Numerical study on the ozone formation inside street canyons using a chemistry box model

Tropospheric ozone is a secondary air pollutant produced in the presence of nitrogen oxides (NO_x),volatile organic compounds (VOCs),and solar radiation.In an urban environment,ground-level vehicular exhaust is the major anthropogenic source of ozone precursors.In the cases of street canyons,pollutant dilution is weakened by the surrounding buildings that creates localized high concentration of NO_x and VOCs,and thus leads to high potential of ozone formation.By considering the major physical and chemica...     

基于航空摄影测量的填埋堆体动态重构精度及影响因素

填埋堆体表面形变监测是填埋场库容管理和堆体失稳等风险分析的核心,其时空高分辨率监测研究近年来引起广泛关注。基于航空摄影的地表测量技术具有采集速度快、时空分辨率高等优点,但在填埋场特殊环境下,面对高频填埋活动、显著的堆体变化以及防雨膜覆盖等干扰时,要同时满足高时空分辨率和耗时短的动态监测要求,无人机的最佳飞行参数设定亟待研究。为此,该研究模拟中等规模危险废物填埋场的规模和日填埋量,利用专业级无人机获取模拟区域图像,空三加密处理生成三维点云数据,利用Arcmap叠加分析多期监测数据,从点位坐标、重构尺度、重构体积、体积差分精度4个角度分析重构误差。结果表明:三维重构的坐标精度可以达到米级;重构尺度误差为2~3 cm,重构体积误差为0.16~0.17 m³,差分体积误差为0.16~0.17 m³;进一步研究发现,高度为25~55 m时,高度越高精度越低,相机倾角为[-53°,-60°]时,精度最高,旁向重叠率大于80%时,误差骤减且基本稳定。考虑到填埋场的填埋作业间隔、无人机续航能力等对飞行时间的约束,为获得最佳精度,建议无人机飞行高度为37 m、相机倾斜角度为[-53°,-60°]、旁向重叠率为80%。     

新化矿区煤矸石中微量元素赋存形态及浸出特征

利用BCR连续提取法和浸泡实验,对贵州省新化煤矿区不同风化程度的煤矸石中微量元素As、Cd、V、Zn、Co、Cr、Cu、Ni、Pb的赋存形态及浸出浓度进行研究。赋存形态研究结果表明:在煤矸石中As和Cd元素主要以酸溶态、可还原态和可氧化态形式赋存,而其他微量元素V、Zn、Co、Cr、Cu、Ni、Pb主要以残渣态形式赋存;除了V元素的赋存形态含量百分比不受煤矸石风化程度影响外,其它微量元素的赋存形态的含量百分比均会受到煤矸石风化程度的影响。煤矸石的浸出实验表明:浸泡时间是影响煤矸石中微量元素释放的一个重要因素;在浸泡过程中,大部分微量元素在浸泡前期的浸出浓度受煤矸石风化程度的影响,Zn和Cu元素则是在整个浸泡过程的浸出浓度均受到煤矸石风化程度的影响;不同粒径大小的煤矸石在浸泡过程中,除微量元素As和Co的浸出浓度不受煤矸石粒径大小的影响,其他微量元素在浸泡前期和中期的浸出浓度均与煤矸石的粒径大小呈反比。     

Characteristics of urban ozone level in Hong Kong

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水溶性有机物电子转移能力与荧光峰强度的关系研究

以不同来源的水溶性有机物（DOM）为供试材料,采用电化学方法和荧光光谱法研究了DOM电子转移能力及其与荧光峰强度的关系.采用库仑安培法测定DOM电子转移能力,其中测得的电子接受能力为635.6～1 049.3μmol.（g.C）-1,电子供给能力为27.3～42.3μmol.（g.C）-1.利用循环伏安法研究DOM电化学活性,发现其氧化还原电位在-731～-996 mV（vs.Ag/AgCl）之间.经过电位跃阶法三次氧化还原循环后电子转移能力仍可维持在232.1～897.2μmol.（g.C）-1之间,电子循环率为36.7%～78.2%,说明DOM具有重复利用、反复转移电子的特性.采用荧光激发发射光谱法（EEMS）测定DOM的类富里酸荧光峰强度并比较其与DOM电子转移能力的关系,发现DOM的类富里酸荧光峰强度与DOM的电子循环率具有显著相关（r2=0.92）.实验结果为理解DOM在元素循环、污染物降解以及生物地球化学循环中的作用提供科学依据.     

Identifying water resources management strategies in adaptation to climate change under uncertainty

In this study, an integrated simulation-based allocation modeling system (ISAMS) is developed for identifying water resources management strategies in response to climate change. The ISAMS incorporates global climate models (GCMs), a semi-distributed land use-based runoff process (SLURP) model, and a multistage interval-stochastic programming (MISP) approach within a general framework. The ISAMS can not only handle uncertainties expressed as probability distributions and interval values but also reveal climate change impacts on water resources allocation under different projections of GCMs. The ISAMS is then applied to the Kaidu-kongque watershed with cold arid characteristics in the Tarim River Basin (the largest inland watershed basin in China) for demonstrating its efficiency. Results reveal that different climate change models corresponding to various projections (e.g., precipitation and temperature) would lead to changed water resources allocation patterns. Variations in water availability and demand due to uncertainties could result in different water allocation targets and shortages. A variety of decision alternatives about water allocations adaptive to climate change are generated under combinations of different global climate models and ecological water release plans. These findings indicate that understanding the uncertainties in water resources system, building adaptive methods for generating sustainable water allocation patterns, and taking actions for mitigating water shortage problems are key adaptation strategies responding to climate change.     

Dietary exposure to di-isobutyl phthalate increases urinary 5-methyl-2′-deoxycytidine level and affects reproductive function in adult male mice

Phthalates are a large family of ubiquitous environmental pollutants suspected of being endocrine disruptors. Epidemiological studies have associated phthalate metabolites with decreased reproductive parameters and linked phthalate exposure with the level of urinary 5-methyl-2′-deoxycytidine(5mdC, a product of methylated DNA). In this study, adult male mice were exposed to 450 mg di-isobutyl phthalate(DiBP)/(kg·day) via dietary exposure for 28 days. Mono-isobutyl phthalate(Mi BP, the urinary metabolite) and reproductive function parameters were determined. The levels of 5mdC and 5-hydroxymethyl-2′-deoxycytidine(5hmdC) were measured in urine to evaluate if their contents were also altered by DiBP exposure in this animal model. Results showed that DiBP exposure led to a significant increase in the urinary 5mdC level and significant decreases in sperm concentration and motility in the epididymis, accompanied with reduced testosterone levels and downregulation of the P450 cholesterol side-chain cleavage enzyme(P450scc) gene in the mice testes. Our findings indicated that exposure to DiBP increased the urinary 5mdC levels,which supported our recent epidemiological study about the associations of urinary 5mdC with phthalate exposure in the male human population. In addition, DiBP exposure impaired male reproductive function, possibly by disturbing testosterone levels; P450scc might be a major steroidogenic enzyme targeted by DiBP or other phthalates.     

Biodegradation of phthalate esters by two bacteria strains

In this study two aerobic phthalic acid ester (PAE) degrading bacteria strains, DK4 and O18, were isolated from river sediment and petrochemical sludge, respectively. The two strains were found to rapidly degrade PAE with shorter alkyl-chains such diethyl phthalate (DEP), dipropyl phthalate (DPrP), di-n-butyl phthalate (DBP), benzylbutyl phthalate (BBP) and diphenyl phthalate (DPP) are very easily biodegraded, while PAE with longer alkyl-chains such as dicyclohexyl phthalate (DCP) and dihexyl phthalate (DHP) and di-(2-ethylhexyl) phthalate (DEHP) are poorly degraded. The degradation rates of the eight PAEs were higher for strain DK4 than for strain O18. In the simultaneous presence of strains DK4 and O18, the degradation rates of the eight PAEs examined were enhanced. When the eight PAEs were present simultaneously, degradation rates were also enhanced. We also found that PAE degradation was delayed by the addition of nonylphenol or selected polycyclic aromatic hydrocarbons (PAHs) at a concentration of 1 microg/g in the sediment. The bacteria strains isolated, DK4 and O18, were identified as Sphigomonas sp. and Corynebacterium sp., respectively.     

Rapid degradation of butachlor in wheat rhizosphere soil

The degradative characteristics of butachlor in non-rhizosphere, wheat rhizosphere, and inoculated rhizosphere soils were measured. The rate constants for the degradation of butachlor in non-rhizosphere, rhizosphere, and inoculated rhizosphere soils were measured to be 0.0385, 0.0902, 0.1091 at 1 mg/kg, 0.0348, 0.0629, 0.2355 at 10 mg/kg, and 0.0299, 0.0386, 0.0642 at 100 mg/kg, respectively. The corresponding half-lives for butachlor in the soils were calculated to be 18.0, 7.7, 6.3 days at 1 mg/kg, 19.9, 11.0, 2.9 days at 10 mg/kg, and 23.2, 18.0, 10.8 days at 100 mg/kg, respectively. The experimental results show that the degradation of butachlor can be enhanced greatly in wheat rhizosphere, and especially in the rhizosphere inoculated with the bacterial community designated HD which is capable of degrading butachlor. It could be concluded that rhizosphere soil inoculated with microorganisms-degrading target herbicides is a useful pathway to achieve rapid degradation of the herbicides in soil.     

Perfluorinated compounds in the Pearl River and Yangtze River of China

A total of 14 perfluorinated compounds (PFCs) were quantified in river water samples collected from tributaries of the Pearl River (Guangzhou Province, south China) and the Yangtze River (central China). Among the PFCs analyzed, perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) were the two compounds with the highest concentrations. PFOS concentrations ranged from 0.90 to 99 ng/l and <0.01–14 ng/l in samples from the Pearl River and Yangtze River, respectively; whereas those for PFOA ranged from 0.85 to 13 ng/l and 2.0–260 ng/l. Lower concentrations were measured for perfluorobutane sulfonate (PFBS), perfluorohexane sulfonate (PFHxS), perfluorooctanesulfoamide (PFOSA), perfluorohexanoic acid (PFHxA), perfluoroheptanoic acid (PFHpA), perfluorononaoic acid (PFNA), perfluorodecanoic acid (PFDA), and perfluoroundecanoic acid (PFUnDA). Concentrations of several perfluorocarboxylic acids, including perfluorododecanoic acid (PFDoDA), perfluorotetradecanoic acid (PFTeDA), perfluorohexadecanoic acid (PFHxDA) and perfluorooctadecanoic acid (PFOcDA) were lower than the limits of quantification in all the samples analyzed. The highest concentrations of most PFCs were observed in water samples from the Yangtze River near Shanghai, the major industrial and financial centre in China. In addition, sampling locations in the lower reaches of the Yangtze River with a reduced flow rate might serve as a final sink for contaminants from the upstream river runoffs. Generally, PFOS was the dominant PFC found in samples from the Pearl River, while PFOA was the predominant PFC in water from the Yangtze River. Specifically, a considerable amount of PFBS (22.9–26.1% of total PFC analyzed) was measured in water collected near Nanjing, which indicates the presence of potential sources of PFBS in this part of China. Completely different PFC composition profiles were observed for samples from the Pearl River and the Yangtze River. This indicates the presence of dissimilar sources in these two regions.