Trophic state and water quality of the Maloe More Strait, Lake Baikal
Articles
DOI: 10.5281/zenodo.11220593

Trophic state and water quality of the Maloe More Strait, Lake Baikal

Limnological Institute Siberian Branch of Russian Academy of Sciences, Irkutsk, 664033, Russia
Irkutsk State University, Irkutsk, 664003, Russia
Baikalian Ecological Museum, Listvyanka vil., Irkutsk District, Irkutsk Region, 664520, Russia
Limnological Institute Siberian Branch of Russian Academy of Sciences, Irkutsk, 664033, Russia
Anthropogenic load change in climatic parameters Lake Baikal phyto- and zooplankton saprobity trophic state

Abstract

The results of a two-year study on the plankton structure and abundance in the Maloe More strait, Lake Baikal, are presented. This place is an area of increased anthropogenic pressure because it is too popular for tourists. The data obtained, in comparison with other previous data, enabled us to identify recent changes in the plankton structure and assess the trophic state of the strait. It was found that in the pelagic zone, the trophic state increases in years of abundant development of cryophilic Baikalian diatoms and decreases in low-productive years, while in the littoral zone, the situation is opposite. The water quality of the strait was assessed using the bioindication method. Water quality in the pelagic zone corresponded to class 1 called “purity” but in the littoral zone to classes 1 and 2 from “purity” to “satisfactory purity”.

Acta Biologica Sibirica 10: 489–505 (2024) doi: 10.5281/zenodo.11220593

Corresponding author: Nina A. Bondarenko (nina@lin.irk.ru)

Academic editor: R. Yakovlev | Received 22 February 2024 | Accepted 14 May 2024 | Published 22 May 2024

http://zoobank.org/840593D7-90B7-4246-83D1-CEB85EAE124A

Citation: Bondarenko NA, Pen'kova OG, Zaitseva YeP, Sheveleva NG (2024) Trophic state and water quality of the Maloe More Strait, Lake Baikal. Acta Biologica Sibirica 10: 489–505. https://doi.org/10.5281/zenodo.11220593

Keywords

Anthropogenic load, change in climatic parameters, Lake Baikal, phyto- and zooplankton, saprobity, trophic state

Introduction

Lake Baikal, the world’s oldest and deepest lake, is situated in Central Siberia, contains 20% of global liquid surface freshwater, and is home to thousands of endemic species including freshwater seals (Kozhov 1963). Lake Baikal is considered to be a secondary or morphometric oligotrophic water body. Its trophogenic zone is usually up to 30 metres deep, sometimes deeper, due to high water transparency and abundant solar radiation. As a result, the phytoplankton primary production exhibits low values in m3 typical for oligotrophic and utraoligotrophic water-bodies but high values under m2 (Votintsev et. al. 1975).

The main feature of the Baikalian, including the Maloe More strait, plankton development in the 20th century was the alternation of high and low productive years. The high productive years were years when large-cell diatom algae of the Baikalian complex, i.e. Aulacoseira baicalensis (K. Meyer) Sim., A. islandica (O. Müll.) Sim., and Stephanodiscus meyeri Genk. et Popovsk. earlier classified in the Melosira genus, intensively bloomed under the ice (Antipova 1974; Popovskaya 1987). These high productive years so called "melosira years" occurred periodically once in 3 or 4 years. Baikalian zooplankton followed such a dynamics of phytoplankton. The zooplanktonic dominant species Cyclops kolensis Lilljeborg directly followed the phytoplankton abundance while another dominant species Epischura baikalensis Sars was depressed in "melosira years" exhibiting number peaks between "melosira years" (Kozhova, Beim 1993; Evstafyev et al. 2010).

The first results on the species composition of the summer plankton in the strait date back to the beginning of the last century (Meyer 1922, 1930; Yasnitsky 1925). More recently, the phytoplankton of the Maloe More strait was studied in detail in the 1950s and 1960s (Kozhova 1959). It was found that the level of development of the pelagic phytoplankton in the strait, as well as in the lake itself, varies greatly from year to year: years of abundant development alternate with years of low productivity. The phytoplankton composition of the open zones of the strait is not identical to that of the Mukhor bay and other shallow bays, where intensive development of cyanoprokaryotes (blue-green algae) was observed during the summer period.

In the 1980s of the last century, changes in phytoplankton of the Maloe More strait were revealed (Popovskaya 1989, 1991). It was found that there was a massive development of cyanoprokaryotes not only in the coastal zone of the strait but also in its open zone in summer. Compared to the 1950s, the phytoplankton biomass increased several times, which the author considered to be a consequence of the increasing anthropogenic load in this zone of Lake Baikal (Popovskaya 1991).

Special studies of the zooplankton of the Maloe More were made sporadically during the last century, and there are few data on this area of the lake. The only main work is the paper by I.K. Vilisova (1959). The author examines the species composition and distribution of zooplankton in different seasons of 1951–1953, both in the open pelagic zone of the strait and in the Mukhor bay. It is noted that the zooplankton abundance in the open zone of the Maloe More strait in spring and autumn is determined by the mass development of epishura. In summer, rotifers and cyclops are especially abundant. The zooplankton of the Mukhor bay was dominated by rotifers and cladocera in all seasons.

Later, L.A. Levkovskaya (1977) studied the zooplankton of the Mukhor bay using the data from 1973–1974. The author notes a decrease in the abundance of zooplankton in the bay during the summer maximum compared to 1951–1953.

Regular studies of zooplankton in the Mukhor bay and the southern part of the Maloe More, started in 1997, showed an increase in zooplankton abundance due to a sharp increase in the number of rotifers (Sheveleva, Pen`kova 2005, 2016, 2020; Sheveleva, Pen`kova and Kirushina 2009).

Recently, many freshwater ecosystems vulnerable to climatic changes and growing anthropogenic loads have undergone alterations in composition of their aquatic communities and biota abundances (Rühland et al. 2008; Lake Onega 1999; Hampton et al. 2018; Reavie et al. 2017; Kurashov et al. 2018; Sterner et al. 2020) and the same was in the ecosystem of Lake Baikal (Timoshkin et al. 2016). It was revealed that the cyclicity of phytoplankton of the “melosira years” in the Maloe More srait as well as round Lake Baikal was violated. Also, the structure of the dominant species was changed (Bondarenko et al. 2023a), so that increasing nitrogen and phosphorus organic forms caused changes in algal size structure towards small cells and nanoplanktonic phytoflagellates. Complex analysis of the state of phyto- and zooplankton of the Maloe More strait showed that changes in the structure of zooplankton are closely associated with the reconstructions in its food base (Bondarenko et al. 2023a).

The paper purposes to assess the current state of the plankton in the Maloe More strait using our data collected for the years 2022 and 2023, in particular to evaluate its trophic state and water quality.

Materials and methods

The Maloe More strait is located between the western shore of Lake Baikal and Olkhon Island. It is 75 km long, including the Mukhor bay, which is 18 km in the widest part and 4 km in the shortest part. Its area is about one thousand km2 and its depth is up to 200 m (Kozhov 1963).

Usually, samples were collected at 2–3 stations in the coastal zone and at 2-3 stations in the pelagic zone (Fig. 1). Sampling was carried out monthly from May to September. Surveys were conducted in March, 2023. The thickness of the ice was from 100 to 120 cm, the snow cover was uneven with patches of pure ice.

We compared our original data collected from 2022 to 2023 with the published data (Kozhova 1959; Popovskaya 1991; Bondarenko et al. 2023а) and the archive data of Drs. Bondarenko N.A. and Sheveleva N.G.

Figure 1.Map of the research area: 1 is the littoral zone of the Mukhor bay; 2 is 4 km from the station 1; 3 is the pelagic zone of the Mukhor Bay; 4 is the pelagic zone; 5 the littoral zone near the Khuzhyr village; 6 the pelagic zone.

Collection and processing of phytoplankton samples

1 L of samples were fixed by Utermóhl’s solution and concentrated by sedimentation. The concentrates were examined by triple counting in a 0.1 ml Nageotte chamber using a light microscope Peraval. The biomass of algae was assessed taking into account individual volumes of their cells (Makarova, Pichkily 1970). Algae were identified according to (Zabelina et al. 1951; Komarek and Anagnostidis 1998; and others). For statistical processing of the experimental data, we used standard computer programs to counter mean values of the samples with a standard error.

Sampling and processing of zooplankton

Juday plankton net (diameter 37.5 cm, mesh size 110 µm) hauls were made in the upper 25m layer in the pelagic zone and in the 3–5m in the Mukhor bay. Desk studies were performed following routine procedure (Kozhova, Melnik 1978). We used individual weights of the Baikal organisms for biomass estimation (Kozhova, Melnik 1978). Average abundance, N total (thousand individuals/m3), abundance of three main taxonomic groups (rotifers, cladocera, and copepods), and total biomass (Β total, mg/m3) were calculated for. The ratio of crustacean and rotifer abundance (Ncr/Nrot) and mean individual weight of an organism (w, mg) were based on average values (Andronikova et al. 2000; Lazareva 2001; 2010). For species identification, we used guides and keys (Kutikova 1970; Einsle 1996; Korovchinsky et al. 2021). Species with a relative abundance over 5% were considered dominant (Lazareva 2001).

The trophic state and water quality

The trophic state of the strait was estimated by parameters such as number of species in communities, sizes of the dominant species, total biomass of phyto- and zooplankton, ratio of phyto- and zooplankton biomasses, biomass ratios of crustaceans and rotifers, ratio of large-cell cladocerae and their total number (k/k), and individual mass of zooplankton organisms (Andronikova 1996; Semenchenko, Razlutsky 2011).

The water quality along the research area has been estimated by the bioindication method, i.e., the saprobity index (S) using species values recognized as pollution indexes. This method is widely used in hydrobiology to assess natural waters based on phyto- and zooplankton data.

Saprobic indexes of the wide-spread species were taken from the sources (Sladecek et al. 1981, 1983; Barinova et al. 2006). Saprobic indexes of the Baikalian algae, crustaceans, and rotifers were assumed to be 0.4 as for xenosaprobic species.

The saprobity of the research area has been carried out by the Pantle-Bukk method in its modification (Sladecek 1973)

S = ∑ (h × s)/ ∑ h,

where h means number of cells per litre for algae and thousand specimens/m3 for zooplankton,

s was the saprobity value for each species.

The estimation of the water quality has been carried out according to the Instruction RD 52.24.309-2016.

Result

The phytoplankton composition of the pelagic zone of the strait in spring 2022 was similar to that of 2019–2021. Stephanodiscus meyeri was the dominant species, although its abundance was lower than in the highly productive year 2021 but higher than in 2019–2020, at 479,000 cells/L. The second representative of the Baikal complex, Aulacoseira islandica, reached a significant abundance in the pelagic zone – 33.4–43.6 thousand cells/L. The abundance of the green alga Koliella longiseta (Vischer) Hind. and the diatom Synedra acus subs. radians (Skabitchev), which dominated the spring plankton in recent years, decreased to 23.1–34.3 thousand/L and 30.7–81.4 thousand/L, respectively. Biomass is higher than in 2019–2020 and 2023 but lower than in 2021, 400–660 mg/ m3 (Table 1). In the Mukhor bay, diatoms also played a dominant role, but the species composition was different: Nitzschia graciliformis (Genk. et Popovsk.), 47.3–304.4 thousand cells/L, and Synedra acus, 49.1–164.6 thousand cells/L. In the littoral zone, two other dominants were added: the euglenophytes Phacus Dujardin (271.5 thousand cells/L) and the diatom Asterionella formosa Hass. (98.7 thousand cells/L). The biomass was high (Table 2).

Season Species number Sizes of dominant species Biomass Biomass ratio
ph z v,μm w, mg ph, mg/m 3 z, mg/m 3 z/ph c/r
Spring 19 6 400–4300 0.005 366 ± 208 17.3 0.047 5.9
Summer 12 4 200–300 0.040 305 ± 119 268 0.88 100
Autumn 11 11 200–300 0.016 157 ± 1 67 0.43 157
Table 1.The plankton parameters in the pelagic zone, the Maloe More strait, 2022: ph means phytoplankton, z – zooplankton, c/r – ratio of crustaceans to rotifers, v – algal cell volume, w – individual cell weight
Season Species number Sizes of dominant species Biomass Biomass ratio
ph z v,μm w, mg ph, mg/m 3 z, mg/m 3 z/ph c/r
Spring 26 14 400–1800 0.003 599 ± 683 129 ± 49 0.21 16
Summer 26 11 140–200 0.030 438 ± 503 267 ± 189 0.61 268
Autumn 34 8 150–200 0.040 719 ± 1180 945 ± 174 1.30 954
Table 2.The plankton parameters in the bay Mukhor, the Maloe More strait, 2022: marked the same as in Table 1

During the under-ice period of 2023, the diatom Stephanodiscus meyeri (46–133 thousand cells/L) and Synedra acus subs. radians (97–146 thousand cells/L) dominated the pelagic plankton of the strait, as in 2022. The green alga Koliella longiseta (45–54 thousand cells/L) was present in a significant quantity. By May, the number of diatoms decreased, and the small-cell K. longiseta became the dominant species (344–715,000 cells/L). The biomass was lower (Table 3).

In the Mukhor bay, the under-ice phytoplankton was dominated by dinoflagellates, up to 97.4% of the total biomass, with diatoms accounting for 2.2%. The phytoflagellates Biecheleria sp. and Woloszynskia sp. have a maximum abundance of 27–32 thousand cells per litre. The biomass was not high (Table 4). In May, the phytoplankton biomass increased sharply. The diatom Nitzschia graciliformis (87–233 thousand cells/L) and the chrysophyte Dinobryon sociale Ehr. (233–316 thousand cells/L) were dominant.

Season Species number Sizes of dominant species Biomass Biomass ratio
ph z v,μm w, mg ph, mg/m 3 z, mg/m 3 z/ph c/r
Under-ice 18 8 300–40000 0.002 508 ± 172 11.0 0.02 2.10
Spring 21 7 200–2000 0.020 337 ± 196 35±12.5 0.10 1.17
Summer 9 10 200–45000 0.010 317 ± 73 25.6 ± 3.9 0.08 13.20
Autumn 18 9 200–45000 0.020 155 ± 96 742 ± 123 4.78 38.00
Table 3.The plankton parameters in the pelagic zone, the Maloe More strait, 2023: marked the same as in Table 1
Season Species number Sizes of dominant species Biomass Biomass ratio
ph z v,μm w, mg ph, mg/m 3 z, mg/m 3 z/ph c/r
Under-ice 6 8 300–40000 0.005 272 ± 81 20.5 0.07 0.13
Spring 20 10 200–9000 0.020 629 ± 470 88.7 0.14 88.67
Summer 12 12 200–45000 0.009 1091 ± 662 218.7 0.20 8.40
Autumn 10 9 200–2000 0.018 151 ± 66 991.7 6.56 35.30
Table 4.The plankton parameters in the bay Mukhor, the Maloe More strait, 2023: marked the same as in Table 1

The summer plankton of the strait were represented by small-cell forms. The dominant species in the coastal zone was Rhodomonas pusilla (Bachm.) Javorn., whose number varied between 224 and 277 thousand cells/L and in the pelagic zone 84 and 312 thousand cells/L. The phytoplankton consisted mainly of picoplanktonic forms (up to 200±2.1 million cells/L). Significant amounts of nanoplanktonic dinoflagellates were registered at some stations (9–31 thousand cells/L). Previously, the abundance of this group did not exceed 1885±691 cells/L.

The composition of phytoplankton in the Mukhor bay had marked distinctions: dominance of colonial cyanoprokaryote forms of the genus Dolichospermum (Ralfs ex Bornet & Flahault) P. Wacklin, L. Hoffmann & J. Komárek (D. lemmermannii (P.G.Richt.) Wacklin, L. Hoffm. & Komárek, D. spiroides (Kleb.) Wacklin, L.Hoffm. & Komárek) (689–802 thousand cells/L) and presence of large-celled dinoflagellate Ceratium hirundinella (O.F. Müller) Schrank (16 thousand cells/L) and diatom Asterionella formosa (70 thousand cells/L).

Observations of the autumn community revealed the development of solely small-sized forms dominated by Rh. pusilla (24–373 thousand cells/L). The number of nanoplanktonic dinoflagellates rose to 13–52 thousand cells/L. Biomass varied from 39 to 194 mg/m3 across the strait, making 441 mg/m3 only in the Kharagoyskaya bay.

By December, the phytoplankton of the strait became poor: single cells of the diatoms Nitzschia graciliformis and Synedra acus were observed in the pelagic zone. Phytoplankton biomass in the littoral zone is slightly higher, 37–40 mg/m3.

It is a well-known fact that the primary production of the pelagic zone of Lake Baikal is provided by the under-ice development of phytoplankton (Votintsev et al. 1975). Phytoplankton biomass during the year in the open part of the strait is also observed in the spring period, and in the Mukhor bay – in the summer-autumn period, i.e. in the pelagic zone of the Maloe More the spring vegetation contributes the main share to the biomass of the year, and in the littoral zone the maximum values of biomass of primary producers are shifted to the summer-autumn period (Table 1–4).

Structural analyses performed during the last century and at the beginning of modern times showed a shift of spring phytoplankton to small-sized species. Large algae with the cell volume attaining ~ 10000 µm3, such as A. baicalensis fell out of the dominant species (Bondarenko et al. 2019; Bondarenko et al. 2023а). Both spring and autumn plankton were dominated by small species with the cell volume ranging from ~ 100 to 2000 µm3, first of all green K. longiseta, diatom Synedra acus subs. radians, haptophyte Chrysochromulina parva Lackey, and cryptophyte Rh. pusilla. In autumn, nanoplanktonic forms of the genera Biecheleria sp. and Woloszynskia sp. joined dominant species.

Zooplankton. The filtrator Epischura baikalensis (96-98%) formed the basis of pelagic zooplankton biomass in 2022 as well as in “melosira year” 2021 in spring and summer. The exception was autumn when only 40% of the copepod biomass was present with Cyclops kolensis accounting for most of the biomass. The role of cladocera in the zooplankton biomass in spring and summer is negligible – not more than 2%. In autumn, the importance of cladocera in the total biomass increased; they accounted for up to 40%. The absolute dominant in the plankton was Bosmina longirostris (O.F. Müller), which is a coarse filtrator and capable of crushing diatoms. The rotifers, due to their low individual mass and insignificant abundance, did not play a significant role after the "melosira year" accounting for 0.3– 0.5% of the total biomass. The Baikal endemics Notholca intermedia Voronkov and Syncheta pachypoida Kutikova et Vassiljeva (0.6 thousand ind./m3) dominated in spring, while Keratella qudrata (O.F. Müller) (0.21 thousand ind./m3) and Conochilus unicornis Rousselet (0.1 thousand ind./m3) dominated in summer and autumn.

In the Mukhor bay of 2022, the zooplankton biomass increased from spring to autumn, mainly due to the abundant development of cladocera in autumn. In spring, copepods were leading in biomass (86%) due to the development of Mesocyclops leuckarti (Claus), while rotifers were dominant in abundance. The biomass of rotifers was comparable to that of cladocera: 8% in each taxonomic group. The number of cladocera increased during the summer and autumn, while the density of rotifers decreased. In summer, the biomass of cladocera was almost equal to that of copepods, and in autumn, their biomass was 2.5 times higher than that of copepods. In summer and autumn, Daphnia galeata Sars was the dominant species (80% of the total zooplankton biomass).

During the 2023 under-ice period in the strait, the composition of zooplankton, both in terms of abundance and biomass, is slightly more than 50% represented by the population of E. baikalensis and rotifers, up to 48%. Among rotifers, the endemic S. pachypoida (0.4 thousand ind./m3) and the year-round Kellicottia longispina (Kellicott) were leading in abundance (0.2 thousand ind./m3). In 2023, the zooplankton biomass was determined by copepods: epishura in spring and cyclopoid copepods in summer. Copepods formed the basis of the autumn biomass: the abundance of cladocera increased, with D. galeata (44%) and B. longirostris (11%) dominating. E. baikalensis represented 28% of the total zooplankton biomass.

In the Mukhor bay, the under-ice and spring zooplankton is quantitatively and qualitatively poor. Zooplankton abundance and diversity increased by autumn. No changes in zooplankton structure were observed as of 2022. The role of the rotifers in the bay is very important. They are the most abundant, up to 50%. Crustaceans were dominant in total biomass, with cladocera accounting for 58% in summer and 37% in autumn, and copepods for 31% and 39%, respectively.

Trophic state of the strait. Changes in the structure of plankton during the studied period continued. The dominance of small algae during the open water period, mainly phytoflagellates (cryptophytes, dinophytes, and haptophytes), which were not previously recorded in the plankton of Maloe More (Kozhova 1959; Popovskaya 1989), became a trigger for further rearrangements not only in the microplankton structure but also in the trophic systems. Fine filtrators were leaders in abundance: rotifiers Keratella cochlearis (Gosse), Polyarthra euryptera Wierzejski, Keratella quadrata, Notholca intermedia, and carnivores Synchaeta pachypoida and S. grandis Zacharias. The first three species are indicators of eutrophic waters (Andronikova 1996). In the littoral zone of the strait, and especially in Mukhor bay, intensive vegetation of colonial cyanoprokaryotes of the genus Dolichospermum was observed in summer in both years, which is also an indicator of increased trophic state.

Quantitative data (Tables 1–4) for the same period show a mixed picture. Due to the dominance of small forms, the biomass of pelagic phytoplankton at this stage does not exceed the limits typical for oligotrophic waters but in the Mukhor bay in summer, during the periods of intensive cyanoprokaryote vegetation, it can be much higher than 1 g/m3. In oligotrophic lakes, the biomass of phytoplankton is lower than the biomass of zooplankton, while in meso- and eutrophic lakes it is equal to or much higher (Andronikova 1996). According to this criterion, the pelagic zone of the strait is characterized as mesotrophic in 2022 and spring-summer 2023 and as oligotrophic only in autumn 2023. The data on the seasonal dynamics of the indicators show a special case in the spring of 2022, when the phytoplankton biomass significantly prevailed the zooplankton biomass, as occurs in the lake during productive years.

In the Mukhor bay, only in the autumn period in both years zooplankton biomass significantly prevailed over phytoplankton biomass in both years.

Total zooplankton biomass (11–742 mg/m3), k/k ratio (0.3–0.46), individual organism mass (0.002–0.04), and the ratio of summer to winter biomass (2.3.) can be considered as more objective indicators. According to these values, the open zone of the strait is characterized as oligotrophic.

In the Mukhor bay, these zooplankton indicators (Table 2, 4) for 2022 and 2023 in the spring and summer periods confirm the oligotrophic state of this part of the water body. During the autumn, the zooplankton biomass reaches almost 1 g/m3, which is characteristic of a higher trophic level. This assessment is also supported by the ratio of summer biomass to winter biomass, 10.7.

The mean zooplankter biomass (w) in the pelagic zone in 2022–2023 was 0.027mg. In the Mukhor bay, the values for this period are unstable, ranging from 0.003 to 0.040.

Water quality. An assessment of the water quality in the strait using the bioindicator method showed that at the time of the study, the plankton in the strait contained 23 species of algae and 27 species of zooplankton – indicators of organic pollution in the water. The saprobic index of algae varies in the range of xeno-alphamesosaprobionts to betamesosaprobionts. The main part (89%) of the species composition, both in the pelagic zone of the Maloe More and Mukhor bay, among zooplanktonic organisms were oligomesosaprobes, oligobetamesosaprobes, and xenosaprobic species.

The saprobic index for phytoplankton in the pelagic zone ranged from 0.79 to 1.58 (Fig. 2), characterizing the open part of the strait at the time of the study from a clean (oligosaprobic) zone to a slightly polluted zone with 2 class water. In the weakly polluted zone, the diversity of species reaches a maximum but the number of individual species is low. The level of water pollution in the pelagic zone of the strait and Mukhor bay increased from spring to summer-autumn. The minimum values of phytoplankton in the pelagic zone were obtained for the under-ice period and the maximum values for the Mukhor bay in autumn.

An assessment of the level of zooplankton pollution indicates that the pelagic waters of the strait had low levels of saprobicity (0.6 – 1.16) during the open water period, which is characteristic of the oligosaprobic zone. During the under-ice period, the water of the strait corresponded to the xenosaprobic zone. This is caused by the fact that the main contribution to the zooplankton abundance belonged to the Baikal endemic E. baikalensis, which has a low saprobic index, 0.4, as for xenosaprobic species.

Figure 2.Saprobity index of phytoplankton and zooplankton in the Maloe More strait, 2022 (А) to 2023 (B). 1 – saprobity index of phytoplankton in the Mukhor bay; 2 – saprobity index of zooplankton in the Mukhor bay; 3 – saprobity index of phytoplankton in the pelagic zone; 4 – saprobity index of zooplankton in the pelagic zone.

In the Mukhor bay of 2022, the average saprobic index during the open water period is 1.47±0.1, with index values decreasing from spring to autumn (Fig. 2), characterizing the bay water as conditionally clean (oligosaprobic). In 2023, the saprobic index values varied from 1.53 (spring) to 1.68 (summer), with a mean of 1.58±0.3. In spring, the leading population in terms of abundance was the β-mesosaprobe population C. kolensis. In summer and autumn, Eudiaptomus graciloides (Lilljeborg) (betaoligomesosaprob) and M. leuckarti (xenosaprob) formed the basis of abundance. Indices of water saprobity in 2023 indicate the prevalence of the “weakly polluted zone” in the whole water area of the bay, which corresponds to quality class 2.

Discussion

In the early 2000s, a sharp increase in the abundance of nanoplanktonic mixotrophic flagellates – indicators of organic pollution of water – was found in the plankton of the strait from spring to autumn as well as in the whole water area of the lake, with the maximum numbers of these organisms noted in places of increased anthropogenic load (Bondarenko et al. 2023a).

Analysis of initial and published data showed that under conditions of intensive anthropogenic load, with redistribution of nitrogen and phosphorus forms towards organic ones (Bondarenko et al. 2023a, b), rearrangements in the taxonomic and size structure of phytoplankton occurred. They caused changes in the zooplankton structure and in the trophic state. While changes in the taxonomic and size structure of the plankton community clearly indicated an increase in the trophic state of the strait, quantitative indicators of phytoplankton and zooplankton did not show such a clear trend (Tables 1–4). For such a unique lake as Lake Baikal, it is difficult to find the right criterion for assessing trophic state. After attempts to find such a criterion, we chose the total biomass of phyto- and zooplankton and the ratio of phyto- and zooplankton biomasses.

In phytoplankton, the tendency to increase trophic state in spring is more pronounced in years with higher concentrations of diatoms of the Baikal complex and less pronounced in years with low productivity; in zooplankton, the reverse is true. During periods when phytoplankton was dominated by small forms, including cryptophytes, haptophytes, and dinophytes, rotifers were abundant, such as in the pelagic zone in 2019 (Bondarenko et al. 2023а). Rotifers become more important as the trophic level of the water body increases but after the highly productive “melosira year” 2021, the importance of rotifers in the plankton of the strait decreases and crustaceans, represented mainly by the endemic Epischura baikalesis, dominate from 2022 onwards. The tendency of the last century, when epishura showed peaks of abundance in “intermelosira years” (Kozhova and Beim 1993; Evstafiev et al. 2010), was evident.

According to the classification (Kitaev 2007), the Mukhor bay is characterized as an alpha-beta oligotrophic or eutrophic water body in different years, while the pelagic zone of the strait either retains its natural oligotrophic state or is characterized as a mesotrophic zone in low productive years. In years with abundant spring vegetation in the psychrophilic Baikal complex, the trophic state of the strait increases (Bondarenko et al. 2023b).

Comprehensive plankton studies conducted in the modern period (Bondarenko et al. 2022) confirm the difference in trophic state between the pelagic zone and Mukhor bay: in summer, the Mukhor bay showed significant values of chlorophyll α (0.56 µg/L) and primary production (56.5 µg C/L.day). At the same time, these values are lower in the pelagic zone of the lake: primary production is 45.2 µg C/L. day and chlorophyll αconcentration is 0.46 µg/L.

Changes in the composition of the biota of many aquatic ecosystems in recent decades have motivated researchers to assess the current state of their trophic state and water quality (Kurashov et al. 2018; Bazhenova, Barsukova 2023; Tekanova et al. 2023; Domysheva et al. 2023). The trophic state and water quality of the coastal zone of South Baikal were assessed in June–December 2020 in the area of the Bolshiye Koty bay using classifications based on the determination of concentrations of total nitrogen, phosphorus, nitrate nitrogen and dissolved phosphorus, Chl α content, and algal biomass (Domysheva et al. 2023). The results showed that the water purity ranges from oligosaprobic to mesosaprobic, corresponding to quality classes 2 and 3, and that the coastal zone of the lake in the study area belongs to the oligotrophic type but with minor elements of mesotrophy.

Another large lake, Lake Onega, also underwent a modern trophic and water quality assessment (Tekanova et al. 2023). It was found that the water body remains oligotrophic in terms of chlorophyll α concentration during summer stratification, and a small amount of easily mineralisable organic matter in the water determines a low level of saprophytic bacterial development, corresponding to xenosaprobic and β-oligosaprobic waters. Only the Kondopoga bay of Lake Onega is characterized by a higher level of trophic (mesotrophic) and saprobic (β-mesosaprobic) water due to pollution by wastewater from the paper mill and trout farm waste.

We apply the bioindication method, which shows that the level of water pollution in the Maloe More strait of Lake Baikal increases from spring to autumn, both in the pelagic zone and in the Mukhor bay. The minimum phytoplankton parameters, in contrast to the trophic parameters, were obtained for the pelagic zone in the under-ice period and the maximum for the Mukhor bay in the autumn period of 2022. The Mukhor bay is classified as either clean, with class 1 water quality (spring and summer 2023), or moderately polluted, with class 2 water quality (summer 2022 and autumn both years). The zooplankton indicators are slightly different: the pelagic zone is oligosaprobic in both years studied (xenosaprobic in the under-ice period), while the Mukhor bay is conditionally clean (oligosaprobic) in 2022 but “weakly polluted” in 2023, corresponding to water quality class 2.

Conclusion

We continued our study in the shallow and pelagic zones of the Maloe More strait during 2022 to 2023, which allowed us to estimate a current state of its plankton, i.e. its trophic state and water quality. These 2-year long studies showed that largecell diatoms Aulacoseira islandica and Stephanodiscus meyeri early belonged to the genus Melosira were abundant in 2021 (a “melosira year”) and then new structural changes occurred in the spring plankton. Spring pelagic small-cell algae decreased their number that caused decreasing rotifer number and simultaneous increasing copepoda number mainly endemic Epischura baikalensis. Earlier Epischura was abundant as a rule in a period between the two “melosira years”. In the summer and autumn plankton, small-cell algae continued to dominate that increased a role of cladocera.

While the changes in taxonomic and size structures of the strait plankton clearly testified to increasing its trophic state, the quantitative data on phyto- and zooplankton did not show the same clear relation. In the pelagic zone, the trophic state has been found to increase in years of intensive under-ice bloom of large-cell diatoms and to decrease in low-productive years while in the littoral zone, it rose in summer and autumn season.

An estimation of the water quality by the bioindication method has showed that the pelagic water was pure of first class during all the seasons excluding the 2023 autumn. The minimal saprobic indexes were observed in the under-ice plankton when cryophilic Baikalian diatoms were dominating. It has been found to increase when wide-spread algae intensively developed in the summer and autumn periods. The water quality of the Mukhor bay has been found to change from pure, 1st class, to slightly polluted, 2nd class.

Acknowledgements

The research was carried out within the state project 0279-2021-0007 of Institute. The authors are thankful to E.M. Timoshkina and Dr. Vladimir Evstafyev for their help in preparing the English version of the manuscript.

References

Andronikova IN (1996) Structural and functional organisation of zooplankton in lacustrine ecosystems. Nauka publisher, Saint-Petersburg, 190 pp. [In Russian]

Andronikova IN, Avinsky VA, Rakhkola M (2000) Zooplankton community characteristics as a tool for monitoring large deep-water lakes. In: Ladoga Lake and other large lakes: Monitoring and assessment of their current state and problems of their service. Petrozavodsk, 2000, 178–188. [In Russian]

Antipova NL (1974) Interannual changes in phytoplankton of Baikal in the region of Bolshye Koty during 1960–1970. Productivity of Baikal and anthropogenic changes of its nature. Irkutsk University Publish, Irkutsk, 75–94. [In Russian]

Barinova SS, Medvedeva LA, Anisimova OV (2006) Algae diversity as an indicator of the environment. Pilies Studio, Tel-Aviv, 498 pp. [In Russian]

Bazhenova OP, Barsukova NN (2023) Phytoplankton of the Ket River (Tomsk region). Acta Biologica Sibirika 9: 55–69. https:// doi.org/10.5281/zenodo.7680101

Bondarenko NA, Ozersky T, Obolkina LA, Tikhonova IV, Sorokovikova EG, Sakirko MV, Potapov SA, Blinov VV, Zhdanov AA, Belykh OI (2019) Recent changes in the spring microplankton of Lake Baikal. Limnologica 75: 19–29. https://doi.org/10.1016/j.limno.2019.01.002

Bondarenko NA, Rusanov II, Chernitsyna CM Shubenkova OV, Zaharenko AS, Pogodaeva TV, Pimenov NV, Zemskaya TI (2022) Structure and production potential of summer phytoplankton of Lake Baikal in the present period. Water Resources 49 (1): 98–108. http://dx.doi.org/10.1134/S0097807822010055

Bondarenko NA, Tomberg IV, Pen'kova OG, Sheveleva NG (2023a) Structural Changes of Phyto- and Zooplankton under the Influence of Climate Change and Anthropogenic Load (Lake Baikal, Russia). Inland Waters Biology 16 (6): 955–966. http://dx.doi.org/10.1134/S1995082923060056

Bondarenko NA, Pen'kova OG, Sheveleva NG (2023b) Assessment of the water-body trophic status on plankton parameters under the anthropogenic pressure: an example of the Maloe More strait, Lake Baikal. Anthropogenic pressure on aquatic organisms and ecosystems. Proceeding All-Russian conference. Borok, 227–230. [In Russian]

Domysheva V, Vorobyeva S, Golobokova L, Netsvetaeva O, Onischuk N, Sakirko M, Kuriganova O, Fedotov A (2023) Assessment of the current trophic status of the Southern Baikal littoral zone. Water. 15: 1139. https://doi.org/10.3390/w15061139

Einsle U (1996) Copepoda: Cyclopoida. Genera Cyclops, Megacyclops, Acanthocyclops. Guides to the identification of the Microinvertebrates of the continental waters of the Wold. SPB Academic Publish., New York, Amsterdam, 112 pp.

Evstafyev VK, Bondarenko NA, Melnik NG (2010) Analysis of long term dynamics of main links of the food web in the Lake Baikal pelagic zone. Bulletin of Irkutsk State University, Biology and Ecology series 3 (1): 3–11. [In Russian]

Hampton SE, McGowan S, Ozersky T, Virdis SG, Thuy VuT, Spanbauer TL, Kraemer BM, Swann G, Mackay AW, Powers SM, Meyer MF, Labou SG, O’Reilly CM, DiCarlo M, Galloway AWE, Fritz SC (2018) Recent ecological change in ancient lakes. Limnology and Oceanography 63 (5): 2277–2304. https://doi.org/10.1002/lno.10938

Instruction RD 52.24.309-2016. Organization and holding routine monitoring of the state and pollution of land surface waters. Rostov on Don, 104 pp. [In Russian]

Kitaev SP (2007) Basic limnology for hydro-biologists and ichthyologists. Petrozavodsk, 395 pp. [In Russian]

Komárek J, Anagnostidis K (1998) Cyanoprokaryota. Chlroococcales. Süßwasserflora von Mitteleuropa. Bd 19/1. Spektrum, Akad. Verl., Heidelberg, Berlin. 548 pp.

Korovchinsky NM, Kotov AA, Sinev AYu (2021) Cladocera (Сrustacea: Cladocera) of Northern Eurasia.Vol. II. Systematic part. KMK Scientific Press, Moscow, 544 pp. [In Russian]

Kozhov MM (1963) Lake Baikal and its Life. Junk Publishers, Netherland, 344 pp.

Kozhova OM (1959) Phytoplankton of Maloe More. Proceedings of the Baikalian limnological station. Nauka publishers, Moscow, Leningrad, 255–274. [In Russian]

Kozhova OM, Melnik NG (1978) Manual to process plankton samples by counting. Irkutsk, 51 pp. [In Russian]

Kozhova OM, Beim AM (1993) Ecological monitoring of Lake Baikal. Ecologia publishers, Moscow, 350 pp. [In Russian]

Kurashov EA, Barbashova MA, Dudakova DS (2018) Ecosystem of Lake Ladoga: the current state and intends of its changes, the end of 20th to beginning of 21st centuries. Biosphere 10 (2): 65–121. https://doi.org/10.24855/BIOSFERA.V1013.439[In Russian]

Kutikova LA (1970) Rotifers in the fauna of the USSR (Rotatoria). Euritatoria subclass (orders Ploimida, Monimotrochida, Paedotrochida). Nauka, Leningrad, 744 pp. [In Russian]

Lazareva VI (2010) Peculiarities of the long-term, 1956 to 2005, zooplankton dynamics in the Rybinsk water-reservoir. Water resources 37 (5): 590–604. [In Russian]

Lazareva VI, Lebedeva IM, Ovchinnikova NK (2001) Changes of the zooplankton community in the Rybinsk water-reservoir along 40 years. Inland Water Biology 4: 46–57. [In Russian]

Levkovskaya LA (1977) Zooplankton of the bays and lakes in the near-shore zone. In: Limnology of the near-shore and shallow zones of Lake Baikal. Nauka publishers, Novosibirsk, 175–191. [In Russian]

Lake Onega. Ecological problems (1999) Karelian Research Center RAS, Petropavlovsk, 151 pp. [In Russian]

Makarova IV, Pichkily LO (1970) To some questions how calculate phytoplankton biomass. Botanical Journal 55 (10): 1488–1492. [In Russian]

Meyer KI (1922) Materials on the algal flora of Lake Baikal. Journal of the Moscow department of Russian Botanical Society 1: 1–27. [In Russian]

Meyer KI (1930) Introduction to the algal flora of Lake Baikal. Bulletin of Moscow Department of Nature Researchers 39 (3-4): 179–392. [In Russian]

Popovskaya GI (1987) Phytoplankton of the deepest Lake in word. Marine and freshwater plankton. Leningrad, 107–115. [In Russian]

Popovskaya GI (1989) Changes in the phytoplankton of the Maloye More. News of the Siberian Branch of the USSR Academy of Sciences 1: 41–47. [In Russian]

Popovskaya GI (1991) Phytoplankton of Lake Baikal and their long-term changes (1958 to 1990). Theses for the degree of Doctor of Biological Sciences. Novosibirsk, 32 pp. [In Russian]

Revie ED, Sgro GV, Estepp LR (2017) Climate warning and changes in Cyclotella sensu latoin the Laurentian Great Lakes. Limnology and Oceanography 62: 768–783. https://doi.org/10.1002/lno.10459

Rühland K, Paterson AM, Smol JO (2008) Hemispheric-scale patterns of climate-related shifts in planktonic diatoms from North American and European lakes. Global Change Biology 14: 2740–2754. http://dx.doi.org/10.1111/j.1365-2486.2008.01670.x

Sheveleva NG, Penkova OG (2005) Zooplankton of the southern area of the Maloe More strait, Lake Baikal. Inland Water Biology 4: 42–49. [In Russian]

Sheveleva NG, Penkova OG (2016) On long-term dynamics of the spring zooplankton of the open part of the Maloye More strait, Baikal Lake. Hydrobiological Journal 52(6): 25–32.

Sheveleva NG, Penkova OG (2020) Long-term dynamics of the zooplankton community in the southern part of Maloye More Strait, Lake Baikal. Limnology and Freshwater Biology 4: 746–747. https://doi.org/10.31951/2658-3518-2020-A-4-746

Sheveleva NG, Penkova OG, Kiprushina KN (2009) Long-term dynamics of the zooplankton number in the open area of the Maloe More strait, Lake Baikal. Bulletin of the Moscow department of nature researchers 114 (3): 505–510. [In Russian]

Sládeček V (1973) System of water quality from the biological point of view. Archiv für Hydrobiologie und Ergebnisse Limnologie 7 (1): 1–218.

Sládeček V (1983) Rotifers as indicators of water quality. Hydrobiologia 100: 169–200.

Sládeček V, Zelinka M, Rothschein J, Moravcova V (1981) Biological analysis of surface waters. Commentary to the Czechoslovak State Norm 83 0532, part 6: Determination of the saprobic index. Vyd. Uradu pro normalizaci a mereni, Praha, 186 pp. [In Czech]

Sterner RW, Reinl KL, Lafrancois BM (2020) A first assessment of cyanobacterial blooms in oligotrophic Lake Superior. Limnology and Oceanography 9999: 1. https://doi.org/10.1101/2020.11.03.366955

Semenchenko VP, Razlutsky VI (2011) Ecological quality of the surface waters. Belaruska navuka publishers, Minsk, 329 pp. [In Russian]

Tekanova EV, Kalinkina NM, Makarova EM, Smirnova VS (2023) The Current Trophic State and Water Quality of Lake Onego. Inland water biology 16 (6): 967–973. https://doi.org/10.1134%2Fs1995082923060251

Timoshkin OA, Samsonov DP, Yamamuro M, Moore MV, Belykh OI, Malnik VV, Sakirko MV, Shirokaya AA, Bondarenko NA, Domysheva VM, Fedorova GA, Kochetkov AI, Kuzmin AV, Lukhnev AG (2016) Rapid ecological change in the coastal zone of Lake Baikal (East Siberia): Is the site of the world’s greatest freshwater biodiversity in danger? Journal of Great Lakes Research 42: 487–497. https://doi.org/10.1016/j.jglr.2016.02.011

Vilisova IK (1959) Zooplankton of Maloe More strait. In: Proceedings of the Baikalian limnological station. Nauka publishers, Moscow, Leningrad, 275–304. [In Russian]

Votintsev КК, Mescheryakova AI, Popovskaya GI (1975) Turnover of the organic substances in Lake Baikal. Nauka publisher, Novosibirsk, 190 pp. [In Russian]

Yasnitsky VN Some results of the hydro-biological studies on Lake Baikal during the summer of 1925. Reports of USSR Academy of Sciences 26–27. [In Russian]

Zabelina MM, Kiseliov IA, Proshkina-Lavrenko AI, Sheshukova VS (1951) Diatom algae: Guide of USSR fresh-water algae. Issue 4. Soviet Science publisher, Moscow, 618 pp. [In Russian]