The Effects of Fuel Evaporation and Biomass Burning on Toluene Concentrations in an Urban Area

Using an automated gas chromatography system coupled with an online sampling/thermal desorption module, benzene, toluene, and their alkylated derivatives were measured in Las Vegas, Nevada from 3 July to 28 August 2008. The levels of hydrocarbons were comparable to those typically found in urban environments. Statistically significant (at 95?% level) higher concentrations were measured on mid-week days as compared with those measured during weekends. This was correlated to a local traffic pattern rather than traffic on highways. The concentrations of aromatic hydrocarbons also increased during periods when transport of smoke from wildfires in central and north California was identified by remote sensing but these levels were comparable to other days with volatile organic compounds concentrations. The high toluene/benzene ratios and the estimated photochemical age of air masses implied the contribution of other local sources. Fuel evaporation accounted for the vast majority of toluene enhanced concentrations in early July (as compared with those measured in June) for sites within the urban grid, but very little for sites located outside the urban area.     

The Relationship Between Indoor, Outdoor and Personal VOC Concentrations in Homes, Offices and Schools in the Metropolitan Region of Kocaeli, Turkey

Human exposure to volatile organic compounds (VOCs) and residential indoor and outdoor VOC levels had hitherto not been investigated in Turkey. This study details investigations of indoor, outdoor, and personal exposure to VOCs conducted simultaneously in 15 homes, 10 offices and 3 schools in Kocaeli during the summer of 2006 and the winter of 2006–2007. All VOC concentrations were collected by passive sampling over a 24-h period and analyzed using thermal desorption (TD) and a gas chromatography/flame ionization detector (GC/FID). Fifteen target VOCs were investigated and included benzene, toluene, m/p-xylene, o-xylene, ethylbenzene, styrene, cyclohexane, 1,2,4-trimethylbenzene, n-heptane, n-hexane, n-decane, n-nonane, n-octane and n-undecane. Toluene levels were the highest in terms of indoor, outdoor, and personal exposure, followed by m/p-xylene, o-xylene, ethylbenzene, styrene, benzene and n-hexane. In general, personal exposure concentrations appeared to be slightly higher than indoor air concentrations. Both personal exposure and indoor concentrations were generally markedly higher than those observed outdoors. Indoor target compound concentrations were generally more strongly correlated with outdoor concentrations in the summer than in winter. Indoor/outdoor ratios of target compounds were generally greater than unity, and ranged from 0.42 to 3.03 and 0.93 to 6.12 in the summer and winter, respectively. Factor analysis, correlation analyses, indoor/outdoor ratios, microenvironment characteristics, responses to questionnaires and time activity information suggested that industry, and smoking represent the main emission sources of the VOCs investigated. Compared with the findings of earlier studies, the level of target analytes in indoor air were higher for several target VOCs, indicating a possible trend toward increased inhalation exposure to these chemicals in residential environments.     

The application of thermal desorption GC/MS with simultaneous olfactory evaluation for the characterization and quantification of odor compounds from a dairy

Few analytical methods exist that combine chemical and sensory analysis of odorous compounds in whole air. Volatile organic compounds were collected by sampling air downwind from a small dairy through sorbent tubes of Tenax TA and Carboxen 569. Samples were analyzed by thermal desorption into a cryotrap and subsequent gas chromatographic separation, followed by simultaneous olfactometry and mass spectrometry. Because compounds are concentrated during sampling, sensory analysis encountered compounds at a concentration 40 times that in air, making this a useful method for identifying trace compounds participating in odor. Twenty odorous and nonodorous compounds were identified and quantified, including straight-chain and aromatic hydrocarbons, chlorinated compounds, alcohols, ketones, aldehydes, and organic acids, at air concentrations of 0.55-320.20 microg/m(3). Compound peaks were characterized by odors ranging from offensive to pleasant, demonstrating the integrative nature of olfaction. This method could be useful in studying many kinds of odors in air.     

Urban BTEX Spatiotemporal Exposure Assessment by Chemometric Expertise

Normative regulations on benzene in fuels and urban management strategies are expected to improve air quality. The present study deals with the application of self-organizing maps (SOMs) in order to explore the spatiotemporal variations of benzene, toluene, ethylbenzene, and xylene levels in an urban atmosphere. Temperature, wind speed, and concentration values of these four volatile organic compounds were measured after passive sampling at 21 different sampling sites located in the city of Trieste (Italy) in the framework of a multi-year long-term monitoring program. SOM helps in defining pollution patterns and changes in the urban context, showing clear improvements for what concerns benzene, toluene, ethylbenzene, and xylene concentrations in air for the 2001–2008 timeframe.     

Volatile Organic Compounds in the Ambient Air of Rousse,Bulgaria

Volatile organic compounds in the ambient air were measured at four locations in Rousse, Bulgaria for a one year period. A gas chromatograph/mass spectrometer equipped with a cryogenic concentrator was used to analyse the air samples. Forty one compounds (aromatic hydrocarbons and halogen-derivatives of aliphatic and aromatic hydrocarbons) were analysed by EPA method TO-14. Aromatic hydrocarbons, benzene, toluene, styrene, isomers of xylene and isomers of trimethyl benzene were the most frequently occurring pollutants. Styrene, isomers of xylene and isomers of trimethyl benzene frequently exceeded the concentration limits. Among the halogen derivatives, the concentration of chloroform was always very high. A concept called ‘degree of pollution’ was proposed to clarify the contribution of each pollutant to the total air-pollution. Suggestions were made on the need to introduce an integral tolerance parameter to describe the total impact on air-pollution.     

Ambient concentration and precipitation scavenging of atmospheric organic pollutants

Trace organic compounds were measured in air and rainfall at a rural site in Texas. Chlorinated hydrocarbons and phthalic acid esters (PAEs) were present at concentrations of ng m^?3 in air and ng L^?1 in precipitation. The most abundant compounds measured in air were PAEs > toxaphene > chlordane > hexachlorocyclohexanes (HCHs) > others. In rainfall the concentration order was PAEs > toxaphene > HCHs > DDTs > chlordane >- PCBs > others. An inverse correlation between concentration and rainfall amount was observed for most compounds. A model of precipitation scavenging of these compounds considered both scavenging of gas-phase and particle-bound compounds from the atmosphere. Good agreement was obtained between theoretical and measured concentrations. Results indicate that scavenging of a small amount of particle-bound compound can account for >98% of wet deposition for insoluble organic pollutants. Gas-phase scavenging is important for the more soluble compounds such as HCH.     

The Chemistry of Intercepted Clouds in Northern Arizona during the North American Monsoon Season

Cloudwater samples have been collected for the first time at a high-elevation site in the US interior Southwest. Cloud samples were collected at the summit of Mt. Elden near Flagstaff, Arizona. The samples were analyzed for pH, ionic composition, trace metals, organic carbon content, and volatile organic compounds. All of the samples showed high pH values (5.12–6.66), which appear to be the result of soil/crustal acid-neutralizing components. Ammonium and nitrate were the dominant ionic species. Organic carbon concentrations ranged from 3 to 18 mg/l. Volatile aromatic compounds (toluene, ethylbenzene, and xylenes) were detected, although they did not contribute significantly to the dissolved organic matter (<1% of dissolved organic carbon). Still, their aqueous-phase concentrations were substantially higher than equilibrium partitioning from the gas phase would suggest. Metal concentrations were high when compared to other cloud studies in remote areas. Overall, with the exception of pH, the cloud chemistry showed marked inter-event variability. The source of the variability was investigated using NOAA HYSPLIT dispersion calculations. Like the cloud composition, the air mass back trajectories differed widely from event to event, and consistently, air masses that passed over highly urbanized areas had higher trace metal, organic, and ion concentrations than more pristine air masses.     

Low volatile chlorinated hydrocarbons in aquatic sediments in Berlin and surrounding areas

Low volatile chlorinated hydrocarbons, especially DDT and HCH, have been used as indicators of the level of pollution in aquatic sediments. These compounds were present in all the sediment samples analysed in this study by gas chromatography. Enrichment factors between the water and sediment were high (K^d = 85-108 for DDT), documenting the strong geoaccumulation of toxic chlorinated hydrocarbons. in contrast with the generally held view, no linear relationship was observed between the concentration of HCH and PCBs and the organic matter content of the sediment. the application of the EVOLON model to determine the kinetics of sorption clearly showed a saturation value. the sorbed amount of low volatile chlorinated hydrocarbons depends to a large extent on the amount of organic matter on the surface of the sediment particles.     

Organic compounds and heavy metals in the atmosphere of the city of Caracas,Venezuela — I: Atmospheric particles

Aliphatic and aromatic hydrocarbons, fatty acids and heavy metals (Pb, Cu, Ni, Zn, Fe and Cd) were analyzed in atmospheric particulate matter in the city of Caracas, Venezuela. Samples were taken from 6 stations within the metropolitan area of Caracas, characterized as industrial (one), urban (two), suburban (two) and rural (one). In addition, the concentration and composition of the organic compounds was monitored over a 5 month period at an urban site to determine seasonal and temporal variabilities. In general terms, the concentrations of pollutants decreased from industrial and urban sites to suburban to rural. A similar trend was observed for preliminary toxicity tests carried out on the particulate extracts. The concentration levels of most of the pollutants were high for the industrial and urban sites, and comparable with those of other major cities worldwide.     

The use of comprehensive two-dimensional gas chromatography and structure–activity modeling for screening and preliminary risk assessment of organic contaminants in soil, sediment, and surface water

Purpose

This article aims to investigate the use and benefits of using comprehensive two-dimensional gas chromatography (GC?×?GC) and structure?Cactivity relationship modeling for screening and prioritization of organic contaminants in complex matrices. The benefit of applying comprehensive screening techniques to samples with high organic contaminant content is primarily that compounds with diverse physicochemical properties can be analyzed simultaneously. Here, a heavily contaminated industrial area was surveyed for organic pollutants by analyzing soil, sediment, and surface water samples. The hazard of the pollutants were ranked using SARs.

Material and methods

The water samples were liquid?Cliquid extracted using dichloromethane and directly analyzed by GC?× GC?Ctime-of-flight mass spectrometry (GC?×?GC?CTofMS). Soil and sediment samples were extracted with dichloromethane in an ultrasonic bath and subjected to gel permeation chromatography to eliminate lipids and humic matter. The low molecular weight fraction was then analyzed with GC?×?GC?CTofMS.

Results and discussion

More than 10,000 components were found in each sample, of which ca. 300 individual compounds were unambiguously identified using the National Institute of Standards and Technology mass spectra library and authentic reference standards. Alkanes, polycyclic aromatic hydrocarbons, and phthalates were generally the most abundant and were found in all matrices. In contrast, chlorinated compounds such as chlorophenols, biphenyls, and chlorinated pesticides were only detected in samples from a few hotspot regions. The toxicities of the most frequently detected compounds and of the compounds detected at the highest concentrations in samples from hotspot regions were estimated by ecological structure?Cactivity relationships. The ratio of the measured concentration to the predicted toxicity level was then calculated for each compound and used for an initial risk assessment in order to prioritize compounds for further transport and fate modeling, complementary measurements, and more advanced risk assessments.

Conclusions

The advantage of using of GC?×?GC?CTofMS for preliminary screenings of contaminated areas was evaluated at a polluted area in northern Sweden. The area was found to carry organic pollutants such as polyaromatic hydrocarbons, aliphatic hydrocarbons, polychlorinated biphenyls, phthalic compounds, and many chlorinated pesticides. Preliminary risk assessments indicate which compounds to use for subsequent remediation experiments based on their availability on the site or toxicity.     

Volatilisation of aromatic hydrocarbons from soil: Part I,fluxes from coal tar contaminated surface soils

The non-steady-state fluxes of aromatic hydrocarbons were measured in the laboratory from the surface of soils contaminated with coal tar. Four soil samples from a former gasworks site were used for the experiments. The fluxes were quantified for 11 selected compounds, 4 mono- and 7 polycyclic aromatic hydrocarbons, for a period of up to 8 or 16 days. The concentrations of the selected compounds in the soils were between 0.2 and 3,100 µg/g. The study included the experimental determination of the distribution coefficient of the aromatic hydrocarbons between the sorbed phase and the water under saturated conditions. The determined distribution coefficients showed that the aromatic hydrocarbons were more strongly sorbed to the total organic carbon including the coal tar pitch — by a factor of 8 to 25 — than expected for natural organic matter. The fluxes were also estimated using an analytical solution of the Fick's diffusion equation and assuming that the compounds diffused independently of each other and that instant equilibrium existed between the air, water and sorbed phases. A relatively good agreement was found between the predicted and the measured flux. The predicted fluxes were between 0.11 and 7.5 time the measured fluxes. The fluxes were overestimated for the monocyclic aromatic hydrocarbons and underestimated for 3-rings-PAHs.     

A New Approach to Calculate EMEA��s Predicted Environmental Concentration for Human Pharmaceuticals in Groundwater at Bank Filtration Sites

Hourly concentrations of non-methane hydrocarbons (NMHCs) recorded between June and August 2006, at two monitoring sites (Gijang and Jin) in Busan were analyzed to examine the characteristics and photochemical reactivity of NMHC sources. The two sites represent urban (Jin) and suburban (Gijang) Busan, which is a typical Korean city. Positive matrix factorization (PMF), applied to identify and apportion the sources of NMHCs, revealed nine sources for Gijang and ten sources for Jin. To explore the contribution of each NMHC source to ozone formation at the two sampling sites, the ozone formation potential was estimated for each source. The largest contributors to ozone formation were sources characterized by 1,2,3-trimethylbenzene (26.4%) at Gijang and by toluene, ethylbenzene, and xylenes (22.5%) at Jin, which were composed mostly of heavy hydrocarbons and aromatics. Secondary sources included two coating sources (20.9%, 12.2%) and vehicle exhaust (10.3%) at Gijang and a source represented by toluene (17.4%), vehicle exhaust (15.9%), and a coating-2 source (9.6%) at Jin. Conditional probability function (CPF) and potential source contribution function (PSCF) analysis methods were used to identify the directions of local sources and to locate potential source regions, respectively. The CPF and PSCF results agreed well for the majority of sources resolved by PMF and thus were very useful in identifying the major sources contributing to ozone formation at the two study sites.     

4种湿地植物根系泌氧由根诱导的pH,Eh和Fe(II)变化和根际土壤中铅和锌的组分研究

A rhizobox experiment was conducted to compare iron (Fe) oxidation and changes of pH, redox potential (Eh) and fractions of zinc (Zn) and lead (Pb) in rhizosphere and non-rhizosphere soils of four emergent-rooted wetland plants (Echinodorus macrophyllus, Eleocharis geniculata, Hydrocotyle vulgaris and Veronica serpyllifolia) with different radial oxygen loss (ROL) from roots. The results indicated that all these wetland plants decreased pH and concentration of Fe(Ⅱ) but increased the Eh in the rhizosphere soils. Pb and Zn were transformed from unstable fractions to more stable fractions in the rhizosphere soils, so decreasing their potential metal mobility factors (MF). Among the four plants, E. macrophyllus, with the highest ROL and root biomass, possessed the greatest ability in formation of Fe plaque and in the reduction of heavy metal MFs in the rhizosphere soil. Wetland plants, with higher ROLs and root biomass, may thus be effective in decreasing potential long-term heavy metal bioavailabilities.     

Investigation of Soil Concentrations of Persistent Organic Pollutants, Trace Elements, and Anions Due to Iron–Steel Plant Emissions in an Industrial Region in Turkey

The spatial distribution of several air pollutants emitted from iron–steel industries in Hatay-Iskenderun industrial region in Turkey was investigated by measuring their concentrations in soil. Collected soil samples (n?=?20) were analyzed for persistent organic pollutants (POPs; i.e., polycyclic aromatic hydrocarbons, polychlorinated biphenyls, polybrominated diphenyl ethers, and polychlorinated naphthalenes), anions, and trace elements. Generally, all measured POP concentrations and marker trace elements for iron–steel industry (Zn, Pb, and Cu) were high relative to those reported previously for rural and urban areas around the world, and they were comparable to those measured recently in a similar industrial region (Aliaga, Izmir, Turkey). For all investigated POPs, elements, and anions, the highest concentrations were measured at points located north of the iron–steel industries where their emissions are transported by the prevailing southerly winds. The spatial distribution and levels of POPs, elemental, and anionic concentrations indicated that the iron–steel plants in Hatay-Iskenderun region are important sources for these pollutants. Statistically significant relationships between several organic and inorganic pollutants further confirmed that they are emitted by common sources (iron–steel plants).     

Einfluß des Belastungsgrades unterschiedlicher Böden an ausgewählten Pestizid wirkenden Chlorkohlenwasserstoffen auf deren Aufnahme durch Möhren im Gefäßversuch

Influence of contamination of selected, pesticid effective hydrocarbons on their uptake by carrots in a pot experiment Exemplary soils from low up to higher grades of contamination with selected pesticid effective hydrocarbons (CHC) were used in a pot experiment on the uptake of these xenobiotica by carrot plants. Carrots are able to take up pesticid effective chlorinated hydrocarbons which was expected because of their oil cells and the lipophilic character of the examined substances. There is a correspondingly higher plant uptake from soils with a higher load of pollutants as from soils with a lower grade of contamination. Despite the high concentrations of beta- and alpha-HCH in the plants from the site Muldenaue (mg/kg dm] the total uptake per pot was relatively small (below 2 mg/pot). The transferfactors soil/plant show in all plant parts no enrichment of organochlorpesticides (foliage 0.021 < carrot body 0.156 < fine roots 0.975).     

The Potted-Plant Microcosm Substantially Reduces Indoor Air VOC Pollution: II. Laboratory Study

Indoor air-borne loads of volatile organic compounds (VOCs) are usually significantly higher than those outdoors, and chronic exposures can cause health problems. Our previous laboratory studies have shown that the potted-plant microcosm, induced by an initial dose, can eliminate high air-borne VOC concentrations, the primary removal agents being potting-mix microorganisms, selected and maintained in the plant/root-zone microcosm. Our office field-study, reported in the preceding paper, showed that, when total VOC (TVOC) loads in reference offices (0 plants) rose above about 100 ppb, levels were generally reduced by up to 75% (to < 100 ppb) in offices with any one of three planting regimes. The results indicate the induction of the VOC removal mechanism at TVOC levels above a threshold of about 100 ppb. The aims of this laboratory dose-response study were to explore and analyse this response. Over from 5 to 9 days, doses of 0.2, 1.0, 10 and 100 ppm toluene and m-xylene were applied and replenished, singly and as mixtures, to potted-plants of the same two species used in the office study. The results confirmed the induction of the VOC removal response at the lowest test dosage, i.e in the middle of the TVOC range found in the offices, and showed that, with subsequent dosage increments, further stepwise induction occurred, with rate increases of several orders of magnitude. At each dosage, with induction, VOC concentrations could be reduced to below GC detection limits (< 20 ppb) within 24 h. A synergistic interaction was found with the binary mixtures, toluene accelerating m-xylene removal, at least at lower dosages. The results of these two studies together demonstrate that the potted-plant microcosm can provide an effective, self-regulating, sustainable bioremediation or phytoremediation system for VOC pollution in indoor air.     

Persistent organic pollutant concentrations in air‐ and freeze‐dried compared to field‐fresh extracted soil samples of an eastern Slovak deposition gradient

Sample preparation affects the results of the determination of persistent organic pollutant (POP) concentrations in soils. We compared the extraction results of POPs from air‐ and freeze‐dried with field‐fresh samples. We determined the concentrations of 21 polycyclic aromatic hydrocarbons (PAHs) and 14 polychlorinated biphenyls (PCBs) in 35 horizons of forest soils (Lithosols and Cambisols) along a deposition gradient caused by a chemical factory in Strá?ske (eastern Slovakia). The organic C (C_org) concentrations of the studied samples ranged 14‐477 g kg^‐1, the sum of 21 PAH (Σ 21PAHs) concentrations 53‐6870 μg kg^‐1, and that of 14 PCBs (Σ 14PCBs) 0.12 96 μg kg^‐1. The benzofluoranthenes were the most abundant PAHs, and the hexa‐chlorinated PCBs 138 and 153 were the most abundant PCBs. The deposition gradient was reflected by decreasing PAH and PCB storages in the organic layer with increasing distance from the chemical factory (Σ 21PAHs: 82‐238, Σ 14PCBs: 0.34‐2.3 g ha^‐1). The PAH concentrations in air‐ and freeze‐dried samples were consistently lower than those in field‐fresh extracted samples. For naphthalene, this was mainly attributable to volatilization losses during drying. Naphthalene losses decreased with increasing C_org concentrations. For all other PAHs, drying reduced the extractability; the latter was correlated with the water content of the samples. The differences in most PCB concentrations among the sample preparation methods were small (within the determination error of ±15 %) and inconsistent. However, PCBs 8, 28, 52, and 209 had markedly higher concentrations in dried than in fieldfresh extracted samples. The increased recovery of low‐chlorinated PCBs in dried samples may be explained by redistribution of PCBs from higher to lower contaminated samples via the drying room atmosphere because there were no PCBs in analytical blanks. This assumption is supported by a close correlation between the octanol‐air distribution coefficient and the up to hexa‐chlorinated PCB concentrations (normalized to those in field‐fresh extracted samples) in air‐ (r = ‐0.90) and freeze‐dried (r = ‐0.86) samples. Our study shows that each sample preparation method has its specific advantages and disadvantages. Sample drying results in a standardization to a well‐defined water content and facilitates homogenization; therefore it increases the reproducibility of POP determinations. Extraction of field‐fresh samples reduces volatilization losses and contamination risks.     

Assessment of the Impact Produced by the Traffic Source on VOC Level in the Urban Area of Canosa di Puglia (Italy)

Volatile organic compounds (VOC) have been monitored in 12 sites of Canosa di Puglia, a city located in the Southern of Italy, in order to identify the main VOC source—vehicular traffic or industrial—and to evaluate the critical situations in the city. Monitoring, carried out by using Radiello® diffusive samplers, has been planned taking into account the traffic density and the architecture of the city. From the study of the data it has been emerged that, among all considered VOC, benzene, toluene, ethylbenzene and xylenes (BTEX) are the pollutants at higher concentration. However no critical situation has appared from the present monitoring. Maps of daily benzene and toluene concentrations have shown that the most significant pollution phenomena happens in the center of the urban area which is in a valley with narrow roads and high buildings that do not allow an efficient dispersion of pollutants. The study of the diagnostic ratios between the toluene and benzene concentrations in the several areas (average T/B?=?3.4) and the high Pearson’s coefficient among the pollutants, and in particular between benzene and toluene concentrations (r?=?0.9505), have suggested that in urban area these pollutants are emitted from the same source: the vehicular traffic.     

Accuracy of seven vapour intrusion algorithms for VOC in groundwater

Background, aim and scope  During the last decade, soil contamination with volatile organic contaminants (VOC) received special attention because of their potential to cause indoor air problems. Moreover, research has shown that people spend 64% to 94% of there time indoors; therefore, the indoor air quality is of a primary importance for exposure to VOC. Human health risks to VOC—in cases of soil contamination—are often dominated by the exposure route ‘inhalation of indoor air’. Exposure is often a result of vapour transport from the soil or groundwater to the indoor air of the building. Within human health risk assessments, a variety of algorithms are available that calculate transfer of soil gas to the indoor air. These algorithms suffer from a relatively high uncertainty due to a lack of representation of spatial and temporal variability. For such an application, these algorithms need to be further verified empirically against field observations so that they can be sufficiently reliable for regulatory purposes. This paper presents the accuracy for seven algorithms by using observed and predicted soil and indoor air concentrations from three sites, where the groundwater had been contaminated with aromatic and chlorinated VOC. Materials and methods  The algorithms for vapour intrusion that are frequently used in European countries were included in this study and were Vlier–Humaan (Flanders), CSoil (Netherlands), VolaSoil (Netherlands), Johnson & Ettinger (USA), Risc (United Kingdom), and the dilution factor (DF) algorithms from Sweden and Norway. Three sites were investigated in more detail and samples were taken synoptically from the groundwater, soil and indoor air on four occasions. On the petroleum sites, the aromatic hydrocarbons benzene, toluene, ethylbenzene and xylenes were analysed and, on the dry cleaning sites, the chlorinated hydrocarbons tetrachloroethylene, trichloroethylene and cis 1,2-dichloroethene. To increase spatial resolution, measurements in groundwater and soil air were taken in three different zones at each site, in the close proximity of or in the building. During sampling, several relevant soil properties were measured like the bulk density, water and air filled porosity, soil temperature and depth of the groundwater. Also, building properties like the dimensions of the building and the quality of the floor were registered. The seven algorithms were applied to compare that observed with the predicted concentrations in soil and indoor air. The groundwater concentrations were used as a source contamination. The results from the algorithms were compared by using performance criteria to assess the accuracy of each algorithm. Results  All calculations are presented in a box plot that contains the predicted soil or indoor air versus the observed concentrations. Results from the applied criteria are presented for each algorithm. Discussion  Differences between predictions and observations were up to three orders of magnitude and can be partially related to the amount of parameters included in each algorithm and the mathematical concept used. For example, the inclusion or exclusion of a capillary fringe or temperature correction for the Henry constant: it is not clear why all algorithms tend to over-predict the soil air concentration. The prediction mostly starts with the calculation of a soil air concentration related to the Henry constant, followed by diffusive and/or convective transport to the soil surface and zone of influence around the building foundation. Further research is needed to investigate the over-predictions and the use of the Henry constant to calculate the soil air concentration should be reviewed. Conclusions  The algorithms with the highest accuracy were the Johnson and Ettinger and the Vlier–Humaan algorithms. The DF algorithms from Sweden and Norway resulted in higher over- and underpredictions than others. Results for the indoor air showed that all the algorithms calculate high and low concentrations in the indoor air when compared to observations. The algorithms with the highest accuracy were JEM, Vlier–Humaan and CSoil. The DF algorithm from Norway calculated concentrations that were frequently higher than observed concentrations and the Swedish DF algorithm showed frequent higher and lower concentration than observed. The conservatism of the most accurate algorithms is sufficient for regulatory purposes, and they can trigger an integrated programme of field observations (monitoring) or/and modelling. Recommendations and perspectives  The dataset used for this paper was derived from three sites with groundwater contamination and further verification of these algorithms should be done for other sites that have a vadose zone contamination.     

Aspects of phytoremediation of organic pollutants

Phytoremediation is a quite novel technique to clean polluted soils using plants. In theory, phytoremediation methods are cheap, are accepted by the public and, compared to physical or chemical approaches, are ecologically advantageous. Until today, however, there are only a few examples of successful applications. One reason is that the processes involved are complex, and a full clean up may require many years. Plants affect the water balance of a site, they change redox potential and pH, and stimulate microbial activity of the soil. These indirect influences may accelerate degradation in the root zone or reduce leaching of compounds to groundwater. Compounds taken up into plants may be metabolised, accumulated, or volatilised into air. Based on these processes, several phytoremediation methods have been developed: Phytoextraction, rhizofiltra-tion, phytostabilisation, rhizo and phytodegradation, pump and tree, land farming, phytovolatilisation, hydraulic control and more. Already in use are plants (and here willow, poplar and grass) for the degradation of petroleum products, aromatic hydrocarbons (BTEX), chlorinated solvents, explosives and cyanides. However, phytotoxicity and pollutant mass balances were rarely documented. Often, the success of the projects was not controlled, and only estimates can be made about the applicability and the potential of phytoremediation. This lack of experience about possibilities and limitations seems to be a hindrance for a broader use of these techniques.