Gonadal maturation and annual reproductive cycle in ovoviviparous oblong rockfish, Sebastes oblangus on the basis of monthly gonadosomatic indices (GSI), hepatosomatic indices (HSI) and histological observations of gonadal tissues. GSI values of female were in a wide range from $0.l5\pm0.0l\;(July)\;to\;58.54\pm3.86$ (December) and began to increase in August and reached the maxium in December, then decreased rapidly thereafter. Male GSI values were in a range from $0.08\pm0.03$ (July) to $1.55\pm0.27$ (September) and began to increase rapidly in July and reached the maximum in September, then decreased gradually, thereafter. Female HSI was in a range from $0.89\pm0.12$ (December) to $3.73\pm0.15$ (October), and male's was from $2.09\pm0.76$ (October) to $3.62\pm0.48$ (August). HSI reached the maximum values one or two months before GSI reached their maxium values in both sex, and then decreased rapidly thereafter. Mature oocytes began to appear in late October as being oocytes began to mature in August, and the type of oocyte development is categorized in the roup-synchronous oocyte development'. Ovulation and fertilization of ripe oocytes occurred in November, and hatched larvae were born from December to January. Maturation of testis was progressed in short term from August to October and spermatozoa were released in October. Sperm balls consisted of many spermatozoa were preserved in ovarian cavity of female after copulation. These results may suggest that the annual reproductive cycle of oblong rockfish could be divided into the following successive stages: growing (August and September), mature (September and October), gestation (November and December), parturition (December and January) and resting (February to July) in female, and growing (August and September), mature (September and October), copulation (October) and resting (November to July) in male.
The present investigation dealt with observation and experiments concerning the growth and differentiation of hop plant, using the varieties of Cascade(C), Shinshuwase(Sh), and Hallertau(H). The results were as follows: (1) Life cycle of hop plants. The annual growth period of hop plant was devided chiefly into 3 phases, dormant, vegetative and reproductive. (2) Growth of main stem. The hop vine begun to grow in the middle of May and grow vigorousely in the middle and latter of June, then gradually decline or stops at the middle of July and the early of August. (3) Growth of lateral vines. By the statistical analysis, it is judged that the varieties of H and Sh were more grown than that of C. H and Sh were not significant, but H and Sh from C were significant in 5% level. (4) Fresh weight and water content of hop cone. Hop cone in fresh weight of C variety was higher than those of other two varieties and water content of hop cone was decreased with time elapse in three races together. (5) Growing point. Histological view of hop varities in each was different. C showed form of sweet potato, H showed form of round, and Sh showed form of ellipse. (6) Shape of the leaf. C and H were 3 lobes, but Sh is 3∼5 lobes. Generally, the color is dark green. (7) Hop cones. Hop cones are as follows.
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.
Annual gonad development of the rock shell, Thais clavigera distributed in Jeju Port was investigated over a 12 month period from March 1998 to February 1999. Monthly change in gonad development was examined using histology. Gametogenesis of T. clavigera in the study area initiated as early as in October and fully ripe eggs could be observed from May to July. Percent gonad area (PGA) also increased rapidly from May to July then dropped in August when the water temperature remained $22.6-24.5^{\circ}C$, suggesting that rock shell released their eggs during this period. All female rock shell collected during the course of study exhibited pseudo-penis in the head, indicating that a certain level of imposex had progressed in the study site. Relative penis size index (RPSI), an indicator of level of imposex phenomenon varied 59.5-173.4% and this value was relatively higher than the index reported from elsewhere. It was believed that such imposex phenomenon observed in T. clavigera was caused by endocrine disruption by chemical contaminants such as TBTs released from biocidal paints in the port environment.
Gametogenesis of the comb pen shell, Atrina pectinata (Linnaeus, 1767) (Bivalvia: Pinnidae) on the southern coast of Ulleungdo Island, Korea was assessed monthly (November 2013 to October 2014) using histology. Gametogenesis commenced in January when the surface water temperature was $12.6^{\circ}C$ and pen shells evidenced an early development phase with small oogonia from January to April, although few females exhibited ripe eggs in their follicular epithelium. In April, the oocyte diameter increased rapidly, and fully mature eggs appeared in May. First spawning males and females were observed in June as the surface water temperature reached $19.3^{\circ}C$ and July ($23.2^{\circ}C$) respectively. The spawning activity continued until the end of September. Histology indicated that the spawning peak of the females in Ulleungdo Island was July to August. During October to January, most of the pen shells were in spent and resting stages. Our data suggested that A. pectinata is a summer spawner, and their annual gametogenesis is closely associated with the seasonal variation in the surface water temperature. The present study is the first provided fundamental information on the life history of A. pectinata in Ulleungdo Island, and this can be put to good use in the management of this pen shell in the study area.
The aim of the present study was to analyze the reductive cycle of the red marbled rockfish Sebastiscus tertius. The analysis was based on annual changes in the gonadosomatic index (GSI), the hepatosomatic index (HSI), histology of the gonadal structure, and plasma sex steroid hormone levels of adult fish from April 1997 to April 1998. GSI of females began to increase in February and peaked ($10.8{\pm}2.72$) in May. HIS levels ($3.41{\pm}0.49$) peaked in February and elevated plasma steroid hormones ($1.47{\pm}0.75$ ng/mL for estradiol-$17{\beta}$ ($E_2$) and $230.7{\pm}27.6$ pg/mL for testosterone (T)) were observed in April. However, in male fish, GSI levels started to increase in August and remained high until November ($0.21{\pm}0.05$). T levels were was also elevated in August and peaked in October ($188.1{\pm}43.5$ pg/mL) and November ($186.8{\pm}28.0$ pg/mL), but started to decline 1 month than the GSI. These results suggest that female ovoviviparious periods span from April to June and amle mating periods occur from November to February.
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.
First sexual maturity, monthly changes in gonadosomatic index and reproductive cycle of viviparous teleost surfperch, Ditrema temmincki were investigated under photomicroscopy. Samples were collected from May 1992 to August 1993 in the vicinity of Suyoung Bay, Pusan, Korea. Body length at the first sexual maturity in female and male were 12.5cm and 13.5cm, respectively. Gonadosomatic index(GSI) in female reached the maximum in June(just before parturition) and male GSI reached the maximum in October(just before copulation). The testis is composed of a number of seminiferous tubules, and spermatogonia are originated from the germinal epithelium on the seminiferous tubule. The ovary consists of several ovigerous folds, and oogonia are originated from the inner surface of the germinal epithelium within the ovigerous fold. Annual reproductive cycle was classified into the following successive periods : in male, growing period from May to August, maturation period from September to October, copulation period from November to December, and degeneration and resting period from January to April, and in female, growing period from September to October, copulation and maturation period from November to December, gestation period from January to June, and resting period from July to August. Hepatosomatic index(HSI) in male appeared to be negatively correlated with gonadosomatic index, but that in female showed to be positively correlated.
The structure of gonads, gametogenesis and reproductive cycle of the jackknife clams, Solen strictus and Solen gordonis were investigated mainly by histological observation. The first species used were monthly sampled at the coastal area of Dadaepo, Pusan, Korea and Naechodo, Kunsan, Korea for one year from February 1982 to January 1983. The second species were monthly sampled at the sand beach of Dadaepo, Pusan, Korea, from February 1982 to January 1983. Sexualities of Solen strictus and Solen gordonis are dioecious, and these species are oviparous. The gonads are irregularly arranged from the subregion of mid-intestinal gland in visceral cavity to reticular connective tissue of foot. The ovary was composed of a number of small ovarian sacs and the testis was composed of several testicular lobuli which from the tubular structure. Early multiplicating oogonium was about $10{\mu}m$ in diamater. Nucleus and nucleolus, at that time, were distinct in appearance. Each of the early growing oocytes made an egg-stalk, connected to the germinal epithelium of the ovarian sac. A great number of undifferentiated mesenchymal tissue and eosinophilic granular cells are abundantly distributed in the ovarian sacs in the early development stages. With the further development of gonad, these tissue and cells gradually disappeared. Then the undifferentiated mesenchymal tissue and eosinophilic granular cells function as nutritive cells in the formation and development of the early stage germ cells. Mature oocytes were free in the lumen of ovarian sacs and gradually become round or oval. Ripe oocyte was about 80 to $90{\mu}m$ in diameter. With the further development of testis, each of the testicular lobuli formed stratified layers composed of spermatogonia, spermatocytes, spermatids and spermatozoa in groups on the germinal epithelium. After spawning, the gonad gradually degenerated, and disorganized completely. Then new differentiated tissues were rearranged next year. The annual reproductive cycle of those species could be classified into five stages; multiplicative, growing, mature, spent, degenerative and resting stage. It seems that the spawning season is closely related to the water temperature, and the spawning of Solen strictus occurs from June to July at above $20^{\circ}C$ in water temperature. The peak spawning season appeared in June at Dadaepo and in July at Kunsan, The spawning of Solen gordonis occurs from May to June with the peak spawning season in June. Percentages of the first maturity in female of Solen strictus ranging from 5.1-6.0 cm and 7.1-8.0 cm in shell length were $50\%$ and $100\%$, respectively.
Gonad development in the sandfish Arctoscopus japonicus was investigated using a histological method. Specimens were collected monthly from April 2003 to March 2004, in the East Sea of Korea. The gonadosomatic index (GSI) of females began to increase in August, reached a maximum in November, and declined sharply in December. By contrast, in males, the GSI began to increase in June and reached a maximum in August. The annual reproductive cycle of A. japonicus can be divided into four successive stages in females: the early growing (January-March), late growing (April-August), ripe and spent (September-November), and recovery (December) stages. Males passed through early growing (January-April), late growing (May-July), ripe and spent (August-November), and recovery (November-December) stages. These results indicate that the spawning season was from October to December. The egg diameter of mature oocytes was 3.12$\pm$0.02 mm. The relationship between fecundity (F$_e$) and body length (BL) was F$_e$=0.4693BL$^{2.6825}$. Fecundity ranged from 483-2,254 eggs in a body length of 14.3-22.9 cm and increased with body length. The body length at 50% maturity was 14.80 cm, which corresponded to an age of 2.40 years.
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