• FISHERIES RESEARCH BOARD OF CANADA Translation Series No.1138 . IH Analysis of the sexual Cycle inielinifemalej By'I.P. Migalovskii . , Original title: Analiz polovogo tsikla samok moivy. From: Trudy Polyarnnogo Nauchno-Issledovatel'skogo i Proektnogo Instituta Morskogo Rybnogo Khozyaistva i Okeanografii im. N.M. Knipovicha (PINRO), Vol. 20, pp. 188-194, 1967. Translated by the Translation Bureau( GNK/WDP) Foreign Languages Division Department of the Secretary. of State of Canada Fisheries Research Board of Canada Biological Station St. John's, Nfld. 1968: 11 pages typescript DEPARTMENT OF THE SECRETARY OF STATE SECRÉTARIAT D'ÉTAT TRANSLATION BUREAU BUREAU DES TRADUÇTIONS FOREIGN LANGUAGES DIVISION CANADA DIVISION DES LANGUES ÉTRANGÈRES INTO - EN • TRANSLATED FROM - TRADUCTION DE English Russian AUTHOR - AUTEUR 1\1i galovsky TITLE IN ENGLISH - TITRE ANGLAIS Analysis of the . Sexual Cycle in Capelin Females. Analiz polovogo tsikla samok . motvy. • RE . FERENCE IN FOREIGN I,ANGUAGE (NAME OF BOOK OR PUBLICATION) IN FULL. TRANSLITERATE FOREIGN CHAeACTERS. REFÉRENCE EN LANGUE ETRANGÉRE (NOM DU LIVRE OU PUBLICATION), AU COMPLET. TRANSCRIRE EN CARACTERES PHONETIQUES. Trudy Polyarnoo nauchno-isslédovatelskogo I proektnogo instituta morskogo rybnogo khozyaystva i okeanografii im. N.M. Knipovicha. (PINRO). REFERENCE IN ENGLISH - RÉFÉRENCE EN , ANGL AIS Transactions of the N.M. Knipovich's Arctic Research and Planning institute of Sea-Fish Economy and Oceanography (PINRO). PAGE NUMBERS IN ORIGINAL NUMEROS DES PAGES DANS L'ORIGINAL PUBLISH ER - EDITEUR . PINRO DATE OF PUBLICATION DATE DE PUBLICATION YEAR ANNÉE PLACE OF PUBLICATION LIEU DE PUBLICATION 67 Mot indicated VOLUME 20 Fisheries REQUESTING DEPARTMENT MINISTÈRE-CLIENT ISSUE NO, NUMÉRO 188 - 194 NUMBER OF TYPED PAGES NOMBRE DE PAGES DACTYLOGRA.PHIÉES 11 TRANSLATION BUREAU NO. NOTRE DOSSIER N° Biological Station, St BRANCH OR DIVISION DIRECTION OU DIVISION - . PERSON f(EQUESTING DEMANDE PAR YOUR NUMBER VOTRE DOSSIER N ° DATE OF REQUEST DATE DE LA DEMANDE • J ohn ' s , TRANSLATOR (INITIALS) TRADUCTEUR (INITIALES) Nfld. . loir. G.H. Winters 76 9-1 8-1 4 . • 1093. 3673 GNK/Revised by W.D.P. (primarily for accuracy) DATE COMPLETED 30 Sept. 1968. ACHEVE LE UNEDITED DRAFT TRANSLATION Only for inforrnafion July 2 , 68. , ' Received by translator: Sept. 5th 68. soS-200- 10.6 (R EV. 2/68) TRADUCTION NON REVISEE Informaion seulement / 3 (S SECRÉTARIAT D'ÉTAT DEPARTMENT OF THE SECRETARY OF STATE TRANSLATION BUREAU BUREAU DES TRADUCTIONS FOREIGN LANGUAGES DIVISION DIVISION DES LANGUES ÉTRANGÈRES CANADA YOUR NO, • VOTRE N O • ' . DEPARTMENT DIVISION/BRANCH CITY MINISTRE DIVISION/DIRECTION VILLE • 1093 769-18-14 Fisheries OUR NO, LANGUAGE NOTRE N ° LANGUE 3673 Biological Station. St. John's Nfld.• TRANSLATOR (INITIALS) TRADUC TILLIR (INI TI A L ES) DATE ,C.NK/Ravised by Russian WDP (primarily fo' 12 Sept. 1968 s . aCIOUraCy "Analysis of the Sexual Cycle in Capelin Femalesn By T. P. Migalovsky i-From: Transactions of the N. M. Knipovich Polar Scienti- fic Research and Planning Institute of Sea Fisheries and Oceanography 4PINR0). No , XX, 1967._7 In this article are presented the results of research into the functional condition of the gonads in the Capelin of the Barents Sea during spawning migration and spawning, and an effort is made to compile a scale for the determination of the maturation stage of the gonads in the Capelin females. The material was'collected in 1963-64. The major part of the material was kindly presented by V. S. Prokho- . A considerable number of samples was fixed totally rov. by formalini and then the gonads were removed and placed into a 4% solution of formalin. A portion of the samples was fixed in Bouin's solution. The fish were weighed and their length measured (according to Smith). Pieces of the gonads were dehydrated by means of alcohols of increasing I S 0 S-200-10-3/ UNEDITED DRAFT TRANSLATION Only for information TRADUCTION. NON REV1SEE information _,sei4ment _ strength and poured into paraffin through-.chloroformparaffin. Gonads with eus, rich in yolk, were either passed through dioxane, or kept in celloidin oil for two to three days. Sections 7-8 millimetres thick were dyed by azan or ferric hematoxylin according to Heidenhain; reactions were carried out for fat (osmium test) and for polysaccharides. Information on collected and processed material is given in the table (the dashes indicate absence of material). A study of histological sections indicated that the ovaries of spawned females contain a complex of cells ranging from ovogonia to ovocytes of the synaptic tract and of the period of Flight growth.furthermore it also indicated a considerable number of empty follicular sacs and individual resorbing eggs which were not spawned. The ovocytes of Lîhe period of2 slight growth have a large nucleus and a relatively small layer of protoplasm. The protoplasm is coloured unevenly (by means of ferric hematoxylin). Around the nucleus,sections of denser and more intensely coloured protoplasm are arranged. There are few nucleoli. They are arranged along the periphery of the nucleus. With the growth of the ovocyte the sections of the intensively coloured protoplasm shift towards the periphery and gradually acquire a more and more porous appearance, and, finally, disappear. The number of the nucleoli in the nucleus increases with the Erowth of the ovocyte. The membrane of the ovocyte is thin, structureless, and is coloured blue by means of. azan. The follicular cells lie upon it. In later ovocytes of the period of small growth a light perinuclear zone is formed around the nucleus; this zone is very sharply delineated from the remaininP; protoplasm. In the Capelin females which • have survived the spawning and migrated to the fattening area two processes take place in the gonads; the destruction /189 of the traces of the concluded spawning and the growth of the ovocytes, which will be spawned in the subsequent year. The females with this condition of the gonads occur from April to July inclusively (fig. 1 and 2). Place and time of material collections for characterization of the maturation stages of the capelin gonads. Sea areas: Motovka Gulf West-Coastal Kildin Bank Jan. Feb. Mar. Apr. May.. um. Jul. Nov. ■ ■ - - IV- IV; VI-II . - . Rybachya Bank _ Finmarken Bank . III-IV Murmansk shallows Murmansk Bank - Southwestern slope . - III-IV Northeastern slope . - Murmansk Spit III Central Trough III - Central Elevation Eastern slope of the . Medvezhya (Bear) Bank - III Novaya Zemlya Bank ▪ - VI-II . , V - VI-II - VI II VI-II - . • «Me - - III - III 21E, VI-II - For the maturation stage III of the capelin'gonads the ovocytes of the synaptic path : and the ovocytes of— the period of small growth are characteristic ]; furthermore, ovocytes of older generation are present which have entered the phase of the trophoplasmatic growth. A deposition of fat and yolk takes place in the ovocytes of the older generation. The fat is initially deposited in the perinuclear zone, the yolk in the nerinherir11 nart of the ovocyte. Fi. 1: "Nest" of ovocytes of the synaptic path in the , ovary of a spawned female (ocular 7+ objective 90; bil immersion). . Gradually. these two processes envelop the entire protoplasm of the ovoCyte, and the latter is filled with yolk and fat inclusions. The nucleus has a round or elongated shape and °couples a central position. The nucleoli are of oval or rounded.shape and are arranged along *the periphery of the nucleus. Simultaneously with the deposition of trophic material the membrane of the ovocyte is . developed. This 1. Such a complex of cells remains during the course of all the subsequent Maturation stages of the ovary. Membrane'is, a double-qayered zona radiatà towards the end of trophoplasmatic growth; it is rather thick and is in tensely dyed bY azan. It also consists of follicular Membrane consisting of a layer of elongated cells. The follicle is covered from the outside by a membrane of connective tissue. Furthermore, remnants of resorbing follicular sacs remain at that time in the ovaries, a phenomenon in full agreement with the statement of V. S. Prokhorov concerning the possibilities that female Capelins may survive spawning and later spawn again. 2 Fig. 2: Ovary of a snawned female. Ovocytes of the period of small growth are visible (ocular 7+ objective 8). The marked growth of ovocytes terminatewhen the ovocytes of the older generation attain definitive size (February or March). is 0 0 7-0.8 microns. The definitive size of the ovocytes Females with maturation state III gonads may occur from November to March (fig. 3-6). 2 Prokhorov 1 V.S. The ecology of Capelin (Màllotus villosus • villosus Milner) of the Barents Sea and the prospects Of its commercial utilization. Transactions of PINRO. Murmansk, 1965. Fig. 3: Ovocytes in the phase of intensive trophoplasmatic growth. Dyed by azan (ocular 71- objective 8).. 7 /191 Fig. 4: Arrangement of fat inclusidns.in the ovocytes of intense trophoplasmatic growth. Osmium tests (oeular 71- objective 8). Fig. 5: Ovocyte filled with yolk. Ovocytes of the slow growth period are visible (ocular 7+ objective 8). Fig. 6: Ovocytes of the end of the trophoplasmatic growth. The resorption of the ovocytes of the trophoplasmatic growth is visible (ocular 7+ objective 8). At the maturation stage IV of the capelin gonads, 8 the ovocyte of the older generation enter the maturing phase. 'Study of histological sections indiented thnt the the ovocytes'ofthe older' ;7eneration ?re - filled'eomnletely with Yolk in which V q e.pO j e7 protlasf of vnrious /192 diametehs are dispersed. gos., gin •\ Fig. 7: Ovocytes of the jective . Fig. 8: Arr?mgement n* e . fl r' ' `.' ' the maturating phjective 8). Fig. :Matu're ovocvtes thnt.,vc. ' P 7: of 9 (ocular 7+ objective). Afterdyeing with azan they remain optically empty, but -after osmium - tests their content is coloured intensively black l indicating the fat nature. The membrane is represented . .hy a double-layered zona radiata - and by a follicular zone. On the outside the follicle is covered with a membrane of connective tissue. • For the first time one may see the formation of micropyle in this maturation stage. This. micronyle is a sar in the zona radiata, into which enter s . the charaCteristic wedre Of the follicular cells. At this time, only the •position of the trophic material and of. the : nucleus change . in the ovocyte. The nucleus, together with the protoplasm's layer surrounding it, moves to. one side of the ovocyte, and lOses its regular shape, its membrane at that time is poorly pronounced, , the number of nucleoli decreases. The nucleoli gradually move into the centré of the nucleus and disappear. Towards the end of this stage the ovocyte has two distinctly pronounced poles: the animal pole, where under the very membrane the nucleus with the . surrounding protoplasm is located, and the vegetative pole, where the trophic materials are concentrated. The matu- ration stage IV continues approximately one month (from March to April) (fig. 7-8). For the maturation stage V of the capelin gonads the exit of ovocytes of the older generation froM the 10 follictès is characteristic. FiF. 10: The ovocyte that came out Arrangement of fat inclusidns i.n mature ovocytes. Osmium tests (ocular 7+ objective 8). of a follicle is characterized by the fact that its entire yolk-fat mass of trophic • substances is surrounded by a layer of protoplasm, which is arranged around the periphery of the ovocyte immediately under the membrane. The thickest layer of the protoplasm is arranged on the animal pole. The yolk grainF are densely united together, but their boundaries are visible. Alonr- the entire yolk mass vacuoles are dispersed; their content, after an osmium test, indicates a fat nature. One does not succeed in detecting a the nucleus as. /mornhologically segregated structure. The membrane is only represented by the zona radiata. Females with gonads of maturation stage V occur from April to June inclusively. (fig• 9-10). During the study of ovogenesis we had the opportunity to observe resorption of certain portions of the ovocytes of the older generation, including maturation stage IV. Because of this, one can for the time being 11 express - an assumption that in the deVelopment of the capelin ovocytes one ObServes a certain asynchronism which is levelled ty meanS of rescirption of the ovocytes . still under- develop- ment. The strUcture of the zona radiata of the capelin ovocyte is interesting and still inexplicable. consists of two layers: This zone zone radiate externa and zona radiate interne. The zone radiata interna remains constant . - along the entire - circumference of the ovocyte, while the zone radiata externa is gradually narrowing, predominantly on one side of the ovocyte. The micropyle and the animal pole are establi shed on the Side where the zona radiata externe , is thinner. Probably the zone radiate of the above-describedstructure serves for attachMent of eggs to the substrate. CONCLUSIONS. 1. The capelin is a fish that spawnsonce only. 2. From the histological studies of the postspawning ovary of the capelin, it follows that some ot the females after the spawning survive and probably participate in spawning for the second time. 3. Discovery of females with gonads of maturation stages III and VI-II in the region of the eastern slope of the Bear Bank permits us to assume that the capelin spawning grounds are present in this area. • e S M A R :11 •. 1 Ac.cording to the character of 5,pawning,' Ole capelin i a once spawning fiSda. hystnlogleal study of the pot spaWhing ovary ()I the eapelin, one 2 As a rinwit :an ste that a part of . the females after spawning survives and spawns for A second tin. • . 1de witti gnnads• of taves of Mann- it y LU and V1 --Il were found on the Eepit slope of the I3ear Is!and hank. and this allows us to make a suppositiOn of the preaence irf soawning grounds In this area. .
© Copyright 2026 Paperzz