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Source Tracking Aerosols Released from Land-Applied Class B Biosolids during High-Wind Events

机译:高风事件期间从土地应用的B类生物固体中释放的气溶胶追踪源

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DNA-based microbial source tracking (MST) methods were developed and used to specifically and sensitively track the unintended aerosolization of land-applied, anaerobically digested sewage sludge (biosolids) during high-wind events. Culture and phylogenetic analyses of bulk biosolids provided a basis for the development of three different MST methods. They included (i) culture- and 16S rRNA gene-based identification of Clostridium bifermentans, (ii) direct PCR amplification and sequencing of the 16S rRNA gene for an uncultured bacterium of the class Chloroflexi that is commonly present in anaerobically digested biosolids, and (iii) direct PCR amplification of a 16S rRNA gene of the phylum Euryarchaeota coupled with terminal restriction fragment length polymorphism to distinguish terminal fragments that are unique to biosolid-specific microorganisms. Each method was first validated with a broad group of bulk biosolids and soil samples to confirm the target's exclusive presence in biosolids and absence in soils. Positive responses were observed in 100% of bulk biosolid samples and in less than 11% of the bulk soils tested. Next, a sampling campaign was conducted in which all three methods were applied to aerosol samples taken upwind and downwind of fields that had recently been land applied with biosolids. When average wind speeds were greater than 5 m/s, source tracking results confirmed the presence of biosolids in 56% of the downwind samples versus 3% of the upwind samples. During these high-wind events, the biosolid concentration in downwind aerosols was between 0.1 and 2 μg/m3. The application of DNA-based source tracking to aerosol samples has confirmed that wind is a possible mechanism for the aerosolization and off-site transport of land-applied biosolids.
机译:开发了基于DNA的微生物源跟踪(MST)方法,用于专门和灵敏地跟踪大风事件中土地施用的,厌氧消化的污水污泥(生物固体)的意外雾化。大量生物固体的培养和系统发育分析为开发三种不同的MST方法提供了基础。它们包括(i)双发酵梭菌的基于培养物和16S rRNA基因的鉴定,(ii)厌氧消化的生物固体中通常存在的未培养细菌绿屈挠菌的16S rRNA基因的直接PCR扩增和测序,以及( iii)直接PCR扩增Euryarchaeota门的16S rRNA基因,并结合末端限制性片段长度多态性,以区分特定于生物固体特异性微生物的末端片段。每种方法都首先通过大量生物固体和土壤样品进行验证,以确认目标物在生物固体中是否存在以及在土壤中是否存在。在100%的大块生物固体样品和不到11%的大块土壤中观察到阳性反应。接下来,开展了一次采样活动,其中将这三种方法都应用于最近在陆地上使用生物固体的田地的上,下风道采集的气溶胶样品。当平均风速大于5 m / s时,源跟踪结果证实,在下风样品中有56%的生物固体存在,而在上风样品中只有3%的生物固体存在。在这些强风事件中,顺风气溶胶中的生物固体浓度在0.1至2μg/ m3之间。将基于DNA的源跟踪应用于气溶胶样品已证实,风是气雾化和陆地施用生物固体的异地运输的一种可能机制。

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