Journal of Environmental Treatment Techniques  
2020, Volume 8, Issue 4, Pages: 1510-1515  
J. Environ. Treat. Tech.  
ISSN: 2309-1185  
Journal web link: http://www.jett.dormaj.com  
https://doi.org/10.47277/JETT/1515  
Characterization of the Fish Population in the  
Southwestern Part of the Onega Lake (Karelia)  
Based on the Results of Long-Term Monitoring  
Irina Mikhailovna Dzyubuk*  
Institute of Biology, Ecology and Agrotechnologies, Petrozavodsk State University, 33 Lenin Ave., Petrozavodsk, 185910, Russia  
Received: 28/06/2020  
Accepted: 27/09/2020  
Published: 20/12/2020  
Abstract  
The results of the long-term ichthyological studies of the southwestern part (the Sheltozero Brusno region) of the Onega Lake performed  
as part of the environmental monitoring have been presented. This is one of the most productive and clean areas in the lake. The fish  
population of the southwestern part of the Onega Lake includes 20 fish species that are representatives of 10 families belonging to six faunistic  
complexes. By the number of the species, the Carp family dominates. By the number of the species in this area of the lake, the Arctic  
freshwater, the boreal plain, and the boreal foothill complexes are equally important. The species of the freshwater Pontian, the Arctic marine,  
and the ancient Late Tertiary complexes together amount to no more than 25 % of the total population. In the southwestern region of the lake,  
there are many valuable commercial species (freshwater salmon (Salmo salar Linnaeus, 1758), lavaret (Coregonus lavaretus lavaretus  
(
(
Linnaeus, 1758)), pikeperch (Sander lucioperca (Linnaeus, 1758)), pike (Esox lucius Linnaeus, 1758), etc. Smelt (Osmerus eperlanus  
Linnaeus, 1758)) and vendace (Coregonus albula (Linnaeus, 1758)) are the most commercially valuable (75  85 %). The population-  
ecological analysis has shown a relatively good state of most studied fish species. For maintaining the existing structure and state of the fish  
population in the southwestern part of the Onega Lake, a set of measures is required, including the preservation and improvement of the fish  
habitat, the conditions for the fish reproduction and feeding; toughening the protective measures during periods with a decrease in the number  
of fish species; regulation of fishing, and increasing the amount of fish artificial reproduction, rearing, and releasing into the lake.  
Keywords: Fishing, fish population, ecological monitoring, population  
1
1
Introduction  
quality of the lake's aquatic environment, which is deteriorated  
due to exerted technogenic, anthropogenic impact. The fish  
population is sensitive to any changes of aquatic environment. In  
the southwestern part of Onega Lake, i.e. in its cleanest area,  
anthropogenic influence manifested itself in the organization and  
functioning of the trout cage farm. The authors studies have  
shown that the operation of the cage farm could cause changes in  
the state of the aquatic ecosystem and the species composition of  
fish in certain areas of the southwestern part of Lake Onega [10-  
11]. Therefore, there are urgent tasks of preventing pollution,  
eutrophicating the water, optimizing capture fishing, and  
developing measures aimed at maintaining the state of the fish  
population in the Onega Lake at the optimal level. The study has  
been aimed at assessing the ecological and biological state of the  
fish population in the southwestern part of the Onega Lake  
Currently, the relevance of studying the fish population of  
freshwater lakes prone to anthropogenic impact remains high [1-  
]. The Onega Lake, the second largest lake in Europe, is valuable  
6
in terms of energy, socio-economic, and environmental  
significance for the development of the North-West of Russia.  
The fish resources of the Onega Lake have always been and will  
remain attractive not only for commercial fishermen and local  
fisherfolk but also for tourists. However, the state of this largest  
fishery pond largely depends on the way these resources are used.  
It is known that irrational, unmonitored fishing decreases the  
population and causes the disappearance of valuable commercial  
species (sturgeon, salmon, lavaret, etc.). The same consequences  
occur when the quality of the aquatic environment changes.  
Salmon population in the southwestern part of Onega Lake, the  
size of which was catastrophically small due to excessive fishing,  
was thoroughly researched. The results of the conducted research  
showed that more than 50% of the catches were artificially bred  
fish, i.e. one of the most effective ways to preserve the species in  
the lake was intensive fish breeding at hatcheries [7-9].  
(
Karelia) based on the results of long-term monitoring.  
2
Materials and methods  
The object of the study was the fish population of the  
Successful existence of fish populations depends on the  
Corresponding author: Irina Mikhailovna Dzyubuk, Institute of Biology, Ecology and Agrotechnologies, Petrozavodsk State University,  
3 Lenin Ave., Petrozavodsk, 185910, Russia. E-mail: dzyubuk.i.m@mail.ru  
3
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Journal of Environmental Treatment Techniques  
2020, Volume 8, Issue 4, Pages: 1510-1515  
southwestern part of the Onega Lake (the Sheltozero  Brusno  
region). The fish were caught in 1998  2016 from May to  
October. The fishing gear was nets (with the mesh of 10 to 70  
mm), seine nets (drag nets, tickler chains), and trail nets. A total  
of about four thousand specimens of various fish species were  
studied.  
Onega Lake belongs to the hydrocarbonate class of the calcium  
group.  
The color of the water is 20 25 degrees; it can reach 40 50  
degrees. The active reaction of the medium is in the range  
between 7.0 and 7.8. The content of oxygen is not less than 9.5  
mg/l. The content of nutrients is not high (the maximum  
concentration of mineral phosphorus is 0.01 mg/l, of ammonia  
nitrogen 0.33 mg/l). The water masses in the southwestern area  
of the lake retain an oligotrophic nature [22]. The fish population  
of the Onega Lake includes 35 species belonging to 15 families  
[21]. The southwestern part of the Onega Lake (the Sheltozero –  
Brusno region) is populated by 20 fish species (57 % of the total  
number of the species in the lake) (Table 1).  
It is known from the local population that sometimes eel  
(Anguilla anguilla (Linnaeus, 1758)), chub (Leuciscus cephalus  
(Linnaeus, 1758)), rudd (Scardinius erythrophthalmus (Linnaeus,  
1758)), and blue bream (Abramis ballerus (Linnaeus, 1758)) are  
found in the catches in this area. Some fish species in the  
southwestern part of the Onega Lake (the Sheltozero  Brusno  
region) are represented by various ecological forms. Of the  
lavaret, Coregonus lavaretus widergeni tsholmygensis and  
Coregonus lavaretus lavaretus ludoga n. Onegi are met.  
Salvelinus lepechini (Gmelin, 1788)) and Salvelinus  
lepechiniprofundicola Berg are also found. The large form of  
whitefish, European cisco (Coregonus albula kiletz  
Michalowsky), is also met.  
During the studies, the species composition of the fish in the  
catches, the age, sex, size, and weight of the fish were determined.  
The Latin name of the fish families and species are given  
according to the literature sources widely used in ichthyological  
research in Russia [12-14]. The fauna associations were given as  
per G. N. Nikolsky [15]. The fish were weighed, measured, their  
age was determined, and the fish were opened using the standard  
methods [16,17]. The caught fish were measured using a tape  
measure and a beam caliper and weighed using an electronic and  
a pharmacy weigher, depending on the size of the fish. The age  
was determined using an MBS-6 binocular microscope and the  
slices of scales, otoliths, and gill covers. To determine the age  
of salmonids, whitefish, cyprinids, and other fish species,  
scales were sampled; for control, otoliths were sampled  
from ruffe and smelt, as well as gill covers from perch.  
When preparing samples, a 10% ammonia solution was used, in  
which the recording structures (scales, gill covers) were kept for  
1
0-15 minutes. Then they were placed on glass slides and  
examined under a binocular microscope.  
All measurements, including weighing, determination of the  
age of the fish population, etc., were carried out personally by the  
author of the article (one researcher) during multi-year  
monitoring, which increases the reliability of the results obtained.  
The author personally prepared and examined about 7,000  
samples by which the age of the fish was determined. On the basis  
of the obtained results of the absolute indicators of the length and  
mass of fish, the dynamics of the absolute indicators for a long-  
term period, the change in the growth rate, the increments in  
length and weight during ontogeny were assessed. Based on the  
study of the age composition of fish in the catches, its changes in  
the long-term aspect were traced. When the fish were dissected,  
the sex of the individuals was determined; on the basis of this, the  
sex composition of the fish population and its dynamics were  
estimated. The collected data were processed using the standard  
methods of analysis of variance [18,19].  
By the number of the species, the Carp family dominates (five  
species). The Salmonidae and Percidae families include three  
species each, the Coregonidae and Gasterosteidae two species  
each, and the Thymallidae, Osmeridae, Esocidae, Lota, and  
Cottidae are represented by one species each. The species in the  
southwestern part of the lake belong to six faunistic complexes.  
By the number of the species, the leading position is taken by the  
Arctic freshwater, boreal plain, and boreal foothill complexes  
(
25 % each). The freshwater Pontian and arctic marine complexes  
account for 10 % each, and the ancient Late Tertiary complex  
accounts for 5 % (Fig.1).  
Further long-term and systematic studies of the species  
composition of fish in Lake Onega will allow assessing the  
stability of the state of faunistic complexes and the fish  
community of the aquatic ecosystem. The population-ecological  
analysis revealed the relatively favorable state of the feeding  
school (Shuiskoye) of freshwater salmon (Salmo salar morpha  
sebago Girard) in the southwestern part of the lake. In the catches,  
the share of commercially reproduced fish reached 53 %. No  
significant difference was found between naturally and  
commercially reproduced fish in terms of the size and weight,  
which were in the range of 33.5  88.0 cm and 0.4  8.8 kg. The  
studies showed a significant reduction in the maximum age of two  
ecological forms of lavaret  fera (C. l. ludoga natio onegi) and  
pit lavaret (C. l. widegreni natio tscholmugensis)  in catches at  
the age of 11+ to 7+ years and 15+ to 9+ years, respectively. The  
length of fera (C. l. ludoga natio onegi) in the catches of 1999 had  
been up to 55 cm, and its weight was up to 1.5 kg; in 2016, these  
indicators in the specimens of the same age did not exceed 40 cm  
and 800 g, respectively. For pit lavaret (C. l. widegreni natio  
tscholmugensis) the maximum length and weight in this period  
had also decreased from 63 cm to 50 cm and from 3.1 kg to 2 kg,  
respectively.  
3
Results and discussion  
The Onega Lake stretches out from the north-west to the  
south-east. The total water area of the lake with islands is 9,943.3  
km², without islands  9,692.6 km². Its maximum length is 290  
km; its width is 82 km. The average depth of the lake is 30 m, the  
greatest depth is 120 m; the depths of 20 to 40 m prevail. Over 50  
rivers and small rivers and about 1,000 streams fall into the Onega  
Lake. The major tributaries are the Vodla, Shuja, Suna, and  
Andoma Rivers. The largest bays of the Onega Lake are the  
Petrozavodsk and the Kondopoga Bays, which have been exposed  
to intense anthropogenic effect [20, 21].  
The southwestern part of the Onega Lake in the Sheltozero –  
Brusno region is one of the purest areas of the water body. All  
water masses of the Onega Lake pass through this area; it is  
connected with the Ladoga Lake, and through the Neva River —  
with the Baltic Sea. The water of the southwestern part of the  
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2020, Volume 8, Issue 4, Pages: 1510-1515  
Table 1: Fish species in the southwestern part of the Onega Lake  
Presence in the southwestern part of the Onega  
Family, species  
Fem. ACIPENSERIDAE Bonaparte, 1831  
Acipenser ruthenus Linnaeus,1758  
Сем.ANGUILLIDAE Rafinesque,1810  
Anguilla anguilla (Linnaeus, 1758)  
Fem.CYPRINIDAE Rafinesque, 1815  
Abramis ballerus (Linnaeus, 1758)  
Abramis brama (Linnaeus, 1758)  
Alburnus alburnus (Linnaeus, 1758)  
Blicca bjoerkna (Linnaeus, 1758)  
Carassius carassius (Linnaeus, 1758)  
Gobio gobio (Linnaeus, 1758)  
-
-
-
+
+
-
-
-
Leuciscus cephalus (Linnaeus, 1758)  
Leuciscus idus (Linnaeus, 1758)  
Leuciscus leuciscus (Linnaeus, 1758)  
Pelecus cultratus (Linnaeus, 1758)  
Phoxinus phoxinus (Linnaeus, 1758)  
Rutilus rutilus (Linnaeus, 1758)  
Scardinius erythrophthalmus (Linnaeus, 1758)  
Fem.BALITORIDAE Swainson,1839  
Barbatula barbatula (Linnaeus, 1758)  
Fem.COBITIDAE Swainson,1838  
Cobitis taenia Linnaeus, 1758  
-
+
-
-
+
+
-
-
-
Fem.SILURIDAE Rafinesque, 1813  
Silurus glanis Linnaeus, 1758  
-
Fem. ESOCIDAE Rafinesque, 1815  
Esox lucius Linnaeus, 1758  
+
+
Fem.OSMERIDAE Regan, 1913  
Osmerus eperlanus (Linnaeus, 1758)  
Fem.СOREGONIDAE Bonaparte, 1845  
Coregonus albula (Linnaeus, 1758)  
Coregonus lavaretus lavaretus (Linnaeus, 1758)  
Fem. THYMALLIDAE Gill, 1885  
Thymallus thymallus (Linnaeus, 1758)  
Fem.SALMONIDAE, Cuver, 1829  
Salmo salar Linnaeus, 1758  
+
+
+
Salmo salar morpha sebago Girard  
Salmo trutta morpha lacustris Linnaeus, 1758  
Salvelinus lepechini (Gmelin, 1788)  
Fem.LOTIDAE Bonaparte, 1835  
Lota lota (Linnaeus, 1758)  
+
+
+
+
Fem.14.GASTEROSTEIDАE Bonaparte, 1831  
Gasterosteus aculeatus Linnaeus, 1758  
Pungitius pungitius (Linnaeus, 1758)  
Fem.COTTIDAE Bonaparte, 1831  
Cottus koshewnikowi Gratzianow, 1907  
Cottus poecilopus Heckel, 1836  
+
+
+
-
Myoxocephalus quadricornis (Linnaeus, 1758)  
-
Fem.PERCIDAE Rafinesque, 1815  
Gymnocephalus cernuus (Linnaeus, 1758)  
Perca fluviatilis Linnaeus, 1758  
+
+
+
Sander lucioperca (Linnaeus, 1758)  
The differences were also significant in the same age groups  
of different generations. The increased catching and the focus of  
lavaret catching on larger specimens had caused changes in the  
age structure of lavaret populations in this area of the lake. It may  
be assumed that changes occurred in the feed base of the species,  
which affected its size and weight. Currently, the issue of  
preserving lavaret in the water bodies in Karelia is very urgent.  
This requires continuing the introduction of lavaret (C. l.  
Lavaretus (L)) to water bodies, breeding the species at fish farms,  
preserving (improving the disturbed) habitat, and reducing the  
catching load on this valuable commercial species.  
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Journal of Environmental Treatment Techniques  
2020, Volume 8, Issue 4, Pages: 1510-1515  
100,0  
80,0  
60,0  
40,0  
20,0  
0,0  
Onega Lake  
south-west part of the Onega lake  
Arctic freshwater  
Ancient Late Tertiary  
Boreal foothill  
Boreal plain  
Freshwater Pontian  
Arctic marine  
Figure 1: The ratio of faunistic complexes by fish species in catches in the southwestern part of the Onega Lake  
The most important place in the fish resources of the lake is  
taken by whitefish (C. albula (L)). Its maximum age in  
commercial catches in the Onega Lake is five years; the life  
expectancy does not exceed six years. Until the end of the 1980s,  
two-year-olds (1+) and three-year-olds (2+) had been of primary  
importance in the catches, later, four-year-olds (3+) and five-  
year-olds (4+) became of primary importance. This might be the  
result of the improved conditions for reproduction and feeding  
due to eutrophication of certain areas in the lake and a decrease in  
the pressure of predators (mainly salmon (S. salar morpha sebago  
Girard) in the southwestern part of the lake) due to their  
intensified catching.  
The Sheltozero region is one of the main distribution  
locations of the large form of vendace - European cisco (C. a.  
kiletz Michalowsky). Due to their scarcity, large commercial  
catches of this species are rarely observed. The authors managed  
to catch and process only 70 European ciscos at the age of 3+ to  
of uncontrolled catching. Bream (A. brama (L)) is one of the most  
important commercial species in Karelia. In the Onega Lake,  
bream has a long life cycle of 29  30 years. In the studies of the  
authors, no specimens older than 20+ years, longer than 45 cm,  
and weighing more than 1,600 g were found. Over many years,  
bream age composition and the size and weight parameters were  
stable. The study showed a reduction in the age of pikeperch (S.  
lucioperca (L)) in the catches at the age of 31+ to 20+ years from  
1950 until the present. The population of pikeperch (S. lucioperca  
(L)) in the lake is not limited by the feed base since the reserves  
of vendace (O. eperlanus (L)) and whitefish (C. albula (L)) are  
sufficient. In the past century, pikeperch (S. lucioperca (L)) could  
reach the length of 80 cm and the weight of 7 kg; currently, its  
size and the weight do not exceed 66 cm and 4,510 g, respectively.  
In terms of the age, size, and weight characteristics, the stable  
state of roach (R. rutilus (L)), striped perch (P. fluviatilis L.),  
Eurasian ruffle (G. cernuus (L)), and other invaluable fish was  
noted in this region of the Onega Lake. Vendace (O. eperlanus  
(L)) (79 %) and whitefish (C. albula (L)) (7 %) prevailed in the  
research catches in the southwestern part of the Onega Lake (the  
Sheltozero  Brusno region). Lavaret (C. l. lavaretus (L)) and  
eelpout (L. lota (L)) account for a large share in the catches  
(7.5 %). Striped perch (P. fluviatilis L), Eurasian ruffle (G.  
cernuus (L)), roach (R. rutilus (L)), and other small fish are  
quantitatively much inferior to vendace (O. eperlanus (L)) (about  
10 %). Pikeperch (S. lucioperca (L)), bream (A. brama (L)), pike  
(E. lucius L), and grayling (T. thymallus (L)) are even less  
common in the catches (up to 10 %). This region remains a place  
for feeding freshwater salmon (S. salar morpha sebago Girard) of  
the Shuya school, whose strength is mainly determined by the  
amounts of reproduction in the artificial conditions. Single  
rainbow trouts (Oncorhynchus mykiss irideus (Walbaum, 1792))  
that left the cages as a result of emergencies at trout farms are  
found in the catches.  
9
+ years, although the maximum age of European cisco (C. a.  
kiletz Michalowsky) is 20 years. The fish aged 5+ to 7+ years  
prevailed in the catches. The maximum size and weight of the fish  
were 39.7 cm and 570 g, respectively. Vendace (O. eperlanus (L))  
is numerous in the southwestern part of the lake, which is also due  
to the presence of spawning grounds. It was found that the age  
limit of vendace (O. eperlanus (L)) had increased from 8+ (before  
1
995) to 10+ years (after 2003). This was the result of improving  
the habitat conditions for the species in this area of the lake. The  
size and weight of vendace (O. eperlanus (L)) in the southwestern  
part of the lake have been stable over the past decade.  
Pike (E. lucius L.) was one of the main objects of commercial  
and recreational fishing. In the trawl catches, pike age was 14+  
years; its length reached 104 cm, and the weight was more than  
1
0 kg. The age composition, the size, and the weight of pike (E.  
lucius L.) in the catches remained stable, which was associated  
with a sufficient feed base (a large population of small invaluable  
fish). It is believed that as a rule, freshwater predatory fish have a  
small population size [23]. However, pike (E. lucius L.) is highly  
resilient and can remain highly abundant in the water body in  
favorable conditions for living and reproduction with the absence  
4
Conclusions  
The development of fisheries in the water bodies of Karelia  
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Journal of Environmental Treatment Techniques  
2020, Volume 8, Issue 4, Pages: 1510-1515  
depends in many respects on successful resolving of the tasks of  
preserving the fish habitat, optimizing capture fishing, especially  
in large water bodies with a significant number of valuable  
commercial species, and maintaining the state of the fish  
population in the lakes at the optimal level. All this is also  
characteristic of the largest fishery reservoir, the Onega Lake,  
which is rich in fish resources and has favorable living conditions  
for valuable commercial species. As a result of the Onega Lake  
monitoring study (1998 to 2016), materials were obtained about  
the state of the fish population in one of the most productive and  
the cleanest part of the lake, the southwestern one. The fish  
population of the southwestern part of the Onega Lake (the  
Sheltozero Brusno region) includes 20 fish species (57 % of the  
total number of species in the lake), representatives of 10 families  
Authors’ contribution  
All authors of this study have a complete contribution for data  
collection, data analyses and manuscript writing.  
References  
1
.
Dzyubuk IM, Klyukina EA. Otsenka mnogoletnei dinamiki vidovogo  
sostava rybnogo naseleniya malykh ozer Karelii s pomoshchyu  
metodov matematicheskoi statistiki [Assessment of the long-term  
dynamics of the species composition of the fish population of small  
lakes in Karelia using the methods of mathematical statistics].  
Scientific notes of Petrozavodsk State University. 2016 Mar;  
2
(155):63-69.  
2
.
Dzyubuk IM, Klyukina EA. Sovremennoe biologicheskoe sostoyanie  
massovykh vidov ryb ozera Konchezero (Kareliya) [The modern  
biological state of mass fish species of the Konchezero Lake  
(
66 % of the number of families characteristic of the lake)  
(Karelia)]. News of the Samara Scientific Center of the Russian  
belonging to six faunistic complexes. In terms of the number of  
species, Cyprinidae (five species) are dominating, followed by  
Salmonidae and Percidae (three species) and Coregonidae and  
Gasterosteidae (two species). Thymallidae, Osmeridae, Esocidae,  
Lota, and Cottidae are represented by one species each. By the  
number of the species, the Arctic freshwater, boreal plain, and  
boreal piedmont complexes are equally important (25 % each).  
The freshwater Pontian, Arctic marine, and ancient Late Tertiary  
complexes together constitute no more than 25%.  
The population-ecological analysis showed the relatively  
good state of most studied fish species in the southwestern part of  
the Onega Lake (the Sheltozero Brusno region). A large number  
of valuable commercial species inhabit the southwestern region  
of the lake, but vendace (O. eperlanus (L)) remains predominant  
in commercial catches in this region of the lake. The catches of  
whitefish (C. albula(L), lavaret (C. l. lavaretus (L)), and burbot  
Academy of Sciences. 2018; 20(5):104109.  
3. Moore JW, Olden JD. Response diversity, nonnative species, and  
disassembly rules buffer freshwater ecosystem processes from  
anthropogenic  
change. Global  
Change  
Biology.  
Available  
4
.
Sterligova OP, Ilmast NV, Milyanchuk NP. Rybnoe naselenie  
malykh vodoemov basseina Onezhskogo ozera i perspektivy ikh  
ispolzovaniya.[Fish population of small water bodies of the Onega  
Lake basin and the perspectives of their use]. Proceedings of the  
Karelian Research Centre of Russian Academy of Sciences. 2018; 10:  
96104.  
5. Estevan LdaS, Ballester ELC, Costa KAda, Scheffer EWdeO, Vaz‐  
dosSantos, AM. Fish community response to environmental  
variations in an impacted Neotropical basin. Ecology of freshwater  
fish. 2018; 27(4):11261139. Available from: doi:10.1111/eff.12420  
6
.
Ngor PB, Grenouillet G, Phem S, So N, Lek S. Spatial and temporal  
variation in fish community structure and diversity in the largest  
tropical floodpulse system of SouthEast Asia. Ecology of  
freshwater fish. 2018; 27(4):10871100. Available from:  
doi:10.1111/EFF.12417  
(
L. lota(L)) are 10 times lower. The catches of perch (P. fluviatilis  
L), pikeperch (S. lucioperca (L)), Eurasian ruffle (G. cernuus  
L)), roach (R. rutilus (L), bream (A. brama (L)), pike (E. lucius  
(
L), and grayling (T. thymallus (L)) are relatively low. To maintain  
the well-being of the populations of valuable commercial species,  
fish-breeding activities (commercial reproduction of fish, release  
of juveniles into the natural environment, etc.) are of great  
importance. With such measures, it is possible to preserve  
freshwater salmon (S. salar morpha sebago Girard) in the  
southwestern part of the lake. It is necessary to reduce the fishing  
load on whitefish (C. l. lavaretus (L)) and to continue its  
commercial reproduction, introduction, and use as an object of  
breeding at fish farms.  
7. Ryzhkov LP, Krupen IM, Elesova NG. Morphophysiological  
characteristics of salmon of Lake Onego. Proceedings of the Fourth  
International Lake Ladoga Symposium. Joensuu 2002; pp. 554 -559.  
8
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Ryzhkov LP, Krupen IM. Morpho-physiological features of lake-  
feeding Salmon from lake Onego. Atlantic salmon: biology,  
conservation and restoration. Petrosavodsk, 2003.  
9
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Dzyubuk IM, Ryzhkov LP. Dinamika sostoyaniya ihtiofauny  
Onezhskogo ozera v XX veke. [Dynamics of the state of the  
ichthyofauna of the Onega Lake in the XX century]. Scientific notes  
of Petrozavodsk State University. 2009; 5:26-31.  
10. Ryzhkov LP, Dzyubuk IM, Gorokhov AV, Marchenko LP,  
Artem’eva NV, Ieshko TA, Ryabinkina MG, Radnaeva VA. The  
State of the Aquatic Environment and Biota during Operation of  
Trout Breeding Pond Farms. Vodnye Resursy. 2011; 38(2):239-247.  
Ethical issue  
Authors are aware of, and comply with, best practice in  
publication ethics specifically with regard to authorship  
1
1. Ryzhkov LP, Dzyubuk IM, Gura VV. Macro-zoobenthos as indicator  
of water ecosystem condition in the area of cage fish farm influence.  
2. Reshetnikov YS. The atlas of freshwater fish of Russia. Vol. I.  
Moscow: Nauka; 2002. 378 p.  
3. Reshetnikov YS, editor. The atlas of freshwater fish of Russia. Vol.  
II. Moscow: Nauka; 2002. 252 p.  
4. Sterligova OP, Ilmast NV, Savosin DS. Cyclostome and freshwater  
fish of Karelia. Petrozavodsk: Karelian Scientific Center of the  
Russian Academy of Sciences; 2016. 224 p.  
(
avoidance of guest authorship), dual submission, manipulation  
of figures, competing interests and compliance with policies on  
research ethics. Authors adhere to publication requirements that  
submitted work is original and has not been published elsewhere  
in any language.  
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1
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Competing interests  
The authors declare that there is no conflict of interest that  
would prejudice the impartiality of this scientific work.  
1
1
5. Nikolsky GV. Struktura vida i zakonomernosti izmenchivosti ryb  
[The structure of the species and patterns of fish variability].  
Moscow: Food industry; 1980. 182 p.  
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7. Kafanova VV. Metody opredeleniya vozrasta i rosta ryb [Methods of  
determining the age and growth of fish]: Handbook. Tomsk:  
Publishing house of the Tomsk University; 1984. 55 p.  
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8. Campana SE. Accuracy, precision and quality control in age  
determination, including a review of the use and abuse of age  
validation methods. Ecology of freshwater fish. 2005; 5(2):197242.  
Available from: doi:10.1111/j.1095-8649.2001.tb00127.x  
9. Ivanter EV, Korosov AV. Elementarnaya biometriya [Elementary  
biometry]: textbook. 3rd ed., rev. and ext. Petrozavodsk: PetrSU  
Publishing house; 2013. 110 p.  
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0. Filatov NN, editor Environmental problems of the Onega Lake.  
Petrozavodsk: KarSC of RAS; 1999. 293 p.  
1. Kukharev VI, Lukin AA, editors.Bioresursy Onezhskogo ozera [The  
biological resources of the Onega Lake].Petrozavodsk: Karelian  
Scientific Center of the Russian Academy of Sciences; 2008. 271 p.  
2. Ryzhkov LP, Dzyubuk IM. Ekologicheskaya bezopasnost sadkovogo  
rybovodstva [Environmental safety of cage fish farming].  
Petrozavodsk: PetrSU; 2014. 98 p.  
3. Forsman A, Tibblin P, Berggren H, Nordahl O, KochSchmidt P,  
Larsson P. Pike Esox lucius as an emerging model organism for  
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Biology. 2015;87(2):472-479. Available from:doi:10.1111/jfb.12712  
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