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Cell evolution and Earth history: stasis and revolution

机译:细胞进化与地球历史:停滞与革命

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This synthesis has three main parts. The first discusses the overall tree of life and nature of the last common ancestor (cenancestor). I emphasize key steps in cellular evolution important for ordering and timing the major evolutionary innovations in the history of the biosphere, explaining especially the origins of the eukaryote cell and of bacterial flagella and cell envelope novelties. Second, I map the tree onto the fossil record and discuss dates of key events and their biogeochemical impact. Finally, I present a broad synthesis, discussing evidence for a three-phase history of life. The first phase began perhaps ca 3.5 Gyr ago, when the origin of cells and anoxic photosynthesis generated the arguably most primitive prokaryote phylum, Chlorobacteria (=Chloroflexi), the first negibacteria with cells bounded by two acyl ester phospholipid membranes. After this 'chlorobacterial age' of benthic anaerobic evolution protected from UV radiation by mineral grains, two momentous quantum evolutionary episodes of cellular innovation and microbial radiation dramatically transformed the Earth's surface: the glycobacterial revolution initiated an oxygenic 'age of cyanobacteria' and, as the ozone layer grew, the rise of plankton; immensely later, probably as recently as ca 0.9 Gyr ago, the neomuran revolution ushered in the 'age of eukaryotes', Archaebacteria (arguably the youngest bacterial phylum), and morphological complexity. Diversification of glycobacteria ca 2.8 Gyr ago, predominantly inhabiting stratified benthic mats, I suggest caused serial depletion of C-13 by ribulose 1,5-bis-phosphate caboxylase/oxygenase (Rubisco) to yield ultralight late Archaean organic carbon formerly attributed to methanogenesis plus methanotrophy. The late origin of archaebacterial methanogenesis ca 720 Myr ago perhaps triggered snowball Earth episodes by slight global warming increasing weathering and reducing CO2 levels, to yield runaway cooling; the origin of anaerobic methane oxidation ca 570 Myr ago reduced methane flux at source, stabilizing Phanerozoic climates. I argue that the major cellular innovations exhibit a pattern of quantum evolution followed by very rapid radiation and then substantial stasis, as described by Simpson. They yielded organisms that are a mosaic of extremely conservative and radically novel features, as characterized by De Beer's phrase 'mosaic evolution'. Evolution is not evenly paced and there are no real molecular clocks.
机译:该综合包括三个主要部分。第一部分讨论了最后一个共同祖先(cenancestor)的整体生命之树和本质。我强调了细胞进化中的关键步骤,这些步骤对于对生物圈历史上的重大进化创新进行排序和计时很重要,尤其是解释了真核细胞以及细菌鞭毛和细胞被膜新奇的起源。其次,我将树映射到化石记录上,并讨论关键事件的日期及其生物地球化学影响。最后,我提出了一个广泛的综述,讨论了生命的三个阶段的历史证据。第一阶段大约在3.5年前开始,当时细胞的起源和缺氧的光合作用产生了可以说是最原始的原核生物门生细菌,即细菌(Chloroflexi),这是第一个带有两个酰基酯磷脂膜结合细胞的负细菌。在底栖厌氧菌进化的这个“氯细菌时代”免受矿物颗粒的紫外线辐射之后,细胞创新和微生物辐射的两个重大量子进化事件极大地改变了地球表面:糖细菌革命引发了蓝藻的氧化“氧时代”,并且臭氧层增加,浮游生物上升;不久之后,大约在0.9 Gyr之前,新村革命引发了“真核生物时代”,古细菌(可以说是最年轻的细菌门)和形态的复杂性。大约2.8年前,糖细菌的多样化,主要居住在分层的底栖垫层上,我建议通过核糖1,5-双磷酸羧化酶/加氧酶(Rubisco)引起C-13的连续消耗,从而产生超轻的古生代晚期有机碳,该碳以前归因于产甲烷作用加上甲烷营养素。大约在720 Myr以前,古细菌甲烷生成的起源较晚,这可能是由于轻微的全球变暖加剧了气候变化并降低了CO2含量,从而引发了雪球状地球事件,从而产生了失控的冷却作用。大约570 Myr之前,厌氧甲烷氧化的起源降低了甲烷的通量,稳定了生代气候。我认为,主要的细胞创新表现出一种量子演化的模式,随后是非常快的辐射,然后是基本停滞,正如辛普森所描述的那样。他们生产出的生物具有极高的保守性和根本性的新颖特征,以戴比尔(De Beer)的“马赛克进化”一词为特征。进化步伐不均衡,也没有真正的分子钟。

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