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Prokaryotic cells of the deep sub-seafloor biosphere identified as living bacteria

机译:深层海底生物圈中的原核细胞被鉴定为活菌

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Chemical analyses of the pore waters from hundreds of deep ocean sediment cores have over decades provided evidence for ongoing processes that require biological catalysis by prokaryotes(1-3). This sub-seafloor activity of microorganisms may influence the surface Earth by changing the chemistry of the ocean and by triggering the emission of methane, with consequences for the marine carbon cycle and even the global climate(4-6). Despite the fact that only about 1% of the total marine primary production of organic carbon is available for deep-sea microorganisms(7,8), subseafloor sediments harbour over half of all prokaryotic cells on Earth(7). This estimation has been calculated from numerous microscopic cell counts in sediment cores of the Ocean Drilling Program(1,9). Because these counts cannot differentiate between dead and alive cells, the population size of living microorganisms is unknown(10,11). Here, using ribosomal RNA as a target for the technique known as catalysed reporter deposition-fluorescence in situ hybridization (CARD-FISH), we provide direct quantification of live cells as defined by the presence of ribosomes. We show that a large fraction of the sub-seafloor prokaryotes is alive, even in very old (16 million yr) and deep (>400 m) sediments. All detectable living cells belong to the Bacteria and have turnover times of 0.25-22 yr, comparable to surface sediments.
机译:数十年来,对数百个深海沉积物核心的孔隙水进行化学分析,为需要原核生物进行生物催化的正在进行的过程提供了证据(1-3)。微生物的这种海底活动可能会通过改变海洋的化学性质和触发甲烷的排放来影响地球表面,从而影响海洋的碳循环甚至全球气候(4-6)。尽管事实上只有约1%的海洋初级有机碳总产量可用于深海微生物(7,8),但海底沉积物却占据了地球上所有原核细胞的一半以上(7)。该估算是根据海洋钻探计划(1,9)沉积物中的大量微观细胞数计算得出的。由于这些计数不能区分死细胞和活细胞,因此尚不知道活微生物的种群大小(10,11)。在这里,使用核糖体RNA作为被称为催化报道分子沉积-荧光原位杂交(CARD-FISH)技术的靶标,我们提供了由核糖体的存在所定义的活细胞的直接定量分析。我们显示,即使在非常老的(1600万年)和深层(> 400 m)沉积物中,大部分海底原核生物仍活着。所有可检测到的活细胞都属于细菌,其周转时间为0.25-22年,与表面沉积物相当。

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