• Title/Summary/Keyword: sexual maturation

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Reproduction of the Shotted halibut in the southern Korean waters (한국 남해에 서식하는 물가자미, Eopsetta grigorjewi (Herzenstein)의 재생산 연구)

  • Cha, Hyung-Kee;Kang, Su-Kyung;Choi, Jung-Hwa;Oh, Taeg-Yun;Seo, Young-Il
    • Journal of the Korean Society of Fisheries and Ocean Technology
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    • v.47 no.3
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    • pp.194-202
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    • 2011
  • Maturation and spawning of the Shotted halibut, Eopsetta grigorjewi was investigated based on the samples captured in South Korean waters from January 2008 to December 2009. Gonadosomatic index began to increase in December, and reached maximum between January to March. After spawning it began to decrease from May. Reproductive season was estimated to January-April, with peak in February. Fecundity was proportional to the size of the female, with the clutch size varying from 170,000 eggs in the smallest female (total length, 28.9cm) to 1,300,000 eggs in the largest (total length, 41.5cm). Size at 50% sexual maturity (TL50), determined from mature females, was 28.8cm. Annual reproductive cycles of this species could be divided into six successive stages; immature stage (May-October), nucleolus stage (November-January), yolk vesicle stage (January-February), vitellogenic and ripe stage (January-April) and spent stage (April-May).

Reproductive ecology of the blackthroat seaperch, Doderleinia berycoides (Hilgendorf) in South Sea of Korean waters (한국 남해에 서식하는 눈볼대, blackthroat seaperch, Doderleinia berycoides (Hilgendorf)의 생식생태연구)

  • Cha, Hyung-Kee;Kang, Su-Kyung;Oh, Taeg-Yun;Choi, Jung-Hwa
    • Journal of the Korean Society of Fisheries and Ocean Technology
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    • v.46 no.4
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    • pp.368-375
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    • 2010
  • Maturation and spawning of the Blackthroat seaperch, Doderleinia berycoides were investigated based on the samples captured in Korean waters from January 2008 to December 2009. Gonadosomatic index began to increase in June, and reached maximum between July to September. After spawning it began to decrease from October. Reproductive season was estimated to July-September, with peak in August. Fecundity was proportional to the size of the female, with the clutch size varying from 115,500 eggs in the smallest female (TL〓28.2cm) to 652,000 eggs in the largest (TL〓33.5cm). Size at 50% sexual maturity ($TL_{50}$), determined from mature females, was 29.6cm. Annual reproductive cycles of this species could be divided into six successive stages; immature stage (October-May), nucleolus stage (June-July), yolk vesicle stage (July-August), vitellogenic stage (June-September), ripe and spent stage (August-October).

Effects of hCG on Sexual Maturation in Korean Loach (hCG가 한국산 미꾸라지(Misgurnus mizolepis)의 성성숙에 미치는 영향)

  • 송기철;이재현;이종영;신재구;윤종만;박홍양
    • Korean Journal of Animal Reproduction
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    • v.16 no.2
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    • pp.157-164
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    • 1992
  • This stduy was carried out to obtain basic information available on ovulation, spawning, fertilization rate, hatching rate, and deformity rate after hCG injection in cyprinid loach, Misgurnus mizolepis. The results obtained in these experiments were as follows: 1. Ovulation and spawning occurred simultaneously and spawing was completed within 1 hour after ovulation. 2. More than 80% of fertilization rates appeared within 12 hours at 21$^{\circ}C$, 8 hours at $25^{\circ}C$, and 4 hours at 29$^{\circ}C$, respectively, following the onset of spawing. Afterwards, the fertilization rates of released eggs sharply decreased in three different water temperatures. 3. More than 70% of hatching rates appeared within 8 hours at 21$^{\circ}C$, 6 hours at $25^{\circ}C$, and 2 hours at 29$^{\circ}C$, respectively, following the onset of spawing. Afterwards, hatching rates of spawned eggs abruptly decreased in three different water temperatures. 4. The deformity rates of hatched larvae were high at $25^{\circ}C$, 8 hours following the onset of spawing. 5. Based on the developmental ability of oocytes, the optimum time of fertilization was 4 hours (stage 5) following the onset of spawing.

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Sexual Maturation Inducement of Striped Knife-Jaw, Oplegnathus fasciatus by Manipulating Environmental Condition (환경조절에 의한 돌돔 Oplegnathus fasciatus 성 성숙 유도)

  • Kim, Sung-Yeon;Bang, In-Chul;Kim, Seok-Min
    • Korean Journal of Ichthyology
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    • v.12 no.1
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    • pp.46-53
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    • 2000
  • Artificial gonadal maturation and spawning inducement of striped knife-jaw Oplegnathus fasciatus were studied. Effects of water temperature and photoperiod under different regims on gonadal activity and maturation of three years old O. fasciatus were investigated histologically. In experiment I (Exp. I), water temperature was gradually increased from $14.5^{\circ}C$ to $21.0^{\circ}C$ and photoperiod was also gradually increased from 10 : 30 L to 15 : 30 L from December 1996 to February 1997 and this conditions were maintained till April. In experiment II (Exp. II), water temperature was increased in the same way from Exp. I and photoperiod was controlled as natural condition till early March and then increased to 15 : 30 L immediately. Control fish were reared in net-cage culture system in the sea from December 1996 to April 1997. Gonadal activity was initiated by increasing water temperature in both Exp. I and II from January. In Exp. I, gonadal maturation and spawning were induced from February when water temperature and photoperiod reached at $21.0^{\circ}C$ and 15 : 30 L, respectively. In Exp. II, complete gonadal maturation was not induced until early March but after treated by compensatory long photoperiod (15 : 30 L), the gonad was matured and subsequently spawning occurred.

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Ecological Study on the Seaweed Porphyra pseudolinearis Originated from the East Sea, Korea (동해안 고유종 긴잎돌김(Porphyra pseudolinearis)의 생태학적 연구)

  • Kim, Young-Dae;Lee, Ju;Son, Yong-Soo;Choi, Jae-Seok;Kim, Dong-Sam;Hong, Yong-Ki
    • Journal of Life Science
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    • v.14 no.2
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    • pp.331-338
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    • 2004
  • Growth and sexual differentiation of the seaweed Porphyra pseudolinearis Ueda have been investigated monthly in the intertidal zone of the East Sea, Korea. Young blades of P. pseudolinearis appeared at the beginning of October. Carp os pores were released at the end of November immediately after carposporangia formation. Then the thalli of P. pseudolinearis were extinguished at the end of March. Young thalli were budded through the stages of conchocelis and conchospore. Thalli showed lanceolate type in shape, cordate type in holdfast, absence of microscopic spinulate process and sexual generation. Ratios of length to width in female thalli ranged from 5.6 to 7.4 at the maturation in December and slightly decreased 3.3 to 4.8 in January and 4.9 to 7.3 in December while the ratios of male thalli ranged from 4.2 to 4.8 in January. On October 12, average five individuals were obsered in a quadrate (30 cm ${\times}$ 30 cm), 238$\pm$18 individuals for the maturation stage in December and then it was reduced to 150 individuals in February and 15 individuals in March. Average sex ratios for female, male and vegetative thalli were 31.3% 46.9% and 21.9% respectively in early December, the beginning time of sex maturation. The sex ratio of female and male thalli in December 17, changed to 69.4%, 30.6% respectively.

Maturation and Spawning of Largehead Hairtail Trichiurus japonicus Near Jeju Island, Korea (한국 제주도 주변해역에 서식하는 갈치(Trichiurus japonicus)의 산란 생태)

  • Kim, Han Ju;Park, Jeong-Ho;Kwon, Dae-Hyeon;Kim, Yeonghye
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.53 no.1
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    • pp.1-8
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    • 2020
  • The reproductive biology of largehead hairtail Trichiurus japonicus, from near Jeju Island, Korea was investigated based on 4,384 individuals collected by commercial vessel from November 2016 to October 2019. There were more female specimens than male specimens (2.64:1). T. japonicus preanal lengths (PL) ranged from 10.5 to 53.5 cm; the relationships between PL and body weight (BW) were BW=0.0103PL3.1293 for females and BW=0.0106PL3.1251 for males. Monthly changes in gonadosomatic index were analyzed to estimate spawning season. The spawning period ranged from June to November. The size-frequency distribution of eggs suggested that T. japonicus exhibits multiple-spawning during a spawning period. The minimum size of females at maturity was 18.2 cm, while the size at sexual maturity was 25.0 cm.

Ovarian Maturation in Female Ruditapes philippinarum on the West Coast of Korea (한국 서해산 바지락, Ruditapes philippinarum의 난소 성숙)

  • Choi, Ki-Ho;Park, Gab-Man;Chung, Ee-Yung
    • Development and Reproduction
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    • v.9 no.2
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    • pp.123-134
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    • 2005
  • Germ cell development during oogenesis, ovarian maturation and first sexual maturity in female Ruditapes philippinarum were investigated by cytological and histological observations. R. philippinarum is dioecious. 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(Februaryto May), ripe stage(April to August), partially spawned stage(May to October), and spent/inactive stage (August to February). Percentages of female clams at first sexual maturity of $15.1{\sim}20.0mm$ in shell length were 52.6%(50% of the rate of group maturity was 17.83mm in length), and 100% for the clams >25.1mm.

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Sexual Maturity and Gonadal Development of Slime Flounder, Microstomus achne (찰가자미, Microstomus achne의 성성숙과 생식소발달)

  • Byun, Soon-Gyu;Kim, Sung-Yeon;Kim, Jin-Do;Lee, Bae-Ik;Lee, Jong-Ha;Han, Kyeong-Ho;Jeong, Min-Hwan
    • Korean Journal of Ichthyology
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    • v.23 no.3
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    • pp.179-186
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    • 2011
  • Slime flounder, Microstomus achne is distributed in the coastal waters of Korea, west sea of Japan, BoHai, Yellow sea and East china sea. They are mainly caught by bottom trawl net during winter, from December to March. Sexual maturation of slime flounder were investigated using samples collected from commercial catch in the southern coast of Korea from November, 2006 to March, 2007. The ovary of the slime flounder is a conical bag in shape and is bilateral structure develops lengthily from the posterior of the abdomen to the end of the anal fin. The testis also is bilateral in structure, usually located in small size in the abdomen. In females, the gonadosomatic index (GSI) were peaked in January (12.46), then decreased rapidly thereafter. Female GSI values plummeted to 2.72 in March just after spawning. Male GSI values were peaked in December (2.46) before in the spawning season, then decreased slowly thereafter. The reproductive cycle would be classified into three successive developmental stages : maturation stage (November to January), ripe and spawning stage (December to February), degenerative and resting stage (February to March). Relationships between the fish sizes in total length (TL) and the number of ovarian eggs (F), the body weights (BW) and the number of ovarian eggs were indicated by the exponential equation respectively: F=29.027TL-767.8 (r$^2$=0.7686), F=0.3998BW+24.288 (r$^2$=0.8919).

Genetic Control of Asexual Sporulation in Fusarium graminearum

  • Son, Hokyoung;Kim, Myung-Gu;Chae, Suhn-Kee;Lee, Yin-Won
    • 한국균학회소식:학술대회논문집
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    • 2014.10a
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    • pp.15-15
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    • 2014
  • Fusarium graminearum (teleomorph Gibberella zeae) is an important plant pathogen that causes head blight of major cereal crops such as wheat, barley, and rice, as well as causing ear and stalk rot on maize worldwide. Plant diseases caused by this fungus lead to severe yield losses and accumulation of harmful mycotoxins in infected cereals [1]. Fungi utilize spore production as a mean to rapidly avoid unfavorable environmental conditions and to amplify their population. Spores are produced sexually and asexually and their production is precisely controlled. Upstream developmental activators consist of fluffy genes have been known to orchestrate early induction of condiogenesis in a model filamentous fungus Aspergillus nidulans. To understand the molecular mechanisms underlying conidiogenesis in F. graminearum, we characterized functions of the F. graminearum fluffy gene homologs [2]. We found that FlbD is conserved regulatory function for conidiogenesis in both A. nidulans and F. graminearum among five fluffy gene homologs. flbD deletion abolished conidia and perithecia production, suggesting that FlbD have global roles in hyphal differentiation processes in F. graminearum. We further identified and functionally characterized the ortholog of AbaA, which is involved in differentiation from vegetative hyphae to conidia and known to be absent in F. graminearum [3]. Deletion of abaA did not affect vegetative growth, sexual development, or virulence, but conidium production was completely abolished and thin hyphae grew from abnormally shaped phialides in abaA deletion mutants. Overexpression of abaA resulted in pleiotropic defects such as impaired sexual and asexual development, retarded conidium germination, and reduced trichothecene production. AbaA localized to the nuclei of phialides and terminal cells of mature conidia. Successful interspecies complementation using A. nidulans AbaA and the conserved AbaA-WetA pathway demonstrated that the molecular mechanisms responsible for AbaA activity are conserved in F. graminearum as they are in A. nidulans. F. graminearum ortholog of Aspergillus nidulans wetA has been shown to be involved in conidiogenesis and conidium maturation [4]. Deletion of F. graminearum wetA did not alter mycelial growth, sexual development, or virulence, but the wetA deletion mutants produced longer conidia with fewer septa, and the conidia were sensitive to acute stresses, such as oxidative stress and heat stress. Furthermore, the survival rate of aged conidia from the F. graminearum wetA deletion mutants was reduced. The wetA deletion resulted in vigorous generation of single-celled conidia through autophagy-dependent microcycle conidiation, indicating that WetA functions to maintain conidia dormancy by suppressing microcycle conidiation in F. graminearum. In A. nidulans, FlbB physically interacts with FlbD and FlbE, and the resulting FlbB/FlbE and FlbB/FlbD complexes induce the expression of flbD and brlA, respectively. BrlA is an activator of the AbaA-WetA pathway. AbaA and WetA are required for phialide formation and conidia maturation, respectively [5]. In F. graminearum, the AbaA-WetA pathway is similar to that of A. nidulans, except a brlA ortholog does not exist. Amongst the fluffy genes, only fgflbD has a conserved role for regulation of the AbaA-WetA pathway.

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Reproduction of the jack mackerel, Trachurus japonicus Temminck et Schlegel in the coastal waters around Jeju Island, Korea: Maturation and spawning (한국 제주 인근해역에 서식하는 전갱이, Trachurus japonicus Temminck et Schlegel의 재생산 연구: 성숙과 산란)

  • Cha, Hyung-Kee;Lee, Jae-Bong;Kang, Su-Kyung;Chang, Dae-Soo;Choi, Jung-Hwa
    • Journal of the Korean Society of Fisheries and Ocean Technology
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    • v.45 no.4
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    • pp.243-250
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    • 2009
  • Maturation and spawning of the jack mackerel, Trachurus japonicus was investigated based on the samples captured in the coastal waters around Jeju Island from January 2007 to December 2008. Gonadosomatic index began to increase in March, and reached a maximum between April to June. After spawning it began to decrease from August. Reproductive season was estimated to March-July, with peak in April. Fecundity was proportional to the size of the female, with the clutch size varying from 33,493 eggs in the smallest female(FL=27.0cm) to 627,061 eggs in the largest(FL=40.6cm). Size at 50% sexual maturity(FL50), determined from mature females, was 26.6cm FL. Annual reproductive cycles of this species could be divided into six successive stages; immature stage(September-December), nucleolus stage(January-February), yolk vesicle stage(February-March), vitellogenic stage(March-April), ripe stage(April-July) and spent stage(July-September).