紫色土N2O排放及氨氧化微生物群落结构对玉米秸秆与化肥减量配施的响应

以紫色土为研究对象,采用静态箱-气相色谱法,通过田间原位试验,设置了对照(CK)、常规施肥(F)、秸秆与全量化肥配施(100FS)、秸秆分别与化肥减量30%(70FS)、40%(60FS)、50%(50FS)处理,观测了玉米秸秆与化肥配施下的菜地土壤N2O排放动态变化特征,并利用克隆技术和实时荧光定量PCR技术,结合土壤理化性质和氨氧化微生物amoA功能基因丰度,分析了秸秆与化肥配施对土壤N2O排放及相关微生物的影响,以期为调控和减缓紫色土N2O排放提供理论依据.结果表明,玉米秸秆与化肥配施处理较F处理提高了土壤N2O排放量和试验期内的累积排放量,其中100FS处理的N2O排放量最高[57.59~6 238.02μg·(m2·h)-1],累积排放量高达60.76 kg·hm-2.与F处理相比,秸秆与化肥配施处理降低了土壤铵态氮和硝态氮含量,提高了土壤有机质含量,但对土壤总氮和pH值没有显著的影响.本试验条件下,土壤AOB amoA基因拷贝数比AOA高出1~2个数量级,其中F处理的AOA amoA基因拷贝数(50.9×103copies·g~(-1))明显高于其他处理,但AOB amoA基因拷贝数最低(1.36×105copies·g~(-1)).100FS处理降低了AOA和AOB amoA基因多样性指数和均匀度,同时也显著降低了AOA amoA基因拷贝数,但秸秆与化肥减量配施可以提高AOA和AOB amoA基因多样性,同时显著增加了AOB amoA基因拷贝数.土壤AOA优势菌群OTU1可能是硝化作用的主要驱动者,直接和间接地影响N2O排放.通过冗余(RDA)分析,土壤铵态氮、有机质和有效磷含量对AOA群落结构存在显著影响(P0.05,蒙特卡罗算法);土壤可溶性有机氮、总氮、速效钾以及有效磷含量显著影响AOB群落结构(P0.05,蒙特卡罗算法),其中AOB对不同环境因子的耐受性和生态位低于AOA.总体上,玉米秸秆配施60%~70%的化肥,在保证蔬菜产量的前提下,有效提高了AOA和AOB amoA基因多样性,在一定程度上减缓了土壤N2O排放.     

缙云山4种森林植被土壤团聚体有机碳分布特征

以重庆市缙云山的竹林、阔叶林、针叶林和针阔叶混交林这4种亚热带森林植被为研究对象,分析不同林分下土壤团聚体及团聚体有机碳在0～20、20～40、40～60和60～100 cm土壤剖面上的分布规律.结果表明,阔叶林土壤 2 mm粒级团聚体含量、平均重量直径(MWD)、几何平均直径(GMD)及 0. 25 mm团聚体含量(R0. 25)均随土层深度的增加而降低,而其他林分在整个土层中则无明显规律.在各土层中,竹林以 2 mm粒级团聚体为主(30. 73%～53. 08%);阔叶林和混交林的2～0. 25 mm粒级团聚体含量较高,为36. 27%～44. 67%和48. 69%～52. 44%;针叶林的优势粒径为2～0. 25 mm和0. 053 mm.总体上,在各土层中,竹林团聚体的MWD、GMD、R0. 25值均高于其他林分,且其分形维数(D)低于其他林分,可见竹林的土壤团聚体稳定性较好.随着土层深度的增加,不同林分(除针叶林外)土壤团聚体有机碳含量逐渐降低,其中竹林团聚体有机碳含量最高,显著高于针叶林和混交林.就不同团聚体粒级而言,4种林分土壤团聚体有机碳在整个土壤剖面上无明显规律,但各土层均以2～0. 25 mm和0. 053 mm粒级团聚体有机碳含量较高.不同林分下土壤团聚体有机碳相对贡献率存在显著差异,其中针叶林中0. 053 mm粒级团聚体有机碳贡献率最高;竹林的 2 mm粒级团聚体有机碳贡献率高达27. 44%～53. 47%;而阔叶林和混交林则以2～0. 25 mm粒级团聚体有机碳贡献率最高.缙云山的4种林分中,竹林的土壤团聚体稳定性较好,而针叶林的较差;在各土层中,竹林土壤各粒级团聚体有机碳含量最高,针叶林最低.     

四斗朱水库蓝藻水华爆发成因分析及治理对策研究

作为饮用水源的小型水库四斗朱连续几年在早春即开始爆发严重束丝藻水华（属于蓝藻）。水质分析发现,四斗朱水库的水质参数如总氮（TN）、总磷（TP）、氨氮（NH4^＋-N）以及BOD和COD浓度并不高,但明显高于其上游的石门塘水库,这说明在四斗朱水库的集水区存在污染源。本文分析了在低营养盐浓度情况下四斗朱水库蓝藻水华爆发的原因,认为由于集水区内的农业、生活、水土淋失以及自然沉降等途径导致水库营养浓度升高。并由于未知营养、气温回升以及水库生态系统失衡等因素,导致蓝藻水华暴发。最后,提出了相应的综合治理对策。     

Heavy metal contamination in surface sediments of Yangtze River intertidal zone: An assessment from different indexes

Surface sediments (0-5 cm) from 59 stations within the Yangtze River intertidal zone (YRIZ) were sampled for metal contamination analysis in April and August 2005. The concentrations ranged (in mg kg⁻¹ dry weight): Al, 40,803-97,213; Fe, 20,538-49,627; Cd, 0.12-0.75; Cr, 36.9-173; Cu, 6.87-49.7; Mn, 413-1,112; Ni, 17.6-48.0; Pb, 18.3-44.1; and Zn, 47.6-154; respectively. Among the 59 sampling stations, enrichment factors (EF) indicate enrichment of Cd (52 stations), Cr (54 stations), Cu (5 stations), Ni (26 stations), Pb (5 stations) and Zn (5 stations). Geoaccumulation indexes (I_geo) also suggest individual metal contamination in localized areas. This study indicates that Cd, Cr and Ni enrichment in the YRIZ sediment is widespread whereas Cu, Mn, Pb and Zn enrichment is localized or nonexistent. Factor and cluster analyses indicate that Cd is associated with total organic carbon whereas Cu, Cr, Ni, Pb and Zn have a close association with Mn.     

Residences with anomalous soil concentrations of dioxin-like compounds in two communities in Michigan, USA: a case study

Most contamination of residential property soil with dioxin-like compounds occurs as a result of proximity to industrial activity that produces such compounds and, outside the industrially impacted zone, the soil concentrations are at background levels. However, as part of the University of Michigan Dioxin Exposure Study, residential properties in the lower peninsula of Michigan, USA, were identified that were located far enough from known sources of these compounds that the soil concentrations should have been at background levels and yet the toxic equivalent (TEQ) of some properties' soil was greater than 2.5 standard deviations above the mean background level. In the three cases presented here from Midland/Saginaw Counties, the anomalously high-TEQ values were primarily due to the presence of polychlorinated dibenzofurans. Based on interviews with the residents and a comparison of soil congener profiles, it was deduced that these values resulted from anthropogenic soil movement from historically contaminated areas. In the cases from Jackson/Calhoun Counties, the unusually high-TEQ values were primarily due to polychlorinated biphenyls. In the case profiled here, it appears that the soil became contaminated through sandblasting to remove paint from the swimming pool. This study identified two mechanisms for soil contamination outside zones of industrial impact; thus, an assumption of background levels of soil contamination outside industrial zones may not be valid.     

Dissolved organic matter with multi-peak fluorophores in landfill leachate

Dissolved organic matter (DOM) sampled from municipal landfill leachate of different ages with/without anoxic or aerobic treatment, was intensively fractionated via size exclusion chromatography (SEC) and hydrophobic resins, and was studied with fluorescence excitation and emission matrix (EEM). Six fluorophores with multiple EEM peaks (fluorophore A-F) were identified based on the collected EEM spectra and validated by bi-variate analysis, principal component analysis, and parallel factor analysis, as follows (excitation wavelength Ex and emission wavelength Em): (Ex 240, 310, 360 nm, Em 460 nm), (Ex 220, 280 nm, Em 340 nm), (Ex 220, 270 nm, Em 300 nm), (Ex 220, 280 nm, Em 360 nm), (Ex 230, 320 nm, Em 420 nm) and (Ex 220, 310 nm, Em 400 nm). The spectral characteristics of these fluorophores were discussed using fractional EEM and apparent molecular weight (AMW) data obtained via SEC analysis. The triple peak flurophore A was pointed at a hydrophobic acid or hydrophobic neutral compound with a pyrenyl functional group of AMW 2500-3500 Da, which displayed an excitation wavelength at 360 nm and a fluorescence intensity ratio of 6.70(+/-1.79):1.70(+/-0.41):1 (fluorescent intensities of Ex 240:Ex 310:Ex 360 nm at Ex 460 nm). This compound is observed to be refractory in landfilling or in anoxic/aerobic treatments, and is specific to this leachate contamination. This paper revealed that the coupling of SEC and EEM can be useful to track the fluorescent DOM fraction in landfill leachate.     

改性甘蔗渣吸附废水中低浓度Cu2+的研究

利用离子液氯化-1-己基-3-甲基咪唑对甘蔗渣进行改性,利用改性甘蔗渣吸附去除模拟废水中低浓度的Cu2+,并对比了较优条件下甘蔗渣改性前后的Cu2+吸附性能.结果表明,溶液pH、改性甘蔗渣投加量、吸附时间对改性甘蔗渣吸附Cu2+均有一定的影响,较佳的溶液pH为5.41、改性甘蔗渣投加量为0.30 g、吸附时间为130 min;吸附温度升高Cu2+吸附率反而降低,因此选择在室温下进行吸附反应为宜;在以上较优条件下,改性甘蔗渣和甘蔗渣的Cu2+吸附率分别为83.20％和53.83％,前者的Cu2+吸附率提高了30.35％.     

Photocatalytic degradation of methyl orange by a multi-layer rotating disk reactor

Introduction

Solar wastewater treatment based on photocatalytic reactions is a green process that utilizes renewable energy resources and minimizes secondary pollution. Reactor design plays an important role in promoting treatment efficiency and throughput density (based on unit volume of the reactor).

Experimental

A rotating disk reactor that significantly increases the process efficiency has been designed and evaluated for application to photocatalytic decomposition of dye pollutants in aqueous solutions. In this process, a novel multi-layer rotating disk reactor (MLRDR) was presented. Photocatalyst (TiO₂) particles are immobilized on the surfaces of disks. Within each layer of the reactor, methyl orange aqueous solution is allowed to flow from the center of the disk in a radial direction along the surface of the disk, which is rotating at high speed and is irradiated with UV lamps. The effluent is then directed to the center of another layer that lies underneath. Up to four stacked layers have been tested in this study, and the effects due to the number of the layers and volumetric flow rate on reaction conversion are investigated.

Results and discussion

The efficiency of this photocatalytic reactor exhibits complex dependence on these parameters. With selected operating conditions, conversions greater than 95% can be achieved within seconds of residence time. Design equations of the reactor have been derived based on fluid dynamics and kinetic models, and the simulation results show promising scale-up potential of the reactor.     

纳米TiO2光催化降解硝基酚类污染物动力学及机理的研究

采用纳米TiO₂(P25)粉末作为催化剂,研究了几种典型硝基取代酚在TiO₂/UV悬浮体系下的光催化降解。研究表明,这些化合物的降解过程符合Langmuir-Hinshelwood动力学方程,其表观速率常数(k_app)的大小为：2-氨基-4硝基酚（2-A,4-NP）＞4-硝基酚（4-NP）＞2-硝基酚（2-NP）＞3-硝基酚（3-NP）＞2,4-二硝基酚（2,4-DNP）＞2,4,6-三硝基酚（2,4,6-TNP）,而吸附平衡常数(KL)却与k_app成反比。苯环上取代基的种类和数目对有机物光催化降解活性有很大的影响,硝基的加入降低了光催化活性,并且k_app与Hammett常数（σ）具有较好的线性关系。     

Aerobic degradation of tetrabromobisphenol-A by microbes in river sediment

This study investigated the aerobic degradation of tetrabromobisphenol-A (TBBPA) and changes in the microbial community in river sediment from southern Taiwan. Aerobic degradation rate constants (k₁) and half-lives (t_1/2) for TBBPA (50 μg g⁻¹) ranged from 0.053 to 0.077 d⁻¹ and 9.0 to 13.1 d, respectively. The degradation of TBBPA (50 μg g⁻¹) was enhanced by adding yeast extract (5 mg L⁻¹), sodium chloride (10 ppt), cellulose (0.96 mg L⁻¹), humic acid (0.5 g L⁻¹), brij 30 (55 μM), brij 35 (91 μM), rhamnolipid (130 mg L⁻¹), or surfactin (43 mg L⁻¹), with rhamnolipid yielding a higher TBBPA degradation than the other additives. For different toxic chemicals in the sediment, the results showed the high-to-low order of degradation rates were bisphenol-A (BPA) (50 μg g⁻¹) > nonylphenol (NP) (50 μg g⁻¹) > 4,4′-dibrominated diphenyl ether (BDE-15) (50 μg g⁻¹) > TBBPA (50 μg g⁻¹) > 2,2′,3,3′,4,4′,5,5′,6,6′-decabromodiphenyl ether (BDE-209) (50 μg g⁻¹). The addition of various treatments changed the microbial community in river sediments. The results also showed that Bacillus pumilus and Rhodococcus ruber were the dominant bacteria in the process of TBBPA degradation in the river sediments.