斑鳜早期性腺分化与发育的组织学观察

    Histological observation on early gonadal differentiation and development of Siniperca scherzeri

    • 摘要:
      目的 探究斑鳜(Siniperca scherzeri)早期性腺分化和发育的组织学特征,为单性别育种提供理论依据。
      方法 以孵化后2~62日龄(dph)的人工繁育斑鳜为研究材料,每5 d采样1次,每次15尾,采用石蜡包埋切片及苏木精-伊红(H.E)染色技术制备性腺组织切片,通过Olympus FX380显微镜和CaseViewer2.4软件进行观察、图片采集及测量。
      结果 7日龄斑鳜原始性腺已形成,成对分布于中肾管与肠道间的体腔膜上;雄斑鳜在17日龄和27日龄分别观察到输精管原基和初级精母细胞,标志着精巢解剖学和细胞学分化的开始;斑鳜精巢属于小叶型结构,发育进程较为迅速,17~27日龄处于Ⅰ期,32日龄进入Ⅱ期,37日龄达到Ⅲ期,62日龄已发育至Ⅳ期。雌斑鳜在22日龄和32日龄分别观察到卵巢腔雏形和初级卵母细胞,标志着卵巢解剖学和细胞学分化的开始;卵巢发育则相对滞后,22~42日龄处于Ⅰ期,47~62日龄处于Ⅱ期。
      结论 在自然水温条件下,斑鳜原始性腺在孵化后1周内形成,精巢发育进程也明显快于卵巢,62日龄精巢已发育至Ⅳ期,卵巢仅发育至Ⅱ期。斑鳜早期性腺分化和组织学发育特征研究,可为斑鳜单性别育种研制提供一定的理论依据。

       

      Abstract:
      Objective This study aims to explore the histological characteristics of early gonadal differentiation and development of Siniperca scherzeri, enrich the reproductive biology data of this species, and provide a theoretical basis for mono-sex breeding.
      Method Artificial breeding S. scherzeri aged 2 to 62 days post-hatching (dph) were taken as the research objects,and 15 individuals were sampled every 5 days. Gonadal tissue sections were prepared by paraffin embedding sectioning and hematoxylin and eosin (H.E) staining techniques. These sections were observed, photographed and measured by Olympus FX380 microscope and CaseViewer2.4 software.
      Results The primitive gonads of S. scherzeri had already formed at 7 dph, distributed in pairs on the coelomic membrane between the mesonephric ducts and the intestines.In male S. scherzeri, the spermaduct anlage and primary spermatocytes were observed at 17 dph and 27 dph respectively, marking the beginning of anatomical and cytological differentiation of the testis. The testis of S. scherzeri belonged to lobular structure,and its development process was relatively rapid: it was in stage I at 17 to 27 dph, entered stage II at 32 dph, reached stage III at 37 dph, and developed to stage IV at 62 dph. In female S. scherzeri,the ovarian cavity and primary oocytes were observed at 22 dph and 32 dph respectively, marking the beginning of anatomical and cytological differentiation of the ovary. Ovarian development was comparatively slower: remaining at stage I from 22 to 42 dph, and progressing to stage II from 47 to 62 dph.
      Conclusion Under natural water temperature conditions, primitive gonads of S. scherzeri had been formed within one week after hatching.The anatomical differentiation of the gonads preceded the cytological differentiation, and the testis differentiation and development were significantly earlier and faster than that of the ovary. The critical period for anatomical differentiation of the gonads was between 7 and 22 dph. By 62 dph, the testis had developed to stage IV, while the ovary had only developed to stage II. This study clarifies the key timeline and histological characteristics of early gonadal differentiation in S. scherzeri, providing a theoretical foundation for its mono-sex breeding practices. In this study, the key time nodes and development characteristics of gonadal differentiation in the early stage of artificial breeding of S. scherzeri were preliminarily clarified, which can provided some theoretical basis for the practice of single-sex breeding of this fish. This study initially clarified the key timeline and histological development characteristics in the early gonadal differentiation of artificial breeding of S. scherzeri, which could provide a theoretical foundation for the development of mono-sex breeding of S. scherzeri.

       

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