Artificial substrates preference for proliferation and immigration in Aurelia aurita (s. l.) polyps

Song Feng; Jianing Lin; Song Sun; Fang Zhang

doi:10.1007/s00343-016-5230-y

Your Location：

Home >

Browse articles >

Artificial substrates preference for proliferation and immigration in Aurelia aurita (s. l.) polyps

OriginalPaper | Updated：2023-05-16

- Artificial substrates preference for proliferation and immigration in Aurelia aurita (s. l.) polyps
- Artificial substrates preference for proliferation and immigration in Aurelia aurita (s. l.) polyps
- 海洋湖沼学报（英文） 2017年35卷第1期页码：153-162
- Affiliations：
  
  1. Key Lab of Marine Ecology and Environmental Sciences Institute of Oceanology Chinese Academy of Sciences
  2. Laboratory for Marine Ecology and Environmental Science Qingdao National Laboratory for Marine Science and Technology
  3. State Key Laboratory of Environmental Criteria and Risk Assessment Chinese Research Academy of Environmental Sciences
  4. Laboratory of Riverine Ecological Conservation and Technology Chinese Research Academy of Environmental Sciences
  5. Jiaozhou Bay Marine Ecosystem Research Station Institute of Oceanology Chinese Academy of Sciences
- Author bio：
- Funds：
  
  Supported by the State Key Program of National Natural Science of China (No.41230963), the Strategic Priority Research Program of the Chinese Academy of Sciences (No.XDA11020305), the Shandong Joint Fund for Marine Ecology and Environmental Sciences (No.U1406403), and the National Natural Science Foundation of China (No.41506144);SUN Song and ZHANG Fang contributed equally to this work.;An erratum to this article is available at;http://dx.doi.org/10.1007/s00343-017-7466-6;.
- DOI：10.1007/s00343-016-5230-y
  中图分类号：
- 网络首发：2016-04-21，
  
  纸质出版：2017
- Accepted：
Scan QR Code
Artificial substrates preference for proliferation and immigration in Aurelia aurita (s. l.) polyps[J]. 海洋湖沼学报（英文）, 2017,35(1):153-162.

Feng, S., Lin, J., Sun, S. et al. Artificial substrates preference for proliferation and immigration in Aurelia aurita (s. l.) polyps., Chin. J. Ocean. Limnol. 35, 153–162 (2017). https://doi.org/10.1007/s00343-016-5230-y
Artificial substrates preference for proliferation and immigration in Aurelia aurita (s. l.) polyps[J]. 海洋湖沼学报（英文）, 2017,35(1):153-162. DOI： 10.1007/s00343-016-5230-y.

Feng, S., Lin, J., Sun, S. et al. Artificial substrates preference for proliferation and immigration in Aurelia aurita (s. l.) polyps., Chin. J. Ocean. Limnol. 35, 153–162 (2017). https://doi.org/10.1007/s00343-016-5230-y DOI：

摘要

Abstract

The increasing amounts of artificial marine substrates

in many parts of the world have been proposed as a potential driver of Aurelia spp. blooms

on account of providing extra habitats for the settlement and the proliferation of the benthic stage (polyps). Previous experiments have mainly focused on the substrate choices of Aurelia spp. planulae. However

substrate preferences for the proliferation and immigration of polyps have not been reported. We monitored the propagation and immigration of Aurelia aurita (s. l.) polyps on two natural and nine artificial substrates at constant temperature (20±0.5°C) and salinity (30±0.5) in beakers and a glass aquarium in the laboratory

respectively. The results showed that

among artificial substrates

the highest number for polyp proliferation and immigration was found on nets

rigid polyvinyl chloride plates (RPVC)

and wood. The lowest density of polyps was present on iron plates. Among natural substrates

the asexual reproduction rate of polyps on Patinopecten yessoensis (Jay

1857) shells was significantly higher than Azumapecten farreri (Jones & Preston

1904). On the account of the distinction in the roughness

chemical properties and biofilms of these material surfaces

bare artificial or natural substrates discriminatively affect the proliferation and the immigration of Aurelia spp. polyps at laboratory. These observations suggest that

even in the natural environment

different materials and texture may influence the composition and the abundance of the fouling communities and the assemblages of polyps and

indirectly

have effects on the amounts of released medusae.

关键词

Keywords

references

Adler L, Jarms G. 2009. New insights into reproductive traits of scyphozoans: special methods of propagation in Sanderia malayensis GOETTE, 1886 (Pelagiidae, Semaeostomeae) enable establishing a new classification of asexual reproduction in the class Scyphozoa. Mar. Biol., 156 (7): 1411–1420.

Arai M N. 1997. A Functional Biology of Scyphozoa. Chapman & Hall, London. 316p.

Arai M N. 2009. The potential importance of podocysts to the formation of scyphozoan blooms: a review. Hydrobiologia, 616 (1): 241–246.

Berrill N J. 1949. Developmental analysis of Scyphomedusae. Biol. Rev., 24 (4): 393–410.

Brewer R H. 1978. Larval settlement behavior in the jellyfish Aurelia aurita (Linnaeus) (Scyphozoa: semaeostomeae). Estuaries, 1 (2): 121–122.

Brewer R H. 1984. The influence of orientation, roughness and wettability of solid surfaces on the behavior and attachment of planulae of Cyanea (Cnidaria: scyphozoa). Biol. Bull., 166 (1): 11–21.

Coyne J A. 1973. An investigation of the dynamics of population growth and control in scyphistomae of the scyphozoan Aurelia aurita. Chesapeake Science, 14 (1): 55–58.

Degarmo E P, Black J, Kohser R. A. 2003. Materials and Processes in Manufacturing. 9th ed. Wiley, Hoboken, NJ, 223p.

Di Camillo C G, Betti F, Bo M, Martinelli M, Puce S, Bavestrello G. 2010. Contribution to the understanding of seasonal cycle of Aurelia aurita (Cnidaria: scyphozoa) scyphopolyps in the northern Adriatic Sea. Journal of the Marine Biological Association of the United Kingdom, 90 (6): 1105–1110.

Dong Z, Liu D, Keesing J K. 2010. Jellyfish blooms in China: Dominant species, causes and consequences. Mar. Pollut. Bull. 60 (7): 954–963.

Duarte C M, Pitt K A, Lucas C H, Purcell J E, Uye S, Robinson K, Brotz L, Decker M B, Sutherland K R, Malej A, Madin L, Mianzan H, Gili J M, Fuentes V, Atienza D, Pagés F, Breitburg D, Malek J, Graham W M, Condon R H. 2013. Is global ocean sprawl a cause of jellyfish blooms? Front. Ecol. Environ., 11 (2): 91–97.

Eckman J E. 1990. A model for passive settlement by planktonic larvae onto bottoms of differing roughness. Limnol. Oceanogr., 35 (4): 887–901.

Fleck J, Fitt W K. 1999. Degrading mangrove leaves of Rhizophora mangle Linne provide a natural cue for settlement and metamorphosis of the upside down jellyfish Cassiopea xamachana Bigelow. Journal of Experimental Marine Biology and Ecology, 234 (1): 83–94.

Graham W M, Gelcich S, Robinson K L, Duarte C M, Brotz L, Purcell J E, Madin L P, Mianzan H, Sutherland K R, Uye S I, Pitt K A, Lucas C H, Bøgeberg M, Brodeur R D, Condon R H. 2014. Linking human well-being and jellyfish: ecosystem services, impacts and socital responses. Front. Ecol. Environ., 12 (9): 515–523.

Hadfield M G. 2011. Biofilms and marine invertebrate larvae: what bacteria produce that larvae use to choose settlement sites. Annu. Rev. Mar. Sci., 3 (1): 453–470.

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 Res earch, 5 (3): 98–105.

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). Mar. Ecol. Prog. Ser. 304: 117–131.

Hofmann D K, Crow G L. 2002. Induction of larval metamorphosis in the tropical scyphozoan Mastigias papua: striking similarity with upside down-jellyfish Cassiopea spp. (with notes on related species). Vieet Milieu, 52 (4): 141–147.

Holst S, Jarms G. 2007. Substrate choice and settlement preferences of planula larvae of five Scyphozoa (Cnidaria) from German Bight, North Sea. Mar. Biol., 151 (3): 863–871.

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.

Hoover R A, Armour R, Dow I, Purcell J E. 2012. Nudibranch predation and dietary preference for the polyps of Aurelia labiata (Cnidaria: scyphozoa). Hydrobiologia, 690 (1): 199–213.

Hoover R A, Purcell J E. 2009. Substrate preferences of scyphozoan Aurelia labiata polyps among common dockbuilding materials. Hydrobiologia, 616 (1): 259–267.

Ishii H, Katsukoshi K. 2010. Seasonal and vertical distribution of Aurelia aurita polyps on a pylon in the innermost part of Tokyo Bay. J. Oceanogr., 66 (3): 329–336.

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 Res earch, 3 (S): 107–113.

Janßen H, Augustin C B, Hinrichsen H H, Kube S. 2013. Impact of secondary hard substrate on the distribution and abundance of Aurelia aurita in the western Baltic Sea. Mar. Pollut. Bull., 75 (1-3): 224–234.

Kakimura, Y. 1975. An experimental study of the life cycle and organ differentiation of Aurelia aurita Lamarck. The Bulletin of the Marine Biological Station of Asamushi, 15 (3): 101–113.

Korean Nuclear Power Plant Operational Performance Information System. 2009. Annual report. Available at: http://opis.kins.re.kr/(accessed on 8 August 2009).

Kramp P L. 1961. Synopsis of the medusae of the world. Journal of the Marine Biological Association of the United Kingdom, 40: 1–469.

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 J. Mar. Sci., 65 (3): 453–461.

Lotan A, Ben-Hillel R, Loya Y. 1992. Life cycle of Rhopilema nomadica: a new immigrant scyphomedusan in the Mediterranean. Mar. Biol., 1 1 2 (2): 237–242.

Lucas C H, Graham W M, Widmer C. 2012. Jellyfish life histories: role of polyps in forming and maintaining scyphomedusa populations. Adv. Mar. Biol., 63: 133–196.

Lucas C H, Horton A A. 2014. Short-term effects of the heavy metals, Silver and copper, on polyps of the common jellyfish, Aurelia aurita. Journal of Experimental Marine Biology and Ecology, 461: 154–161.

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.

Makabe R, Furukawa R, Takao M, Uye S I. 2014. Marine artificial structures as amplifiers of Aurelia aurita s.l. blooms: a case study of a newly installed floating pier. J. Oceanogr., 70 (5): 447–455.

Makabe R, Kurihara T, Uye S I. 2012. Spatio-temporal distribution and seasonal population dynamics of the jellyfish Aurelia aurita s.l. studied with Dual-frequency IDentification SO Nar (DIDSON). J. Plankton Res., 34 (11): 936–950.

Malej A, Kogovšek T, Ramšak A, Catenacci L. 2012. Blooms and population dynamics of moon jellyfish in the northern Adriatic. Cahiers de Biologie Marine, 53 (3): 337–342.

McNamara M E, Lonsdale D J, Cerrato R M. 2013. Top-down control of mesozooplankton by adult Mnemiopsis leidyi influences microplankton abundance and composition enhancing prey conditions for larval ctenophores. Estuarine, Coastal and Shelf Science, 133: 2–10.

Miyake H, Terazaki M, Kakinuma Y. 2002. On the polyps of common jellyfish Aurelia aurita in Kagoshima Bay. J. Oceanogr., 58 (3): 451–459.

Müller W A, Leitz T. 2002. Metamorphosis in the Cnidaria. Canadian Journal of Zoology, 80 (10): 1755–1771.

Pitt K A. 2000. Life history and settlement preferences of the edible jellyfish Catostylus mosaicus (Scyphozoa: rhizostomeae). Mar. Biol., 136 (2): 269–279.

Purcell J E, Atienza D, Fuentes V, Olariaga A, Tilves U, Colahan C, Gili J M. 2012. Temperature effects on asexual reproduction rates of scyphozoan species from the northwest Mediterranean Sea. Hydrobiologia, 690 (1): 169–180.

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. Ecol. Prog. Ser., 375: 139–149.

Purcell J E, Uye S I, Lo W T. 2007. Anthropogenic causes of jellyfish blooms and their direct consequences for humans: a review. Mar. Ecol. Prog. Ser., 350: 153–174.

Purcell J E. 1997. Pelagic cnidarians and ctenophores as predators: selective predation, feeding rates, and effects on prey populations. Annales de L’ Institut Océanographique, 73 (2): 125–137.

Purcell J E. 2007. Environmental effects on asexual reproduction rates of the scyphozoan Aurelia labiat a. Mar. Ecol. Prog. Ser., 348: 183–196.

Purcell J E. 2012. Jellyfish and ctenophore blooms coincide with human proliferations and environmental perturbations. Annu. Rev. Mar. Sci., 4 (1): 209–235.

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 Ecol. Evol., 24 (6): 312–322.

Schiariti A, Melica V, Kogovšek T, Malej A. 2015. Densitydependent effects control the reproductive strategy and population growth of Aurelia aurita s.l. scyphistomae. Mar. Biol., 162 (8): 1665–1672.

Schiariti A, Morandini A C, Jarms G, Paes R V G, Franke S, Mianzan H. 2014. Asexual reproduction strategies and blooming potential in Scyphozoa. Mar. Ecol. Prog. Ser., 510: 241–253.

Takao M, Okawachi H, Uye S I. 2014. Natural predators of polyps of Aurelia aurita s.l. (Cnidaria: scyphozoa: semaeostomeae) and their predation rates. Plankton Benthos Res earch, 9 (2): 105–113.

Thein H, Ikeda H, Uye S I. 2012. The potential role of podocysts in perpetuation of the common jellyfish Aurelia aurita s.l. (Cnidaria: scyphozoa) in anthropogenically perturbed coastal waters. Hydrobiologia, 690 (1): 157–167.

Tinta T, Kogovšek T, Malej A, Turk V. 2012. Jellyfish modulate bacterial dynamic and community structure. PLoS One, 7 (6): e39274.

Toyokawa M, Aoki K, Yamada S, Yasuda A, Murata Y, Kikuchi T. 2011. Distribution of ephyrae and polyps of jellyfish Aurelia aurita (Linnaeu. 1758. sensu lato in Mikawa Bay, Japan. J. Oceanogr., 67 (2): 209–218.

Toyokawa M, Furota T, Terazaki M. 2000. Life history and seasonal abundance of Aurelia aurita medusae in Tokyo Bay, Japan. Plankton Biol. Ecol., 47 (1): 48–58.

Uye S I. 2011. Human forcing of the copepod-fish-jellyfish triangular trophic relationship. Hydrobiologia, 666 (1): 71–83.

Vagelli A A. 2007. New observations on the asexual reproduction of Aurelia aurita (Cnidaria, Scyphozoa) with comments on its life cycle and adaptive significance. Invertebrate Zoologiya, 4 (2): 111–127.

Wang S W, Zhang G T, Sun S, Wang Y T, Zhao Z X. 2012. Population dynamics of three scyphozoan jellyfish species during summer of 2011 in Jiaozhou Bay. Oceanologia et Limnologia Sinica, 43 (3): 471–479. (in Chinese with English abstract)

Watanabe T, Ishii H. 2001. In situ estimation of ephyrae liberated from polyps of Aurelia aurita using settling plates in Tokyo Bay, Japan. Hydrobiologia, 451 (1-3): 247–258.

Willcox S, Moltschaniwskyj N A, Crawford C M. 2008. Population dynamics of natural colonies of Aurelia sp. scyphistomae in Tasmania, Australia. Mar. Biol., 154 (4): 661–670.

浏览量

Downloads

CSCD

文章被引用时，请邮件提醒。

Submit

工具集

关联资源

Molecular identification, expression pattern, and in-vitro bioactivity analysis of insulin-like growth factor 2 in olive flounder Paralichthys olivaceus

Natural predators of polyps of three scyphozoans: Nemopilema nomurai, Aurelia coerulea, and Rhopilema esculentum

Intraguild predation by polyps of three scyphozoan jellyfish: Nemopilema nomurai, Aurelia coerulea, and Rhopilema esculentum

Analysis of expressed sequence tags from the Ulva prolifera (Chlorophyta)

Effect of nitrogen to phosphorus ratios on cell proliferation in marine micro algae