Impacts of Pollution from Different Sources on Ecological Quality of a Multiple-use Coast

Investigation of pollution sources and their impacts on ecosystems is important, not only for better understanding the responses of an ecosystem to pollutants, but also for making practicable prevention and control plans. In this study, ecological quality of three areas which received different source pollutants in Shanghai coast were evaluated and compared in four seasons using Shannon–Wiener index (H′), a benthic diversity index as an indicator of ecological quality of coastal waters. The genotoxicity and physical-chemical variables of water samples were also analyzed. The H′ value indicated the ecological quality of Shanghai coastal waters was seriously impacted, and the ecological quality of two areas receiving waste discharges were significantly worse than that of the natural protection zone but not significantly different in four seasons. The positive genotoxic response was detected in most samples from two discharge zones but not detected in the samples from the natural protection zone. However, no significant difference was observed in water quality variables in the different coastal areas. Our study suggested that the point source pollution had significantly contributed to the genotoxicity of the coastal waters and impaired benthic assemblages, while the deterioration of ecological quality status was also critically impacted by the stressors from other sources.     

Quantitative evaluation of elbe river-derived organic marker compounds in sediment samples from the german bight

Background, Goal and Scope  A large share of anthropogenic contamination of the coastal zone is a result of riverine contributions. Accordingly, the pollution of North Sea estuaries and coastal areas by organic xenobiotics is dominantly characterized by land-derived contamination. In a previous study, we identified a high number of organic contaminants in sediments of the German Bight emitted by industrial and municipal sources, primarily as a result of riverine contributions. Furthermore, a group of contaminants was identified representing Elbe-specific marker compounds. However, quantitative analyses are more adequate to describe the source specificity via the spatial distribution as compared to qualitative analyses. Hence, in the present investigation, the determination of various anthropogenic contaminants has been performed in order to evaluate the proposed Elbe-specific marker compounds. Methods  Numerous anthropogenic contaminants were quantified in seven surface sediment samples from the German Bight by means of gas chromatographic — mass spectrometric analyses. The analytical procedure includes extraction, reI moval of sulphur, fractionation, concentration and addition of internal standard. Results and Discussion  Two groups of Elbe-derived contaminants were differentiated. Substances of the first group appear only at sampling locations directly influenced by the Elbe river and include hexachlorobutadiene and alkylsulfonic acid phenyl esters. The second group consists of compounds, which occur additionally in minor concentrations at sites situated at a greater distance from the coastal area, which are therefore only influenced to a minor-degree by the Elbe river. However, their spatial and quantitative distribution characterizes them clearly as Elbe river-derived components. Compounds of the second group are tetra- to hexachlorinated benzenes, mono- and disubstituted chloronaphthalenes, tetrabutyltin, 4,4’-dichlorodiphenylsulfide and DDT related compounds In order to discern the discussed Elbe marker compounds from non-marker substances, several nonspecific contaminants were analyzed additionally. These contaminants include galaxolide, tonalide, tri-n-butylphosphate, 2,4,4-trimethylpentane-l,3-dioldi-iso-butyrate and 2,2,4,4,6,8,8-heptamethylnonane. No significant accumulation of these compounds was observed at sampling locations mainly influenced by either the Elbe river, or the Ems and Weser rivers. Conclusions  For the evaluation of the proposed Elbe marker compounds, the quantitative and spatial distribution was investigated and successfully discussed as the most important criterion to define their source specificity. Generally, these results illustrate how quantitative data on source-specific organic contaminants and the corresponding spatial distribution can be used to trace individual riverine contributions to the pollution of coastal areas. This approach might be especially useful to differentiate the contribution of several rivers discharging close together into the marine environment. Fingerprinting, the individual riverine contribution additionally allows one to quantify the individual, river-derived contamination. Subsequently, the level of coastal zone contaminations can be reduced more effectively. Further comprehensive analyses on numerous coastal and estuarine areas have to be done to support this approach.     

An integrative method to quantify contaminant fluxes in the groundwater of urban areas

Background, Aims, and Scope  Groundwater in urban areas is often contaminated and emission sources can be located close to groundwater wells. The delineation of contaminant plumes is difficult because of the various potential emission sources. Thus, detection, quantification and remediation of contaminated sites in a city need more integrative approaches. Methods  A method has been developed which allows quantification of mass fluxes of contaminants in groundwater between control planes. Budget zones along the flow path are defined to calculate a contaminant balance and to quantitatively reveal input areas. Concentrations and water budgets are used to calculate mass balances for each contaminant. The city of Darmstadt (Germany) was chosen to evaluate the method. Results  The groundwater monitoring wells (GMWs) upstream of the city showed anthropogenically superposed background values for all naturally occurring inorganic species. The contaminant concentrations increased in the city (probably influenced by road traffic, gas stations, leaking sewers, etc.). Downstream from the city, concentrations usually decreased. Organic compounds typical for urban environments, such as polycyclic aromatic hydrocarbons (PAH), locally exceeded drinking water regulations. In GMWs with high concentrations of organic contaminants in the city or downstream from industrial areas, a significant increase in Fe²⁺ and Mn²⁺ could be observed, in some cases coinciding with a decrease in NO₃, SO₄ and an increase in NH₄. Discussion  For typical urban contaminants, a positive budget was calculated in several zones, which shows that emissions from urban sources are reaching the groundwater. Negative budgets can be mainly explained with diving plumes and degradation. The input calculated from the individual budget zones is usually higher than the input estimated from urban emissions. Differences between the calculated and the estimated input can be explained with additional sources or (bio)degradation processes. Conclusions  It was confirmed that high concentrations of contaminants do not necessarily correlate with high fluxes. Integrative approaches can reveal areas of high contaminant mass input. The results obtained with the new method are plausible compared to the land use and the estimated urban input. The concentration pattern of Fe²⁺, Mn²⁺, SO₄ and NO₃ is partly due to natural processes, triggered by the degradation of organic matter and organic contaminants. Recommendations  Since this method includes mass balances and flux calculations, avoiding an overestimation of single point contaminant concentration, it is recommended to use this approach to quantify groundwater contamination in cities. Further research is focusing on the role of urban soils as natural reservoirs for the input of contaminants.     

Sediments as Archives of Industrialisation: Evidence of Atmospheric Pollution in Coastal Wetlands of Southern Sydney,Australia

The history of heavy metal pollution in southern Sydney was reconstructed from wetland sediments using chemical analysis. Seven wetlands along the Pacific coast were examined for present day concentrations of acid-extractable Cd, Cu, Fe, Pb and Zn. Additionally, four of these sites were cored in order to assess past levels of these metal contaminants, changes in organic content and magnetic susceptibility variations. The low nutrient status and closed catchments of the study sites suggested that the pollutants were predominantly derived from atmospheric sources. Surficial sediments were enriched with Cd, Cu, Fe, Pb and Zn levels 5.0, 16.4, 22.7, 8.2 and 22.5 times baseline levels, respectively. In some cases, the concentrations of trace metals were in excess of environmentally acceptable levels. The results show a strong spatial association between sources and levels of pollutants, and the increase in metals levels in sedimentary records corresponds well to documentary historical evidence.This study demonstrates the utility of coastal wetlands in the reconstruction of atmospheric pollution histories, and their particular vulnerability to contamination from airborne pollutants in urban areas.     

Redistribution of organic pollutants in river sediments and alluvial soils related to major floods

Background, Aims, and Scope  More frequent occurrence of stronger floods in Europe as well as in other parts of the world in recent years raises major concern about the material damages, but also an important issue of contamination of the affected areas through flooding. The effects of major floods on levels and distribution of contamination with hydrophobic organic pollutants were examined from the continuous set of data for floodplain soils and sediments from a model industrial area in the Czech Republic where a 100-year flood occurred in 1997. The goal of this study was to evaluate the risk related to contamination associated with such extensive natural events and characterize the spatial and temporal distribution and dynamics of pollutants related to a major flooding shortly after the floods and also in the time period several years after floods. Methods  Sediments and alluvial soils from fourteen sites each were repeatedly sampled during the period from 1996 until 2005. The sampling sites represented five regions. Collected top-layer sediment and soil samples were characterized and analyzed for hydrophobic organic pollutants PCBs, OCPs and HCB using GC-ECD and PAHs using a GC-MS instrument. Spatial and temporal differences as well as the relative distribution of the pollutants were examined in detail by statistical analysis including multivariate methods with special emphases placed on the changes related to floods. Results  The organic pollutants levels in both alluvial soils and sediments exceeded the safe environmental limits at numerous sites. Pollutants concentrations and relative distribution as well as organic carbon content in both sediment and floodplain soils were significantly affected by the flooding, which resulted in a decrease of all studied contaminants in sediments and significant rise of the PAH pollution in the flooded soils. There was a unique and highly conserved PAH pattern in soils regardless of the floods and greater changes in PAH pattern in sediments related to floods. The relative distribution of individual PAHs reflected a combustion generated PAH profile. PAH levels in the river sediments rose again at the sites with continuous sources several years after floods. Discussion  The results showed different dynamics of PAHs and PCBs during the floods when PAHs were redistributed from the sediments to alluvial soils while PCBs have been washed out of the study regions. The data reveal longer contamination memory and consistent contamination pattern in soils, whereas sediments showed more dynamic changes responding strongly to the actual situation. The stable PAH pattern within the regions also indicates that a relative amount of all compounds is comparable across the samples and, thus, that the sources at different sites have similar character. Conclusions  Sediments have the potential to function as a secondary source of contamination for the aquatic ecosystem, but also for the floodplain soils and other flooded areas. The floods served as a vector of PAHs contamination from sediments to soils. The reloading of river sediments in time, namely with PAHs, due to present sources increases their risk as a potential source in the next bigger flood event both to the downstream river basin and affected alluvial soils. Recommendations and Perspectives  The results stress the importance of including the floodplain soil contamination in the risk assessment focused on flood effects. Floodplain soils have stable long-term environmental memory related to contamination levels, pattern and distribution, whereby they can provide relevant information on the overall contamination of the area. The sediments will continue to serve as a potential source of contaminants and alluvial soils as the catchment media reflecting the major flood events, especially until effective measures are taken to limit contamination sources. ESS-Submission Editor: Dr. Henner Hollert (Hollert@uni-heidelberg.de) This article is openly accessible!     

Best management practices for storm water at industrial facilities

Contaminated storm water runoff has been identified as a significant source of degradation to our nation's waterways. Industrial and construction activities are primary sources of this contamination. After identifying this problem, Congress passed the Clean Water Act Amendments of 1987 which required EPA to publish regulations to control storm water discharges from certain activities. As a result, industrial facilities subject to the program are required to obtain permits and implement controls referred to as Best Management Practices (BMPs) to reduce the pollutants in the storm water runoff from their sites. BMPs can be implemented to reduce contaminants from entering storm water (source controls) or to treat storm water after it has contacted industrial areas (treatment controls). In general, source controls are more effective in reducing pollutant levels in storm water runoff, and are therefore, preferred by EPA and other regulatory agencies. This paper provides an overview of the EPA Storm Water Program which also applies to most state programs and discusses methods to identify and implement BMPs.     

Atmospheric Transport and Air-Surface Exchange of Pesticides

Atmospheric transport and exchange of pesticides with soil, vegetation, water and atmospheric particles are discussed, with an emphasis on applying physicochemical properties of the compound to describe environmental partitioning. The octanol-air partition coefficient is promoted as a unifying property for describing volatilization of pesticides from soil and sorption to aerosols. Present-day sources of organochlorine (OC) pesticides to the atmosphere are continued usage in certain countries and volatilization from contaminated soils where they were used in the past. Models are available to predict volatilization from soil; however, their implementation is hampered by lack of soil residue data on a regional scale. The need to differentiate "new" and "old" sources is increasing, as countries negotiate international controls on persistent organic pollutants (POPs). A new technique, based on the analysis of individual pesticide enantiomers, is proposed to follow emission of chiral OC pesticides from soil and water. Air monitoring programs in the Arctic show the ubiquitous presence of OC pesticides, PCBs and other POPs, and recently a few "modern" pesticides have been identified in fog and surface seawater. Atmospheric loadings of POPs to oceans and large lakes take place mainly by air-water gas exchange. In the case of OC pesticides and PCBs, aquatic systems are often near air-water equilibrium or even oversaturated. Measurement of water/air fugacity ratios suggests revolatilization of PCBs and several OC pesticides in the Great Lakes and, for α-hexachloroacyclohexane (α-HCH), in the Arctic Ocean. Outgassing of α-HCH in large lakes and arctic waters has been confirmed by enantiomeric tracer studies. The potential for pesticides to be atmospherically transported depends on their ability to be mobilized into air and the removal processes that take place enroute: wet and dry deposition of gases and particles and chemical reactions in the atmosphere. Measurement of reaction rate constants for pesticides in the gas and particle phase at a range of environmental temperatures is a critical research need. The transport distance of a chemical is related to its overall environmental persistence, determined by the partitioning among different compartments (water, sediment, soil, air), degradation rates in each compartment and mode of emission (into water, soil, air). Several pesticides found in the arctic environment have predicted lifetimes in the gas phase of only a few days in temperate climates, pointing out the need for monitoring and evaluation of persistence in cold regions.     

Toxic Metals (As, Cd, Ni and Pb) and PM2.5 in Air Concentration of a Model Ceramic Cluster

The relationship between ambient concentrations of fine particulate matter and detrimental health effects remains a highly controversial issue. Increased incidence of mortality and morbidity due to cardiopulmonary complications has been associated with elevated levels of urban air particles with an aerodynamic of <2.5 ??m (PM2.5). The main aim of this paper was to present the assessment of the temporal and spatial variations of the PM2.5 fraction and its contents in arsenic, cadmium, nickel and lead in order to identify possible emission sources of these pollutants. Daily ambient aerosol samples (PM2.5) were taken in the province of Castellón from 2008 to 2009. Particle concentration levels were determined by gravimetry, and the As, Cd, Ni and Pb levels in the samples were determined by inductively coupled plasma mass spectroscopy. The season variation of these pollutants differs according to the emission source and the factors involved in dispersion. In the weekly trend, there were no significant differences in levels among sampling sites in relation to the day activity (working vs. non-working) due to chemical pollutants that are found in fine particulate fractions residing in the atmosphere longer than coarse particles, resulting in a more homogeneous concentration of pollutants over time. In order to identify similar behaviour between chemical pollutants and PM2.5, an assessment of the correlation between them was carried out. This behaviour study shows whether the source of contaminants is the same. A statistical analysis of the levels of PM2.5 and the presence of As, Cd, Ni and Pb in the different sampling sites was performed in order to evaluate the influence of the sampling point on the concentrations of these pollutants.     

Polycyclic aromatic hydrocarbons (PAHs) in marine sediments of the Hellenic coastal zone, eastern Mediterranean: levels, sources and toxicological significance

Purpose  

Polycyclic aromatic hydrocarbons (PAHs) are widespread in sediments, particularly near areas of intense human activities. Due to their mutagenic and carcinogenic behaviour, PAHs are classified as priority contaminants to be monitored in environmental quality control schemes. The purpose of this study was to determine the levels of PAHs in major coastal areas of Greece that receive various pressures, investigate their sources and evaluate their potential toxicity by comparison against effects-based Sediment Quality Guidelines (SQG).     

Quality Assessment of Three Industry-Derived Organic Amendments for Agricultural Use

The quality of three types of treated sludges (sludge from the paper recycling industry, and sewage sludge treated by composting with pruning waste and thermally dried) was assessed in this work. The amendments were physicochemically characterized and evaluated for their microbiological quality and for contamination with pollutants. All three organic amendments showed an absence of pathogens, so they are microbially suitable for agricultural use. The pollutants studied in the amendments included eight heavy metals and 83 organic compounds. Heavy metals, pesticides, polycyclic aromatic hydrocarbons, octylphenol, bisphenol A, and parabens were found in the organic amendments. The amount and type of contaminants depended on the sample sources and differed between samples from a single origin. The presence of some of the pollutants found has not been previously reported in organic amendments. The germination assay showed that these amendments may be applied to soil in controlled doses. As far as we know, this is the first reported study that has evaluated a great variety of pollutants (heavy metals, pesticides, persistent and emerging organic pollutants) in sludge from the recycled paper industry; moreover, studies in other waste products in which such a broad range of pollutants has been evaluated have been scarce until now due to the complexity of these matrices.     

The use of moss,lichen and pine bark in the nationwide monitoring of atmospheric heavy metal deposition in Finland

Mosses, lichens and pine bark were compared as indicators of atmospheric heavy metal deposition in Finland. The samples were collected from the nationwide sampling network systematically covering the country as a whole. All three bioindicators showed a fairly similar result concerning heavy metal deposition. The major emission sources and the areas affected were reflected in the metal concentrations in the samples. However, there were differences between the accumulation of metals. The correlation between concentrations in mosses and lichens was generally higher than that between mosses and bark or lichens and bark. Concentrations in lichens were the highest and lichens reflected the regional differences in background areas as well as the local emission sources. The concentrations in the mosses were slightly lower than those in lichens and also the mosses pinpointed the emission sources and the extend of the areas polluted. Bark had the lowest concentrations and bark did not generally reveal regional differences as well as mosses and lichens. In spite of the differences, all three bioindicators proved to be suitable for monitoring atmospheric heavy metal deposition.     

Nickel Uptake and its Effect on Some Nutrient Levels, Amino Acid Contents and Oxidative Status in Matricaria chamomilla Plants

Ustica is an island relatively far from continental, industrial and urban settlements and it has been designated as a marine protected area with the aim of preserving the natural diversity of flora and fauna of the surrounding sea. In such an environment, the assessment of the levels and origin of persistent organic pollutants such as polycyclic aromatic hydrocarbons (PAHs) can shed light on the mechanisms and effects of pollutant long-distance transport in the western Mediterranean Sea. PAHs concentrations resulted relatively low when compared with those of other coastal areas of the Mediterranean Sea. The low values of the ratio between low- and high-molecular-weight (LMW and HMW, respectively) PAHs and the fluoranthene and pyrene ratios underlined a pyrolytic origin of these contaminants. The prevalence of HMW-PAHs, however, may also be due to the effect of LMW-PAH preferential degradation during transport and burial into sediments. On the other hand, petrogenic sources prevailed in the past. Whilst PAHs concentrations showed a recent increase, especially at the site close to the port, the estimated sedimentary fluxes of PAHs ranged from 0.5 to 25 μg m^?2 year^?1.     

Source and Fate of Heavy Metals in Marine Sediments from a Semi-Enclosed Deep Embayment Subjected to Severe Anthropogenic Activities

Urban and industrial activities are major sources of pollution to marine environments. Sediments can act as sink and reservoir for a wide range of contaminants, including heavy metals. Environmental quality assessment in this compartment can provide useful information to control pollution in coastal areas. Lately, implementation of Environmental Legislative Frameworks within the European Community is increasing awareness about the importance of marine sediment quality in order to achieve a ??Good Environmental Status.?? In this work, the study of superficial marine sediments allowed assessment of source and fate of heavy metals in a semi-enclosed deep embayment that is subjected to severe anthropogenic activities. Results indicated that accumulation of heavy metals takes place mainly in proximity to anthropogenic sources (industrial area and harbors), but pollution can also spread to greater depths affecting the whole ecosystem. Multivariate statistics helped identify source and fate of several elements, showing evidence of pollutants transfer from urban wastewaters, industrial effluents, and atmospheric emissions to marine sediments. Results provided useful information for the implementation and development of Environmental Management Strategies under European Legislative Frameworks.     

Air Pollutant Transport Analysis Based on Hourly Winds in the City of La Plata and Surroundings, Argentina

The city of La Plata and its surroundings are a very populated area, which has an important Industrial Pole and intense traffic activity but environmental studies have been rare so far. This article presents and discusses the importance of wind frequencies and velocities for the transport of air pollutants. The study emphasizes the importance of knowing wind patterns on an hourly basis that can be helpful for designing a monitoring network as well as for preventing exposure to pollutants. Correlation between monthly SO₂ concentrations and wind frequencies and velocities are discussed for a particular set of directions NNW–NE that carry pollutants from industrial sources toward populated areas. As a result, averaged wind frequencies have been found to be very important for determining patterns influencing pollutants transport; the influence of averaged velocities has shown low variability (hourly and monthly). Hierarchical cluster analysis applied to wind roses provided a useful approach for analyzing and describing the general daily occurrence of winds.     

Soil contamination by organic and inorganic pollutants at the regional scale: the case of Piedmont,Italy

Background, aim, and scope  

Diffuse soil contamination has often been neglected in scientific literature, as most studies focus on contaminants from point-sources (either of industrial or agricultural origin). However, soil pollution from diffuse sources is recognized as one of the major soil threats by the EU Soil Thematic Strategy. In fact, some pollutants are nowadays ubiquitarious in the soil system, and they have to be considered for the implementation of environmental legislation, the definition of clean-up values in remediation activities and, more generally, for a sustainable management of rural areas. In the literature large scale studies on diffuse contamination are few and scattered and often do not consider a wide range of contaminants, the effect of land use, the vertical variability and the potential natural contribution. Aim of this work was to provide an overview of the diffuse soil contamination on a regional scale for a large set of contaminants. Soil inorganic (Cd, Cr, Ni, Pb, Cu, Zn) and organic contaminants (polychlorinated dibenzo-p-dioxins(PCDD), polychlorinated biphenyls (PCBs), and polycyclic aromatic hydrocarbons (PAHs) as well as other soil general parameters were investigated on a 18 × 18 km grid covering a whole Italian region heavily industrialized and intensively cultivated. Soils were sampled at different depths both for natural–undisturbed soil and for agricultural–plow soil. Differences in the trends of investigated contaminants, as a consequence of land use, vertical variability, natural or geogenic origin, relationships among contaminants, and with main soil properties, were explored by means of enrichment factors, bi- and multi-variate statistics.     

Persistent Organic Pollutants in Singapore's Coastal Marine Environment: Part II,Sediments

Polycyclic aromatic hydrocarbons (PAHs) can enter the marine environment from a variety of anthropogenic sources. As some PAHs are known or suspected carcinogens and mutagens, their potential hazard to human health and the natural environment warrants investigation. This is the first reported study on the prevalence and concentration of PAHs in marine sediments from Singapore's coastal environment, and accompanies the report by Basheer et al. (2003) on the measurement of persistent organic pollutants (POPs) in seawater. The concentration of 16 PAH, classified as USEPA priority pollutants were analysed in sediments from 22 sample stations located within the northeastern and southwestern regions of Singapore's marine waters. The total PAH concentration varied between 15.22 μg g^-1 and 82.41 μg g^-1 in the northeastern region and between 13.63 μg g^-1 and 84.92 μg g^-1in the southwestern region. The highest concentration of total PAH i.e. 84.92 μg g^-1 was recorded at a site adjacent to a petrochemical refinery. Among the sixteen individual PAHs, chrysene, indeno[1,2,3-cd]pyrene and benzo[a]anthracene were most prevalent in the sediments. The relatively low kinetic/thermodynamic isomer ratios for PAHs suggest that PAHs of pyrogenic origin are predominant in Singapore's coastal environment. The distribution of higher molecular weight i.e. (4–5 ring) individual PAHs corresponded to mixture profiles typical of those originating from high temperature combustion processes subjected to photolytic degradation during long-range atmospheric transportation. A comparison of total PAH concentration data for sediments collected from Singapore relative to those reported for other countries indicates a moderate level of PAH contamination in Singapore's coastal marine sediments.     

Re-shaping the “original SIN”: a need to re-think sediment management and policy by introducing the “buffer zone” concept

Purpose

The effects of long-standing industrialization processes and poor environmental management practices have often left a harmful legacy for marine-coastal sites worldwide, causing a wide range of unforeseen impacts on the ecosystem and on human health. A critical revision of available data from three highly contaminated Italian sites (Augusta Bay, Sicily; Cagliari Gulf, Sardinia; Pozzuoli Bay, Campania) revealed the crucial role of biogeochemical/physical dynamics and potential widespread delivery of contaminants as key components for a wider comprehensive sediment management.

Materials and methods

Datasets of organic pollutants (ΣPAHs, ΣPCBs), heavy metals (As, Cd, Co, Cr, Cu, Hg, Ni, Pb, V, and Zn), radionuclides, and grain size composition of marine sediments of all three sites were critically reviewed and seafloor bathymetric data were analyzed.

Results and discussion

A critical review of available physical and chemical information of sediments collected from the three marine sites provides a better understanding of the physical and biogeochemical dynamics of large-scale dispersion of contaminants in those areas, as well as new insights in terms of improved sediments management policies with actions of larger scale monitoring of the “buffer zone” confining with the national relevance and highly contaminated site to trace inputs and accumulation effects of pollutants deriving from the point-source.

Conclusions

This study demonstrates how the presence of polluted sediments on the coastal areas can have, also after the closure of anthropogenic activities, a potential impact at a large scale. Then to better evaluate the effective impact, we suggest the adoption of a buffer zone contiguous to the national relevance sites (SIN) area. While SINs are optimized to define the state of the art of the near-source pollution, buffer zones may help to outline the rate of delivery of pollutants to the deep sea. Buffer zones must be designed by taking into account the local hydrodynamics, sedimentology, and geomorphology, and should be monitored, even if at a lower resolution, like SINs.

     

Phytovolatilisation of organic chemicals

Features

Independently of the volatilisation of the contaminants from the nutrient solution, the emission rates were determinated under defined, approximated natural conditions by using a dynamic gas exchange chamber. To detect traces of contaminants in air samples with high relative humidity, a purge & trap technology was used. An estimation of the specific emission rates of different materials was made with a transportation model. The model was used to ascertain what compounds are most likely to be emitted by plants due to their physical characteristics.

Results and Conclusions

In experiments with 2,6-Dimethylphenol and Trichloroethylene, a clear link was observed between contaminant emission and the lighting intensity likely to be due to the stomata aperture. The absolute values of the emission rates were very low and in the range of nmol/h m² foliar surface. The calculation of the emission rates in different scenarios shows lowly higher emission rates for materials with lower n-octanol-water partition coefficients

Recommendations and Outlook

Phytovolatilisation is particularly suitable for eliminating volatile compounds in shallow groundwater contaminations, but the experimental proof of an increased net emission of planted areas with volatile soil contaminants near the surface compared with unplanted areas is still pending. On the basis of the model computations it is rather to be expected that the net emission of volatile lipophilic materials should be reduced into the atmosphere by using plants.     

Subsonic jet aircraft and stratospheric pollution

A significant number of thepresent long-range subsonic jet aircraft flights are in the stratosphere. Based on fuel consumption, an equivalent of 107 SST aircraft (Concorde) have been flying in the stratosphere each year from 1960 to 1970 (620 equivalent SST in 1990). Subsonic jets in 1990 will burn about 1.6 times as much fuel in the stratosphere as SST aircraft. Based on a Concorde emission index of 12.5 for NO, the amount of NO_x emitted by subsonic jets in the stratosphere from 1960 to 1970 is equivalent to an average of 20 Concordes (444 Concordes in 1990). Available information concerning mixing and transport in the atmosphere indicates that both subsonic jets and the SST will fly in the same atmospheric environment in the upper troposphere and lower stratosphere insofar as dissipation of their exhaust pollutants is concerned. The tropopause is not an effective barrier to mixing of stratospheric and tropospheric air. Many processes contribute to mixing in the lower stratosphere where the residence time of contaminants is of the order of months instead of years.     

Ecotoxicity of Snowpack Collected from Selected Sites in Québec, Canada

Sampling was conducted at seven sites on, and at varying distances adjacent to, the Island of Montréal (Québec, Canada), and as far as 1,100 km away in Northern Québec, to explore the hazard potential of snowpacks in remote, rural, and urban environments. Ecotoxic effects of melted snow were ascertained with a suite of small-scale bioassays representing several aquatic taxonomic groups (bacteria, micro-algae, micro-invertebrates, fish liver cells) as well as with biomarker measurements determined with a rainbow trout primary hepatocyte (RTPH) assay. Bioassays undertaken with the cnidarian Hydra attenuata and RTPH cell assays, and to a lesser extent with the micro-alga Pseudokirchneriella subcapitata, proved particularly sensitive to infer the presence of bio-available pollutants in snow samples collected from all sites, thereby suggesting their contamination (at least) via atmospheric sources. Furthermore, biomarker responses indicated that snow samples presumably included metals (free Zn biomarker), organics (CYP 1A1 biomarker), estrogens (alkali-labile phosphate biomarker) as well as chemicals capable of causing oxidative stress (LPO biomarker), depending on the site being considered. Overall, effects data acquired during this preliminary investigation on the ecotoxicity of snowpacks submit that adverse impact toward aquatic biota is conceivable at some sites during spring meltdown. Because snow has a recognized affinity for sequestering solids and contaminants of atmospheric origin, future studies aimed at identifying sources and chemicals implicated in observed effects are legitimate endeavors.