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A 3D imaging and visualization workflow, using confocal microscopy and advanced image processing for brachyuran crab larvae

机译:3D成像和可视化工作流程,使用共聚焦显微镜和Brachyuran Crab幼虫的高级图像处理

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摘要

Confocal laser scanning microscopy is an excellent tool for nondestructive imaging of arthropods and can provide detailed information on morphology including fine surface detail. A methodology is presented here for the visualization by confocal microscopy of arthropods, using brachyuran crab zoeal stages as examples and postprocessing techniques derived from micro-CT protocols to improve the final images. This protocol is divided into description of the preprocessing steps (cleaning, staining, digesting and mounting), confocal laser scanning microscopy and data visualization using open-source, freeware programs ImageJ and Drishti. The advantages of using ImageJ to standardize stack data and Drishti for surface rendering are discussed. The methodology has been comprehensively tested using data acquired from all four brands of confocal microscope (Leica, Nikon, Olympus and Zeiss).
机译:共聚焦激光扫描显微镜是节肢动物非破坏性成像的优秀工具,可以提供有关细节的细节的详细信息。 这里介绍一种通过节肢动物的共聚焦显微镜来表达一种方法,使用Brachyuran蟹Zoeal阶段作为从微型CT协议导出以改善最终图像的示例和后处理技术。 该协议分为预处理步骤的描述(清洁,染色,消化和安装),共聚焦激光扫描显微镜和使用开源的数据可视化,免费软件程序ImageJ和Drishti。 讨论了使用imagej来标准化堆栈数据和DRISHTI进行表面渲染的优点。 通过从所有四个品牌的共聚焦显微镜(Leica,Nikon,Olympus和Zeiss)获得的数据全面测试了该方法。

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