• Title/Summary/Keyword: Annual cycle of seminiferous epithelium

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Annual Cycle of the Seminiferous Epithelium of Miniopterus schreibersi fuliginosus

  • Kang Mu-Shik;Lee Jung-Hun
    • Biomedical Science Letters
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    • v.10 no.4
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    • pp.435-445
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    • 2004
  • The characteristics of the testis and the annual cycle of the seminiferous epithelium of the Miniopterus schreibersi fuliginosus were examined by optical microscopy. The testis weight and diameter of the seminiferous tubules were increased gradually from May to July, and the highest activity was observed in August. The size then decreased rapidly from October. Spermatogenesis began in May, peaked in August, and was suspended from October to April in the following year. Spermatocytogenesis were produced from May to July. Spermiogenesis occurred from August to September. In particular, immature spematogenic cells in the seminiferous tubules were engulfed by the phagocytosis of Sertoli cells in October. From November to April, the seminiferous tubuly contained only Sertoli cells and Ad spermatogonia. Therefore, the periodic changes in the seminiferous epithelium of M. S. fuliginosus suggest that a long hibernation is an adaptive strategy for the preservation of energy and the regulation of the breeding cycle.

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Seminiferous Epithelium Cycle in the Korea Squirrel, Tamias sibiricus

  • Jung Tae-Dong;Lee Jung-Hun
    • Biomedical Science Letters
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    • v.10 no.3
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    • pp.275-283
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    • 2004
  • The annual changes in testis weight and diameter of seminiferous tubules, and the seminiferous epithelium cycle of Tamias sibiricus were studied by light microscope. Testis weight and diameter of seminiferous tubule are significantly increased from January to July, and decreased rapidly to the size from August to December. Spermatogenesis occurs from January to July, and spermatocytogenesis are produced from August to December. The cycle of the seminiferous epithelium was divided into 12 stages during the development of spermatids as a changes of the nucleus and acrosomal structure, presence and/or absence of residual body, appearance and/or absence of sperm tail and meiotic figure and spermiation. The dark type spermatogonia (Ad) are appeared in all stages (I ~ XII), and the spermatids of step 10 are observed at I, II, X and XII stages. The spermatids of step 11 are appeared in III and IV stages, only the step 12 spermatid observed in V stage.

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Studies on the reproductive pattern in the male of Korean greater horseshoe bat, Rhinolophus ferrumequinum korai I. The cycle of seminiferous epithelium and histological changes of testis. (한국산 관박쥐 (Rhinolophus ferrumequinum korai)의 웅성생식 pattern에 관한 연구 1. 세정관상피의 주기 및 정소의 조직변화)

  • 이정훈;손성원
    • The Korean Journal of Zoology
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    • v.36 no.1
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    • pp.36-50
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    • 1993
  • 한국산 관박쥐(Rhinolophusfewmequinum Jroma의 웅성생식 pattern을 알아보기 위하여 정소의 형태변화와 세정관 정상피의 1년주기를 조사하여 다음과 같은 결론을 얻었다. 정자형성은 5월에 시작되어 10월말에 완료되었다. 7월초부터 10월중순까지는 정자변태과정이며, 정자형성과정의 활성도가 가장 높은 달은 8월 중순경이었다. 또한 교미가 끝난 11월경부터 세정관내에는 미성숙한 정자세포가 Sertoli cell의 식작용과정의 일환으로 포식되어졌고, 91년 12월부터 92년 1월, 2월, 3월, 그리고 동면각성기인 4월의 실험군에서도 역시 점진적으로 식작용 과정을 관찰할 수 있었다. 교미가 끝난 후의 세정관 내에는 새로운 정자를 만들기 위한 준비단계로서 미성숙된 정자들이 Sertoli cell의 식작용에 의해 정화(cleaning)되므로 이 기간을 정화기간(cleaning time)이라 볼 수 있다. 따라서 정소내 세정관의 1년 주기를 볼 때 정화기간은 동면 개시기인 11월부터 익년 4월까지 약 6개월에 걸쳐 이루어 진다. 이상의 결과로 볼때, 정자형성은 동면각성 직후부터 시작하여 10월경에 완료되며 교미개시기에는 정지되고, 동면기 동안 정자형성이 일어나지 않는 점으로 보아 한국산 관박쥐는 'Pipistnfluspottem'에 속한다고 할 수 있다.

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Sexual Maturation of Viviparous Teleost Surfperch, Ditrema temmincki (태생 경골어류 망상어, Ditrema temmincki의 성성숙)

  • Lee, Jung-Sick;An, Cheul-Min;Chin, Pyung
    • Korean Journal of Ichthyology
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    • v.7 no.2
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    • pp.150-159
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    • 1995
  • 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.

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Reproductive Cycle of Small Filefish, Rudarius ercodes (그물코쥐치, Rudarius ercodes의 생식주기)

  • LEE Taek Yuil;HANYU Isao
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.17 no.5
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    • pp.423-435
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    • 1984
  • The reproductive cycle of the small filefish, Rudarius ercodes was investigated based on the annual variations of gonadosomatic index(GSI) and hepatosomatic index(HSI) by electronic and photic microscophy. The specimens used were collected at the coastal area of Benden island, Sizuokagen, Japan, from September 1982 to August 1983. GSI began to increase from March, starting season of longer daylength and higher water temperature, and reached the maximum value between June and August. It began to decrease from September with the lowest value appearing between November and February without any evident variation. The annual variations of HSI were not distinct in male filefish and were negatively related to GSI in female : HSI decreased in the summer season when the ovary was getting mature and reached the maximum in the winter season when the ovary was getting retrogressive. The ovary consisted of a pair of saccular structure with numerous ovarian sacs branched toward the median cavity. Oogonia divided and proliferated along the germinal epithelium of the ovarian sac. Young oocytes with basophile cytoplasm showed several scattering nucleoli along the nuclear membrane. when the oocytes growing to about 300 ${\mu}m$, nuclear membrane to disappear with nucleus migrating toward the animal pole. The regions of protoplasm were extremely confined within the animal hemisphere in which most of cytoplasms were filled with yolk materials and oil drops. After ovulation, residual follicles and growing oocytes remaining in the ovarian sacs degenerated. But perinucleatic young oocytes without follicles formed were not degenerated, and growing continuously still in the next year. Mitochondria and endoplasmic reticula in the cytoplasm remarkably increased with oocytes maturing and yolk accumulating. Those were considered to be functionally related to the yolk accumulation. Five or six layers of possible vitellogenin, oval-shaped disc structures with high electron density, appeared in the apex of follicular processes stretching to the microvilli pits of mature oocytes. Testis consisting of a pair of lobular structures in the right and left were united in the posterior seminal vesicle, Cortex of testis was composed of several seminiferous tubules, and medulla consisting of many sperm ducts connected with tubules. Steroid hormone-secreting cells with numerous endoplasmic reticula and large mitochondria of well developed cristae were recognized in the interstitial cells of the growing testis. Axial filament of spermatozoon invaginated deeply in the central cavity of the nucleus and the head formed U-shape with acrosome severely lacking, mitochondria formed large globular paranuclei at the posterior head, and microtubular axoneme of the tail represented 9+9+2 type. The annual reproductive cycles could be divided into five successive stages : growth(March to July), maturation(May to September), Spawning(mid May to early October) and resting stages(October to February). The spawning peak occurred from June to August.

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