建立我国生态环境标准体系的初步构想

我国的生态环境标准极其薄弱，建立生态环境标准体系是我国生态环境保护的迫切需要。借鉴我国目前针对污染防治的环境标准体系，提出了我国生态环境标准体系的基本框架，以及生态环境标准制订的原则和重点。     

江西武夷成矿带铜多金属矿产资源远景评价与展望

华南武夷山地区处于扬子、华夏两大构造单元交接叠加地段,构造变形复杂,中生代岩浆活动强烈,具有十分优越的成矿条件,矿产资源潜力巨大.本文以正在武夷山成矿带开展的矿产远景调查工作和资源评价工作所取得的阶段性成果为基础,分析了武夷山成矿带的成矿地质背景、主要矿床类型及近几年的找矿勘查成果,并对武夷成矿带江西省境内铜多金属矿产资源潜力进行了初步评价,划分了十七个找矿远景区.     

生态气象监测评估业务平台的设计与应用

  针对目前生态气象监测轨道业务的特点，结合工作的实际需要，运用C和C++语言建立了生态气象监测评估业务平台。在程序设计中，采用了生成中间交换文件的结构组织，能够对各模块的输出结果进行详尽直观的分析，并提供了等值线色斑图与区域填充等多种图形绘制方式。该系统可处理AVHRR和EOS/MODIS卫星遥感资料，对气象观测报文进行解译、数据分类管理和质量控制，统计计算水体密度指数、湿润指数、植被覆盖指数、土地退化指数、灾害指数和生态质量综合评价指标，以图形、图像的形式输出生态气象监测评估产品，实现了卫星遥感与生态气象地面监测数据的有效组织和智能化管理。将系统应用于湖南省生态质量气象评价，业务化运行的结果表明，该系统具有较好的业务实用性。〖HJ1〗〖HJ〗
〖HT5”H〗     

基于层次分析法的城市河流生态修复评估

城市的发展改变了许多河流的自然水文环境，并导致河流生态系统中水质、物理生境和生物完整性下降。评估受损河流水体修复的效果，需要结合物理、化学的参数，以及对生物结构、多样性和过程的影响。构建了包含河流水力、水质、水生生物、河岸带及物理结构5个方面15个指标的城市河流生态修复评估指标体系，运用群组决策的层次分析法(AHP)，确定了各指标的权重，重要性排序前5位依次为：水质污染指数、鱼类IBI、水源补给量、藻类多样性、透明度。并以我国南方城市岐江河整治修复状况为例进行综合评价，结果表明,河流生态系统修复评估结果为可以接受，体现了河流整治工程使河流水质、生态的状况有所改善，但河流生态系统恢复需要较长的周期，修复初期生态系统仍处于受损状态。〖     

Kinetic limitations on tracer partitioning in ganglia dominated source zones

Quantification of the relationship between dense nonaqueous phase liquid (DNAPL) source strength, source longevity and spatial distribution is increasingly recognized as important for effective remedial design. Partitioning tracers are one tool that may permit interrogation of DNAPL architecture. Tracer data are commonly analyzed under the assumption of linear, equilibrium partitioning, although the appropriateness of these assumptions has not been fully explored. Here we focus on elucidating the nonlinear and nonequilibrium partitioning behavior of three selected alcohol tracers - 1-pentanol, 1-hexanol and 2-octanol in a series of batch and column experiments. Liquid-liquid equilibria for systems comprising water, TCE and the selected alcohol illustrate the nonlinear distribution of alcohol between the aqueous and organic phases. Complete quantification of these equilibria facilitates delineation of the limits of applicability of the linear partitioning assumption, and assessment of potential inaccuracies associated with measurement of partition coefficients at a single concentration. Column experiments were conducted under conditions of non-equilibrium to evaluate the kinetics of the reversible absorption of the selected tracers in a sandy medium containing a uniform entrapped saturation of TCE-DNAPL. Experimental tracer breakthrough data were used, in conjunction with mathematical models and batch measurements, to evaluate alternative hypotheses for observed deviations from linear equilibrium partitioning behavior. Analyses suggest that, although all tracers accumulate at the TCE-DNAPL/aqueous interface, surface accumulation does not influence transport at concentrations typically employed for tracer tests. Moreover, results reveal that the kinetics of the reversible absorption process are well described using existing mass transfer correlations originally developed to model aqueous boundary layer resistance for pure-component NAPL dissolution.     

Refinement of the density-modified displacement method for efficient treatment of tetrachloroethene source zones

A novel method to remediate dense nonaqueous phase liquid (DNAPL) source zones that incorporates in situ density conversion of DNAPL via alcohol partitioning followed by displacement with a low interfacial tension (IFT) surfactant flood has been developed. Previous studies demonstrated the ability of the density-modified displacement (DMD) method to recover chlorobenzene (CB) and trichloroethene (TCE) from heterogeneous porous media without downward migration of the dissolved plume or free product. However, the extent of alcohol (n-butanol) partitioning required for in situ density conversion of high-density NAPLs, such as tetrachloroethene (PCE), could limit the utility of the DMD method. Hence, the objective of this study was to compare the efficacy of two n-butanol delivery approaches: an aqueous solution of 6% (wt) n-butanol and a surfactant-stabilized macroemulsion containing 15% (vol) n-butanol in water, to achieve density reduction of PCE-NAPL in two-dimensional (2-D) aquifer cells. Results of liquid-liquid equilibrium studies indicated that density conversion of PCE relative to water occurred at an n-butanol mole fraction of 0.56, equivalent to approximately 5 ml n-butanol per 1 ml of PCE when in equilibrium with an aqueous solution. In 2-D aquifer cell studies, density conversion of PCE was realized using both n-butanol preflood solutions, with effluent NAPL samples exhibiting density reductions ranging from 0.51 to 0.70 g/ml. Although the overall PCE mass recoveries were similar (91% and 93%) regardless of the n-butanol delivery method, the surfactant-stabilized macroemulsion preflood removed approximately 50% of the PCE mass. In addition, only 1.2 pore volumes of the macroemulsion solution were required to achieve in situ density conversion of PCE, compared to 6.4 pore volumes of the 6% (wt) n-butanol solution. These findings demonstrate that use of the DMD method with a surfactant-stabilized macroemulsion containing n-butanol holds promise as an effective source zone remediation technology, allowing for efficient recovery of PCE-DNAPL while mitigating downward migration of the dissolved plume and free product.     

接种不同普通活性污泥培养厌氧氨氧化污泥的研究

采用厌氧氨氧化反应器（ASBR）,分别以普通厌氧活性污泥、混合污泥、好氧活性污泥为种泥,通过对氨氮,NO2^--N等指标监测、分析及污泥颜色的观察,研究采用不同普通活性污泥为种泥启动ASBR的可行性及差异。结果表明．ASBR反应器A和B成功启动,C因反应器故障．启动失败。采用厌氧活性污泥为接种污泥（反应器A）,当进水N的容积负荷为kg／（m^3·d）时,氨氮平均去除率为14.4％。P（NO2^--N）：p（NH4^＋-N）变化量为1．24。采用混合污泥为接种污泥（反应器B）．N的容积负荷于前者相同时,氨氮去除率平均29．7％,p（NO2^--N）：p（NH4^＋-N）变化量为1．27。采用混合普通活性污泥作为种泥培养厌氧氨氧化污泥优于单一厌氧普通活性污泥。     

Evaluation of trichloroethene recovery processes in heterogeneous aquifer cells flushed with biodegradable surfactants

The ability of two biodegradable surfactants, polyoxyethylene (20) sorbitan monooleate (Tween 80) and sodium dihexyl sulfosuccinate (Aerosol MA), to recover a representative dense non-aqueous-phase liquid (DNAPL), trichloroethene (TCE), from heterogeneous porous media was evaluated through a combination of batch and aquifer cell experiments. An aqueous solution containing 3.3% Aerosol MA, 8% 2-propanol and 6 g/l CaCl(2) yielded a weight solubilization ratio (WSR) of 1.21 g TCE/g surfactant, with a corresponding liquid-liquid interfacial tension (IFT) of 0.19 dyn/cm. Flushing of aquifer cells containing a TCE-DNAPL source zone with approximately two pore volumes of the AMA formulation resulted in substantial (>30%) mobilization of TCE-DNAPL. However, a TCE mass recovery of 81% was achieved when the aqueous-phase flow rate was sufficient to displace the mobile TCE-DNAPL toward the effluent well. Aqueous solutions of Tween 80 exhibited a greater capacity to solubilize TCE (WSR=1.74 g TCE/g surfactant) and exerted markedly less reduction in IFT (10.4 dyn/cm). These data contradict an accepted empirical correlation used to estimate IFT values from solubilization capacity, and indicate a unique capacity of T80 to form concentrated TCE emulsions. Flushing of aquifer cells with less than 2.5 pore volumes of a 4% T80 solution achieved TCE mass recoveries ranging from 66 to 85%, with only slight TCE-DNAPL mobilization (<5%) occurring when the total trapping number exceeded 2 x 10(-5). These findings demonstrate the ability of Tween 80 and Aerosol MA solutions to efficiently recover TCE from a heterogeneous DNAPL source zone, and the utility of the total trapping number as a design parameter for a priori prediction of DNAPL mobilization and bank angle formation when flushing with low-IFT solutions. Given their potential to stimulate microbial reductive dechlorination at low concentrations, these surfactants are well-suited for remedial action plans that couple aggressive mass removal followed by enhanced bioremediation to treat chlorinated solvent source zones.