scholarly journals Age and growth of European flounder from the Chupa Inlet (Kandalaksha Bay, the White Sea)

2019 ◽  
Vol 323 (2) ◽  
pp. 93-104 ◽  
Author(s):  
P.N. Yershov ◽  
A.A. Matvienko ◽  
D.A. Aristov

We studied age structure, growth and distribution of European flounder Platichthys flesus at the sea in Chupa Inlet (Kandalaksha Bay, the White Sea). Immature and mature fishes fed at shallows of Chupa Inlet and adjacent open sea area in June-August. Size-age and sex composition of fishes in catches are presented in the paper. Individuals of 17–27 cm length and 4–5 year age constituted the majority of catches (45%). On the whole, males numerically predominated over females in the samples. Analysis of sexual differences of growth has shown that females grew faster than males. The most intensive growth took place in July–August, according to the increments on the otoliths. Growth rate of the flounder from Chupa Inlet appeared to be similar to the growth rate of the flounder from other open shore sites of Kandalaksha Bay. We have compared also peculiarities of growth and age structure of flounder populations from Kandalaksha Bay to those from other bays of the White Sea. Significant differences of the growth rate were found between flounders from Kandalaksha, Onega, Dvina and Mezen' Bays. Both males and females from Onega Bay grew faster than other. Growth rate of fish decreased towards the north (Kandalaksha Bay) and the north-east (Mezen' Bay). The most slow-growing flounder inhabited shallows of Mezen' Bay. Statistical analysis has shown that age structure of flounder populations varied in different bays of the White Sea, and observed regional variations were characteristic for both males and females. Flounder population in Onega Bay was characterized by the dominance of the younger individuals compared to populations in other bays. The greatest mean age of flounder was registered in populations from the north-west (Kandalaksha Bay) and the north-east (Mezen' Bay) parts of the White Sea. Males and females in populations from Onega and Dvina Bays differed significantly in the mean age, and as a rule females were older. No age differences between sexes were found in flounder population of Mezen' Bay. We suppose that temperature conditions were among the main factors influencing regional differences in growth rate and age structure of the flounder populations in the White Sea.

2021 ◽  
Vol 325 (3) ◽  
pp. 273-277
Author(s):  
G.V. Fuks ◽  
P.N. Yershov ◽  
V.M. Khaitov

Interannual variation in proportion of left-sided individuals has been studied in the populations of the European flounder from Onega (2002–2019), Mezen (2010–2016), and Dvina (2005–2019) bays of the White Sea. It was found that the flounder populations show no statistically significant and consistent changes in this character. The frequency of left-sided individuals in the local populations and the character of interpopulation differences in different years of the observation period remain relatively constant. The comparison of the results of this study with those of earlier studies reveals a similarity in proportions of left-sided fish over the past 40–60 years in flounder populations of the Kandalaksha Bay and Onega Bay. These results highlight the importance of the proportion of left-sided morphs for the analysis of population differentiation of the European flounder in the White Sea.


2019 ◽  
Vol 323 (2) ◽  
pp. 105-111
Author(s):  
P.N. Yershov ◽  
A.A. Matvienko ◽  
E.P. Voronina

Squamation of the European flounder Platichthys flesus is formed by the common cycloid scales and the bony plates. The number of the bony plates and their localization on the body vary considerably in the flounders from different parts of their range. Study of the variability of bony plates coverage in the European flounder are of importance for understanding structural diversity and for use of this character for morphological differentiation of the local populations. We compared the bony plates on the eye side of the body in the flounders from Chupa Inlet (Kandalaksha Bay) and from the delta of the North Dvina River (Dvina Bay). The localization and the number of the bony plates near the bases of dorsal, anal, pectoral fins and above/below of the lateral line were analyzed. Our results clearly showed that the compared samples can be characterized by certain phenotypes, differing by number and location of the bony plates on the eye side of the fish body. The individuals of one phenotype were found in Chupa Inlet only. Small amount of the bony plates on the body and the presence of relatively wide aggregation of the bony plates near the pectoral fin are the traits of this phenotype. Three phenotypes were distinguished among fishes from the North Dvina delta. The absence of the bone plates on the most part of the body is typical for the prevalent phenotype. Individuals of the second phenotype were similar to the flounder from Chupa Inlet. Large amount of the bony plates covering the whole eye side of the body is characteristic for the third phenotype. The obtained results complement the existing data on the variability of squamation of the White Sea flounders, and indicate the importance of this character in the study of the differences between local populations in this region.


2019 ◽  
Vol 53 (1) ◽  
pp. 39-65
Author(s):  
T. A. Mikhaylova

In 2016–2018, during the summer period, the first detail studies of the red algal belt of the White Sea were carried out time with SCUBA diving at the Chupa Inlet, near the Cape Kartesh, and at the Kolvitsa Inlet (the Kandalaksha Bay), in the vicinity of Sonostrov Island (the White Sea Basin) and Bolshoy Zhuzhmuy Island (the Onega Bay). The upper boundary of the red algal belt lies at a depth of about 7 m, and the lower boundary, at a depth of about 20 m. In the White Sea, the algae distribution in the lower part of the photic zone depends on the geomorphological structure of the bottom and on the composition of the accompanying sedentary fauna, so the lower boundary may vary in the depth range from 14 down to 23 m. In total, 87 species of algae belonging to the three large taxonomic groups have been registered: Chlorophyta (13), Phaeophyceae (33), and Rhodophyta (41). Significant richness of the species composition, vertical zoning, and a variety of phytocoenoses of the red algal belt in different parts of the White Sea have been found. Phytocoenoses of the red algal belt refer to three associations: ass. Odonthalia dentata(–Pseudolithoderma extensum), ass. Phycodrys rubens+Coccotylus truncatus(–Pseudolithoderma extensum), and ass. Lithothamnion glaciale. Nineteen species of macrophytes were the most common and characteristic representatives of the red algal belt, including thirteen species of red algae, four species of brown algae, and two species of green algae. It has been found that abundant and characteristic species of the red algal belt have an additional edificatory function in the studied phytocoenoses, being the consorts that carry rich epiflora and form favorable conditions for increasing the species diversity of algae in the lower phytal zone. The observed rapid shrinkage of the depth range of the kelp and red algal belts, as well as the changes in the vertical distribution of some other algal species in the White Sea, require specific attention concerning altering of their habitat conditions.


2020 ◽  
Author(s):  
Natalia Kosevich ◽  
Ivan Lebedev ◽  
Tanya Bagdasaryan

<p>We have studied the AMS of metamorphic rocks (gneiss, granitoids, dykes) and soft sediments (mainly marine sediments or reworked diamicton) from the Kandalaksha and Onega Bay’s Islands of the White sea. The objects of research are located within the White sea mobile belt, represented by large tectonic nappes.</p><p>The magnetic susceptibility in soft sediment samples ranges from 78.6 E-6 to 1525E-6 (Km), and the degree (P) from 1.8% to 4.1%. Ellipsoids have a predominantly flattened type, such a distribution of AMS is typical for sedimentary rocks. At the same time, in a number of samples (from the Islands of Joker, Ipanchinikha and Olenevsky), the maximum axis is directed in a North-Westerly direction, which may indicate the flow direction. This is especially evident in flattened-triaxial ellipsoids (T=0.2-0.3). Values that have a T greater than 0.5 have a predominantly northerly direction and the orientation of minerals of the magnetic fraction and the direction of paleoflow is less pronounced.</p><p>The study of the anisotropy of the magnetic susceptibility of the Archean complexes composing the Islands of the Kandalaksha Bay of the White sea showed a high magnetic susceptibility-5E-6-1E-3 (Km), which confirms the change in the petrographic composition of gneiss. The degree of anisotropy (P) is 9% on average. It was found that the distribution of the main axes of the magnetic susceptibility ellipsoid coincides with shale and banding in the root outlets, while the maximum axis of the ellipsoid coincides with the West-North-West stretch of the regional fault. In the Onega Bay we sampled paleoproerozoic dykes, and there are AMS is coincided as contacts of studied dykes.</p><p>We done alternating field and thermal demagnetization of pilot collection which contains samples from all studied complexes. And it gives us not good results because of bad paleomagnetic record. Most of samples contain only low coercive or low temperature components and it mainly has modern direction.</p>


1873 ◽  
Vol 10 (111) ◽  
pp. 413-415
Author(s):  
Joshua Wilson

It must be admitted that if during the Glacial period an arctic current, similar to that which now sweeps along the east coast of North America, were to pass over the submerged portions of our island, there is no reason why the climate of this country should not assimilate to that of Labrador, where there is now perpetual frozen ground in the latitude of Liverpool. The question then is, what evidence have we that such a current existed at the commencement of the Glacial epoch ? Have we not the evidence of the striæ on the rocks and mountains of the Scandinavian peninsula, as well as on those of our own country, to show that, during the period of the submergence of these districts, icebergs were driven by an arctic current from the north-east to the south-west ?—that the Polar Sea extended from the White Sea to the entrance of the Baltic, spreading southward over Germany to the confines of Switzerland, which can be traced by the deposited boulders and other ice-transported materials ? Then, as to the cause of this return current. It must be evident that the Gulf-stream at that date could not have flowed in its present direction. The arctic current coming down the Baltic must have thrown it further to the west, so that in all probability in its northern progress it would impinge on the east coast of Greenland and the Island of Spitzbergen; then being deflected by the polar ice, it would return by the way of the White Sea and the Baltic, so completing the circuit.


2019 ◽  
Vol 59 (6) ◽  
pp. 1089-1092
Author(s):  
I. V. Miskevich ◽  
A. V. Leshchev ◽  
D. S. Moseev ◽  
A. S. Lokhov

In the winter low water season in March and the first week of April 2019, complex hydrological and hydrochemical studies were carried out at the mouths of two small rivers of the White Sea catchment basin (the Mudyuga river, which flows into the Dvina Bay, and the Tamitsa river, which flows into the Onega Bay). The results indicate significant differences in the short-period variability of hydrological and hydrochemical parameters in the winter in the studied river mouths compared with the characteristics observed in the tidal estuaries of large and medium rivers, as well as in the mouths of small rivers of the southern seas.


Oceanology ◽  
2008 ◽  
Vol 48 (2) ◽  
pp. 255-267 ◽  
Author(s):  
Yu. S. Dolotov ◽  
N. N. Filatov ◽  
V. P. Shevchenko ◽  
M. P. Petrov ◽  
A. V. Tolstikov ◽  
...  

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