Auxospore fine structure and development in the surirelloid diatom Campylodiscus cf. neofastuosus (Bacillariophyta).

IF 3.4 3区 生物学 Q1 MARINE & FRESHWATER BIOLOGY
Masahiko Idei, David G Mann, Tsuyoshi Watanabe, Shinya Sato
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Abstract

The development of the auxospore is reported in the surirelloid diatom Campylodiscus cf. neofastuosus. As in most pennate diatoms, growth of the auxospore is accompanied and constrained by the formation of a transverse perizonium composed of finely structured bands, which are added one after another as the auxospore expands. However, unlike in most pennate diatoms, in which the transverse perizonium develops bidirectionally from a hoop-like or shortly cylindrical primary band formed around the equator of the zygote, in C. cf. neofastuosus, development is unidirectional, outward from a heart-shaped cap at one end of the auxospore. Limited evidence from other surirelloid diatoms suggests that unidirectional perizonium development may be typical of the group. This developmental pattern correlates with the profound symmetry shifts that have occurred during the evolution of the circumferential raphe system of Surirellaceae and may have a common origin with these, despite the difference in life-cycle stage. The longitudinal perizonium of Campylodiscus also exhibits differences from the arrangement typical of most raphid diatoms, since it comprises three concentrically organized bands, including a unique, heavily silicified secondary band, which runs around the whole circumference of the wide primary band. In this and some other Surirellaceae, the longitudinal perizonium seems to play an important role in the morphogenesis of the initial cells by controlling the shape of the protoplast during a contraction before the formation of the initial epivalve. Small extra perizonial elements, unlike any reported previously in raphid diatoms, were detected beneath the suture formed by the ends of the transverse perizonial bands.

水生硅藻Campylodiscus cf. neofastousus的副孢子精细结构和发育。
报道了生存类硅藻弯曲硅藻(Campylodiscus cf. neofastousus)的副孢子发育。与大多数pennate硅藻一样,副孢子的生长伴随着并受到横向周层形成的限制,横向周层由结构精细的条带组成,随着副孢子的扩张,这些条带一个接一个地增加。然而,与大多数pennate硅藻不同的是,在大多数pennate硅藻中,横向周胞体是从围绕合子赤道形成的环状或短圆柱形初级带向双向发育的,而在c.c.c . neofastuosus中,发育是单向的,从副孢子一端的心形帽向外发育。来自其他存活硅藻的有限证据表明,单向生周发育可能是该群体的典型特征。这种发育模式与生存科周缘系统的进化过程中发生的深刻的对称性变化有关,尽管生命周期阶段不同,但可能与这些变化有共同的起源。弯曲硅藻的纵向周层也表现出与大多数raphid硅藻的典型排列不同,因为它包括三个同心组织的条带,包括一个独特的,重度硅化的次级条带,它环绕着宽的初级条带的整个圆周。在这个和其他一些存活科中,纵向周层似乎在初始细胞形成前的收缩过程中通过控制原生质体的形状在初始细胞的形态发生中起重要作用。与以往报道的任何快速硅藻不同,在横向水平带末端形成的缝合线下检测到小的额外水平元素。
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来源期刊
Journal of Phycology
Journal of Phycology 生物-海洋与淡水生物学
CiteScore
6.50
自引率
3.40%
发文量
69
审稿时长
2 months
期刊介绍: The Journal of Phycology was founded in 1965 by the Phycological Society of America. All aspects of basic and applied research on algae are included to provide a common medium for the ecologist, physiologist, cell biologist, molecular biologist, morphologist, oceanographer, taxonomist, geneticist, and biochemist. The Journal also welcomes research that emphasizes algal interactions with other organisms and the roles of algae as components of natural ecosystems. All aspects of basic and applied research on algae are included to provide a common medium for the ecologist, physiologist, cell biologist, molecular biologist, morphologist, oceanographer, acquaculturist, systematist, geneticist, and biochemist. The Journal also welcomes research that emphasizes algal interactions with other organisms and the roles of algae as components of natural ecosystems.
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