基于数字流域的水文过程模拟研究

考虑流域下垫面空间变异性,基于数字高程模型构建了数字流域,并在此基础上对描述流域水文物理过程的数学方法进行了探讨,文章认为,数字水文模型是一种有物理基础的包含大容量信息的现代模拟灌河实例研究表明,数字水文模型可以十分方便地输出水文要素和状态变量的空间分布与时间序列,这对充分利用现有观测信息进行水文信息的深层挖掘创新了条件。     

Anthropogenic lead distribution in soils under arable land and permanent grassland estimated by Pb isotopic compositions

The role of land use on fate of metals in soils is poorly understood. In this work, we studied the incorporation of lead in two neighboring soils with comparable pedogenesis but under long-term different agricultural management. Distributions of anthropogenic Pb were assessed from concentrations and isotopic compositions determined on bulk horizon samples, systematical 5-10 cm increment samples, and on 24-h EDTA extracts. Minor amounts of anthropogenic lead were detected until 1-m depth under permanent grassland, linked to high earthworm activity. In arable land, exogenous Pb predominantly accumulated at depths <60 cm. Although the proximity between the two sites ensured comparable exposition regarding atmospheric Pb deposition, the isotopic compositions clearly showed the influence of an unidentified component for the cultivated soil. This work highlights the need for exhaustive information on historical human activities in such anthropized agrosystems when fate of metal pollution is considered.     

Photochemical behaviour of musk tibetene

BACKGROUND: Synthetic musk compounds are widely used as additives in personal care and household products. The photochemical degradation of musk tibetene in aqueous solutions or in acetonitrile/water mixtures under different conditions was studied in order to assess its environmental fate. METHODS: Musk tibetene dissolved (or suspended) in water and/or acetonitrile/water mixtures was irradiated at different times by UV-light and by solar light. The irradiation mixtures were analyzed by NMR and TLC. The photoproducts formed were identified by GC-MS and NMR data. RESULTS: The experimental results indicated that musk tibetene was photodegradable in water or acetonitrile/water mixtures with half-life reaction times close to 20 minutes. The irradiation mixtures were separated by chromatographic techniques yielding three photoproducts (3,3,5,6,7-pentamethyl-4-nitro-3H-indole, 3,3,5,6,7-pentamethyl-4-nitro-1H-indoline and 3,3,5,6,7-pentamethyl-4-nitro-3H-indolinone) identified by means of spectroscopic analysis. DISCUSSION: The numerical modelling of the photodegradation concentration-time profiles gave (8.13 +/- 0.15) x 10(-2) and (1.34 +/- 0.04) x 10(-2) mol/E for the overall primary quantum yield of direct photolysis for musk tibetene and the major intermediate (3,3,5,6,7-pentamethyl-4-nitro-3H-indolinone), respectively, in the wavelength range 305-366 nm. The half-life times of photodegradation of the both substances varied from 1-1.5 hours at 20 degrees N during the summer season to 6-10 hours for highest latitudes in winter. CONCLUSIONS: Under solar light, musk tibetene was photolabile in acetonitrile and acetonitrile/water 1/1, while it was slowly degraded when suspended in water. In all media, musk tibetene was photodegraded into three photoproducts. By using a kinetic model, the overall primary quantum yields of direct photolysis of musk tibetene and its main photoproduct, in the wavelength range 305-366 nm, were estimated, indicating that the photodegradation rate for musk tibetene is faster than the photolysis rate of the major by-product. RECOMMENDATIONS AND PERSPECTIVES: The results indicate that, in order to assess the environmental impact of musk tibetene on the aquatic ecosystem, great attention should be focused on the major photoproduct which is proved to be more persistent than the parent compound under light irradiation. The predicted half-life times of direct photolysis for both substances ranged from 1-1.5 hours at 20 degrees N during the summer season to about 6-10 hours for highest latitudes in winter, indicating that, from a photochemical point of view, the environmental persistence of these substances increases by increasing the latitudes and during the cold seasons, making more realistic an intake of these xenobiotic molecules into the food chain of aquatic living organisms. Tanabe reports in his Editorial (Tanabe 2005) that "It is necessary to have knowledge of the global picture of synthetic musk pathways. So, it is conceivable that now is the time to study the transport, persistency, distribution, bioaccumulation and toxic potential of this new environmental menace on a global scale, especially in developing countries". Therefore, the future environmental analysis and investigations on the eco-toxicity of nitro musk compounds should take into account not only the presence of the parent compounds but also their photochemical intermediates or end-by-products.     

WATERSHED FUNCTIONS1

ABSTRACT: Watershed functions that dominate the hydrologic environment are identified and discussed. Hydrological and ecological functions are considered in relation to the storm and annual hydrographs, and to water quality. Two integrative watershed responses to these functions are also articulated. Since most of the Earth's water is in storage, consideration of the hydrologic cycle as movement between water storage sites enhances this functional and response characterization of the watershed which, in turn, suggests guidance and direction for the restoration of watershed functions.     

Degradation and removal methods of antibiotics from aqueous matrices--a review

Over the past few years, antibiotics have been considered emerging pollutants due to their continuous input and persistence in the aquatic ecosystem even at low concentrations. They have been detected worldwide in environmental matrices, indicating their ineffective removal from water and wastewater using conventional treatment methods. To prevent this contamination, several processes to degrade/remove antibiotics have been studied. This review addresses the current state of knowledge concerning the input sources, occurrence and mainly the degradation and removal processes applied to a specific class of micropollutants, the antibiotics. In this paper, different remediation techniques were evaluated and compared, such as conventional techniques (biological processes, filtration, coagulation, flocculation and sedimentation), advanced oxidation processes (AOPs), adsorption, membrane processes and combined methods. In this study, it was found that ozonation, Fenton/photo-Fenton and semiconductor photocatalysis were the most tested methodologies. Combined processes seem to be the best solution for the treatment of effluents containing antibiotics, especially those using renewable energy and by-products materials.     

国内硝基苯废水治理的研究进展

硝基苯具有很高的毒性且难以生物降解,严重威胁环境和人类健康.综述了近年来国内硝基苯废水治理的研究现状,介绍了硝基苯废水的主要处理方法化学法、生物法和物理法,并指出今后的发展方向.     

聚糖原菌富集实验及其内源过程探究

细胞衰减是微生物内源过程的一个重要组成部分,可分为由细胞死亡引起的数量衰减和由细胞活性降低引起的活性衰减两部分.通过挥发性脂肪酸（VFA）吸收速率(VFAUR)测定、荧光原位杂交技术（FISH）以及LIVE/DEAD细胞染色技术,研究了富集聚糖原菌（GAOs）在序批式反应器（SBR）系统中好氧环境下的衰减特征.结果表明,当T=30℃、进料中m(COD)∶m(P)=100时,SBR系统中GAOs富集比例达94%.测定和计算表明,SBR富集系统中GAOs衰减速率和死亡速率分别为0.132 d^-1和0.034 d^-1,其数量衰减和活性衰减占其细胞总衰减比例分别为26%和74%.可见,GAOs数量衰减只占其细胞总衰减中很小一部分,而绝大部分衰减由活性衰减所引起.     

秋季典型光化学污染过程的分析

通过一个月的Ｏ３－ＮＯｘ同步观测和有关气象资料的分析,研究了光化学污染特点和及其和气象的关系,发现秋季的光化学污染过程,既有冬夏两季局地源产生和积累的机制,也有春季外来源造成的高浓度Ｏ３污染特点。Ｏ３的最大浓度和日最大值平均浓度分别为１６８．７μｇ／ｍ＾３和１１４．８μｇ／ｍ＾３。     

春季生物作用对山地岩溶池水地球化学特征的影响

岩溶水文系统对外界环境变化敏感,使得岩溶区水质存在昼夜、小时甚至分钟等尺度的变化.许多地表水体都会经历p H值、溶解性气体、微量元素以及其他水化学指标的昼夜变化.重庆金佛山水房泉及受其补给的水池地处海拔2 050 m的山地岩溶区,具有温带气候特征.通过对水房泉泉水(以下简称泉水)及水池进行为期3 d的昼夜监测,以期探究春季生物作用对岩溶池水地球化学的影响.研究发现,在昼夜时间尺度上,泉水地球化学指标基本稳定,未表现出昼夜变化,池水地球化学指标化学表现出了昼夜波动,但水温、溶解氧、p H值、电导率等物理化学指标昼夜变化幅度较小.在不同的天气条件下,水温、溶解氧、Cl-等昼夜变化幅度存在差别;池水二氧化碳分压(p CO2)、Ca2+、DIC白天降低、晚上升高,方解石饱和指数(SIc)相反;这些指标的变化受控于温度、碳酸盐岩矿物的溶解与沉淀、水生植物光合作用与呼吸作用;通过亨利常数的计算,发现水温变化对p CO2变化的影响仅占0.79%~10.01%,水温、碳酸盐岩沉淀等物理因素对DIC损失量的贡献率为39%,水生植物光合作用的贡献率为61%.