Persistent Organic Pollutants In Air Research Articles

Spatial and Temporal Trends of Persistent Organic Pollutants across Europe after 15 Years of MONET Passive Air Sampling.

The Global Monitoring Plan of the Stockholm Convention on Persistent Organic Pollutants (POPs) was established to generate long-term data necessary for evaluating the effectiveness of regulatory measures at a global scale. After 15 years of passive air monitoring (2003-2019), MONET is the first network to produce sufficient data for the analysis of continuous long-term temporal trends of POPs in air across the entire European continent. This study reports long-term concentrations of 20 POPs monitored at 32 sites in 27 European countries. As of January 1, 2019, the concentration ranges (pg/m3) were 1.1-52.8 (∑6PCB), 0.3-8.5 (∑12dl-PCB), 0.007-0.175 (∑17PCDD/F), 0.02-2.2 (∑9PBDE), 0.4-24.7 (BDE 209), 0.5-247 (∑6DDT), 1.7-818 (∑4HCH), 15.8-74.7 (HCB), and 5.9-21.5 (PeCB). Temporal trends indicate that concentrations of most POPs have declined significantly over the past 15 years, with median annual decreases ranging from -8.0 to -11.5% (halving times of 6-8 years) for ∑6PCB, ∑17PCDD/F, HCB, PeCB, and ∑9PBDE. Furthermore, no statistically significant differences were observed in either the trends or the concentrations of specific POPs at sites in Western Europe (WEOG) compared to sites in Central and Eastern Europe (CEE), which suggests relatively uniform compound-specific distribution and removal at the continental scale.

Preliminary results from the Tunisian monitoring program on POPs in air under the Stockholm Convention

Persistent organic pollutants (POPs) have been measured using passive air samplers (PASs) over two years (2017–2018) in the city of Tunis within the framework of the UNEP/GEF GMP2 projects to support Stockholm Convention implementation. Several POPs, although banned for a long time from Tunisia, were registered in relatively high amounts in the atmospheric compartment. The most unexpected compound is hexachlorobenzene (HCB), with concentrations ranging from 5.2 ng/PUF to 16 ng/PUF. Furthermore, the current results seem to confirm the presence of dichlorodiphenyltrichloroethane (DDT) and its transformation products and hexachlorocyclohexanes (HCHs) at relatively high concentrations (4.6 ng/PUF to 9.4 ng/PUF and 2.7 ng/PUF to 5.1 ng/PUF, respectively), followed by hexabromocyclododecane (HCBD), which varies from 1.5 ng/PUF to 7.7 ng/PUF. Nondioxin-like PCB (ndl-PCB) concentrations in Tunis were very high (62.0 ng/PUF to 419.3 ng/PUF), higher than those in other African countries participating in this project. Uncontrolled combustion seems to be one of the most important sources of the emanation of dioxin compounds dl-PCBs and Polychlorinated dibenzodioxins PCDD/polychlorinated dibenzofurans PCDF. Toxic equivalents (TEQs) ranged from 4.1 pg WHO-TEQ/PUF to 6.4 pg WHO-TEQ/PUF. The perfluorinated compounds (PFAS) and congeners of polybrominated diphenyl ethers (PBDEs) show relatively low amounts that remain below the African continent average. The PFAS pattern suggests a local source rather than long-range transport. These results constitute the first exhaustive work capable of providing an overview of the levels of POPs in the air in Tunis. As a result, it will be possible to set up an adequate monitoring program with specific investigations and experimental studies.

Persistent organic pollutants in air from Asia, Africa, Latin America, and the Pacific

In support of the United Nations Environment Programme (UNEP) global monitoring plan under the Stockholm Convention concentrations of persistent organic pollutants (POPs) were determined during two years in air from 42 countries in Asia, Africa, Latin America, and the Pacific by using polyurethane foams installed in passive samplers. The compounds included were polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), polybrominated diphenylethers (PBDEs), one polybrominated biphenyl and hexabromocyclododecane (HBCD) diastereomers. Total-DDT and PCBs were the highest in concentrations in about 50% of the samples, which shows their high persistency. Total DDT in air from the Solomon Islands ranged from 200 to 600 ng/polyurethane foam disk (PUF). However, at most locations, a decreasing trend is observed for PCBs, DDT and most other OCPs. Patterns varied per country with e.g. elevated dieldrin in air from Barbados and chlordane in air from the Philippines. A number of OCPs, such as heptachlor and its epoxides, some other chlordanes, mirex and toxaphene have decreased down to almost undetectable levels. PBB153 was hardly found and penta and octa--mix related PBDEs were also relatively low at most locations. HBCD and the decabromodiphenylether were more prominent at many locations and may even still increase. To draw more holistic conclusions more colder climate countries should be included in this program.

Preliminary trends over ten years of persistent organic pollutants in air - Comparison of two sets of data in the same countries

In two series of ambient air measurement campaigns to support the implementation of the global monitoring plan (GMP) component of the Stockholm Convention on Persistent Organic Pollutants (POPs), passive air samplers (PAS) using polyurethane foams were implemented by the United Nations Environment Programme (UNEP). With the same laboratories responsible for the chemical analyses of the different groups of POPs, a total of 423 PUFs were analyzed for organochlorine pesticides (OCPs) including hexachlorobenzene (HCB) and polychlorinated biphenyls (PCB); 242 for dioxin-like POPs. For trend analysis, to compare amounts of POPs in the PUFs during the first phase in 2010/2011 and the second phase from 2017 to 2019, only results were assessed that were generated in the same country and for the same POP in both campaigns. Finally, there were 194 PUFs available for OCPs (GMP1 = 67 and GMP2 = 127), 297 for PCB (GMP1 = 103, GMP2 = 194), 158 for polychlorinated dibenzodioxins and polychlorinated dibenzofurans (PCDD, PCDF) (GMP1 = 39, GMP2 = 119), and 153 for dl-PCB (GMP1 = 34, GMP2 = 119). Indicator PCB and dioxin-like POPs were quantified in all countries at all times; decreases of about 30% based on median values were determined. A 50% increase was found for HCB. By scale, DDT remained with the highest values, although more than 60% decrease was found; mainly due to smaller values in the Pacific Islands region. Our assessment showed that on relative scale – per PUF – trend analysis was achieved and that such approach should be undertaken at regular intervals, not necessarily on an annual basis.

Spatial variability and temporal changes of POPs in European background air

Concentration data on POPs in air is necessary to assess the effectiveness of international regulations aiming to reduce the emissions of persistent organic pollutants (POPs) into the environment. POPs in European background air are continuously monitored using active- and passive air sampling techniques at a limited number of atmospheric monitoring stations. As a result of the low spatial resolution of such continuous monitoring, there is limited understanding of the main sources controlling the atmospheric burdens of POPs across Europe. The key objectives of this study were to measure the spatial and temporal variability of concentrations of POPs in background air with a high spatial resolution (n = 101) across 33 countries within Europe, and to use observations and models in concert to assess if the measured concentrations are mainly governed by secondary emissions or continuing primary emissions. Hexachlorobenzene (HCB) was not only the POP detected in highest concentrations (median: 67 pg/m3), but also the only POP that had significantly increased over the last decade. HCB was also the only POP that was positively correlated to latitude. For the other targeted POPs, the highest concentrations were observed in the southern part of Europe, and a declining temporal trend was observed. Spatial differences in temporal changes were observed. For example, γ-HCH (hexachlorocyclohexane) had the largest decrease in the south of Europe, while α-HCH had declined the most in central-east Europe. High occurrence of degradation products of the organochlorine pesticides and isomeric ratios indicated past usage. Model predictions of PCB-153 (2,2’,4,4’,5,5’-hexachlorobiphenyl) by the Global EMEP Multi-media Modelling System suggest that secondary emissions are more important than primary emissions in controlling atmospheric burdens, and that the relative importance of primary emissions are more influential in southern Europe compared to northern Europe. Our study highlights the major advantages of combining high spatial resolution observations with mechanistic modelling approaches to provide insights on the relative importance of primary- and secondary emission sources in Europe. Such knowledge is considered vital for policy makers aiming to assess the potential for further emission reduction strategies of legacy POPs.

Highly efficient adsorptive removal of persistent organic pollutants using NPD-acid combined modified NaY zeolites

Adsorption method is an effective way to remove persistent organic pollutants in air. In this study, nanosecond pulsed discharge plasma combined acid was employed to modify the NaY zeolites with the purpose of adsorbing persistent organic pollutants, comparing with the adsorption capacity of NaY zeolites modified by the solo acid and solo plasma treatment. The waveforms of pulse voltage and discharge current, and gas temperature of discharge were collected to investigate the plasma characteristics. The physical structure and chemical active sites of raw and modified zeolites were characterized by means of N2 adsorption–desorption analysis, Scanning Electron Microscopy, Fourier Transform Infrared Spectrum, Pyridine Infrared Spectrum, and X-ray Photoelectron Spectroscopy. It was found that the adsorption capacity of zeolites modified by NPD-acid combined system increased by 167%, 56%, and 40%, respectively, compared with the raw, solo 3 mol/L of acid and solo NPD modified zeolites, with the conditions of 3 mol/L of acid concentration, 1 mg/L of naphthalene initial concentration, 25 min of treatment time, and 30 kV of pulse peak voltage. This result can be ascribed to the increased acid sites (Brønsted and Lewis acid), O element content, specific surface area, and number of micropores and mesopores, which all played an important role in naphthalene adsorption. Additionally, the adsorption kinetics and mass transfer of raw and modified zeolites could be described by pseudo-second-order and intra-particle diffusion models.

Tracking POPs in Global Air from the First 10 Years of the GAPS Network (2005 to 2014).

The Global Atmospheric Passive Sampling (GAPS) network, initiated in 2005 across 55 global sites, supports the global monitoring plan (GMP) of the Stockholm Convention on Persistent Organic Pollutants (POPs) by providing information on POP concentrations in air on a global scale. These data inform assessments of the long-range transport potential of POPs and the effectiveness evaluation of chemical regulation efforts, by observing changes in concentrations over time. Currently, measurements spanning 5–10 sampling years are available for 40 sites from the GAPS Network. This study was the first time that POP concentrations in air were reported on a global scale for an extended time period and the first to evaluate worldwide trends with an internally consistent sample set. For consistency between sampling years, site- and sample specific sampling rates were calculated with a new, public online model, which accounts for the effects of wind speed variability. Concentrations for legacy POPs in air between 2005 and 2014 show different trends for different organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs). The POPs discussed in this study were chosen due to being the most frequently detected, with detection at the majority of sites. PCB, endosulfan, and hexachlorocyclohexane (HCH) concentrations in air are decreasing at most sites. The global trends reflect global sources and recycling of HCH, ongoing emissions from old stockpiles for PCBs, and recent use restrictions for endosulfan. These chlorinated OCPs continue to present exposure threat to humans and ecosystems worldwide. Concentrations of other OCPs, such as chlordanes, heptachlor and dieldrin, are steady and/or declining slowly at the majority of sites, reflecting a transition from primary to secondary sources (i.e., re-emission from reservoirs where these POPs have accumulated historically) which now control ambient air burdens.

Research progress on analytical methods for the determination of hexachlorobutadiene

六氯丁二烯是一种持久性有机污染物,于2015年和2017年分别被列入《斯德哥尔摩公约》附件A和附件C的受控污染物名单中。六氯丁二烯的来源、环境赋存和影响等研究对控制该新增受控持久性有机污染物污染具有重要意义,而灵敏可靠的六氯丁二烯分析方法是开展相关研究的前提和基础。近年来已有不少学者将六氯丁二烯作为分析目标物之一进行了检测或方法学研究。基于这些研究成果,该文综述了六氯丁二烯分析方法的研究进展,其中重点介绍了空气、水体、土壤、污泥、生物组织等多种介质中六氯丁二烯的样品前处理方法,并比较了各方法的优缺点,以期为该领域的进一步研究提供参考。空气中六氯丁二烯主要由泵抽气通过吸附管而采集,再经热脱附后进行仪器分析,检出限在ng/m3水平。也有研究应用聚氨酯泡沫被动采样器和吸附剂填充聚氨酯泡沫被动采样器采集大气中六氯丁二烯及其他污染物。基于吸附剂填充聚氨酯泡沫被动采样器的分析方法灵敏度较高,其对六氯丁二烯的检出限低至0.03 pg/m3。然而目前被动采样体积仅根据六氯丁二烯的log KOA系数估算,未来仍需进一步实验校正。水体样品前处理通常也较简单,通过吹扫捕集、液-液萃取或固相萃取目标物后进行仪器分析。固相萃取法能够同步实现目标物的提取、净化和浓缩,在水样中六氯丁二烯分析方面具有明显优势。固相萃取柱类型以及干燥步骤中柱中残留水分去除率均会影响六氯丁二烯的回收率。灰尘、土壤、沉积物、污泥和生物组织等固体介质样品基质最为复杂,需联合多种方法进行前处理。固体样品中六氯丁二烯提取方法包括索氏提取,加速溶剂萃取和超声萃取,其中超声萃取法应用最为广泛。固体基质净化方面主要采用层析柱色谱法,多根净化柱联用或多层复合柱能够提升净化效果。仪器分析方面,六氯丁二烯主要采用气相色谱和质谱联用检测,高性能质谱检测器如串联质谱能够大大提高六氯丁二烯的检测灵敏度,具有较大的应用潜力。

Trends of Diverse POPs in Air and Water Across the Western Atlantic Ocean: Strong Gradients in the Ocean but Not in the Air.

Oceans have remained the least well-researched reservoirs of persistent organic pollutants (POPs) globally, due to their vast scale, difficulty of access, and challenging (trace) analysis. Little data on POPs exists along South America and the effect of different currents and river plumes on aqueous concentrations. Research cruise KN210-04 (R/V Knorr) offered a unique opportunity to determine POP gradients in air, water, and their air-water exchange along South America, covering both hemispheres. Compounds of interest included polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), polybrominated diphenylethers (PBDEs), and polycyclic aromatic hydrocarbons (PAHs). Remote tropical Atlantic Ocean atmospheric concentrations varied little between both hemispheres; for HCB, BDEs 47 and 99, they were ∼5 pg/m3, PCBs were ∼1 pg/m3, α-HCH was ∼0.2 pg/m3, and phenanthrene and other PAHs were in the low 100s pg/m3. Aqueous concentrations were dominated by PCB 52 (mean 4.1 pg/L), HCB (1.6 pg/L), and β-HCH (1.9 pg/L), with other compounds <1 pg/L. Target PCBs tended to undergo net volatilization from the surface ocean, while gradients indicated net deposition for a-HCH. In contrast to atmospheric concentrations, which were basically unchanged between hemispheres, we detected strong gradients in aqueous POPs, with mostly nondetects in the tropical western South Atlantic. These results highlight the importance of currents and loss processes on ocean scales for the distribution of POPs.

Occurrence of persistent organic pollutants in air at different sites in the province of Córdoba, Argentina.

The occurrence of persistent organic pollutants (POPs) and polycyclic aromatic hydrocarbons (PAHs) in the atmosphere of six sites with different emission sources in the province of Córdoba, Argentina, was analyzed. The sites included urban, industrial, agricultural, and mountain areas. Samples were collected using passive air samplers (PAS) consisting of polyurethane foam disks (PUF). Samples were analyzed for 12 PAHs, 31 polychlorinated biphenyls (PCBs), 12 organochlorine pesticides (OCPs), and 11 polybrominated diphenyl ethers (PBDEs). The concentrations of PAHs in the atmosphere were elevated at urban sites and were even higher at the industrial site. With respect to OCPs, it was observed that the concentrations of endosulfan were greater at the agricultural site (AGR) (416 ± 4pgm-3). For hexachlorocyclohexanes (HCHs), only the alpha isomer was detected and there were minimal differences between the different sampling sites (5.9-13.3pgm-3). In the case of dieldrin, the highest concentrations (33.6pgm-3) were found at the mountain site, which may have been due to its use for insect control. Although heptachlor epoxide was not detected, the concentration of heptachlor was significantly higher at the agricultural and downtown sites (∼3.6pgm-3). Regarding DDTs, the isomers p,p'-DDT and p,p'-DDE showed the highest concentrations at the mountain site (ΣDDT 120 ± 12pgm-3) and downtown site (ΣDDT 157 ± 62pgm-3). The relationship between the isomers suggested that at the downtown site, the contribution of this pesticide to the environment was recent, probably for the control of diseases vectors. The congener pattern of PBDEs was dominated by BDE-47, and BDE-99 at all sites, with the downtown site having the highest concentrations of compound esters (ΣPBDEs 118 ± 38pgm-3). Finally, high concentrations of PCBs were found at the industrial site (ΣPCBs 1677 ± 134pgm-3), and the predominating homologs were 5-Cl and 6-Cl, in contrast to the other sites where PCBs were dominated by 3-Cl and 4-Cl. This is the first study of POPs carried out in the province of Córdoba.

A Comprehensive Review of Analytical Methods for Determining Persistent Organic Pollutants in Air, Soil, Water and Waste

The Persistent Organic Pollutants (POPs) are compounds (i.e., Polycyclic Aromatic Hydrocarbons PAHs, Polychlorinated Biphenyls PCBs, Polychlorinated dibenzodioxins/ dibenzofurans PCDD/Fs, PBDDs, Polybrominated diphenyl ethers PBDEs, hexachlorocyclohexane isomers HCHs, etc.) with precise physical and chemical properties such that they remain intact for long periods. Because of their persistence, POPs bioaccumulate with potential significant impacts on human health and the environment. Since the last decades, the scientific community has felt the need to investigate such compounds at very low levels and so it has developed novel analytical protocols based on extraction and clean-up procedures followed by Gas Chromatography/High Performance Liquid Chromatography- Mass Spectrometry (GC/HPLC-MS) analysis. This review would like to focus the attention on analytical methodologies set up during the last 5 years (2012-2016): the main papers reporting significant advancements in the analytical protocols for analyzing POPs in different environmental matrices such as air, soil, water and waste, will be illustrated and discussed. Keywords: Review, POPs, analytical methods, chromatography, air, soil, water, waste.

Assessment of POPs in air from Spain using passive sampling from 2008 to 2015. Part I: Spatial and temporal observations of PBDEs

The Stockholm Convention (SC) on Persistent Organic Pollutants (POPs) calls for the Parties' effectiveness evaluation of those measures taken to meet the reduction and eventual elimination of POPs from the environment. With that goal, air concentrations of different POP families have been measured uninterruptedly since 2008 under the Spanish Monitoring Program (SMP) by means of passive air sampling. This work focuses on data for polybrominated diphenyl ethers (PBDEs) determined in a total of 321 samples collected seasonally each year in 5 urban and 7 background sites. Neither significant temporal trends nor significant seasonal variations for total PBDE air burdens were detected. In contrast, significant variations were found among PBDE congeners. Those related to the octa-PBDE formulation significantly decreased in the study period. However, PBDEs related to the penta-formulation showed steady concentrations while PBDE-209, the congener found at the greatest levels, showed increasing or steady levels in most sampling sites. Seasonal variations were also markedly different among congeners. Concentrations of the lightest PBDEs (tri- to penta-substituted) were highly influenced by ambient temperature (T), showing maximum values in summer probably due to higher volatilization rates compared to those of heavier PBDEs. Contrarily, no clear seasonal trends were found for hexa- to deca-PBDEs, which were negatively related to precipitation; thereby, indicating an efficient atmospheric wash out by wet deposition episodes. Regarding spatial patterns, overall significant greater PBDE levels were found in cities compared to background areas, pointing out the role of highly populated areas as sources for these pollutants in Spain. Yet and especially in the case of PBDE-209, our results suggested the presence of significant unknown sources of PBDEs in some background sites. Further monitoring efforts are needed to assess potential unknown sources in the sampling network as well as to ensure temporal trends of these pollutants in Spain.

Low concentrations of persistent organic pollutants (POPs) in air at Cape Verde

Ambient air is a core medium for monitoring of persistent organic pollutants (POPs) under the Stockholm Convention and is used in studies of global transports of POPs and their atmospheric sources and source regions. Still, data based on active air sampling remain scarce in many regions. The primary objectives of this study were to (i) monitor concentrations of selected POPs in air outside West Africa, and (ii) to evaluate potential atmospheric processes and source regions affecting measured concentrations. For this purpose, an active high-volume air sampler was installed on the Cape Verde Atmospheric Observatory at Cape Verde outside the coast of West Africa. Sampling commenced in May 2012 and 43 samples (24h sampling) were collected until June 2013. The samples were analyzed for selected polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), hexachlorobenzene (HCB) and chlordanes. The concentrations of these POPs at Cape Verde were generally low and comparable to remote sites in the Arctic for several compounds. Seasonal trends varied between compounds and concentrations exhibited strong temperature dependence for chlordanes. Our results indicate net volatilization from the Atlantic Ocean north of Cape Verde as sources of these POPs. Air mass back trajectories demonstrated that air masses measured at Cape Verde were generally transported from the Atlantic Ocean or the North African continent. Overall, the low concentrations in air at Cape Verde were likely explained by absence of major emissions in areas from which the air masses originated combined with depletion during long-range atmospheric transport due to enhanced degradation under tropical conditions (high temperatures and concentrations of hydroxyl radicals).

Persistent organic pollutants in the Atlantic and southern oceans and oceanic atmosphere.

Persistent organic pollutants (POPs) continue to cycle through the atmosphere and hydrosphere despite banned or severely restricted usages. Global scale analyses of POPs are challenging, but knowledge of the current distribution of these compounds is needed to understand the movement and long-term consequences of their global use. In the current study, air and seawater samples were collected Oct. 2007-Jan. 2008 aboard the Icebreaker Oden en route from Göteborg, Sweden to McMurdo Station, Antarctica. Both air and surface seawater samples consistently contained α-hexachlorocyclohexane (α-HCH), γ-HCH, hexachlorobenzene (HCB), α-Endosulfan, and polychlorinated biphenyls (PCBs). Sample concentrations for most POPs in air were higher in the northern hemisphere with the exception of HCB, which had high gas phase concentrations in the northern and southern latitudes and low concentrations near the equator. South Atlantic and Southern Ocean seawater had a high ratio of α-HCH to γ-HCH, indicating persisting levels from technical grade sources. The Atlantic and Southern Ocean continue to be net sinks for atmospheric α-, γ-HCH, and Endosulfan despite declining usage.

Assessing levels of POPs in air over the South Atlantic Ocean off the coast of South America

The occurrence of persistent organic pollutants (POPs) in the atmosphere of the near-coast South Atlantic Ocean was studied. Air samples were collected using a high-volume air sampler (filter and polyurethane foam) on board the Argentinean research cruise R/V Puerto Deseado (CONICET). Samples were analyzed for 50 polychlorinated biphenyl (PCBs), 22 organochlorine pesticides (OCPs) and 14 polybrominated diphenyl ethers (PBDEs). These POPs classes showed a trend of decreasing levels from near-shore to open ocean sites. OCPs and PCBs were in the same order of magnitude (2.71–87.1pg/m3 and 9.56–130pg/m3, respectively) while PBDEs levels were significantly lower (0.69–2.58pg/m3). Dichlorodiphenyltrichloroethanes (DDTs), endosulfans, chlordanes, hexachlorocyclohexanes (HCHs) and heptachlors were between 0.20 and 17.8pg/m3, while drines and hexachlorobenzene (HCB) were at lower levels (0.28–3.71pg/m3). The most frequently detected PCBs were congeners 32, 28, 44, 52, 95, representing >50% of the total. The PBDEs congener pattern was dominated by congener 209 (70%), followed by 47 and 99 (16% and 7%, respectively). Air parcel back trajectories for the study period provided few insights as trajectories mainly stemmed from the open ocean with limited inputs from continental sources. These results indicate that the concentration of POPs (namely PCBs, OCPs, and PBDEs) in air remain elevated in the near-shore environment and then drop-off substantially beyond a distance of about 400km. This has implications for the loading of POPs and delivery to the marine environment in the near coastal zone.

Evaluation of passive air sampler calibrations: Selection of sampling rates and implications for the measurement of persistent organic pollutants in air

Polyurethane foam (PUF) passive air samplers (PAS) are a common and highly useful method of sampling persistent organic pollutants (POP) concentrations in air. PAS calibration is necessary to obtain reasonable and comparable semi-quantitative measures of air concentrations. Various methods are found in the literature concerning PAS calibration. 35 studies on PAS use and calibration are examined here, in conjunction with a study involving 10 PAS deployed concurrently in outdoor air with a low-volume air sampler in order to measure the sampling rates of PUF-PAS for polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), polycyclic musks (PCMs), and polycyclic aromatic hydrocarbons (PAHs). Based on this analysis it is recommended that (1) PAS should be assumed to represent bulk rather than gas-phase compound concentrations due to the sampling of particle-bound compounds, (2) calibration of PAS sampling rates is more accurately achieved using an active low-volume air sampler rather than depuration compounds since the former measures gas- and particle-phase compounds and does so continuously over the deployment period of the PAS, and (3) homolog-specific sampling rates based on KOA groupings be used in preference to compound/congener-specific or single sampling rates.

Recent trends of persistent organic pollutants in air in central Europe - Air monitoring in combination with air mass trajectory statistics as a tool to study the effectivity of regional chemical policy

We use air mass back trajectory analysis of persistent organic pollutant (POP) levels monitored at a regional background site, Košetice, Czech Republic, as a tool to study the effectiveness of emission reduction measures taken in the last decade in the region. The representativity of the chosen trajectory starting height for air sampling near ground was ensured by excluding trajectories starting at time of inversions lower than their starting height. As the relevant pollutant sources are exclusively located in the atmospheric boundary layer, trajectory segments above this layer were also excluded from the analysis. We used a linear time weight to account for the influence of dispersion and deposition on trace components abundances and to quantify the ground source loading, a continuous measure for the influence of surface emissions. Hexachlorocyclohexanes (HCHs), hexachlorobenzene (HCB), polychlorinated biphenyls (PCBs), DDT, and two time periods, the years 1997–1999 and 2004–2006, were studied. The pollutant levels transported to Košetice decreased for all substances except HCB. Except for lindane seasonal emissions were insignificant. Increasing emissions of HCB were at least partly linked to the 2002 floods in the Danube basin. Major emissions of 1997–1999 which decreased significantly were in France (lindane), western Poland, Hungary and northern ex-Yugoslavia (technical HCH), and the Czech Republic (DDT). Emissions remaining in 2004–2006 include HCB and DDT in the northern Czech Republic, HCB and PCBs in Germany. Besides changes in emission strength meteorological factors influence the level of transported pollutant concentrations. The prevailing air flow pattern limits the geographic coverage of this analysis to central Europe and parts of western Europe. However, no POP monitoring stations exist in areas suitable for a possible extension of the study area.

Levels of persistent organic pollutants in air in China and over the Yellow Sea

The occurrence of persistent toxic substances (PTS) in China and possibly their regional transport in the Yellow and East China Seas region was studied. Organochlorines in atmospheric gas-phase and particulate matter were collected by high-volume sampling (filters and polyurethane foams) during 2 weeks in June 2003 (dry season) simultaneously at a Yellow Sea coastal site in an urban area, Qingdao, China, and a rural island site, Gosan, Jeju Island, Korea. Using GC methods, the samples were analysed for 9 persistent organic pollutants (POPs) regulated under the global POP convention, namely aldrin, chlordane ( cis- and trans-isomers CC and TC), DDT and metabolites ( o, p′-DDT, p, p′-DDD, and p, p′-DDE), dieldrin, endrin, heptachlor, hexachlorobenzene (HCB), mirex and PCB (congeners number 28, 52, 101, 153 and 180), and for hexachlorocyclohexane ( α-, β- and γ-isomers), a PTS and now considered for regulation under the convention, too. At the coastal site additionally o, p′-DDE and -DDD, β-endosulfan, isodrin, heptachlorepoxide and δ-HCH, and at the island site additionally p, p′-DDT and 12 additional PCB congeners were analysed. 9 samples were collected at the coastal and 15 (for PCBs 5) at the island site. Long-range advection pathways were determined based on analysed back-trajectory calculations. The mean concentrations of DDT and its metabolites, HCB, HCH, and PCB at the coast were in the 100–1000 pg m −3 range. Higher concentrations prevailed during nighttime. The levels were in general lower at the island site, but not for DDT. Local sources are likely. PCBs were even 2 orders of magnitude lower, suggesting that PCBs are not subject to regional transport but elevated concentrations in air are limited to the source areas. Organochlorine pesticide levels on the other hand were seemingly determined by regional transport over Mainland China rather than by emissions in the coastal area. The currently used pesticides mirex and chlordane were found at elevated levels, i.e. 79 (6.6–255) and 36 (<6–71) pg m −3, respectively, at the coast but not over the island. The POPs pesticides aldrin, dieldrin and endrin, never registered in China, were mostly found at <10 pg m −3 except for endrin at the coastal site (up to 400 pg m −3) and aldrin at the island site (up to 50 pg m −3).