evolution of asexuality in mammals. Studies on species with occasional, deficient parthenogenesis indicate that the relative importance of these constraints may vary widely. The intimate evolutionary relations between haplodiploidy and parthenogenesis as well as implications for the clade selection hypothesis of the maintenance of sexual reproduction are also discussed.     

Effects of low dissolved oxygen on survival and asexual reproduction of scyphozoan polyps (Chrysaora quinquecirrha)

Hypoxic conditions are common in many coastal environments such as Chesapeake Bay. While medusae appear to be quite tolerant of low dissolved oxygen (DO) concentrations, the effects of hypoxia on the benthic polyp stages are unknown. Chrysaora quinquecirrha (DeSor) polyps, and were subjected to 5 DO treatments (air-saturated [control], 3.5, 2.5, 1.5 and 0.5 mg l^–1) in the laboratory. Polyp survival and development were documented over 24 d. Virtually no mortality occurred in any treatment during the first 5 d. Total polyp mortality after 24 d was 59.3% at the lowest DO concentration, whereas <3% mortality was observed in the air-saturated treatment. Formation of stolons and strobilae occurred in all treatments, however, the proportions of polyps undergoing stolonation and strobilation were significantly greater in all DO concentrations above 0.5 mg l^–1. Polyp encystment was not observed in any treatment over the course of the 24 d experiment. These results indicate that polyps can survive and asexually propagate even during prolonged exposure to hypoxic conditions.     

Population dynamics of Aurelia aurita (Scyphozoa) from an isolated brackish lake, with particular reference to sexual reproduction

The annual cycle of abundance, growth and sexual reproductionof the scyphomedusa Aurelia aurita was examined over a 12 monthperiod in an isolated, shallow, brackish, man-made body of water:Horsea Lake, England. Strobilation started in December and ephyraewere present through June in varying numbers, suggesting a 7month period of near-continuous recruitment. Horsea Lake hasa dense A.aurita population, with the peak abundance of 24.9m^–3 occurring in mid-May. Medusae (>10 mm) were presentin the water column from March through January. Maximum belldiameter of 105 mm was observed in late September. However,medusa growth was very poor (G ranged between –0.03 and0.07 day^–1 over a 12 month period), and monthly mean belldiameters were typically <50 mm. For most of the year, theabundant A.aurita population was most likely severely food limitedas a result of a numerically and species-poor mesozooplanktoncommunity dominated by the calanoid copepods Acartia margalefiand Acartia tonsa. Nevertheless, the very small A.aurita medusaewere still able to attain sexual maturity and reproduce. Ripefemale medusae carrying fertilized eggs and planula larvae werefirst observed in May and June, although the main period ofplanula larva production was September-December. In November,all females were ripe, the smallest being 19–20 mm belldiameter. At both Horsea Lake and a nearby productive estuary,Southampton Water, planula larva production increased linearlywith wet weight, although compared with the larger A.auritamedusae from Southampton Water, reproductive output at HorseaLake was low. Aurelia aurita in Horsea Lake showed plasticityin its population characteristics in response to environmentalconditions, with both fecundity and size to maturity varyingon a seasonal basis. Medusae appeared to partition the availablefood resources into either somatic growth when food was abundantor reproductive effort when food was scarce.     

Size-based Prey Selectivity and Dietary Shifts in the Jellyfish, Aurelia aurita

Gut content analyses on field-caught Aurelia aurita showed bothquantitative and qualitative change in diet as a function ofmedusa size. Larger medusae tended towards greater numbersand diversity of prey (up to 1550 individual prey representingas many as 13 different prey groups). We also found that medusasize was a good predictor of prey diversity recovered from themedusa gut. While a shift toward greater prey diversity inlarger medusae might be explained by increased contact rateswith 'rare' prey taxa, we also found size-based prey selectivitychanges in A. aurita. We used in situ gut content data to describeselectivity by A. aurita for three prey types representing varyingdegrees of swimming or escape velocity. Fish eggs were usedas a non-swiming prey, and small (     

Food and feeding of Aurelia aurita in Tokyo Bay with an analysis of stomach contents and a measurement of digestion times

In situ seasonal variations in stomach contents of Aurelia aurita (L.) in Tokyo Bay, Japan, were analyzed. Copepods, such as Oithona davisae Ferrari & Orsi were the predominant food items of A. aurita from June to November. The mean digestion time measured in incubation experiments was 0.95 h. Daily rations calculated using stomach content data and digestion times were 2.2–21.8 mg C ind^–1 corresponding to 0.58–5.56% of body carbon. The ingestion rate increased significantly with an increase in medusa size, although no significant relationship was found between medusa size and carbon specific daily ration. The zooplankton community in Tokyo Bay is characterized by the significant dominance of O. davisae and it is assumed that the prosperity of A. aurita is caused by the high abundance of the O. davisae population. It is suggested that a food chain comprised of microflagellates, cyclopoid copepods O. davisae, and A. aurita is the most significant one in Tokyo Bay and only a small portion of production is transferred to fish.