广州地区酸雨状况及其影响因素探讨

对广州地区降水酸度、酸雨频率的年际变化进行了研究,发现近十几年来广州地区的酸雨污染有所减缓,但2001-2003年有恶化的趋势.为探究原因,追溯主要酸雨污染物来源,并对各酸雨污染物进行综合评价,结论表明,广州地区的大气环境已从过去的以SO2为主的煤烟型污染转变为以NOX为主的氧化型污染.还讨论了广州地区气象条件对酸雨形成的影响.     

Interactions between precipitation and Scots pine canopies along a heavy-metal pollution gradient

Bulk precipitation and stand throughfall were collected during 1992-96 at distances of 0.5, 4 and 8 km from the Harjavalta Cu-Ni smelter, southwestern Finland. The amounts of heavy metals (Cu, Ni, Zn, Fe) and mineral nutrients in bulk precipitation and throughfall were highest at 0.5 km. Although the canopy coverage was low at 0.5 km, the amounts of heavy metals intercepted by the canopy were extremely high. The proportion of foliar leaching relative to the wash-off of dry deposition from the needle surfaces decreased on moving towards the smelter for all elements, except for K. The high rate of K leaching from the needle tissues close to the smelter demonstrated that the K throughfall flux has been greatly altered by the heavy pollution load.     

Cartographic modelling of aerotechnogenic pollution in snow cover in the landscapes of the Kola Peninsula

The goal of this work was to develop computational techniques for sulphates, nickel and copper accumulation in the snow in the local pollution zone. The main task was to reveal the peculiarities of formation and pollution of snow cover on the region with complex cross-relief. A digital cartographic model of aerotechnogenic pollution of snow cover in the landscapes of the local zone has been developed, based on five-year experimental data. Data regarding annual emissions from the industrial complex, information about distribution of wind and the sum of precipitation from meteostation "Nikel" for the winter period, allowed the model to ensure: * material presentation in the form of maps of water capacity and accumulation of sulphates, nickel and copper in the snow over any winter period in retrospective; * calculation of water capacity and accumulation of pollutants for watersheds and other natural-territorial complexes; * solution of the opposite problem about the determination of the emissions of sulphates, nickel and copper from the enterprise by measuring snow pollution in datum points. The model can be used in other northern regions of the Russian Federation with similar physical-geographical and climatic conditions. The relationships between the sum of precipitation and water capacity in the landscapes of the same type and also the relationships between pollution content in snow and relief, pollution content in snow and distance from the source of emissions, were used as the basis for the model.     

The influence of meteorological conditions on the behavior of pollutants concentrations in S?o Paulo, Brazil.

The observed behavior of pollution concentrations to the prevailing meteorological conditions has been studied for the period from June 13 to September 2, 1994, for the Metropolitan Area of Sao Paulo (MASP). The synoptic conditions, which prevailed during the period, have been identified. The behavior of these large-scale systems namely the relative positions, the nature and the types of the anticyclone or cold front (CF) has been investigated, and for each identified synoptic situation, trace elements concentrations have been determined. During the CF synoptic condition, the elements presented low concentrations associated with intense ventilation, precipitation and high relative humidity. It is seen that for both the synoptic conditions namely the South Atlantic Subtropical High and Polar High, high values of concentrations prevailed due to weak ventilation, low relative humidity and absence of precipitation. The micro and mesoscale meteorological conditions have also been studied for a day with low and a day with high concentration of particulate pollutants. Finally, applying receptor modeling to the fine aerosol mass concentration data set, five categories of emission sources in the MASP were identified: vehicles, garbage incineration, vegetation, suspend soil dust and burning of fuel oil.     

Impact of airborne pollution on the drainage area of subarctic lakes and fish

Within the period from 1989 to 1993, the impact of heavy metals and acid oxides on lakes, more than 100 km distant from the nearest source of pollution (enterprises of the copper-nickel industry), has been investigated. On the basis of complex investigations (chemical composition of snowpack and lake sediments, state of fish organisms and populations), it was discovered that there is intensive precipitation of heavy metals and acid oxides within the catchment of the lake Kochejavr. The catchment is characterized by a natural buffer capacity to neutralize acid precipitation. Active accumulation of heavy metals is observed in lake sediments. Metal accumulation causes subtoxic effects on the lake fish. The levels of precipitation of nickel and copper of 0.9 mg/m2 per year over long periods was found to be dangerous for biological systems of freshwater catchments.     

Indications for changing deposition patterns in central Europe

The German Federal Environmental Agency (Umweltbundesamt) currently runs a network of 17 air pollution monitoring stations in rural areas within the Federal Republic of Germany. Since 1982, daily bulk precipitation samples have been collected and analysed at five of these stations. As no changes in sampling and chemical analysis techniques have been introduced in this time period, an interpretation with respect to trends is possible. An increase in pH is most obvious at Deuselbach in the western part of Germany. It is related to a decrease in sulphate ions. Reduced SO2 emissions in the western part of Europe have resulted in decreasing ambient air concentrations mainly in the western part of Germany, whereas changes in concentrations close to the eastern border of West Germany were not as pronounced. Part of the decrease, however, was a consequence of three mild winters in sequence at the end of the period, with little easterly air flow. Estimated dry deposition fluxes of sulphur at 3 rural stations in West Germany were lower in 1988/1989 compared to 1980-1987 by 44-69%. Wet deposition showed between 8% increase and 25% decrease. The resulting reduction in total sulphur deposition ranged from 17-54%. Deposition via interception of fog droplets was not measured.     

湖南省酸性降水现状、成因及对策研究

本文在对湖南省近十年的降水监测数据进行综合分析的基础上 ,研究了本省酸性降水的污染特征和变化趋势 ,分析了酸雨的成因 ,并提出了防治酸雨污染的对策和建议。     

Air pollution and mortality: A history

Mortality is the most important health effect of ambient air pollution and has been studied the longest. The earliest evidence relates to fog episodes but with the development of more precise methods of investigation it is still possible to discern short-term temporal associations with daily mortality at the historically low levels of air pollution that now exist in most developed countries. Another early observation was that mortality was higher in more polluted areas. This has been confirmed by modern cohort studies that account for other potential explanations for such associations. There does not appear to be a threshold of effect within the ambient range of concentrations. Advances in the understanding of air pollution and mortality have been driven by the combined development of methods and biomedical concepts. The most influential methodological developments have been in time-series techniques and the establishment of large cohort studies, both of which are underpinned by advances in data processing and statistical analysis. On the biomedical side two important developments can be identified. One has been the application of the concept of multifactorial disease causation to explaining how air pollution may affect mortality at low levels and why thresholds are not obvious at the population level. The other has been an increasing understanding of how air pollution may plausibly have pathophysiological effects that are remote from the lung interface with ambient air. Together, these advances have had a profound influence on policies to protect public health. Throughout the history of air pollution epidemiology, mortality studies have been central and this will continue because of the widespread availability of mortality data on a large population scale and the weight that mortality carries in estimating impacts for policy development.     

Ionic composition of wet precipitation over the southern slope of central Himalayas,Nepal

Severe atmospheric pollution transported to Himalayas from South Asia may affect fragile ecosystem and can be harmful for human health in the region. In order to understand the atmospheric chemistry in the southern slope of central Himalayas, where the data is limited, precipitation has been sampled at four sites: Kathmandu (1,314 m), Dhunche (2,065 m), Dimsa (3,078 m), and Gosainkunda (4,417 m) in Nepal for over a 1-year period characterized by an urban, rural, and remote sites, respectively. HCO₃ ^? is the dominant anion, while the NH₄ ⁺ is the dominant cation in precipitation at the four sites. Generally, most of ions (e.g., SO₄ ^2?, NO₃ ^?, NH₄ ⁺, HCO₃ ^?, and Ca²⁺) have higher concentrations in urban site compared to the rural sites. Neutralization factor calculation showed that precipitation in the region is highly neutralized by NH₄ ⁺ and Ca²⁺. Empirical orthogonal function and correlation analysis indicated that the precipitation chemistry was mostly influenced by crustal, anthropogenic, and marine sources in Nepal. Among different sites, urban area was mostly influenced by anthropogenic inputs and crustal dusts, whereas remote sites were mostly from marine and crustal sources. Seasonal variations show higher ionic concentrations during non-monsoon seasons mainly due to limited precipitation amount. On the other hand, lower ionic concentrations were observed during monsoon season when higher amount of precipitation washes out aerosols. Thus, precipitation chemistry from this work can provide a useful database to evaluate atmospheric environment and its impacts on ecosystem in the southern slope of central Himalayas, Nepal.     

Assessment of environmental impact zones in the Kola Peninsula forest ecosystems

This paper describes the condition of forest ecosystems subjected to smelter pollution in the Kola peninsula. This assessment is based on the parameters of the biogeochemical cycle. The defoliation index was used to delimit three basic forest states: background, defoliating, sparse. Close to the smelter, due to expansion of the area not covered by vegetation, a fourth type of state, so-called "industrial deserts", has been observed. The concentrations of sulphur, copper and nickel in the precipitation in the forests generally declined with distance from the smelter. The defoliating forests are noted for the highest Ca, Mg, K concentrations in the summer precipitation. In sparse forests and industrial deserts a decrease in the Ca, Mg, K concentrations in the summer precipitation in comparison with the defoliating forests, despite the particle emissions, could be attributed to the reduction in forest biomass. The higher levels of soil and soil leachate carbon and acidity in the defoliating forests was due to higher litterfall and to the higher dissolution of fulvic acids by the acidic precipitation. This increase in organic matter levels affects soil cation exchange capacity and cation saturation. The pine trees demonstrated significant changes in the uptake of elements in all types of forests under pollution. Elevated levels of S, Ni, Cu and K and reduced levels of Mg, Mn and Zn were found in the needles of different age classes.     

Sampling and physico-chemical analysis of precipitation: a review

Wet deposition is one of two processes governing the transfer of beneficial and toxic chemicals from the atmosphere on to surfaces. Since the early 1970s, numerous investigators have sampled and analyzed precipitation for their chemical constituents, in the context of "acidic rain" and related atmospheric processes. Since then, significant advances have been made in our understanding of how to sample rain, cloud and fog water to preserve their physico-chemical integrity prior to analyses. Since the 1970s large-scale precipitation sampling networks have been in operation to broadly address regional and multi-regional issues. However, in examining the results from such efforts at a site-specific level, concerns have been raised about the accuracy and precision of the information gathered. There is mounting evidence to demonstrate the instability of precipitation samples (e.g. with N species) that have been subjected to prolonged ambient or field conditions. At the present time precipitation sampling procedures allow unrefrigerated or refrigerated collection of wet deposition from individual events, sequential fractions within events, in situ continuous chemical analyses in the field and even sampling of single or individual rain, cloud and fog droplets. Similarly analytical procedures of precipitation composition have advanced from time-consuming methods to rapid and simultaneous analyses of major anions and cations, from bulk samples to single droplets. For example, analytical techniques have evolved from colorimetry to ion chromatography to capillary electrophoresis. Overall, these advances allow a better understanding of heterogeneous reactions and atmospheric pollutant scavenging processes by precipitation. In addition, from an environmental perspective, these advances allow better quantification of semi-labile (e.g. NH4+, frequently its deposition values are underestimated) or labile species [e.g. S (IV)] in precipitation and measurements of toxic chemicals such as Hg and PCBs (polychlorinated biphenyls). Similarly, methods now exist for source-receptor studies, using for example, the characterization of reduced elemental states and/or the use of stable isotopes in precipitation as tracers. Future studies on the relationship between atmospheric deposition and environmental impacts must exploit these advances. This review provides a comprehensive and comparative treatment of the state of the art sampling methods of precipitation and its physico-chemical analysis.     

Concentrations and fluxes of organic compounds in the atmosphere of the Swedish west coast

Measurements of organic compounds in air and deposition have been carried out in parallel on the Swedish west coast. In this investigation the importance of long-range transport for the occurrence of organic compounds in deposition has been studied. Air samples were collected using a high volume sampler (HVS) and the deposition was sampled on a 1 m² Teflon-coated horizontal surface with runoff for the precipitation to an adsorbent. The samples were analyzed in order to identify and quantify different semivolatile compounds such as PAH and petrogenic hydrocarbons and chlorinated compounds such as PCB, HCH and HCB. Qualitative differences between the content of organic compounds in air and deposition during periods with varying levels of air pollution and different meteorological conditions have been studied and a comparison with other air pollutants, such as soot, has been carried out. The results of the measurements show that deposition of PAH and other hydrocarbons takes place continuously but the greatest amounts are measured in the deposition in connection with episodes together with heavy precipitation. The highest concentrations of PCB and HCH in the air were obtained during a warm dry period in May and the greatest amounts were deposited in a period in May with heavy precipitation.     

Heavy metal pollution and forest health in the Ukrainian Carpathians

The Ukrainian Carpathians are characterized by high air pollution caused by emissions from numerous industries. We have been monitoring the state of forests in this region since 1989. The highest levels of tree defoliation (>30%) are found close to industrial emission sources and in the upper mountain forests of the Ivano-Frankivsk and Chernivtsi regions. This is caused by a combination of strong anthropogenic influences (pollution, illegal uses, recreation) as well as poor site and climatic conditions. In the Ivano-Frankivsk region, Cd and Mo accumulate in forest soils; Cr, Mo and Zn soil concentrations are higher than their limit levels; and Pb concentrations exceed toxic levels close to industrial areas (10% of the region territory). Local background levels of heavy metals are greatly exceeded in snow close to industrial regions. Analysis of correlation matrices shows that the chemical elements Ba, Cd, Co, Cr, Cu, Mo, Ni, Pb, V and Zn occur at pollution levels in natural ecosystems in the Ukrainian Carpathians. Maximum concentrations of toxic elements occur in the oak forest zone; the most industrially developed area of the region. Toxic heavy metals in the Ukrainian Carpathians forests enter with precipitation and dustfall, then become fixed in soil and accumulate in leaves, needles of vascular plants and mosses. Concentrations of these metals decrease with altitude: highest in the oak forests, less in beech, and lowest in the spruce forest zones. However, some chemical elements have the highest concentrations in spruce forests; V in needles, As in snow, and Ba and Al in soils.     

UASB-SBR组合工艺处理畜禽养殖废水的研究

近年来,随着中国畜禽养殖业的快速发展,落后的养殖模式和污染防治设施,使畜禽养殖污染日趋严重,畜禽养殖污染已居农业污染源之首,已成为中国环境污染的重要因素,对环境质量乃至人体健康都会产生不良影响。文中采用UASB—SBR组合工艺处理畜禽养殖废水,通过试验探讨SBR反应器启动方法及最佳运行模式,同时研究UASB反应器的启动方法。结果表明,SBR运行的最佳模式为进水0.5 h、反应8 h、沉淀1 h、出水0.5 h、闲置14 h。经过一段时间的启动,UASB和SBR反应器均成功启动,UASB—SBR组合工艺在处理畜禽养殖废水时可获得稳定的处理效果,COD、氨氮、总磷等出水水质均达到《畜禽养殖业污染物排放标准》(GB18596-2001)要求,为畜禽养殖废水处理的工程化应用提供了参考依据。     

Air pollution and forest health: toward new monitoring concepts

It is estimated that 49% of forests (17 million km(2)) will be exposed to damaging concentrations of tropospheric O(3) by 2100. Global forest area at risk from S deposition may reach 5.9 million km(2) by 2050, despite SO(2) emission reductions of 48% in North America and 25% in Europe. Although SO(2) levels have decreased, emissions of NO(x) are little changed, or have increased slightly. In some regions, the molar SO(4)/NO(3) ratio in precipitation has switched from 2/1 to near 1/1 during the past two decades. Coincidentally, pattern shifts in precipitation and temperature are evident. A number of reports suggest that forests are being affected by air pollution. Yet, the extent to which such effects occur is uncertain, despite the efforts dedicated to monitoring forests. Routine monitoring programmes provide a huge amount of data. Yet in many cases, these data do not fit the conceptual and statistical requirements for detecting status and trends of forest health, nor for cause-effect research. There is a clear need for a re-thinking of monitoring strategies.     

沉淀法回收聚苯乙烯泡沫塑料的工艺研究

研究沉淀法回收聚苯乙烯泡沫塑料（EPS）的工艺，利用石油裂解副产物为溶剂回收废旧聚苯乙烯泡沫塑料，以废治废，回收利用。溶剂低毒，对聚苯乙烯泡沫塑料溶解速度快，溶解量大，价廉易得。采用转式间歇投料并附加溶剂挥发分z收装置的工艺，溶剂回收率高，无二次污染，可循环使用。聚苯乙烯塑料（PS）回收率可达99％。     

沉淀法回收聚苯乙烯泡沫塑料的工艺研究

研究沉淀法回收聚苯乙烯泡沫塑料(EPS)的工艺,利用石油裂解副产物为溶剂回收废旧聚苯乙烯泡沫塑料,以废治废,回收利用。溶剂低毒,对聚苯乙烯泡沫塑料溶解速度快,溶解量大,价廉易得。采用转式间歇投料并附加溶剂挥发分回收装置的工艺,溶剂回收率高,无二次污染,可循环使用。聚苯乙烯塑料(PS)回收率可达99%。     

Scale-dependent spatial variability in peatland lead pollution in the southern Pennines, UK

Increasingly, within-site and regional comparisons of peatland lead pollution have been undertaken using the inventory approach. The peatlands of the Peak District, southern Pennines, UK, have received significant atmospheric inputs of lead over the last few hundred years. A multi-core study at three peatland sites in the Peak District demonstrates significant within-site spatial variability in industrial lead pollution. Stochastic simulations reveal that 15 peat cores are required to calculate reliable lead inventories at the within-site and within-region scale for this highly polluted area of the southern Pennines. Within-site variability in lead pollution is dominant at the within-region scale. The study demonstrates that significant errors may be associated with peatland lead inventories at sites where only a single peat core has been used to calculate an inventory. Meaningful comparisons of lead inventories at the regional or global scale can only be made if the within-site variability of lead pollution has been quantified reliably.     

Why Industry Needs Performance Standard Zoning

The trend toward increased use of central refuse incinerators is inevitably contributing to urban air pollution. Eventually sampling ports, emission sensing and recording equipment will be required; and more detailed data will be available. But, tradilionally, discharges have been estimated by means of emission factors for nominal design loadings. Such estimates may be unreliable, especially under highly variable processing rates.

Preliminary evidence suggests lhat actual emission factors are higher when the incinerator is charged at greater rates, and vice versa. Observations at the Boston municipal incinerator indicate considerable day-to-day variability in refuse loading. No measurements of emissions are made, but daily input loading records for several years are available.

This study focuses upon the variability in daily loadings. Several functions relating emission factors to charging rates are assumed in order to estimate variability in discharges to the atmosphere. Four years of daily records were analyzed for day-of-week and seasonal components, as well as secular trends. Further analysis suggested that some of the remaining variation in observations could be explained in connection with holidays and precipitation.

The implications of conventionally designed holding pits and charging policies on air pollution problems are discussed in view of such variability, and alternatives are suggested.     

Methyl tert-butyl ether (MTBE) in urban and rural precipitation in Germany

The use of the oxygenate methyl tert-butyl ether (MTBE) in gasoline has led to detectable concentrations in urban and rural air up to 160 ppbV. Results from MTBE measurement in precipitation have not been reported so far. In the present study, 120 samples of precipitation collected at 17 sampling locations all over Germany have been analyzed for their MTBE content. Analysis is performed by a combination of headspace-solid-phase microextraction (HS-SPME) and gas chromatography/mass spectrometry (GC-MS). A 75 μm poly(dimethylsiloxane)/Carboxene fiber and a cryostat is used for SPME. The detection limit is 10 ng/l. In precipitation samples, MTBE was detected in wintertimes only with a maximum concentration of 85 ng/l. Measurement at Frankfurt/M City from 6 September 2000 to 12 March 2001 provided for 49% of the data concentrations in the range of 30–85 ng/l (n=17). Sampling in winter 2000/2001 at several German cities and rural locations showed that MTBE is more often detectable in urban (86%, n=78) than in rural (18%, n=42) precipitation. By comparing the results with corresponding temperatures and amounts of precipitation it can be concluded that the detection of MTBE in urban precipitation is observed at ambient temperatures lower than about 10–15°C. Moreover, the first precipitation after a dry period accumulates more MTBE than precipitation during or at the end of a wet period (wash-out effect). Highest concentrations occurred in snow samples. Corresponding mean air equilibrium concentrations of 0.04 ppbV (urban samples) and 0.01 ppbV (rural samples) are calculated. This is about one magnitude lower than year round and summertime measurements in the US and in Switzerland. Urban runoff (n=12) and corresponding precipitation sampling indicate that urban runoff might be composed of about 20% MTBE that is already transported by air and precipitation, whereas about 80% may be attributed to direct uptake of vehicle emissions and leakage near the road during precipitation.