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A benign approach to the preparation of freshwater bryozoan statoblasts for scanning electron microscopy (SEM) imaging

机译:用于扫描电子显微镜(sEm)成像的淡水苔藓成核细胞的良性制备方法

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摘要

Several different species of freshwater Bryozoa, belonging to the genera Plumatella, Rumarcanella and Fredericella, were detected within the Northern Mallee Pipeline (NMP) system in Victoria, Australia, that required definitive identification. These organisms produce asexual buds called statoblasts, with valves composed of sclerotised chitin that bear minute micro-ornamentations of considerable taxonomical significance. Imaging and analysis of these distinctive micro-ornamentations using scanning electron microscopy (SEM) is often employed for species identification. Meticulous preparation of statoblast samples is therefore required that necessitates the removal of adhering debris, dehydration and drying—whilst mitigating specimen damage and distortion. This technical note describes an approach whereby each of these three steps have been individually designed to be as benign as possible, using mild detergent/sonication to remove debris, a gradual and gentle dehydration procedure using ethanol, and critical point drying. For the overall process, these methods are chosen to optimise control and to minimise the use of harsh and hazardous chemicals.
机译:在澳大利亚维多利亚州的北马利管道(NMP)系统中发现了几种不同种类的淡水Bryozoa,分别属于Plumatella,Rumarcanella和Fredericella属,需要进行最终鉴定。这些生物产生无性芽,称为无核芽细胞,其瓣膜由硬化的几丁质组成,具有微小的微装饰,具有重要的分类学意义。这些独特的微装饰物的成像和分析通常使用扫描电子显微镜(SEM)进行物种鉴定。因此,需要细致地制备成层母细胞样品,这需要除去粘附的碎屑,脱水和干燥,从而减轻样品的损坏和变形。本技术说明介绍了一种方法,通过使用温和的去污剂/超声处理来去除碎屑,使用乙醇进行逐步平缓的脱水过程以及临界点干燥,将这三个步骤中的每一个都设计得尽可能地好。对于整个过程,选择这些方法是为了优化控制并最大程度地减少使用刺激性和危险化学品。

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