生态系统健康与环境管理

环境管理和生态系统健康是密不可分的,生态系统健康是环境管理的目的,生态系统健康为环境管理提供了新的思路、新的方法,健康的生态系统为实现区域可持续发展提供技术支撑和发展基础.生态系统健康的发展演替过程是优化环境管理的步骤.优化的环境管理为生态系统健康发展提供宏观决策和社会经济保障.本文从学科发展的角度论述了生态系统健康产生的背景、理论基础和应用途径;从学科交叉的角度论述了生态系统健康的评价和与环境管理的关系.提出了环境管理的目标:健康的生态系统→健康的环境→健康的食品→健康的人类生态系统→健康的社会发展.     

生物多样性在路域植被恢复中的应用

从生物多样性的特点出发 ,根据公路路域的特点以及近年来公路绿化成功与失败的经验 ,探讨植物多样性在公路植被恢复中的应用。自然界中植物通过多种多样的组合体而存在 ,多样性是自然形成 ;利用植物多样性原理可以提高路域植被的恢复水平和景观效果     

明胶厂剩余高钙污泥作为燃煤固硫剂的应用研究

明胶生产产业在废水处理工艺中产生大量剩余高钙污泥,采用该剩余污泥作为燃煤固硫剂,在高温管式电阻炉内进行燃烧实验,通过测定燃烧前和燃烧后样品中的硫含量确定该剩余污泥的固硫效果。通过单因素研究煤粉粒径、剩余污泥粒径和剩余污泥/煤样%等影响因素对固硫率的影响。在单因素试验的基础上通过正交设计法优选达到较高固硫率的实验条件。实验结果表明:影响固硫率的因素从大到小依次为燃烧温度>剩余污泥/煤样%>煤粉粒径>剩余污泥粒径。以剩余污泥作为固硫剂,固硫率最高的实验条件为:燃烧温度800℃,剩余污泥/煤样为3%,煤粉粒径60⁹0目,剩余污泥粒径9090目,剩余污泥粒径90¹20目。并且,当温度达到1150℃,煤粉粒径90120目。并且,当温度达到1150℃,煤粉粒径90¹20目,剩余污泥粒径为60120目,剩余污泥粒径为60⁹0目,污泥/煤样(质量比)为3%时,固硫率可达62.78%,说明在高温下该剩余污泥保持较高的固硫率。将明胶厂剩余污泥作为固硫剂是较为合适的再利用方法,可有效缓解当前该污泥大量堆积污染环境的状况。     

废弃SCR脱硝催化剂的再生及其脱硝性能研究

对废弃脱硝催化剂处理后重新加工再生,研究了添加剂对其粉体成型和再生催化剂脱硝活性的影响,探讨了反应温度、空速、n(NH3)∶n(NO)摩尔比、氧含量、H2O和SO2对再生催化剂NH3选择性催化还原(SCR)NO的影响。结果表明:最佳再生条件是使用5%羧甲基纤维素和10%无机粘结剂辅助成型;废弃催化剂再生利用率高达90%;再生催化剂抗压强度为4.73 MPa,优于商用催化剂;空速5 000 h-1、氨氮摩尔比1、氧含量6%时,脱硝活性温度窗口为310⁴50℃,350℃时活性最高为94%;350℃时,单独通入1 000×10-6SO2或10%H2O对再生催化剂活性均有一定抑制作用,最低活性分别为70%和81%,停止通入SO2或H2O后其活性逐渐恢复;同时通入1 000×10-6SO2和10%H2O,再生催化剂活性下降至63%并于1 h内保持相对稳定,停止通入SO2和H2O 2 h后,活性逐渐恢复到73%。     

Risk assessment of heavy metals in road and soil dusts within PM2.5, PM10 and PM100 fractions in Dongying city, Shandong Province, China

15 road and 14 soil dust samples were collected from an oilfield city, Dongying, from 11/2009-4/2010 and analyzed by inductively coupled plasma-mass spectroscopy (ICP-MS) for V, Cr, Mn, Co, Ni, Cu, Zn, As, Cd and Pb within PM(2.5), PM(10) and PM(100) fractions synchronously. Metal concentrations, sources and human health risk were studied. Results showed that both soil and road dust exhibited higher values for Mn and Zn and lower values for Co and Cd for the three fractions. Mass concentration ratios of PM(2.5)/PM(10) and PM(10)/PM(100) for metals in road and soil dust indicate that most of the heavy metals tend to concentrate in fine particles. Geoaccumulation index and enrichment factors analysis showed that Cu, Zn and Cd exhibited moderate or heavy contamination and significant enrichment, indicating the influence of anthropogenic sources. Vanadium, Cr, Mn and Co were mostly not enriched and were mainly influenced by crustal sources. For Ni, As and Pb, they ranged from not enriched to moderately enriched and were influenced by both crustal materials and anthropogenic sources. The conclusions were confirmed by multivariate analysis methods. Principle component analysis revealed that the major sources were vehicle emission, industrial activities, coal combustion, agricultural activities and crustal materials. The risk assessment results indicated that metal ingestion appeared to be the main exposure route followed by dermal contact. The most likely cause for cancer and other health risks are both the fine particles of soil and road dusts.     

Chemical compositions and sources of atmospheric PM10 in heating, non-heating and sand periods at a coal-based city in northeastern China

Mass concentrations and chemical components (18 elements, 9 ions, organic carbon [OC] and elemental carbon [EC]) in atmospheric PM(10) were measured at five sites in Fushun during heating, non-heating and sand periods in 2006-2007. PM(10) mass concentrations varied from 62.0 to 226.3 μg m(-3), with 21% of the total samples' mass concentrations exceeding the Chinese national secondary standard value of 150 μg m(-3), mainly concentrated in heating and sand periods. Crustal elements, trace elements, water-soluble ions, OC and EC represented 20-47%, 2-9%, 13-34%, 15-34% and 13-25% of the particulate matter mass concentrations, respectively. OC and crustal elements exhibited the highest mass percentages, at 27-34% and 30-47% during heating and sand period. Local agricultural residuals burning may contribute to EC and ion concentrations, as shown by ion temporal variation and OC and EC correlation analysis. Heavy metals (Cr, Ni, Zn, Cu and Mn) from coal combustion and industrial processes should be paid attention to in heating and sand periods. The anion/cation ratios exhibited their highest values for the background site with the influence of stationary sources on its upper wind direction during the sand period. Secondary organic carbon were 1.6-21.7, 1.5-23.0, 0.4-17.0, 0.2-33.0 and 0.2-21.1 μg m(-3), accounting for 20-77%, 44-88%, 4-77%, 8-69% and 4-73% of OC for the five sampling sites ZQ, DZ, XH, WH and SK, respectively. From the temporal and spatial variation analysis of major species, coal combustion, agricultural residual burning and industrial emission including dust re-suspended from raw material storage piles were important sources for atmospheric PM(10) in Fushun at heating, non-heating and sand periods, respectively. It was confirmed by principal component analysis that coal combustion, vehicle emission, industrial activities, soil dust, cement and construction dust and biomass burning were the main sources for PM(10) in this coal-based city.     

Occurrence and characterization of selected organochlorine contaminants in outdoor dust collected from Xinxiang,a fast developing city in North China

As facile “environmental media”, the outdoor dust may reflect the changes of contaminants in environment more promptly. In the present study, selected organochlorine contaminants (OCs) include hexachlorocyclohexanes (HCHs), dichlorodiphenyltrichloroethanes (DDTs), hexachlorobenzene (HCB), and pentachlorobenzene (PeCB) were detected in 20 outdoor dust samples collected from Xinxiang City. The concentrations of ΣHCHs, ΣDDTs, HCB, and PeCB in dust were in the range of 0.18–5.05 ng/g dry weight, 0.44–13.50 ng/g dry weight, 0.13–51.61 ng/g dry weight and ND-0.74 ng/g dry weight, respectively. Long-range transport, historical use, and recent impact of impure pesticides might be the main sources of OCs in the outdoor dust. The results of this study indicated that impure pesticide application maybe an important source of DDTs and HCB in the environment.     

Effects of input uncertainty and variability on the modelled environmental fate of organic pollutants under global climate change scenarios

Global climate change (GCC) is expected to influence the fate, exposure and risks of organic pollutants to wildlife and humans. Multimedia chemical fate models have been previously applied to estimate how GCC affects pollutant concentrations in the environment and biota, but previous studies have not addressed how uncertainty and variability of model inputs affect model predictions. Here, we assess the influence of climate variability and chemical property uncertainty on future projections of environmental fate of six polychlorinated biphenyl congeners under different GCC scenarios using a spreadsheet version of the ChemCAN model and the Crystal Ball® software. Regardless of emission mode, results demonstrate: (i) uncertainty in degradation half-lives dominates the variance of modelled absolute levels of PCB congeners under GCC scenarios; (ii) when the ratios of predictions under GCC to predictions under present day climate are modelled, climate variability dominates the variance of modelled ratios; and (iii) the ratios also indicate a maximum of about a factor of 2 change in the long-term average environmental concentrations due to GCC that is forecasted between present conditions and the period between 2080 and 2099. We conclude that chemical property uncertainty does not preclude assessing relative changes in a GCC scenario compared to a present-day scenario if variance in model outputs due to chemical properties and degradation half-lives can be assumed to cancel out in the two scenarios.     

The residues, distribution, and partition of organochlorine pesticides in the water, suspended solids, and sediments from a large Chinese lake (Lake Chaohu) during the high water level period

The levels of organochlorine pesticides (OCPs) in the water, suspended solids, and sediments from Lake Chaohu during the high water level period were measured by a solid-phase extraction gas chromatograph–electron capture detector. The spatial distributions of the three phases and the water/suspended solids and sediment/water partition coefficients were analyzed. The results showed the following: (1) The mean contents of OCPs in the water, suspended solids, and sediments were 132.4?±?432.1 ng/L, 188.1?±?286.7 ng/g dry weight (dw), and 13.7?±?9.8 ng/g dw, respectively. The dominant OCP components were isodrin (85.1 %) for the water, DDTs (64.4 %) for the suspended solids, and both isodrin (48.5 %) and DDTs (31.8 %) for the sediments. (2) β-HCH was the primary isomer of HCHs in the water and sediments, and the proportions were 61.7 and 41.3 %; γ-HCH was the primary isomer in the suspended solids, accounting for 49.3 %; p,p′-DDT was the dominant content of DDTs in the water and suspended solids, whereas p,p′-DDD was the main metabolite of DDTs in the sediments. (3) The concentrations of contaminants in the water from the western lake were greater than those from the eastern lake, but the concentrations in the suspended solids from the western lake were less than those from the eastern lake. (4) There was no significant correlation between the water–suspended solids partition coefficient K _d and the n-octanol–water partition coefficient K _ow, and between the sediment–water organic-C weighted sorption coefficients K _oc and K _ow.     

改善环保疏浚底泥脱水干化效能的实验研究

采用以硫酸亚铁(FeSO4)为主要成分的复合脱水剂作为疏浚泥浆脱水剂(以下简称脱水剂),黄沙、炉渣、煤灰、石灰和粉煤灰分别作为疏浚底泥干化改良剂进行实验研究。结果表明,在脱水剂投加量为100 mg/L条件下,可以提高沉淀效率约20%;在投加脱水剂及5%石灰、粉煤灰、炉渣改良剂的条件下,底泥比阻值下降50%～70%;初期渗水速率提高6%～68%;与原泥相比,以黄沙、炉渣、煤灰为改良剂的底泥,经过4个月干化期后,承载力提高了30%～150%。本研究为疏浚底泥快速脱水干化提供了一种可行的技术途径。