西北植物学报
西北植物學報
서북식물학보
ACTA BOTANICA BOREALI-OCCIDENTALIA SINICA
2005年
4期
761-769
,共9页
曹建国%何群%王全喜%田国伟%包文美
曹建國%何群%王全喜%田國偉%包文美
조건국%하군%왕전희%전국위%포문미
绵马鳞毛蕨%精母细胞%游动精子%超微结构
綿馬鱗毛蕨%精母細胞%遊動精子%超微結構
면마린모궐%정모세포%유동정자%초미결구
Dryopteris crassirhizoma Nakai.%spermatocyte%spermatozoid%ultra-structure
应用电镜技术对蕨类植物绵马鳞毛蕨(Dryopteris crassirhizoma Nakai)精母细胞和游动精子的超微结构特征进行了研究.精母细胞为多边形,细胞质内含有丰富的线粒体、质体、内质网、高尔基体等常见的细胞器,在细胞质中还可见到一些同心圆膜状结构,位于质膜的附近或精母细胞的角偶.同心圆膜状结构由双层膜环绕构成,外被1层单位膜.精母细胞与精子器的璧细胞之间形成了分离腔,在精母细胞质膜外形成了嗜锇层,这些结构的形成说明精母细胞已经开始与雄配子体逐渐分离,进入独立发育的阶段.尽管精母细胞之间也有嗜锇层的形成,但嗜锇层是不连续的,其上有一些空隙,精母细胞之间可通过空隙进行物质和信息的交流.成熟的精子细胞外被1层透明的薄膜,里面为游动精子,螺旋状,由环状细胞器环绕3~4圈构成,这些环状细胞器包括多层结构、微管带、巨大线粒体、鞭毛带和1个长形浓缩的细胞核.游动精子的后端为一些泡囊化的细胞质,其中包括一些残存的线粒体、造粉质体及大的囊泡等.当成熟的精子细胞排出精子器后,其内的游动精子挣脱透明质膜的束缚,摆脱后端的囊泡,成为1条游动精子.本文还对绵马鳞毛蕨和其它蕨类植物精子的超微结构特征进行了比较.
應用電鏡技術對蕨類植物綿馬鱗毛蕨(Dryopteris crassirhizoma Nakai)精母細胞和遊動精子的超微結構特徵進行瞭研究.精母細胞為多邊形,細胞質內含有豐富的線粒體、質體、內質網、高爾基體等常見的細胞器,在細胞質中還可見到一些同心圓膜狀結構,位于質膜的附近或精母細胞的角偶.同心圓膜狀結構由雙層膜環繞構成,外被1層單位膜.精母細胞與精子器的璧細胞之間形成瞭分離腔,在精母細胞質膜外形成瞭嗜鋨層,這些結構的形成說明精母細胞已經開始與雄配子體逐漸分離,進入獨立髮育的階段.儘管精母細胞之間也有嗜鋨層的形成,但嗜鋨層是不連續的,其上有一些空隙,精母細胞之間可通過空隙進行物質和信息的交流.成熟的精子細胞外被1層透明的薄膜,裏麵為遊動精子,螺鏇狀,由環狀細胞器環繞3~4圈構成,這些環狀細胞器包括多層結構、微管帶、巨大線粒體、鞭毛帶和1箇長形濃縮的細胞覈.遊動精子的後耑為一些泡囊化的細胞質,其中包括一些殘存的線粒體、造粉質體及大的囊泡等.噹成熟的精子細胞排齣精子器後,其內的遊動精子掙脫透明質膜的束縳,襬脫後耑的囊泡,成為1條遊動精子.本文還對綿馬鱗毛蕨和其它蕨類植物精子的超微結構特徵進行瞭比較.
응용전경기술대궐류식물면마린모궐(Dryopteris crassirhizoma Nakai)정모세포화유동정자적초미결구특정진행료연구.정모세포위다변형,세포질내함유봉부적선립체、질체、내질망、고이기체등상견적세포기,재세포질중환가견도일사동심원막상결구,위우질막적부근혹정모세포적각우.동심원막상결구유쌍층막배요구성,외피1층단위막.정모세포여정자기적벽세포지간형성료분리강,재정모세포질막외형성료기철층,저사결구적형성설명정모세포이경개시여웅배자체축점분리,진입독립발육적계단.진관정모세포지간야유기철층적형성,단기철층시불련속적,기상유일사공극,정모세포지간가통과공극진행물질화신식적교류.성숙적정자세포외피1층투명적박막,리면위유동정자,라선상,유배상세포기배요3~4권구성,저사배상세포기포괄다층결구、미관대、거대선립체、편모대화1개장형농축적세포핵.유동정자적후단위일사포낭화적세포질,기중포괄일사잔존적선립체、조분질체급대적낭포등.당성숙적정자세포배출정자기후,기내적유동정자쟁탈투명질막적속박,파탈후단적낭포,성위1조유동정자.본문환대면마린모궐화기타궐류식물정자적초미결구특정진행료비교.
The electron microscopic technique was adopted to study spermatocyte and spermatozoid ultra-structures of Dryopteris crassirhizoma Nakai. The spermatocytes were polygonal and contained many commonly-observed organelles such mitochondria, plastids, endoplasmic reticula, Golgi bodies; in their cytoplasm some concentric membrane-like structures were seen to stand near the plasmalemma or corner areas. The concentric structures consisted of self-encircled double-layer membrane covered by a single-layer unit membrane. There formed segregating cavities between spermatocyte cell-wall and spermogonium cell-wall and osmiophillic layers outside spermatocyte cytoplasmalemma, which indicated that the spermatocytes had begun to gradually break away from the male gametophytes and embark on independent development. Although osmiophillic layers also developed between spermatocyte and gametophytes, they were interrupted by pores for substance and signal exchanges. Mature gametophytes, wrapped by a transparent membrane, contained spermatozoids and spiral-shape bodies composed of ring-shape organelles that encircle themselves in 3~4 folds; the ring-shaped organelles included multi-layer structures, microtubule ribbon, megamitochondria, flagellum bands, a long dolichomorphic concentrated nucleus. At the back end of the spermatozoids there existed some vacuolated cytoplasm that contained residual mitochondria, amyloplasts and some big vesicles. When mature spermatids released from the antheridia, the spermatozoids overcame the binding of the transparent membrane and broke away from the vesicles at the back end to become free. In addition, the ultra-structures of Dryopteris crassirhizoma Nakai. were compared with those of other ferns.