Research Article |
Corresponding author: NG Otchenasch ( tatarva812@yandex.ru ) Academic editor: Yuliya V. Bespalaya
© 2019 NG Otchenasch, GA Dvoryankin, EN Imant.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Otchenash NG , Dvoryankin GA, Imant EN (2019) State of spring phytoplankton and quality of the Kenozero waters in 2018. Arctic Environmental Research 19(1): 43-48. https://doi.org/10.3897/issn2541-8416.2019.19.1.43
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Phytoplankton constitutes a key part of all aquatic ecosystems. It produces organic matter, thus forming the first level of food chains in water bodies. In addition, phytoplankton plays a major role in the water quality formation. The studies of algocoenosis always remain relevant, since the obtained data provides important information on the ecological status of water bodies. This information can subsequently be used for planning and implementing environmental measures, which are particularly significant for water bodies located in specially protected areas. National parks existing for the purposes of nature preservation, education and research are also designed for tourism, which makes their ecosystems more vulnerable. Population residing in such territories and its economic activity may also carry some environmental risks, which necessitates regular complex observations. This paper covers the state of spring phytoplankton community of Lake Kenozero in 2018, its qualitative and quantitative characteristics (species composition, abundance and biomass). In the course of research, we identified 70 phytoplankton taxa belonging to seven divisions: Bacillariophyta, Dinophyta, Chlorophyta, Cyanophyta, Chrysophyta, Xanthophyta and Euglenophyta. The dominant species complex included diatoms (Asterionella formosa, Melosira granulata, Tabellaria fenestrata), representatives of Dinophyta (Gymnodinium sp.), as well as small euglenoids. Species diversity was estimated using the Shannon-Weaver index. Aquatic environment contamination was assessed, i.e. the saprobity index was calculated and the class of surface water quality was determined. According to the water quality classification of water bodies and watercourses by hydrobiological indicators, Lake Kenozero was assigned the second class of water quality (moderately polluted).
Lake Kenozero, phytoplankton, abundance, biomass, surface water quality, saprobity index
Lake Kenozero is one of the largest lakes in the Arkhangelsk Region, as well as the biggest one in the Kenozersky National Park. It has a total area of approximately 75 km2, with water surface covering 66.3 km2. Numerous islands and peninsulas divide the lake into separate stretches and bays (Fig.
Hydrobiological research was carried out within the programme for hydrobiological and ecological study of Lake Kenozero (Kenozersky National Park).
Samples for the quantitative and qualitative analysis of phytoplankton were taken from the surface water in a volume of 1 litre; the material was fixed with 40% formaldehyde solution. The samples were concentrated up to 1 ml using the traditional sedimentary method (
where S – total area of the coverslip; Sc – area of the coverslip under which phytoplankton was counted; n – number of counted cells; Vconc – volume of the concentrated sample; Vin – initial sample volume (1 litre); Vsub – subsample volume (0.05 ml); а – number of calculated subsamples (
The Shannon-Weaver index was calculated as follows
Н’ – index; рi – proportion of individuals belonging to the j-th species. The true value of pi in samples is unknown, but is estimated as ni/N (where N – abundance, ind./m3; ni – number of individuals of one species, ind./m3).
The contamination of aquatic environment was estimated by calculating the saprobity index S according to the Pantle–Buck’s method modified by Sladechek using the following formula
where S – indicator value of each species (Unified methods for the study of water quality1977a, b); h –relative frequency of occurrence.
The higher the saprobity index, the higher the level of water pollution is. The saprobity indices for five classes of water quality are as follows: class I (conditionally clean) – less than 1.5; class II (moderately polluted) – from 1.5 up to 2.5; class III (polluted) – from 2.5 up to 3.5; class IV (dirty) – from 3.5 up to 4.0; class V (extremely dirty) – more than 4.07 (RD 52.24.309-2016). Previously, this method was successfully used on the territory of the Arkhangelsk Region to determine the water quality of the Northern Dvina in 2014 (
The composition of phytoplankton species was determined using identifiers of microalgae. The biomass was calculated using the tables for phytoplankton size and weights (mass) (
Hydrobiological studies of phytoplankton were carried out on 13–14 June (hydrobiological spring) in the Kenozero water area. Samples were taken from the surface water at 15 points over the entire surface of the water body (Fig.
The number of identified microalgae at individual stations ranged from 14 (station 14) to 35 (station 5) averaging 22 species.
The most common types of planktonic algae included Melosira granulata and Fragilaria crotonensis (present at all stations), as well as Tabellaria fenestrata, Gymnodinium sp., Asterionella formosa, Closterium acutum and Protoperidinium bipes, which were encountered less frequently (Table
The presence of golden algae (Dinobryon), which prefer water bodies having a minimum content of inorganic phosphorus, indicates oligotrophic conditions throughout most of the lake (
The total abundance of planktonic microalgae in Kenozero (June 2018) varied from 3,520 to 50,960 cells/L. The highest and the lowest abundances were registered at stations 3 and 15, respectively. Such a significant difference is due to the complex bottom relief and strong coastline indentation, which result in local hydrological and hydrochemical features and, consequently, variations in the phytoplankton community. The average abundance amounted to a very low value of 23750 cells/L, characteristic of oligotrophic water bodies, whose algal flora is outside the vegetation peaks (Fig.
The total biomass of phytoplankton organisms in the studied area varied from 8.01 to 138.56 µg/L. The highest value of total biomass was registered at station 3, located in the northern part of the lake, whereas station 15 showed the smallest value. The average phytoplankton biomass amounted to 47.61 µg/L (Fig.
Representatives of Bacillariophyta (Melosira granulata, Asterionella formosa) and euglenoids, whose species could not be identified, were found to be the most numerous at all stations of the studied area. In addition, a significant number of Fragilaria, Tabellaria and Nitzschia representatives were found. At most stations, the maximum biomass was observed for representatives of Bacillariophyta (Melosira granulata, Tabellaria fenestrata), Euglenophyta and Dinophyta. It should be noted that representatives of Euglenophyta were predominant at stations 1, 2, 3 and 11. Euglenophyta grow in areas affected by organic pollution (
The values of the Shannon-Weaver diversity index by phytoplankton abundance ranged from 1.9 (station 3) to 3.6 (station 12), whereas calculated by biomass it varied from 1.9 (stations 3 and 14) to 3.5 (station 6). The diversity indices by abundance and by biomass averaged 2.9 and 2.8, respectively.
The saprobity index according to V. Sladechek ranged from 1.57 to 1.8 (station 1) averaging 1.6. The saprobic state of the Kenozero waters corresponded to the oligo-β-mesosaprobic conditions (saprobity index 1.5–2.5), or class II of water quality (moderate content of organic substances) (
Taxon | Occurrence |
---|---|
Bacillariophyta | |
Achnanthes sp. | 60% |
Amphoracoffeaeformis (C.Agardh) Kützing, 1844 | 60% |
Amphora exigua Gregory, 1857 | 7% |
Amphora ovalis (Kützing) Kützing, 1844 | 20% |
Asterionella formosa Hassall, 1850 | 87% |
Caloneis bacillum (Grunow) Cleve, 1894 | 27% |
Caloneis silicula (Ehrenberg) Cleve, 1894 | 47% |
Caloneis sp. | 20% |
Cocconeis sp. | 20% |
Cyclotella bodanica Eulenstein ex Grunow, 1878 | 13% |
Cyclotella comta (Ehrenberg) Kützing, 1849 | 33% |
Cyclotella planctonica Brunnthaler, 1901 | 47% |
Cyclotella sp. | 13% |
Cymbella ventricosa (C.Agardh) C.Agardh, 1830 | 7% |
Diatoma hiemale (Lyngb.) Heiberg, 1863 | 33% |
Diploneis interrupta (Kützing) Cleve, 1894 | 7% |
Diploneis ovalis (Hilse) Cleve, 1891 | 13% |
Eunotia pectinalis (Kützing) Rabenhorst, 1864 | 20% |
Eunotia praerupta Ehrenberg, 1843 | 7% |
Eunotia sp. | 40% |
Fragilaria bicapitata Mayer, 1917 | 7% |
Fragilaria capucina Desmazières, 1830 | 53% |
Fragilaria construens (Ehrenberg) Grunow, 1862 | 7% |
Fragilaria crotonensis Kitton, 1869 | 100% |
Gomphonema acuminatum Ehrenberg, 1832 | 7% |
Gomphonema gracile Ehrenberg, 1838 | 13% |
Gyrosigma acuminatum (Kützing) Rabenhorst, 1853 | 7% |
Melosira granulata (Ehrenberg) Ralfs, 1861 | 100% |
Meridion circulare (Greville) C.Agardh, 1831 | 13% |
Navicula gastrum Lauby, 1910 | 7% |
Navicula lanceolata Ehrenberg, 1838 | 13% |
Navicula mutica (Kützing) Frenguelli, 1924 | 40% |
Navicula placentula Pantocsek, 1902 | 20% |
Navicula sp. | 20% |
Navicula tuscula Pantocsek, 1902 | 40% |
Nitzschia acuminata (W.Smith) Grunow, 1880 | 7% |
Nitzschia gracilis Brébisson ex H.L. Smith, 1874–1879 | 27% |
Nitzschia holsatica Hustedt, 1930 | 53% |
Nitzschia linearis W.Smith, 1853 | 40% |
Nitzschia longissima (Brébisson) Ralfs, 1861 | 40% |
Nitzschia palea (Kützing) W.Smith, 1856 | 27% |
Nitzschia sigmoidea (Nitzsch) W.Smith, 1853 | 7% |
Nitzschia sp. | 7% |
Nitzschia subtilis (Kützing) Grunow, 1880 | 7% |
Nitzschia tryblionella Hantzsch, 1860 | 7% |
Nitzschia vermicularis (Kützing) Hantzsch, 1860 | 13% |
Stauroneis anceps Ehrenberg, 1843 | 13% |
Stephanodiscus hantzschii Grunow, 1880 | 13% |
Synedra ulnasensu Hustedt, 1942 | 53% |
Tabellaria fenestrata (Lyngbye) Kützing, 1844 | 93% |
Chlorophyta | |
Ankistrodesmus convolutus Corda, 1838 | 13% |
Ankistrodesmus falcatus (Corda) Ralfs, 1848 | 7% |
Closterium acutum Brébisson, 1848 | 87% |
Closterium sp. | 13% |
Crucigenia tetrapedia (Kirchner) Kuntze, 1898 | 7% |
Dictyosphaerium sp. | 20% |
Scenedesmus quadricauda (Turpin) Brébisson, 1835 | 13% |
Chrysophyta | |
Dinobryon spirale Iwanoff, 1899 | 73% |
Dinobryon divergens O.E.Imhof, 1887 | 60% |
Mallomonas sp. | 60% |
Cyanophyta | |
Anabaena sp. | 27% |
Aphanizomenon flos-aquae (Linnaeus) Ralfs ex Bornet & Flahault, 1888 | 7% |
Gloeocapsa sp. | 7% |
Microcystis sp. | 7% |
Dinophyta | |
Gymnodinium sp. | 93% |
Peridinium sp. | 7% |
Protoperidinium bipes (Paulsen, 1904) Balech, 1974 | 80% |
Euglenophyta | |
Euglena sp. | 33% |
Xanthophyta | |
Centritractus sp. | 40% |
Tribonema sp. | 7% |
Saprobity index according to V. Sladechek. Shannon-Weaver diversity index by abundance and by biomass
Station number | S | HꞋ1 | HꞋ2 |
---|---|---|---|
1 | 1.805 | 3.16 | 3.088 |
2 | 1.715 | 3.086 | 2.745 |
3 | 1.541 | 1.933 | 1.945 |
4 | 1.63 | 3.554 | 3.402 |
5 | 1.679 | 3.379 | 3.152 |
6 | 1.564 | 3.232 | 3.526 |
7 | 1.648 | 3.335 | 3.167 |
8 | 1.57 | 2.402 | 2.704 |
9 | 1.691 | 2.318 | 2.354 |
10 | 1.603 | 2.013 | 2.043 |
11 | 1.64 | 3.435 | 3.26 |
12 | 1.626 | 3.573 | 3.19 |
13 | 1.569 | 2.349 | 2.17 |
14 | 1.567 | 2.063 | 1.929 |
15 | 1.594 | 3.194 | 2.84 |
Average value | 1.629 | 2.868 | 2.768 |
The obtained data show that the dominant phytoplankton complex of Kenozero in June 2018 was represented by diatoms (Melosira granulata, Fragilaria crotonensis, Tabellaria fenestrata, Asterionella Formosa), by dinoflagellates (Gymnodinium sp, Protoperidinium bipes), green algae (Closterium acutum) and, zonally, by small small euglenoids. Quantitative indicators of phytoplankton were extremely low. In addition, the values of species diversity indices were also modest.
Therefore, Lake Kenozero belongs to floristically depleted oligotrophic water bodies with a significant predominance of diatoms and low quantitative indicators (abundance and biomass). A slight zonal pollution of the water body by organic wastewater can be assumed. In order to identify the vegetation peaks in the development of phytoplankton community in Kenozero, to collect more information on its species composition and quantitative indicators, as well as to monitor the ecological state of the lake, extensive year-round research is required.