Abundance and diversity of ammonia-oxidizing archaea in response to various habitats in Pearl River Delta of China, a subtropical maritime zone

Ammonia-oxidizing archaea (AOA) are widely considered key to ammonia oxidation in various environments. However, little work has been conducted to simultaneously investigate the abundance and diversity of AOA as well as correlations between archaeal amoA genotypes and environmental parameters of different ecosystems at one district. To understand the abundance, diversity, and distribution of AOA in Pearl River Delta of China in response to various habitats, the archaeal amoA genes in soil, marine, river, lake, hot spring and wastewater treatment plant (WWTP) samples were investigated using real-time fluorescent quantitative PCR and clone libraries. Our analyses indicated that the diversity of AOA in various habitats was different and could be clustered into five major clades, i.e., estuary sediment, marine water/sediment, soil, hot spring and Cluster 1. Phylogenetic analyses revealed that the structure of AOA communities in similar ecological habitats exhibited strong relation. The canonical correspondence method indicated that the AOA community structure was strongly correlated to temperature, pH, total organic carbon, total nitrogen and dissolved oxygen variables. Assessing AOA amoA gene copy numbers, ranging from 6.84×10⁶ to 9.45×10⁷ copies/g in dry soil/sediment, and 6.06×10⁶ to 2.41×10⁷ copies/L in water samples, were higher than ammonia-oxidizing bacteria (AOB) by 1-2 orders of magnitude. However, AOA amoA copy numbers were much lower than AOB in WWTP activated sludge samples. Overall, these studies suggested that AOA may be a major contributor to ammonia oxidation in natural habitats but play a minor role in highly aerated activated sludge. The result also showed the ratio of AOA to AOB amoA gene abundance was positively correlated with temperature and less correlated with other environmental parameters. New data from our study provide increasing evidence for the relative abundance and diversity of ammonia-oxidizing archaea in the global nitrogen cycle.     

耕地质量监测中合理样本量配置及不确定性分析——以陕西省宝鸡市为例

耕地质量监测样本量的优化配置对降低成本,实现可持续土地资源监测与利用有重要指导价值。以陕西省宝鸡市为例,采用2018年耕地质量监测数据,运用传统统计学和地统计学方法,探讨耕地质量监测中土壤监测指标的合理样本量及不确定性。研究表明：样本变异性大小与样本量的关系并不是绝对的。样本代表性评价方法和地统计学方法较Cochran方法能有效降低样本的不确定性;样本代表性评价法适用性更广,但研究结果缺乏稳定性;地统计学方法的适用性存在局限性,可降低中等变异性指标的不确定性,但对低、高变异性指标适用性较低。中等变异性指标宜采用地统计学方法确定合理样本量;低、高变异性指标宜采用代表性评价方法确定合理样本量。     

氯/氯胺和紫外顺序消毒对管网抗性基因的去除

为探究供水系统中氯/氯胺与低压紫外顺序消毒对抗生素抗性基因(ARGs)分布特征的影响,采用生物膜反应器模拟供水管网,对管网出水和生物膜进行60mJ/cm²低压紫外线(254nm)消毒,并利用高通量定量PCR技术检测模拟管网进、出水及生物膜内的典型ARGs和遗传原件(MGEs).结果表明,管网反应器运行150d,氯和氯胺管网出水ARGs总相对丰度分别为0.13和0.137,生物膜ARGs分别为2.45和0.277,表明供水管网中低剂量的氯或氯胺可有效降低水相和生物膜相中ARGs的相对丰度达90%,且氯胺消毒对生物膜中的ARGs控制作用更显著.氯和氯胺消毒后管网出水再经低压紫外线照射后,ARGs相对丰度分别为0.0682和0.0537,管网生物膜中ARGs的相对丰度分别为2.01和0.194.ARGs与MGEs间的相关性发生显著变化,转座子与strB和mepA的相关性增强,与ermX和tetM相关性减弱,而整合子与acrF、cmlA1-01、oprJ及tolC-01的相关性增强.研究表明,将紫外线消毒工艺设置在用水终端可以显著降低氯和氯胺管网水中ARGs丰度,但对管网生物膜中的ARGs影响较小.     

颗粒+絮体污泥CANON工艺的启动与SRT影响研究

为缩短工程应用中CANON工艺的启动时间及指导实际工程排泥控制,利用两个相同规格的SBR反应器接种不同比例厌氧氨氧化(anaerbic ammonium oxidation,ANAMMOX)颗粒污泥,研究了CANNON工艺启动规律与不同絮体SRT对工艺运行的影响.试验过程中,温度控制在30℃±1℃,pH 7~8.结果表明,接种5%和10%ANAMMOX颗粒污泥的两反应器在初始FA浓度大于44 mg·L~(-1)条件下,不利于工艺的快速启动.接种15%和20%ANAMMOX颗粒污泥的两反应器,分别在运行的第46 d和35 d成功启动了CANON工艺.当絮体SRT分别为30 d、90 d和不主动排泥时,系统总氮去除负荷均能维持在0.35kg·(m3·d)-1;定量PCR数据显示,随污泥龄的延长,AOB丰度相对稳定,ANAMMOX菌丰度略有增加,但是NOB丰度显著增加.因此,选择性地排出絮体有利于NOB的淘洗和系统的长期运行稳定性.     

磺胺抗性消长与堆肥进程的交互特征

基于添加和不添加磺胺药[m(磺胺二甲嘧啶SM2)∶m(磺胺-6-甲氧嘧啶SMM)=1∶1]的好氧堆肥试验,分析堆肥过程中鸡粪理化性质、微生物群落代谢特征、磺胺抗生素以及5种抗性基因变化,探明磺胺抗性消长与堆肥过程的交互特征.结果表明,磺胺药添加抑制了堆肥基础呼吸,延长了堆体达到高温的时间,减缓了养分转化速度,显著影响堆肥中期微生物群落结构特征.鸡粪中SMM和SM2在堆肥14 d内即可完全降解,且SMM降解速率高于SM2.随堆肥进行,sul1和sul2呈先下降后轻微回升的趋势,磺胺药添加对sul1和Int I1丰度无明显提高作用,但可促进sul2扩散.堆肥过程中,tet Q和tet W变化与磺胺抗性基因不同,但磺胺药添加亦增加tet Q和tet W相对丰度.冗余分析结果显示,温度与sul1、sul2和Int I1明显负相关,与tet Q和tet W无明显相关性;5种抗性基因相对丰度均与碳氮比和硝态氮含量负相关,与p H、含水率和铵态氮含量正相关.     

盐生杜氏藻烯醇酶基因启动子的克隆分析及胁迫转录应答

为了解盐生杜氏藻(Dunaliella salina)烯醇酶(Enolase)在渗透耐受中的具体功能,利用基因组步行方法和巢式PCR,从D.salina中克隆了烯醇酶基因DsENO 5’上游约2 000 bp的调控序列,并对其进行序列分析.分析表明,它包含多个与转录调控有关的保守序列(如CAAT-box,TATA-box),富含光﹑干旱及其它胁迫应答元件.利用实时荧光定量PCR的方法,研究了高渗﹑高温以及低温外界胁迫条件下DsENO的转录情况,发现其受高渗强烈抑制,高温显著诱导而低温微弱诱导.