Reproductive cycles in oregon populations of the echlnoid, Strongylocentrotvs purpuratus (Stimpson). I. Annual gonad growth and ovarian gametogenic cycles

Four annual reproductive cycles were followed in the echinoid, Strongylocentrotus purpuratus (Stimpson), at three places on the central Oregon coast near 44°45′N lat., where intermittent upwelling depresses coastal sea temperatures from June through September. Monthly measurements were made of the gonad index of samples of 30 urchins and the relative frequency of five stages in oogenesis were determined from sectioned ovaries from these samples.Individuals in these populations are synchronous in their annual cycle of gonad growth, oogenesis, and spawning, the latter taking place between late December and March. The population usually undergoes one major, complete spawning within a period of 30 days. When large reserves of stored nutrients are present, ova continue to mature over a longer period and may be present in quantity from December into April. Gonad weight does not change significantly from March through June. From July through November the gonad undergoes its annual growth at a mean instantaneous relative growth rate of ≈ 1 % per day. Gonad growth is not significantly correlated with sea temperature. Variable temperatures resulting from upwelling do not result in erratic fluctuations in the reproductive cycle, probably because of the annual change in feeding rate, the seasonal shift in energy utilization, and the constancy of the amount of food assimilated during gonad growth. Gonad size and annual growth rates may differ significantly between years and locations, indicating that both are influenced by local environmental factors, probably food availability and degree of wave action.The frequency of oogonial clusters is least in mid-winter, increases after spawning, reaches an annual maximum in June and declines in the fall. Primary oocyte growth is very slow until October, when it increases abruptly, and some oocytes become ova as early as late October. When stored nutrients are low, many oocytes do not complete growth by January, and are not spawned until May. Prolongation of the spawning period delays the increase in frequency of oogonial clusters in the following new cycle. The timing of the annual increase in oogonial cluster frequency and of the onset of rapid oocyte growth did not otherwise vary between places and years. In these populations, entrainment or synchronization of the reproductive cycle to seasonal environmental events probably occurs at the beginning of one or all of these critical annual events: oogonial proliferation, annual gonad growth and rapid oocyte growth.     

Oogonial proliferation and early oocyte dynamics during the reproductive cycle of two Clupeiform fish species

Although oogonial proliferation continues in mature females in most teleosts, its dynamics and the transformation of oogonia to early meiotic oocytes during the reproductive cycle have received little attention. In the present study, early oogenesis was examined throughout the reproductive cycle in two Clupeiform fishes, the Mediterranean sardine, Sardina pilchardus, and the European anchovy, Engraulis encrasicolus. Observations using confocal laser scanning microscopy (CLSM) provided extensive information on markers of oogonial proliferation (mitotic divisions, oogonia nests) and meiotic prophase I divisions of oocyte nests (leptotene, zygotene, pachytene, diplotene) in ovaries of different reproductive phases. In sardine, oogonial proliferation persisted throughout the entire reproductive cycle, whereas in anchovy, it was more pronounced prior to (developing ovaries) and after (resting ovaries) the spawning period. Anchovy exhibited a higher rate of meiotic activity in developing ovaries, whereas sardine exhibited a higher rate in resting ovaries. The observed differences between the two species can potentially be attributed to different seasonal patterns of energy allocation to reproduction and the synchronization between feeding and the spawning season.     

Control of oocyte recruitment: regulative role of follicle cells through the release of a diffusible factor

To determine whether oogonial proliferation and oocyte recruitment are under control of hypophyseal and/or ovarian factors, we carried out a series of investigations using Podarcis sicula, a lizard inhabiting the temperate lowlands of Europe in which oocyte recruitment occurs throughout the year, as animal model. Germinal beds containing oogonia and oocytes in prefollicular stages were cocultured with different ovarian compartments in presence/absence of FSH, and the effects of different treatments were evaluated by counting the number of prelepto-leptotene oocytes. Results revealed that oocyte recruitment from the pool of oogonia is under the control of a factor released by follicle cells while FSH has an indirect effect on modulating oogonial proliferation. SDS-PAGE analyses carried out on media conditioned by follicles suggest that the factor involved in the control of oocyte recruitment may be a small protein (about 21 kDa) and that its release is dependent on the period of the ovarian cycle but apparently not on the circulating levels of FSH.     

Ecological investigations of the zooplankton community of Balsfjorden,northern Norway: Population structure and breeding biology of the chaetognath Sagitta elegans Verrill

The population dynamics of the chaetognath Sagitta elegans Verrill has been followed in Balsfjorden in 1976 and 1977. Seasonal variation in abundance, length-frequency distribution, growth in total length, and maturity stages are presented and discussed in relation to changes in hydrography.An annual generation of S. elegans was found, with a protracted and more or less continuous breeding season from May until October during 1977. The 1976 year-class consisted of two distinct length groups, both of which participated in the 1977 spawning. This spawning gave rise to possibly four sub-populations during 1977. The variation in numbers of sub-populations produced during the spawning season in 1976 and 1977 is discussed in relation to the hydrographical conditions in Balsfjorden. From November 1976 to March 1977 the abundance of S. elegans varied between 1 and 8 ind. · m^?3. The lowest value was recorded in May (0.9 ind. · m^?3). From September to December 1977 the population abundance was ≈2 ind. · m^?3.     

Gametogenesis, spawning and fecundity of Platygyra daedalea (Scleractinia) on equatorial reefs in Kenya

The reproductive ecology of the hermaphroditic broadcast spawning scleractinian reef coral Platygyra daedalea was studied on lagoonal reefs in Kenya. While single annual gametogenic cycles occurred in 84% of colonies, biannual gametogenic cycles were recorded in 16% of colonies and these patterns occurred in two morphotypes. In colonies with a single annual cycle, oogenesis occurred for 6–7 months from September to March and spermatogenesis for 5 months from November to March. In biannually spawning colonies, oogenic cycles overlapped for at least 2 months prior to gamete release. The major spawning period occurred in February and March, with minor spawning also occurring in August–October in biannually spawning colonies. Reproductive effort was lower during the minor winter compared to the major summer spawning, with fewer colonies reproducing (12.5–19.2%), not all mesenteries producing oocytes (32.5%) and less than half of the mesenteries with mature oocytes had associated spermaries (48.1%).     

Expression of activin subunits and receptors in the developing human ovary: activin A promotes germ cell survival and proliferation before primordial follicle formation

The formation of the essential functional unit of the ovary, the primordial follicle, occurs during fetal life in humans. Factors regulating oogonial proliferation and interaction with somatic cells before primordial follicle formation are largely unknown. We have investigated the expression, localisation and functional effects of activin and its receptors in the human fetal ovary at 14-21 weeks gestation. Expression of mRNA for the activin betaA and betaB subunits and the activin receptors ActRIIA and ActRIIB was demonstrated by RT-PCR. Expression of betaA mRNA increased 2-fold across the gestational range examined. Activin subunits and receptors were localised by immunohistochemistry. The betaA subunit was expressed by oogonia, and the betaB subunit and activin receptors were expressed by both oogonia and somatic cells. BetaA expression was increased in larger oogonia at later gestations, but was low in oocytes within newly formed primordial follicles. Treatment of ovary fragments with activin A in vitro increased both the number of oogonia present and oogonial proliferation, as detected by bromodeoxyuridine (BrdU) incorporation. These data indicate that activin may be involved in the autocrine and paracrine regulation of germ cell proliferation in the human ovary during the crucial period of development leading up to primordial follicle formation.     

Seasonal histological changes in the ovaries of a mountain stream teleost, Schizothorax richardsonii (Gray and Hard).

In S. richardsonii, unlike its testis, the whole of the ovary is fertile. The oogonia pass through seven maturation stages to form the ripe ova. The residual oogonia are responsible for the development of the new crop of oogonia. The zonation of the ooplasm reveals that a majority of the oocytes have a darkly stained inner and a lightly stained outer zone. The yolk nucleus probably has some relationship with the process of vitellogenesis. The nucleoli are produced by the division and fragmentation of the nucleolus. Extrusion of nucleoli appears to be associated with the formation of yolk. The formation of yolk globules in the oocyte begins in the periphery of the ooplasm and moves inward till the whole of the ooplasm in impregnated with yolk. As the yolk vesicles are PAS-positive in this fish, they contain mucopolysaccharides. The ovarian cycle can be divided into five stages. The ovary becomes much enlarged and distended in the month of October and delicate and thin in March. The spawning season extends from late October to December and the ovary exhibits asynchronism.     

Involvement of GnRH neuron in the spermatogonial proliferation of the scallop, Patinopecten yessoensiss

The aim of this study was to quantitatively analyze a pattern of proliferation of gonial cells and to demonstrate neural involvement in spermatogonial proliferation of the scallop by the in vitro experiment. Immunocytochemistry for incorporated BrdU was used to identify mitotically active gonial cells. The pattern of proliferation of gonial cells was divided into two phases: phase I; oogonia and spermatogonia slowly proliferate through the growing stage: phase II; oogonia develop into oocytes and spermatogonia start to proliferate rapidly from the mature stage through the spawning stage. The neurons detected with anti-mammalian (m)GnRH antibody were distributed sparsely in the pedal ganglion and predominantly in the cerebral ganglion of both sexes at the growing stage. The extracts from the cerebral and pedal ganglion (CPG) of both sexes collected at the growing stage promoted proliferation of spermatogonia in the in vitro culture of the testicular tissue as well as mGnRH. However, CPG extract had no effect on oogonial proliferation. The increased mitotic activity induced by CPG and mGnRH was abolished by the addition of mGnRH antagonists and anti-mGnRH antibody, suggesting that the spermatogonial proliferation is regulated by GnRH-like peptide in CPG of the scallop. The same mitotic activity as CPG extract and mGnRH was observed in the hemocyte lysate, but not in the serum. These findings suggest that the spermatogonial proliferation at phase II in the scallop may be under the neuroendocrine control by GnRH neuron in CPG.     

Histological studies on early oogenesis in barfin flounder (Verasper moseri)

There is much information on oogenesis from the resumption of the first meiotic division to oocyte maturation in many vertebrates; however, there have been very few studies on early oogenesis from oogonial proliferation to the initiation of meiosis. In the present study, we investigated the histological changes during early oogenesis in barfin flounder (Verasper moseri). In fish with a total length (TL) of 50mm (TL 50mm fish), active oogonial proliferation was observed. In TL 60mm fish, oocytes with synaptonemal complexes were observed. Before the initiation of active oogonial proliferation, somatic cells which surrounded a few oogonial germ cells, started to proliferate to form the oogonial cysts that accompanied oogonial proliferation. In TL 70mm fish, however, the cyst structure of the oocyte was gradually broken by the invagination of somatic cells, and finally the oocyte became a single cell surrounded by follicle cells. Upon comparison of nuclear size, DNA-synthesizing germ cells could be divided into two types: small nuclear cells and large nuclear cells. Based on histological observation, we propose that the small nuclear cells were in the mitotic prophase of oogonia and the large nuclear cells were in the meiotic prophase of oocytes, and that the nuclear size increases upon the initiation of meiosis.     

Formation of germ cell cluster in tubuliferan thrips (Thysanoptera)

The ovarian structure and oogenesis in the larval stages of 2 tubuliferan species, Bactrothrips brevitubus (Idolothripinae) and Holothrips yuasai (Phlaeothripinae) of the Thysanoptera were examined using ultrathin serial sections, with special reference to the cluster formation of germ cells. No cells identifiable as stem cells were found in the ovarian rudiments of the 1st and 2nd-instar larvae. The clusters of oogonial cells were observed frequently in the 1st-instar, but scarcely in the 2nd-instar larvae: all the oogonial clusters observed were composed of 2 cells. In the 2nd-instar larvae, the ovarian region posterior to the germarium, or the vitellarium, contained both solitary and clustered oocytes. The oocyte clusters were composed of less than 5 cells. The oocytes, located in the posterior region of the vitellarium, were all solitary and at the previtellogenic stages.A protuberance was found in some solitary germ cells. The structure may represent a remnant of the intercellular bridge, previously formed between the germ cells. The number of oocytes composing a cluster is small but does not always fit the 2ⁿ-rule. One possible explanation is the accelerated detachment process of oocytes from a cluster. The cluster formation of germ cells has been confirmed in the Tubulifera as well as in the Terebrantia, and this phenomenon can be recognized as a general feature of the panoistic ovaries of the Thysanoptera.     

Proliferation of Oogonia and folliculogenesis in the viviparous teleost Ilyodon whitei (Goodeidae)

Oogonial proliferation in fishes is an essential reproductive strategy to generate new ovarian follicles and is the basis for unlimited oogenesis. The reproductive cycle in viviparous teleosts, besides oogenesis, involves development of embryos inside the ovary, that is, intraovarian gestation. Oogonia are located in the germinal epithelium of the ovary. The germinal epithelium is the surface of ovarian lamellae and, therefore, borders the ovarian lumen. However, activity and seasonality of the germinal epithelium have not been described in any viviparous teleost species regarding oogonial proliferation and folliculogenesis. The goal of this study is to identify the histological features of oogonial proliferation and folliculogenesis during the reproductive cycle of the viviparous goodeid Ilyodon whitei. Ovaries during nongestation and early and late gestation were analyzed. Oogonial proliferation and folliculogenesis in I. whitei, where intraovarian gestation follows the maturation and fertilization of oocytes, do not correspond to the late oogenesis, as was observed in oviparous species, but correspond to late gestation. This observation offers an example of ovarian physiology correlated with viviparous reproduction and provides elements for understanding the regulation of the initiation of processes that ultimately result in the origin of the next generation. These processes include oogonia proliferation and development of the next batch of germ cells into the complex process of intraovarian gestation. J. Morphol. 275:1004–1015, 2014. © 2014 Wiley Periodicals, Inc.     

An analysis of the reproductive pattern in the sea star Astropecten irregularis (Pennant) from the Bristol Channel

Summary

The reproductive cycle in Astropecten irregularis is described, making use of a range of statistical techniques detailed previously. Analysis of gonad weights proved more satisfactory than the use of gonad indices, as the latter are not independent of animal size. When examining the course of oogenesis, standardised residuals in an (R × C) contingency table are much easier to interpret than size/frequency polygons.

The species has an annual cycle with spawning in June or July, but the gonads are small even when the animals are gravid, and the annual cycle in gonad weights is more marked in males. Proliferation of oogonia may apparently occur at any time of year, and the ripe ovary contains many small, previtellogenic oocytes. There is an annual cycle of small magnitude in the size of the pyloric caecum, with a peak in December.     

Sexual Maturation, Annual Reproductive Cycle, and Spawning Periodicity of the Shore Scorpionfish, Scorpaenodes littoralis

The ovarian structure, sexual maturation, annual reproductive cycle, and spawning periodicity of the shore scorpionfish, Scorpaenodes littoralis, in Uchiura Bay, central Japan, were examined using specimens collected between May 1995 and March 1998 and fishes reared in laboratory. The ovarian stroma and blood vessels run longitudinally through the center of each ovarian lobe. The ovarian peduncles radiate from the central stroma. During the spawning season, gelatinous material is secreted from the epithelia of both the ovarian peduncle and ovarian wall, and the epithelia show morphological changes accompanying the ovarian maturation cycle. The minimum standard length at maturity was 55.2mm for males and 40.2mm for females. Males with mature testes were collected from March to November. Females in the mature or post spawning stages were collected between May and October, when the mean gonadosomatic indices were also high. This indicates that the spawning season of this species occurs between May and October. Four successive types of oocytes were grouped in the mature ovary, comprised of mature, late and early vitellogenic and previtellogenic oocytes respectively, suggesting that this species is a multiple spawner. Four captive females spawned repeatedly at intervals of 2–8 days over a prolonged period (4–8 months); a 2-day spawning interval was the most common for all females. This suggests that female S. littoralis have a 48-h spawning cycle in captivity.     

The annual reproductive cycle of the freshwater mussel Dreissena polymorpha Pallas in lakes

Summary The annual development of the gonads of Dreissena polymorpha was studied at three sampling sites in two lakes over 3 and 1 1/2 years, respectively. A resting stage occurred after the last spawning in summer/autumn. Oogenesis (accompanied by multiplying segmentation of the oogonia and early growth processes of its oocytes) restarted in specimens at least 1 year old at low temperatures (below 10° C) during winter and early spring. At one location (Fühlinger See) the onset of the spawning season was correlated with an increase of water temperatures above 12° C. At 2 m depth, two main spawning periods in May and August were normally recognized, the first at temperatures of 12–16° C, the second at 16–21° C. It was clearly demonstrated for the first time in Dreissena polymorpha that the oocytes became mature in successive cohorts within one gonad. A female mussel may spawn several times during the reproductive season. At 9 m depth, the onset of spawning also started at about 12° C; this occurred in late summer, with two spawning periods within 1 month at a temperature range of 12–16° C. At another location (Heider Bergsee) the size of the gonads and the oocytes was reduced during April of both years studied, when food supply was low simultaneously with rapidly rising water temperatures in this shallow lake. There was no spawning period during spring. The major spawning period was delayed until July (temperatures 19–22°C). This shows (1) the synchronizing influence of low winter temperatures on the annual reproductive cycle and (2) a temperature threshold of at least 12° C for the start of the spawning processes. The results are discussed with regard to the geographical limits of further spread of Dreissena polymorpha.     

REPRODUCTION SEXUÉE D'UNE ASTÉRIE FISSIPARE,SCLERASTERIAS RICHARDI (PERRIER, 1882) / SEXUAL REPRODUCTION IN A FISSIPAROUS ASTEROID,SCLERASTERIAS RICHARDI (PERRIER, 1882)

Sclerasterias richardi, a relatively deep sea asteroid (140–200 m) from the border of the Mediterranean continental shelf, is characterized by an asexual reproduction by fissiparity concomitant with a functional sexuality.

A monthly sampling of a population from Calvi (Corsica) has allowed a study of the complete sexual cycle from 354 histologically-treated specimens.

The 218 sexually defined animals (62% males, 38% females) show strict gonochorism. In males, spermatogenesis is cyclic and sexual maturity seems to be reached before that of the females. In females, the different stages of oogenesis are well marked: oogonia and parietal oocytes disappear only at maturity. Oligolecithic oocytes (120–150 μn) show a synchronous growth.

The annual reproductive cycle is well defined in both sexes with one spawning period from mid-September to mid-October.

After spawning, a resting period (from mid-October to mid-January) occurs during which unspawned oocytes are phagocytized by more or less isolated accessory cells. These phagocytic cells have never been found in male specimens.

Each month the presence of specimens without gonads or unsexable individuals is one of the characteristics of this cycle. Their high proportion during the organization stage and after spawning can be easily explained. In March they are frequent too, owing to the infestation of gonads by Ciliates.

As shown by our samples, the bottom water temperature is nearly the same during the whole year and cannot be directly involved as the dominant exogenous variable stimulating spawning.

As a consequence of fissiparity which affects the main part of the population there is a great inter- and intra-individual variability.

The reproductive potentiality is low: as a female emits approximatly 400–500 ova whose development produces planktotrophic larvae with a long pelagic life, it is clear that sexual reproduction is accessory in comparison with asexual reproduction by fission.     

Relationship between Marteilioides chungmuensis infection and reproduction in the Pacific oyster, Crassostrea gigas

Marteilioides chungmuensis, a protozoan paramyxean parasite, infects the oocytes of the Pacific oyster, Crassostrea gigas. The effects of infection on the reproductive cycle of C. gigas were investigated over two consecutive years at Okayama Prefecture, Japan. In male oysters, gonadal development began during February/March, maturity was achieved in June and spawning activity extended from July to September. In November and December, male oysters were not seen, probably because their gonads regressed to connective tissue and they transformed into undifferentiated oysters. By contrast, female oysters, in which parasite spore formation occurred, were still carrying oocytes until the following March and the spawning process of female oysters took 5 months longer than that of males in epizootic areas. The prevalence of M. chungmuensis infection increased from July to September, when most female oysters had their spawning period, and declined from October to the following April when oysters were at the spent stage. The prevalence of infection increased again in May of the following year and high prevalence was observed in the following July. When prevalence was compared between oysters of different age classes, higher prevalence was detected in older than in younger oysters. Histological examination showed that infected oysters produced oocytes continuously and spawned repeatedly from October to March, during which period healthy oysters were reproductively inactive. Parasites can infect the oocytes of infected oysters throughout the longer spawning period. These observations suggest that M. chungmuensis extends the reproductive period of infected oysters for its own reproductive benefit.     

Oocytes develop from interconnected cystocytes in the panoistic ovary of Nemoura sp. (Pictet) (Plecoptera : Nemouridae)

The 2 ovaries of Nemoura sp. (Plecoptera : Nemouridae) are comb-like and house about 60–70 ovarioles each. By ultrathin serial sections through a whole ovariole of a last-larval instar, we gathered information on its ultrastructure and 3-dimensional architecture. The germarial region contains several clusters of interconnected oogonia or oocytes. The intercellular bridges (ring canals) are filled with fusomes. Most of the fusomes assemble to polyfusomes and some of the intercellular bridges move together and their cells assemble to rosettes. Results indicate that existence of polyfusomes is not sufficient for rosette formation. The oogonia or oocytes of each cluster develop synchronously. Oocytes detach from clusters next to intercellular bridges. A transdetermination of oogonia to nurse cells does not occur. Thus, the stone flies remain true panoists.     

Cyclical Changes in the Testis of the Hagfish Eptatretus burgeri (Cyclostomata)

The development of the spermatogenetic stages in the testis of the hagfish Eptatretus burgeri was studied by means of histological techniques. These animals have an annual reproductive cycle with a spawning season in October. Spermatocytes begin to appear in January and reach a maximum in March. The development of spermatids of stage I and stage II starts in April and June, respectively. In August about 35% of the testicular follicles contain spermatids of stage II. The gonadosomatic index shows a more or less constant increase from November until August. During the spawning season, no animals with well developed testis could be trapped. About 10% of male hagfish bear undeveloped gonads.     

Phylogenetic significance of the structure of adult ovary and oogenesis in a primitive chilognathan diplopod,Hyleoglomeris japonica Verhoeff (Glomerida,Diplopoda)

Some histological details of the adult ovary of Hyleoglomeris japonica are described for the first time in the glomerid diplopods. The ovary is a single, long sac-like organ extending from the 4th to the 12th body segment along the median body axis, lying between the alimentary canal and the ventral nerve cord. The ovarian wall consists of a layer of thin ovarian epithelium which surrounds a wide ovarian lumen. A pair of longitudinal “germ zones,” including female germ cells, runs in the lateral ovarian wall. Each germ zone consists of two types of oogenetic areas: 1) 8–12 narrow patch-shaped areas for oogonial proliferation, arranged metamerically in a row along each of the dorsal and ventral peripheries, and 2) the remaining wide area for oocyte growth. Oogonial proliferation areas include oogonia, very early previtellogenic oocytes, and young somatic interstitial cells, among the ovarian epithelial cells. The larger early previtellogenic oocytes in the oogonial proliferation areas are located nearer to the oocyte growth area, and migrate to the oocyte growth area. They are surrounded by a layer of follicle cells and are connected with the ovarian epithelium of the oocyte growth area by a portion of their follicles. They grow into the ovarian lumen, but their follicles are still connected with the oocyte growth area. Various sizes of the previtellogenic and vitellogenic oocytes in the ovarian lumen are connected with the oocyte growth area; the smaller oocytes are connected nearer to the dorsal and ventral oogonial proliferation areas, while the larger ones are connected nearer to the longitudinal middle line of the oocyte growth area. Following the completion of vitellogenesis and egg membrane formation in the largest primary oocytes, the germinal vesicles break down. Ripe oocytes are released from their follicles directly into the ovarian lumen to be transported into the oviducts. Ovarian structure and oogenesis of H. japonica are very similar to those of other chilognathan diplopods. At the same time, however, some characteristic features of the ovary of H. japonica are helpful for understanding the structure and evolution of the diplopod ovaries. Some aspects of the phylogenetic significance in the paired germ zones of H. japonica are discussed. J. Morphol 231:277–285, 1997. © 1997 Wiley-Liss, Inc.     

Seasonal changes in the hypothalamo-hypophyseal-ovarian system in the catfish,Heteropneustes fossilis (Bloch)*

The annual reproductive cycle of the catfish, H. fossilis (Bloch) is divided into the preparatory period (February-April), the prespawning period (May-June), the spawning period (July-August) and the postspawning period (September-January). During the early postspawning period (September-November), the hypothalamo-hypophyseal-ovarian system shows a gradual regression. In January, the hypothalamic nuclei, the pars magnocellularis (PMC), the pars parvocellularis (PPC) of the nucleus preopticus (NPO), and the nucleus lateralis tuberis (NLT) show renewed activity, as shown by a significant increase in their nuclear diameters and an accumulation of neurosecretory material (NSM) in their cell bodies. The hypophysis and the ovary remain quiescent. During the preparatory period, all the hypothalamic neurons studied indicate decreased activity but simultaneously show an accumulation of NSM in their cell bodies. The number of granulated basophils in the proximal pars distalis (PPD) of the hypophysis remains low but ovarian weights increase, presumably due to the multiplication of oogonia. In the prespawning period, there is a marked accumulation of NSM in the cell bodies of the hypothalamic neurons and at the same time the number of granulated basophils in the PPD of the hypophysis dramatically increases with concomitant increase in vitellogenic activity in the ovary. During the spawning period, the hypothalamic neurons continue to store NSM in their cell bodies and simultaneously there is a tremendous increase in the number of granulated basophils in the PPD of the hypophysis and the ovary has a large proportion of yolky primary oocytes. Spawning is associated with a significant degranulation of the granulated basophils in the PPD of the hypophysis. The significance of the results is discussed in relation to the environmental and hormonal regulation of seasonal ovarian activity.