Toporski Jan K W, Steele Andrew, Westall Frances, Thomas-Keprta Kathie L, McKay David S
School of Earth, Environmental and Physical Sciences, Astrobiology Group, University of Portsmouth, Portsmouth, UK.
Astrobiology. 2002 Spring;2(1):1-26. doi: 10.1089/153110702753621312.
Evidence of microbial life on Earth has been found in siliceous rock formations throughout the geological and fossil record. To understand the mechanisms of silicification and thus improve our search patterns for evidence of fossil microbial life in rocks, a series of controlled laboratory experiments were designed to simulate the silicification of microorganisms. The bacterial strains Pseudomonas fluorescens and Desulphovibrio indonensis were exposed to silicifying media. The experiments were designed to determine how exposure time to silicifying solutions and to silicifying solutions of different Si concentration affect the fossilization of microbial biofilms. The silicified biofilms were analyzed using transmission electron microscopy (TEM) in combination with energy-dispersive spectroscopy. Both bacterial species showed evidence of silicification after 24 h in 1,000 ppm silica solution, although D. indonensis was less prone to silicification. The degree of silicification of individual cells of the same sample varied, though such variations decreased with increasing exposure time. High Si concentration resulted in better preservation of cellular detail; the Si concentration was more important than the duration in Si solution. Even though no evidence of amorphous silica precipitation was observed, bacterial cells became permineralized. High-resolution TEM analysis revealed nanometer-sized crystallites characterized by lattice fringe-spacings that match the (10-11) d-spacing of quartz formed within bacterial cell walls after 1 week in 5,000 ppm silica solution. The mechanisms of silicification under controlled laboratory conditions and the implication for silicification in natural environments are discussed, along with the relevance of our findings in the search for early life on Earth and extraterrestrial life.
在整个地质和化石记录中,已在硅质岩层中发现了地球上微生物生命的证据。为了了解硅化作用机制,从而改进我们在岩石中寻找化石微生物生命证据的搜索模式,设计了一系列对照实验室实验来模拟微生物的硅化过程。将荧光假单胞菌和印尼脱硫弧菌菌株暴露于硅化介质中。这些实验旨在确定暴露于硅化溶液的时间以及不同硅浓度的硅化溶液如何影响微生物生物膜的石化过程。使用透射电子显微镜(TEM)结合能量色散光谱对硅化生物膜进行了分析。在1000 ppm二氧化硅溶液中培养24小时后,两种细菌均显示出硅化迹象,不过印尼脱硫弧菌较不易发生硅化。同一样本中单个细胞的硅化程度各不相同,不过随着暴露时间的增加,这种差异会减小。高硅浓度能更好地保存细胞细节;硅浓度比在硅溶液中的持续时间更为重要。尽管未观察到无定形二氧化硅沉淀的证据,但细菌细胞发生了完全矿化。高分辨率TEM分析显示,在5000 ppm二氧化硅溶液中培养1周后,细菌细胞壁内形成了纳米级微晶,其晶格条纹间距与石英的(10-11)d间距相匹配。本文讨论了在对照实验室条件下的硅化作用机制及其对自然环境中硅化作用的影响,以及我们的研究结果在寻找地球早期生命和外星生命方面的相关性。