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Distribution of macrozoobenthos in an Arctic estuary (Pechora Bay, SE Barents Sea) during the spring flood period

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Abstract

Pechora Bay, located in the permafrost area of the Russian European Arctic, is characterised by highly variable environments due to its shallowness, complex system of water currents, and extensive freshwater input. The results of several benthic surveys carried out in the 1990s showed the stability of distribution of macrozoobenthos in summer. The aim of this study is to assess the status and distribution of the macrozoobenthos during the spring flood period, when the volume of the Pechora River discharge shows a 5- to 7-fold increase, and to determine the relationship of macrozoobenthos distribution to environmental factors. The intensive river runoff provokes ice scouring of the bottom sediments in shallow areas, causing low species richness, abundance and biomass. It was found that estuarine species spread to the entrance of the bay in flood time but the dominant species in five determined communities remain stable. The strongest driver for species richness and biomass is sediment granulometric composition. Shannon diversity (H′) negatively correlated with the organic matter content of the sediments. Assessing the status of the macrozoobenthos showed that it is slightly disturbed only in the small area close to the Pechora River mouth, influenced both by ice scouring and enormous freshwater discharge.

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References

  • Andersin AB, Lassig J, Sandler H (1984) On the biology and production of Pontoporeia affinis Lindstr. in the Gulf of Bothnia. Limnology 15:395–401

    Google Scholar 

  • Beukema JJ (1988) An evolution of ABC-Method (Abundance-Biomass Comparison) as applied to macrobenthic communities living in tidal flats in the Dutch Wadden Sea. Mar Biol 99:425–433

    Article  Google Scholar 

  • Biryukov VYu, Ogorodov SA (2005) Bathymetry-based seafloor morphology of the Pechora Sea. Ber Polarforsch Meeresforsch 501:85–90

    Google Scholar 

  • Borja A, Franco J, Perez V (2000) A marine biotic index to establish the ecological quality of bottom benthos within European estuarine and coastal environments. Mar Pollut Bull 40:1100–1114

    Article  CAS  Google Scholar 

  • Borja A, Aguirrezabalaga F, Martinez J, Sola JC, Garcıa-Arberas L, Gorostiaga JM (2004) Benthic communities, biogeography and resources management. In: Borja A, Collins M (eds) Oceanography and Marine Environment of the Basque Country, Elsevier Oceanography Series, 70. Elsevier, Amsterdam, pp 455–492

    Chapter  Google Scholar 

  • Bray RJ, Curtis JT (1957) An ordination of the upland forest communities of southern Wisconsin. Ecol Monogr 27:325–349

    Article  Google Scholar 

  • Brey T (1990) Estimating productivity of macrobenthic invertebrates from biomass and mean individual weight. Meeresforschung 32:329–343

    Google Scholar 

  • Brown TM, Edinger EN, Hooper RG, Belliveau K (2011) Benthic Marine fauna and flora of two nearshore coastal locations in the western and central Canadian Arctic. Arctic 64:281–301

    Article  Google Scholar 

  • Burkovskiy IV, Stolyarov AP, Kolobov MYu (2002) Spatial organization and functioning of the marine (estuarine) littoral ecosystem. Biol Bull Rev 122:316–325 (In Russian)

    Google Scholar 

  • Chertoprud MV, Udalov AA, Stolyarov AP, Borisov RR (2004) Diversity of macrobenthic communities in the White Sea estuaries. Oceanology 44:845–855

    Google Scholar 

  • Clarke KR (1990) Comparison of dominance curves. J Exp Mar Biol Ecol 138:143–157

    Article  Google Scholar 

  • Conlan KE, Lenihan NS, Kvitek RG, Oliver JS (1998) Ice scour disturbance to benthic communities in the Canadian High Arctic. Mar Ecol Prog Ser 166:1–16

    Article  Google Scholar 

  • Conlan K, Aitken A, Hendrycks E, McClelland Ch, Melling H (2008) Distribution patterns of Canadian Beaufort Shelf macrobenthos. J Mar Syst 74:864–886

    Article  Google Scholar 

  • Czekanowski J (1909) Zur differential Diagnose der Neandertalgruppe. Korrespbl Dtsch Ges Anthropol 40:44–47

    Google Scholar 

  • Dauer DM, Llanso RJ, Lane MF (2008) Depth–related patterns in benthic community condition along an estuarine gradient in Chesapeake Bay, USA. Ecol Ind 8:417–424

    Article  Google Scholar 

  • Denisenko SG (2006) Shannon’s information measure and its use for biodiversity assessment (as exemplified by marine macrozoobenthos). In: Sirenko BI, Vasilenko SV (eds) Marine invertebrates of Arctic, Antarctic, and sub-Antarctic. Explorations of the fauna of the seas, 56(64), ZIN RAS, St. Petersburg, pp 35–46 (In Russian)

    Google Scholar 

  • Denisenko NV (2009) Composition and distribution of sublittoral macrozoobenthos in Kemskaya Bay of the White Sea. Oceanology 49:788–800

    Article  Google Scholar 

  • Denisenko NV (2010) The description and prediction of benthic biodiversity in high arctic and freshwater-dominated marine areas: the southern Onega Bay (the White Sea). Mar Pollut Bull 61:224–233

    Article  CAS  PubMed  Google Scholar 

  • Denisenko SG (2013) Biodiversity and bioresources of macrozoobenthos in the Barents Sea. Nauka, Staint Petersburg (In Russian)

    Google Scholar 

  • Denisenko NV, Denisenko SG (1990) Biomass, density of populations and their contribution in productivity of bottom communities. In: Anonymous (ed) Problems of nature preservation in the northern areas. Abstracts of Lectures of All Union Science Conference of Young Scientists and Specialists. Apatity, 29–30 Jan 1990. KSC USSR Academy of Science, Murmansk, pp 53–54 (In Russian)

  • Denisenko S, Sandler H, Denisenko N, Rachor E (1999) Current state in two estuarine bays of the Barents and Kara Seas. ECES J Mar Sci 56(Suppl):187–193

    Article  Google Scholar 

  • Denisenko SG, Denisenko NV, Lehtonen KK, Andersin A-B, Laine AO (2003a) Macrozoobenthos of the Pechora Sea (SE Barents Sea): community structure and spatial distribution in relation to environmental conditions. Mar Ecol Prog Ser 258:109–123

    Article  Google Scholar 

  • Denisenko NV, Rachor E, Denisenko SG (2003b) Benthic fauna of the southern Kara Sea. In: Stein R, Fahl K, Fütterer DK, Galimov EM, Stepanets OV (eds) Siberian River Runoff in the Kara Sea: characterization, quantification variability and environmental significance. Proceedings in Marine Science. Elsevier, Amsterdam, pp 213–236

    Google Scholar 

  • Denisenko NV, Denisenko SG, Frolov AA (2006) Zoobenthos of the Gorlo and Voronka Straits of the White Sea: composition and distribution patterns in the coastal areas of the Kola Peninsula. In: Sirenko BI, Vasilenko SV (eds) Marine invertebrates of the Arctic, Antarctic and sub-Antarctic. Explorations of the fauna of the seas, ZIN RAS, St-Petersburg, pp 15-36 (In Russian)

    Google Scholar 

  • Denisenko NV, Denisenko SG, Lehtonen K, Andersin A-B, Sandler H (2007) Macrozoobenthos of the Cheshskaya bay (southeastern Barents Sea) spatial distribution and community structure in relation to environmental factors. Polar Biol 30:735–746

    Article  Google Scholar 

  • Denisenko SG, Barbashova MA, Skvortsov VV, Belyakov VP, Kurashov EI (2013) The Results of an assessment of the ecological state of zoobenthos communities according to the difference of evenness index. Inland Water Biol 1:46–55

    Google Scholar 

  • Dorovskikh GN, Stepanov VG (2015) Parasite fauna and the structure of parasites component communities of the minnow Phoxinus phoxinus (Linneus, 1758) in conditions of oil pollution of waterstream. Parazitologia 49:412–427 (In Russian)

    CAS  PubMed  Google Scholar 

  • Dunton KH, Schonberg SV, Cooper LW (2012) Food web of the Alaskan nearshore shelf and estuarine lagoons of the Beaufort Sea. Estuar Coasts 35:416–435

    Article  CAS  Google Scholar 

  • Elliott M, Kingston PF (1987) The sublittoral benthic fauna of the estuary and Firth of Forth, Scotland. In: McLusky DS (ed) The natural environment of the estuary and Firth of Forth. Proc R Soc Edin B 93(3/4), pp 449–466

    Google Scholar 

  • Elliott M, McLusky DS (2002) The need for definition in understanding estuaries. Estuar Coast Shelf Sci 55:815–827

    Article  Google Scholar 

  • Elliott M, Quintino VM (2007) The estuarine quality paradox, environmental homeostasis and the difficulty of detecting anthropogenic stress in naturally stressed areas. Mar Pollut Bul 54:640–645

    Article  CAS  Google Scholar 

  • Elliott M, Burdon D, Hemingway KL, Apitz SE (2007) Estuarine, coastal and marine ecosystem restoration: confusing management and science – a revision of concepts. Estuar Coast Shelf Sci 74:349–366

    Article  Google Scholar 

  • Golikov AN, Scarlato OA, Averintsev BG, Menshutkina TV, Novikov OK, Sheremetevskiy AM (1990) Ecosystems of the New Siberian Shoal, their distribution and functioning. In: Golikov AN (ed) Ecosystems of the New Siberian Shoal and the fauna of the Laptev Sea and adjacent waters. Explorations of the fauna of the seas 37(45). Nauka, Leningrad, pp 4-79 (In Russian)

    Google Scholar 

  • Golikov AN, Anisimova NA, Golikov AA, Denisenko NV, Kaplina TV, Menshutkin VV, Menshutkina TV, Novikov OK, Panteleeva NN, Frolova EA (1993) Bottom communities and biocenoses of the Yarnyshnaya Inlet and their seasonal dynamic. Kola Science Center of Russian Academy of Sciences, Apatity (In Russian)

    Google Scholar 

  • Gordeev VV (2000) River input of water, sediment, major ions, nutrients and trace metals from Russian territory to the Arctic Ocean. In: Lewis EL (ed) Freshwater budget of the Arctic Ocean. Kluwer, Dordrecht, pp 297–322

    Chapter  Google Scholar 

  • Gordeev VV, Rachold V (2003) River input. In: Stein R, McDonald RW (eds) Organic carbon cycle in the Arctic Ocean: present and past. Springer, Berlin, pp 33–41

    Google Scholar 

  • Grall J, Glémarec M (1997) Using biotic indices to estimate macrobenthic community perturbations in the Bay of Brest. Estuar Coast Shelf Sci 44:43–53

    Article  Google Scholar 

  • Gray JS, Elliott M (2009) Ecology of marine sediments: science to management, 2nd edn. Oxford University Press, Oxford

    Google Scholar 

  • Grönlund L, Kuznetsov L, Druzhkov N (1996) Hydrography, water chemistry, plankton production and plankton species composition in the Pechora Bay in 1995. Pechora Bay ecological study in1995. Finnish-Russian offshore technology work group, Helsinki, pp 3–35

    Google Scholar 

  • Hemmingsen AM (1960) Energy metabolism as relation to body size and respiratory surface, and its evolution. Reports Steno Memorial Hospital 13, Copenhagen, pp 1–110

  • Herman PMJ, Middelburg JJ, Van De Koppel J, Heip CHR (1999) Ecology of estuarine macrobenthos. Adv Ecol Res 29:195–240

    Article  Google Scholar 

  • Hummel H, Bogaards R, Bek T, Polishchuk L, Amiard Triquet C, Bachelet G, Desprez M, Strelkov P, Sukhotin A, Naumov A, Dahle S, Denisenko S, Gantsevich M, Sokolov K, de Wolf L (1997) Sensitivity to stress in the bivalve Macoma balthica from the most northern (Arctic) to the most southern (French) populations: low sensitivity in Arctic populations because of genetic adaptations. Hydrobiology 355:127–138

    Article  Google Scholar 

  • Hummel H, Günther C-P, Bogaards RH, Fedyakov V (1998) Variation in genetic traits of the Baltic clam Macoma balthica from a tidal gradient in the subarctic. Polar Biol 19:342–347

    Article  Google Scholar 

  • Hyland JL, Balthis WL, Rosey M, Hackney CT, Alphin TD (2004) The soft bottom macrobenthos of North Carolina estuaries. Estuary 27:501–514

    Article  Google Scholar 

  • Jorgensen LL, Pearson TH, Anisimova NA, Gulliksen B, Dahle S, Denisenko S, Matishov GG (1999) Environmental influence on benthic fauna associations of the Kara Sea (Arctic Russia). Polar Biol 22:395–416

    Article  Google Scholar 

  • Josefson AB, Hansen JLS (2004) Species richness of benthic macrofauna in Danish estuaries and coastal areas. Global Ecol Biogeogr 13:273–288

    Article  Google Scholar 

  • Kozlovskiy VV, Chikina MV, Kucheruk NV, Basin AB (2011) Structure of the macrozoobenthic communities in the southwestern Kara Sea. Oceanology 51:1072–1081

    Article  Google Scholar 

  • Krebs CJ (1999) Ecological methodology. 2nd ed. Harper & Row, New York

    Google Scholar 

  • Kucheruk NV, Mokievskiy VO, Denisov NE (1998) Macrobenthos of the coastal shallow zone in the southwestern part of the Kara Sea. Oceanology 38:86–94 (In Russian)

    Google Scholar 

  • Kuznetsov AP (1984) Ecology of the bottom communities of shelf zones of the World Ocean (trophic structure of marine bottom fauna). Nauka, Moscow (In Russian)

    Google Scholar 

  • Magurran AE (1988) Ecological diversity and its measurement. Croom Helm, London

    Book  Google Scholar 

  • Magurran AE (2004) Measuring biological diversity. Blackwell, Malden

    Google Scholar 

  • McLusky DS, Elliott M (2004) The estuarine ecosystems. Ecology, threats and management. Oxford University Press, Oxford

    Book  Google Scholar 

  • McManus JW, Pauly D (1990) Measuring ecological stress: variations on a theme by R.M.Warwick. Mar Biol 106:305–308

    Article  Google Scholar 

  • Muniz P, Venturini N, Pires-Vanin AMS, Tommasi LR, Borja A (2005) testing the applicability of a marine biotic index (AMBI) to assessing the ecological quality of soft-bottom benthic communities, in the South America Atlantic region. Mar Pollut Bull 50:624–637

    Article  CAS  PubMed  Google Scholar 

  • Muxika I, Borja A, Bald J (2007) Using historical data, expert judgment and multivariate analysis in assessing reference conditions and benthic ecological status, according to the European Water Framework Directive. Mar Pollut Bull 55:19–31

    Article  CAS  Google Scholar 

  • Naumov AD (2013) Long-term fluctuations of soft-bottom intertidal community structure affected by ice cover at two small sea bights in the Chupa Inlet (Kandalaksha Bay) of the White Sea. Hydrobiology 706:159–173

    Article  Google Scholar 

  • Ogorodov SA (2005) The role of sea ice in coastal and sea bottom dynamics of the Pechora Sea. Ber Polarforsch Meerforsch 501:113–124

    Google Scholar 

  • Palmer TA, Montagna PA, Pollack JB, Kalke RD, DeYoe HR (2011) The role of freshwater inflow in lagoons, rivers, and bays. Hydrobiology 667:49–67

    Article  CAS  Google Scholar 

  • Pearson TH, Rosenberg R (1978) Macrobenthic succession in relation to organic enrichment and pollution of the marine environment. Oceanogr Mar Biol Ann Rev 16:229–311

    Google Scholar 

  • Pesenko YA (1982) Rules and methods of quantitative analysis in faunistic investigations. Nauka, Moscow (In Russian)

    Google Scholar 

  • Petrova VI, Batova GI, Galishev MA, Ivanov GI (1999) The Pechora Bay, an experience of geoanalitical monitoring. Oceanology 39:539–547 (In Russian)

    CAS  Google Scholar 

  • Pielou ES (1984) The interpretation of ecological data. Wiley, New York

    Google Scholar 

  • Pogrebov VB, Kiyko OA, Stogov IA, Chernova NV (2003) Composition, structure and multi-years dynamic of the Pechora Bay ecosystem. Selected papers of the seminar in Narian-Mar, 16–19 Sept. Narian-Mar, pp 36–39 (In Russian)

  • Polonsky VF (2012) Influence of tidal cycles on re-distribution of fresh water discharge in delta of the Pechora River. Arctic 2:20-27 (In Russian)

    Google Scholar 

  • Puente A, Diaz RJ (2008) Is it possible to assess the ecological status of highly stressed natural estuarine environments using macro invertebrates indices? Mar Pollut Bull 56:1880–1889

    Article  CAS  PubMed  Google Scholar 

  • Remane A (1934) Die Brackwasserfauna. Verh Dtsch Zool Ges 36:34–74

    Google Scholar 

  • Romankevich EA, Vetrov AA (2001) Carbon cycle in the Arctic seas of Russia. Nauka, Moscow (In Russian)

    Google Scholar 

  • Rosenberg R, Loo L-O, Möller P (1992) Hypoxia, salinity and temperature as structuring factors for marine benthic communities in a eutrophic area. Neth J Sea Res 30:121–129

    Article  Google Scholar 

  • Sanders HL (1968) Marine benthic diversity: a comparative study. Am Nat 102:243–282

    Article  Google Scholar 

  • Savel’yeva CP, Potanin VA, Pavlov BK, Savchenko EM (1987) To study of water dynamic in the Pechora Bay of the Barents Sea. In: Study of the hydrometeorological regime of the Northern Seas. Proc AARI. Gidrometeoizdat, Leningrad, pp 97–105 (In Russian)

  • Shannon CE (1948) The mathematical theory of communication. University of Illinois Press, Urbana

    Google Scholar 

  • Sørensen T (1948) A method of establishing groups of equal amplitude in plant sociology based on similarity of species and its application to analyses of the vegetation on Danish commons. Kngl Dan Videnskab Selskab, Biol Skr 5:1–34

    Google Scholar 

  • Terziev FS, Zatuchnaya BM, Shevchenko AV, Vlasenko PV, Berezina ON (eds) (1992) Hydrochemical and oceanographic basics of forming of biological productivity. Gidrometizdat, St Petersburg (In Russian)

    Google Scholar 

  • Tscharntke T, Tylianakis JM, Rand TA, Didham RK, Fahrig L, Batáry P, Bengtsson J, Clough Y, Crist TO, Dormann CF, Ewers RM, Fründ J, Holt RD, Holzschuh A, Klein AM, Kleijn D, Kremen C, Landis DA, Laurance W, Lindenmayer D, Scherber C, Sodhi N, Steffan-Dewenter I, Thies C, van der Putten WH, Westphal C (2012) Landscape moderation of biodiversity patterns and processes—eight hypotheses. Biol Rev 87:661–685

    Article  PubMed  Google Scholar 

  • Umnov AA, Alimov AF (1979) The ratio of production to the total energy flow through the population. In: Vinberg GG (ed) General basis for the study of aquatic ecosystems. Nauka, Leningrad, pp 133–139 (In Russian)

    Google Scholar 

  • Varushkina TS (1967) Benthos of the Korovinskaya Inlet. Proceedings of fishery research in the Northern basin, 9. PINRO, Murmansk, pp 42–51 (In Russian)

  • Vedenin A, Galkin SV, Kozlovskiy VV (2015) Macrobenthos of the Ob Bay and adjacent Kara Sea shelf. Polar Biol 38:829–844

    Article  Google Scholar 

  • Vilenkin BYa, Vilenkina MN, (1979) Respiration of aquatic invertebrates. In: Zaika VE (ed) Results of science and technology. Ser. Zoology, Moscow, pp 125–143 (In Russian)

    Google Scholar 

  • Warwick RM (1986) A new method for detecting pollution effects on marine macrobenthos communities. Mar Biol 92:557–562

    Article  Google Scholar 

  • Warwick RM, Pearson TH, Ruswahyuni H (1987) Detection of pollution effects on marine macrobenthos: further evaluation of the species abundance biomass method. Mar Biol 95:193–200

    Article  Google Scholar 

  • Weisberg SB, Ranasinghe JA, Dauer DM, Schaffner LC, Diaz RJ, Frithsen JB (1997) An estuarine benthic index of biotic integrity (B-IBI) for the Chesapeake Bay. Estuaries 20:149–158

    Article  Google Scholar 

  • Whitfield AK, Elliott M, Basset A, Blaber SJM, West RJ (2012) Paradigms in estuarine ecology—a review of the Remane diagram with a suggested revised model for estuaries. Estuar Coast Shelf Sci 97:78–90

    Article  Google Scholar 

  • Włodarska-Kowalczuk M, Renaud PE, Wesławski JM, Cochrane SKJ, Denisenko SG (2012) Species diversity, functional complexity and rarity in Arctic fjordic versus open shelf benthic systems. Mar Ecol Prog Ser 463:73–87

    Article  Google Scholar 

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Acknowledgements

The authors are grateful to the administration and scientists of the Murmansk Marine Biological Institute RAS for support in the organisation of expeditions and species identification of polychaetes, crustaceans and echinoderms. Mr. Henrik Sandler is gratefully thanked for help in sampling. The authors are also thankful to Dr. Mayya Gogina and two anonymous reviewers for their constructive comments and suggestions. The main part of the study was financed by the Neste Oil Company (now Fortum), Finland, and the Ministry of Education and Science of the Russian Federation (N AAAA-A17–117030310207-3), and the Program of Russian Academy of Sciences ‘Fundamental Research to the Development of the Arctic’ (Project ‘Biodiversity and vulnerability of the Pechora Sea ecosystems’).

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  1. Zoological Institute, Russian Academy of Sciences, Universitetskaya emb. 1, St.-Petersburg, Russia, 199034

    N. V. Denisenko & S. G. Denisenko

  2. Marine Research Centre, Finnish Environment Institute, Agnes Sjöbergin katu 2, 00790, Helsinki, Finland

    K. K. Lehtonen

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This article belongs to the special issue on the "Ecology of the Pechora Sea", coordinated by Alexey A. Sukhotin.

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Denisenko, N.V., Denisenko, S.G. & Lehtonen, K.K. Distribution of macrozoobenthos in an Arctic estuary (Pechora Bay, SE Barents Sea) during the spring flood period. Polar Biol 42, 1667–1684 (2019). https://doi.org/10.1007/s00300-018-02452-6

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