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Gelatinous macroplankton in the Black Sea in the autumn of 2010

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Abstract

In October and November of 2010, the gelatinous macroplankton in the northwestern Black Sea and at the Crimean shelf was represented by the scyphozoan jellyfish Aurelia aurita, three species of ctenophores (Beroe ovata, Mnemiopsis leidyi, and Pleurobrachia pileus), and three species of hydromedusae. A. aurita was more common at the shelf, M. leidyi and P. pileus prevailed at the deeper sea stations, and B. ovata was almost ubiquitous with a biomass from below 1 to 49 g/m2 A. aurita, which had an average biomass of 82–224 g/m2, was dominant at all the stations. M. leidyi, which had a biomass from below 1 to 115 g/m2, was recorded in October at only 14 of the 52 stations and in November at 20 of the 46 stations. The highest biomass of M. leidyi in October (105 to 116 g/m2) was recorded in the deep sea areas; in November, it was also the highest in these areas, but it reached at most 100 g/m2. The average daily ration of Aurelia ranged from 19.4 to 27.3 mg/m2 in October and from 7.0 to 17.2 mg/m2 in November; in both cases, it was insufficient to provide for the minimal physiological requirements. The average daily ration of the Mnemiopsis population (2.8–20.5 mg of zooplankton per m2) was invariably more than sufficient to provide for the minimal physiological requirements. Both predatory species together consumed less than 5% of the daily zooplankton production of the sea.

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References

  1. B. E. Anninsky, G. I. Abolmasova, and N. A. Datsyk, “Influence of jelly raptorial animals on food reserves of small pelagic fishes, 9.2.2. Eat away of mesoplankton by Aurelia aurita L. in the Black Sea,” in Commercial Bioresources of the Black and Azov Seas, Ed. by V. N. Eremeev (EKOSI-Gidrofizika, Sevastopol, 2011), pp. 276–282.

    Google Scholar 

  2. B. E. Anninsky and F. Timofte, “Distribution of zooplankton in Western Black Sea in October of 2005,” Morsk. Ekol. Zh. 8(1), 17–31 (2009).

    Google Scholar 

  3. M. E. Vinogradov, E. A. Shushkina, and G. G. Nikolaeva, “Conditions of zoocene in open regions of the Black Sea by the late summer of 1992,” Okeanologiya (Moscow, Russ. Fed.) 33(3), 382–387 (1993).

    Google Scholar 

  4. M. E. Vinogradov, T. A. Shiganova, and V. S. Khoroshilov, “Conditions of basic elements of plankton community in the Black Sea,” Okeanologiya (Moscow, Russ. Fed.) 35(3), 418–422 (1995).

    Google Scholar 

  5. A. V. Kovalev, V. V. Mel’nikov, N. A. Ostrovskaya, and I. Yu. Prusova, “Mesoplankton,” in Plankton of the Black Sea, Ed. by A. V. Kovalev and Z. Z. Finenko (Naukova Dumka, Kiev, 1993), pp. 183–193.

    Google Scholar 

  6. A. V. Kovalev, Yu. A. Zagorodnyaya, and N. A. Gavrilova, “Study of the Black Sea zooplankton,” in Geological Studies of 47th Cruise of R/V Professor Vodyanitskii in the Black Sea, Ed. by E. F. Shnyukov (Otd. Morsk. Geol. Osad. Rudoobraz., Kiev, 1995), pp. 155–165.

    Google Scholar 

  7. T. S. Petipa, “Average weight of zooplankton in the Black Sea,” Tr. Sevastop. Biol. Stn., Akad. Nauk Ukr. SSR 9, 39–57 (1957).

    Google Scholar 

  8. A. V. Temnykh, Yu. N. Tokarev, V. V. Mel’nikov, and Yu. A. Zagorodnyaya, “Diurnal dynamics and vertical distribution of pelagic Copepoda in open waters of southwestern Crimea (Black Sea) in autumn of 2010,” Morsk. Ekol. Zh. 11(2), 75–84 (2012).

    Google Scholar 

  9. G. A. Finenko, G. I. Abolmasova, N. A. Datsyk, and B. E. Anninsky, “Mnemiopsis leidyi: nutrition rate of sea walnuts in a sea and food burden on zooplankton,” Morsk. Ekol. Zh. 9(1), 73–83 (2010).

    Google Scholar 

  10. G. A. Finenko, Z. A. Romanova, G. I. Abolmasova, B. E. Anninsky, T.V. Pavlovskaya, L. Bat, and A. Kideys, “Ctenophores invaders and their role in the trophic dynamics of the planktonic community in the coastal regions off the Crimean coasts of the Black Sea (Sevastopol Bay),” Okeanologiya (Moscow, Russ. Fed.) 46(4), 472–482 (2006).

    Google Scholar 

  11. E. A. Shushkina and G. N. Arnautov, “Jellyfish Aurelia found in the Black Sea plankton in May 1984,” in Current Condition of the Black Sea Ecosystem, Ed. by M. E. Vinogradov and M. V. Flint (Nauka, Moscow, 1987), pp. 186–196.

    Google Scholar 

  12. E. A. Shushkina and M. E. Vinogradov, “Changes in plankton communities of open waters of the Black Sea affected by Mnemiopsis (1978–1989),” in Variability of the Black Sea Ecosystem Caused by Natural and Anthropogenic Factors, Ed. by M. E. Vinogradov (Nauka, Moscow, 1991), pp. 248–262.

    Google Scholar 

  13. E. A. Shushkina and E. I. Musaeva, “A role of jellyfishes in activity of plankton communities in the Black Sea,” Okeanologiya (Moscow, Russ. Fed.) 23(1), 125–130 (1983).

    Google Scholar 

  14. B. E. Anninsky, “Organic composition and ecological energetics of jellyfish Aurelia aurita L. (Cnidaria, Scyphozoa) under the Black Sea conditions,” in Trophic Relationships and Food Supply of Heterotrophic Animals in the Pelagic Ecosystem of the Black Sea, Ed. by G. E. Shulman, et al. (Black Sea Comm. Publ., Istanbul, 2009), pp. 99–160.

    Google Scholar 

  15. B. E. Anninsky, A. E. Kideys, Z. A. Romanova, et al., “The ecological and physiological state of the ctenophore Mnemiopsis leidyi (Agassiz) in the Black Sea in autumn 1996,” in Ecosystem Modeling as a Management Tool for the Black Sea, Ed. by L. I. Ivanov, T. Oguz et al. (Kluwer, Dordrecht, 1998), Vol. 1, pp. 249–262.

    Google Scholar 

  16. K. Barz and H.-J. Hirche, “Seasonal development of scyphozoa medusae and predatory impact of Aurelia aurita on the zooplankton community in the Bornholm Basin (central Baltic Sea),” Mar. Biol. 147, 465–476 (2005).

    Article  Google Scholar 

  17. G. A. Finenko, B. E. Anninsky, G. I. Abolmasova, et al., “Functional role of the ctenophores-invaders Mnemiopsis leidyi Agassiz and Beroe ovata Mayer in inshore planktonic communities,” in Trophic Relationships and Food Supply of Heterotrophic Animals in the Pelagic Ecosystem of the Black Sea, Ed. G. E. Shulman, et al. (Black Sea Comm. Publ., Istanbul, 2009), pp. 161–221.

    Google Scholar 

  18. L. J. Hansson, O. Moeslund, T. Kiørboe, and H. U. Riisgärd, “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 (2005)

    Article  Google Scholar 

  19. A. E. Kideys and Z. A. Romanova, “Distribution of gelatinous macrozooplankton in the southern Black Sea during 1996–1999,” Mar. Biol. 139, 535–547 (2001).

    Article  Google Scholar 

  20. A. Malej, V. Turk, D. Lučić, and A. Benović, “Direct and indirect trophic interactions of Aurelia sp. (Scyphozoa) in stratified marine environment (Mljet Lakes, Adriatic Sea),” Mar. Biol. 151, 827–841 (2006).

    Article  Google Scholar 

  21. H. Möller, “Scyphomedusae as predators and food competitors of larval fish,,” Meeresforsch. 28, 90–100 (1980).

    Google Scholar 

  22. E. Mutlu, “Distribution and abundance of cteno-phores, and their zooplankton food in the Black Sea. II. Mnemiopsis leidyi,” Mar. Biol. 135, 603–613 (1999).

    Article  Google Scholar 

  23. E. Mutlu, F. Bingel, A. C. Gücü, et al., “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 (1994).

    Article  Google Scholar 

  24. B. Öztürk, V. Mihneva, and T. V. Shiganova, “First records of Bolinopsis vitrea (L. Agassiz, 181860) (Ctenophora: Lobata) in the Black Sea,” Aquat. Invasion 6(3), 355–360 (2011).

    Article  Google Scholar 

  25. J. E. Purcell, “Climate effects on formation of jellyfish and ctenophore blooms,” J. Mar. Biol. Assoc. UK 85, 461–476 (2005).

    Article  Google Scholar 

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

    Article  Google Scholar 

  27. A. J. Richardson, A. Bakun, G. C. Hays, and M. J. Gibbons, “The jellyfish joyride: causes, consequences and management responses to a more gelatinous future,” Trends Ecol. Evol. 24(6), 312–322 (2009).

    Article  Google Scholar 

  28. T. A. Shiganova, J. V. Bulgakova, S. P. Volovik, et al., “A new invader, Beroe ovata Mayer 1912 and its effect on the ecosystems of the Black and Azov seas,” Hydrobiologia 451, 187–197 (2001).

    Article  Google Scholar 

  29. D. Stoecker, A. E. Michaels, and L. H. Davies, “Grazing by the jellyfish, Aurelia aurita, on microzooplankton,” J. Plankton Res. 9, 901–915 (1987).

    Article  Google Scholar 

  30. B. K. Sullivan, J. R. Garcia, and G. Klein-MacPhee, “Prey selection by the scyphomedusan predator Aurelia aurita,” Mar. Biol. 121, 335–341 (1994).

    Article  Google Scholar 

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Correspondence to B. E. Anninsky.

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Original Russian Text © B.E. Anninsky, G.A. Finenko, N.A. Datsyk, S.M. Ignatyev, 2013, published in Okeanologiya, 2013, Vol. 53, No. 6, pp. 758–768.

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Anninsky, B.E., Finenko, G.A., Datsyk, N.A. et al. Gelatinous macroplankton in the Black Sea in the autumn of 2010. Oceanology 53, 676–685 (2013). https://doi.org/10.1134/S0001437013060015

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