斑鳜早期性腺分化与发育的组织学观察

    Histological observation on the 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(HE)染色技术制备性腺组织切片,通过Olympus FX380显微镜和CaseViewer 2.4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日龄分别被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日龄分别被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,精巢发育进程明显快于卵巢,62日龄精巢已发育至Ⅳ期,此时卵巢仅发育至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 Artificially bred 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 (HE) staining techniques. These sections were observed, photographed and measured using an Olympus FX380 microscope and CaseViewer 2.4 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. For 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 at stage Ⅰ from 17 to 27 dph, entered stage Ⅱ at 32 dph, reached stage Ⅲ at 37 dph, and developed to stage Ⅳ at 62 dph. For 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 formed within one week after hatching, and the developmental process of testis was significantly faster than that of ovary. At 62 dph, the testis had developed to stage Ⅳ, while the ovary had only reached stage Ⅱ. This study on the early gonadal differentiation and histological development characteristics of S. scherzeri could provide a theoretical foundation for the development of mono-sex breeding techniques for this species.

       

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