Mercury in fish in Swedish lakes

The aim of this work has been to try to obtain a picture of the past, present and future mercury situation in fish in Swedish lakes, to make an estimate of the number of lakes threatened by 'blacklisting', and to see if the data can be used to reveal anything about the impact of liming on the Hg content in pike. The register contains a broad set of data from 1456 lakes. The main results are as follows. Trend analyses indicate that the Hg content in 1-kg pike seems to increase with time. This is interesting since there has been a significant decrease in mercury emissions from Swedish industries during the last two decades. High Hg contents in 1-kg pike appear in a very characteristic pattern, linked to specific sources of Hg emission. The data indicate that old Swedish 'sins' are still causing a lot of problems. The factors governing the leakage of Hg from soils to water ought to be a very important topic for further studies. The Hg content in pike shows the highest correlation with the following parameters: Hg in surficial sediments, pH, distance from point source and water hardness, lake water alkalinity and conductivity, water retention time, size of drainage area and lake surface. A formula which provides the best possible degree of explanation (r2 = 0.78) has been derived. At present there are about 250 lakes 'blacklisted' in Sweden due to high Hg content in fish. Our data show that there are at least 9400 lakes that ought to be 'blacklisted' today. A successful liming operation will alter the chemical conditions in lakes and also decrease the Hg content in fish.     

Pesticide levels in surface waters in an agricultural-forestry basin in Southern Chile

Residues of five pesticides in surface water were surveyed during 2001 and 2003 in the Traiguen river basin in Southern Chile. Simazine, hexazinone, 2,4-D, picloram herbicides and carbendazim fungicide were selected through a pesticide risk classification index. Six sampling stations along the river were set up based on agricultural and forestry land use. The water sampling was carried out before and after the pesticide application periods and in correspondence to some rain events. Pesticides were analyzed by HPLC with DAD detection in a multiresidue analysis. During 2001, in the first sampling campaign (March), the highest concentrations of pesticides were 3.0 microg l(-1) for simazine and hexazinone and 1.8 microg l(-1) for carbendazim. In the second sampling (September), the highest concentration were 9.7 microg l(-1) for 2,4-D, 0.3 microg l(-1) for picloram and 0.4 microg l(-1) for carbendazim. In the last sampling period (December), samples indicated contamination with carbendazim fungicide at levels of up to 1.2 microg l(-1). In sampling carried out on May 2003, no pesticides were detected. In October 2003, the highest concentrations of pesticides were 4.5 microg l(-1) for carbendazim and 2.9 microg l(-1) for 2,4-D. Data are discussed in function of land use and application periods of the products, showing a clear seasonal pattern pollution in the Traiguen river. Risk assessment for these pesticides was calculated by using a risk quotient (RQ = PNEC/PEC). For picloram the calculated RQ < was 0, which indicates that no adverse effects may occur due to the exposure to this herbicide in the Traiguen river basin. For 2,4-D, simazine, hexazinone, carbendazim RQ > 1, meaning that adverse effects could occur and it is necessary to reduce pesticide exposure in surface waters. It is recommended to continue with a pesticide monitoring program and the implementation of ecotoxicological testing with local and standardized species in order to consider the probability of effects occurrence, with less uncertainty. Thus, it will be more feasible to make some recommendations to regulatory agencies regarding the pesticide use.     

Large-scale spatial variation in mercury concentrations in cattle in NW Spain

Mercury (Hg) is a highly toxic environmental contaminant and man-made emissions account for between a quarter and a third of total atmospheric levels. Point discharges, particularly coal-burning power stations, are major sources of atmospheric Hg and can result in marked spatial variation in mercury deposition and subsequent uptake by biota. The aims of this study were to quantify the extent to which major point and diffuse sources of atmospheric Hg emissions affected accumulation of Hg by biota throughout Galicia and Asturias, two of the major regions in northwest Spain. We did this by relating renal Hg concentrations in locally reared cattle (n=284) to the proximity of animals to point and diffuse sources of Hg emissions. Mercury residues in calf kidneys ranged between non-detected and 89.4 g/kg wet weight. Point discharges from coal-fired power plants in Galicia had the most dominant impact on Hg accumulation by calves in Galicia, affecting animals throughout the region and explaining some two-thirds of the variation in renal residues between animals located directly downwind from the plants. The effects of more diffuse emission sources on Hg accumulation in calves were not distinguishable in Galicia but were detected in cattle from neighbouring Asturias. The impact of both point and diffuse sources in elevating environmental levels of bioavailable Hg and subsequent accumulation by cattle extended to approximately 140-200 km downwind from source.     

基因芯片在环境毒理学研究中的应用进展

基因芯片可以将大量的DNA信息集成到 1cm2 左右的芯片上 ,对生命信息具有大规模平行处理的能力 ,为环境毒理学研究提供了一个理想的平台。基因芯片可以精确地完成污染物对人类基因表达影响的分析 ,并对污染物进行分类与分级 ,筛选毒物靶标和确定毒性机理。本文描述了基因芯片技术、毒理学应用研究现状及应用前景。引用文献 2 9篇。     

Evaluation and in situ assessment of photodegradation of polyaromatic hydrocarbons in semipermeable membrane devices deployed in ocean water

Semipermeable membrane devices (SPMDs) were deployed in water using four different methods: a typical SPMD cage with and without a mesh cover, a bowl chamber and without any protection. In addition to routinely used performance reference compounds (PRCs), perdeuterated dibenz[a,h]anthracene was added. Due to its high sampler to water partition coefficient no measurable clearance due to diffusion was expected during the deployment period, hence any observed loss could be attributed to photodegradation. The loss of PRCs was measured and SPMD-based water concentrations determined. Results showed that a typical SPMD deployment cage covered with mesh provided the best protection from photodegradation. Samplers which had undergone the highest photodegradation underestimated PAH water concentrations by up to a factor of 5 compared to the most protected SPMDs. This study demonstrates that the potential for photodegradation needs to be addressed when samplers are deployed in water of low turbidity.     

Trends in summer sulphate in Europe

A trend analysis of the sulphate concentration in Europe in the summer half-year was performed. Data from various measuring networks were analysed, but only stations with quality assured sampling methods and a record of more than 10 years were included in the study. 1978 served as the reference year for the trend, because in that year most stations started operation. The relatively dense network in Belgium provided the most valuable data, as evidenced by the fact that two sites at a distance of only 10 km apart correlated better than 95% over a month. The two sites also show a correlation of better than 90% over a season with two other stations at distances of 45 and 95 km. The relative decrease in summer-sulphate at the four stations in Belgium, as analysed by linear regression, was 3.3% per year which corresponds to an absolute decrease of 0.42 μgm⁻³ per year. In the Netherlands the average yearly decrease in summer-sulphate at two stations was 3.5% (−0.34 μgm⁻³). In other countries stations were further apart or only a single site wits in use, which limits the representativeness of the data. In northwestern Germany, a region with several monitoring stations, a yearly averaged decrease of 3.0% occurred. The lower absolute decrease (0.25 μgm⁻³) per year compared to that in the two neighbouring countries reflects the lower summer-time sulphate concentrations. In the remainder of Germany the average decrease was 1.6%. In South-Scandinavia the yearly relative decrease at two sites was 2.6% (0.13 μgm⁻³ absolute). There was no significant trend in the U.K. Al the Polish station the levels increased, it decreased at the Hungarian and Austrian station and remained constant at the Czechoslovakian site. Reasons for omission of the data from France from the trend analysis are discussed.     

城市污水管网对水质的生化改善特性

研究建立了一套长1 200 m的城市污水模拟管网,分析研究了城市污水管网对水质的生化改善特性。研究表明,污水经过1 200 m管网输送后,水中TCOD、NO3--N和NH3-N含量均发生了变化,其中TCOD、NO3--N含量分别由292~420 mg·L-1、0.26~0.6 mg·L-1降低至205~315 mg·L-1、0.13~0.29 mg·L-1,NH3-N含量由31~50 mg·L-1上升为35~66 mg·L-1。采用三维荧光分析了水中有机物的变化情况,结果表明,蛋白质及腐殖质的含量均沿程减少,而蛋白质发生了蓝移,腐殖质则发生了红移,表明其物质的化学结构发生了改变。结合有机物的分子量分析可知污水中高分子量(蛋白质等)及部分中等分子量有机物(腐殖质)向小分子量有机物(乙酸等)转化。进一步的研究表明,管网中微生物改变了水中有机物的构成,将不饱和性有机物转变为易于生物利用的饱和性物质,从而提高了污水的生化性。     

Air distribution in the Borden aquifer during in situ air sparging

A field experiment was conducted at Canadian Forces Base Borden (CFB Borden) to assess the air distribution from a single in situ air sparging injection point. This aquifer consists of fine to medium sand deposited in horizontal layers. The permeability at the study location varied from 10(-10) to 10(-14) m2 and distinct low permeability horizons were present at approximately 1.2, 2.0, and 2.9 m below the water table. Prior to air injection, a 15x15-m portion of the vadose zone was excavated to the water table (approximately 1 m below ground surface) in order to visually observe air release distribution at the water table. The water table was actively maintained 5 cm above the excavated surface. The sparging system operated for a period of 7 days with an injection flow rate of 200 m3/days (5 scfm). The resulting subsurface air distribution was assessed using a variety of techniques including neutron logging, borehole and surface ground penetrating radar, piezometric head measurements, surface visualization, and hydraulic testing. Through this combination of tests, it was demonstrated that variations in permeability and, hence, capillary pressure at the site were sufficient to cause the injected air to spread laterally, forming stratigraphically trapped air pockets beneath the low permeability horizons. The formation of these air pockets eventually resulted in a buildup of capillary pressure that exceeded the air entry pressure and allowed some air to migrate up through the lower permeability layers. Each of the assessment techniques employed generated information at different spatial scales that prevented a direct comparison of the results from the various techniques; however, the results from all techniques proved to be critical in the interpretation of the experimental data. As a consequence, the different assessment techniques should not be viewed as alternatives, but rather as complimentary techniques.     

Response types in Collembola towards copper in the microenvironment

Laboratory studies were carried out to cast light on differences in density responses among collembolan species to copper (Cu)-polluted environments. In a recolonisation experiment, mesofauna originating from a copper (Cupolluted arable field were allowed to colonise defaunated Cu-contaminated and uncontaminated soil cores for 3 months. The abundances of Pseudosinella alba and gamasid mites were higher in the uncontaminated soil, whereas the majority of other collembolans tended to be more abundant in the Cu-enriched soil. Behavioural experiments were conducted to test the ability of single Collembola species to distinguish between filter paper and food soaked in water, Cu, and calcium (Ca) solutions. Onychiurus armatus avoided both Cu and Ca, whereas Folsomia quadrioculata and Folsomia manolachei showed a significant preference for Cu. Isotomurus palustris was not able to distinguish between Cu and water. The results are compared and discussed with regard to other studies on the occurrence and behaviour of Collembola in Cu-contaminated environments. We suggest that microsite selection according to preference or avoidance of high salinity of pore water may partly explain the community structure of Collembola in Cu-polluted soils which are characterised by an increase of euedaphic species. More studies have to be carried out to generalise this concept and to explore to what extent reduced predation by gamasid mites contribute to the success of certain Collembola in Cu-contaminated sites.     

Comparison of in vitro and in vivo acute fish toxicity in relation to toxicant mode of action

Acute toxicity to fish hepatoma cell line PLHC-1 and to juvenile rainbow trout was examined for 18 plant protection products. The main objective was to explore whether hepatoma cells could be used to predict acute toxicity in fish taking into account the mode of toxic action and compound properties. Acute fish toxicity was determined using the OECD guideline test 203 and compared to predicted baseline LC50 of acute fish toxicity calculated with a quantitative structure-activity relationship (QSAR) derived for guppy fish. Cytotoxicity was determined through the inhibition of neutral red uptake (NR(50)) into lysosomes and compared to predicted baseline cytotoxicity derived for goldfish GFS cells. In general, NR50 values were higher by a factor ranging from 3 to 3000 than the corresponding acute LC50. A weak correlation between NR50 and LC50 values was found (log/log: r2=0.62). Also the lipophilicity (log K(ow)) was not a good predictor for cytotoxicity (r2=0.43) and lethality (r2=0.57) of these pesticides. The neutral red assay is detecting general baseline toxicity only. Comparing LC50 data to QSAR results, the compounds can be classified to act as narcotics or reactive compounds with a specific mode of toxic action in fish. The results indicate that limitation of the neutral red assay in predicting acute fish toxicity. A promising alternative might be the assessment of toxicity in a set of in vitro systems addressing also cell-specific functions which are related to the mode of toxic action of the compound.     

Response to heavy nitrogen applications in fertilizer experiments in British forests

Increasing concern over the level of nitrogen inputs to forests in polluted rain has led to a number of suggestions of possible adverse consequences under the general heading of nitrogen saturation. A saturated ecosystem may be one (a) in which the trees show no growth response to the addition of further nitrogen, (b) in which addition of further nitrogen leads to growth disturbances or reduction, or (c) in which elevated nitrogen inputs lead to increased losses of nitrate in streamwater. Experience gained from forest fertilizer experiments is used to examine each of these suggestions. A definition involving a lack of growth response (a) is shown to be based on a lack of understanding of the continuing changing patterns of nitrogen demand and mineralization in even-aged forests. Similarly, using growth disturbances (b) is unsatisfactory because, it is suggested, these are either secondary deficiencies that appear once growth accelerates with added nitrogen or are a consequence of changing growth with increasing size. A definition based on increased loss of nitrate is, by analogy with the situation for sulphate, at least superficially attractive. However, the fact that nitrate retention is predominantly biological, rather than chemical, makes for difficulties and the limited evidence available suggests that many exceptions and variations may exist. Whilst experience with forest fertilizers might not be entirely apposite, for example foliar uptake from polluted rain may be a factor, it is urged that at least any hypothesis put forward should be compatible with information gained from fertilizer trials.     

Changes in concentration levels of selected VOCs in newly erected and remodelled building in Gdansk

Volatile organic compounds such as benzene, toluene, butyl acetate, ethylbenzene, m-xylene, styrene and m-dichlorobenzene were measured in three newly erected and remodelled dwellings. The present study also attempted to examine the time dependence of concentrations of selected VOCs in each investigated dwelling. This was accomplished by at least triplicate measurements of the IAQ. To collect a series of air samples the active and passive methods were used. In both cases activated charcoal was applied as a sorption medium. The samples were recovered by solvent extraction, and analysed by capillary column gas chromatography, employing a flame ionisation detector. The experimental results showed that MAC values for analysed VOCs were exceeded (even a few orders of magnitude) for the measurements made before inhabiting of the occupants, in every investigated dwelling. The concentrations of the investigated VOCs decreased significantly with time, which should be expected, although in some cases the levels of selected VOCs remained still high. Our experience indicates that parallel application of two different indoor air sampling techniques to determine analytes of interest, though more laborious and time consuming, can lead to significant conclusions concerning indoor air quality in monitored spaces.     

Characteristics of indoor aerosols in residential homes in urban locations: a case study in Singapore

As part of a major study to investigate the indoor air quality in residential houses in Singapore, intensive aerosol measurements were made in an apartment in a multistory building for several consecutive days in 2004. The purpose of this work was to identify the major indoor sources of fine airborne particles and to assess their impact on indoor air quality for a typical residential home in an urban area in a densely populated country. Particle number and mass concentrations were measured in three rooms of the home using a real-time particle counter and a low-volume particulate sampler, respectively. Particle number concentrations were found to be elevated on several occasions during the measurements. All of the events of elevated particle concentrations were linked to indoor activities based on house occupant log entries. This enabled identification of the indoor sources that contributed to indoor particle concentrations. Activities such as cooking elevated particle number concentrations < or =2.05 x 10(5) particles/cm3. The fine particles collected on Teflon filter substrates were analyzed for selected ions, trace elements, and metals, as well as elemental and organic carbon (OC) contents. To compare the quality of air between the indoors of the home and the outdoors, measurements were also made outside the home to obtain outdoor samples. The chemical composition of both outdoor and indoor particles was determined. Indoor/outdoor (I/O) ratios suggest that certain chemical constituents of indoor particles, such as chloride, sodium, aluminum, cobalt, copper, iron, manganese, titanium, vanadium, zinc, and elemental carbon, were derived through migration of outdoor particles (I/O <1 or - 1), whereas the levels of others, such as nitrite, nitrate, sulfate, ammonium, cadmium, chromium, nickel, lead, and OC, were largely influenced by the presence of indoor sources (I/O >1).     

Targeting lead in the multimedia environment in the continental United States

The U.S. Environmental Protection Agency's (EPA) lead attainment strategy for air is being expanded to address geographic areas with the potential for multimedia, multipathway exposures to lead. Geographic Information Systems (GIS) technology is used to coordinate information from various databases to identify areas of potential concern. The data retrieval and decision processes used in identifying priority sources from each medium and in evaluating identified areas of concern are described in this paper. Only EPA databases with reliable locational information were used to facilitate accurate mapping and allow correlation with other data sources. The sources of lead loadings to air, water, and soils were mapped using either latitude and longitude or zip code, or county centroids for data lacking longitudinal and latitudinal coordinates (such as the drinking water data). A multimedia cluster of lead sources was identified at the county level, since all the facility data in the five databases could be mapped to this level. An impact factor and weighting system was devised to combine the information on the number of facilities and their relative size in developing a ranking of the multimedia lead clusters of concern in each region. The counties with the highest number of points were considered clusters of highest concern for multimedia lead sources. Two separate lists of the clusters were developed according to a point system. One identified 10 multimedia lead clusters in each of the 10 EPA regions, and the other identified the 100 clusters of highest concern in the country as a whole. The project is designed to be a first step in targeting future efforts to identify potential environmental problems associated with lead. The analyses presented in this paper provide a first look at the areas in the country where there is a potential for multimedia exposure to lead. A more refined analysis at the zip code level was subsequently developed to provide a good understanding of the issues pertaining to potential exposure at the neighborhood level. The results of this analysis will ultimately help the EPA and the states to target implementation and enforcement in areas of high potential lead exposures.     

Polychlorinated biphenyl residues in sandstorm depositions in Beijing, China

Sandstorms, which distribute many particles, are a special atmospheric occurrence and are frequent in northern China. We conducted this study to determine, for the first time, the concentration of polychlorinated biphenyls (PCBs) in sandstorm depositions. We collected 13 samples from urban areas of Beijing, and we measured a total of 144 PCB congeners. Thirteen samples all contained PCB residues. The total PCB concentration ranged from 1.6 to 15.6ngg(-1) (median, 4.8ngg(-1), dry weight), with trichlorinated biphenyls as the predominant homologue (>50.4%). Furthermore, we observed increasing PCB contamination from northwest to east Beijing. We later explored possible factors affecting contamination of the sandstorm depositions, which revealed a significant correlation between SigmaPCBs and the minimum particle size of the sandstorm deposition samples. Principal-component analysis revealed that the major source of PCBs in Beijing may be potentially associated with the number-one commercial PCB through the long-range transmission. In previous results, PCBs were not a severe component of contamination in sandstorm depositions of Beijing. However, this study suggested that sandstorm deposition may be a potential source of exposure to PCBs for the residents of Beijing, China.     

Pesticides in rainfall in Europe

Papers and published reports investigating the presence of pesticides in rainfall in Europe were reviewed. Approximately half of the compounds that were analysed for were detected. For those detected, most concentrations were below about 100 ng/l, but larger concentrations, up to a few thousand nanograms per litre, were detected occasionally at most monitoring sites. The most frequently detected compounds were lindane (gamma-HCH) and its isomer (alpha-HCH), which were detected on 90-100% of sampling occasions at most of the sites where they were monitored. For compounds developed more recently, detection was usually limited to the spraying season. A classification of pesticides according to their deposition pattern is proposed.     

Characteristics of Indoor Aerosols in Residential Homes in Urban Locations: A Case Study in Singapore

Abstract

As part of a major study to investigate the indoor air quality in residential houses in Singapore, intensive aerosol measurements were made in an apartment in a multistory building for several consecutive days in 2004. The purpose of this work was to identify the major indoor sources of fine airborne particles and to assess their impact on indoor air quality for a typical residential home in an urban area in a densely populated country. Particle number and mass concentrations were measured in three rooms of the home using a real-time particle counter and a low-volume particulate sampler, respectively. Particle number concentrations were found to be elevated on several occasions during the measurements. All of the events of elevated particle concentrations were linked to indoor activities based on house occupant log entries. This enabled identification of the indoor sources that contributed to indoor particle concentrations. Activities such as cooking elevated particle number concentrations ≤2.05 × 10⁵ particles/cm³. The fine particles collected on Teflon filter substrates were analyzed for selected ions, trace elements, and metals, as well as elemental and organic carbon (OC) contents. To compare the quality of air between the indoors of the home and the outdoors, measurements were also made outside the home to obtain outdoor samples. The chemical composition of both outdoor and indoor particles was determined. Indoor/outdoor (I/O) ratios suggest that certain chemical constituents of indoor particles, such as chloride, sodium, aluminum, cobalt, copper, iron, manganese, titanium, vanadium, zinc, and elemental carbon, were derived through migration of outdoor particles (I/O<1 or ≈1), whereas the levels of others, such as nitrite, nitrate, sul-fate, ammonium, cadmium, chromium, nickel, lead, and OC, were largely influenced by the presence of indoor sources (I/O >1).     

Colloid migration in symmetrical non-uniform fractures: particle tracking in three dimensions

A three-dimensional model for the migration of colloids in a saturated fracture is presented, which considers the motion of colloids as a result of advection and diffusion, as well as colloid-surface interactions at the fracture walls. This model is successfully incorporated into a three-dimensional particle tracking algorithm that tracks particles within a continuum and allows consideration of the migration of colloids in symmetrical, three-dimensional, non-uniform fractures. The framework is general enough to incorporate non-local interactions that provide colloid motion relative to the fluid. The algorithm is verified against classical Taylor dispersion, and its generalization to a sorbing phase, in a uniform fracture and shows excellent agreement with theory. A simple, non-uniform fracture that has an analytically tractable velocity field is also considered, and both quantitative and qualitative comparisons are made with the uniform fracture case. The modelling of more complex fracture geometries is also discussed and a particular case is implemented within the particle tracking framework.     

Bioaccumulation of decamethylcyclopentasiloxane in perch in Swedish lakes

Decamethylcyclopentasiloxane (D5), a high production volume chemical used in personal care products, enters the environment both via air and sewage treatment plant (STP) recipients. It has been found in fish, and there is concern that it may be a bioaccumulative substance. In this work D5 was analyzed in perch from six Swedish lakes that did not receive STP effluent, and in perch and sediment from six lakes that received STP effluent. In the lakes receiving the STP effluent, the D5 concentrations in sediment varied over three orders of magnitude and were correlated with the number of persons connected to the STP normalized to the surface area of the receiving body. In the lakes not receiving effluent, the D5 levels in perch were all below the LOQ, while D5 was above the LOQ in almost all perch from lakes that received effluent. The D5 concentrations in perch and sediment from the lakes receiving STP effluent were correlated. This shows that STP effluent is a much more important source of D5 to aquatic ecosystems than atmospheric deposition, and that the risk of adverse effects of D5 on aquatic life will be greatest in small recipients receiving large amounts of STP effluent. The bioaccumulation of D5 was compared to that of PCB 180 on the basis of multimedia bioaccumulation factors (mmBAFs), which describe the fraction of the contaminant present in the whole aquatic environment (i.e. water and surface sediment) that is transferred to the fish. In four of the six lakes the mmBAF of D5 was >0.3 of the mmBAF of PCB 180. Given that PCB 180 is a known highly bioaccumulative chemical, this indicates that the bioaccumulation of D5 in perch is considerable.     

Relation between lead in air and in petrol in two urban areas of Britain

The recent reduction in the lead content of petrol in the United Kingdom, following government legislation, has been used to investigate the relationship between lead in petrol and in outside air in urban environments. In parts of London and Manchester, the airborne lead concentration closely followed the petrol lead concentration, within a time resolution of about 1 month. These results indicate that, in these areas, the petrol lead content has a fairly direct and prompt effect on the urban air lead concentration, i.e. any environmental lead reservoirs in the pathway from petrol to air (and hence to man by inhalation) are not significant on this timescale. A small component of the airborne lead, apparently independent of the petrol lead, was also observed.