农业土地利用转变对土壤团聚体组成及碳、氮含量的影响

为探究农业土地利用转变对土壤团聚体组成、稳定性及有机碳（SOC）、全氮（TN）含量变化的影响,选取玉米地、玉米地转变为姜地、稻田和稻田转变为姜地4种农业土地利用类型为研究对象,对土壤水稳性团聚体的组成、稳定性及SOC、TN含量进行测定与分析.结果表明： ①玉米地转变为姜地后,>0.25 mm粒级的大团聚体减少21.48%（p<0.01）,>0.25 mm稳定性团聚体的含量（DR_0.25）显著降低53.39%;稻田转变为姜地后,大团聚体差异不显著,<0.053 mm粒级的粉黏团聚体增加8.93%（p<0.01）;冗余分析和相关分析表明,土壤含水量是团聚体组成和 稳定性的重要影响因素;②玉米地转变为姜地后,0.25~1 mm粒级团聚体中SOC、TN含量分别减少52.68%、50.98%,粉黏团聚体（<0.053 mm）中SOC和TN含量增加约2倍（p<0.01）;稻田转变为姜地后,>0.25 mm的大团聚体和0.053~0.25 mm的微团聚体中的SOC、TN含量均减少（p<0.05）,其中,大团聚体碳氮比与团聚体组成和稳定性存在相关关系（p<0.05）;③所有处理均为大团聚体SOC、TN贡献率最高,转变后的姜地较玉米地、稻田的土壤粉黏团聚体的SOC、TN贡献率显著增加,尤其是较玉米地的粉黏团聚体SOC、TN贡献率增加3倍（p<0.01）;④平均质量 直径（MWD）和几何平均直径（GMD）与大团聚体的SOC、TN含量呈显著正相关（p<0.05）,分形维数（D）与MWD及1~2 mm粒级大团聚体的SOC、TN含量呈显著负相关（p<0.01）,DR_0.25与大团聚体的SOC、TN含量呈显著正相关（p<0.01）.总体上,玉米地和稻田两种用地转变为姜地后,土壤团聚体的组成发生较大变化,团聚体稳定性变化虽不显著,但大团聚体中SOC、TN含量降低,粉黏团聚体中SOC、TN含量增加.本研究的开展对农田科学管理和可持续生产具有重要的指导意义.     

生物酶对初沉污泥厌氧发酵产短链脂肪酸的调控研究

旨在通过生物酶调节(碱性蛋白酶、中性蛋白酶和α-淀粉酶)提高初沉污泥的厌氧发酵效率,并通过微生物群落结构解析,SCFAs (short-chain fatty acids,SCFAs)组分分析等揭示其调控机理.结果表明,3种生物酶均可增强初沉污泥水解和产酸作用,碱性蛋白酶调控系统对初沉污泥厌氧发酵的促进效果最为明显,发酵第4d SCFAs的产量和产率分别达到1508mg COD/L和0.174g COD/g VSS.对比控制组,SCFAs的产量和产率分别增加了1129mg COD/L和0.13g COD/g VSS.微生物群落结构分析表明,在碱性蛋白酶调控发酵系统中,Lentimicrobium、Proteiniphilum和Bacteroides等发酵相关菌群的相对丰度得到了改善,Methanosaeta、Methanospirillum等产甲烷古菌的活性受到了抑制.同时,生物酶调控对促进发酵过程乙酸占比也有促进作用.     

低NOx环境异戊二烯促进甲苯生成甲基丁烯二醛的模拟实验

在低NO_x浓度条件下开展甲苯和异戊二烯复合体系的烟雾箱模拟实验,使用高时间分辨率的在线质子转移反应飞行时间质谱(PTR-TOF-MS)实时监测混合体系中反应物与产物的浓度变化情况,探究人为源与天然源交汇过程中, 自然源挥发性有机物 (BVOCs)对人为挥发性有机物(AVOCs)化学降解的影响.结果表明,异戊二烯与甲苯竞争OH自由基,从而抑制了甲苯的化学降解,该竞争反应开始得越早,抑制效果越显著.研究还发现异戊二烯会增强甲苯RO₂降解途径产物的产量,生成更多1,4不饱和-二羰基化合物(如丁烯二醛和甲基丁烯二醛)与二羰基化合物(如乙二醛和甲基乙二醛),其中甲基丁烯二醛增量最高可达38.6%.此外,异戊二烯快速氧化生成的RO₂自由基碳数更少,可能与甲苯氧化生成的RO₂自由基发生了快速的交叉反应,有利于甲苯RO自由基的生成及裂解,最终导致甲苯RO₂途径裂解产物的增加.     

三峡水库水动力分区及总磷标准研究

采用EFDC模型计算2010~2018年三峡水库流域水龄.结果表明,三峡水库水龄由上游库尾至下游库首愈来愈大,尤其坝前水龄高达100余天,湖泊属性增强,坝前支流受库区影响大,大坝调度对水龄影响较大,高水位运行期水龄将增长至2~4倍.基于水龄空间分布将三峡水库及其17条主要支流划分为河流型、河湖过渡型和湖泊型.水龄影响因素定量分析表明,水龄与水位呈正相关,与流量呈负相关,泄水期变化速率较蓄水期明显,单位流量与水位内水龄变化幅度高达6~7d,变化区间介于30~100d之间.最后,提出基于水龄权重法的河湖过渡区总磷评价标准,该标准可揭示库区水体总磷的时空变化特征.     

Potassium ferrate pretreatment promotes short chain fatty acids yield and antibiotics reduction in acidogenic fermentation of sewage sludge

During the acidogenic fermentation converting waste activated sludge (WAS) into short-chain fatty acids (SCFA), hydrolysis of complex organic polymers is a limiting step and the transformation of harmful substances (such as antibiotics) during acidogenic fermentation is unknown. In this study, potassium ferrate (K₂FeO₄) oxidation was used as a pretreatment strategy for WAS acidogenic fermentation to increase the hydrolysis of sludge and destruct the harmful antibiotics. Pretreatment with K₂FeO₄ can effectively increase the SCFA production during acidogenic fermentation and change the distribution of SCFA components. With the dosage of 0.2 g/g TS, the maximum SCFA yield was 4823 mg COD/L, which is 28.3 times that of the control group; acetic acid accounts for more than 90% of the total SCFA. The higher dosage (0.5 g/g TS) can further increase the proportion of acetic acid, but inhibit the overall performance of SCFA production. Apart from the promotion of hydrolysis and acidogenesis, K₂FeO₄ pretreatment can also simultaneously oxidizes and degrades part of the antibiotics in the sludge. When the dosage is 0.5 g/g TS, the degradation efficacy of antibiotics is the most significant, and the contents of ofloxacin, azithromycin, and tetracycline in the sludge are reduced by 69%, 42%, and 50%, respectively. In addition, K₂FeO₄ pretreatment can also promote the release of antibiotics from sludge flocs, which is conducive to the simultaneous degradation of antibiotics in the subsequent biological treatment process.     

Relationships between regulated DBPs and emerging DBPs of health concern in U.S. drinking water

A survey was conducted at eight U.S. drinking water plants, that spanned a wide range of water qualities and treatment/disinfection practices. Plants that treated heavily-wastewater-impacted source waters had lower trihalomethane to dihaloacetonitrile ratios due to the presence of more organic nitrogen and HAN precursors. As the bromide to total organic carbon ratio increased, there was more bromine incorporation into DBPs. This has been shown in other studies for THMs and selected emerging DBPs (HANs), whereas this study examined bromine incorporation for a wider group of emerging DBPs (haloacetaldehydes, halonitromethanes). Moreover, bromine incorporation into the emerging DBPs was, in general, similar to that of the THMs. Epidemiology studies that show an association between adverse health effects and brominated THMs may be due to the formation of brominated emerging DBPs of heath concern. Plants with higher free chlorine contact times before ammonia addition to form chloramines had less iodinated DBP formation in chloraminated distribution systems, where there was more oxidation of the iodide to iodate (a sink for the iodide) by the chlorine. This has been shown in many bench-scale studies (primarily for iodinated THMs), but seldom in full-scale studies (where this study also showed the impact on total organic iodine. Collectively, the THMs, haloacetic acids, and emerging DBPs accounted for a significant portion of the TOCl, TOBr, and TOI; however, ∼50% of the TOCl and TOBr is still unknown. The correlation of the sum of detected DBPs with the TOCl and TOBr suggests that they can be used as reliable surrogates.     

Wall losses of oxygenated volatile organic compounds from oxidation of toluene: Effects of chamber volume and relative humidity

Vapor wall losses can affect the yields of secondary organic aerosol. The effects of surface-to-volume (S/V) ratio and relative humidity (RH) on the vapor-wall interactions were investigated in this study. The oxygenated volatile organic compounds (OVOCs) were generated from toluene-H₂O₂ irradiations. The average gas to wall loss rate constant (k_gw) of OVOCs in a 400 L reactor (S/V = 7.5 m⁻¹) is 2.47 (2.41 under humid conditions) times higher than that in a 5000 L reactor (S/V = 3.6 m⁻¹) under dry conditions. In contrast, the average desorption rate constant (k_wg) of OVOCs in 400 L reactor is only 1.37 (1.20 under humid conditions) times higher than that in 5000 L reactor under dry conditions. It shows that increasing the S/V ratio can promote the wall losses of OVOCs. By contrast, the RH effect on k_gw is not prominent. The average k_gw value under humid conditions is almost the same as under dry conditions in the 400 L (5000 L) reactor. However, increasing RH can decrease the desorption rates. The average k_wg value under dry conditions is 1.45 (1.27) times higher than that under humid conditions in the 400 L (5000 L) reactor. The high RH can increase the partitioning equilibrium timescales and enhance the wall losses of OVOCs.     

三峡水库藻类“水华”预测

根据三峡库区江段16条一级支流以及重庆市35座大中型〖JP2〗水库的调查资料，分析天然河流与水库两种不同水流条件下，水体叶绿素a浓度与总磷和透明度的关系。结果发现,在水库环境中，水体叶绿素a的浓度与总磷以及与透明度都具有较好的相关性，但在河流条件下则没有明显的关系。由于三峡库区江段大多数支流的营养水平已达到富营养化状况，当三峡水库建成、水流条件发生变化后，在支流河口等水域存在爆发“水华”的风险。为此，我们根据1998年枯水期，在三峡库区长江江段流域面积大于100 km2的40条支流河口实测的总磷浓度，利用所建立的水库环境中总磷与叶绿素a 浓度的关系，对三峡成库后在局部水域爆发“水华”的可能性和程度进行了分析，并提出了相应的对策。     

我国沿海地区水污染区域治理探讨

本文分析了我国当前水污染区域治理的难度，沿海地区水污染的主要问题，探讨了污染区域治理的基本原则，提出了水污染治理的重点区域和水污染区域治理的主要途径，并以浑河流域沈阳地区２０００年水污染物总量控制为例，概述总量控制方法和目标     

乌江流域梯级水库入出库河流中总汞和甲基汞的时空分布

2006年1~12月，每月采集乌江流域梯级水库入出库河流水样，用两次金汞齐-冷原子荧光光谱法和蒸馏-乙基化结合GC CVAFS法测定了水中总汞和甲基汞的浓度。结果表明：（1）入出库河流中总汞年均加权浓度分别为317和 2.34 ng/L，甲基汞为014和 0.18 ng/L。（2）不同水库入出库河流中总汞和甲基汞的时空分布特征不同，位于上游第一级的普定和洪家渡水库入库河流中总汞有明显的季节变化趋势，且显著低于出库河流；而甲基汞的季节变化在出库河流中较为明显，而且库龄大的普定、东风、乌江渡水库出库河流中甲基汞浓度显著高于入库河流。（3）相关分析发现水库入库河流中总汞、甲基汞浓度主要受悬浮颗粒物的影响，而与水量间的相关性因水库所处位置的不同而有差异，上游的普定和洪家渡水库中呈显著正相关，其它水库中呈负相关。