2013-2015年上海市霾污染事件潜在源区贡献分析

统计分析2013-2015年上海市每个月不同空气质量等级天数比重,根据HYSPLIT（Hybrid Single Particle Lagrangian Integrated Trajectory）后向轨迹模型对3年内的12月份影响上海地区的污染气团进行了综合聚类分析和逐年聚类分析.在综合12次严重霾事件的后向轨迹基础上,结合上海实时公布的PM_2.5小时浓度资料,对潜在源贡献因子PSCF（Potential Source Contribution Function）和浓度权重轨迹CWT（Concentration-weighted Trajectory）进行分析与比较,研究重霾期间影响上海PM_2.5质量浓度的潜在源区及不同源区对PM_2.5质量浓度的贡献差异.结果显示,上海市3年期间12月份霾颗粒物外来源主要输送渠道为西北路径和北方路径,源自于西北方向的气团比重占总气团的50.4%,北方向的气团几乎都经过海洋后进入上海地区.影响上海地区PM_2.5质量浓度的潜在源区主要分布在安徽、江苏和山东地区,此外江西北部、浙江北部、河北南部及山西少部分地区也对重霾事件中的污染物颗粒有一定程度的贡献.     

Mitochondrial toxicity and in vitro biological effects of ambient PM2.5 from an urban site in China

Abstract

The roles of PM_2.5-induced mitochondrial damage and oxidative stress on mast cell degranulation were examined in vitro. Mast cells were treated with suspensions of PM_2.5 in Dulbecco’s modified Eagle’s medium at concentrations from 25 to 200?mg/L in the absence or presence of 10?mmol/L N-acetyl-L-cysteine. Biological effects and mitochondrial function were assessed by determining cell viability, β-hexosaminidase release, interleukin-4 secretion, reactive oxygen species generation, adenosine triphosphate production, potential alteration of mitochondrial membrane, and activities of mitochondrial electron transport chain complexes I and III. Exposure of mast cells to PM_2.5 induced reduction of adenosine triphosphate production, collapse of mitochondrial membrane potential, and inhibition of the activity of complex III. Co-treatment of mast cells exposed to PM_2.5 with N-acetyl-L-cysteine attenuated cytotoxicity and the production of reactive oxygen species, and decreased the release of β-hexosaminidase and interleukin-4. Evidently, PM_2.5-induced oxidative stress plays an essential role in mitochondrial toxicity and mast cell activation.     

千岛湖水源水微生物安全性评价

千岛湖作为国家战略水源地,其微生物安全直接关系到千万居民的用水安全.为了研究千岛湖湖水的生物安全性,于2018-2019年采集了金竹牌取水口不同深度的水样,并检测了水样的可生物降解溶解性有机碳(BDOC)、细菌再生长的潜力(BGP)、可培养细菌数、潜在的条件致病菌和细菌群落结构.结果显示,千岛湖水质属地表水Ⅱ～Ⅲ类水,...     

南海重点海洋倾倒区表层沉积物富集特征及其潜在生态风险评价

根据2005南海三个重点海洋倾倒区,即九澳岛重点海洋倾倒区、黄茅岛重点海洋倾倒区、汕头重点海洋倾倒区的监测,分析其表层沉积物重金属的监测资料,采用富集系数法和Hakanson潜在生态危害系数法对其富集度和潜在生态危害程度进行了分析和评价.结果表明:在三个倾倒区表层沉积物所监测的重金属中,Cu和Pb元素的富集度相对最高,Hg和Cd元素的富集度较低,从空间上看,潜在生态危害系数评价结果显示,南海三个重点海洋倾倒区表层沉积物中的重金属对海洋生态系统的潜在生态危害非常轻微,均属于轻微潜在生态危害范畴,其中轻微潜在生态危害程度相对较重的是Cd和Hg元素,Cu和Pb元素的轻微生态危害程度较轻.     

Transformations of particles, metal elements and natural organic matter in different water treatment processes

Characterizing natural organic matter （NOM）, particles and elements in different water treatment processes can give a useful information to optimize water treatment operations. In this article, transformations of particles, metal elements and NOM in a pilot-scale water treatment plant were investigated by laser light granularity system, particle counter, glass-fiber membrane filtration, inductively coupled plasma-optical emission spectroscopy, ultra filtration and resin absorbents fractionation. The results showed that particles, NOM and trihalomethane formation precursors were removed synergistically by sequential treatment of different processes. Preozonation markedly changed the polarity and molecular weight of NOM, and it could be conducive to the following coagulation process through destabilizing particles and colloids; mid-ozonation enhanced the subsequent granular activated carbon （GAC） filtration process by decreasing molecular weight of organic matters. Coagulation-flotation and GAC were more efficient in removing fixed suspended solids and larger particles; while sand-filtration was more efficient in removing volatile suspended solids and smaller particles. Flotation performed better than sedimentation in terms of particle and NOM removal. The type of coagulant could greatly affect the performance of coagulation-flotation. Pre-hydrolyzed composite coagulant （HPAC） was superior to FeCl3 concerning the removals of hydrophobic dissolved organic carbon and volatile suspended solids. The leakages of flocs from sand-filtration and microorganisms from GAC should be mitigated to ensure the reliability of the whole treatment system.     

Topsoil organic carbon mineralization and CO2 evolution of three paddy soils from South China and the temperature dependence

Carbon mineralization and its response to climatic warming have been receiving global attention for the last decade. Although the virtual influence of temperature effect is still in great debate, little is known on the mineralization of organic carbon （SOC） of paddy soils of China under warming. SOC mineralization of three major types of China＇s paddy soils is studied through laboratory incubation for 114 d under soil moisture regime of 70% water holding capacity at 20℃ and 25℃ respectively. The carbon that mineralized as CO2 evolved was measured every day in the first 32 d and every two days in the following days. Carbon mineralized during the 114 d incubation ranged from 3.51 to 9.22 mg CO2-C/gC at 20℃ and from 4.24 to 11.35 mg CO2-C/gC at 25℃ respectively; and a mineralizable C pool in the range of 0.24 to 0.59 gC/kg, varying with different soils. The whole course of C mineralization in the 114 d incubation could be divided into three stages of varying rates, representing the three subpools of the total mineralizable C： very actively mineralized C at 1-23 d, actively tnineralized C at 24--74 d and a slowly mineralized pool with low and more or less stabilized C mineralization rate at 75-114 d. The calculated Q10 values ranged from 1.0 to 2.4, varying with the soil types and N status. Neither the total SOC pool nor the labile C pool could account for the total mineralization potential of the soils studied, despite a well correlation of labile C with the shortly and actively mineralized C, which were shown in sensitive response to soil warming. However, the portion of microbial C pool and the soil C/N ratio controlled the C mineralization and the temperature dependence. Therefore, C sequestration may not result in an increase of C mineralization proportionally. The relative control of C bioavailability and microbial metabolic activity on C mineralization with respect to stabilization of sequestered C in the paddy soils of China is to be further studied.     

Denitrification potential enhancement by addition of external carbon sources in a pre-denitrification process

The aim of this study is to investigate the denitrification potential enhancement by addition of external carbon sources and to estimate the denitrification potential for the predenitrification system using nitrate utilization rate （NUR） batch tests. It is shown that the denitrification potential can be substantially increased with the addition of three external carbon sources, i.e. methanol, ethanol, and acetate, and the denitrification rates of ethanol, acetate, and methanol reached up to 9.6, 12, and 3.2 mgN/（g VSS.h）, respectively, while that of starch wastewater was only 0.74 mgN/（g VSS,h）. By comparison, ethanol was found to be the best external carbon source. NUR batch tests with starch wastewater and waste ethanol were carried out. The denitfification potential increased from 5.6 to 16.5 mg NO3-N/L owing to waste ethanol addition. By means of NUR tests, the wastewater characteristics and kinetic parameters can be estimated, which are used to determine the denitrification potential of wastewater, to calculate the denitrification potential of the plant and to predict the nitrate effluent quality, as well as provide information for developing carbon dosage control strategy.     

红壤稻田系统有机物循环再利用潜力及增产作用

10年田间试验结果表明：红墩妥田系统有机养分循环再利用潜力大，水稻收获，年均从稻田系统中输出NPK的总量最大可达到224.7,53.0和271.4kg/hm^2，有机物循环再利用，年均可归N，P，K量最大分别为115.1,35.8和231.5kg/hm^2，占系统输总量的51.2%,67.5%g和85.3%，保持稻田系统内有机物循环再利用可提高系统生产力，在不施化肥的情况下，增产3056kg/hm^2，增施N肥，增产2753kg/hm^2，增施N，P肥，增产1543kg/hm^2；NPK配合，增产984kg/hm^2；有机物循环再利用还可增强稻田系统的稳产性能，降低稻谷产量的年际变异系数；有机物循环再利用对水稻的增产有着明显的残效叠加作用，在施用N，P，K化肥基础上圾机物养分循环再利用水稻增产率在试验期间的前5年为7．2％，后5年平均为9．4％。     

长江中上游防护林体系森林植被碳贮量及固碳潜力估算

基于“八五”期间长江中上游流域各省的森林资源调查资料,结合经典的材积源生物量法估算了长江中上游防护林体系生物量碳密度和碳贮量,并根据不同树种生物量-生产力回归关系推算了该地区当前的固碳潜力。结果表明：长江中上游地区森林平均碳密度为2575 t/hm2;碳贮量为1 39459 Tg (1 Tg = 1012 g),其中林分（包括经济林）碳贮量为1 20430 Tg,灌木林为13437 Tg,竹林为5592 Tg,三者分别占总碳贮量的8636%、963%和401%。整个防护林体系森林植被的固碳潜力为36856 Tg/a。位于本区西部的四川盆地嘉陵江流域和西部高山峡谷区,其森林碳密度、碳贮量和固碳潜力较高,而东部地区的川鄂山地长江干流、鄱阳湖水系以及洞庭湖水系相对较低,因此,长江中上游森林碳密度、碳贮量和固碳潜力总体上呈现自西向东逐渐降低的趋势。     

Study on the hydrolysis/precipitation behavior of Keggin Al13 and Al30 polymers in polyaluminum solutions

The hydrolysis/precipitation behaviors of Al³⁺, Al₁₃ and Al₃₀ under conditions typical for flocculation in water treatment were investigated by studying the particulates' size development, charge characteristics, chemical species and speciation transformation of coagulant hydrolysis precipitates. The optimal pH conditions for hydrolysis precipitates formation for AlCl₃, PAC_Al13 and PAC_Al30 were 6.5–7.5, 8.5–9.5, and 7.5–9.5, respectively. The precipitates' formation rate increased with the increase in dosage, and the relative rates were AlCl₃ ? PAC_Al30 > PAC_Al13. The precipitates' size increased when the dosage increased from 50 μM to 200 μM, but it decreased when the dosage increased to 800 μM. The Zeta potential of coagulant hydrolysis precipitates decreased with the increase in pH for the three coagulants. The iso-electric points of the freshly formed precipitates for AlCl₃, PAC_Al13 and PAC_Al30 were 7.3, 9.6 and 9.2, respectively. The Zeta potentials of AlCl₃ hydrolysis precipitates were lower than those of PAC_Al13 and PAC_Al30 when pH > 5.0. The Zeta potential of PAC_Al30 hydrolysis precipitates was higher than that of PAC_Al13 at the acidic side, but lower at the alkaline side. The dosage had no obvious effect on the Zeta potential of hydrolysis precipitates under fixed pH conditions. The increase in Zeta potential with the increase in dosage under uncontrolled pH conditions was due to the pH depression caused by coagulant addition. Al–Ferron research indicated that the hydrolysis precipitates of AlCl₃ were composed of amorphous Al(OH)₃ precipitates, but those of PAC_Al13 and PAC_Al30 were composed of aggregates of Al₁₃ and Al₃₀, respectively. Al³⁺ was the most un-stable species in coagulants, and its hydrolysis was remarkably influenced by solution pH. Al₁₃ and Al₃₀ species were very stable, and solution pH and aging had little effect on the chemical species of their hydrolysis products. The research method involving coagulant hydrolysis precipitates based on Al–Ferron reaction kinetics was studied in detail. The Al species classification based on complex reaction kinetic of hydrolysis precipitates and Ferron reagent was different from that measured in a conventional coagulant assay using the Al–Ferron method. The chemical composition of Al_a, Al_b and Al_c depended on coagulant and solution pH. The Al_b measured in the current case was different from Keggin Al₁₃, and the high Al_b content in the AlCl₃ hydrolysis precipitates could not used as testimony that most of the Al³⁺ was converted to highly charged Al₁₃ species during AlCl₃ coagulation.