橡胶坝对河流沉积物氮转化功能基因丰度和营养盐的影响

沉积物氮转化功能微生物是河流脱氮和水体净化的重要生物因素.为探讨橡胶坝对沉积物氮转化功能基因丰度及氮营养盐的影响，本研究以沂河沂水城区蓄水段为研究对象，从橡胶坝前不同距离采集沉积物，利用实时荧光定量PCR（qPCR）方法研究了沉积物的反硝化功能基因（nirS、nirK、nosZ）、厌氧氨氧化功能基因（AMX）和反硝化型甲烷厌氧氧化功能基因（pmoA）的丰度及沉积物营养盐特征.结果表明：橡胶坝促进了沉积物中nirK、nirS、nosZ和pmoA基因的聚集，反硝化功能基因nirK、nirS、nosZ丰度在坝前120 ~330 m范围内较高；橡胶坝促进了沉积物NH4+、NO3-、TN、TP、TOC、有机质（OM）等营养盐的滞留，主要在120 ~360 m区域聚集，多元线性回归模型拟合度较高.相关分析表明，16S rRNA、nirK、nirS、nosZ、pmoA基因丰度与环境因子NH4+、NO3-、TN、OM、TOC、孔隙度呈正相关；PCA分析结果表明，随着沉积物环境因子主成分的增长，氮转化功能基因丰度主成分呈升高趋势.橡胶坝可促进沂河沉积物氮素等营养盐的滞留和氮转化功能微生物的聚集.     

不同配比农业废物堆肥过程中堆肥的阴阳离子和大分子对种子发芽的影响

为揭示不同配比农业废物堆肥过程中阴阳离子和大分子对植物毒性的影响机理，开展了以鸡粪和猪粪为主料，稻草秸秆为辅料的条垛堆肥试验，设置的试验处理包括：等质量的鸡粪+稻草秸秆+包菜（1∶1∶1）处理（T1）、鸡粪+稻草秸秆（1∶1）处理（T2）、大量猪粪+少量稻草秸秆（85∶15）处理（T3）.测定了各处理的堆温、堆肥的水溶性无机阴阳离子和有机大分子变化，以及对大白菜（Brassica rapa L.）和水堇（Lepidium sativum. L.）种子发芽指数（Germination Index， GI）等指标变化的影响.试验结果表明，T3处理堆肥的高温（>55 ℃）持续期最长，杀灭病原微生物和杂草种子的能力最好，且其堆肥的Cl^-、SO42-、K⁺、Na⁺、Ca²⁺和Mg²⁺浓度最低；T2处理堆肥的NH4+ 浓度最低.T1和T2处理堆肥过程中堆肥的脂肪烃可转化为稳定的芳香烃.T3处理堆肥对大白菜和水堇的种子发芽指数大于80%.堆肥中抑制种子发芽的阴阳离子及大分子浓度分别为：Ca²⁺浓度>0.98 mmol·L^-1，Mg²⁺浓度>0.92 mmol·L^-1，NH4+浓度均>5.75 mmol·L^-1，芳香C/多糖比值>0.33，羧基C/多糖比值>0.30.堆肥中脂肪族大分子增加、多糖类大分子减少可抑制种子发芽.综上所述，猪粪与稻草秸秆的质量配比为85∶15、初始C/N比为25、初始水分含量为60%、 堆肥期周为35 d是条垛式堆肥处理猪粪和稻草秸秆的最佳工艺参数.大白菜比水堇种子更能准确反映农业废物堆肥的植物毒性.本研究可为优化不同畜禽粪便与农作物秸秆的条垛堆肥工艺参数、减少土地利用的风险提供重要的决策支持.     

基于QAR数据的中国民航飞行排放清单估计研究

近年来中国民用航空迅速发展，产生了大量的排放物，需要准确的排放清单来评估民航行业对环境的影响.针对现有的研究在估算精度与覆盖范围上存在的不足，本文利用了飞机QAR数据构建了估算单次飞行燃油消耗量与包括HC、CO、NOx、PM、SO2以及CO2在内的排放物生成量的方法，并采用自下而上的方法，对2018年1月—2021年11月在中国国内民航活动产生的排放物进行了统计.在估算时考虑了机型、起飞机场和降落机场对飞行各阶段持续时间的影响.从排放模式来看，不同机场的飞行在LTO阶段的平均排放量存在差异，总的来说，机场规模越大，单次飞行排放量越多，大多数排放物在CCD阶段排放且该阶段的排放量与飞行时间存在明显的线性关系.2018年和2019年的排放量保持了上升，CO2排放量分别为73.17 ×10⁶ t和76.85 ×10⁶ t，但自从2019年12月受到新冠疫情影响后，排放量与航班量随疫情控制情况波动，2020年和2021年1月—11月CO2排放量分别为61.51 ×10⁶ t和60.08 ×10⁶ t.为了探究新冠疫情对排放物的影响，采用差分整合移动平均自回归模型对无疫情时2019年12月之后的排放量进行了估计，结果表明新冠疫情爆发后，到2021年11月为止各种排放物的排放量减少了20%左右.     

Competitive role of nitrogen functionalities of N doped GO and sensitizing effect of Bi2O3 QDs on TiO2 for water remediation

The promising solar irradiated photocatalyst by pairing of bismuth oxide quantum dots (BQDs) doped TiO₂ with nitrogen doped graphene oxide (NGO) nanocomposite (NGO/BQDs-TiO₂) was fabricated. It was used for degradation of organic pollutants like 2,4-dichlorophenol (2,4-DCP) and stable dyes, i.e. Rhodamine B and Congo Red. X-ray diffraction (XRD) profile of NGO showed reduction in oxygenic functional groups and restoring of graphitic crystal structure. The characteristic diffraction peaks of TiO₂ and its composites showed crystalline anatase TiO₂. Morphological images represent spherical shaped TiO₂ evenly covered with BQDs spread on NGO sheet. The surface linkages of $\text{NO}?\mathrm{O}?\text{Ti}$, $\mathrm{C}?\mathrm{O}?\text{Ti}$, $\mathrm{B}\mathrm{i}?\mathrm{O}?\text{Ti}$ and vibrational modes are observed by Fourier transform infrared spectroscopy (FTIR) and Raman studies. BQDs and NGO modified TiO₂ results into red shifting in visible region as studied in diffused reflectance spectroscopy (DRS). NGO and BQDs in TiO₂ are linked with defect centers which reduced the recombination of free charge carriers by quenching of photoluminescence (PL) intensities. X-ray photoelectron spectroscopy (XPS) shows that no peak related to $\mathrm{C}?\mathrm{O}$ in NGO/BQDs-TiO₂ is observed. This indicated that doping of nitrogen into GO has reduced some oxygen functional groups. Nitrogen functionalities in NGO and photosensitizing effect of BQDs in ternary composite have improved photocatalytic activity against organic pollutants. Intermediate byproducts during photo degradation process of 2,4-DCP were studied through high performance liquid chromatography (HPLC). Study of radical scavengers indicated that ${\mathrm{O}}_2^{·?}$ has significant role for degradation of 2,4-DCP. Our investigations propose that fabricated nanohybrid architecture has potential for degradation of environmental pollutions.     

Modeling of spatial and temporal variations of ozone-NOx-VOC sensitivity based on photochemical indicators in China

Comprehensive air quality model with extensions (CAMx)-decoupled direct method (DDM) was used to simulate ozone-NO_x-VOCs sensitivity of for May–November in 2016–2018 in China. Based on the relationship between the simulated ozone (O₃) sensitivity values and the ratio of formaldehyde (HCHO) to NO₂ (FNR) and the ratio of production rate of hydrogen peroxide (H₂O₂) to production rate of nitric acid (HNO₃) ($P_{{\mathrm{H}}_2{\mathrm{O}}_2}/P_{\text{HN}{\mathrm{O}}_3}$), the localized range of FNR and $P_{{\mathrm{H}}_2{\mathrm{O}}_2}/P_{\text{HN}{\mathrm{O}}_3}$ thresholds in different regions in China were obtained. The overall simulated FNR values are about 1.640–2.520, and $P_{{\mathrm{H}}_2{\mathrm{O}}_2}/P_{\text{HN}{\mathrm{O}}_3}$ values are about 0.540–0.830 for the transition regime. Model simulated O₃ sensitivities or region specific FNR or $P_{{\mathrm{H}}_2{\mathrm{O}}_2}/P_{\text{HN}{\mathrm{O}}_3}$ thresholds should be applied to ensure the accurate local O₃ sensitivity regimes. Using the tropospheric column FNR values from ozone monitoring instrument (OMI) satellite data as an indicator with the simulated threshold values, the spatial distributions of O₃ formation regimes in China are determined. The O₃ sensitivity regimes from eastern to central China are gradually from VOC-limited, transition to NO_x-limited spatially, and moving toward to transition or NO_x-limited regime from 2005 to 2019 temporally.     

Chemical and olfactive impacts of organic matters on odor emission patterns from the simulated construction and demolition waste landfills

The explosive increase of construction and demolition waste (CDW) caused the insufficient source separation and emergency disposal at domestic waste landfills in many developing countries. Some organic fractions were introduced to the CDW landfill process and resulted in serious odor pollution. To comprehensively explore the impacts of organic matters on odor emission patterns, five CDW landfills (OIL), with organic matters/ inert CDW components (O/I) from 5% to 30%, and the control group only with inert components (IL) or organics (OL) were simulated at the laboratory. The chemical and olfactive characters of odors were evaluated using the emission rate of 94 odorants content (ER_total), theory odor concentration (TOC_total), and e-nose concentration (ER_ENC), and their correlations with waste properties were also analyzed. It was found that the main contributors to ER_total (IL: 93.0% NH₃; OIL: 41.6% sulfides, 31.0% NH₃, 25.9% oxygenated compounds) and TOC total (IL: 64.1% CH₃SH, 28.2% NH₃; OIL: 71.7% CH₃SH, 24.8% H₂S) changed significantly. With the rise of O/I, ER_total, TOC_total, and ER_ENC increased by 10.9, 20.6, and 2.1 times, respectively. And the organics content in CDW should be less than 10% (i.e., DOC<101.3 mg/L). The good regressions between waste properties (DOC, DN, pH) and ${\mathrm{ER}}_{\stackrel{?}{\mathrm{ENC}}}$ (r=0.86, 0.86, -0.88, p<0.05), ${\mathrm{TOC}}_{\stackrel{?}{\mathrm{total}}}$ (r=0.82, 0.79, -0.82, p<0.05) implied that the carbon sources and acidic substances relating to organics degradation might result in that increase. Besides, the correlation analysis results (${\mathrm{ER}}_{\stackrel{?}{\mathrm{ENC}}}$ vs. ${\mathrm{TOC}}_{\stackrel{?}{\mathrm{total}}}$, r=0.96, p<0.01; vs. ${\mathrm{ER}}_{\stackrel{?}{\mathrm{total}}}$, r=0.86, p<0.05) indicated that e-nose perhaps was a reliable odor continuous monitoring tool for CDW landfills.     

Origins of black carbon from anthropogenic emissions and open biomass burning transported to Xishuangbanna, Southwest China

Black carbon (BC) has importance regarding aerosol composition, radiative balance, and human exposure. This study adopted a backward-trajectory approach to quantify the origins of BC from anthropogenic emissions ($\mathrm{B}{\mathrm{C}}_{\text{An}}$) and open biomass burning ($\mathrm{B}{\mathrm{C}}_{\text{BB}}$) transported to Xishuangbanna in 2017. Haze months, between haze and clean months, and clean months in Xishuangbanna were defined according to daily PM_2.5 concentrations of >75, 35–75, and <35 µg/m³, respectively. Results showed that the transport efficiency density (TED) of BC transported to Xishuangbanna was controlled by the prevailing winds in different seasons. The yearly contributions to the effective emission intensity of $\mathrm{B}{\mathrm{C}}_{\text{An}}$ and $\mathrm{B}{\mathrm{C}}_{\text{BB}}$ transported to Xishuangbanna were 52% and 48%, respectively. However, when haze occurred in Xishuangbanna, the average $\mathrm{B}{\mathrm{C}}_{\text{An}}$ and $\mathrm{B}{\mathrm{C}}_{\text{BB}}$ contributions were 23% and 77%, respectively. This suggests that open biomass burning (BB) becomes the dominant source in haze months. Myanmar, India, and Laos were the dominant source regions of BC transported to Xishuangbanna during haze months, accounting for 59%, 18%, and 13% of the total, respectively. Furthermore, India was identified as the most important source regions of $\mathrm{B}{\mathrm{C}}_{\text{An}}$ transported to Xishuangbanna in haze months, accounting for 14%. The two countries making the greatest contributions to $\mathrm{B}{\mathrm{C}}_{\text{BB}}$ transported to Xishuangbanna were Myanmar and Laos in haze months, accounting for 55% and 13%, respectively. BC emissions from Xishuangbanna had minimal effects on the results of the present study. It is suggested that open BB in Myanmar and Laos, and anthropogenic emissions in India were responsible for poor air quality in Xishuangbanna.     

外源Cd（Ⅱ）胁迫Alcaligenes faecalis过程中阴离子对 EPS产量及其特性的影响

微生物产生EPS受多种因素影响，其中重金属阳离子的作用较为明显，但其对应的阴离子的作用仍不明确.研究了SO₄^2-、NO₃^-和Cl^-对应的3种Cd（Ⅱ）化合物胁迫/诱导下Alcaligenes faecalis EPS的产量、组分变化及其吸附性能.结果表明，20 mg·L^-1 Cd（NO₃）₂的胁迫效果最为明显，EPS产量达到109.17 mg·g^-1，其中蛋白质含量达到89.46 mg·g^-1，较Control-EPS提高50%以上.在此条件下，Cd（NO₃）₂-EPS对Cd（Ⅱ）吸附量最高，达到300.20 mg·g^-1，较胁迫前增加41.83%.三维荧光（3D-EEM）、红外光谱（FTIR）和X射线光电子能谱（XPS）分析表明，胁迫后的EPS，尤其是Cd（NO₃）₂-EPS中C?O、C-O/C-N含量增幅明显，在吸附Cd（Ⅱ）中发挥了重要作用.实验结果表明，在Cd（NO₃）₂胁迫/诱导下，Alcaligenes faecalis可产生特异EPS，具有优异的吸附性能.本文为制备生物制剂以处理含重金属废水提供了重要理论指导.     

Enhanced phosphate removal using zirconium hydroxide encapsulated in quaternized cellulose

Zirconium-based materials are efficient adsorbent for aqueous phosphate removal. However, current zirconium-based materials still show unsatisfied performance on adsorption capacity and selectivity. Here, we demonstrate a zirconium hydroxide encapsulated in quaternized cellulose (QC–Zr) for the selective phosphate removal. Zirconium hydroxide nanoparticles were simultaneously generated in situ with the QC framework and firmly anchored in the three-dimensional (3D) cross-linked cellulose chains. The maximum P adsorption capacity of QC–Zr was 83.6 mg P/g. Furthermore, the QC–Zr shows high P adsorption performance in a wide pH range, generally due to the electrostatic effects of quaternized cellulose. The enhanced adsorption of P was also achieved in the presence of competing anions (including Cl^?, NO₃^?, ${\text{SO}}_4^{2?}$, ${\text{SO}}_4^{\mathrm{4}?}$) and humic acid (HA) even at a molar ratio up to 20 levels. The column adsorption capacity of QC–Zr reached 4000 bed volumes (BV) at EBCT = 0.5 min as the P concentration decreased from 2.5 to 0.5 mg/L. Mechanism study revealed that both –N⁺(CH₃)₃ groups and zirconium hydroxide were involved in phosphate adsorption via electrostatic interactions between –N⁺(CH₃)₃ and phosphate, and the formation of zirconium hydrogen phosphate (Zr(HPO₄)x). The ³¹P nuclear magnetic resonance (NMR) study implied that P surface–precipitated and inner–sphere complexed with zirconium hydroxide at a ratio of 3:1.     

Experimental and theoretical studies on NO selective catalytic oxidation over α-MnO2

Based on the experimental and theoretical methods, the NO selective catalytic oxidation process was proposed. The experimental results indicated that lattice oxygen was the active site for NO oxide over the $\mathrm{\alpha }$-MnO₂(110) surface. In the theoretical study, DFT (density functional theory) and periodic slab modeling were performed on an $\mathrm{\alpha }$-MnO₂(110) surface, and two possible NO oxidation mechanisms over the surface were proposed. The non-defect $\mathrm{\alpha }$-MnO₂(110) surface showed the highest stability, and the surface O_s (the second layer oxygen atoms) position was the most active and stable site. O₂ molecule enhanced the joint adsorption process of two NO molecules. The reaction process, including O₂ dissociation and O=N-O-O-N=O formation, was calculated to carry out the NO catalytic oxidation mechanism over $\mathrm{\alpha }$-MnO₂(110). The results showed that NO oxidation over the $\mathrm{\alpha }$-MnO₂(110) surface exhibited the greatest possibility following the route of O=N-O-O-N=O formation. Meanwhile, the formation of O=N-O-O-N=O was the rate-determining step.     

微囊藻毒素-LR的臭氧降解研究

采用不同的臭氧投加量,考察了微囊藻毒素-LR(MC-LR)的降解效果,并通过对臭氧氧化过程中产生的8种主要降解产物的相对分子质量分析,推测其降解途径.结果表明,臭氧氧化降解MC-LR主要通过Adda途径和Mdha途径来完成对MC-LR的降解和脱毒作用.臭氧氧化的Adda途径是通过对MC-LR上Adda侧链的进攻,断开具有活性的Adda支链,而达到脱毒的目的;臭氧氧化的Mdha途径是通过对MCs肽环上面Mdha和Ala的断键,打开环状肽链,使藻毒素失去活性,在整个过程中Adda途径占主导地位.在O3∶MC为6时,MC-LR的去除率最高可达到92%.     

假单胞菌N7的萘降解特性及其降解途径研究

应用HPLC和UV分析技术,以萘为代表性多环芳烃污染物,研究了假单胞菌N7对水中萘的降解特性.结果表明,营养盐、微量元素的添加可使萘的降解率提高23.65%;溶解氧高于4.3 mg/L时萘降解率达95.66%并趋于稳定;随萘浓度增加降解率逐渐下降;在中性和弱碱性环境下,降解效果较好,萘降解率均在82.88%以上.在30℃、转速为165 r/min的摇床中处理pH7.5、萘浓度为100 mg/L的水样72 h,其最大降解率为95.66%.通过检测菌株N7处理含不同底物水样时其吸光度、pH和底物的变化情况,证实菌株N7亦能降解甲苯、二甲苯、苯酚、2,4-二硝基苯酚、苯甲酸、1-萘酚和水杨酸,并以其为唯一的碳源和能源生长繁殖,表明该菌株能适应环境中芳烃类物质种类的变化,具有很好的降解多样性.经UV-Vis和GC-MS分析各降解阶段的中间产物,初步确定了该菌对萘的降解途径:一条是邻苯二甲酸途径;另一条是水杨酸途径,萘先被氧化为1,2-二羟基萘,再开环生成水杨酸、邻苯二酚和2-羟基粘康酸半醛,最终进入三羧酸循环(TCA).     

睾丸酮丛毛单胞菌对喹啉的微生物降解途径的研究

从油制气废水的活性污泥中分离得到一株可以在好氧条件下利用喹啉作为唯一碳源和能源的睾丸酮丛毛单胞菌 (Co mamonastestosteroni,编号为Q10 ) .浓度为 2 5 0mg L的喹啉可被该菌完全降解 ,TOC去除率为 70 % .实验结果表明喹啉首先降解为 1H— 2 氧喹啉 ,然后继续转化为 6 羟基— 1H— 2 氧喹啉、5 ,6 二羟基— 1H— 2 氧喹啉和 5 羟基— 6 (2 羧基乙烯基 )—1H— 2 吡啶酮 ,由此提出该菌降解喹啉的一种可能途径 .样品中还发现少量的 8 羟基— 1H— 2 氧喹啉 ,表明菌Q10 对喹啉的降解可能是通过以一种途径为主的多种途径进行的 .     

两种不同形态MnO2降解卡马西平的效果及途径对比

研究了两种不同形态MnO₂（δ-MnO₂和胶体MnO₂）对难降解有机药物卡马西平（carbamazepine,CBZ）的去除效果,并通过液相色谱质谱联用技术（LC/MS）分析了不同pH值条件下δ-MnO₂和胶体MnO₂氧化转化CBZ的产物,探究其氧化转化途径.结果表明,δ-MnO₂和胶体MnO₂能通过化学氧化作用在2h内去除约1mg/L CBZ,相比之下,胶体MnO₂受pH影响较小且单位质量Mn对CBZ具有更好的去除效果.δ-MnO₂和胶体MnO₂与CBZ反应过程中各检出7种和4种产物.胶体MnO₂具有更强的氧化能力,越过了多种中间产物的产生步骤,使CBZ的降解途径更加简明.     

环境雌激素及其降解途径

结合近期国内外以及作者对环境雌激素降解的研究,指出环境雌激素可以通过多种途径迁移、降解,环境雌激素主要降解途径为生物降解和光解;一般情况下多数不易降解,易富集,研究其降解具有重要的意义。     

北京边界层外来污染物输送通道

由京、津、冀气候站历史资料及激光雷达资料分析,在稳定天气条件下,北京市外来污染物各类尺度的输入通道流场分为边界层西南气流、东南气流和东风气流风带型,其中对形成北京输送汇风带的统计表明,西南风带汇发生频率占45%,东南风带汇占36%,东风风带汇占19%。输送通道是指空间和时间稳定性风带,是区域尺度、局地尺度的范围内相继出现的欧拉风场,且有多频率发生的特征。按城市间尺度流型可分为城市间东风、西南风、东南风输送通道。具有一定空间尺度和时间尺度的相继性、接续性输送特征,按配置的天气系统可分为大陆高压南部偏东风输送通道系统、海上高压后部东南风输送通道系统、河套倒槽前西南风输送通道系统、东北低槽前部偏南风输送通道系统等。3个风带流经地区恰好位于华北平原3个主要排放源群地区。      

炔雌醇氯化反应的动力学和机制研究

对典型内分泌干扰物炔雌醇(EE2)在模拟饮用水氯化过程中的反应行为进行了深入研究.结果发现,EE2的氯化反应符合二级反应动力学.表观速率常数kapp随pH的变化规律证明EE2分子中的酚环是氯原子攻击的首选位置.EE2的转换是由不同形态的EE2和HClO之间的3个基元反应控制.去质子化的EE2阴离子明显比其中性共轭体更具活性.高效液相色谱/质谱(HPLC/MS)分析表明氯原子可以通过亲电取代反应接到EE2分子中的酚羟基的邻位,先后生成一氯和二氯代EE2,第三个氯原子的取代导致苯环结构的破坏,分子不稳定发生水解.本研究的结果对全面了解EE2在饮用水氯化消毒过程中的反应规律,为评价EE2对人体的潜在暴露提供了依据.     

贵州西南地区慢性铊中毒途径研究

铊中毒区土壤、植物中铊含量均很高，铊中毒途径主要是食用高铊蔬菜，进入人体长期积累，导致慢性铊中毒。     

微生物在生物煤层气形成中的作用及影响因素研究进展

在当今能源紧缺和环境污染严重的前提下,煤层气作为一类非常规天然气,越来越受到人们的重视。传统观点认为煤层甲烷多由高温热解产生,但是根据甲烷的同位素特征来判断,世界很多地方(包括我国鄂尔多斯、淮南等地)的煤层气多属生物成因或者生物和热成因混合。同时,越来越多的生物学证据也表明种类多样的产甲烷相关微生物广泛存在于煤层伴生地层水中或者煤层样品中。这也说明生物成因的煤层气仍然在不断地产生,这也为利用生物方法促进煤层气产生和利用提供了良好的契机。本文将介绍产甲烷微生物种群构成与功能、产气途径、影响产气速率的因素,探讨我国微生物强化产煤层气并实现产业化的应用前景。     

喹啉及其衍生物微生物降解研究进展

喹啉类氮杂环化合物在水、土壤环境中普遍存在，受其污染的水、土壤环境生物修复是目前环境治理领域的重要课题。介绍了近年来喹啉类氮杂环化合物微生物降解的国内外研究进展，主要包括可利用喹啉类氮杂环化合物作为碳源、氮源和能源的微生物资源、微生物降解的有氧代谢和无氧代谢两大途径，以及喹啉类化合物的降解动力学。在此基础上，提出了需要进一步研究的方向。