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The effect of estuarine system on the meiofauna and nematodes in the East Siberian Sea

  • 1.

    Stein, R. & Macdonald, R. W. Organic carbon budget: Arctic Ocean vs. global ocean. In The Organic Carbon Cycle in the Arctic Ocean (eds Stein, R. & Macdonald, R. W.) (Springer, 2004).

    Chapter 

    Google Scholar 

  • 2.

    Barber, D. G. & Massom, R. A. The role of sea ice in Arctic and Antarctic polynyas. Oceanogr. Ser. 74, 1–54. https://doi.org/10.1016/S0422-9894(06)74001-6 (2007).

    Article 

    Google Scholar 

  • 3.

    Sheremetevskiy, A. M. Role of meiobenthos of the South Sakhalin shelf, Eastern Kamchatka, and Novosibirsk shallow water area. Issledovaniya Fauny Morei 35, 43 (1987).

    Google Scholar 

  • 4.

    Golikov, A. N. Ecosystems of the New Siberian shoals and fauna of the Laptev Sea and adjacent waters of the Arctic Ocean (in Russian). Explor. Fauna Seas 37, 4 (1990).

    Google Scholar 

  • 5.

    Golikov, A. N. Fauna of the East Siberian Sea. Part III. Explor. Fauna Seas 49, 57 (1994).

    Google Scholar 

  • 6.

    Sirenko, B. I. & Denisenko, S. G. Fauna of the East Siberian Sea, distribution patterns and structure of bottom communities. Explor. Fauna Seas 66, 74 (2010).

    Google Scholar 

  • 7.

    Sirenko, B. I. List of species of free-living invertebrates of Eurasian Arctic seas and adjacent deep waters. Explor. Fauna Seas 51(59), 1–76 (2001).

    Google Scholar 

  • 8.

    Schmidt-Rhaesa, A. Handbook of Zoology: Gastrotricha, Cycloneuralia, Gnathifera Vol. 2, 608 (De Gruyter, 2020).

    Google Scholar 

  • 9.

    Udalov, A. et al. Integrity of benthic assemblages along the arctic estuarine-coastal system. Ecol. Indic. 121, 107115. https://doi.org/10.1016/j.ecolind.2020.107115 (2021).

    Article 

    Google Scholar 

  • 10.

    Portnova, D., Fedyaeva, M., Udalov, A. & Tchesunov, A. Community structure of nematodes in the Laptev Sea shelf with notes on the lives of ice nematodes. Reg. Stud. Mar. Sci. 31, 100757. https://doi.org/10.1016/j.rsma.2019.100757 (2019).

    Article 

    Google Scholar 

  • 11.

    Gallucci, F., Moens, T. & Fonseca, G. Small-scale spatial patterns of meiobenthos in the Arctic deep sea. Mar. Biodivers. 39(1), 9–25. https://doi.org/10.1007/s12526-009-0003-x (2009).

    Article 

    Google Scholar 

  • 12.

    Lei, Y., Stumm, K., Volkenborn, N., Wickham, S. A. & Berninger, U. G. Impact of Arenicola marina (Polychaeta) on the microbial assemblages and meiobenthos in a marine intertidal flat. Mar. Biol. 157(6), 1271–1282. https://doi.org/10.1007/s00227-010-1407-7 (2010).

    Article 

    Google Scholar 

  • 13.

    Flint, M. V., Poyarkov, S. G. & Rymsky-Korsakov, N. A. Ecosystems of the Siberian Arctic Seas-2017 (Cruise 69 of the R/V Akademik Mstislav Keldysh). Oceanology 58(2), 315–318. https://doi.org/10.1134/S0001437018020042 (2018).

    ADS 
    Article 

    Google Scholar 

  • 14.

    Garlitska, L. A. & Azovsky, A. I. Benthic harpacticoid copepods of the Yenisei Gulf and the adjacent shallow waters of the Kara Sea. J. Nat. Hist. 50, 2941–2959. https://doi.org/10.1080/00222933.2016.1219410 (2016).

    Article 

    Google Scholar 

  • 15.

    Portnova, D., Garlitska, L., Udalov, A. & Kondar, D. Meiobenthos and nematode community in the Yenisei Bay and adjacent parts of the Kara Sea shelf. Oceanology 57(1), 1–15. https://doi.org/10.1134/S0001437017010155 (2017).

    Article 

    Google Scholar 

  • 16.

    Carmack, E. et al. Toward quantifying the increasing role of oceanic heat in sea ice loss in the new Arctic. Bull. Am. Meteorol. Soc. 96(12), 2079–2105. https://doi.org/10.1175/BAMS-D-13-00177.1 (2005).

    ADS 
    Article 

    Google Scholar 

  • 17.

    Peterson, B. J. et al. Increasing river discharge to the Arctic Ocean. Science 298(5601), 2171–2173. https://doi.org/10.1126/science.1077445 (2002).

    ADS 
    CAS 
    Article 
    PubMed 

    Google Scholar 

  • 18.

    Polukhin, A. The role of river runoff in the Kara Sea surface layer acidification and carbonate system changes. ERL 14(10), 105007. https://doi.org/10.1088/1748-9326/ab421e (2019).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 19.

    Lisitzin, A. P. Marginal filter of the oceans. Oceanology 34(5), 735–743 (1994).

    CAS 

    Google Scholar 

  • 20.

    Moens, T., Braeckman, U., Derycke, S., Fonseca, G., Gallucci, F., Gingold, R., Guilini, Katja, Ingles, J., Leduc, D., Vanaverbeke, J., Van Colen, C., Vanreusel, A, & Vincx, M. Ecology of free-living marine nematodes. In Volume 2 Nematoda, 109–152. De Gruyter (2013)

  • 21.

    Aller, J. Y. & Aller, R. C. General characteristics of benthic faunas on the Amazon inner continental shelf with comparison to the shelf off the Changjiang River, East China Sea. Cont. Shelf Res. 6(1–2), 291–310. https://doi.org/10.1016/0278-4343(86)90065-8 (1986).

    ADS 
    Article 

    Google Scholar 

  • 22.

    Soetaert, K., Vincx, M., Wittoeck, J. & Tulkens, M. Meiobenthic distribution and nematode community structure in five European estuaries. Hydrobiologia 311(1), 185–206. https://doi.org/10.1007/BF00008580 (1995).

    Article 

    Google Scholar 

  • 23.

    Tank, S. E. et al. The processing and impact of dissolved riverine nitrogen in the Arctic Ocean. Estuaries Coast 35, 401–415. https://doi.org/10.1007/s12237-011-9417-3 (2012).

    CAS 
    Article 

    Google Scholar 

  • 24.

    Galtsova, V. V., Lukina, T. G. & Vladimirov, M. V. Meiobenthos of Chaunskaya Bay, East Siberian Sea. Issledovaniya Fauny Morei 48(56), 67–97 (1994).

    Google Scholar 

  • 25.

    Coull, B. C. Role of meiofauna in estuarine soft‐bottom habitats. Austral Ecol. 24(4), 327–343 (1999).

    Article 

    Google Scholar 

  • 26.

    Vincx, M., Meire, P., & Heip, C. The distribution of nematodes communities in the Southern Bight of the North Sea. Cah Biol Mar. 31(1), 107–129 (1990).

  • 27.

    Vanaverbeke, J., Gheskiere, T., Steyaert, M., & Vincx, M. Nematode assemblages from subtidal sandbanks in the Southern Bight of the North Sea: effect of small sedimentological differences. J. Sea Res. 48(3), 197–207. https://doi.org/10.1016/S1385-1101(02)00165-X (2002)

    ADS 
    Article 

    Google Scholar 

  • 28.

    Steyaert, M., et al. The importance of fine-scale, vertical profiles in characterising nematode community structure. Estuar Coast Shelf Sci. 58(2), 353–366 (2003).

    ADS 
    Article 

    Google Scholar 

  • 29.

    Alves, A. S., Adão, H., Patrício, J., Neto, J. M., Costa, M. J., & Marques, J. C. Spatial distribution of subtidal meiobenthos along estuarine gradients in two southern European estuaries (Portugal). J. Mar. Biol. Assoc. U. K. 89(8), 1529–1540 (2009).

    CAS 
    Article 

    Google Scholar 

  • 30.

    Garlitska, L. A., Chertoprud, E. S., Portnova, D. A. & Azovsky, A. I. Benthic harpacticoida of the Kara Sea: Species composition and bathymetrically related distribution. Oceanology 59(4), 541–551. https://doi.org/10.1134/S0001437019040064 (2019).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 31.

    Huang, D. et al. Preliminary study on community structures of meiofauna in the middle and eastern Chukchi Sea. Acta Oceanol. Sin. 40(6), 83–91. https://doi.org/10.1007/s13131-021-1777-3 (2021).

    ADS 
    Article 

    Google Scholar 

  • 32.

    Giere, O. Meiobenthology: The Microscopic Motile Fauna in Aquatic Sediments 2nd edn. (Springer, 2009).

    Google Scholar 

  • 33.

    Semiletov, I. et al. The East Siberian Sea as a transition zone between Pacific-derived waters and Arctic shelf waters. Geophys. Res. Lett. https://doi.org/10.1029/2005GL022490 (2005).

    Article 

    Google Scholar 

  • 34.

    Miroshnikov, A. Y. et al. Ecological state and mineral-geochemical characteristics of the bottom sediments of the East Siberian Sea. Oceanology 60(4), 595–610. https://doi.org/10.31857/S0030157420040152 (2020).

    Article 

    Google Scholar 

  • 35.

    Frontalini, F. et al. The response of cultured meiofaunal and benthic foraminiferal communities to lead exposure: Results from mesocosm experiments. Environ. Toxicol. Chem. 37(9), 2439–2447. https://doi.org/10.1002/etc.4207 (2018).

    CAS 
    Article 
    PubMed 

    Google Scholar 

  • 36.

    Fonseca, G. & Soltwedel, T. Deep-sea meiobenthic communities underneath the marginal ice zone off Eastern Greenland. Polar Biol. 30, 607–618. https://doi.org/10.1007/s00300-006-0220-8 (2007).

    Article 

    Google Scholar 

  • 37.

    Portnova, D. & Polukhin, A. Meiobenthos of the eastern shelf of the Kara Sea compared with the meiobenthos of other parts of the sea. Reg. Stud. Mar. Sci. 24, 370–378. https://doi.org/10.1016/j.rsma.2018.10.002 (2018).

    Article 

    Google Scholar 

  • 38.

    Alexeev, D. K., & Galtsova, V. V. Effect of radioactive pollution on the biodiversity of marine benthic ecosystems of the Russian Arctic shelf. Polar Sci. 6(2), 183–195 (2012).

    ADS 
    Article 

    Google Scholar 

  • 39.

    Grzelak, K. & Sørensen, M. V. Diversity and community structure of kinorhynchs around Svalbard: First insights into spatial patterns and environmental drivers. Zool. Anz. 282, 31–43. https://doi.org/10.1016/j.jcz.2019.05.009 (2019).

    Article 

    Google Scholar 

  • 40.

    Landers, S. C. et al. Kinorhynch communities from Alabama coastal waters. Mar. Biol. Res. 16(6–7), 494–504. https://doi.org/10.1080/17451000.2020.1789660 (2020).

    Article 

    Google Scholar 

  • 41.

    Holovachov, O. New and known species of the genus Campylaimus Cobb, 1920 (Nematoda: Araeolaimida: Diplopeltidae) from North European marine habitats. Biodivers. Data J. https://doi.org/10.3897/BDJ.7.e46545 (2007).

    Article 

    Google Scholar 

  • 42.

    Sharma, J. & Bluhm, B. A. Diversity of larger free-living nematodes from macrobenthos (> 250 μm) in the Arctic deep-sea Canada Basin. Mar. Biodivers. 41(3), 455–465. https://doi.org/10.1007/s12526-010-0060-1 (2010).

    Article 

    Google Scholar 

  • 43.

    Kotwicki, L., Grzelak, K. & Bełdowski, J. Benthic communities in chemical munitions dumping site areas within the Baltic deeps with special focus on nematodes. Deep Sea Res. II 128, 123–130. https://doi.org/10.1016/j.dsr2.2015.12.012 (2016).

    CAS 
    Article 

    Google Scholar 

  • 44.

    Netto, S. A., Pagliosa, P. R., Colling, A., Fonseca, A. L. & Brauk, K. M. Benthic estuarine assemblages from the Southern Brazilian marine ecoregion. Braz. Estuaries. https://doi.org/10.1007/978-3-319-77779-5_6 (2018).

    Article 

    Google Scholar 

  • 45.

    Broman, E., et al. Uncovering diversity and metabolic spectrum of animals in dead zone sediments. Commun. Biol. 3(1), 1–12 (2020).

  • 46.

    Zeppilli, D., et al. Characteristics of meiofauna in extreme marine ecosystems: a review. Mar. Biodiver. 48(1), 35–71 (2018).

  • 47.

    Pérez-García, J. A. et al. Nematode diversity of freshwater and anchialine caves of Western Cuba. PBSW 131(1), 144–155. https://doi.org/10.2988/17-00024 (2018).

    Article 

    Google Scholar 

  • 48.

    Bezzubova, E. M., Seliverstova, A. M., Zamyatin, I. A. & Romanova, N. D. Heterotrophic bacterioplankton of the Laptev and East Siberian Sea shelf affected by freshwater inflow areas. Oceanology 60, 62–73. https://doi.org/10.1134/S0001437020010026 (2020).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 49.

    Vanreusel, A. et al. Meiobenthos of the central Arctic Ocean with special emphasis on the nematode community structure. Deep Sea Res. I 47, 1855–1879. https://doi.org/10.1016/S0967-063728002900007-8 (2000).

    Article 

    Google Scholar 

  • 50.

    Tahseen, Q. Nematodes in aquatic environments: Adaptations and survival strategies. Biodivers. J. 3(1), 13–40 (2012).

    Google Scholar 

  • 51.

    Williams, W. J. & Carmack, E. C. The ‘interior’ shelves of the Arctic Ocean: Physical oceanographic setting, climatology and effects of sea-ice retreat on cross-shelf exchange. Prog. Ocean 139, 24–41. https://doi.org/10.1016/j.pocean.2015.07.008 (2015).

    Article 

    Google Scholar 

  • 52.

    Magritsky, D. V. et al. Long-term changes of river water inflow into the seas of the Russian Arctic sector. Polarforschung 87(2), 177–194. https://doi.org/10.2312/polarforschung.87.2.177 (2018).

    Article 

    Google Scholar 

  • 53.

    Anderson, L. G. et al. East Siberian Sea, an Arctic region of very high biogeochemical activity. Biogeosciences 4, 6. https://doi.org/10.5194/bg-8-1745-2011 (2011).

    CAS 
    Article 

    Google Scholar 

  • 54.

    Dmitrienko, I. A. et al. Impact of the Arctic Ocean Atlantic water layer on Siberian shelf hydrography. J. Geophys. Res. Oceans. https://doi.org/10.1029/2009JC006020 (2010).

    Article 

    Google Scholar 

  • 55.

    Stein, R. Arctic Ocean Sediments: Processes, PROXIES, and Paleoenvironment (Elsevier, 2008).

    Google Scholar 

  • 56.

    Petrova, V. I., Batova, G. I., Kursheva, A. V. & Litvinenko, I. V. Geochemistry of organic matter of bottom sediments in the rises of the central Arctic Ocean. Russ. Geol. Geophys. 51(1), 88–97. https://doi.org/10.1016/j.rgg.2009.12.008 (2010).

    ADS 
    Article 

    Google Scholar 

  • 57.

    Millero, F. J. Thermodynamics of the carbon dioxide system in oceans. GCA 59(4), 661–677. https://doi.org/10.12691/wjce-3-6-1 (1995).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 58.

    Pavlova, G. Y. et al. Intercalibration of Bruevich’s method to determine the total alkalinity in seawater. Oceanology 48, 438. https://doi.org/10.1134/S0001437008030168 (2008).

    ADS 
    Article 

    Google Scholar 

  • 59.

    Dickson, A. G. & Goyet, C. Handbook of Methods for the Analysis of the Various Parameters of the Carbon Dioxide System in Sea Water. Version 2 (No. ORNL/CDIAC-74) (1994).

  • 60.

    Dickson, A. G., Afghan, J. D. & Anderson, G. C. Reference materials for oceanic CO2 analysis: A method for the certification of total alkalinity. Mar. Chem. 80, 185–197. https://doi.org/10.1016/S0304-4203(02)00133-0 (2003).

    CAS 
    Article 

    Google Scholar 

  • 61.

    Lewis, E. & Wallace, D. W. R. Program Developed for CO2 System Calculations. ORNL/CDIAC-105 (Carbon Dioxide Information Analysis Center, Oak Ridge National Laboratory, U.S. Department of Energy, 1998).

    Book 

    Google Scholar 

  • 62.

    Shiklomanov, A. I., Holmes, J. W., McClelland, S. E., Tank, R. & Spencer, G.M. Arctic Great Rivers Observatory. Discharge Dataset, Version 20200801 (2020).

  • 63.

    Niemistö, L. A gravity corer for studies of soft sediments. Merentutkimuslait. Julk./Havsforskningsinst. Skr. 238, 33–38 (1974).

    Google Scholar 

  • 64.

    Eleftheriou, A. Methods for the Study of Marine Benthos (Wiley, 2013).

    Book 

    Google Scholar 

  • 65.

    Wieser, W. Beziehungen zwischen Mundhöhlengestalt, Ernährungsweise und Vorkommen bei freilebenden, marinen Nematoden. Ark. Zool. 2, 439–484 (1953).

    Google Scholar 

  • 66.

    Hammer, Ø., Harper, D. A. T. & Ryan, P. D. PAST paleontological statistics software package for education and data analysis. Palaeontol. Electron. 4, 1–9 (2001).

    Google Scholar 

  • 67.

    Heip, C. & Herman, P. Indices of diversity and evenness. Oceanis 24(4), 61–88 (2001).

    Google Scholar 


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