Journal of Oceanology and Limnology

, Volume 36, Issue 6, pp 2216–2230 | Cite as

Carbon distribution strategy of Aurelia coerulea polyps in the strobilation process in relation to temperature and food supply

  • Nan Wang (王楠)
  • Chaolun Li (李超伦)Email author
  • Yantao Wang (王彦涛)
  • Song Feng (冯颂)


Mass occurrences of moon jellyfish have been observed in coastal waters. Strobilation directly determines the initial population size of adult jellyfish, but energy distribution during the strobilation process is not well understood. In this study, strobilation was induced in polyp of Aurelia coerulea by elevating temperature. The different stages in the strobilation process, including polyp budding, strobilation and body growth, were investigated at six temperature levels (8, 10, 13, 15, 17 and 19°C) and five food supply levels (0, 30, 60, 100 and 150 μg C/L). The results showed that the duration of strobilation preparation stage (SP) remarkably decreased with increasing temperature. Food level positively affected the production of buds and ephyrae and the body growth of parent polyps. Of the six temperatures tested, 13°C was optimal for strobilation. At 13°C, strobilation activity was enhanced, and this treatment resulted in the greatest energy distribution, highest ephyrae production and longest duration of strobilation stage (SS). Polyps tended to allocate 6.58%–20.49% carbon to buds with sufficient food supply regardless of temperature. The body growth of parent polyps was highest at lower temperatures and higher food levels. This study is the first to provide information on carbon-based energy distribution strategy in the polyp strobilation process. We concluded that budding reproduction is a lower-risk strategy for A. coerulea polyps to increase populations. Even during strobilation season, polyps prioritize budding, but at the optimal strobilation temperature, polyps utilize a portion of the energy stored for budding to release ephyrae. The body carbon content of parent polyps may be considered as strategic energy reserves, which could help to support budding activities and strobilation during harsh conditions.


Aurelia coerulea temperature food supply carbon distribution strategy strobilation 


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We thank Ms. ZHANG Zhenghua for caring for the polyps. We are grateful to WANG Shiwei and WANG Pengpeng for help with sampling A. coerulea medusae. Editing services were provided by Wiley editing services.


  1. Bakun A, Weeks S J. 2006. Adverse feedback sequences in exploited marine systems: are deliberate interruptive actions warranted? Fish & Fisheries, 7 (4): 316–333.CrossRefGoogle Scholar
  2. Båmstedt U, Lane J, Martinussen M B. 1999. Bioenergetics of ephyra larvae of the scyphozoan jellyfish Aurelia aurita in relation to temperature and salinity. Marine Biology, 135 (1): 89–98.CrossRefGoogle Scholar
  3. Chi X P, Javidpour J. 2016. Combined effects of food quality, food quantity and temperature on somatic growth, asexual reproduction and fatty acid composition of Aurelia aurita polyps. jellyfish%20bloom%20conference_poster_XCHI_JJ.pdf.Google Scholar
  4. Condon R H, Duarte C M, Pitt K A, Robinson K L, Lucas C H, Sutherland K R, Mianzan H W, Bogeberg M, Purcell J E, Decker M B, Uye S–i, Madin L P, Brodeur R D, Haddock S H D, Malej A, Parry G D, Eriksen E, Quiñones J, Acha M, Harvey M, Arthur J M, Graham W M. 2013. Recurrent jellyfish blooms are a consequence of global oscillations. Proceedings of the National Academy of Sciences of the United States of America, 110 (3): 1 000–1 005.CrossRefGoogle Scholar
  5. Feng S, Zhang F, Sun S, Wang S W, Li C L. 2015. Effects of duration at low temperature on asexual reproduction in polyps of the scyphozoan Nemopilema nomurai (Scyphozoa: Rhizostomeae). Hydrobiologia, 754 (1): 97–111.CrossRefGoogle Scholar
  6. Han C H, Uye S I. 2010. Combined effects of food supply and temperature on asexual reproduction and somatic growth of polyps of the common jellyfish Aurelia aurita s.l. Plankton and Benthos Research, 5 (3): 98–105.CrossRefGoogle Scholar
  7. Hansson L J, Moeslund O, Kiørboe T, Riisgård H U. 2005. Clearance rates of jellyfish and their potential predation impact on zooplankton and fish larvae in a neritic ecosystem (Limfjorden, Denmark). Marine Ecology Progress Series, 304: 117–131.CrossRefGoogle Scholar
  8. Hong H P, Han C H, Yoo J K. 2013. Population dynamics of jellyfish Aurelia aurita (s. l.) in Sihwa Lake. Ocean and Polar Research, 35 (3): 205–217.CrossRefGoogle Scholar
  9. Hoover R A, Purcell J E. 2009. Substrate preferences of scyphozoan Aurelia labiata polyps among common dockbuilding materials. Hydrobiologia, 616 (1): 259–267.CrossRefGoogle Scholar
  10. Ikeda H, Mizota C, Uye S I. 2017. Bioenergetic characterization in Aurelia aurita (Cnidaria: Scyphozoa) polyps and application to natural polyp populations. Marine Ecology Progress Series, 568: 87–100.CrossRefGoogle Scholar
  11. Ishii H, Ohba T, Kobayashi T. 2008. Effects of low dissolved oxygen on planula settlement, polyp growth and asexual reproduction of Aurelia aurita. Plankton and Benthos Research, 3 (S): 107–113.Google Scholar
  12. Keen S L, Gong A J. 1989. Genotype and feeding frequency affect clone formation in a marine cnidarian ( Aurelia aurita Lamarck 1816). Functional Ecology, 3 (6): 735–745.CrossRefGoogle Scholar
  13. Liu W C, Lo W T, Purcell J E, Chang H H. 2009. Effects of temperature and light intensity on asexual reproduction of the scyphozoan, Aurelia aurita (L.) in Taiwan. Hydrobiologia, 616 (1): 247–258.CrossRefGoogle Scholar
  14. Lo W T, Purcell J E, Hung J J, Su H M, Hsu P K. 2008. Enhancement of jellyfish ( Aurelia aurita ) populations by extensive aquaculture rafts in a coastal lagoon in Taiwan. ICES Journal of Marine Science., 65 (3): 453–461.CrossRefGoogle Scholar
  15. Lucas C H, Gelcich S, Uye S I. 2014. Living with jellyfish: Management and adaptation strategies. In: Pitt K, Lucas C eds. Jellyfish Blooms. Springer, Dordrecht, Netherlands. p.129–150.Google Scholar
  16. Lucas C H. 1996. Population dynamics of Aurelia aurita (Scyphozoa) from an isolated brackish lake, with particular reference to sexual reproduction. Journal of Plankton Research, 18 (6): 987–1007.CrossRefGoogle Scholar
  17. Lucas C H. 2001. Reproduction and life history strategies of the common jellyfish, Aurelia aurita, in relation to its ambient environment. Hydrobiologia, 451 (1–3): 229–246.CrossRefGoogle Scholar
  18. Ma X P, Purcell J. 2005. Temperature, salinity, and prey effects on polyp versus medusa bud production by the invasive hydrozoan Moerisia lyonsi. Marine Biology, 147 (1): 225–234.CrossRefGoogle Scholar
  19. Mangum C P, Oakes M J, Shick J M. 1972. Rate–temperature responses in scyphozoan medusae and polyps. Marine Biology, 15 (4): 298–303.CrossRefGoogle Scholar
  20. Miyake H, Iwao K, Kakinuma Y. 1997. Life history and environment of Aurelia aurita. South Pacific Study, 17 (2): 273–285.Google Scholar
  21. Möller H. 1980. Scyphomedusae as predators and food competitors of larval fish. Meeresforschung, 28: 1–17.Google Scholar
  22. Pascual M, Fuentes V, Canepa A, Atienza D, Gili J M, Purcell J E. 2015. Temperature effects on asexual reproduction of the scyphozoan Aurelia aurita s.l.: differences between exotic (Baltic and Red seas) and native (Mediterranean Sea) populations. Mar ine Ecology, 36 (4): 994–1 002.CrossRefGoogle Scholar
  23. Prieto L, Astorga D, Navarro G, Ruiz J. 2010. Environmental controlof phase transition and polyp survival of a massive–outbreaker jellyfish. PLoS One, 5 (11): e13793.CrossRefGoogle Scholar
  24. Purcell J E, Hoover R A, Schwarck N T. 2009. Interannual variation of strobilation by the scyphozoan Aurelia labiata in relation to polyp density, temperature, salinity, and light conditions in situ. Mar ine Ecology Prog ress Ser ies, 375: 139–149.CrossRefGoogle Scholar
  25. Purcell J E, Uye S I, Lo W T. 2007. Anthropogenic causes of jellyfish blooms and their direct consequences for humans: a review. Mar ine Ecology Prog ress Ser ies, 350: 153–174.CrossRefGoogle Scholar
  26. Purcell J E. 2007. Environmental effects on asexual reproduction rates of the scyphozoan Aurelia labiata. Mar ine Ecology Prog ress Ser ies, 348: 183–196.CrossRefGoogle Scholar
  27. Richardson A J, Bakun A, Hays G C, Gibbons M J. 2009. The jellyfish joyride: causes, consequences and management responses to a more gelatinous future. Trends in Ecology & Evolution, 24 (6): 312–322.CrossRefGoogle Scholar
  28. Russel F S. 1970. The Medusae of the British Isles. Vol. II. Pelagic Scyphozoa, with A Supplement to Vol. I. Cambridge University Press, London, UK.Google Scholar
  29. Schiariti A, Morandini A C, Jarms G, von Glehn Paes R, Franke S, Mianzan H. 2014. Asexual reproduction strategies and blooming potential in Scyphozoa. Mar ine Ecology Prog ress Ser ies, 510: 241–253.CrossRefGoogle Scholar
  30. Schneider G, Weisse T. 1985. Metabolism measurements of Aurelia aurita planulae larvae, and calculation of maximal survival period of the free swimming stage. Helgolä nder Meeresuntersuchungen, 39 (1): 43–47.CrossRefGoogle Scholar
  31. Shi Y, Yu Z G, Zhen Y, Wang G S, Wang X G, Mi T Z. 2017. Effect of decreasing temperature on the strobilation of Aurelia sp. 1. Chinese Journal of Oceanology and Limnology,–017–6210–6.Google Scholar
  32. Sokołowski A, Brulińska D, Olenycz M, Wołowicz M. 2016. Does temperature and salinity limit asexual reproduction of Aurelia aurita polyps (Cnidaria: Scyphozoa) in the Gulf of Gdańsk (southern Baltic Sea)? An experimental study. Hydrobiologia, 773 (1): 49–62.CrossRefGoogle Scholar
  33. Sun M, Dong J, Fu Z L, Li Y L. 2012. The effect of light intensity on survival and growth of scyphistomae in jellyfish, Aurelia sp. 1. Fish eries Sci ence, 31 (4): 211–215. (in Chinese with English abstract)Google Scholar
  34. Sun M, Dong J, Purcell J E, Li Y L, Duan Y, Wang A Y, Wang B. 2015a. Testing the influence of previous–year temperature and food supply on development of Nemopilema nomurai blooms. Hydrobiologia, 754 (1): 85–96.CrossRefGoogle Scholar
  35. Sun S, Sun X X, Jenkinson I R. 2015b. Preface: Giant jellyfish blooms in Chinese waters. Hydrobiologia, 754 (1): 1–11.CrossRefGoogle Scholar
  36. Thein H, Ikeda H, Uye S I. 2013. Ecophysiological characteristics of podocysts in Chrysaora pacifica (Goette) and Cyanea nozakii Kishinouye (Cnidaria: Scyphozoa: Semaeostomeae): effects of environmental factors on their production, dormancy and excystment. Journal of Experimental Marine Biology and Ecology, 446: 151–158.CrossRefGoogle Scholar
  37. Toyokawa M, Furota T, Terazaki M. 2000. Life history and seasonal abundance of Aurelia aurita medusae in Tokyo Bay, Japan. Plankton Biology and Ecology, 47 (1): 48–58.Google Scholar
  38. Uye S, Shimauchi H. 2005. Population biomass, feeding, respiration and growth rates, and carbon budget of the scyphomedusa Aurelia aurita in the Inland Sea of Japan. Journal of Plankton Research, 27 (3): 237–248.CrossRefGoogle Scholar
  39. Vagelli A. 2007. New observations on the asexual reproduction of Aurelia aurita (Cnidaria, Scyphozoa) with comments on its life cycle and adaptive significance. Invertebrate Zoology, 4 (2): 111–127.Google Scholar
  40. Wan A Y, Zhang G T. 2012. Annual occurrence of moon jellyfish Aurel i a sp. 1 in the Jiaozhou Bay and its impacts on zooplankton community. Oceanologia et Limnologia Sinica, 43 (3): 494–501. (in Chinese with English abstract)Google Scholar
  41. Wang B, Dong J, Wang W B, Li Y L, Liu X Z, Fu J. 2012. The quantity distribution of giant jellyfish and its relationship to seawater temperature and salinity in inshore waters of the northern Liaodong Bay region. Oceanologia et Limnologia Sinica, 43 (3): 568–578. (in Chinese with English abstract)Google Scholar
  42. Wang N, Li C L, Liang Y, Shi Y Q, Lu J L. 2015a. Prey concentration and temperature effect on budding and strobilation of Aurelia sp. 1 polyps. Hydrobiologia, 754 (1): 125–134.CrossRefGoogle Scholar
  43. Wang N, Li C L. 2015. The effect of temperature and food supply on the growth and ontogeny of Aurelia sp. 1 ephyrae. Hydrobiologia, 754 (1): 157–167.CrossRefGoogle Scholar
  44. Wang Y T, Sun S. 2015. Population dynamics of Aurelia sp. 1 ephyrae and medusae in Jiaozhou Bay, China. Hydrobiologia, 754 (1): 147–155.CrossRefGoogle Scholar
  45. Wang Y T, Zheng S, Sun S, Zhang F. 2015b. Effect of temperature and food type on asexual reproduction in Aurelia sp. 1 polyps. Hydrobiologia, 754 (1): 169–178.CrossRefGoogle Scholar
  46. Webster C N, Lucas C H. 2012. The effects of food and temperature on settlement of Aurelia aurita planula larvae and subsequent somatic growth. Journal of Experimental Marine Biology and Ecology, 436–437: 50–55.Google Scholar
  47. Willcox S, Moltschaniwskyj N A, Crawford C. 2007. Asexual reproduction in scyphistomae of Aurelia sp.: Effects of temperature and salinity in an experimental study. Journal of Experimental Marine Biology and Ecology, 353 (1): 107–114.CrossRefGoogle Scholar
  48. Winans A K, Purcell J E. 2010. Effects of pH on asexual reproduction and statolith formation of the scyphozoan, Aurelia labiata. Hydrobiologia, 645 (1): 39–52.CrossRefGoogle Scholar

Copyright information

© Chinese Society for Oceanology and Limnology, Science Press and Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  • Nan Wang (王楠)
    • 1
    • 2
    • 4
  • Chaolun Li (李超伦)
    • 1
    • 2
    • 3
    • 4
    Email author
  • Yantao Wang (王彦涛)
    • 1
    • 2
    • 4
  • Song Feng (冯颂)
    • 1
    • 2
    • 4
  1. 1.Key Laboratory of Marine Ecology and Environmental Sciences, Institute of OceanologyChinese Academy of SciencesQingdaoChina
  2. 2.Laboratory for Marine Ecology and Environmental ScienceQingdao National Laboratory for Marine Science and TechnologyQingdaoChina
  3. 3.University of Chinese Academy of SciencesBeijingChina
  4. 4.Center for Ocean Mega-ScienceChinese Academy of SciencesQingdaoChina

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