• The Korean Journal of Malacology
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• v.1 no.1
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• pp.5-12
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• 1985

The maturity of gonads, early development of the fertilized egg, spawning period, and morphogenesis of larvae in Limnoperua fortunei were studied from October, 1981 to November, 1982 as on attempt to identify its life cycle. 1) Active motility of its sperm was observed at late May, and matured egg could be found at late June. 2) It was estimated that the spawning was occured from late August. This species was belong to the short-term breeder because it finished its spawning within 20 days. 3) It has free-living trochophore and D-shaped larva stage. The shell lengths of early, middle, and D-larval stage were $140.0{\mu}m$, $167.6{\mu}m$ and $210.0{\mu}m$, respectively. The shell heigths of each stage were $97.3{\mu}m$, $137.6{\mu}m$ and $178.2{\mu}m$, respectively.

• The Korean Journal of Malacology
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• v.21 no.2 s.34
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• pp.95-105
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• 2005

Gonadosomatic index, reproductive cycle, spermatogenesis and first sexual maturity of Chlamys farreri were investigated by cytological and histological observations, from January 1998 to December 1999. The gonadosomatic index (GSI) rapidly increased in April and reached a maximum in May when seawater temperature rapidly increase. Then the GSI gradually decreased from June to August when spawning occur. Accordingly, monthly changes in the GSI in males coincide with the reproductive cycle. The spermatozoon of Chlamys farreri is the primitive type found in external fertilization species. The head of the spermatozoon is approximately $2.75{\mu}m$ in length including the acrosome measuring about $0.50{\mu}m$ in length, and its tail was approximately $20{\mu}m$, the axoneme of the tail flagellum consists of nine pairs of microtubules at the periphery and a pair at the center. Five spherical mitochondria around the centriole (the satellite body) appear in the middle piece of the sperm. The spawning period was from June to August and the main spawning occurs from July to August when seawater temperatures are greater than $20^{\circ}C$ The reproductive cycle of this species can be categorized into five successive stages; early active stage (January to March), late active stage (March to April), ripe stage (April to August), partially spawned stage (June to August), and spent/inactive stage (August to January). Over 50% of male scallops attained first sexual maturity between 50.0 and 60.0 mm in shell height, and 100% of those over 60.0 mm in shell height achieved maturity. Accordingly, we assume that male individuals begin reproduction at three years of age.

• Journal of The Korean Society of Agricultural Engineers
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• v.64 no.4
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• pp.55-64
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• 2022

The objectives of this study were to assess physical habitat suitability of fish species for different life cycle stages and to suggest appropriate ecological stream flows in a Bokha downstream reach. A dominant species of Zacco platypus was selected as the study fish of which three stages of spawning, juvenile and adult in life cycle were considered into assessment. The stream hydraulic environment was calibrated with HEC-RAS before the PHABSIM simulation. The hydraulics of flow velocity and depth were used to estimate Weighted Usable Area (WUA) by multiplying respective habitat suitability indices with stream area. Overall the WUAs tend to be great in gentle slopes with relatively shallow water depth regions. Maximum WUAs, ie, candidate for ecological flow rates were 1 m³/s, 7 m³/s and 8 m³/s for the respective spawning, juvenile and adult stages of Zacco platypus. Since the ecological flow rates for juvenile and adult stages appeared to be is greater than the abundant flow rate (3.67 m³/s) for the study reach, additional water supply may be needed but should be cautious to avoid the spawning period of Apr through May from the stream water management perspective.

• Proceedings of the Korean Society of Developmental Biology Conference
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• 2005.07a
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• pp.52-52
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• 2005

Oogenesis, the gonadosomatic index (GSI), reproductive cycle and first sexual maturation of the female Neptunea (Barbitonia) arthritica cumingii have been investigated by light and electron microscope observations. In the early vitellogenic oocyte, the Golgi complex and mitochondria were involved in the formation of glycogen, lipid droplets and yolk granules. In late vitellogenic oocytes, the rough endoplasmic reticulum and multivesicular bodies were involved in the formation of proteid yolk granules in the cytoplasm. In particular, compared with the results of other gastropods, it is a different result that appearances of cortical granules at the cortical layer and microvilli on the vitelline envelope, which is associated with heterosynthetic vitellogenesis, were not observed in vitellogenic oocytes during oogenesis. A mature yolk granule was composed of three components: main body (central core), superficial layer, and the limiting menbrane, Monthly changes in the gonadosomatic index in females were studied in 2002 and 2003 were closely associated with ovarian developmental phases. Spawning occurred between May and August in 2002 and 2003 and the main spawning occurred between June and July when the seawater temperature rose to approximately 18${\sim}$23${\circ}$C. The female reproductive cycle can be classified into five successive stages: early activestage (Septmber to October), late active stage ( November to February), ripe stage (February to June), partially spawned stage (May to Aygust), and recovery stage (June to August).

• The Korean Journal of Malacology
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• v.22 no.1 s.35
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• pp.51-61
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• 2006

Oogenesis and the reproductive cycle in female Ruditapes philippinarum were investigated by cytological and histological observations. R. philippinarum is dioecious and oviparous. During vitellogenesis, the Golgi complex, glycogen particles and mitochondria were involved in the formation of lipid droplets and lipid granules in the cytoplasm of the early vitellogenic oocyte. In the late vitellogenic oocyte, cortical granules, the endoplasmic reticulum, and mitochondria were involved in the formation of proteid yolk granules in the cytoplasm. At this time, exogenous lipid granular substance and glycogen particles in the germinal epithelium passed into the oocyte through the microvilli of the vitelline envelope. The spawning period was once a year between early June and early October, and the main spawning occurred between July and August when seawater temperature was approximately $20^{\circ}C$. The reproductive cycle of this species can be categorized into five successive stages: early active stage (January to March), late active stage (February to May), ripe stage (April to August), partially spawned stage (May to October), and spent/inactive stage (August to February). Percentages of female clams at frst sexual maturity of 15.1-20.0 mm in shell length were 52.6% (50% of the rate of group maturity was 17.83 mm in length), and 100% for the clams > 25.1 mm.

• Fisheries and Aquatic Sciences
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• v.1 no.1
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• pp.82-93
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• 1998

Monthly changes of the gonad follicle index (GFI), reproductive cycle, egg-diameter composition, first sexual maturity of the Pacific oyster, Crassostrea gigas, were studied based on the samples which have been collected from the intertidal zone of Poryong west coast of Korea, from January to December, 1996. C. gigas, is dioecious, while a few individuals are alternatively hermaphroditic. Monthly variation of gonad follicle index (GFI) used for determination of spawning period, coincided with the reproductive cycle. GFI increased from April when seawater temperatures gradually increased and reached the maximum in May. And then, GFI sharply decreased from June to September due to spawning. Reproductive cycle of this species can be divided into five successive stages: in females, early active stage (March to April), late active stage (April to May), ripe stage (May to August), partially spawned stage (June to September) and spent/inactive stage (September to February); in males, early active stage (February to March), late active stage (April to May), ripe stage (May to September), partially spawned stage (June to September) and spent/ inactive stage (September to February). The diameter of fully mature eggs are approximately 50um. Spawning occurred from June to September, and two spawning peaks were observed in June and August when the seawater temperature was above $20^{\circ}C$. Percentages of the first sexual maturity of males of 20.1-25.0 mm in shell height were over $50\%$, while those of females of 25.1-30.0 mm in shell height were over $50\%$. All the males of > 30.1 mm and all the females of ^gt; 35.1 mm completed their first sexual maturity. The results suggest that C. gigas has a protandry phenomenon. Sex ratios of 919 oysters observed were 453 females $(49.29\%)$, 429 males $(46.68\%)$, 16 hermaphrodites $(1.74\%)$, and 21 indeterminate individuals $(2.29\%)$. In age class I, sex ratio of males were $64.00\%$, thus, a higher percentage than that of females. It was noted that $64.00\%$ of the young males (age class I) were more functional than females in age class I, but 2-3 year-old oysters showed higher percentage of females. Percentages of hemaphrodites in 2-3 year classes were relatively higher than those in other year classes. Histological pattern of hermaphrodites can be divided into two types: Type I (hermaphrodite having a number of newly formed developing oocytes on the oogenic tissues within a degenerating spermatogenic follicle after discharge of numerous spermatozoa) and Type II (hermaphrodite having two separate follicles in the same gonad).

• Development and Reproduction
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• v.1 no.2
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• pp.173-180
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• 1997

This study has been conducted to investigate the molting behavior and the effects of rearing temperature and day length on molting in the behavior and the effects of rearing temperature and day length on molting in the giant freshwater prawn, Macrobrachium rosenbergii reared in the laboratory. The results obtained were summarized as follow: 1. After pre-spawning molting, the protopodites of 1st, 2nd, 3rd, and 4th except 5th pleopod bore new breeding setae which conserve eggs in the brooding chamber and the basis of 3rd, 4th, and 5th pereiopods bore new breeding dresses which transport the ovulated eggs into the brooding chamber. 2. Adult females reared in 27.5-$29.4^{\circ}C$ molted 10-12 times per year at interval of 27-35 days, of which four or six moltings were common molting for growth and another four or five moltings were pre-spawning molting for spwaning and brooding. In winter season, pre-spawning molting did not happen to most of adult females in spite of the same temperature. 3. Duration of intermolt cycle was 31-38 days and 26-30 days at 25.3- $26.5^{\circ}C$ and 28.7- $30.4^{\circ}C$ of rearing temperature, respectively.

• Development and Reproduction
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• v.25 no.3
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• pp.157-171
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• 2021

To determine whether the reproductive processes of sea bass, Lateolabrax japonicus, proceed normally after transportation from an outdoor net-cage into indoor tanks, we examined changes in the gonadosomatic index (GSI), histological gonadal tissue, and plasma levels of sex hormones (testosterone and estradiol-17ß) during their annual reproductive cycle. We also measured maturation and spawning across two sea water salinity levels (full and low salinity). Fecundity was estimated by the relationship between egg number and body size in female sea bass. Monthly changes in the GSI, histological gonadal tissues, and oocyte size showed both male and female sea bass reach final maturation in January and February, respectively, indicating that the spermiation of males occurs earlier than the spawning of females. The histological results indicated that the sea bass is a multiple spawner, similar to many marine teleosts, exhibiting group-synchronous oocyte development. Female maturation and spawning were enhanced in lower salinity seawater (29.6-31.0 psu) compared to that of normal salinity (34.5-35.1 psu). These results confirm that sea bass reproduction can occur successfully in captivity and imply that fertilized eggs can be collected from February to March. Additionally, our results show that lower salinity enhances oocyte maturation and spawning of female sea bass.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.17 no.6
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• pp.523-528
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• 1984

The small filefish, Rudarius ercodes, generally spawning from mid May to early October in the natural habitat, was exposed to various photoperiod and temperature regimes. These environmental effects on the gonad activity, regression and recrudescence were experimentally investigated based on the mechanism of reproductive cycle. Spawning season was initiated in the early spring with the gonad activated by long photoperiod(13L) and stimulated by compensatory temperature rising. Even when the gonad activated readily at the above critical daylength (12L to 13L)was kept back at the below if, it went on maturing. At the end of spawning period (mid September), since the shortening of daylength (12L) resulted in the gonad regression regardless of temperature, the short daylength might be related to the termination of spawning in situ. When the regressive gonad at the post spawning period was treated by the above 13L: $20^{\circ}C$ condition, it could recrudesce and bring forth even spawning. From this fact, the feasible control of annual reproductive cycle of small filefish was recognized. But even in the long daylength, the temperature above $28^{\circ}C$ was preventive of gonad maturation.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.8 no.4
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• pp.234-241
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• 1975

Reproductive cycle of Haliotis discus hannai Ino was studied based on the samples which were collected in Yeosu area from January, 1973 to December, 1974. Particular emphasis was paid on the seasonal variation of gonad maturity factor, coefficieot of gonad maturity, fatnesss, and relationship of gonad weight to growth of the abalone. seasonal fluctuation of water temperature and induction of artificial spawnings were also checked. The abalone of this area spawns twice a year: spring spawning(early May-late July) and Autumn spawning(early September-late November). peak spawning occurs from late May to middle of June for spring spawning: it occurs from late September to early November for Autumn spawning. Gonad maturity factor was closely related to the spawning seasons. For the spring spawning Gonad maturity factor reached to its maximum value as 18.84 in April; for the Autumn spawning it reached to its maximum value as 22.65 in September. Annual minimum value was 12.65 in January. Annual maximum values of coefficient of gonad maturity were 44.10 in May and 49.05 in September and the annual minimum was 10.09 in January. Fatnesswas highest in July as 0.221 and it was lowest in October as 0.1058. Ratios of shell length to gonad weight were formulated as follows : $$In\;September\;GW=0.000003710SL^{3.7860}$$ $$In\;January\;GW=0.000021198SL^{2.8564}$$ $$Annual\;mean\;GW=0.00000005013SL^{4.2273}$$ Relations of total weight to gonad weight were formulated as follows : In September GW=0.1918TW-4.9231 In January GW=0.0992TW-0.1759 Annual maan GW=0.1568UW-3.5256.