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Soil Microbe Active Community Composition and Capability of Responding to Litter Addition after 12 Years of No Inputs

机译:12年无输入后土壤微生物活性群落组成及对凋落物响应的能力

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One explanation given for the high microbial diversity found in soils is that they contain a large inactive biomass that is able to persist in soils for long periods of time. This persistent microbial fraction may help to buffer the functionality of the soil community during times of low nutrients by providing a reservoir of specialized functions that can be reactivated when conditions improve. A study was designed to test the hypothesis: in soils lacking fresh root or detrital inputs, microbial community composition may persist relatively unchanged. Upon addition of new inputs, this community will be stimulated to grow and break down litter similarly to control soils. Soils from two of the Detrital Input and Removal Treatments (DIRT) at the H. J. Andrews Experimental Forest, the no-input and control treatment plots, were used in a microcosm experiment where Douglas-fir needles were added to soils. After 3 and 151 days of incubation, soil microbial DNA and RNA was extracted and characterized using quantitative PCR (qPCR) and 454 pyrosequencing. The abundance of 16S and 28S gene copies and RNA copies did not vary with soil type or amendment; however, treatment differences were observed in the abundance of archaeal ammonia-oxidizing amoA gene abundance. Analysis of ~110,000 bacterial sequences showed a significant change in the active (RNA-based) community between day 3 and day 151, but microbial composition was similar between soil types. These results show that even after 12 years of plant litter exclusion, the legacy of community composition was well buffered against a dramatic disturbance.
机译:对于土壤中存在的高微生物多样性的一种解释是,它们含有大量的非活性生物质,能够长期在土壤中持续存在。通过提供特殊功能的库,当条件改善时,这种持久的微生物级分可以在营养不足的情况下帮助缓冲土壤群落的功能。设计了一项研究以检验该假设:在缺乏新鲜根或碎屑输入的土壤中,微生物群落组成可能会保持相对不变。添加新的投入后,将像刺激土壤一样刺激这个社区生长和分解垃圾。 H. J.安德鲁斯实验森林的两种碎屑输入和清除处理(DIRT)的土壤(无输入和对照处理区)用于微观实验,在其中将花旗松针添加到土壤中。孵育3天和151天后,提取土壤微生物DNA和RNA,并使用定量PCR(qPCR)和454焦磷酸测序进行表征。 16S和28S基因拷贝和RNA拷贝的丰度并没有随土壤类型或改良而变化。然而,在古细菌氨氧化的amoA基因丰度上观察到治疗差异。对约110,000个细菌序列的分析显示,在第3天和第151天之间,活动(基于RNA)的群落发生了显着变化,但土壤类型之间的微生物组成相似。这些结果表明,即使在排除植物凋落物12年之后,社区组成的遗产也可以很好地缓冲以防发生严重的干扰。

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