Concentrations Of HCHs Research Articles

Elevated Concentrations of Pesticides and PCBs in Soils at the Southern Caspian Sea (Iran) are Related to Land Use

Soil contamination by organochlorine pesticides or PCBs is almost undocumented for Iran. Here we report a soil survey in Mazandaran and Guilan provinces that hold >30% of the agricultural areas of Iran where pesticide use is widespread. Concentration of DDTs, HCHs, cyclodienes, and PCBs were measured in 45 soil samples from different agricultural land uses and forest land. The average concentrations of ∑DDT (37 μg kg−1) and ∑HCH (21 μg kg−1) in agricultural soils are among the largest ever reported and exceed international soil screening standards. All residues were larger in agricultural than in forest soil. Within agricultural land, ∑DDT were largest for tea gardens, lindane was largest in rice fields, and cyclodiens largest in citrus orchards. The ratio of (DDD + DDE)/DDT is an index of the extent of DDT degradation in soil and was lower in tea gardens than in other soils (0.7 versus 2–5), indicating either ongoing DDT input or lower degradation rate in the tea gardens that are more acid than the other soils (pH 4.5 versus 6.5–7.0). The o,p′–DDT/p,p′–DDT ratio was about 3 in forest soils, suggesting that DDT is derived from dicofol application and not from technical DDT as in agricultural soils. The PCB 28, 180, and 138 showed the highest mean concentration compared with other PCB congeners in all land uses. This survey is the first of this kind for Iran and illustrates that concentrations of organochlorine pesticide in soil are relatively large.

Contamination and risk assessment of organochlorines in surface sediments of Egyptian Mediterranean coast

The levels of 20 organochlorine pesticides (OCPs) in addition to 10 polychlorinated biphenyls (PCBs) in sediments of Egyptian Mediterranean coast were investigated to evaluate their pollution potential on the environment. The OCPs were HCHs, DDTs and cyclodienes (aldrin, dieldrin, endrin, endrin aldehyde, endrin ketone, heptachlor, heptachloro epoxide, γ-chlordane, α-chlordane, methoxychlor, endosulfan I, endosulfan II and endosulfan sulfate). Concentrations of PCBs, HCHs, DDTs and cyclodienes ranged from 0.31 to 1.95, 0.09 to 3.31, 0.08 to 3.31 and 0.23 to 2.51ng/g dry weight, respectively. Investigation of OCPs leads to the fact, that DDTs have greater potential for distribution than both HCHs and cyclodienes. Risk assessment of organochlorines in surface sediment was conducted and the results indicate that the concentrations of some OCPs contaminated in the sediments may pose few risks to the local aquatic system. Principal component factor and cluster analysis concluded that it is impossible to predict the distribution patterns of the OCPs in contaminated area, and there is a lack of correlation between PCBs and most of OCPs. This explains the variety of organochlorines input sources to studied locations.

Polychlorinated Biphenyls and Chlorinated Pesticides in Sediments along the Semi-Closed Areas of Alexandria, Egypt

The residues of 19 EPA-organochlorine pollutants were analyzed in sediments collected from 49 different locations along the semi-closed areas of Alexandria, Egypt. The pollutants studied were 7 individual polychlorinatedbiphenyl (PCB) congeners, α,β,γ-hexachlorocyclohexane (HCHs), cyclodienes (aldrin, endrin, dieldrin) and dichlorodiphenyltrichloroethanes (DDTs) (o,p-DDE, p,p-DDE, o,p-DDD, p,p-DDD, o,p-DDT, p,p-DDT). The concentration of total DDTs ranged between ND and 123.76 ng.g-1 (dry wt) whereas the concentration of PCBs, HCHs and cyclodienes ranged from ND to 192.24 ng.g-1; ND to 20.78 ng.g-1 and ND to 8.04 ng.g-1 dry wt, respectively. The average total organic carbon (TOC) percent was varied from 0.04 to 7.65%.

Using PUF disk passive samplers to simultaneously measure air concentrations of persistent organic pollutants (POPs) across the Tuscany Region, Italy

Passive air samplers consisting of polyurethane foam (PUF) disks were deployed simultaneously over 2–4 month periods from April to July 2008 at 19 locations throughout the Tuscany Region at urban (n=9), rural (n=7) and agricultural sites (n=3). The purpose of the study was to assess the gas–phase air concentrations of PCBs, OCPs, PBDEs and PAHs on a local and regional scale. Derived air concentrations (pg m−3) ranged from below detection limit (BDL) to 300 for Σ6PCBs and from BDL to 30 for Σ3PBDEs. As expected, the highest PCB concentrations (pg m−3) were observed at urban sites, peaking in Piombino (300). PBDEs, however, exhibited a “reverse gradient” (i.e. rural>agricultural>urban) with highest air concentration at the rural site, Arcidoso (30). Levels of OCPs showed less distinct differences among the three site types. The most frequently detected OCPs were Endosulfan I, γ–HCH and α–HCH. Endosulfan I ranged from BDL to 2 200pg m−3, α–HCH from BDL to 610, and γ–HCH from BDL to 1 100. The high air concentrations of HCHs were surprising and possibly due to continued and illegal use – especially at agricultural and urban sites that exhibited the highest levels in air. PAHs showed highest concentrations (pg m−3) at agricultural and urban sites, ranging from 290 to 4 700 and were generally consistent with other data sets from Europe. PAHs were dominated by the 3–ring PAHs (76±6)%, with phenanthrene alone accounting for (45±11%) of the total PAHs. This study demonstrates the feasibility of using PUF disks as time–integrating passive air samplers for assessing local and regional scale concentrations of a wide range of POPs in central Italy. Given their low cost and simplicity, passive air samplers are the preferred option for conducting concurrent sampling at multiple sites for monitoring and research purposes.

Organochlorine pesticides and polychlorinated biphenyls in sediments and fish from freshwater cultured fish ponds in different agricultural contexts in north-eastern France

Organochlorine pesticides (HCB, HCH with α-, β-, and γ isomers, heptachlor, cis-heptachlor epoxyde, trans-heptachlor epoxyde, endosulfan with α- and β isomers, sulfate endosulfan, o, p′-DDT, p, p′-DDT, o, p′-DDE, p, p′-DDE, o, p′-DDD, p, p′-DDD, chlorothalonil, alachlor, aldrin, dieldrin, methoxychlor, oxychlordane, chlordane with α- and γ isomers, p, p′-dicofol and o, p′-dicofol) and indicators PCBs (IUPAC nos. 28, 52, 101, 118, 138, 153, and 180) were studied both in sediments and muscles of farmed fish species ( Cyprinus carpio and Perca fluviatilis). Samples were collected from fish ponds located in the hydrographic basin of the Moselle River (Lorraine Region, France). OCPs and PCBs were present at low concentrations both in sediments and fish muscles. Concerning sediments, ∑DDTs revealed concentrations ranging from 0.2 to 2.30 ng g −1 dw and ∑PCBs ranged from 0.3 to 3.5 ng g −1 dw. Concerning fish muscles, the highest concentrations in OCPs were those of p, p′-DDE, with average concentrations of 0.57±0.44 ng g −1 ww for carp and 0.58±0.29 ng g −1 ww for perch. The contamination profiles proved to be different depending on the fish species. Indeed, HCH-isomers, HCB, and dieldrin were detected only for the carp and always at low concentrations. For example, the highest concentration of HCHs was observed for β-HCH with a mean value of 0.64±0.15 ng g −1 ww for carp. As for PCBs, the levels of ∑PCBs ranged from 0.3 to 6.4 ng g −1 ww in carp muscles and from 0.90 to 5.60 ng g −1 ww in perch muscles.

Concentrations and classification of HCHs and DDTs in soil from the lower reaches of the Jiulong River, China

Soil is an important source to other environmental media and organisms for organochlorine pesticides (OCPs) bioaccumulation. Twenty-four representative surface soil samples were collected from the lower reaches of the Jiulong River, China, in 2009. The concentrations of hexachlorocyclohexane isomers (HCHs) ranged from 0.38 to 39.52 ng·g−1, with a mean value of 9.51 ng·g−1. The concentrations of dichlorodiphenyltrichloroethanes (DDTs) and their metabolites were within the ranges of 0.94–700.99 ng·g−1, with a mean value of 71.17 ng·g−1. The concentrations of HCHs and DDTs in the soil were lower than the first grade level (50 ng·g−1) of the Chinese Environmental Quality Standard (GB15618-1995). Hierarchical Cluster Analysis (HCA) and Pearson’s bivariate Correlations Analysis (PCA) were used to analyse the distribution and contamination levels of OCPs in this region. The results showed that DDTs were the major contaminants and there were no significant correlations between various OCPs concentrations and the total organic carbon (TOC) contents. A significant positive correlation was observed between HCHs and DDTs (p<0.01), which indicates that HCHs and DDTs may have similar sources and fate in the study area.

Organochlorine pesticides in sediments of Laizhou Bay and its adjacent rivers, North China

Organochlorine pesticides (HCHs, DDTs and HCB) have been investigated in sediments of Laizhou Bay and its adjacent rivers. The average concentrations of HCHs, DDTs and HCBs are 0.09ng/gdw, 0.59 and 0.05 for marine sediments and 0.55, 8.6 and 1.1 for riverine sediments, respectively. Laizhou Bay is less contaminated by HCHs and DDTs in comparison with other coastal regions around the world, including the other two biggest bays in Bohai Sea. Fresh input of lindane and dicofol-type DDT were found in several riverine sites. Relatively strong TOC-dependence of HCB distribution in the entire studied area suggested no point source existed and/or water–sediment equilibrium achieved. No significant difference of α/γ-HCH ratios have been observed between marine and riverine sediments. However, o,p′-DDT/p,p′-DDT ratios varied largely between the two regions.

Effects of different treatments on soil-borne DDT and HCH dynamics and plant uptake

Pot experiments were conducted to examine the effects of various fertilizers, as well as soil dilution treatments on the dynamics of soil-borne DDTs [sum of dichlorodiphenyltrichloroethane (DDT), chlorodiphenyldichloroethylene (DDE) and di- chlorodiphenyldichloroethane (DDD)] and hexachlorocyclohexanes (HCHs, sum of α-HCH, β-HCH, γ-HCH and δ-HCH) and their subsequent impacts on the uptake of DDTs and HCHs by a test plant. The results show that the soil residual DDTs and HCHs concentrations in the iron-rich fertilizer-treated soil were significantly lower than those in other fertilizer-treated soils. There was a close relationship between the soil residual DDTs and the plant tissue DDTs. This suggests that the uptake rate of DDTs by the plant was dependent on the concentration of soil-borne DDTs. A less close relationship between soil residual HCHs and plant tissue HCHs was also observed. Dilution of pesticide-contaminated soil with the non-contaminated soil not only physically reduced the concentration of pesticides in the soil but also enhanced the loss of soil-borne pesticides, possibly through the improvement of soil conditions for microbial degradation. Soil dilution had a better effect on promoting the loss of soil-borne HCHs, relative to soil-borne-DDTs. The research findings obtained from this study have implications for management of heavily contaminated soils with DDTs and HCHs. Remediation of DDTs and HCHs-contaminated soils in a cost-effective way can be achieved by incorporating treatment techniques into conventional agricultural practices. Applications of iron-rich fertilizer and soil dilution treatments could cost-effectively reduce soil-borne DDTs and HCHs, and subsequently the uptake of these organochlorine pesticides by vegetables.

Passive air sampling of organochlorine pesticides in a northeastern state of India, Manipur

Abstract Thirty-six polyurethane foam disk passive air samplers (PUF-PAS) were deployed over a year during January to December, 2009 at three locations, i.e., Imphal (urban site), Thoubal (rural site) and Waithou (alpine site) of Manipur, to assess the seasonal local atmospheric emission of selected organochlorine pesticides (OCPs). The average concentration of HCHs monitored at mountain site during hot season (Mar, Apr, and May) and rainy seasons (Jun, Jul, Aug, and Sep) were 403 and 349 pg/m 3, respectively. DDTs had a high concentration with 384 pg/m 3 at rural site and 379 pg/m 3 at urban site during hot seasons. Endosulfans and chlordane were found high in concentration during hot seasons (260 pg/m 3) and low during retreating monsoon seasons (44 pg/m 3) at rural site. Most of the OCPs concentrations were high during cultivation period. The OCP concentrations of rainy season were highly correlated (p < 0.01) with OCPs of hot seasons. Further, positive correlation ( p < 0.05) was also obtained between cold seasons and retreating monsoon. Principal component analysis showed a significant correlation among the four seasons and distribution pattern of OCPs in air. Back trajectory analysis by using HYPSLIT model showed a long range air transport of OCPs to the present study area. Present OCP levels at Manipur is an outcome of both local emission and also movement of air mass by long range atmospheric transport.

Halogenated POPs and PAHs in Blood Plasma of Hong Kong Residents

The objective of this study was to quantify organic chlorinated pesticides (OCPs), polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), and polycyclic aromatic hydrocarbons (PAHs) in blood plasma collected from 111 healthy residents in Hong Kong to assess the levels of these pollutants in the general population during the period of March to April, 2008. Concentrations of these residues in blood plasma obtained from the Hong Kong Red Cross Blood Transfusion Service were determined by gas chromatography-mass spectrometry. Naphthalene, phenanthrene, p,p'-DDE, PCB-180, and PBDE-47 were detected in 100% of the participants. Females had significantly greater concentrations of acenaphthylene (female: 93.3 ng/g lipid; male: 39.8, p < 0.05), anthracene (22.3; 15.3, p < 0.05), fluoranthene (138; 125, p < 0.05), p,p'-DDE, p,p'-DDT, PCB-183, BDE-99 than males. Blood of smokers contained significantly greater (p < 0.05) concentrations of acenaphthene, benzo(a)pyrene, p,p'-DDE, p,p'-DDT, PCB-138, BDE-47, and BDE-99 than did blood of nonsmokers. Positive correlations were found between concentrations of each class of pollutant, with respect to seafood diet habit, Body Mass Index (BMI), and age. Concentrations of HCHs and DDTs in blood plasma of healthy Hong Kong residents were greater than those of other countries, and it was found that smoking, consumption of a seafood diet, BMI, and age could influence concentrations in human blood.

Health risk assessment of organochlorine pesticides with emphasis on DDTs and HCHs in abandoned agricultural soils

The aim of this study was to evaluate the consequence of changing land use from agriculture land to other use purposes with respect to OCPs non-cancer and cancer risk on human health, based on concentrations of DDTs and HCHs in soils collected from 55 locations representing 12 different land use types. There were no non-cancer risks of DDTs and γ-HCHs on adults and children, and there were very low cancer risks of DDD, o,p'-DDE, DDT, α-HCH, β-HCH, γ-HCH based on their total concentrations in all samples. Nonetheless, there were significant correlations of DDT to its metabolites (DDE and DDD) (r = 0.506 and r = 0.648) and DDE to DDD (r = 0.438) both at p < 0.01. OCP levels should be routinely monitored in different environmental media and food in order to verify whether there is fresh input. Their potential risks on human health should also be assessed.

Distribution of HCHs and DDTs in Agricultural Soil of Pudong New Area, Shanghai

To study HCHs and DDTs contents and their spatial distribution in the agricultural soil of Pudong, Shanghai, the residue amounts of HCHs and DDTs in 238 surface soil samples were determined. The results showed that concentrations of HCHs ranged from 0.001 to 0.050 mg/kg and DDTs ranged from 0.001 to 0.067 mg/kg, with both occurrences of 100%. The spatial analysis indicated that there was the obvious regional differentiation in soil pollution. Compared with HCHs, soil quality was contaminated more seriously by DDTs in the study area. In addition, areas with high contents of HCHs were mainly located in Jichang, Chuansha and Sanlin, whereas areas with high concentrations of DDTs mainly lied in Sanlin, Jichang, Tang, Chuansha and Caolu.

Persistent organic pollutants in food items collected in Hong Kong

This study aims to investigate levels of POPs in meat, edible oils, nuts, milk and wine collected from Hong Kong. Naphthalene, pp-DDE, beta-, gamma-HCH and PBDE 47 were detected in most of the food items. Goose liver accumulated the highest PAHs (47.9 ng g −1 wet wt), DDTs (25.6), HCHs (13.0), PCBs (4.17), PBDEs (468 pg g −1 wet wt) among all the selected food. Meat and nut groups had significant ( p < 0.01 or 0.05) correlations between lipid contents and concentrations of PAHs (meat: r = 0.878), HCHs (meat: r = 0.753), DDTs (meat: r = 0.937; nuts: r = 0.968) and PCBs (meat: r = 0.832; nut: r = 0.946). The concentrations of DDTs, HCHs and PCBs in vegetable oil were lower, but HCHs in fish oil were higher, when compared with other countries. The concentrations of PAHs, DDTs, PCBs and PBDEs in food tested in the present study were all below various safety guidelines.

Organochlorine pesticides (HCHs and DDTs) in soils along the north coastal areas of the Bohai Sea, China

A systematic survey of organochlorine pesticides (OCPs) including hexachlorocyclohexane isomers (α-HCH, β-HCH, γ-HCH, δ-HCH and ΣHCH) and dichlorodiphenyltrichloroethane metabolites (p,p′-DDT, p,p′-DDE, o,p′-DDT, p,p′-DDD and ∑DDT) in soils along the north coastal areas of the Bohai Sea, China, has been lacking. In this study, 31 representative surface soil samples were collected along the north coastal and riverine areas of the Bohai Sea to characterise the potential for adverse effects of ∑HCH, ∑DDT and their individual isomers and transformation products. Concentrations of ΣHCH and ΣDDT in soils ranged from less than the limit of detection (<LOD) to 3.0 × 101 ng · g−1 dw (mean: 3.5 ng · g−1 dw) and<LOD to 2.6 × 102 ng · g−1 dw (mean: 1.7 × 101 ng · g−1 dw), respectively. Compared with studies of OCPs in soils from other locations, concentrations of HCHs and DDTs observed in this study were moderate. Concentrations of OCPs observed in soils were generally less than proposed reference values. HCH residues were a mixture of historical technical HCH and current lindane sources. The pattern of DDTs was consistent with historical releases of technical DDTs. Selected soil physicochemical properties did not explain the sorption and/or partitioning of HCHs or DDTs.

Occurrence and source identification of organochlorine pesticides in the surrounding surface soils of the Ittehad Chemical Industries Kalashah Kaku, Pakistan

Surface soil and sediment samples were collected from the surroundings of the Ittehad Chemical Industries Kalashah Kaku industrial zone to assess residual level of 19 organochlorine pesticides (OCPs) and identify their sources. DDTs and HCHs were most prevalent OCPs and general pattern of contamination followed the order: ∑DDT > ∑HCH > dicofol > endrin > heptachlor > dieldrin > endosulfan II. Total measured concentrations of HCHs (6.38–121.71 ng/g) and DDTs (759.65–1811.98 ng/g) were greater in the soil samples collected from fodder/rice fields irrigated with the factory effluents and in the surrounding of waste disposal site. Ratios of β to γ-HCH highlighted an old mixed source of technical HCH and lindane in surface soils. Predominance of p,p′-DDT and p,p′-DDE among isomers and metabolites showed that large quantity of technical grade DDT is still present in the surrounding surface soils. Six soil samples were categorized as heavy polluted soils (class III category of DDT > 1,000 ng/g), two soil samples into less polluted soil between class I and II (50–500 ng/g) and 28 soil samples as non-polluted (<50 ng/g) according to environmental quality standards for surface soils. Six soil samples were categorized as less polluted between class I and II of HCHs (50–500 ng/g). Greater concentration of DDTs and HCHs above quality guideline poses potential exposure risk to biological organisms, safety of agricultural products and human health in the surrounding of the Ittehad Chemical Industries.

Variations of organochlorine pesticides and polychlorinated biphenyls in atmosphere of the Tibetan Plateau: Role of the monsoon system

Monsoon transport is an important process that influences the global transport of persistent organic pollutants. Only a few studies focused on the influence of monsoon on organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) levels in the Tibetan Plateau. In this study, 19 samples were collected in Lhasa, the capital of Tibet Autonomous Region, using a high-volume air sampler. The average concentrations of α-HCH, γ-HCH, p-p′-DDT, p-p′-DDE, o-p′-DDT, α-endosulfan, β-endosulfan and PCBs (including PCB-28, 101, and 118) were 2.3, 10.3, 3.2, 2.9, 5.8, 6.3, 2.2, and 10.6 pg m −3, respectively. The weak correlation coefficients between ln p (natural logarithm of partial pressure) and 1/T (reciprocal temperature) were obtained for DDTs and β-endosulfan ( r 2 values ranged from 0.13 to 0.41). However, no significant correlations were obtained for HCHs and PCBs. These results suggested that both local emission and long-range atmospheric transport (monsoon) may influence the distribution of OCPs at Lhasa. In this study, peak concentrations of DDTs, endosulfans and PCBs were found in August, when Eastern Monsoon system occurred. However, the maximum concentrations of HCHs appeared in June (Indian Monsoon is the dominant air circulation pattern). Monthly variation of OCP/PCB levels was likely associated with the different air sources of monsoon system.

Reproductive performance in East Greenland polar bears ( Ursus maritimus) may be affected by organohalogen contaminants as shown by physiologically-based pharmacokinetic (PBPK) modelling

Polar bears ( Ursus maritimus) feed mainly on ringed seal ( Phoca hispida) and consume large quantities of blubber and consequently have one of the highest tissue concentrations of organohalogen contaminants (OHCs) worldwide. In East Greenland, studies of OHC time trends and organ system health effects, including reproductive, were conducted during 1990–2006. However, it has been difficult to determine the nature of the effects induced by OHC exposures on wild caught polar bears using body burden data and associated changes in reproductive organs and systems. We therefore conducted a risk quotient (RQ) evaluation to more quantitatively evaluate the effect risk on reproduction (embryotoxicity and teratogenicity) based on the critical body residue (CBR) concept and using a physiologically-based pharmacokinetic (PBPK) model. We applied modelling approaches to PCBs, p, p′-DDE, dieldrin, oxychlordane, HCHs, HCB, PBDEs and PFOS in East Greenland polar bears based on known OHC pharmacokinetics and dynamics in laboratory rats ( Rattus rattus). The results showed that subcutaneous adipose tissue concentrations of dieldrin (range: 79–1271 ng g −1 lw) and PCBs (range: 4128–53 923 ng g −1 lw) reported in bears in the year 1990 were in the range to elicit possible adverse health effects on reproduction in polar bears in East Greenland (all RQs ⩾ 1). Similar results were found for PCBs (range: 1928–17 376 ng g −1 lw) and PFOS (range: 104–2840 ng g −1 ww) in the year 2000 and for dieldrin (range: 43–640 ng g −1 lw), PCBs (range: 3491–13 243 ng g −1 lw) and PFOS (range: 1332–6160 ng g −1 ww) in the year 2006. The concentrations of oxychlordane, DDTs, HCB and HCHs in polar bears resulted in RQs < 1 and thus appear less likely to be linked to reproductive effects. Furthermore, sumRQs above 1 suggested risk for OHC additive effects. Thus, previous suggestions of possible adverse health effects in polar bears correlated to OHC exposure are supported by the present study. This study also indicates that PBPK models may be a supportive tool in the evaluation of possible OHC-mediated health effects for Arctic wildlife.

Current status and historical trends of organochlorine pesticides in the ecosystem of Deep Bay, South China

To characterize the current status and historical trends in organochlorine pesticides (OCPs) contamination in Deep Bay, an important water body between Hong Kong and mainland China with a Ramsar mangrove wetland (Maipo), samples from seawater, suspended particulate matter (SPM), surface sediment, sediment core and fish were collected to determine the OCPs concentrations. Sediment core dating was accomplished using the 210Pb method. The average concentrations of DDTs, HCHs and chlordanes in water were 1.96, 0.71, 0.81 ng l −1, while in SPM were 36.5, 2.5, 35.7 ng g −1 dry weight, in surface sediment were 20.2, 0.50, 2.4 ng g −1 dry weight, and in fish were 125.4, 0.43, 13.1 ng g −1 wet weight, respectively. DDTs concentrations in various matrices of Deep Bay were intermediate compared with those in other areas. Temporal trends of the targeted OCPs levels in sediment core generally increased from 1948 to 2004, with the highest levels in top or sub-surface sediment. Both DDT composition and historical trends indicated an ongoing fresh DDT input. A positive relationship between the bioconcentration factor (BCF) of target chemicals and the corresponding octanol–water partition coefficient ( K ow), and between the biota-sediment accumulation factors (BSAF) and the K ow were observed in the Bay. The risk assessment indicated that there were potential ecological and human health risks for the target OCPs in Deep Bay.

International Pellet Watch: Global monitoring of persistent organic pollutants (POPs) in coastal waters. 1. Initial phase data on PCBs, DDTs, and HCHs

Samples of polyethylene pellets were collected at 30 beaches from 17 countries and analyzed for organochlorine compounds. PCB concentrations in the pellets were highest on US coasts, followed by western Europe and Japan, and were lower in tropical Asia, southern Africa and Australia. This spatial pattern reflected regional differences in the usage of PCBs and was positively correlated with data from Mussel Watch, another monitoring approach. DDTs showed high concentrations on the US west coast and in Vietnam. In Vietnam, DDT was predominant over its metabolites (DDE and DDD), suggesting the principal source may be current usage of the pesticide for malaria control. High concentrations of pesticide HCHs were detected in the pellets from southern Africa, suggesting current usage of the pesticides in southern Africa. This study demonstrates the utility and feasibility of the International Pellet Watch approach to monitor POPs at a global scale.

Feasibility of poplar foliages as bio-monitors for organochlorine pesticides in air

The feasibility of poplar (P. tomentosa) foliages as passive biomonitors for organochlorine pesticides in air was explored. The accumulation patterns of poplar foliages for HCHs, DDTs and HCB were similar, the amount of HCHs, DDTs and HCB increased with foliage growth in spring, and decreased thereafter. There was no obvious distinction in the accumulation styles between the adult leaf and the leaf-litter. This accumulation pattern is likely related to the growing process of the poplar foliage, and was observed for the first time in our work, giving an evidence for the “bud burst effect” in plants. The technical HCH and DDT were used largely in history and not used in recent years, but there was a little usage of lindane and new input of o,p’-DDT in recent years, and dicofol usage may be the main source of o,p’-DDT. Concentrations of HCHs, DDTs and HCB in poplar foliages were similar to those in pine needles at the corresponding period, and there is a positive strong correlation between OCP concentration data of two kinds of trees. It presents no difference in the accumulation style between two kinds of trees. The level of OCPs in the poplar foliage reflected the pollution status of OCPs in air. The result of this work showed that the poplar foliage can be used as the bio-monitor of OCPs in air.