Urban air pollution and atmospheric diffusion research in China

Air pollution has become a serious problem in China as a result of that country's efforts in the last 30 years to become a great industrial power. The burning of coal, which currently provides over 70% of all China's energy needs, is a major source of air pollution. Because Chinese coal is high in sulfur and ash content and because most combustion devices in China have low efficiencies, SO₂ and particulate emissions are a serious problem and are comparable to or exceed those found in many countries that are much more industrialized. Although most coal is burned in North China, acid precipitation is most severe in South China because of the lack of buffering loess dust found in the former region.The Chinese government has already taken major steps to mitigate air pollution, such as relocating polluting industries, supplying coal with lower sulfur content, using gas instead of coal for residential heating, and levying fines on industries that exceed pollution standards. Atmospheric environmental impact assessment (AEIA) is also required for all major new projects. This article describes three types of mathematical diffusion models and field and wind-tunnel experiments that are used in such assessments.The Chinese authorities believe that a range of technological, managerial, locational, and behavioral changes must be effected before the air of Chinese cities can be significantly improved.     

Management strategy for acidic deposition in Western and Northern Canada

The governments of British Columbia, Alberta, Saskatchewan, Manitoba, Northwest Territories, and Canada held joint consultations in 1980 to review the available information on acid rain from Western and Northern Canada. It was concluded that acid rain might become a problem in the future and, hence, a research, monitoring, and management strategy for acidic deposition was needed. An overview of the joint governments' management strategy, organization of research and monitoring programs, and accomplishments to date are discussed in this article.The authors are members of the Technical Committee for the Long Range Transport of Atmospheric Pollutants (LRTAP)/Acid Deposition in Western and Northern Canada, and represent Alberta and British Columbia, respectively.     

Monitoring the results of Canada/U.S.A acid rain control programs: some lake responses

Aquatic acidification by deposition of airborne pollutants emerged as an environmental issue in southeastern Canada during the 1970s. Drawing information from the extensive research and monitoring programs, a sequence of issue assessments demonstrated the necessity of reducing the anthropogenic emissions of acidifying pollutants, particularly sulphur dioxide (SO₂). The 1991 Canada-U.S. Air Quality Agreement (AQA) was negotiated to reduce North American SO₂ emissions by 40% relative to 1980 levels by 2010, and at present, both countries have reduced emissions beyond their AQA commitment. In response to reduced SO₂ emissions, atmospheric deposition of sulphate (SO₄ ^2–) and SO₄ ^2– concentrations in many lakes have declined, particularly in south-central Ontario and southern Québec. Sulphate deposition still exceeds aquatic critical loads throughout southeastern Canada however. Increasing pH or alkalinity (commonly deemed recovery) has been observed in only some lakes. Several biogeochemical factors have intervened to modify the lake chemistry response to reduced SO₄ ^2– input, notably release of stored SO₄ ^2– from wetlands following periods of drought and reduction in the export of base cations from terrestrial soils. Three examples from Ontario are presented to illustrate these responses. Significant increases in pH and alkalinity have been observed in many lakes in the Sudbury area of Ontario due to the large reductions in local SO₂ emissions; early-stage biological recovery is evident in these lakes. An integrated assessment model predicts that AQA emission reductions will not be sufficient to promote widespread chemical or biological recovery of Canadian lakes. Monitoring and modeling are mutually supporting assessment activities and both must continue.     

The Precision of Precipitation Chemistry Measurements in the Canadian Air and Precipitation Monitoring Network (CAPMoN)

Precision estimates are presented for precipitation chemistry and depth measurements made by the Canadian Air and Precipitation Monitoring Network (CAPMoN). The estimates were made for daily measurements of ion concentration and precipitation depth as well as for weekly, 28-day, seasonal and annual precipitation-weighted mean concentrations and depths. The data on which the estimates are based were collected from collocated samplers at five CAPMoN sites during the period 1985 to 1993. The data pairs from the collocated samplers were used to calculate the between-instrument error defined as 1/2 times the difference between the paired sample concentrations (or depths). For all of the ion concentrations and depths, the between-sampler errors were found not to be normally distributed, but the normality of the distributions improved with the length of the (volume-weighting) time period considered. A set of quantitative measures of overall network precision were derived in absolute (mg L^-1) and relative (%) units. These included the Modified Median Absolute Deviation (M.MAD), the P90% probability values and the Coefficient of Variation (CoV). The latter, defined as the percent ratio of the M.MAD to the median concentration (or depth), represents the relative precision at the center of the error and concentration (and depth) distributions. Based on the CoV values, the relative precision of the CAPMoN measurements was very high (better than 4%) for SO ₄ ^2- , NO ₃ ^- , pH, H⁺, NH ₄ ⁺ , sample depth and standard gauge depth, and not as high (between 10 and <35%) for Cl^-, Na⁺, Ca²⁺, Mg²⁺, and K⁺. The ions with the lowest median concentrations had the poorest relative precision since so many of the concentrations were at or near the analytical detection limit. Except for the sample and standard gauge depths, both the absolute and relative precision improved with the length of the precipitation-weighting period. Detailed statistical testing established that the precision of the daily measurements is dependent on a number of factors, the most dominant being sample depth and concentration, i.e., the absolute precision improves with increasing sample depth and decreasing concentration. The strength of these relationships diminished with the length of the precipitation-weighting period being considered. Laboratory-related sources of imprecision were found to account for less than 4% of the overall daily measurement imprecision for most species, while field-related sources of imprecision accounted for the balance. Specialized plots are shown which allow data users to estimate the absolute and relative precision at any concentration and depth value.     

宜昌市酸雨的成因

根据近１０年１０７７个降水样品监测结果，进行统计分析，阐明了宜昌市存在酸雨污染，且日趋严重的趋势。从大气污染、气象、地形等因素方面初步探讨了该市酸雨的成因。     

中越边界—河口酸沉降的来源和发展趋势分析

河口当地无工业。燃料结构以柴禾为主，但８０年代降水酸度ＰＨ值为３．８０－５．１２平均为４．４，频率高达１００％。相距五年后，９０年代进行三年连续监测，酸 雨ＰＨ值为３．８２－６．９０，平均为４．９３，频率为９７．６％。     

"九五"期间昆明市盘龙区酸雨状况分析

本文通过对盘龙区‘‘九五"期间降水监测结果进行评价,得出昆明市中心区酸雨的变化趋势,并加以分析,提出对策建议.     

我国酸雨状况和对策

我国酸雨区面积占国土面积的30％，是世界第3大酸雨区，为控制酸雨发展，应将其防治工作纳入经济和社会发展计划，调整能源结构，治理工业排放，研发治理技术和设备，加强环境管理。     

二氧化硫浓度的垂直分布对云下雨水酸化的影响

用一物理化学模式讨论了云下雨水的酸化过程.参照重庆地区的实际情况,讨论了SO_2随高度指数分布和其它分布对酸化的影响及近地面层高浓度SO_2对酸化的影响.SO_2平均浓度与实际垂直分布相比较,地面雨水成份相差较小,用平均浓度代替实际垂直分布是可行的.