• Journal of Aquaculture
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• v.21 no.4
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• pp.252-258
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• 2008

Gonadal development and reproductive cycle of the ark shell Scarpharca subcrenata were investigated by histological observations. Samples were collected monthly from March 2007 to February 2008 in the Yeoja Bay, Yeosu, Jeollanam-do, Korea. S. subcrenata was dioecious. The gonads consist of a number of oogenic follicle and acinus. Monthly changes in the gonad index reached a maximum in June and a minimum in September. Monthly changes in the condition index reached a maximum in April and a minimum in September. The reproductive cycle of this species can be divided into five successive stages: early active stage (January to April), late active stage (March to June), ripe stage (May to August), spent stage (July to September) and recovery and resting stage (September to March). The main spawning of S. subcrenata occurred in July and August in Yeoja Bay. The sex ratio of female to male was not significantly different from 1:1.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.37 no.5
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• pp.393-399
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• 2004

Annual reproductive cycle of Siganus canaliculatus was studied based on monthly variation of gonadosomatic index (GSI) and histological changes of gonads. Samples were monthly collected by a set net along the southern coast of Jeju Island, Korea from January to December, 1996. Variation of the monthly mean GSI values showed similar trends in female and male. The GSI values increased from June and reached a peak in the spawning season in July $(9.65{\pm}1.96\;in\;females,\;10.00{\pm}4.27\;in\;males)$, and decreased rapidly thereafter. Female hepatosomatic index (HSI) values ranged from $1.26{\pm}0.22\;(in\;April)\;to\;2.34{\pm}0.39$ (in July), and male HSI values ranged from $1.27{\pm}0.21\;(in\;April)\;to\;1.87{\pm}0.30$ (in October). Annual reproductive cycle was classified into the following successive stages: in female, growing stage (from February to June), mature stage (from June to July), ripe and spawning stage (from July to August), recovery stage (from August to March); and in male, growing stage (from January to June), mature stage (from June to July), ripe and spent stage (from July to August), and recovery stage (from August to April). Based on these data, this species has a group-synchronous oocyte development and one spawning season a year.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.35 no.3
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• pp.201-206
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• 2002

Reproductive cycle of the bay scallop, Argopecten irradians, transplanted from China on 16 August 1996, was investigated monthly until August 1997 in the Deukyang Bay, Jangheung-gun, Jeollanam-do, Korea. Sexuality of this species is hermaphrodite and oviparous, Monthly changes in the soft part weight index and adductor muscle weight (g) began to increase from October and reached the maximum in November, and then the values gradually decreased from December to August, The gonadosomatic index (GI) began to increase in March and reached the maximum in April. Thereafter, the values gradually decreased from May to December, The reproductive cycle of this species, transplanted in the south coast of Korea could be divided into 5 successive stages; early active (October to February), late active (November to May), ripe (February to May), spawning (May to June) with a peak in May, and spent/inactive stage (June to August).

• Journal of Fisheries and Marine Sciences Education
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• v.24 no.6
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• pp.1003-1012
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• 2012

The gonadosomatic index (GSI), sex steroid hormones and gonadal development of roughscale sole Clidoderma asperrimum cultured in indoor tank were investigated to evaluate its sexual maturation and reproductive cycle. The highest GSI values of female and male were $6.91{\pm}4.03$ (May) and $0.16{\pm}0.08$ (August), respectively. The reproductive cycle would be classified into four successive developmental stages: growing stage (December to February), maturation stage (March to April), ripe and spawning stage (May to June), recovery and resting stage (July to November). The highest plasma testosterone (T) and estradiol-$17{\beta}$ ($E_2$) levels of female were $259.4{\pm}76.8$ and $633.3{\pm}182.5$ pg/mL, respectively in May. Also $17{\alpha}$, $20{\beta}$-dihydroxy-4-pregen-3-one ($17{\alpha}$, $20{\beta}$-OHP) levels of female peaked in April before spawning season ($244.2{\pm}42.5$ pg/mL). The highest plasma testosterone (T) and 11-ketotestosterone levels of male were $231.0{\pm}46.0$ and $273.9{\pm}54.5$ pg/mL, respectively in April. But there was no significant difference in $17{\alpha}$, $20{\beta}$-OHP.

• Journal of Aquaculture
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• v.16 no.3
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• pp.179-186
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• 2003

Reproductive cycle, gonadal development and the spawning period of the Korean anchovy Coilia nasus were investigated by histologhical observations. Samples were collected at the coastal area of Geumgang dyke which is connected to Gunsan and Janghang, Korea, from February 2002 to January 2003. C. nasus is dioecious; the ovary consists of a pair of saccular structure with many ovarian lobules, and the testis consists of a pair of lobular structure with many testicular lobules and connected to the posterior seminal vesicle. Monthly changes in the gonadosomatic index (GSI) began to increase in April when seawater temperature increased and reached the maximum in June when the ovary was getting mature, the summer season of longer day length with higher water temperature. The reproductive cycle can be classified into five successive stage in females: early growing stage (February to March), late growing stage (March to April), mature stage (May to June), ripe and spent stage (June to July), and recovery and resting stage (July to January): in males, the cycle can be divided into four successive stages; growing stage (February to April), mature stage (May to July), ripe and spent (June to July), and recovery and resting stages (July to January). According to the frequency distributions of egg diameters in the spawning season. C. nasus is presumed to be summer spawning species and polycyclic species to spawn 2 times or more during the spawning season.

• Journal of Microbiology and Biotechnology
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• v.17 no.3
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• pp.398-402
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• 2007

Abstract Female mice post weaning were exposed to 20 kHz sawtooth electric and magnetic fields (EMF) with $6.25{\mu}T$ peak intensity for 6 weeks. Estrous cycles were checked using vaginal smears over the last 10 days of the experimental period. The vaginal smears from EMF-exposed mice revealed an increase in the frequency of one or two phases persisting. The number of estrous cycles less than 1 was more in the EMF-exposed group than in the sham control group. Furthermore, in the EMF-exposed group, the duration of proestrous and metestrous stages of the estrous cycle was significantly increased compared with the control group. In conclusion, our results suggest that exposure to 20 kHz sawtooth EMF may affect normal cycling of the estrous cycle by disrupting the female reproductive endocrine physiology. We should not disregard the possible adverse reproductive effect of the 20 kHz sawtooth EMF generated under the occupational exposure situation in females.

• The Korean Journal of Malacology
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• v.11 no.2
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• pp.147-163
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• 1995

The unionid family Unionidae contains several genera in Korea, among which occru considerable variations in life histories and sexual conditions. Seven species from the Korea(Anodonta arcaeformis flavotincta, A. woodiana, Unio douglaseae, U. douglasiae sinuolatus, Lamprotula gottschei, Lanceolaria acrorhyncha, Solenaia triangularis)were stueide in order to identify and describe the seasonal gonadal activity and the visceral sex. The gonads of seven species were histologically examined by using the paraffin block technique for sectioning. All seven species were uniformly dioecious and testicular activity in six species except one species, S. triangularis, generated sperm-morulae(multinucleated cell). The annual reproductive cycle of the seven species could be classified into five successive stages; multicative, growing, mature, spent, deginerative and resting stages. The breeding season of six species was the summer and that of A. a. flavotincta was the winter.

• Reproductive and Developmental Biology
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• v.30 no.2
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• pp.99-105
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• 2006

The growing oocytes become progressively capable of resuming meiosis, and full meiotic competence appear when they are about 80% of the size of fully grown oocytes. As hormonal influences vary at different stages of reproductive cycle, the size of oocytes may vary according to the reproductive stages. The present study was designed to compare the diameter between the ovulated and freshly collected immature canine oocytes. The ovulated oocytes were collected 72 hr after ovulation by oviductal tube flushing by laparotomy under general anesthesia. Immature oocytes were collected by ovarian slicing method. Diameter of all oocytes was measured directly using epiflurescence microscope with a calibrated micro-eyepiece micrometer at ${\times}200$ magnification. The thickness of zona pellucida and diameter of cytoplasm were measured separately and recorded. A total of 2209 zona intact oocytes were collected, among them 628 from anestrus, 675 from follicular, 838 from luteal and 68 by fallopian tubes flushing methods. The average number of oocytes was 104.7, 168.8, 119.7 and 11.3 for anestrus, follicular, luteal and fallopian tubes flushing methods, respectively. The average diameters of the ooplasm and oocyte were significantly varied in different reproductive stages as well as with ovulated oocytes (P<0.05). The average diameter of ooplasm and oocyte was 115.6 and 127.7, 143.0 and 162.0, 134.6 and 150.6, 159.6 and 185.6 for anestrus, follicular, luteal and ovulated oocytes, respectively. Highest number of oocytes with larger diameter could be collected from the follicular and luteal stages. In conclusion, the follicular and luteal ovaries are the best sources of oocytes for canine IVM.

• Fisheries and Aquatic Sciences
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• v.14 no.4
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• pp.379-388
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• 2011

The mechanism by which gonadotropin-releasing hormone (GnRH) and dopamine (DA) control gonadotropin (GTH) release was studied in male and female rainbow trout using cultured pituitary cells obtained at different reproductive stages. The mechanisms of follicle-stimulating hormone (FSH) release by GnRH and DA could not be determined yet. However, basal and salmon-type GnRH (sGnRH)- or chicken-II-type GnRH (cGnRH-II)- induced luteinizing hormone (LH) release increased with gonadal maturation in both sexes. LH release activity was higher after sGnRH stimulation than cGnRH-II stimulation at maturing stages in both sexes. The GnRH antagonist ([Ac-3, 4-dehydro-$Pro^1$, D-p-F-$Phe^2$, D-$Trp^{3,6}$] GnRH) suppressed LH release by sGnRH stimulation in a dose-dependent manner, although the effect was weak in maturing fish. The role of DA as a GTH-release inhibitory factor differs during the reproductive cycle: the inhibition of sGnRH-stimulated LH release by DA was stronger in immature fish than in maturing, ovulating, or spermiated fish. DA did not completely inhibit sGnRH-stimulated LH release, and DA alone did not alter basal LH release. Relatively high doses ($10^{-6}$ or $10^{-5}M$) of domperidone (DOM, a DA D2 antagonist) increased LH release, which did not change with reproductive stage in either sex. The potency of DOM to enhance sGnRH-stimulated LH release was higher in maturing and ovulated fish than in immature fish. These data suggest that LH release from the pituitary gland is controlled by dual neuroendocrine mechanisms by GnRH and DA in rainbow trout, as has been reported in other teleosts. The mechanism of control of FSH release, however, remains unknown.

• Reproductive and Developmental Biology
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• v.32 no.2
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• pp.89-95
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• 2008

The present study was undertaken to identify changes of plasminogen activators (PAs) in porcine oviductal epithelial cells (POECs) during the estrous cycle classified with post-ovulatory stages (Post-Ov), early to mid-luteal stages (Early-mid L) and pre-ovulatory (Pre-Ov) stages. The urokinase-type plasminogen activator (uPA) was only observed on day 5 and day 7 of culture in the POECs on all the estrous cycles and gradually increased according to increasing culture times, but not Early-mid L. In POECs-conditioned medium, uPA, tissue-type (tPA) and tPA-PA inhibitor (tPA-PAI) activity were observed at all culture times during estrous cycles. The uPA activity of POECs-conditioned medium on Post-Ov stage were significantly (p<0.05) decreased during prolonged cultures. On the other hand, the tPA activity of POECs-conditioned medium at Post-Ov stage was significantly (p<0.05) higher on day 5 than compared to the other days. Although was higher on day 1 at Post-Ov stage, the tPA-PAI activity of POECs-conditioned medium was significantly (p<0.05) higher on day 7 at all stage than that of day 5 of the culture. Taken together, these results suggest that uPA, tPA and tPA-PAI are produced by POECs, and the variations of the PAs activity are regulated in the different stages of the estrous cycle.