Diatom Morphogenesis. Группа авторов

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Diatom Morphogenesis - Группа авторов

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chapters were contributed by experts on morphological diatoms. The authors stem from the USA, Russia, Denmark, Germany, Greece, Israel, and Portugal.

      Topics include computer simulation of morphogenesis, silicic acid to silica frustules, inhibition in valve morphogenesis, pores within frustules, mesopores of pennate diatoms, frustule photonics and light harvesting, clonal chains, silica cell wall, geometric models of centric diatoms, morphology, surface features, buckling of valve morphogenesis, on mantle profiles, genetic-biochemical approaches, modeling silicon pools, valve morphogenesis, diatom teratology in taxonomy, phenotypic plasticity, geometric and morphometric analysis, silica morphogenesis in sister algae, and the uncanny symmetry of some diatoms.

      This volume is the third book in the series Diatoms: Biology and Applications. The first book, Diatoms: Fundamentals and Applications appeared in 2019, and was edited by Joseph Seckbach and Richard Gordon. The second book, Diatom Gliding Motility, was published in September 2021 and is edited by Stanley A. Cohn, Kalina M. Manoylov and Richard Gordon.

      We would like to thank the authors, the reviewers, the guest editor (Vadim V. Annenkov), and our publisher Martin Scrivener of Massachusetts, USA.

      Joseph Seckbach Hebrew University Jerusalem, Israel September 2021

Part 1 GENERAL ISSUES

      1

      Introduction for a Tutorial on Diatom Morphology

       Kalina Manoylov1* and Mohamed Ghobara2

       1Dept. of Biological & Environmental Sciences, Georgia College and State University, Milledgeville, GA, United States

       2Department of Physics, Freie Universitat Berlin, Berlin, Germany

       Abstract

      Diatoms are an exceptionally successful group of unicellular microalgae with a large contribution of global primary production in aquatic environments and contributing a significant amount of oxygen to both hydro- and atmospheres. They are fascinating throughout their life and even after death, thanks to their unique cell walls made from ornamented silica. The diatoms include centric species, which may have radial or polar symmetry, and pennates, which include araphid, monoraphid, and biraphid species. Several applications have utilized diatomite, i.e., the fossil form of diatom frustules. To date, many diatoms’ secrets have been understood; however, there are still more hidden. Thus, there is a need for more research on diatom basic biology and applications. Seeking this goal, more people should be encouraged to work on diatoms. Often novice researchers are overwhelmed by the terminology associated with the diverse morphology, the discrepancy between expected features for published descriptions, and the actual observation of those complex 3D organisms, which can be a barrier for more progress. Here, we provide a brief introduction to the beginners with a guide to approach the complex diatom morphology focusing on the tools that can be used for its study.

      Keywords: Diatom morphology, tutorial, LM and SEM, frustule morphology

      Diatoms are a unique group of microalgae for several reasons, but one of the most notable and unique differences is the glass cell walls they possess [1.45]. This cell wall is called the “frustule” and is composed of amorphous hydrated silica that gives it unique properties. In general, the frustule is composed of two pieces that fit together like a petri-dish, meaning that the lower part of the frustule, called the hypotheca, sits inside of the upper part of the frustule, called the epitheca. The frustule volume extends by adding strips of silica called girdle bands (cingulum) to the mantle, i.e., the curved edge of the valve. It should be noted that there are plenty of frustule morphologies that vary between taxa.

      Diatoms reproduce both asexually (visible in Figure 1.6) and sexually. Most of the time, they reproduce asexually via binary fission through adding new hypovalves to the parent valves. Those new hypovalves are synthesized inside the silica deposition vesicle (SDV). Only after the new hypovalves have completely synthesized and the protoplast cleavage, as well as the exocytosis of siliceous parts, has occurred, the final splitting apart will occur, leaving two daughter diatoms in place. Because the SDV forms inside of each new cell before splitting into two, each new cell creates a new interior of the petri-dish structure. What this means is that the cell that originally contained the upper part of the petri dish (the epitheca) remains the same size, whereas the cell that originally contained the lower part of the petri-dish (the hypotheca) becomes smaller, since it has now built a smaller hypovalve to fit into it. Repeated cell division, therefore, leads to some part of the resulting population becoming smaller and smaller. Were asexual reproduction the only method by which diatoms reproduces, this could lead the population eventually to become vulnerable to dying out, but diatoms are ingenious and have gotten around this problem. At some point, sexual reproduction is initiated by a number of steps, including meiotic divisions to produce male and female gametes. These cells can find each other, fuse to form a zygote and create a structure known as an auxospore, out of which a new large cell of the diatom species will form, restoring its optimal size, which also depends on the environmental circumstances surrounding the auxospores. Some new research proposes chemical communication with pheromones between the male and female gametes [1.20].

Photos depict living diatoms as observed under LM, brightfield.

      Figure 1.1 Living diatoms as observed under LM, brightfield. (a) Two living cells of Actinoptychus senarius (Ehrenberg) Ehrenberg at the valve view. (b) The valve view of a single living cell of Coscinodiscus wailesii Gran and Angst. (c) The girdle view of a single living cell of Coscinodiscus granii L.F. Gough. (d) Two living cells of Achnanthes brevipes C. Agardh at the girdle view attached to each other with a prolonged stalk for the attachment to the substrate. (e) A living colony of Stephanopyxis turris (Greville) Ralfs with visible linking spines. (f) A living colony of Odontella longicruris (Greville) M.A. Hoban with discoid chloroplasts. Copyright reserved Mary Ann Tiffany, used with her permission. The identification was carried out by Mary Ann Tiffany. All the scale bars are 50 μm.

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