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Jellyfish blooms: are populations increasing globally in response to changing ocean conditions?

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Abstract

By the pulsed nature of their life cycles, gelatinous zooplankton come and go seasonally, giving rise in even the most undisturbed circumstances to summer blooms. Even holoplanktonic species like ctenophores increase in number in the spring or summer when planktonic food is available in greater abundance. Beyond that basic life cycle-driven seasonal change in numbers, several other kinds of events appear to be increasing the numbers of jellies present in some ecosystems. Over recent decades, man's expanding influence on the oceans has begun to cause real change and there is reason to think that in some regions, new blooms of jellyfish are occurring in response to some of the cumulative effects of these impacts. The issue is not simple and in most cases there are few data to support our perceptions. Some blooms appear to be long-term increases in native jellyfish populations. A different phenomenon is demonstrated by jellyfish whose populations regularly fluctuate, apparently with climate, causing periodic blooms. Perhaps the most damaging type of jellyfish increase in recent decades has been caused by populations of new, nonindigenous species gradually building-up to `bloom' levels in some regions. Lest one conclude that the next millennium will feature only increases in jellyfish numbers worldwide, examples are also given in which populations are decreasing in heavily impacted coastal areas. Some jellyfish will undoubtedly fall subject to the ongoing species elimination processes that already portend a vast global loss of biodiversity. Knowledge about the ecology of both the medusa and the polyp phases of each life cycle is necessary if we are to understand the true causes of these increases and decreases, but in most cases where changes in medusa populations have been recognized, we know nothing about the field ecology of the polyps.

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References

  • Angel, M. V. & A. de C. Baker, 1982. Vertical distribution of the standing crop of plankton and micronekton at three stations in the northeast Atlantic. Biol. Oceanogr. 2: 1–30.

    Google Scholar 

  • Arai, M. N., 2001. Pelagic coelenterates and eutrophication: a review. Hydrobiologia 451 (Dev. Hydrobiol. 155): 69–87.

    Google Scholar 

  • Båmstedt, U., J. H. Fosså, M. B. Martinussen & A. Fosshagen, 1998. Mass occurrence of the physonect siphonophore Apolemia uvaria (Lesueur) in Norwegian waters. Sarsia 83: 79–85.

    Google Scholar 

  • Benović, A., D. Justić & A. Bender, 1987. Enigmatic changes in the hydromedusan fauna of the northern Adriatic Sea. Nature 326: 597–600.

    Google Scholar 

  • Benović, A., D. Lučcić & V. Onofri, in press. Does change in an Adriatic hydromedusan fauna indicate an early phase of marine ecosystem destruction? P.S.Z.N.:Mar. Ecol.

  • Bingel, F., D. Avsar & A. C. Gücu, 1991. Occurrence of jellyfish in Mersin Bay. In Jellyfish Blooms in the Mediterranean, Proceedings of the II Workshop on Jellyfish in the Mediterranean Sea. MAP Technical Reports Series No. 47, UNEP, Athens: 65–71.

    Google Scholar 

  • Boero, F., 1991. Contribution to the understanding of blooms in the marine environment. In Jellyfish Blooms in the Mediterranean, Proceedings of the IIWorkshop on Jellyfish in theMediterranean Sea. MAP Technical Reports Series No. 47, UNEP, Athens: 72–76.

    Google Scholar 

  • Brodeur, R. D., C. E. Mills, J. E. Overland, G. E. Walters & J. D. Schumacher, 1999. Evidence for a substantial increase in gelatinous zooplankton in the Bering Sea, with possible links to climate change. Fish. Oceanogr. 8: 296–306.

    Google Scholar 

  • Buecher, E. & M. J. Gibbons, 2000. Interannual variation in the composition of the assemblages of medusae and ctenophores in St Helena Bay, southern Benguela ecosystem. Sci. mar. 64(Supl.1): 123–124.

    Google Scholar 

  • Buecher, E., J. Goy, B. Planque, M. Etienne & S. Dallot, 1997. Long-term fluctuations of Liriope tetraphylla in Villefranche Bay between 1966 and 1993 compared to Pelagia noctiluca pullulations. Oceanol. Acta 20: 145–157.

    Google Scholar 

  • Burd, B. J. & R. E. Thomson, 2000. Distribution and relative importance of jellyfish in a region of hydrothermal venting. Deep Sea Res. Pt. I: Oceanogr. Res. 47: 1703–1721.

    Google Scholar 

  • Calder, D. R. & V. G. Burrell Jr., 1967. Occurrence of Moerisia lyonsi (Limnomedusae, Moerisiidae) in North America. Am. midl. Nat. 78: 540–541.

    Google Scholar 

  • Calder, D. R. & V. G. Burrell Jr., 1969. Brackish water hydromedusa Maeotias inexpectata in North America. Nature 222: 694–695.

    Google Scholar 

  • Dawson, M. N & L. E. Martin, 2001. Geographic variation and ecological adaptation in Aurelia (Scyphozoa, Semaeostomeae): some implications from molecular phylogenetics. Hydrobiologia 451 (Dev. Hydrobiol. 155): 259–273.

    Google Scholar 

  • Edwards, M., A. W. G. John, H. G. Hunt & J. A. Lindley, 1999. Exceptional influx of oceanic species into the North Sea late 1997. J. mar. biol. Ass. U.K. 79: 737–739.

    Google Scholar 

  • Eiane, K. & E. Bagøien, 1999. Fish or jellies – a question of visibility? Limnol. Oceanogr. 44: 1352–1357.

    Google Scholar 

  • Estes, J. A., M. T. Tinker, T. M. Williams & D. F. Doak, 1998. Killer whale predation on sea otters linking oceanic and nearshore ecosystems. Science 282: 473–476.

    PubMed  Google Scholar 

  • Fearon, J. J., A. J. Boyd & F. H. Schülein, 1992. Views on the biomass and distribution of Chrysaora hysoscella (Linné, 1766) and Aequorea aequorea (Forskål, 1775) off Namibia, 1982–1989. Sci. mar. 56: 75-84 & 383–384 (errata).

    Google Scholar 

  • Finenko, G. A., B. E. Anninsky, Z. A. Romanova, G. I. Abolmasova & A. E. Kideys, 2001. Chemical composition, respiration and feeding rates of the new alien ctenophore, Beroe ovata, in the Black Sea. Hydrobiologia 451 (Dev. Hydrobiol. 155): 177–186.

    Google Scholar 

  • Fosså, J. H., 1992. Mass occurrence of Periphylla periphylla (Scyphozoa, Coronatae) in a Norwegian fjord. Sarsia 77: 237–251.

    Google Scholar 

  • Galil, B. S., E. Spanier & W. W. Ferguson, 1990. The scyphomedusae of the Mediterranean coast of Israel, including two Lessepsian migrants new to the Mediterranean. Zool. Meded. (Leiden) 64: 95–105.

    Google Scholar 

  • Goy, J., S. Dallot & P. Morand, 1989a. Les proliférations de la méduse Pelagia noctiluca et les modifications associées de la composition du macroplancton gélatineux. Oceanis 15: 17–23.

    Google Scholar 

  • Goy, J., P. Morand & M. Etienne, 1989b. Long term fluctuation of Pelagia noctiluca (Cnidaria, Scyphomedusa) in the western Mediterranean Sea. Prediction by climatic variables. Deep-Sea Res. 36: 269–279.

    Google Scholar 

  • Graham, W. M., 2001. Numerical increases and distributional shifts of Chrysaora quinquecirrha (Desor) and Aurelia aurita (Linné ) (Cnidaria: Scyphozoa) in the northern Gulf of Mexico. Hydrobiologia 451 (Dev. Hydrobiol. 155): 97–111.

    Google Scholar 

  • Graham, W. M., Pagès, F. & W. M. Hamner, 2001 A physical context for gelatinous zooplankton aggregations: a review. Hydrobiologia 451 (Dev. Hydrobiol. 155): 199–212.

    Google Scholar 

  • Greve, W., 1994. The 1989 German Bight invasion of Muggiaea atlantica. ICES J. mar. Sci. 51: 355–358.

    Google Scholar 

  • Gröndahl, F., 1988. A comparative ecological study on the scyphozoans Aurelia aurita, Cyanea capillata and C. lamarckii in the Gullmar Fjord, western Sweden, 1982 – 1986. Mar. Biol. 97: 541–550.

    Google Scholar 

  • Hay, S. J. & J. R. G. Hislop, 1980. The distribution and abundance of scyphomedusae in the North Sea during the summer of 1979. Int. Counc. Explor. Sea, Comm. Meet. (Oceanogr. Biol. Comm.) L: 1–7.

    Google Scholar 

  • Hirasaka, K., 1915. Medusae of Tokyo Bay. Jap. J. Zool. 27: 164 (in Japanese)

    Google Scholar 

  • Ishii, H. & F. Tanaka, 2001. Food and feeding of Aurelia aurita in Tokyo Bay with an analysis of stomach contents and a measurement of digestion times. Hydrobiologia 451 (Dev. Hydrobiol. 155): 311–320.

    Google Scholar 

  • Jarms, G., U. Båmstedt, H. Tiemann, M. B. Martinussen & J.H. Fosså, 1999. The holoplanktonic life cycle of the deep-sea medusa Periphylla periphylla (Scyphozoa, Coronata). Sarsia 84: 55–65.

    Google Scholar 

  • Kideys, A. E. & A. C. Gücü, 1995. Rhopilema nomadica: a lessepsian scyphomedusan new to the Mediterranean coast of Turkey. Israel J. Zool. 41: 6145–617.

    Google Scholar 

  • Kideys, A. E., A. V. Kovalev, G. Shulman, A. Gordina & F. Bingel, 2000. A review of zooplankton investigations of the Black Sea over the last decade. J. mar. Systems 24: 355–371.

    Google Scholar 

  • Kishinouye, K., 1891. Mizu-Kurage. Jap. J. Zool. 3: 289–291 (in Japanese).

    Google Scholar 

  • Kovalev, A. V. & S. A. Piontkovski, 1998. Interannual changes in the biomass of the Black Sea gelatinous zooplankton. J. Plankton Res. 20: 1377–1385.

    Google Scholar 

  • Kramp, P. L., 1961. Synopsis of the medusae of the world. J. mar. biol. Ass. U. K. 40: 1–469.

    Google Scholar 

  • Loeb, V., V. Siegel, O. Holm-Hansen, R. Hewitt, W. Fraser, W. Trivelpiece & S. Trivelpiece, 1997. Effects of sea-ice extent and krill or salp dominance on the Antarctic food web. Nature 387: 897–900.

    Google Scholar 

  • Lotan, A., R. Ben-Hillel & Y. Loya, 1992. Life cycle of Rhopilema nomadica: a new immigrant scyphomedusan in the Mediterranean. Mar. Biol. 112: 237–242.

    Google Scholar 

  • Lotan, A., M. Fine & R. Ben-Hillel, 1994. Synchronization of the life cycle and dispersal pattern of the tropical invader scyphomedusan Rhopilema nomadica is temperature dependent. Mar. Ecol. Prog. Ser. 109: 59–65.

    Google Scholar 

  • Lucas, C. H., 2001. Reproduction and life history strategies of the common jellyfish, Aurelia aurita, in relation to its ambient environment. Hydrobiologia 451 (Dev. Hydrobiol. 155): 229–246.

    Google Scholar 

  • Madin, L. P., S. M. Bollens, E. Horgan, M. Butler, J. Runge, B. K. Sullivan, G. L. Klein-MacPhee, E. Durbin, A. G. Durbin, D. Van Keuren, S. Plourde, A. Bucklin & M. E. Clarke, 1996. Voracious planktonic hydroids: unexpected predatory impact on a coastal marine ecosystem. Deep-Sea Res. II 43: 1823–1829.

    Google Scholar 

  • Matsueda, N., 1969. Presentation of Aurelia aurita at thermal power station. Bull. mar. biol. Sta. Asamushi 13: 187–191.

    Google Scholar 

  • Mills, C. E., 1995. Medusae, siphonophores and ctenophores as planktivorous predators in changing global ecosystems. ICES J. mar. Sci. 52: 575–581.

    Google Scholar 

  • Mills, C. E. & J. T. Rees, 2000. New observations and corrections concerning the trio of invasive hydromedusae Maeotias marginata (=M. inexpectata), Blackfordia virginica and Moerisia sp. in the San Francisco Estuary. Sci. mar. 64(Suppl. 1): 151–155.

    Google Scholar 

  • Mills, C. E. & F. Sommer, 1995. Invertebrate introductions in marine habitats: two species of hydromedusae (Cnidaria) native to the Black Sea, Maeotias inexspectata and Blackfordia virginica, invade San Francisco Bay. Mar. Biol. 122: 279–288.

    Google Scholar 

  • Mlot, C., 1997. Unusual fish threat afloat in the Atlantic. Sci. News 152: 325.

    Google Scholar 

  • Möller, H., 1980. Population dynamics of Aurelia aurita medusae in Kiel Bight, Germany (FRG). Mar. Biol. 60: 123–128.

    Google Scholar 

  • Möller, H., 1984a. Effects on jellyfish predation by fishes. Proceedings of the Workshop on Jellyfish Blooms in the Mediterranean, Athens 1983. UNEP 1984: 45–59.

  • Möller, H., 1984b. Reduction of a larval herring population by jellyfish predator. Science 224: 621–622.

    Google Scholar 

  • Morand, P. & S. Dallot, 1985. Variations annuelle et pluriannuelles de quelques espèces du macroplancton cotier de la Mer Ligure (1898–1914). Rapp. Comm. Int. Mer Méd. 29: 295–297.

    Google Scholar 

  • Mutlu, E., F. Bingel, A. C. Gücü, V. V. Melnikov, U. Nierman, N.A. Ostr & V. E. Zaika, 1994. Distribution of the new invader Mnemiopsis sp. and the resident Aurelia aurita and Pleurobrachia pileus populations in the Black Sea in the years 1991–1993. ICES J. mar. Sci. 51: 407–421.

    Google Scholar 

  • National Research Council, 1996. The Bering Sea Ecosystem: Report of the Committee on the Bering Sea Ecosystem. National Academy Press, Washington, D.C.: 307 pp.

    Google Scholar 

  • Omori, M., H. Ishii & A. Fujinaga, 1995. Life history strategy of Aurelia aurita (Cnidaria, Scyphomedusae) and its impact on the zooplankton community of Tokyo Bay. ICES J. mar. Sci. 52: 597–603.

    Google Scholar 

  • Omori, M. & E. Nakano, 2001. Jellyfish fishery in southeast Asia Hydrobiologia 451 (Dev. Hydrobiol. 155): 19–26.

    Google Scholar 

  • Pagès, F., 1997. The gelatinous zooplankton in the pelagic system of the Southern Ocean: a review. Ann. Inst. océanogr., Paris 73: 139–158.

    Google Scholar 

  • Papathanassiou, E., P. Panayotidis & K. Anagnostaki, 1987. Notes on the biology and ecology of the jellyfish Aurelia aurita Lam. in Elefsis Bay (Saronikos Gulf, Greece). P. S. Z. N. I.: Mar. Ecol. 8: 49–58.

    Google Scholar 

  • Pauly, D., V. Christensen, J. Dalsgaard, R. Froese & F. Torres Jr., 1998. Fishing down marine food webs. Science 279: 860–863.

    PubMed  Google Scholar 

  • Purcell, J. E. & M. N. Arai, 2001. Interactions of pelagic cnidarians and ctenophores with fish: a review. Hydrobiologia 451 (Dev. Hydrobiol. 155): 27–44.

    Google Scholar 

  • Purcell, J. E., U. Båmstedt & A. Båmstedt, 1999a. Prey, feeding rates and asexual reproduction rates of the introduced oligohaline hydrozoan Moerisia lyonsi. Mar. Biol. 134: 317–325.

    Google Scholar 

  • Purcell, J. E., D. L. Breitburg, M. B. Decker, W. M. Graham, M. J. Youngbluth & K. A. Raskoff, 2001b. Pelagic cnidarians and ctenophores in low dissolved oxygen environments: a review. In Rabalais, N. N. & R. E. Turner (eds), Coastal Hypoxia: Consequences for Living Resources and Ecosystems, American Geophysical Union. Coastal & Estuar. Stud. 58: 77–100.

  • Purcell, J. E., A. Malej & A. Benović, 1999b. Potential links of jellyfish to eutrophication and fisheries. In Malone, T. C., A. Malej, L. W. Harding Jr., N. Smodlana & R. E. Turner (eds), Ecosystems at the Land-Sea Margin: Drainage Basin to Coastal Sea. Coastal and Estuar. Stud. 55: 241–263.

  • Purcell, J. E., T. A. Shiganova, M. B. Decker & E. D. Houde, 2001a. The ctenophore Mnemiopsis in native and exotic habitats: U.S. estuaries versus the Black Sea basin. Hydrobiologia 451 (Dev. Hydrobiol. 155): 145–175.

    Google Scholar 

  • Purcell, J. E., J. R. White, D. A. Nemazie & D. A. Wright, 1999c. Temperature, salinity and food effects on asexual reproduction and abundance of the scyphozoan Chrysaora quinquecirrha. Mar. Ecol. Prog. Ser. 180: 187–196.

    Google Scholar 

  • Rajagopal, S., K. V. K. Nair & J. Azariah, 1989. Some observations on the problem of jelly fish ingress in a power station cooling system at Kalpakkam, east coast of India. Mahasagar Quart. J. Oceanogr., Nat. Inst. Oceanogr, Goa, India 22: 151–158.

    Google Scholar 

  • Raskoff, K. A., 2001 The impact of El Niño events on populations of mesopelagic hydromedusae. Hydrobiologia 451 (Dev. Hydrobiol. 155): 121–129.

    Google Scholar 

  • Rees, J. T. & L. A. Gershwin, 2000. Non-indigenous hydromedusae in California's upper San Francisco Estuary: life cycles, distribution, and potential environmental impacts. Sci. Mar. 64(Suppl.1): 73–86.

    Google Scholar 

  • Rees, J. T. & R. J. Larson, 1980. Morphological variation in the hydromedusa genus Polyorchis on the west coast of North America. Can. J. Zool. 58: 2089–2095.

    Google Scholar 

  • Robison, B. & J. Connor, 1999. The Deep Sea. Monterey Bay Aquarium Press, Monterey, California: 80 pp.

    Google Scholar 

  • Rogers, C. A., D. C. Biggs & R. A. Cooper, 1978. Aggregation of the siphonophore Nanomia cara in the Gulf of Maine: observations from a submersible. Fish. Bull. 76: 281–284.

    Google Scholar 

  • Schneider, G. & G. Behrends, 1994. Population dynamics and the trophic role of Aurelia aurita medusae in the Kiel Bight and western Baltic. ICES J. mar. Sci. 51: 359–367.

    Google Scholar 

  • Shiganova, T. A., 1998. Invasion of the Black Sea by the ctenophore Mnemiopsis leidyi and recent changes in pelagic community structure. Fish. Oceanogr. 7: 305–310.

    Google Scholar 

  • Shiganova, T. A., Yu. V. Bulgakova, S. P. Volovik, Z. A. Mirzoyan & S. I. Dudkin, 2001. The new invader Beroe ovata Mayer, 1912 and its effect on the ecosystem in the northeastern Black Sea. Hydrobiologia 451 (Dev. Hydrobiol. 155): 187–197.

    Google Scholar 

  • Shimomura, T., 1959. On the unprecedented flourishing of 'Echizen-Kurage', Stomolophus nomurai (Kishinouye), in the TsushimaWarm Current regions in autumn, 1958. Bull. Jap. Sea Reg. Fish. Res. Lab. 7: 85–107.

    Google Scholar 

  • Smith, R. I & J. T. Carlton (eds), 1975. Light's Manual: Intertidal Invertebrates of the Central California Coast. University of California Press, Berkeley: 716 pp.

    Google Scholar 

  • Sparks, C., E. Buecher, A. S. Brierley, B. E. Axelsen, H. Boyer & M. J. Gibbons, 2001. Observations on the distribution and relative abundance of the scyphomedusan Chrysaora hysoscella (Linné, 1776) and the hydrozoan Aequorea aequorea (Forskål, 1775) in the northern Benguela ecosystem. Hydrobiologia 451 (Dev. Hydrobiol. 155): 275–286.

    Google Scholar 

  • Studenikina, Ye. I., S. P. Volovik, I. A. Mirzoyan & G. I. Luts, 1991. The ctenophore Mnemiopsis leidyi in the Sea of Azov. Oceanology 31: 722–725.

    Google Scholar 

  • Thorne-Miller, B. & J. Catena, 1991. The Living Ocean: Understanding and Protecting Marine Biodiversity. Island Press, Washington, D.C., 180 pp.

    Google Scholar 

  • Thurston, M. H., 1977. Depth distributions of Hyperia spinigera Bovallius, 1889 (Crustacea: Amphipoda) and medusae in the North Atlantic Ocean, with notes on the associations between Hyperia and coelenterates. In Angel, M. (ed.), A Voyage of Discovery: George Deacon 70th Anniversary Volume. Pergamon Press, Ltd., Oxford: 499–536.

    Google Scholar 

  • Uchida, T., 1927. Studies on Japanese Hydromedusae. 1. Anthomedusae. J. Fac. Sci. imp. Univ. Tokyo. IV. Zool. 1: 145–241, pls. 10, 11.

    Google Scholar 

  • Uye, S. & T. Kasuya, 1999. Functional roles of ctenophores in the marine coastal ecosystem. In Okutani, T., S. Ohta & R. Ueshima (eds) Update Progress in Aquatic Invertebrate Zoology. Tokai University Press, Tokyo: 57–76 (in Japanese with English Abstract).

    Google Scholar 

  • Vinogradov, M. Ye., E. A. Shushkina, E. I. Musayeva & P. Yu. Sorokin, 1989. A newly acclimated species in the Black Sea: the ctenophore Mnemiopsis leidyi (Ctenophora: Lobata). Oceanology 29: 220–224.

    Google Scholar 

  • Volovik, S. P., (ed), 2000. Ctenophore Mnemiopsis leidyi (A. Agassiz) in the Azov and Black Seas: its Biology and Consequences of its Intrusion. State Unitary Enterprize Research Institute of the Azov Sea Fishery Problems (GUP AzNIIRKH), Rostov-on-Don, Russia, 497 pp. (in Russian with English Contents, Introduction and Concluding Remarks).

    Google Scholar 

  • Vućetić, T., 1983. Some causes of the blooms and unusual distribution of the jellyfish Pelagia noctiluca in the Mediterranean (Adriatic). In Proceedings of the Workshop on Jellyfish Blooms in the Mediterranean, Athens 1983. UNEP 1984: 167–176.

  • Wilkerson, F. P. & R. C. Dugdale, 1984. Possible connections between sewage effluent, nutrient levels and jellyfish blooms. In Proceedings of the Workshop on Jellyfish Blooms in the Mediterranean, Athens 1983. UNEP 1984: 195–201.

  • Yasuda, T., 1988. Unusually gregarious occurrences of jellyfishes in Japanese waters. Saishu to Shiiku 50: 338–346 (in Japanese).

    Google Scholar 

  • Youngbluth, M. & U. Båmstedt, 2001. Distribution, abundance, behavior and metabolism of Periphylla periphylla, a mesopelagic coronate medusa in a Norwegian fjord. Hydrobiologia 451 (Dev. Hydrobiol. 155): 321–333.

    Google Scholar 

  • Zaitsev, Yu. P., 1992. Recent changes in the trophic structure of the Black Sea. Fish. Oceanogr. 1: 180–189.

    Google Scholar 

  • Zaitsev, Yu. & V. Mamaev, 1997, Marine biological diversity in the Black Sea: a study of change and decline. United Nations Publications, New York: 208 pp.

    Google Scholar 

  • Zavodnik, D., 1987. Spatial aggregations of the swarming jellyfish Pelagia noctiluca (Scyphozoa). Mar. Biol. 94: 265–269.

    Google Scholar 

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Mills, C.E. Jellyfish blooms: are populations increasing globally in response to changing ocean conditions?. Hydrobiologia 451, 55–68 (2001). https://doi.org/10.1023/A:1011888006302

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