Spawning cycle and fecundity of a multiple spawner round herring Etrumeus teres off southern Japan: Oocyte growth and maturation analysis

2017 ◽  
Vol 122 ◽  
pp. 11-18 ◽  
Author(s):  
Mitsuo Nyuji ◽  
Akinori Takasuka
1997 ◽  
Vol 63 (1) ◽  
pp. 15-21 ◽  
Author(s):  
Benjamin Jareta Gonzales ◽  
Nobuhiko Taniguchi ◽  
Osamu Okamura

ISRN Zoology ◽  
2011 ◽  
Vol 2011 ◽  
pp. 1-12 ◽  
Author(s):  
Alaa G. M. Osman ◽  
El Sayed H. Akel ◽  
Mahmoud M. S. Farrag ◽  
Mohsen A. Moustafa

Maturity stages of round herring Etrumeus teres were divided anatomically into six stages. Monthly distribution of such maturity stages showed that E. teres had prolonged spawning season extended from December to May for females and to July for males. The observed sex ratio was 1 : 2 (male: female). Gonadosomatic index (GSI) values were high during breeding season for both sexes. Hepatosomatic index (HIS) values for females increased from December to April and from December to July for males. Both sexes of E. teres showed the same correlation between GSI and HSI during their breeding season. The absolute and relative fecundity increased with increasing of length and weight. Histologically, the ovarian cycle of E. teres was classified into six stages and the testicular cycle into five stages. Female of E. teres was a multiple spawner and had prolonged spawning season with a group-synchronous ovarian which contained oocytes at all stages of development. Also, different sizes of spermatocytes at different developmental stages of maturation were observed during the same season. This may reflect the suitability of the specific reproductive behavior of male and its adaptation to the prolonged spawning season with females.


2014 ◽  
Author(s):  
Akihiko Sakashita ◽  
Yosuke Iseki ◽  
Mei Nakajima ◽  
Takuya Wakai ◽  
Hisato Kobayashi ◽  
...  

Circulation ◽  
1970 ◽  
Vol 41 (4s1) ◽  
Author(s):  
NOBORU KIMURA ◽  
ANCEL KEYS
Keyword(s):  

Zygote ◽  
2008 ◽  
Vol 16 (3) ◽  
pp. 239-247 ◽  
Author(s):  
T. Metoki ◽  
H. Iwata ◽  
M. Itoh ◽  
M. Kasai ◽  
A. Takajyo ◽  
...  

SummaryWe examined the effect of supplementing the culture medium with follicular fluid (FF) on the growth of porcine preantral follicles and oocytes. Firstly, preantral follicles were retrieved from ovaries and then FF was collected from all antral follicles that were 2–7 mm in diameter (AFF), which included large follicles of 4–7 mm in diameter (LFF) and small follicles of 2–3 mm in diameter (SFF). When preantral follicles with a diameter of 250 μm were cultured in medium containing AFF, the growth of follicles and oocytes was greater than when follicles were cultured in medium containing fetal calf serum (FCS). When this growth-promoting effect in AFF was compared for LFF and SFF, the LFF were shown to be significantly more effective than SFF. This LFF effect was lost, however, when the concentration of LFF in the medium was decreased from 5% to 0.5% or when LFF were heat treated (60 °C for 30 min) or trypsin was added. In contrast, a decrease in SFF concentration from 5% to 0.5% and heat treatment of the SFF enhanced preantral follicle growth. Furthermore, proteins obtained from LFF that had molecular weights greater than 10 kDa (LFF > 10 kDa) had similar, but relatively reduced, growth-promoting properties. The remaining three LFF protein fractions (<10 kDa or <100 kDa or >100 kDa), however, did not have these growth-promoting properties. In conclusion, the supplementation of medium with LFF, rather than serum, enhanced preantral follicle and oocyte growth. Factors that enhanced follicle development in LFF and factors that suppressed follicle development in SFF were proteins and these LFF factors ranged in size from 10 kDa to over 100 kDa.


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