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Concurrent imaging of chlorophyll fluorescence, Chlorophyll a content and green fluorescent proteins-like proteins of symbiotic cnidarians

机译:共生刺胞的叶绿素荧光,叶绿素a含量和绿色荧光蛋白样蛋白的同时成像

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摘要

Research on photosynthetic cnidarians has been mainly focused on the symbiosis established between the cnidarian host and its dinoflagellates endosymbionts from genus Symbiodinium. Despite the potential of imaging techniques for assessing the spatial distribution of key parameters of cnidarian photobiology, such as photochemical activity, chlorophyll a content or green fluorescent proteins (GFPs), to our best knowledge, no study has ever attempted to simultaneous map these three features. In this study, we developed a modified imaging pulse amplitude fluorometer by applying excitation light of different wavelengths and selectively detecting short spectral bands through bandpass filters. The imaging system was used to sequentially excite and quantify chlorophyll variable fluorescence (maximum quantum yield of photosystem II, F-v/F-m), Chl a content (normalized difference vegetation index) and relative content of GFPs. The spatial distribution of these photophysiological parameters was mapped both horizontally, across the surface of the soft corals Sarcophyton cf. glaucum and Sinularia flexibilis and the zoanthid Protopalythoa sp., and vertically, throughout a vertical section of S. cf. glaucum. Results showed bleached areas within each individual coral colony and registered photophysiological changes with S. cf. glaucum tissue depth. Analysis of Protopalythoa sp. polyps' expansion revealed differential surface patterns of NDVI and GFP concentration, and a negative relation between these latter parameters within each polyp. This novel non-invasive approach allowed a high-resolution characterization of the spatial relationship between these key parameters through the analysis of image information on a pixel-by-pixel basis, which has great potential for investigating the physiological state of symbiotic associations.
机译:光合刺胞的研究主要集中在刺胞宿主与其共生菌属的鞭毛内共生体之间建立的共生关系。尽管成像技术有潜力评估cnidarian光生物学关键参数的空间分布,例如光化学活性,叶绿素a含量或绿色荧光蛋白(GFPs),据我们所知,还没有研究试图同时绘制这三个特征。在这项研究中,我们通过施加不同波长的激发光并通过带通滤波器选择性地检测短光谱带,开发了一种改进的成像脉冲幅度荧光计。成像系统用于顺序激发和定量叶绿素可变荧光(光系统II的最大量子产率,F-v / F-m),Chla含量(归一化差异植被指数)和GFP的相对含量。这些光生理学参数的空间分布在水平方向上横跨软珊瑚Sarcophyton cf.青草和柔毛Sinularia flexibilis和zoanthid Protopalythoa sp。,垂直于整个S. cf.的垂直部分。青豆。结果显示每个单个珊瑚群落内的漂白区域和S.cf.记录的光生理变化。青草组织深度。分析Protopalythoa sp。息肉的扩张显示出NDVI和GFP浓度的表面差异,每个息肉中这些参数之间呈负相关。这种新颖的非侵入性方法允许通过逐个像素地分析图像信息来高分辨率表征这些关键参数之间的空间关系,这对于研究共生关联的生理状态具有巨大的潜力。

著录项

  • 来源
    《Marine ecology》 |2015年第3期|572-584|共13页
  • 作者单位

    Univ Aveiro, Dept Biol, P-3810193 Aveiro, Portugal|Univ Aveiro, CESAM, P-3810193 Aveiro, Portugal|Univ Georgia, Skidaway Inst Oceanog, Savannah, GA USA;

    Univ Nantes, LUNAM Univ, Mer Mol Sante EA 2160, Fac Sci & Tech, Nantes, France|Univ Nova Lisboa, Fac Ciencias, Ctr Biodiversidade Genom Integrat & Func BioFIG, P-1200 Lisbon, Portugal;

    Univ Aveiro, Dept Biol, P-3810193 Aveiro, Portugal|Univ Aveiro, CESAM, P-3810193 Aveiro, Portugal;

    Univ Aveiro, Dept Biol, P-3810193 Aveiro, Portugal|Univ Aveiro, CESAM, P-3810193 Aveiro, Portugal;

    Univ Aveiro, Dept Biol, P-3810193 Aveiro, Portugal|Univ Aveiro, CESAM, P-3810193 Aveiro, Portugal;

    Univ Nova Lisboa, Fac Ciencias, Ctr Oceanog, P-1200 Lisbon, Portugal;

    Univ Aveiro, Dept Biol, P-3810193 Aveiro, Portugal|Univ Aveiro, CESAM, P-3810193 Aveiro, Portugal;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Chl a; fluorescence; imaging-PAM; Symbiodinium; symbiosis;

    机译:Chl a;荧光;成像-PAM;共生素;共生;
  • 入库时间 2022-08-18 03:33:33

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