Abstract
The species distribution of heterotrophic flagellates has been investigated in accordance with the zonation of the White Sea silty-sandy intertidal flat. In Gryaznaya Bay of the Chernaya River Estuary (Kandalaksha Bay), 64 species and forms of flagellates have been identified. Three species (Ploeotia tenuis, Salpingoeca tuba, and Thecamonas trahens) are newly recorded for the White Sea. The species diversity, abundance, and biomass of heterotrophic flagellates were the highest in the upper and lower littoral horizons, as compared to the middle littoral and transitional zones. The species composition and community structure of heterotrophic flagellates depend on the local combinations of salinity and Eh rather than on the littoral zone and related sediments and the type and amount of organic material. The heterotrophic flagellate community within the intertidal zone has been subdivided into three groups: 1) species preferring biotopes of higher salinity at lower and upper boundaries of the mid intertidal zone, 2) species tending to silty sediments of the upper intertidal zone with lower salinity and Eh, and 3) species preferring the well-aerated slightly silted sands of the lower intertidal zone.
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A. I. Azovsky, I. V. Burkovsky, M. Yu. Kolobov, M. V. Chertoprud, N. V. Kucheruk, F. V. Sapozhnikov, A. A. Udalov, and M. A. Saburova, “Self-similar properties of the spatial structure of intertidal macroand microbenthic communities,” Zh. Obshch. Biol. 68 (3), 180–194 (2007).
A. I. Azovsky and Yu. A. Mazei, “Structure of subtidal and intertidal communities of psammophilous ciliates of the Pechora Sea,” Oceanology (Engl. Transl.) 47 (1), 60–67 (2007).
I. V. Burkovsky, Structure, Functions, and Stability of Marine Bottom Communities (Moscow State University, Moscow, 1992) [in Russian].
I. V. Burkovsky, Marine Biogeocenology. Structure of Communities and Ecosystems (KMK, Moscow, 2006) [in Russian].
I. V. Burkovsky and D. E. Aksenov, “Structure of community of marine psammophilous ciliates in different spatial scale studies,” Usp. Sovrem. Biol. 116 (2), 218–230 (1996).
I. V. Burkovskii, A. S. Esaulov, and Y. A. Mazei, “Influence of the period of existence of a biotope on the formation of the species structure of a marine psammophilous ciliate community,” Russ. J. Mar. Biol. 37 (3), 177–184 (2011).
I. V. Burkovsky, A. P. Stolyarov, and M. Yu. Kolobov, “Spatial heterogeneity of macrobenthic structure of the sand-silty littoral of the White Sea,” Usp. Sovrem. Biol. 117 (4), 466–479 (1997).
M. Yu. Kolobov and I. V. Burkovsky, “Microspatial organization of Priapulus caudatus and Halicriptus spinulosus (Priapulida) populations in a tidal gradient,” Zool. Zh. 81 (12), 1439–1447 (2002).
Yu. A. Mazei, D. V. Tikhonenkov, and A. P. Myl’nikov, “The species structure of a community and abundance of heterotrophic flagellates in small freshwater bodies,” Zool. Zh. 84 (9), 1027–1041 (2005).
Yu. A. Mazei and D. V. Tikhonenkov, “Heterotrophic flagellates in the littoral and sublittoral zones of the southeast part of the Pechora Sea,” Oceanology (Engl. Transl.) 46 (3), 368–375 (2006).
M. A. Saburova, I. V. Burkovsky, and I. G. Polikarpov, “Spatial distribution of microphytobenthos on the sand littoral of the White Sea,” Usp. Sovrem. Biol. 111 (6), 882–889 (1991).
A. P. Stolyarov, I. V. Burkovsky, and A. A. Udalov, “Spatial structure and energy flows in the ecosystem of sandy-silty littoral of the White Sea,” Usp. Sovrem. Biol. 125 (Ç), 274–290 (2005).
D. V. Tikhonenkov and Yu. A. Mazei, “Distribution of heterotrophic flagellates at the littoral of estuary of Chernaya River (Kandalaksha Bay, White Sea),” Russ. J. Mar. Biol. 32 (5), 276–283 (2006).
D. V. Tikhonenkov and Yu. A. Mazei, “Spatial structure of communities of heterotrophic flagellates from a sphagnum bog,” Zh. Obshch. Biol. 70 (1), 78–93 (2009).
D. V. Tikhonenkov and Yu. A. Mazei, “Distribution of benthic heterotrophic flagellates along salinity gradient: correlation between active and cryptic species diversity in the White Sea estuary,” Usp. Sovrem. Biol. 133 (2), 178–190 (2013).
D. V. Tikhonenkov, Yu. A. Mazei, and E. A. Embulaeva, “Degradation succession of heterotrophic flagellate communities in microcosms,” Zh. Obshch. Biol. 69 (1), 57–64 (2008).
S. M. Adl, A. G. B. Simpson, M. A. Farmer, et al., “The new higher level classification of eukaryotes with emphasis on the taxonomy of protists,” J. Eukaryotic Microbiol. 52, 399–432 (2005).
F. Azam, T. Fenchel, J. G. Field, et al., “The ecological role of water-column microbes in the sea,” Mar. Ecol.: Progr. Ser. 10, 257–263 (1983).
A. I. Azovsky, “Species-area and species-sampling effort relationships: disentangling the effects,” Ecography 34, 18–30 (2011).
A. I. Azovsky, E. S. Chertoprood, M. A. Saburova, and I. G. Polikarpov, “Spatio-temporal variability of microand meiobenthic communities in a White Sea intertidal sandflat,” Estuarine, Coastal Shelf Sci. 60, 663–671 (2004).
A. I. Azovsky, M. A. Saburova, D. V. Tikhonenkov, et al., “Composition, diversity, and distribution of microbenthos across the intertidal zones of the Ryazhkov Island (the White Sea),” Eur. J. Protistol. 49, 500–515 (2013).
T. Cavalier-Smith, “Flagellates megaevolution. The basis for eukaryote diversification,” in The Flagellates: Unity, Diversity, and Evolution (Taylor and Francis, London, 2000), pp. 316–239.
K. Clarke, “Non-parametric multivariate analyses of changes in community structure,” Aust. J. Ecol. 18, 117–143 (1993).
K. Clarke and R. Gorley, PRIMER v. 6: User Manual/Tutorial (PRIMER-E, Plymouth, 2006).
K. Clarke and R. Warwick, Change in Marine Communities: An Approach to Statistical Analysis and Interpretation, 2nd ed. (PRIMER-E, Plymouth, 6).
T. Crist and J. Veech, “Additive partitioning of rarefaction curves and species-area relationships: unifying alpha-, beta-, and gamma-diversity with sample size and habitat area,” Ecol. Lett. 9, 923–932 (2006).
T. Crist, J. Veech, and J. Gering, “Partitioning species diversity across landscapes and regions: a hierarchical analysis of alpha, beta, and gamma diversity,” Am. Nat. 162, 734–743 (2003).
I. Domaizon, S. Viboud, and D. Fontvieille, “Taxonspecific and seasonal variations in flagellates grazing on heterotrophic bacteria in the oligotrophic Lace Annecy–importance of mixotrophy,” FEMS Microbiol. Ecol. 46, 317–329 (2003).
T. Fenchel, “Flagellate design and function,” in The Biology of Free-Living Heterotrophic Flagellates (Clarendon, Oxford, 1991), pp. 7–19.
T. Fenchel, C. Bernard, G. Esteban, et al., “Microbial diversity and activity in a Danish fjord with anoxic deep water,” Ophelia 43 (1), 45–100 (1995).
O. Hammer, D. A. T. Harper, and P. D. Ryan, “PAST: Palaeontological Statistics software package for education and data analysis,” Palaeontol. Electron. 4 (1), art. 4 (2001). http://palaeo-electronica.org/2001-1/ past/issue1-01.htm
Yu. Mazei, “Biodiversity patterns in protozoan communities: linking processes and scales,” Protistology 5, 268–280 (2008).
M. A. Saburova, I. G. Polikarpov, and I. V. Burkovsky, “Spatial structure of an intertidal sandflat microphytobenthic community as related to different spatial scales,” Mar. Ecol.: Progr. Ser. 129, 214–232 (1995).
D. V. Tikhonenkov, Yu. A. Mazei, and A. P. Mylnikov, “Species diversity of heterotrophic flagellates in the White Sea littoral sites,” Eur. J. Protistol. 42, 191–200 (2006).
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Original Russian Text © D.V. Tikhonenkov, I.V. Burkovsky, Yu.A. Mazei, 2015, published in Okeanologiya, 2015, Vol. 55, No. 5, pp. 787–800.
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Tikhonenkov, D.V., Burkovsky, I.V. & Mazei, Y.A. Is there a relation between the distribution of heterotrophic flagellates and the zonation of a marine intertidal flat?. Oceanology 55, 711–723 (2015). https://doi.org/10.1134/S0001437015050173
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DOI: https://doi.org/10.1134/S0001437015050173