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Penetration of fluorescent microspheres into the NEEM (North Eemian) Greenland ice core to assess the probability of microbial contamination

机译:荧光微球渗透到NEEM(北艾米亚)格陵兰冰芯中,以评估微生物污染的可能性

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摘要

The validation of microbiological results from non-aseptically drilled deep ice cores is challenging because exogenous microbial cells can be transported into the core interior and compromise the existing microbial populations. The NEEM (North Eemian) ice core in Greenland provided a first-time opportunity to use fluorescent microspheres as tracers for assessing potential microbial contamination of glacial ice. We developed specific procedures to coat the surfaces of selected NEEM core samples representing bubbly (93-100 m), brittle (633-644 m) and clathrated (1,730 and 2,050 m) ice with melamine-based carboxylated fluorescent microspheres and tracked periodically their penetration into the core interior for 2.5 years using flow cytometry. Sufficient ice surface coating was achieved by immersing retrieved cores in plastic bags containing suspensions of pre-counted 1-and 10-μm microspheres or by down-hole microsphere deployment in plastic sleeves attached to the drill barrel and liberated during drilling. We examined the relationship between microspheres penetration and ice core depth, structure and time after coating. One consistent observation for all cores (except the brittle ice) was that removing a few millimeters of the outer layer drastically reduced micro-sphere counts, independent of timing, indicating that penetration was mostly limited to the surface layers. Any deeper penetration was found to be microsphere size dependent. The brittle ice showed significant microsphere penetration possibly due to micro fractures. Overall, the use of fluorescent microspheres as tracers and microbial surrogates proved to be a sensitive approach for testing potential contamination during deep core projects.
机译:非无菌钻孔深冰芯的微生物学结果的验证具有挑战性,因为外源性微生物细胞可被转运到内核内部并损害现有微生物种群。格陵兰岛的NEEM(北艾米亚)冰芯首次提供了使用荧光微球作为示踪剂评估冰川冰潜在微生物污染的机会。我们开发了特定程序,以选定的NEEM核心样品的表面涂覆三聚氰胺基羧化荧光微球,这些样品分别代表泡状(93-100 m),脆性(633-644 m)和笼状(1,730和2,050 m)冰,并定期跟踪其渗透使用流式细胞仪进入核心内部2.5年。通过将回收的岩芯浸入装有预先计数的1和10μm微球悬浮液的塑料袋中,或通过将井下微球部署在与钻杆连接并在钻探过程中释放的塑料套管中,可以实现足够的冰面涂层。我们检查了微球渗透与包衣后冰芯深度,结构和时间之间的关系。对所有核心(脆冰除外)的一个一致观察结果是,除去几毫米的外层,与时间无关,从而大大减少了微球数,表明渗透主要限于表层。发现任何更深的渗透都取决于微球尺寸。脆冰显示可能由于微破裂而显着地渗透了微球。总体而言,荧光微球作为示踪剂和微生物替代物的使用被证明是测试深层核心项目潜在污染的灵敏方法。

著录项

  • 来源
    《Polar biology》 |2014年第1期|47-59|共13页
  • 作者单位

    Department of Biochemistry and Molecular Biology, The Pennsylvania State University, 211 South Frear, University Park, PA 16802, USA;

    Department of Geosciences, Earth and Environment Systems Institute, The Pennsylvania State University, University Park, PA 16802, USA;

    Department of Biochemistry and Molecular Biology, The Pennsylvania State University, 211 South Frear, University Park, PA 16802, USA;

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

    Ice core; NEEM Greenland; Microbial contamination; Fluorescent microspheres; Penetration;

    机译:冰芯;NEEM格陵兰岛;微生物污染;荧光微球;渗透;

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