The relationship between indoor and outdoor airborne particles in the residential environment

The relationship between indoor and outdoor airborne particles was investigated for 16 residential houses located in a suburban area of Brisbane, Australia. The submicrometer particle numbers were measured using the Scanning Mobility Particle Sizer, the larger particle numbers using the Aerodynamic Particle Sizer and an approximation of PM_2.5 was also measured using a DustTrak. The measurements were conducted for normal and minimum ventilation conditions using simultaneous and non-simultaneous measurement methods designed for the purpose of the study. Comparison of the ratios of indoor to outdoor particle concentrations revealed that while temporary values of the ratio vary in a broad range from 0.2 to 2.5 for both lower and higher ventilation conditions, average values of the ratios were very close to one regardless of ventilation conditions and of particle size range. The ratios were in the range from 0.78 to 1.07 for submicrometer particles, from 0.95 to 1.0 for supermicrometer particles and from 1.01 to 1.08 for PM_2.5 fraction. Comparison of the time series of indoor to outdoor particle concentrations shows a clear positive relationship existing for many houses under normal ventilation conditions (estimated to be about and above 2 h⁻¹), but not under minimum ventilation conditions (estimated to be about and below 1 h⁻¹). These results suggest that for normal ventilation conditions, outdoor particle concentrations could be used to predict instantaneous indoor particle concentrations but not for minimum ventilation, unless air exchange rate is known, thus allowing for estimation of the “delay constant”.     

环境DNA在监测表层沉积物中的运用及其与环境变量的关系

环境DNA技术是近几年出现的新兴环境生态监测技术,为研究环境变量对表层沉积物中环境DNA变化的影响,通过小试实验模拟海水环境并以日本大螯蜚作为目标生物,引入4组不同的生物丰度,运用环境DNA技术研究了表层沉积物中环境DNA含量变化与周边环境变量的关系。在小试装置中养殖日本大螯蜚4 d后全部取出,之后启动实验。在实验启动后的第0、6、12、18、24、72、144、264、384小时进行取样,提取出的环境DNA片段含量通过实时荧光进行定量PCR检测。结果表明,表层沉积物中的环境DNA在源生物移除后72 h内降低至较低含量水平,与水体中的环境DNA有较为相似的变化特征。通过广义线性回归分析,发现环境DNA降解速率与水质盐度呈显著负相关(P=0.000 5),与pH呈显著正相关(P=0.04),说明表层沉积物中的环境DNA对于周边环境变化具有一定指示意义。上述结果为进一步推动环境DNA技术的应用及其对环境变量影响作用的深入研究提供参考。     

完善中国环境与健康关系的法律制度——基于健康权视角

中国环境污染损害事件呈现高发、频发的态势,公众健康权益受到较大威胁。中国政府历来重视环境与健康工作,已采取诸多措施并取得显著成效,但环境与健康法律制度面临较多困境。因此,需进一步完善环境与健康法律制度,其关键点在于树立并践行健康权理念,具体包括:将健康权写入《宪法》,加强环境与健康立法,建立环境与健康标准体系,构建公众环境与健康素养教育制度,完善环境健康损害赔偿制度,形成有效的环境健康监管协作机制等措施,从而切实保障公众的健康权益。     

Managing soil remediation problems

Soil remediation has only a short history but the problem addressed is a significant one. Cost estimates for the clean-up of contaminated sites in the European Union and the United States are in the order of magnitude of 1,400 billion ECU. Such an enormous operation deserves the best management it can get. Reliable cost estimations per contaminated site are an important prerequisite. This paper addresses the problems related to site-wise estimations. When solving soil remediation problems, we have to deal with a large number of scientific disciplines. Too often solutions are presented from the viewpoint of only one discipline. In order to benefit from the combined disciplinary knowledge and experience, we think that it is necessary to describe the interrelations between these disciplines. This can be realized by developing an adequate model of the desired process which enables to consider and evaluate the essential factors as interdependent components of the total system. The resulting model provides a binding paradigm to the contributing disciplines which will result in improved efficiency and effectivity of the decision and the cost estimation process. In the near future, we will release the “Biosparging and Bioventing Expert Support System”, an expert support system for problem owners, consultants and authorities dealing with the design and operation of a biosparging and/or a bioventing system.     

PCDTs in the environment

Polychlorinated dibenzothiophenes (PCDTs) are sulfur analogues of polychlorinated dibenzofurans. Recently, PCDTs have been found in stack gas and fly ash samples, pulp mill effluents, sediments and in some aquatic organisms. PCDTs have been analyzed by high resolution GC/MS and by other GC-MS techniques. Combustion is until now the major known source of PCDTs in the environment. Tri-, tetra- and pentaCDTs in concentrations approaching those of PCDTs have been analyzed in some samples from waste incineration and metal reclamation. Concentrations of PCDTs in pulp mill effluents have been found to be quite low. 2378-TeCDT was found to be the major TeCDT isomer in some pulp mill effluents. Preliminary toxicological investigations have shown that PCDTs possess some kind of dioxin type toxicity.     

Predicting and Managing the Health Risks of Sour-Gas Wells

The development of sour-gas resources in Canada and the United States has prompted concerns about the public health risks of accidental releases of gas contaminated with hydrogen sulfide (H₂S) from wells. This paper focuses on methods for improving the prediction and management of those risks. Data associated with the health effects of hydrogen sulfide are examined, and it is suggested that sublethal effects should be addressed in risk assessments of sour-gas wells along with the life-threatening effects normally considered. The demarcation of hazard zones around wells can be improved by using a statistical approach for estimating an upper-bound H₂S release rate; this rate can then be used in an atmospheric dispersion model to estimate maximum distances to downwind concentrations for lethal (300 ppmv) and sublethal (50 ppmv) effects resulting from an accidental release. A vertical release is found to have little impact, especially under stable atmospheric conditions; horizontal releases, on the other hand, result in the greatest downwind distances for health impacts. Management of health risks depends on a mix of safety technologies and contingency actions, such as well-ignition options and provision for post-release monitoring and assessment of ambient H₂S concentrations.     

大学环境教育与环境建设

从中国生态环境的现状和大学传授学生知识、确立学生观念的特殊地位说明了在高校进行环境教育的必要性。环境教育是让学生了解人类生活和文明发展历程中的环境状况和问题，思考环境保护的意义和价值，进而确立环境观念。提出了建设环境友好型大学。建议在高校中建立讲座、选修、必修三位一体的环境教育教学体系。     

World trade and the environment

This paper is the text of a speech given by the author at a recent conference. As the title implies, it discusses the relationship between economic activity and the environment, and emphasises that they are not incompatible. Indeed, a reduction in the former decreases the resources necessary to protect the latter. He concludes by arguing the case for flexibility in international standards, in order to allow Third World countries to compete more equally and to cope with local differences.     

Trichloroacetic acid in the environment

Suppositions that the trichloroacetic acid (TCA, CCl3C(O)OH) found in nature was a consequence solely of the use of chlorinated hydrocarbon solvents prompted this critical review of the literature on its environmental fluxes and occurrences. TCA is widely distributed in forest soils (where it was rarely used as an herbicide) and measurements suggest a soil flux of 160 000 tonnes yr(-1) in European forests alone. TCA is also produced during oxidative water treatment and the global flux could amount to 55 000 tonnes yr(-1) (from pulp and paper manufacture, potable water and cooling water treatments). By contrast, the yields of TCA from chlorinated hydrocarbon solvents are small: from tetrachloroethene 13 600 tonnes yr(-1) and from 1,1,1-trichloroethane 4300 tonnes yr(-1) on a global basis, at the atmospheric burdens and removal rates typical of the late 1990s. TCA is ubiquitous in rainwater and snow. Its concentrations are highly variable and the variations cannot be connected with location or date. However, there is no significant difference between the concentrations found in Chile and in eastern Canada (by the same analysts), or between Malawi and western Canada, or between Antarctica and Switzerland, nor any significant difference globally between the concentrations in cloud, rain and snow (although local enhancement in fog water has been shown). TCA is present in old ice and firn. At the deepest levels, the firn was deposited early in the 19th century, well before the possibility of contamination by industrial production of reactive chlorine, implying a non-industrial background. This proposition is supported by plume measurements from pulp mills in Finland. TCA is ubiquitous in soils; concentrations are very variable but there are some indications that soils under coniferous trees contain higher amounts. The concentrations of TCA found in plant tissue are region-specific and may also be plant-specific, to the extent that conifers seem to contain more than other species. TCA is removed from the environment naturally. There is abundant evidence that soil microorganisms dehalogenate TCA and it is lost from within spruce needles with a half-life of 10 days. There is also recent evidence of an abiotic aqueous decarboxylation mechanism with a half-life of 22 days. The supposedly widespread effects of TCA in conifer needles are not shown in controlled experiments. At concentrations in the needles of Scots pine similar to those observed in needles in forest trees, changes consequent on TCA treatment of field laboratory specimens were almost all insignificant.     

Pollution in the upland environment

As part of a study on the effects of pollutants on forests, a long-term monitoring programme has been operating at two sites (602 and 275 m above sea level (a.s.l.)) in Glentress Forest, south-east Scotland, since June 1987. At these sites, equipment has been recording 20-min data for weather parameters, and cloud and rain event frequency, duration and intensity. The chemical composition of bulk cloud and rainwater has been measured. Cloudwater detection and collection has been made using passive 'Harp wire' gauges (with a cross-sectional area of 0.047 m2) strung with polypropylene filament and having a typical collection efficiency of 29% when compared with independent measurements of windspeed and liquid water content. During 1988, the annual rainfall at the upper site was 1213 mm, occurring over 1776 h. The equivalent cloudwater deposition to a forest with a drag coefficient of 0.06 was estimated to be 375 mm over 1936 h. A 'typical cloud event' lasted 4.5 h and would deposit to forests at a rate of 0.2 mm h(-1). There were significantly higher loadings of suspended particulate material (> 0.2 microm) in cloudwater (mean 18.42, max. 94.5 mg litre(-1)) compared with rainwater (mean 2.6, max. 25.6 mg litre(-1)). There were similar differences in ion concentrations, e.g. for H+ in cloudwater (mean 163, max. 1259 microm) and in rainwater (mean 33, max. 262 microM). It is concluded that cloudwater deposition represents a major pathway for pollutant transfer to the upland environment, especially where the surface vegetation is efficient at capturing cloudwater, i.e. forests. The consequences of this increased pollutant loading to forests and water catchments are yet to be assessed.